PAPERS CITING THE AGRE CONSORTIUM


Constantino J.
Data from the Baby Siblings Research Consortium confirm and specify the nature of the female protective effect in autism: A commentary on Messinger et al.
Molecular Autism. 2016 June 29; 7:32. doi: 10.1186/s13229-016-0092-x.
PDF

Molenhuis R, Bruining H, Remmelink E, Visser L, Loos M, Burbach P, Kas M.
Limited impact of Cntn4 mutation on autism-related traits in developing and adult C57BL/6J mice.
Journal of Neurodevelopmental Disorders. 2016 Mar 2; 8:6. doi: 10.1186/s11689-016-91402.
PDF

Tao Y, Gao H, Ackerman B, Guo W, Saffen D, Shugart YY.
Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders.
BMC Genomics. 2016 Mar 1;17(1):163. doi: 10.1186/s12864-016-2475-y.
PMID: 26931105

Poopal Ac, Schroeder LM, Horn PS, Bassell GJ, Gross C.
Increased expression of the P13K catalytic subunit p110δ underlies elevated S6 phosphorylation and protein synthesis in an individual with autism from a multiplex family.
Mol Autism. 2016 Jan 14;7:3. doi: 10.1186/s13229-015-0066-4. eCollection 2016.
PMID: 26770665

Aldinger KA, Lane CJ, Veenstra-VanderWeele J, Levit P.
Patterns of Risk for Multiple Co-Occurring Medical Conditions Replicate Across Distinct Cohorts of Children with Autism Spectrum Disorder.
Autism Res. 2015 Dec;8(6):771-81. doi: 10.1002/aur.1492. Epub 2015 May 24.
PMID: 26011086

Werling DM, Geschwind DH.
Recurrence rates provide evidence for sex-differential, familial genetic liability for autism spectrum disorders in multiplex families and twins.
Mol Autism. 2015 May 13;6:27. doi: 10.1186/s13229-015-0004-5. eCollection 2015.
PMID: 25973164

Eicher JD, Gruen JR.
Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders.
Autism Res. 2015 Apr;8(2):229-34. doi: 10.1002/aur.1436. Epub 2014 Dec 1.
PMID: 25448322

Lowe JK, Werling DM, Constantino JN, Cantor RM, Geschwind DH.
Social responsiveness, an autism endophenotype: genomewide significant linkage to two regions on chromosome 8.
Am J Psyciatry. 2015 Mar 1;172(3):266-75. doi: 10.1176/appi.ajp.2014.14050576. Epub 2014 Nov 7.
PMID: 25727539

Yuan H, Dougherty JD.
Investigation of maternal genotype effects in autism by genome-wide association.
Autism Res. 2014 Apr;7(2):245-53. doi: 10.1002/aur.1363. Epub 2014 Feb 25.
PMID: 24574247

Carayol J, Schellenberg GD, Dombroski B, Amiet C, Genin B, Fontaine K, Rousseau F, Vazart C, Cohen D, Frazier TW, Hardan AY, Dawson G, Rio Frio T.
A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism.
Front Genet. 2014 Feb 18;5:33. doi: 10.3389/fgene.2014.00033. eCollection 2014.
PMID: 24600472

Werling DM, Lowe JK, Luo R, Cantor RM, Geschwind DH.
Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder.
Mol Autism. 2014 Feb 17;5(1):13. doi: 10.1186/2040-2392-5-13.
PMID: 24533643

Bruining H, Eijkemans MJ, Kas MJ, Curran SR, Vortsman JA, Bolton PF.
Behavioral signatures related to genetic disorders in autism.
Mol Autism. 2014 Feb 11;5(1):11. doi: 10.1186/2040-2392-5-11.
PMID: 24517317

Amiet C, Gourfinkel-AN I, Laurent C, Bodeau N, Genin B, Leguern E, Tordjman S, Cohen D.
Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?
Mol Autism. 2013 Dec 1;4(1):47. doi: 10.1186/2040-2392-4-47.
PMID: 24289166

Main PA, Thomas P, Esterman A, Fenech MF.
Necrosis is increased in lymphoblastoid cell lines from children with autism compared with their non-autistic siblings under conditions of oxidative and nitrosative stress.
Mutagenesis. 2013 Jul;28(4):475-84. doi: 10.1093/mutage/get025.
PMID: 23766106

Vardarajan BN, Eran A, Jung JY, Kunkel LM, Wall DP.
Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder.
Transl Psychiatry. 2013 May 28;3:e262. doi: 10.1038/tp.2013.38.
PMID: 23715297

Yang W, Liu J, Zheng F, Jia M, Zhao L, Lu T, Ruan Y, Zhang J Ye W, Zhang D, Wang L.
The evidence for association of ATP2B2 polymorphisms with autism in Chinese Han population.
PLoS One. 2013 Apr 19;8(4):e61021. doi: 10.1371/journal.pone.0061021. Print 2013.
PMID: 23620727

Dougherty JD, Maloney SE, Wozniak DF, Rieger MA, Sonnenblick L, Coppola G, Mahieu NG, Zhang J, Cai J, Patti GJ, Abrahams BS, Geschwind DH, Heintz N.
The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons results in autism-related behaviors.
J Neurosci. 2013 Feb 13;33(7):2732-53. doi: 10.1523/JNEUROSCI.4762-12.2013.
PMID: 23407934

Lu AT, Dai X, Martinez-Agosto JA, Cantor RM.
Support for calcium channel gene defects in autism spectrum disorders.
Mol Autism. 2012 Dec 15;3(1):18. doi: 10.1186/2040-2392-3-18.
PMID: 23241247

Martin LA, Horriat NL.
The effects of birth order and birth interval on the phenotypic expression of autism spectrum disorder.
PLoS One. 2012;7(11):e51049. doi: 10.1371/journal.pone.0051049. Epub 2012 Nov 30.
PMID:23226454

Anitha A, Thanseem I, Nakamura K, Yamada K, Iwayama Y, Toyota T, Iwata Y, Suzuki K, Sugiyama T, Tsujii M, Yoshikawa T, Mori N.
Protocadherin a (PCDHA) as a novel susceptibility gene for autism.
J Psychiatry Neurosci. 2012 Oct 2;37(6):120058. doi: 10.1503/jpn.120058. [Epub ahead of print]
PMID:23031252

Skafidas E, Testa R, Zantomio D, Chana G, Everall IP, Pantelis C.
Predicting the diagnosis of autism spectrum disorder using gene pathway analysis.
Mol Psychiatry. 2012 Sep 11. doi: 10.1038/mp.2012.126. [Epub ahead of print]
PMID:22965006

Wall DP, Dally R, Luyster R, Jung JY, Deluca TF.
Use of artificial intelligence to shorten the behavioral diagnosis of autism.
PLoS One. 2012;7(8):e43855. Epub 2012 Aug 27.
PMID:22952789

Wall DP, Kosmicki J, Deluca TF, Harstad E, Fusaro VA.
Use of machine learning to shorten observation-based screening and diagnosis of autism.
Transl Psychiatry. 2012 Apr 10;2:e100. doi: 10.1038/tp.2012.10.
PMID:22832900

Ramos PS, Sajuthi S, Langefeld CD, Walker SJ.
Immune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder.
Mol Autism. 2012 Jun 9;3(1):4. [Epub ahead of print]
PMID:22681640

Hall D, Huerta MF, McAuliffe MJ, Farber GK.
Sharing Heterogeneous Data: The National Database for Autism Research.
Neuroinformatics. 2012 May 24. [Epub ahead of print]
PMID:22622767

Shi J, Li P.
An integrative segmentation method for detecting germline copy number variations in SNP arrays.
Genet Epidemiol. 2012 May;36(4):373-83.
PMID:22539397

Meyer WK, Arbeithuber B, Ober C, Ebner T, Tiemann-Boege I, Hudson RR, Przeworski M.
Evaluating the Evidence for Transmission Distortion in Human Pedigrees.
Genetics. 2012 Feb 29. [Epub ahead of print]
PMID:22377632

Lu AT, Yoon J, Geschwind DH, Cantor RM.
QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders.
Mol Psychiatry. 2011 Nov 22. [Epub ahead of print].
PMID:22105621

Carayol J, Schellenberg GD, Dombroski B, Genin E, Rousseau F, Dawson G.
Autism risk assessment in siblings of affected children using sex-specific genetic scores.
Mol Autism. 2011 Oct 21;2(1):17 [Epub ahead of print].
PMID:22017886

Abuhatzira L, Shamir A, Schones DE, Schäffer AA, Bustin M.
The Chromatin-binding Protein HMGN1 Regulates the Expression of Methyl CpG-binding Protein 2 (MECP2) and Affects the Behavior of Mice.
J Biol Chem. 2011 Dec 9;286(49):42051-62. Epub 2011 Oct 17.
PMID:22009741

Thanseem I, Nakamura K, Anitha A, Suda S, Yamada K, Iwayama Y, Toyota T, Tsujii M, Iwata Y, Suzuki K, Matsuzaki H, Iwata K, Sugiyama T, Yoshikawa T, Mori N.
Association of transcription factor gene LMX1B with autism.
PLoS One. 2011;6(8):e23738. Epub 2011 Aug 25.
PMID:21901133

Norris M, Lecavalier L, Edwards MC.
The Structure of Autism Symptoms as Measured by the Autism Diagnostic Observation Schedule.
J Autism Dev Disord. 2011 Aug 20 [Epub ahead of print].
PMID:21858586

Liu X, Malenfant P, Reesor C, Lee A, Hudson ML, Harvard C, Qiao Y, Persico AM, Cohen IL, Chudley AE, Forster-Gibson C, Rajcan-Separovic E, Lewis MS, Holden JJ.
2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism .
Eur J Hum Genet. 2011 Jul 13. [Epub ahead of print].
PMID:21750575

Carayol J, Sacco R, Tores F, Rousseau F, Lewin P, Hager J, Persico AM.
Converging Evidence for an Association of ATP2B2 Allelic Variants with Autism in Male Subjects.
Biol Psychiatry. 2011 Jul 12. [Epub ahead of print].
PMID:21757185

Hussman JP, Chung RH, Griswold AJ, Jaworski JM, Salyakina D, Ma D, Konidari I, Whitehead PL, Vance JM, Martin ER, Cuccaro ML, Gilbert JR, Haines JL, Pericak-Vance MA.
A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism.
Mol Autism. Volume 2, Issue 1. Jan 19 2011.
PMID:21247446

Hallmayer J, Cleveland S, Torres A, Phillips J, Cohen B, Torigoe T, Miller J, Fedele A, Collins J, Smith K, Lotspeich L, Croen LA, Ozonoff S, Lajonchere C, Grether JK, Risch N.
Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism.
Arch Gen Psychiatry. 2011 Jul 4. [Epub ahead of print].
PMID:21727249

Bowers K, Li Q, Bressler J, Avramopoulos D, Newschaffer C, Fallin MD
Glutathione pathway gene variation and risk of autism spectrum disorders.
J Neurodev Disord. Volume 3, Issue 2, 132-43, June 2011.
PMID:21484198

Wang LW, Tancredi DJ, Thomas DW
The prevalence of gastrointestinal problems in children across the United States with autism spectrum disorders from families with multiple affected members.
J Dev Behav Pediatr. Volume 32, Issue 5, 351-60, June 2011.
PMID:21555957

Rosenspire A, Yoo W, Menard S, Torres AR.
Autism spectrum disorders are associated with an elevated autoantibody response to tissue transglutaminase-2.
Autism Res. 2011 Apr 19. doi: 10.1002/aur.194. [Epub ahead of print]
PMID: 21506289

Allen-Brady K, Cai G, Cannon D, Robison R, McMahon WM, Coon H, Buxbaum JD.
No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set.
Autism Res. 2011 Apr 12. doi: 10.1002/aur.195. [Epub ahead of print]
PMID: 21491612

Yaspan BL, Bush WS, Torstenson ES, Ma D, Pericak-Vance MA, Ritchie MD, Sutcliffe JS, Haines JL
Genetic analysis of biological pathway data through genomic randomization.
JL.Hum Genet. 2011 Jan 30. [Epub ahead of print]
PMID: 21279722

Salyakina D, Ma DQ, Jaworski JM, Konidari I, Whitehead PL, Henson R, Martinez D, Robinson JL, Sacharow S, Wright HH, Abramson RK, Gilbert JR, Cuccaro ML, Pericak-Vance MA.
Variants in several genomic regions associated with asperger disorder.
Autism Res. 2010 Dec;3(6):303-10. doi: 10.1002/aur.158.
PMID: 21182207

Chang SC, Pauls DL, Lange C, Sasanfar R, Santangelo SL.
Common genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disorders.
Am J Med Genet B Neuropsychiatr Genet. 2010 Dec 16.
PMID:21165891

Kistner-Griffin E, Brune CW, Davis LK, Sutcliffe JS, Cox NJ, Cook EH Jr.
Parent-of-origin effects of the serotonin transporter gene associated with autism.
Am J Med Genet B Neuropsychiatr Genet. 2010 Dec 8. [Epub ahead of print]
PMID:21154434

Lu AT, Cantor RM.
Allowing for sex differences increases power in a GWAS of multiplex Autism families.
Mol Psychiatry. 2010 Dec 14. [Epub ahead of print]
PMID:21151189

Flax JF, Hare A, Azaro MA, Vieland VJ, Brzustowicz LM.
Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci.
J Neurodev Disord. 2010 Dec;2(4):210-223. Epub 2010 Oct 12.
PMID:21125004

Schwender H, Bowers K, Fallin MD, Ruczinski I.
Importance measures for epistatic interactions in case-parent trios.
Ann Hum Genet. 2011 Jan;75(1):122-32. doi: 10.1111/j.1469-1809.2010.00623.x. Epub 2010 Nov 30.
PMID: 21118192

Jacob S, Brune CW, Badner JA, Ernstrom K, Courchesne E, Lord C, Leventhal BL, Cook EH, Kim SJ.
Family-based association testing of glutamate transporter genes in autism.
Psychiatr Genet. 2010 Nov 16. [Epub ahead of print]
PMID:21085054

Devlin B, Melhem N, Roeder K.
Do common variants play a role in risk for autism? Evidence and theoretical musings.
Brain Res. 2010 Nov 12.[Epub ahead of print]
PMID:21078308

Liu X, Solehdin F, Cohen IL, Gonzalez MG, Jenkins EC, Lewis ME, Holden JJ.
Population- and Family-Based Studies Associate the MTHFR Gene with Idiopathic Autism in Simplex Families.
J Autism Dev Disord. 2010 Nov 12. [Epub ahead of print]
PMID:21069446

Pagnamenta AT, Khan H, Walker S, Gerrelli D, Wing K, Bonaglia MC, Giorda R, Berney T, Mani E, Molteni M, Pinto D, Le Couteur A, Hallmayer J, Sutcliffe JS, Szatmari P, Paterson AD, Scherer SW, Vieland VJ, Monaco AP
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
J Med Genet. 2011 Jan;48(1):48-54. Epub 2010 Oct 23.
PMID: 20972252

Lajonchere CM; AGRE Consortium.
Changing the landscape of autism research: the autism genetic resource exchange.
Neuron. 2010 Oct 21;68(2):187-91.
PMID:20955925

Noor A, Whibley A, Marshall CR, Gianakopoulos PJ, Piton A, Carson AR, Orlic-Milacic M, Lionel AC, Sato D, Pinto D, Drmic I, Noakes C, Senman L, Zhang X, Mo R, Gauthier J, Crosbie J, Pagnamenta AT, Munson J, Estes AM, Fiebig A, Franke A, Schreiber S, Stewart AF, Roberts R, McPherson R, Guter SJ, Cook EH Jr, Dawson G, Schellenberg GD, Battaglia A, Maestrini E; Autism Genome Project Consortium, Jeng L, Hutchison T, Rajcan-Separovic E, Chudley AE, Lewis SM, Liu X, Holden JJ, Fernandez B, Zwaigenbaum L, Bryson SE, Roberts W, Szatmari P, Gallagher L, Stratton MR, Gecz J, Brady AF, Schwartz CE, Schachar RJ, Monaco AP, Rouleau GA, Hui CC, Lucy Raymond F, Scherer SW, Vincent JB.
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
Sci Transl Med. 2010 Sep 15;2(49):49ra68.
PMID:20844286

Fradin D, Cheslack-Postava K, Ladd-Acosta C, Newschaffer C, Chakravarti A, Arking DE, Feinberg A, Fallin MD.
Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs.
PLoS One. 2010 Sep 2;5(9). pii: e12513.
PMID:20824079

McInnes LA, Nakamine A, Pilorge M, Brandt T, Jiménez González P, Fallas M, Manghi ER, Edelmann L, Glessner J, Hakonarson H, Betancur C, Buxbaum JD.
A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region.
Mol Autism. 2010 Mar 19;1(1):5.
PMID:20678247

Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Carson AR, Casallo G, Casey J, Chu S, Cochrane L, Corsello C, Crawford EL, Crossett A, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green A, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Melhem NM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Piven J, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Rickaby J, Roberts W, Roeder K, Roge B, Rutter ML, Bierut LJ, Rice JP, Salt J, Sansom K, Sato D, Segurado R, Senman L, Shah N, Sheffield VC, Soorya L, Sousa I, Stoppioni V, Strawbridge C, Tancredi R, Tansey K, Thiruvahindrapduram B, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Wallace S, Wang K, Wang Z, Wassink TH, Wing K, Wittemeyer K, Wood S, Yaspan BL, Zurawiecki D, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Gallagher L, Geschwind DH, Gill M, Haines JL, Miller J, Monaco AP, Nurnberger JI Jr, Paterson AD, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vicente AM, Vieland VJ, Wijsman EM, Devlin B, Ennis S, Hallmayer J.
A genomewide scan for common alleles affecting risk for autism.
Hum Mol Genet. 2010 Jul 27.
PMID: 20663923

Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Bryson SE, Carson AR, Casallo G, Casey J, Chung BH, Cochrane L, Corsello C, Crawford EL, Crossett A, Cytrynbaum C, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green A, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Pilorge M, Piven J, Ponting CP, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Rickaby J, Roberts W, Roeder K, Roge B, Rutter ML, Bierut LJ, Rice JP, Salt J, Sansom K, Sato D, Segurado R, Sequeira AF, Senman L, Shah N, Sheffield VC, Soorya L, Sousa I, Stein O, Sykes N, Stoppioni V, Strawbridge C, Tancredi R, Tansey K, Thiruvahindrapduram B, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Wallace S, Wang K, Wang Z, Wassink TH, Webber C, Weksberg R, Wing K, Wittemeyer K, Wood S, Wu J, Yaspan BL, Zurawiecki D, Zwaigenbaum L, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Devlin B, Ennis S, Gallagher L, Geschwind DH, Gill M, Haines JL, Hallmayer J, Miller J, Monaco AP, Nurnberger Jr JI, Paterson AD, Pericak-Vance MA, Schellenberg GD, Szatmari P, Vicente AM, Vieland VJ, Wijsman EM, Scherer SW, Sutcliffe JS, Betancur C.
Functional impact of global rare copy number variation in autism spectrum disorders.
Nature. 2010 Jun 9.
PMID: 20531469

Munesue T, Yokoyama S, Nakamura K, Anitha A, Yamada K, Hayashi K, Asaka T, Liu HX, Jin D, Koizumi K, Islam MS, Huang JJ, Ma WJ, Kim UH, Kim SJ, Park K, Kim D, Kikuchi M, Ono Y, Nakatani H, Suda S, Miyachi T, Hirai H, Salmina A, Pichugina YA, Soumarokov AA, Takei N, Mori N, Tsujii M, Sugiyama T, Yagi K, Yamagishi M, Sasaki T, Yamasue H, Kato N, Hashimoto R, Taniike M, Hayashi Y, Hamada J, Suzuki S, Ooi A, Noda M, Kamiyama Y, Kido MA, Lopatina O, Hashii M, Amina S, Malavasi F, Huang EJ, Zhang J, Shimizu N, Yoshikawa T, Matsushima A, Minabe Y, Higashida H.
Two genetic variants of CD38 in subjects with autism spectrum disorder and controls.
Neurosci Res. 2010 Jun;67(2):181-91. Epub 2010 May 1.
PMID: 20435366

Nguyen A, Rauch TA, Pfeifer GP, Hu VW.
Global methylation profiling of lymphoblastoid cell lines reveals epigenetic contributions to autism spectrum disorders and a novel autism candidate gene, RORA, whose protein product is reduced in autistic brain.
FASEB J. 2010 Apr 7.
PMID: 20375269

Sarachana T, Zhou R, Chen G, Manji HK, Hu VW.
Investigation of post-transcriptional gene regulatory networks associated with autism spectrum disorders by microRNA expression profiling of lymphoblastoid cell lines.
Genome Med. 2010 Apr 7;2(4):23.
PMID: 20374639

van der Zwaag B, Staal WG, Hochstenbach R, Poot M, Spierenburg HA, de Jonge MV, Verbeek NE, van 't Slot R, van Es MA, Staal FJ, Freitag CM, Buizer-Voskamp JE, Nelen MR, van den Berg LH, van Amstel HK, van Engeland H, Burbach JP.
A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder.
Am J Med Genet B Neuropsychiatr Genet. 2009 Dec 22.
PMID: 20029941

Babatz TD, Kumar RA, Sudi J, Dobyns WB, Christian SL.
Copy number and sequence variants implicate APBA2 as an autism candidate gene.
Autism Res. 2009 Dec;2(6):359-64.
PMID: 20029827

Russo AJ, Krigsman A, Jepson B, Wakefield A.
Decreased Serum Hepatocyte Growth Factor (HGF) in Autistic Children with Severe Gastrointestinal Disease.
Biomark Insights. 2009 Nov 27;4:181-90.
PMID: 20029653

Ronald A, Butcher LM, Docherty S, Davis OS, Schalkwyk LC, Craig IW, Plomin R.
A Genome-Wide Association Study of Social and Non-Social Autistic-Like Traits in the General Population Using Pooled DNA, 500 K SNP Microarrays and Both Community and Diagnosed Autism Replication Samples.
Behav Genet.
PMID: 20012890

Hilton CL, Fitzgerald RT, Jackson KM, Maxim RA, Bosworth CC, Shattuck PT, Geschwind DH, Constantino JN.
Brief Report: Under-Representation of African Americans in Autism Genetic Research: A Rationale for Inclusion of Subjects Representing Diverse Family Structures.
J Autism Dev Disord. 2009 Nov 20
PMID: 19936905

Delahanty RJ, Kang JQ, Brune CW, Kistner EO, Courchesne E, Cox NJ, Cook EH Jr, Macdonald RL, Sutcliffe JS.
Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism.
Mol Psychiatry. 2009 Nov 24.
PMID: 19935738

Weiss LA.
Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
Expert Rev Mol Diagn. 2009 Nov;9(8):795-803.
PMID: 19895225

Nishiyama T, Notohara M, Sumi S, Takami S, Kishino H.
Major contribution of dominant inheritance to autism spectrum disorders (ASDs) in population-based families.
J Hum Genet. 2009 Nov 6.
PMID: 19893580

McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O, Krause V, Kumar RA, Grozeva D, Malhotra D, Walsh T, Zackai EH, Kaplan P, Ganesh J, Krantz ID, Spinner NB, Roccanova P, Bhandari A, Pavon K, Lakshmi B, Leotta A, Kendall J, Lee YH, Vacic V, Gary S, Iakoucheva LM, Crow TJ, Christian SL, Lieberman JA, Stroup TS, Lehtimäki T, Puura K, Haldeman-Englert C, Pearl J, Goodell M, Willour VL, Derosse P, Steele J, Kassem L, Wolff J, Chitkara N, McMahon FJ, Malhotra AK, Potash JB, Schulze TG, Nöthen MM, Cichon S, Rietschel M, Leibenluft E, Kustanovich V, Lajonchere CM, Sutcliffe JS, Skuse D, Gill M, Gallagher L, Mendell NR; Wellcome Trust Case Control Consortium, Craddock N, Owen MJ, O'Donovan MC, Shaikh TH, Susser E, Delisi LE, Sullivan PF, Deutsch CK, Rapoport J, Levy DL, King MC, Sebat J.
Microduplications of 16p11.2 are associated with schizophrenia.
Nat Genet. 2009 Nov;41(11):1223-7. Epub 2009 Oct 25.
PMID: 19855392

Weiss LA, Arking DE; Gene Discovery Project of Johns Hopkins & the Autism Consortium, Daly MJ, Chakravarti A.
A genome-wide linkage and association scan reveals novel loci for autism.
Nature. 2009 Oct 8;461(7265):802-8.
PMID: 19812673

Roberson ED, Pevsner J.
Visualization of shared genomic regions and meiotic recombination in high-density SNP data.
PLoS One. 2009 Aug 21;4(8):e6711.
PMID: 19696932

Russo AJ, Neville L, Wroge C.
Low Serum Alpha-1 Antitrypsin (AAT) in Family Members of Individuals with Autism Correlates with PiMZ Genotype.
Biomark Insights. 2009 Mar 18;4:45-56.
PMID: 19652762

Benayed R, Choi J, Matteson PG, Gharani N, Kamdar S, Brzustowicz LM, Millonig JH.
Autism-Associated Haplotype Affects the Regulation of the Homeobox Gene, ENGRAILED 2.
Biol Psychiatry. 2009 Jul 16.
PMID: 19615670

Serajee FJ, Huq AH.
Association of Y Chromosome Haplotypes With Autism.
J Child Neurol. 2009 Jul 15.
PMID: 19605777

Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, Sonnenblick LI, Alvarez Retuerto AI, Imielinski M, Hadley D, Bradfield JP, Kim C, Gidaya NB, Lindquist I, Hutman T, Sigman M, Kustanovich V, Lajonchere CM, Singleton A, Kim J, Wassink TH, McMahon WM, Owley T, Sweeney JA, Coon H, Nurnberger JI, Li M, Cantor RM, Minshew NJ, Sutcliffe JS, Cook EH, Dawson G, Buxbaum JD, Grant SF, Schellenberg GD, Geschwind DH, Hakonarson H.
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
PLoS Genet. 2009 Jun;5(6):e1000536. Epub 2009 Jun 26.
PMID: 19557195

Ma D, Salyakina D, Jaworski JM, Konidari I, Whitehead PL, Andersen AN, Hoffman JD, Slifer SH, Hedges DJ, Cukier HN, Griswold AJ, McCauley JL, Beecham GW, Wright HH, Abramson RK, Martin ER, Hussman JP, Gilbert JR, Cuccaro ML, Haines JL, Pericak-Vance MA.
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
Ann Hum Genet. 2009 May;73(Pt 3):263-73.
PMID: 19456320

Campbell DB, Warren D, Sutcliffe JS, Lee EB, Levitt P.
Association of MET with social and communication phenotypes in individuals with autism spectrum disorder.
Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 22
PMID: 19548256

Kumar RA, Sudi J, Babatz TD, Brune CW, Oswald D, Yen M, Nowak NJ, Cook EH, Christian SL, Dobyns WB.
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.
J Med Genet. 2009 Jun 21.
PMID: 19546099

Goin-Kochel RP, Porter AE, Peters SU, Shinawi M, Sahoo T, Beaudet AL.
The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations.
Autism Res. 2009 Apr;2(2):98-108.
PMID: 19455642

Hu VW, Sarachana T, Kim KS, Nguyen A, Kulkarni S, Steinberg ME, Luu T, Lai Y, Lee NH.
Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism.
Autism Res. 2009 May 5.
PMID: 19418574

Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman PM, Chiavacci R, Annaiah K, Thomas K, Hou C, Glaberson W, Flory J, Otieno F, Garris M, Soorya L, Klei L, Piven J, Meyer KJ, Anagnostou E, Sakurai T, Game RM, Rudd DS, Zurawiecki D, McDougle CJ, Davis LK, Miller J, Posey DJ, Michaels S, Kolevzon A, Silverman JM, Bernier R, Levy SE, Schultz RT, Dawson G, Owley T, McMahon WM, Wassink TH, Sweeney JA, Nurnberger JI, Coon H, Sutcliffe JS, Minshew NJ, Grant SF, Bucan M, Cook EH, Buxbaum JD, Devlin B, Schellenberg GD, Hakonarson H.
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Nature. 2009 Apr 28.
PMID: 19404257

Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, Korvatska O, Piven J, Sonnenblick LI, Alvarez Retuerto AI, Herman EI, Dong H, Hutman T, Sigman M, Ozonoff S, Klin A, Owley T, Sweeney JA, Brune CW, Cantor RM, Bernier R, Gilbert JR, Cuccaro ML, McMahon WM, Miller J, State MW, Wassink TH, Coon H, Levy SE, Schultz RT, Nurnberger JI, Haines JL, Sutcliffe JS, Cook EH, Minshew NJ, Buxbaum JD, Dawson G, Grant SF, Geschwind DH, Pericak-Vance MA, Schellenberg GD, Hakonarson H.
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Nature. 2009 Apr 28
PMID: 19404256

Talebizadeh Z, Butler MG, Theodoro MF.
Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism.
Autism Res. 2008 Aug;1(4):240-50.
PMID: 19360674

Campbell DB, Li C, Sutcliffe JS, Persico AM, Levitt P.
Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.
Autism Res. 2008 Jun;1(3):159-68.
PMID: 19360663

James SJ, Rose S, Melnyk S, Jernigan S, Blossom S, Pavliv O, Gaylor DW.
Cellular and mitochondrial glutathione redox imbalance in lymphoblastoid cells derived from children with autism.
FASEB J. 2009 Mar 23.
PMID: 19307255

Campbell DB, Buie TM, Winter H, Bauman M, Sutcliffe JS, Perrin JM, Levitt P.
Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions.
Pediatrics. 2009 Mar;123(3):1018-24.
PMID: 19255034

Kumar RA, Marshall CR, Badner JA, Babatz TD, Mukamel Z, Aldinger KA, Sudi J, Brune CW, Goh G, Karamohamed S, Sutcliffe JS, Cook EH, Geschwind DH, Dobyns WB, Scherer SW, Christian SL.
Association and mutation analyses of 16p11.2 autism candidate genes.
PLoS ONE. 2009;4(2):e4582. Epub 2009 Feb 26.
PMID: 19242545

Burbach JP, van der Zwaag B.
Contact in the genetics of autism and schizophrenia.
Trends Neurosci. 2009 Jan 8.
PMID: 19135727

Ramoz N, Cai G, Reichert JG, Silverman JM, Buxbaum JD.
An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene.
Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5.
PMID: 18348195

Cai G, Edelmann L, Goldsmith JE, Cohen N, Nakamine A, Reichert JG, Hoffman EJ, Zurawiecki DM, Silverman JM, Hollander E, Soorya L, Anagnostou E, Betancur C, Buxbaum JD.
Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a novel microduplication in ASMT.
BMC Med Genomics. 2008 Oct 16.
PMID: 18925931

Conroy J, Cochrane L, Anney RJ, Sutcliffe JS, Carthy P, Dunlop A, Mullarkey M, O'hici B, Green AJ, Ennis S, Gill M, Gallagher L.
Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32.
Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 7.
PMID: 18846500

Miller DT, Shen Y, Weiss LA, Korn J, Anselm I, Bridgemohan C, Cox GF, Dickinson H, Gentile J, Harris DJ, Hegde V, Hundley R, Khwaja O, Kothare S, Luedke C, Nasir R, Poduri A, Prasad K, Raffalli P, Reinhard A, Smith SE, Sobeih M, Soul J, Stoler J, Takeoka M, Tan WH, Thakuria J, Wolff P, Yusupov R, Gusella JF, Daly MJ, Wu BL.
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatirc disorders.
J Med Genet. 2008 Sep 19.
PMID: 18805830

Alvarez Retuerto AI, Cantor RM, Gleeson JG, Ustaszewska A, Schackwitz WS, Pennacchio LA, Geschwind DH.
Association of common variants in the Joubert syndrome gene (AHI1) with autism.
Hum Mol Genet. 2008 Sep 9.
PMID: 18782849

Liu X, Novosedlik N, Wang A, Hudson ML, Cohen IL, Chudley AE, Forster-Gibson CJ, Lewis SM, Holden JJ.
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders.
Eur J Hum Genet. 2008 Aug 27.
PMID:18728693

Virkud YV, Todd RD, Abbacchi AM, Zhang Y, Constantino JN.
Familial aggregation of quantitative autistic traits in multiplex versus simplex autism.
Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 10. [Epub ahead of print]
PMID:18618672

Palmieri L, Papaleo V, Porcelli V, Scarcia P, Gaita L, Sacco R, Hager J, Rousseau F, Curatolo P, Manzi B, Militerni R, Bravaccio C, Trillo S, Schneider C, Melmed R, Elia M, Lenti C, Saccani M, Pascucci T, Puglisi-Allegra S, Reichelt KL, Persico AM.
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.
Mol Psychiatry. 2008 Jul 8.
PMID:18607376

Nakamura K, Anitha A, Yamada K, Tsujii M, Iwayama Y, Hattori E, Toyota T, Suda S, Takei N, Iwata Y, Suzuki K, Matsuzaki H, Kawai M, Sekine Y, Tsuchiya KJ, Sugihara GI, Ouchi Y, Sugiyama T, Yoshikawa T, Mori N.
Genetic and expression analyses reveal elevated expression of syntaxin 1A ( STX1A) in high functioning autism.
Int J Neuropsychopharmacol. 2008 Jul 2:1-12.
PMID:18593506

Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, Lifton RP, State MW.
Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.
Am J Hum Genet. 2008 Jun;82(6):1385.
PMID:18551756

Loat C, Curran S, Lewis C, Abrahams B, Duvall J, Geschwind D, Bolton P, Craig I.
Methyl - CpG - binding protein (MECP2) polymorphisms and vulnerability to autism.
Genes Brain Behav. 2008 Jun 2.
PMID:18518921

Jill James S, Melnyk S, Jernigan S, Hubanks A, Rose S, Gaylor DW.
Abnormal Transmethylation/transsulfuration Metabolism and DNA Hypomethylation Among Parents of Children with Autism.
J Autism Dev Disord. 2008 May 30.
PMID:18512136

Maussion G, Carayol J, Lepagnol-Bestel AM, Tores F, Loe-Mie Y, Milbreta U, Rousseau F, Fontaine K, Renaud J, Moalic JM, Philippi A, Chedotal A, Gorwood P, Ramoz N, Hager J, Simonneau M.
Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism.
Hum Mol Genet. 2008 Aug 15;17(16):2541-51. Epub 2008 May 20.
PMID:18492799

Bureau A, Labbe A, Croteau J, Mèrette C.
Using disease symptoms to improve detection of linkage under genetic heterogeneity.
Genet Epidemiol. 2008 Mar 10;
PMID:18330904

Wallace AE, Anderson GM, Dubrow R.
Obstetric and parental psychiatric variables as potential predictors of autism severity.
J Autism Dev Disord. 2008 Mar 7.
PMID: 18348195

Lee LC, Newschaffer CJ, Lessler JT, Lee BK, Shah R, Zimmerman AW.
Variation in season of birth in singleton and multiple births concordant for autism spectrum disorders.
Paediatr Perinat Epidemiol. 2008 Mar;22(2):172-9.
PMID:18298692

Anitha A, Nakamura K, Yamada K, Suda S, Thanseem I, Tsujii M, Iwayama Y, Hattori E, Toyota T, Miyachi T, Iwata Y, Suzuki K, Matsuzaki H, Kawai M, Sekine Y, Tsuchiya K, Sugihara GI, Ouchi Y, Sugiyama T, Koizumi K, Higashida H, Takei N, Yoshikawa T, Mori N.
Genetic analyses of Roundabout (ROBO) axon guidance receptors in autism.
Am J Med Genet B Neuropsychiatr Genet. 2008 Feb 12
PMID:18270976

Martin LA, Ashwood P, Braunschweig D, Cabanlit M, Van de Water J, Amaral DG.
Stereotypies and hyperactivity in rhesus monkeys exposed to IgG from mothers of children with autism.
Brain Behav Immun. 2008 Feb 7
PMID:18262386

Hettinger JA, Liu X, Schwartz CE, Michaelis RC, Holden JJ
A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families.
Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 18;
PMID:18205172

Wendland JR, Deguzman TB, McMahon F, Rudnick G, Detera-Wadleigh SD, Murphy DL.
SERT Ileu425Val in autism, Asperger syndrome and obsessive-compulsive disorder.
Psychiatr Genet. 2008 Feb;18(1):31-9.
PMID:18197083

Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira MA, Green T, Platt OS, Ruderfer DM, Walsh CA, Altshuler D, Chakravarti A, Tanzi RE, Stefansson K, Santangelo SL, Gusella JF, Sklar P, Wu BL, Daly MJ; the Autism Consortium.
Association between Microdeletion and Microduplication at 16p11.2 and Autism.
N Engl J Med. 2008 Jan 9; [Epub ahead of print]
PMID:18184952

Kim HG, Kishikawa S, Higgins AW, Seong IS, Donovan DJ, Shen Y, Lally E, Weiss LA, Najm J, Kutsche K, Descartes M, Holt L, Braddock S, Troxell R, Kaplan L, Volkmar F, Klin A, Tsatsanis K, Harris DJ, Noens I, Pauls DL, Daly MJ, Macdonald ME, Morton CC, Quade BJ, Gusella JF.
Disruption of neurexin 1 associated with autism spectrum disorder.
Am J Hum Genet. 2008 Jan;82(1):199-207.
PMID:18179900

Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, Biederer T, Gunel M, Lifton RP, State MW.
Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders.
Am J Hum Genet. 2008 Jan 10;82(1):165-173.
PMID:18179895

Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH Jr, Chakravarti A.
A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism.
Am J Hum Genet. 2008 Jan;82(1):160-4.
PMID:18179894

Alarcón M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH.
Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene.
Am J Hum Genet. 2008 Jan 10;82(1):150-159.
PMID:18179893

Stephan DA.
Unraveling autism.
Am J Hum Genet. 2008 Jan;82(1):7-9.
PMID:18179879

Kumar RA, Karamohamed S, Sudi J, Conrad DF, Brune C, Badner JA, Gilliam TC, Nowak NJ, Cook EH Jr, Dobyns WB, Christian SL.
Recurrent 16p11.2 microdeletions in autism.
Hum Mol Genet. 2007 Dec 21; [Epub ahead of print]
PMID:18156158

Philippi A, Tores F, Carayol J, Rousseau F, Letexier M, Roschmann E, Lindenbaum P, Benajjou A, Fontaine K, Vazart C, Gesnouin P, Brooks P, Hager J.
Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.
BMC Med Genet. 2007 Dec 6;8(1):74 [Epub ahead of print]
PMID:18053270

Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SF, Hakonarson H, Bucan M
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Genome Res. 2007 Nov;17(11):1665-74. Epub 2007 Oct 5.
PMID: 17921354

Goin-Kochel RP, Mazefsky CA, Riley BP.
Level of Functioning in Autism Spectrum Disorders: Phenotypic Congruence Among Affected Siblings.
J Autism Dev Disord. 2007 Oct 30; [Epub ahead of print]
PMID:17968643

Silverman JM, Buxbaum JD, Ramoz N, Schmeidler J, Reichenberg A, Hollander E, Angelo G, Smith CJ, Kryzak LA.
Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism.
Am J Med Genet B Neuropsychiatr Genet. 2007 Sep 25; [Epub ahead of print]
PMID:17894412

Zhao X, Leotta A, Kustanovich V, Lajonchere C, Geschwind DH, Law K, Law P, Qiu S, Lord C, Sebat J, Ye K, Wigler M.
A unified genetic theory for sporadic and inherited autism.
Proc Natl Acad Sci U S A. 2007 Jul 31;104(31):12831-6. Epub 2007 Jul 25.
PMID:17652511

Sacco R, Militerni R, Frolli A, Bravaccio C, Gritti A, Elia M, Curatolo P, Manzi B, Trillo S, Lenti C, Saccani M, Schneider C, Melmed R, Reichelt KL, Pascucci T, Puglisi-Allegra S, Persico AM.
Clinical, Morphological, and Biochemical Correlates of Head Circumference in Autism.
Biol Psychiatry. 2007 Jul 17
PMID:17644070

Toyoda T, Nakamura K, Yamada K, Thanseem I, Anitha A, Suda S, Tsujii M, Iwayama Y, Hattori E, Toyota T, Miyachi T, Iwata Y, Suzuki K, Matsuzaki H, Kawai M, Sekine Y, Tsuchiya K, Sugihara GI, Ouchi Y, Sugiyama T, Takei N, Yoshikawa T, Mori N.
SNP analyses of growth factor genes EGF, TGFbeta-1, and HGF reveal haplotypic association of EGF with autism.
Biochem Biophys Res Commun. 2007 Jun 18;
PMID:17626784

Ashley-Koch AE, Jaworski J, Ma DQ, Mei H, Ritchie MD, Skaar DA, Robert Delong G, Worley G, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA.
Investigation of potential gene-gene interactions between apoe and reln contributing to autism risk.
Psychiatr Genet. 2007 Aug;17(4):221-226.
PMID:17621165

Frazier TW, Youngstrom EA, Kubu CS, Sinclair L, Rezai A.
Exploratory and Confirmatory Factor Analysis of the Autism Diagnostic Interview-Revised.
J Autism Dev Disord. 2007 Jul 6;
PMID:17619129

Nishimura Y, Martin CL, Lopez AV, Spence SJ, Alvarez-Retuerto AI, Sigman M, Steindler C, Pellegrini S, Schanen NC, Warren ST, Geschwind DH.
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways.
Hum Mol Genet. 2007 May 21
PMID:17519220

Martin CL, Duvall JA, Ilkin Y, Simon JS, Arreaza MG, Wilkes K, Alvarez-Retuerto A, Whichello A, Powell CM, Rao K, Cook E, Geschwind DH.
Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism.
Am J Med Genet B Neuropsychiatr Genet. 2007 May 14
PMID:17503474

Goin-Kochel RP, Abbacchi A, Constantino JN, Autism Genetic Resource Exchange Consortium.
Lack of evidence for increased genetic loading for autism among families of affected females: A replication from family history data in two large samples.
Autism. 2007 May;11(3):279-86.
PMID:17478580

Cantor RM, Yoon JL, Furr J, Lajonchere CM.
Paternal age and autism are associated in a family-based sample.
Mol Psychiatry. 2007 May;12(5):419-421.
PMID:17453057

Buxbaum JD, Cai G, Chaste P, Nygren G, Goldsmith J, Reichert J, Anckarsater H, Rastam M, Smith CJ, Silverman JM, Hollander E, Leboyer M, Gillberg C, Verloes A, Betancur C.
Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly.
Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 10;
PMID:17427195

Duvall JA, Lu A, Cantor RM, Todd RD, Constantino JN, Geschwind DH.
A quantitative trait locus analysis of social responsiveness in multiplex autism families.
Am J Psychiatry. 2007 Apr;164(4):656-62.
PMID:17403980

Sadakata T, Washida M, Iwayama Y, Shoji S, Sato Y, Ohkura T, Katoh-Semba R, Nakajima M, Sekine Y, Tanaka M, Nakamura K, Iwata Y, Tsuchiya KJ, Mori N, Detera-Wadleigh SD, Ichikawa H, Itohara S, Yoshikawa T, Furuichi T.
Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients.
J Clin Invest. 2007 Apr;117(4):931-43. Epub 2007 Mar 22.
PMID:17380209

Stone JL, Merriman B, Cantor RM, Geschwind DH, Nelson SF.
High Density SNP Association Study of a Major Autism Linkage Region on Chromosome 17.
Hum Mol Genet. 2007 Mar 21;
PMID:17376794

Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimaki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King MC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M.
Strong Association of De Novo Copy Number Mutations with Autism.
Science. 2007 Mar 15;
PMID:17363630

Nishimura K, Nakamura K, Anitha A, Yamada K, Tsujii M, Iwayama Y, Hattori E, Toyota T, Takei N, Miyachi T, Iwata Y, Suzuki K, Matsuzaki H, Kawai M, Sekine Y, Tsuchiya K, Sugihara GI, Suda S, Ouchi Y, Sugiyama T, Yoshikawa T, Mori N.
Genetic analyses of the brain-derived neurotrophic factor (BDNF) gene in autism.
Biochem Biophys Res Commun. 2007 Mar 5;
PMID:17349978

Hettinger JA, Liu X, Holden JJ.
The G22A Polymorphism of the ADA Gene and Susceptibility to Autism Spectrum Disorders.
J Autism Dev Disord. 2007 Mar 6; [Epub ahead of print]
PMID:17340203

The Autism Genome Project Consortium; Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, Marshall CR, Scherer SW, Vieland VJ, Bartlett C, Mangin LV, Goedken R, Segre A, Pericak-Vance MA, Cuccaro ML, Gilbert JR, Wright HH, Abramson RK, Betancur C, Bourgeron T, Gillberg C, Leboyer M, Buxbaum JD, Davis KL, Hollander E, Silverman JM, Hallmayer J, Lotspeich L, Sutcliffe JS, Haines JL, Folstein SE, Piven J, Wassink TH, Sheffield V, Geschwind DH, Bucan M, Brown WT, Cantor RM, Constantino JN, Gilliam TC, Herbert M, Lajonchere C, Ledbetter DH, Lese-Martin C, Miller J, Nelson S, Samango-Sprouse CA, Spence S, State M, Tanzi RE, Coon H, Dawson G, Devlin B, Estes A, Flodman P, Klei L, McMahon WM, Minshew N, Munson J, Korvatska E, Rodier PM, Schellenberg GD, Smith M, Spence MA, Stodgell C, Tepper PG, Wijsman EM, Yu CE, Roge B, Mantoulan C, Wittemeyer K, Poustka A, Felder B, Klauck SM, Schuster C, Poustka F, Bolte S, Feineis-Matthews S, Herbrecht E, Schmotzer G, Tsiantis J, Papanikolaou K, Maestrini E, Bacchelli E, Blasi F, Carone S, Toma C, Van Engeland H, de Jonge M, Kemner C, Koop F, Langemeijer M, Hijimans C, Staal WG, Baird G, Bolton PF, Rutter ML, Weisblatt E, Green J, Aldred C, Wilkinson JA, Pickles A, Le Couteur A, Berney T, McConachie H, Bailey AJ, Francis K, Honeyman G, Hutchinson A, Parr JR, Wallace S, Monaco AP, Barnby G, Kobayashi K, Lamb JA, Sousa I, Sykes N, Cook EH, Guter SJ, Leventhal BL, Salt J, Lord C, Corsello C, Hus V, Weeks DE, Volkmar F, Tauber M, Fombonne E, Shih A.
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Nat Genet. 2007 Mar;39(3):319-28. Epub 2007 Feb 18.
PMID:17322880

Nicholas B, Rudrasingham V, Nash S, Kirov G, Owen MJ, Wimpory DC.
Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing hypothesis.
Mol Psychiatry. 2007 Jan 30;
PMID:17264841

Cheslack-Postava K, Fallin MD, Avramopoulos D, Connors SL, Zimmerman AW, Eberhart CG, Newschaffer CJ.
beta(2)-Adrenergic receptor gene variants and risk for autism in the AGRE cohort.
Mol Psychiatry. 2007 Jan 2;
PMID:17199132

Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.
Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
Mol Psychiatry. 2006 Dec 19;
PMID:17179998

Harvey CG, Menon SD, Stachowiak B, Noor A, Proctor A, Mensah AK, Mnatzakanian GN, Alfred SE, Guo R, Scherer SW, Kennedy JL, Roberts W, Srivistava AK, Minassian BA, Vincent JB.
Sequence variants within exon 1 of MECP2 occur in females with mental retardation.
Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 14;
PMID:17171659

Muscarella LA, Guarnieri V, Sacco R, Militerni R, Bravaccio C, Trillo S, Schneider C, Melmed R, Elia M, Mascia ML, Rucci E, Piemontese MR, D'Agruma L, Persico AM.
HOXA1 gene variants influence head growth rates in humans.
Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 14.
PMID:17171652

Sakurai T, Ramoz N, Reichert JG, Corwin TE, Kryzak L, Smith CJ, Silverman JM, Hollander E, Buxbaum JD.
Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive-compulsive or self-stimulatory behaviors.
Psychiatr Genet. 2006 Dec;16(6):251-7.
PMID:17106428

Lee LC, Zachary AA, Leffell MS, Newschaffer CJ, Matteson KJ, Tyler JD, Zimmerman AW.
HLA-DR4 in Families With Autism.
Pediatr Neurol. 2006 Nov;35(5):303-7.
PMID:17074598

Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P.
A genetic variant that disrupts MET transcription is associated with autism.
Proc Natl Acad Sci U S A. 2006 Oct 19;.
PMID:17053076

Petek E, Schwarzbraun T, Noor A, Patel M, Nakabayashi K, Choufani S, Windpassinger C, Stamenkovic M, Robertson MM, Aschauer HN, Gurling HM, Kroisel PM, Wagner K, Scherer SW, Vincent JB.
Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome.
Mol Genet Genomics. 2006 Oct 17; .
PMID:17043892

Ramoz N, Cai G, Reichert JG, Corwin TE, Kryzak LA, Smith CJ, Silverman JM, Hollander E, Buxbaum JD
Family-based association study of TPH1 and TPH2 polymorphisms in autism.
Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 6;.
PMID:16958027

Tierney E, Bukelis I, Thompson RE, Ahmed K, Aneja A, Kratz L, Kelley RI
Abnormalities of cholesterol metabolism in autism spectrum disorders.
Am J Med Genet B Neuropsychiatr Genet. 2006 Jul 27;.
PMID:16874769

Walker SJ, Segal J, Aschner M.
Cultured lymphocytes from autistic children and non-autistic siblings up-regulate heat shock protein RNA in response to thimerosal challenge.
Neurotoxicology. 2006 Jun 16; [Epub ahead of print]
PMID:16870260

Zandi PP, Kalaydjian A, Avramopoulos D, Shao H, Fallin MD, Newschaffer CJ.
Rh and ABO maternal-fetal incompatibility and risk of autism.
Am J Med Genet B Neuropsychiatr Genet. 2006 Jul 19; [Epub ahead of print]
PMID:16856119

Baron CA, Liu SY, Hicks C, Gregg JP.
Utilization of Lymphoblastoid Cell Lines as a System for the Molecular Modeling of Autism.
J Autism Dev Disord. 2006 Jul 15; [Epub ahead of print]
PMID:16845580

Collins AL, Ma D, Whitehead PL, Martin ER, Wright HH, Abramson RK, Hussman JP, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA.
Investigation of autism and GABA receptor subunit genes in multiple ethnic groups.
Neurogenetics. 2006 Jul;7(3):167-74. Epub 2006 Jun 13.
PMID:16770606

Spence SJ, Cantor RM, Chung L, Kim S, Geschwind DH, Alarcon M.
Stratification based on language-related endophenotypes in autism: Attempt to replicate reported linkage.
Am J Med Genet B Neuropsychiatr Genet. 2006 Jun 2; [Epub ahead of print]
PMID:16752361

Weiss LA, Kosova G, Delahanty RJ, Jiang L, Cook EH, Ober C, Sutcliffe JS
Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility.
Eur J Hum Genet. 2006 May 17;.
PMID:16724005

Hu VW, Frank BC, Heine S, Lee NH, Quackenbush J
Gene expression profiling of lymphoblastoid cell lines from monozygotic twins discordant in severity of autism reveals differential regulation of neurologically relevant genes.
BMC Genomics. 2006 May 18;7(1):118.
PMID:16709250

Ashley-Koch AE, Mei H, Jaworski J, Ma DQ, Ritchie MD, Menold MM, Delong GR, Abramson RK, Wright HH, Hussman JP, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA.
An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder.
Ann Hum Genet. 2006 May;70(Pt 3):281-92.
PMID:16674551

Talebizadeh Z, Lam DY, Theodoro MF, Bittel DC, Lushington GH, Butler MG.
Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism.
J Med Genet. 2006 May;43(5):e21.
PMID:16648374

Ramoz N, Reichert JG, Corwin TE, Smith CJ, Silverman JM, Hollander E, Buxbaum JD.
Lack of Evidence for Association of the Serotonin Transporter Gene SLC6A4 with Autism.
Biol Psychiatry. 2006 Apr 6
PMID:16616719

Constantino JN, Lajonchere C, Lutz M, Gray T, Abbacchi A, McKenna K, Singh D, Todd RD
Autistic social impairment in the siblings of children with pervasive developmental disorders.
Am J Psychiatry. 2006 Feb;163(2):294-6.
PMID:16449484

Baron CA, Tepper CG, Liu SY, Davis RR, Wang NJ, Schanen NC, Gregg JP
Genomic and Functional Profiling of Duplicated Chromosome 15 Cell Lines Reveal Regulatory Alterations in UBE3A-associated Ubiquitin-Proteasome Pathway Processes.
Hum Mol Genet. 2006 Jan 30.
PMID:16446308

Connors SL, Crowell DE, Eberhart CG, Copeland J, Newschaffer CJ, Spence SJ, Zimmerman AW.
beta2-Adrenergic Receptor Activation and Genetic Polymorphisms in Autism: Data from Dizygotic Twins.
J Child Neurol. 2005 Nov;20(11):876-84.
PMID:16417856

Yonan AL, Palmer AA, Gilliam TC.
Hardy-Weinberg disequilibrium identified genotyping error of the serotonin transporter (SLC6A4) promoter polymorphism.
Psychiatr Genet. 2006 Feb;16(1):31-4.
PMID:16395127

Richler E, Reichert JG, Buxbaum JD, McInnes LA.
Autism and ultraconserved non-coding sequence on chromosome 7q.
Psychiatr Genet. 2006 Feb;16(1):19-23.
PMID:16395125

Serajee FJ, Zhong H, Mahbubul Huq AH.
Association of Reelin gene polymorphisms with autism.
Genomics. 2005 Nov 24; [Epub ahead of print]
PMID:16311013

Ylisaukko-Oja T, Alarcon M, Cantor RM, Auranen M, Vanhala R, Kempas E, von Wendt L, Jarvela I, Geschwind DH, Peltonen L.
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.
Ann Neurol. 2005 Nov 15; [Epub ahead of print]
PMID:16288458

Sahoo T, Shaw CA, Young AS, Whitehouse NL, Schroer RJ, Stevenson RE, Beaudet AL.
Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements.
Am J Med Genet A. 2005 Nov 11; [Epub ahead of print]
PMID:16284940

Hamilton SP, Woo JM, Carlson EJ, Ghanem N, Ekker M, Rubenstein JL. Analysis of four DLX homeobox genes in autistic probands.
BMC Genet. 2005 Nov 2;6(1):52 [Epub ahead of print]
PMID:16266434

Benayed R, Gharani N, Rossman I, Mancuso V, Lazar G, Kamdar S, Bruse SE, Tischfield S, Smith BJ, Zimmerman RA, DiCicco-Bloom E, Brzustowicz LM, and Millonig JH
Support for the Homeobox Transcription Factor Gene ENGRAILED 2 as an Autism Spectrum Disorder Susceptibility Locus
Am J Hum Genet. 2005 Nov 77(5):851-68.
PMID:16252243

Faham M, Zheng J, Moorhead M, Fakhrai-Rad H, Namsaraev E, Wong K, Wang Z, Chow SG, Lee L, Suyenaga K, Reichert J, Boudreau A, Eberle J, Bruckner C, Jain M, Karlin-Neumann G, Jones HB, Willis TD, Buxbaum JD, Davis RW.
Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays.
Proc Natl Acad Sci U S A. 2005 Oct 11;102(41):14717-22. Epub 2005 Oct 3.
PMID:16203980

Chen GK, Kono N, Geschwind DH, Cantor RM
Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder.
Mol Psychiatry 2005 Sep 27
PMID:16189504

Talebizadeh Z, Bittel DC, Veatch OJ, Kibiryeva N, Butler MG.
Brief Report: Non-Random X Chromosome Inactivation in Females with Autism.
J Autism Dev Disord. 2005 Sep 16;:1-7
PMID:16167093

Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA.
Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism.
Am J Hum Genet. 2005 Sep;77(3):377-88. Epub 2005 Jul 15.
PMID:16080114

Prasad HC, Zhu CB, McCauley JL, Samuvel DJ, Ramamoorthy S, Shelton RC, Hewlett WA, Sutcliffe JS, Blakely RD.
Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase.
Proc Natl Acad Sci U S A. 2005 Aug 9;102(32):11545-50. Epub 2005 Jul 29.
PMID:16055563

Philippi A, Roschmann E, Tores F, Lindenbaum P, Benajou A, Germain-Leclerc L, Marcaillou C, Fontaine K, Vanpeene M, Roy S, Maillard S, Decaulne V, Saraiva JP, Brooks P, Rousseau F, Hager J.
Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism.
Mol Psychiatry. 2005 Jul 19;
PMID:16027742

D'Amelio M, Ricci I, Sacco R, Liu X, D'Agruma L, Muscarella LA, Guarnieri V, Militerni R, Bravaccio C, Elia M, Schneider C, Melmed R, Trillo S, Pascucci T, Puglisi-Allegra S, Reichelt KL, Macciardi F, Holden JJ, Persico AM.
Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.
Mol Psychiatry. 2005 Jul 19;
PMID:16027737

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD.
Allelic Heterogeneity at the Serotonin Transporter Locus (SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors.
Am J Hum Genet. 2005 Jul 1;77(2)
PMID:15995945

Molloy CA, Keddache M, Martin LJ
Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression.
Mol Psychiatry 2005 May 10;.
PMID:15940295

Alarcon M, Yonan AL, Gilliam TC, Cantor RM, Geschwind DH.
Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.
Mol Psychiatry. 2005 Apr 12; [Epub ahead of print]
PMID:15824743

Cantor RM, Kono N, Duvall JA, Alvarez-Retuerto A, Stone JL, Alarcon M, Nelson SF, Geschwind DH.
Replication of Autism Linkage: Fine-Mapping Peak at 17q21.
Am J Hum Genet. 2005 Apr 1;76(6) [Epub ahead of print]
PMID:15806440

Butler MG, Dasouki MJ, Zhou XP, Talebizadeh Z, Brown M, Takahashi TN, Miles JH, Wang CH, Stratton R, Pilarski R, Eng C.
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
J Med Genet. 2005 Apr;42(4):318-21.
PMID:15805158

Bartlett CW, Gharani N, Millonig JH, Brzustowicz LM.
Three autism candidate genes: a synthesis of human genetic analysis with other disciplines.
Int J Dev Neurosci. 2005 Apr-May;23(2-3):221-34.
PMID:15749247

Bartlett CW, Goedken R, Vieland VJ.
Effects of Updating Linkage Evidence across Subsets of Data: Reanalysis of the Autism Genetic Resource Exchange Data Set.
Am J Hum Genet. 2005 Feb 23;76(4)
PMID:15729670

Odell D, Maciulis A, Cutler A, Warren L, McMahon WM, Coon H, Stubbs G, Henley K, Torres A.
Confirmation of the association of the C4B null allelle in autism.
Hum Immunol. 2005 Feb;66(2):140-5.
PMID:15694999

McCauley JL, Li C, Jiang L, Olson LM, Crockett G, Gainer K, Folstein SE, Haines JL, Sutcliffe JS.
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.
BMC Med Genet. 2005 Jan 12;6(1):1
PMID:15647115

Talebizadeh Z, Bittel DC, Veatch OJ, Butler MG, Takahashi TN, Miles JH.
Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?
J Autism Dev Disord. 2004 Dec;34(6):735-6.
PMID: 15679194

Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA.
Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes.
Neurosci Lett. 2004 Dec 6;372(3):209-14.
PMID:15542242

Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, Delong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA.
Analysis of the RELN gene as a genetic risk factor for autism.
Mol Psychiatry. 2004 Nov 23
PMID:15558079

Junaid MA, Kowal D, Barua M, Pullarkat PS, Sklower Brooks S, Pullarkat RK.
Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor.
Am J Med Genet. 2004 Nov 15;131A(1):11-7.
PMID:15386471

Stone JL, Merriman B, Cantor RM, Yonan AL, Gilliam TC, Geschwind DH, Nelson SF.
Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder.
Am J Hum Genet. 2004 Oct 5;75(6) [Epub ahead of print]
PMID:15467983

Serajee FJ, Nabi R, Zhong H, Huq M.
Polymorphisms in xenobiotic metabolism genes and autism.
J Child Neurol. 2004 Jun;19(6):413-7.
PMID:15446388

McCauley JL, Olson LM, Delahanty R, Amin T, Nurmi EL, Organ EL, Jacobs MM, Folstein SE, Haines JL, Sutcliffe JS.
A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism.
Am J Med Genet. 2004 Aug 24 [Epub ahead of print]
PMID:15389768

Jiang YH, Sahoo T, Michaelis RC, Bercovich D, Bressler J, Kashork CD, Liu Q, Shaffer LG, Schroer RJ, Stockton DW, Spielman RS, Stevenson RE, Beaudet AL.
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A.
Am J Med Genet. 2004 Aug 30 [Epub ahead of print]
PMID:15389703

Vincent JB, Kolozsvari D, Roberts WS, Bolton PF, Gurling HM, Scherer SW.
Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands.
Am J Med Genet. 2004 Aug 15;129B(1):82-4.
PMID:15274046

Kolevzon A, Smith CJ, Schmeidler J, Buxbaum JD, Silverman JM.
Familial symptom domains in monozygotic siblings with autism.
Am J Med Genet. 2004 Aug 15;129B(1):76-81.
PMID:15274045

Persico AM, D'Agruma L, Zelante L, Militerni R, Bravaccio C, Schneider C, Melmed R, Trillo S, Montecchi F, Elia M, Palermo M, Rabinowitz D, Pascucci T, Puglisi-Allegra S, Reichelt KL, Muscarella L, Guarnieri V, Melgari JM, Conciatori M, Keller F.
Enhanced APOE2 transmission rates in families with autistic probands.
Psychiatr Genet. 2004 Jun;14(2):73-82.
PMID:15167692

McCauley JL, Olson LM, Dowd M, Amin T, Steele A, Blakely RD, Folstein SE, Haines JL, Sutcliffe JS.
Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.
Am J Med Genet. 2004 May 15;127B(1):104-12.
PMID:15108191

Ramoz N, Reichert JG, Smith CJ, Silverman JM, Bespalova IN, Davis KL, Buxbaum JD.
Linkage and Association of the Mitochondrial Aspartate/Glutamate Carrier SLC25A12 Gene With Autism.
Am J Psychiatry. 2004 Apr;161(4):662-9.
PMID:15056512

Gharani N, Benayed R, Mancuso V, Brzustowicz LM, Millonig JH.
Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder.
Mol Psychiatry. 2004 Mar 16 :1-11 [Epub ahead of print]
PMID:15024396

Conciatori M, Stodgell CJ, Hyman SL, O'Bara M, Militerni R, Bravaccio C, Trillo S, Montecchi F, Schneider C, Melmed R, Elia M, Crawford L, Spence SJ, Muscarella L, Guarnieri V, D'Agruma L, Quattrone A, Zelante L, Rabinowitz D, Pascucci T, Puglisi-Allegra S, Reichelt KL, Rodier PM, Persico AM.
Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism.
Biol Psychiatry. 2004 Feb 15;55(4):413-9.
PMID:14960295

Nabi R, Serajee FJ, Chugani DC, Zhong H, Huq AH.
Association of tryptophan 2,3 dioxygenase gene polymorphism with autism.
Am J Med Genet. 2004 Feb 15;125B(1):63-8.
PMID:14755447

Raiford KL, Shao Y, Allen IC, Martin ER, Menold MM, Wright HH, Abramson RK, Worley G, DeLong GR, Vance JM, Cuccaro ML, Gilbert JR, Pericak-Vance MA.
No association between the APOE gene and autism.
Am J Med Genet. 2004 Feb 15;125B(1):57-60.
PMID:14755445

Vincent JB, Thevarkunnel S, Kolozsvari D, Paterson AD, Roberts W, Scherer SW.
Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism.
Am J Med Genet. 2004 Feb 15;125B(1):54-6.
PMID:14755444

Buxbaum JD, Silverman J, Keddache M, Smith CJ, Hollander E, Ramoz N, Reichert JG.
Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.
Mol Psychiatry. 2004 Feb;9(2):144-150.
PMID:14699429

Serajee FJ, Nabi R, Zhong H, Mahbubul Huq AH.
Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism.
J Med Genet. 2003 Nov;40(11):e119.
PMID:14627686

Yonan AL, Alarcon M, Cheng R, Magnusson PK, Spence SJ, Palmer AA, Grunn A, Juo SH, Terwilliger JD, Liu J, Cantor RM, Geschwind DH, Gilliam TC.
A genomewide screen of 345 families for autism-susceptibility loci. Am J Hum Genet. 2003 Oct;73(4):886-97. Epub 2003 Sep 17.
PMID:13680528

Yonan AL, Palmer AA, Smith KC, Feldman I, Lee HK, Yonan JM, Fischer SG, Pavlidis P, Gilliam TC.
Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction.
Genes Brain Behav. 2003 Oct;2(5):303-20.
PMID:14606695

Nabi R, Zhong H, Serajee FJ, Huq AH.
No association between single nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism.
Am J Med Genet 2003 May 15;119B(1):98-101.
PMID:12707945

Serajee FJ, Zhong H, Nabi R, Huq AH.
The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism.
J Med Genet 2003 Apr;40(4):e42.
PMID:12676915

Cisternas FA, Vincent JB, Scherer SW, Ray PN.
Cloning and characterization of human CADPS and CADPS2, new members of the Ca(2+)-dependent activator for secretion protein family.
Genomics 2003 Mar;81(3):279-91.
PMID:12659812

Weiss LA, Escayg A, Kearney JA, Trudeau M, MacDonald BT, Mori M, Reichert J, Buxbaum JD, Meisler MH.
Sodium channels SCN1A, SCN2A and SCN3A in familial autism.
Mol Psychiatry 2003 Feb;8(2):186-94.
PMID:12610651

Zhong H, Serajee FJ, Nabi R, Huq AH.
No association between the EN2 gene and autistic disorder.
J Med Genet 2003 Jan;40(1):e4.
PMID:12525552

Vincent JB, Petek E, Thevarkunnel S, Kolozsvari D, Cheung J, Patel M, Scherer SW.
The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript system.
Genomics 2002 Sep;80(3):283-94.
PMID:12213198

Yamagata T, Aradhya S, Mori M, Inoue K, Momoi MY, Nelson DL.
The human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autism.
Genomics 2002 Aug;80(2):185-94.
PMID:12160732

Torres AR, Maciulis A, Stubbs EG, Cutler A, Odell D.
The transmission disequilibrium test suggests that HLA-DR4 and DR13 are linked to autism spectrum disorder.
Hum Immunol 2002 Apr;63(4):311-6.
PMID:12039413

Fatemi SH.
The role of Reelin in pathology of autism.
Mol Psychiatry 2002;7(9):919-20.
PMID:12399938

Zhang H, Liu X, Zhang C, Mundo E, Macciardi F, Grayson DR, Guidotti AR, Holden JJ.
Reelin gene alleles and susceptibility to autism spectrum disorders.
Mol Psychiatry 2002;7(9):1012-7.
PMID:12399956

Fatemi SH, Stary JM, Egan EA.
Reduced blood levels of reelin as a vulnerability factor in pathophysiology of autistic disorder.
Cell Mol Neurobiol. 2002 Apr;22(2):139-52
PMID:12363196

Buxbaum JD, Silverman JM, Smith CJ, Greenberg DA, Kilifarski M, Reichert J, Cook EH Jr, Fang Y, Song CY, Vitale R.
Association between a GABRB3 polymorphism and autism.
Mol Psychiatry 2002;7(3):311-6.
PMID:11920158

Silverman JM, Smith CJ, Schmeidler J, Hollander E, Lawlor BA, Fitzgerald M, Buxbaum JD, Delaney K, Galvin P; Autism Genetic Research Exchange Consortium.
Symptom domains in autism and related conditions: evidence for familiality.
Am J Med Genet 2002 Jan 8;114(1):64-73
PMID:11840508

Alarcon M, Cantor RM, Liu J, Gilliam TC, Geschwind DH; Autism Genetic Research Exchange Consortium.
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.
Am J Hum Genet 2002 Jan;70(1):60-71
PMID:11741194

Greenberg DA, Hodge SE, Sowinski J, Nicoll D.
Excess of twins among affected sibling pairs with autism: implications for the etiology of autism.
Am J Hum Genet 2001 Nov;69(5):1062-7
PMID:11590546

Cheung J, Petek E, Nakabayashi K, Tsui LC, Vincent JB, Scherer SW
Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.
Genomics. 2001 Nov; 78(1-2):7-11.
PMID:11707066

Geschwind DH, Sowinski J, Lord C, Iversen P, Shestack J, Jones P, Ducat L, Spence SJ; AGRE Steering Committee.
The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions.
Am J Hum Genet. 2001 Aug;69(2):463-6.
PMID:11452364

Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P, Hoh J, Ott J, Gilliam TC; Autism Genetic Resource Exchange Consortium.
A genomewide screen for autism susceptibility loci.
Am J Hum Genet. 2001 Aug;69(2):327-40. Epub 2001 Jul 10.
PMID:11452361

Buxbaum JD, Silverman JM, Smith CJ, Kilifarski M, Reichert J, Hollander E, Lawlor BA, Fitzgerald M, Greenberg DA, Davis KL.
Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity.
Am J Hum Genet 2001 Jun;68(6):1514-20.
PMID:11353400

Copyright © 2016 Autism Speaks, all rights reserved.