Comprehensive List of Publications Using the AGRE Database
Showing 1 to 30 of 205       |  | 1 2 3 4 5 6 7 |  | 
Anitha A, Thanseem I, Nakamura K, Yamada K, Iwayama Y, Toyota T, Iwata Y, Suzuki K, Sugiyama T, Tsujii M, Yoshikawa T, Mori N. Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH.
Protocadherin α (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


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 May;191(1):215-32. Epub 2012 Feb 29.
PMID: 22377632


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


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


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


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


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


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


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


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


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


Showing 1 to 30 of 205       |  | 1 2 3 4 5 6 7 |  |