Comprehensive List of Publications Using the AGRE Database
Showing 1 to 30 of 226       |  | 1 2 3 4 5 6 7 8 |  | 

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.


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.


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

St Pourcain B, Haworth CM, Davis OS, Wang K, Timpson NJ, Evans DM, Kemp JP, Ronald A, Price T, Meaburn E, Ring SM, Golding J, Hakonarson H, Plomin R, Davey Smith G.
Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.
Hum Genet. 2015 Jun;134(6):539-51. doi: 10.1007/s00439-014-1514-5. Epub 2014 Dec 17.

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

Simpson C, Kim Y, Hansen N, Bailey-Wilson J.
No Evidence of Excess of De Novo Mutations in Autistic Children from Multiplex Families.
Conference: 2014 International Meeting for Autism Research. 2014 May. doi: 268143366.

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

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.

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]

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

Showing 1 to 30 of 226       |  | 1 2 3 4 5 6 7 8 |  |