Rita M. Cantor

发表

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Robert T. Schultz, Margaret A. Pericak-Vance, Takeshi Sakurai, 2009, Nature.

Amerindian-specific regions under positive selection harbour new lipid variants in Latinos

Markus Perola, Markku Heliövaara, Bogdan Pasaniuc, 2014, Nature Communications.

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, American journal of human genetics.

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Kathryn Roeder, Murim Choi, Eric M. Morrow, 2011, Neuron.

Genetic Analysis Workshop 19: methods and strategies for analyzing human sequence and gene expression data in extended families and unrelated individuals

Ellen M. Wijsman, Justo Lorenzo Bermejo, Laura Almasy, 2016, BMC Proceedings.

Offering to Share: How to Put Heads Together in Autism Neuroimaging

Guido Gerig, Anders M. Dale, Robert T. Schultz, 2008, Journal of autism and developmental disorders.

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

John A. Sweeney, Geraldine Dawson, Daniel H. Geschwind, 2009, PLoS genetics.

Familial Combined Hyperlipidemia in Mexicans: Association With Upstream Transcription Factor 1 and Linkage on Chromosome 16q24.1

Päivi Pajukanta, Teresa Tusie-Luna, Aldons J. Lusis, 2005, Arteriosclerosis, thrombosis, and vascular biology.

Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia

Eleazar Eskin, René S. Kahn, Serghei Mangul, 2016, bioRxiv.

QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders

Daniel H. Geschwind, A. Lu, D. Geschwind, 2013, Molecular Psychiatry.

Genome-wide association study identifies five new schizophrenia loci

Anders D. Børglum, Peter Donnelly, Jianxin Shi, 2011, Nature Genetics.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

Anatomic Brain Asymmetry in Vervet Monkeys

Roger P. Woods, Zvart Abaryan, Matthew J. Jorgensen, 2011, PloS one.

Title : Total RNA Sequencing reveals microbial communities in human blood and disease specific effects

Eleazar Eskin, René S. Kahn, Serghei Mangul, 2016 .

Individual common variants exert weak effects on the risk for autism spectrum disorders

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2012, Human molecular genetics.

Association of the APOLIPOPROTEIN A 1 / C 3 / A 4 / A 5 Gene Cluster With Triglyceride Levels and LDL Particle Size in Familial Combined Hyperlipidemia

Päivi Pajukanta, Janet S. Sinsheimer, Aldons J. Lusis, 2004 .

“High Density SNP Association Study of the 17q21 Chromosomal Region Linked to Autism Identifies CACNA1G as a Novel Candidate Gene”

Barry Merriman, Stanley F. Nelson, Daniel H. Geschwind, 2009, Molecular Psychiatry.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.