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Human Molecular Genetics|January 11, 2011
Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genesSwarkar Sharma, Xiaochong Gao, Douglas Londono, et al.Molecular Biology and Evolution|August 6, 2011
Crohn's disease and genetic hitchhiking at IBD5Chad D Huff, David J Witherspoon, Yuhua Zhang, et al.Journal of Child Psychology and Psychiatry, and Allied Disciplines|April 11, 2015
The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborativeMonica E Calkins, Kathleen R Merikangas, Tyler M Moore, et al.Cancer Letters|March 3, 2024
CRISPR/Cas9 screenings unearth protein arginine methyltransferase 7 as a novel essential gene in prostate cancer metastasisMaria Rodrigo-Faus, Africa Vincelle-Nieto, Natalia Vidal, et al.The American Journal of Psychiatry|January 26, 2016
Common and Dissociable Mechanisms of Executive System Dysfunction Across Psychiatric Disorders in YouthSheila Shanmugan, Daniel H Wolf, Monica E Calkins, et al.Science Immunology|May 3, 2024
Oxidative phosphorylation regulates B cell effector cytokines and promotes inflammation in multiple sclerosisRui Li, Yanting Lei, Ayman Rezk, et al.Plos Genetics|October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyriaSamin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.The American Journal of Psychiatry|March 3, 2018
Polygenic Risk Score for Alzheimer's Disease: Implications for Memory Performance and Hippocampal Volumes in Early LifeLuiza K Axelrud, Marcos L Santoro, Daniel S Pine, et al.BMC Urology|October 23, 2016
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidismYanping Wang, Jin Li, Thomas F Kolon, et al.Diabetes|July 14, 2009
Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight geneJianhua Zhao, Mingyao Li, Jonathan P Bradfield, et al.Pageof 91