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American Journal of Human Genetics|April 19, 2016
A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control StudiesCorneliu A Bodea, Benjamin M Neale, Stephan Ripke, et al.Genome Biology|October 26, 2018
PINES: phenotype-informed tissue weighting improves prediction of pathogenic noncoding variantsCorneliu A Bodea, Adele A Mitchell, Alex Bloemendal, et al.Molecular Neuropsychiatry|March 10, 2017
Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31Corneliu A Bodea, Frank A Middleton, Nadine M Melhem, et al.The Journal of Allergy and Clinical Immunology|May 28, 2025
Type 2 cytokines pleiotropically modulate sensory nerve architecture and neuroimmune interactions to mediate itchMithilesh Kumar Jha, Yingnan Han, Zhipeng Liu, et al.Nature Genetics|July 21, 2014
Most genetic risk for autism resides with common variationTrent Gaugler, Lambertus Klei, Stephan J Sanders, et al.Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.Pageof 1