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European Journal of Human Genetics : EJHG|September 7, 2017
Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencingIngrid P Vogelaar, Rachel S van der Post, J Han Jm van Krieken, et al.
BMC Genomics|February 1, 2014
Finding the missing honey bee genes: lessons learned from a genome upgradeChristine G Elsik, Kim C Worley, Anna K Bennett, et al.
Genome Research|April 10, 2014
Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel linesWen Huang, Andreas Massouras, Yutaka Inoue, et al.
Circulation. Genomic and Precision Medicine|May 13, 2018
Common Coding Variants in SCN10A Are Associated With the Nav1.8 Late Current and Cardiac ConductionVincenzo Macri, Jennifer A Brody, Dan E Arking, et al.
Nature|February 10, 2012
The Drosophila melanogaster Genetic Reference PanelTrudy F C Mackay, Stephen Richards, Eric A Stone, et al.
American Journal of Human Genetics|December 30, 2019
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry CohortsLaura M Raffield, Apoorva K Iyengar, Biqi Wang, et al.
JAMA Pediatrics|October 4, 2017
Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical ManagementLinyan Meng, Mohan Pammi, Anirudh Saronwala, et al.
American Journal of Human Genetics|April 6, 2022
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed programXiaowei Hu, Dandi Qiao, Wonji Kim, et al.
Genome Research|January 6, 2005
Comparative genome sequencing of Drosophila pseudoobscura: chromosomal, gene, and cis-element evolutionStephen Richards, Yue Liu, Brian R Bettencourt, et al.
HGG Advances|January 20, 2022
Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variabilityChaofan Zhang, Angad Jolly, Brian J Shayota, et al.
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