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European Heart Journal|October 18, 2011
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studiesHarald Grallert, Josée Dupuis, Joshua C Bis, et al.
Plos Genetics|September 21, 2021
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Plos Genetics|July 29, 2021
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
The Lancet. Neurology|October 15, 2017
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysisBarbara Schormair, Chen Zhao, Steven Bell, et al.
American Journal of Human Genetics|February 25, 2025
Identification of genes associated with testicular germ cell tumor susceptibility through a transcriptome-wide association studyEmilio Ugalde-Morales, Rona Wilf, John Pluta, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 25, 2017
Homologous Recombination DNA Repair Pathway Disruption and Retinoblastoma Protein Loss Are Associated with Exceptional Survival in High-Grade Serous Ovarian CancerDale W Garsed, Kathryn Alsop, Sian Fereday, et al.
The Journal of Physical Chemistry Letters|March 25, 2021
X-ray Free Electron Laser-Induced Synthesis of ε-Iron Nitride at High PressuresHuijeong Hwang, Taehyun Kim, Hyunchae Cynn, et al.
Genome Medicine|December 26, 2018
Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controlsJung Kim, Wen Luo, Mingyi Wang, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 9, 2022
TRACEBACK: Testing of Historical Tubo-Ovarian Cancer Patients for Hereditary Risk Genes as a Cancer Prevention Strategy in Family MembersRachel Delahunty, Linh Nguyen, Stuart Craig, et al.
Science Translational Medicine|September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityAbdul Noor, Annabel Whibley, Christian R Marshall, et al.
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