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Biochimica Et Biophysica Acta|June 19, 2016
Understanding the genetic and epigenetic basis of common variable immunodeficiency disorder through omics approachesJin Li, Zhi Wei, Yun R Li, et al.
American Journal of Human Genetics|May 4, 2010
Interpretation of association signals and identification of causal variants from genome-wide association studiesKai Wang, Samuel P Dickson, Catherine A Stolle, et al.
HGG Advances|March 29, 2022
Maternal effect genes as risk factors for congenital heart defectsFadi I Musfee, Omobola O Oluwafemi, A J Agopian, et al.
Nature Communications|December 10, 2025
Transformer-based deep learning enhances discovery in migraine GWASZiang Meng, Yingchao Song, Yue Jiang, et al.
Applied Clinical Informatics|February 26, 2025
A Comprehensive Approach to Clinical Decision Support in the Return of Genome Informed Risk Assessments to Primary Care PediatriciansDean Karavite, Shannon Terek, John J Connolly, et al.
Human Molecular Genetics|February 8, 2011
Neutral mitochondrial heteroplasmy and the influence of agingNeal Sondheimer, Catherine E Glatz, Jack E Tirone, et al.
European Heart Journal|January 24, 2006
Familial aggregation of atrial fibrillation in IcelandDavid O Arnar, Sverrir Thorvaldsson, Teri A Manolio, et al.
Congenital Heart Disease|May 21, 2013
The prevalence of 16p12.1 microdeletion in patients with left-sided cardiac lesionsLisa C A D'Alessandro, Petra Werner, Hongbo M Xie, et al.
Pediatric Pulmonology|December 19, 2013
DENND1B gene variants associate with elevated exhaled nitric oxide in healthy high-risk neonatesBo L K Chawes, Anne Louise Bischoff, Eskil Kreiner-Møller, et al.
Molecular Genetics & Genomic Medicine|May 11, 2022
Saudi Arabian CML patient with a novel four-way translocation at t(9;22;5;2)(q34;q11.2;p13;q44)Walid Dridi, Solaf Kanfar, Patrick M A Sleiman, et al.
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