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Scientific Reports|March 29, 2018
Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathiesIker Sanchez-Navarro, Luciana R J da Silva, Fiona Blanco-Kelly, et al.Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|July 10, 2007
Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's diseaseRobert N Baldassano, Jonathan P Bradfield, Dimitri S Monos, et al.European Journal of Human Genetics : EJHG|April 30, 2015
Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP arraySantiago Rodriguez, Tom R Gaunt, Yiran Guo, et al.Journal of Medical Genetics|March 18, 2025
Clinicogenetic characterisation of SLC29A3-related syndromes: a case series, tracing ancestral variants and molecular dynamics simulationSajjad Biglari, Mohammad Shahrooei, Fatemeh Vahidnezhad, et al.The American Journal of Psychiatry|February 3, 2011
Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplicationsDouglas F Levinson, Jubao Duan, Sang Oh, et al.American Journal of Human Genetics|May 11, 2020
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic GroupsOzan Dikilitas, Daniel J Schaid, Matthew L Kosel, et al.Nature Genetics|February 11, 2004
The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and strokeAnna Helgadottir, Andrei Manolescu, Gudmar Thorleifsson, et al.Human Genomics|September 10, 2024
The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetesMahmoud Amiri Roudbar, Seyed Milad Vahedi, Jin Jin, et al.Nature Genetics|March 9, 2010
Common variants at 5q22 associate with pediatric eosinophilic esophagitisMarc E Rothenberg, Jonathan M Spergel, Joseph D Sherrill, et al.Clinical Epigenetics|April 29, 2019
Gene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndromeEric G Bend, Erfan Aref-Eshghi, David B Everman, et al.Pageof 91