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JAMA Cardiology|June 9, 2021
Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen StudyTafadzwa Machipisa, Michael Chong, Babu Muhamed, et al.International Journal of Cardiology|February 19, 2021
Rationale and design of the African Cardiomyopathy and Myocarditis Registry Program: The IMHOTEP studySarah M Kraus, Gasnat Shaboodien, Veronica Francis, et al.American Journal of Human Genetics|January 10, 2015
Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanismsHansjörg Baurecht, Melanie Hotze, Stephan Brand, et al.Circulation Research|December 25, 2018
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of FallotDonna J Page, Matthieu J Miossec, Simon G Williams, et al.Plos One|March 12, 2014
Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohortsAnna L Mitchell, Katie D R Macarthur, Earn H Gan, et al.Human Molecular Genetics|January 9, 2013
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of FallotHeather J Cordell, Ana Töpf, Chrysovalanto Mamasoula, et al.The Journal of Allergy and Clinical Immunology|October 3, 2013
Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjectsSean P Saunders, Christabelle S M Goh, Sara J Brown, et al.Journal of Hepatology|December 23, 2021
Macrophage scavenger receptor 1 mediates lipid-induced inflammation in non-alcoholic fatty liver diseaseOlivier Govaere, Sine Kragh Petersen, Nuria Martinez-Lopez, et al.The Pharmacogenomics Journal|May 26, 2018
Genome-wide association study of response to methotrexate in early rheumatoid arthritis patientsJohn C Taylor, Tim Bongartz, Jonathan Massey, et al.The Journal of Clinical Investigation|March 24, 2015
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity geneJoshua W Knowles, Weijia Xie, Zhongyang Zhang, et al.Pageof 27