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Cell Reports|March 21, 2019
In Vivo Generation of Post-infarct Human Cardiac Muscle by Laminin-Promoted Cardiovascular ProgenitorsLynn Yap, Jiong-Wei Wang, Aida Moreno-Moral, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2018
Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disordersYasmin Bylstra, Jyn Ling Kuan, Weng Khong Lim, et al.
The Journal of Clinical Investigation|August 8, 2017
Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremiaJames S Ware, Louise V Wain, Sarath K Channavajjhala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 10, 2018
Correction: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disordersYasmin Bylstra, Jyn Ling Kuan, Weng Khong Lim, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 10, 2018
Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trialsDorothea Buck, Till Fm Andlauer, Wilmar Igl, et al.
Gut|April 2, 2022
Interleukin-11 drives human and mouse alcohol-related liver diseaseMaria Effenberger, Anissa A Widjaja, Felix Grabherr, et al.
The Lancet. Neurology|September 5, 2009
250 microg or 500 microg interferon beta-1b versus 20 mg glatiramer acetate in relapsing-remitting multiple sclerosis: a prospective, randomised, multicentre studyPaul O'Connor, Massimo Filippi, Barry Arnason, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|March 9, 2021
Cardiovascular magnetic resonance predictors of heart failure in hypertrophic cardiomyopathy: the role of myocardial replacement fibrosis and the microcirculationClaire E Raphael, Frances Mitchell, Gajen Sunthar Kanaganayagam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert PanelMelissa A Kelly, Colleen Caleshu, Ana Morales, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 12, 2018
Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yieldKate L Thomson, Elizabeth Ormondroyd, Andrew R Harper, et al.
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