Multiple HABP2 variants in familial papillary thyroid carcinoma: Contribution of a group of “thyroid-checked” controls

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

Sue Richards, Nazneen Aziz, Sherri J. Bale et al. · Genetics in Medicine · 2015 · 32.2K citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Analysis of protein-coding genetic variation in 60,706 humans

Monkol Lek, Konrad J. Karczewski, Eric Vallabh Minikel et al. · Nature · 2016 · 10.3K citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Endometrial gene expression analysis at the time of embryo implantation in women with unexplained infertility

Signe Altmäe, José Antonio Martínez-Conejero, Andres Salumets et al. · Molecular Human Reproduction · 2009 · 177 citations · Full text

Medicine, Gynecology, Molecular Biology +10

Germline<i>HABP2</i>Mutation Causing Familial Nonmedullary Thyroid Cancer

Sudheer Kumar Gara, Maria J. Merino, Sunita Agarwal et al. · New England Journal of Medicine · 2015 · 154 citations · Full text

Medicine, Genetics, Molecular Genetics +17

The G534E polymorphism of the gene encoding the factor VII–activating protease is associated with cardiovascular risk due to increased neointima formation

Daniel Sedding, Jan‐Marcus Daniel, Lars Muhl et al. · The Journal of Experimental Medicine · 2006 · 75 citations · Full text

Medicine, Cardiology, Molecular Genetics +13