Martin C. Gregory

Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome

David F. Barker, Sirkka Liisa Hostikka, Jing Zhou et al. · Science · 1990 · 872 citations

Nonmuscle Myosin Heavy Chain IIA Mutations Define a Spectrum of Autosomal Dominant Macrothrombocytopenias: May-Hegglin Anomaly and Fechtner, Sebastian, Epstein, and Alport-Like Syndromes

Karen E. Heath, Ángel Campos‐Barros, Amos Toren et al. · The American Journal of Human Genetics · 2001 · 297 citations · Full text

Autosomal Dominant Macrothrombocytopenias, Mendelian Disorder, Autoimmune Disease +10

Genotype–Phenotype Correlation in X-Linked Alport Syndrome

Mir Reza Bekheirnia, Berenice Reed, Martin C. Gregory et al. · Journal of the American Society of Nephrology · 2010 · 273 citations

Genetic Testing, Mendelian Disorder, Genetic Disorder +12

Metabolic Clearance and Plasma Half-Disappearance Time of Exogenous Somatostatin in Man*

Michael C. Sheppard, Brahm Shapiro, B. L. Pimstone et al. · The Journal of Clinical Endocrinology & Metabolism · 1979 · 203 citations · Full text

Immunology, Pharmacotherapy, Metabolic Clearance +24

X-linked nephrogenic diabetes insipidus mutations in North America and the Hopewell hypothesis.

Daniel G. Bichet, Marie‐Françoise Arthus, Michèle Lonergan et al. · Journal of Clinical Investigation · 1993 · 151 citations · Full text

Genetics, Genetic Epidemiology, Human Polymorphism +19