Howard Feit

PTEN Mutation Spectrum and Genotype-Phenotype Correlations in Bannayan-Riley-Ruvalcaba Syndrome Suggest a Single Entity With Cowden Syndrome

Deborah J. Marsh, Jennifer B. Kum, Kathryn L. Lunetta et al. · Human Molecular Genetics · 1999 · 605 citations

Genotype-phenotype Correlations, Mendelian Disorder, Malignant Disease +15

Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

Arkadiusz Piotrowski, Jing Xie, Ying F Liu et al. · Nature Genetics · 2013 · 315 citations

Developmental Anomaly, Rare Diseases, Somatic Variant +12

Progesterone is neuroprotective after transient middle cerebral artery occlusion in male rats

Ning Jiang, Michael Chopp, Donald G. Stein et al. · Brain Research · 1996 · 234 citations

Cerebral Vascular Regulation, Neuroanatomy, Medicine +12

COLCHICINE‐BINDING ACTIVITY IN PARTICULATE FRACTIONS OF MOUSE BRAIN¹

Howard Feit, S H Barondes · Journal of Neurochemistry · 1970 · 188 citations

Neurophysiology, Medicine, Physiology +12

Autosomal-Dominant Distal Myopathy Associated with a Recurrent Missense Mutation in the Gene Encoding the Nuclear Matrix Protein, Matrin 3

Jan Senderek, Sean M. Garvey, Michael J. B. Krieger et al. · The American Journal of Human Genetics · 2009 · 175 citations · Full text

Rare Diseases, Recurrent Missense Mutation, Mendelian Disorder +9