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 · 613 citations

Medicine, Molecular Genetics, Oncology +17

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

Janel O. Johnson, Erik P. Pioro, Ashley Boehringer et al. · Nature Neuroscience · 2014 · 443 citations · Full text

Life Sciences, Genetics, Neuroscience +12

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 · 322 citations

Life Sciences, Genetics, Molecular Genetics +15

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

Medicine, Neurology, Neuroscience +14

COLCHICINE‐BINDING ACTIVITY IN PARTICULATE FRACTIONS OF MOUSE BRAIN¹

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

Life Sciences, Biochemistry, Neuroscience +6