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HF

Howard Feit

Credentials: ·

History

Neurology

Research

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
Human Molecular Genetics · 1999 · 453 citations
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
Nature Neuroscience · 2014 · 386 citations
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas
Nature Genetics · 2014 · 232 citations

Michael Shelanski
4 papers · 2 as a resident
Steven Levine
4 papers · 3 as a fellow
MG
Mark Glasberg
3 papers
SK
Stuart Kieran
3 papers · 3 as a resident
Bruce Korf
2 papers
ET
Erwin Thal
2 papers
SE
Stanton Elias
2 papers
AP
Alan Pestronk
1 paper
Alice Silbergleit
1 paper
Amanda Bergner
1 paper
Andrew Russman
1 paper
BP
Barbara Pober
1 paper