Back to Search
NEHA LIMAYE, M.D.
M.D.
Hospitalist Physician
NPI: 1871025155IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hospitalist PhysicianPrimary
Hospitalist
Code: 208M00000X
317173(NY)
CMS Specialties
PrimaryHOSPITALIST
Education
PERELMAN SCHOOL OF MED AT THE UNIVERSITY OF PENNSYLVANIA
Class of 2017
Research & Publications (19)
Cutaneous venous malformations in familial cerebral cavernomatosis caused by KRIT1 gene mutations.
PMID 19182478·Dermatology·2009
8-other
Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations.
PMID 19079259·Nat Genet·2009
8-other
Genome profiling of chondrosarcoma using oligonucleotide array-based comparative genomic hybridization.
PMID 19596254·Cancer Genet Cytogenet·2009
8-other
From germline towards somatic mutations in the pathophysiology of vascular anomalies.
PMID 19297403·Hum Mol Genet·2009
6-review
Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma.
PMID 18931684·Nat Med·2008
8-other
Prevalence and evolutionary origins of autoimmune susceptibility alleles in natural mouse populations.
PMID 18094711·Genes Immun·2008
7-preclinical
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383590·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383589·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383588·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383587·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18380023·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383593·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383597·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383596·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383595·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383594·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383591·Hum Genet·2007
8-other
Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupus.
PMID 15589166·Immunity·2004
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1 GUSTAVE L LEVY PL
NEW YORK, NY 10029 - Phone
- (212) 241-0896
Quick Facts
- NPI
- 1871025155
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 9
- Publications
- 19
Are you this provider?
Claim Your Profile