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RICHARD HOFSTRA, M.D.
M.D.
Anesthesiology Physician
NPI: 1639170756IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anesthesiology PhysicianPrimary
Anesthesiology
Code: 207L00000X
35067160(OH)
CMS Specialties
PrimaryANESTHESIOLOGY
Education
UNIVERSITY OF MICHIGAN MEDICAL SCHOOL
Class of 1990
Research & Publications (20)
Complex pathogenesis of Hirschsprung's disease in a patient with hydrocephalus, vesico-ureteral reflux and a balanced translocation t(3;17)(p12;q11).
PMID 19300444·Eur J Hum Genet·2009
5-case
Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association.
PMID 19306335·Hum Mutat·2009
8-other
Mononucleotide precedes dinucleotide repeat instability during colorectal tumour development in Lynch syndrome patients.
PMID 19521971·J Pathol·2009
4-observational
Medullary thyroid carcinoma and biomarkers: past, present and future.
PMID 19522831·J Intern Med·2009
6-review
Long-term follow-up of patients with recessive dystrophic epidermolysis bullosa in the Netherlands: expansion of the mutation database and unusual phenotype-genotype correlations.
PMID 19665875·J Dermatol Sci·2009
8-other
Do microsatellite instability profiles really differ between colorectal and endometrial tumors?
PMID 19373783·Genes Chromosomes Cancer·2009
8-other
Survival-related profile, pathways, and transcription factors in ovarian cancer.
PMID 19192944·PLoS Med·2009
8-other
TP53 germline mutations in Portugal and genetic modifiers of age at cancer onset.
PMID 19468865·Fam Cancer·2009
8-other
Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome.
PMID 19156873·Genes Chromosomes Cancer·2009
8-other
PMS2 involvement in patients suspected of Lynch syndrome.
PMID 19132747·Genes Chromosomes Cancer·2009
8-other
Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome.
PMID 19455606·Genes Chromosomes Cancer·2009
8-other
A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy.
PMID 19569224·Hum Mutat·2009
8-other
Somatic mutations in mismatch repair genes in sporadic gastric carcinomas are not a cause but a consequence of the mutator phenotype.
PMID 18206535·Cancer Genet Cytogenet·2008
8-other
Assessment of functional effects of unclassified genetic variants.
PMID 18951449·Hum Mutat·2008
8-other
A database to support the interpretation of human mismatch repair gene variants.
PMID 18951442·Hum Mutat·2008
8-other
Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes.
PMID 18951438·Hum Mutat·2008
8-other
C. elegans model identifies genetic modifiers of alpha-synuclein inclusion formation during aging.
PMID 18369446·PLoS Genet·2008
7-preclinical
A new perspective on transcriptional system regulation (TSR): towards TSR profiling.
PMID 18297136·PLoS One·2008
7-preclinical
Tumor characteristics as an analytic tool for classifying genetic variants of uncertain clinical significance.
PMID 18951447·Hum Mutat·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 18101 LORAIN AVE
CLEVELAND, OH 44111 - Phone
- (216) 476-7052
Quick Facts
- NPI
- 1639170756
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 36
- Publications
- 20
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