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MARK BULMAN, M.D.
M.D.
Orthopaedic Surgery Physician
NPI: 1770556664Individual
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
56939(MA)
Research & Publications (20)
The study of cystic fibrosis transmembrane conductance regulator gene mutations in a group of patients from Romania.
PMID 18467194·J Cyst Fibros·2008
8-other
Probability of BRCA1/2 mutation varies with ovarian histology: results from screening 442 ovarian cancer families.
PMID 18312450·Clin Genet·2008
8-other
BRCA1/2 mutation analysis in male breast cancer families from North West England.
PMID 17636422·Fam Cancer·2008
8-other
Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening.
PMID 17079251·J Med Genet·2007
8-other
A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO.
PMID 15173236·J Med Genet·2004
4-observational
Haplotype and cancer risk analysis of two common mutations, BRCA1 4184del4 and BRCA2 2157delG, in high risk northwest England breast/ovarian families.
PMID 14757871·J Med Genet·2004
8-other
Sensitivity of BRCA1/2 mutation testing in 466 breast/ovarian cancer families.
PMID 12960223·J Med Genet·2003
8-other
A genome-wide scan in families with maturity-onset diabetes of the young: evidence for further genetic heterogeneity.
PMID 12606533·Diabetes·2003
8-other
Abnormal splicing of hepatocyte nuclear factor 1 alpha in maturity-onset diabetes of the young.
PMID 12378390·Diabetologia·2002
8-other
Evidence for haploinsufficiency of the human HNF1alpha gene revealed by functional characterization of MODY3-associated mutations.
PMID 12530534·Biol Chem·2002
8-other
Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1alpha gene mutation carriers.
PMID 12453975·Diabetes Care·2002
8-other
High detection rate for BRCA2 mutations in male breast cancer families from North West England.
PMID 14574168·Fam Cancer·2001
4-observational
A distant upstream promoter of the HNF-4alpha gene connects the transcription factors involved in maturity-onset diabetes of the young.
PMID 11590126·Hum Mol Genet·2001
7-preclinical
Hepatocyte nuclear factor-1beta: a new kindred with renal cysts and diabetes and gene expression in normal human development.
PMID 11562418·J Am Soc Nephrol·2001
5-case
beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors.
PMID 11272211·Diabetes·2001
8-other
beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutations.
PMID 11272165·Diabetes·2001
8-other
Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease.
PMID 11085914·Am J Hum Genet·2001
8-other
R127W in HNF4alpha is a loss-of-function mutation causing maturity-onset diabetes of the young (MODY) in a UK Caucasian family.
PMID 11043869·Diabetologia·2000
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
- 143 LONGWATER DR
NORWELL, MA 02061 - Phone
- (781) 792-4191
Quick Facts
- NPI
- 1770556664
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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