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JAMES RAMSER, MD
MD
Orthopaedic Surgery Physician
NPI: 1982621439IndividualAccepts Medicare
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
101045458(VA)
CMS Specialties
PrimaryORTHOPEDIC SURGERY
Education
VIRGINIA COMMONWEALTH UNIVERSITY, SCHOOL OF MEDICINE
Class of 1987
Research & Publications (20)
Decreased expression of angiogenesis antagonist EFEMP1 in sporadic breast cancer is caused by aberrant promoter methylation and points to an impact of EFEMP1 as molecular biomarker.
PMID 19115204·Int J Cancer·2009
8-other
Identification of brain- and bone-specific breast cancer metastasis genes.
PMID 19114293·Cancer Lett·2009
8-other
Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophy.
PMID 18179898·Am J Hum Genet·2008
8-other
The reduced expression of the HADH2 protein causes X-linked mental retardation, choreoathetosis, and abnormal behavior.
PMID 17236142·Am J Hum Genet·2007
8-other
Allelic loss analysis by denaturing high-performance liquid chromatography and electrospray ionization mass spectrometry.
PMID 17109391·Hum Mutat·2007
4-observational
A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.
PMID 17033686·Eur J Hum Genet·2007
5-case
Classification of non-bacterial osteitis: retrospective study of clinical, immunological and genetic aspects in 89 patients.
PMID 16782988·Rheumatology (Oxford)·2007
8-other
Validation of mRNA/EST-based gene predictions in human Xp11.4 revealed differences to the organization of the orthologous mouse locus.
PMID 16341673·Mamm Genome·2005
4-observational
A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor.
PMID 15746149·Hum Mol Genet·2005
8-other
A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9).
PMID 15342698·J Med Genet·2004
8-other
Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly.
PMID 15024694·Am J Hum Genet·2004
8-other
Refinement of the physical location and the genomic characterization of the CRSP2 (EXLM1) gene on Xp11.4.
PMID 12825353·DNA Seq·2003
8-other
Chromosomal region 15q21.1 is a frequent target of allelic imbalance in advanced breast carcinomas.
PMID 12794759·Int J Cancer·2003
8-other
Honeybee (Apis mellifera L.) mrjp gene family: computational analysis of putative promoters and genomic structure of mrjp1, the gene coding for the most abundant protein of larval food.
PMID 12559578·Gene·2003
7-preclinical
Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22.
PMID 11973628·Eur J Hum Genet·2002
8-other
An integrated, functionally annotated gene map of the DXS8026-ELK1 interval on human Xp11.3-Xp11.23: potential hotspot for neurogenetic disorders.
PMID 11944989·Genomics·2002
8-other
X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15.
PMID 11857109·Am J Hum Genet·2002
8-other
ACRC codes for a novel nuclear protein with unusual acidic repeat tract and maps to DYT3 (dystonia parkinsonism) critical interval in xq13.1.
PMID 11714101·Neurogenetics·2001
8-other
DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements.
PMID 11702207·Hum Genet·2001
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 52 W SHIRLEY AVE
WARRENTON, VA 20186 - Phone
- (540) 347-9220
Quick Facts
- NPI
- 1982621439
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 39
- Publications
- 20
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