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ANNE ANTONELLIS, M.D.
M.D.
Obstetrics & Gynecology Physician
NPI: 1619389053IndividualAccepts Medicare
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
EC141074(ME)276409(MA)
CMS Specialties
PrimaryOBSTETRICS/GYNECOLOGY
Education
UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL
Class of 2014
Research & Publications (18)
Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish.
PMID 18773071·PLoS Genet·2008
7-preclinical
The role of aminoacyl-tRNA synthetases in genetic diseases.
PMID 18767960·Annu Rev Genomics Hum Genet·2008
6-review
Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axons.
PMID 17035524·J Neurosci·2006
4-observational
Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome.
PMID 16330480·Hum Mol Genet·2006
4-observational
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.
PMID 12690580·Am J Hum Genet·2003
8-other
A method for developing high-density SNP maps and its application at the type 1 angiotensin II receptor (AGTR1) locus.
PMID 11863362·Genomics·2002
8-other
Gpnmb is a melanoblast-expressed, MITF-dependent gene.
PMID 18983539·Pigment Cell Melanoma Res·2009
7-preclinical
An evolutionarily conserved intronic region controls the spatiotemporal expression of the transcription factor Sox10.
PMID 18950534·BMC Dev Biol·2008
7-preclinical
Evidence of a founder haplotype refines the X-linked Charcot-Marie-Tooth (CMTX3) locus to a 2.5 Mb region.
PMID 18458969·Neurogenetics·2008
8-other
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness.
PMID 16385457·Am J Hum Genet·2006
4-observational
Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations.
PMID 16014653·Brain·2005
5-case
Detection of potential GDF6 regulatory elements by multispecies sequence comparisons and identification of a skeletal joint enhancer.
PMID 15979840·Genomics·2005
7-preclinical
SAP regulates T(H)2 differentiation and PKC-theta-mediated activation of NF-kappaB1.
PMID 15539155·Immunity·2004
7-preclinical
Direct interaction of Sox10 with the promoter of murine Dopachrome Tautomerase (Dct) and synergistic activation of Dct expression with Mitf.
PMID 15250937·Pigment Cell Res·2004
7-preclinical
Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect.
PMID 12453976·Diabetes Care·2002
8-other
Leukocyte adhesion deficiency (LAD) type II/carbohydrate deficient glycoprotein (CDG) IIc founder effect and genotype/phenotype correlation.
PMID 12116250·Am J Med Genet·2002
8-other
Mutation of melanosome protein RAB38 in chocolate mice.
PMID 11917121·Proc Natl Acad Sci U S A·2002
7-preclinical
Aldose reductase gene polymorphisms and susceptibility to diabetic nephropathy in Type 1 diabetes mellitus.
PMID 10746480·Diabet Med·2000
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 725 CONCORD AVE STE 1200
CAMBRIDGE, MA 02138 - Phone
- (617) 926-2414
Quick Facts
- NPI
- 1619389053
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 3
- Years in Practice
- 12
- Publications
- 18
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