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CLARA KEEGAN, MD
MD
Family Medicine Physician
NPI: 1770542631IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
219879(MA)042-0012154(VT)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
COLUMBIA UNIVERSITY COLLEGE OF PHYSICIANS AND SURGEONS
Class of 2002
Research & Publications (20)
Caudal regression in adrenocortical dysplasia (acd) mice is caused by telomere dysfunction with subsequent p53-dependent apoptosis.
PMID 19660449·Dev Biol·2009
7-preclinical
Identification of critical regions for clinical features of distal 10q deletion syndrome.
PMID 19558528·Clin Genet·2009
5-case
The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia.
PMID 18925679·Am J Med Genet A·2008
5-case
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.
PMID 18414210·Genet Med·2008
4-observational
Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromes.
PMID 17466001·Clin Endocrinol (Oxf)·2007
4-observational
Tpp1/Acd maintains genomic stability through a complex role in telomere protection.
PMID 18185984·Chromosome Res·2007
7-preclinical
Prenatal ascertainment of OEIS complex/cloacal exstrophy - 15 new cases and literature review.
PMID 17702047·Am J Med Genet A·2007
6-review
Telomere protection by mammalian Pot1 requires interaction with Tpp1.
PMID 17632522·Nat Struct Mol Biol·2007
7-preclinical
IMAGe association and congenital adrenal hypoplasia: no disease-causing mutations found in the ACD gene.
PMID 16504561·Mol Genet Metab·2006
7-preclinical
Household remedies: new narratives of queer containment in the television movie.
PMID 16873217·J Lesbian Stud·2006
8-other
Craniofacial dyssynostosis in two boys with apparently normal cognitive development.
PMID 16691590·Am J Med Genet A·2006
5-case
Urogenital and caudal dysgenesis in adrenocortical dysplasia (acd) mice is caused by a splicing mutation in a novel telomeric regulator.
PMID 15537664·Hum Mol Genet·2005
7-preclinical
Microcephaly, jejunal atresia, aberrant right bronchus, ocular anomalies, and XY sex reversal.
PMID 14994240·Am J Med Genet A·2004
5-case
Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia.
PMID 12457340·Am J Hum Genet·2003
4-observational
Mouse knockout solves endocrine puzzle and promotes new pituitary lineage model.
PMID 12651886·Genes Dev·2003
6-review
Acute extrapyramidal syndrome in mild ornithine transcarbamylase deficiency: metabolic stroke involving the caudate and putamen without metabolic decompensation.
PMID 12647200·Eur J Pediatr·2003
5-case
SF-1, DAX-1, and acd: molecular determinants of adrenocortical growth and steroidogenesis.
PMID 12530669·Endocr Res·2002
6-review
Recent insights into organogenesis of the adrenal cortex.
PMID 12185666·Trends Endocrinol Metab·2002
6-review
Steroidogenic factor-1 is essential for compensatory adrenal growth following unilateral adrenalectomy.
PMID 12130578·Endocrinology·2002
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
- 3 TIMBER LN
SOUTH BURLINGTON, VT 05403 - Phone
- (802) 847-8500
Quick Facts
- NPI
- 1770542631
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 24
- Publications
- 20
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