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ELIZABETH PUGH, M.D.
M.D.
Psychiatry Physician
NPI: 1487751194Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
72313(MA)
Research & Publications (20)
Unconventional superconductivity and novel quantum order.
PMID 14667294·Philos Trans A Math Phys Eng Sci·2003
8-other
Comparison of variance components, ANOVA and regression of offspring on midparent (ROMP) methods for SNP markers.
PMID 11793780·Genet Epidemiol·2001
8-other
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results.
PMID 19521098·Hum Hered·2009
8-other
Home away from home? A case study of bedside objects in a hospice.
PMID 19537536·Int J Palliat Nurs·2009
8-other
A profile of the belief system and attitudes to end-of-life decisions of senior clinicians working in a National Health Service Hospital in the United Kingdom.
PMID 19073784·Palliat Med·2009
8-other
Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
PMID 18985386·Hum Genet·2009
8-other
Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in mice.
PMID 19409519·Am J Hum Genet·2009
7-preclinical
Ezetimibe for the treatment of primary (heterozygous-familial and non-familial) hypercholesterolaemia: NICE technology appraisal guidance.
PMID 18411354·Heart·2008
8-other
Nrl-knockout mice deficient in Rpe65 fail to synthesize 11-cis retinal and cone outer segments.
PMID 18326740·Invest Ophthalmol Vis Sci·2008
7-preclinical
Mouse cones require an arrestin for normal inactivation of phototransduction.
PMID 18701071·Neuron·2008
7-preclinical
Altered visual function in monocarboxylate transporter 3 (Slc16a8) knockout mice.
PMID 18524945·Am J Physiol Cell Physiol·2008
7-preclinical
Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women.
PMID 18505370·J Bone Miner Res·2008
8-other
Common variants in the GDF5-UQCC region are associated with variation in human height.
PMID 18193045·Nat Genet·2008
4-observational
Safety and efficacy of gene transfer for Leber's congenital amaurosis.
PMID 18441370·N Engl J Med·2008
3-trial
Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genes.
PMID 18678618·Diabetes·2008
8-other
New models of collaboration in genome-wide association studies: the Genetic Association Information Network.
PMID 17728769·Nat Genet·2007
8-other
Evolution of the vertebrate eye: opsins, photoreceptors, retina and eye cup.
PMID 18026166·Nat Rev Neurosci·2007
6-review
Novel distribution of junctional adhesion molecule-C in the neural retina and retinal pigment epithelium.
PMID 17853450·J Comp Neurol·2007
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
- 156 MOUNT AUBURN ST
CAMBRIDGE, MA 02138 - Phone
- (617) 484-7245
Quick Facts
- NPI
- 1487751194
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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