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JESSICA NEIDHARDT, M.D.
M.D.
Emergency Medicine Physician
NPI: 1689061343IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
27851(WV)
CMS Specialties
PrimaryEMERGENCY MEDICINE
Education
WEST VIRGINIA UNIVERSITY SCHOOL OF MEDICINE
Class of 2015
Research & Publications (18)
Therapeutic strategy to rescue mutation-induced exon skipping in rhodopsin by adaptation of U1 snRNA.
PMID 18837008·Hum Mutat·2009
5-case
Overexpression of RPGR leads to male infertility in mice due to defects in flagellar assembly.
PMID 18579752·Biol Reprod·2008
7-preclinical
Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing.
PMID 18552978·Mol Vis·2008
8-other
Vascular changes in the cerebellum of Norrin /Ndph knockout mice correlate with high expression of Norrin and Frizzled-4.
PMID 18547247·Eur J Neurosci·2008
7-preclinical
Identification and functional characterization of a novel rhodopsin mutation associated with autosomal dominant CSNB.
PMID 18487375·Invest Ophthalmol Vis Sci·2008
8-other
Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria.
PMID 18304496·Am J Hum Genet·2008
8-other
Semi-quantitative chemical analysis of hard coatings by Raman micro-spectroscopy: the aluminium chromium nitride system as an example.
PMID 17932660·Anal Bioanal Chem·2007
8-other
Identification and characterization of a novel RPGR isoform in human retina.
PMID 17405150·Hum Mutat·2007
8-other
Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking.
PMID 17405131·Hum Mutat·2007
7-preclinical
Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy.
PMID 17033974·Am J Hum Genet·2006
5-case
Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.
PMID 16877424·Invest Ophthalmol Vis Sci·2006
7-preclinical
Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes.
PMID 16565402·Invest Ophthalmol Vis Sci·2006
8-other
Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
PMID 16249515·Invest Ophthalmol Vis Sci·2005
8-other
[Viral and nonviral gene therapy for treatment of retinal diseases].
PMID 16012813·Ophthalmologe·2005
6-review
Tenascin-N: characterization of a novel member of the tenascin family that mediates neurite repulsion from hippocampal explants.
PMID 12812753·Mol Cell Neurosci·2003
7-preclinical
Imaging of fullerene-like structures in CNx thin films by electron microscopy; sample preparation artefacts due to ion-beam milling.
PMID 12524186·Ultramicroscopy·2003
8-other
Cross-linked nano-onions of carbon nitride in the solid phase: existence of a novel C(48)N(12) aza-fullerene.
PMID 11736407·Phys Rev Lett·2001
8-other
Review and evaluation of anatomy sites on the Internet (updated 1999).
PMID 10959677·Surg Radiol Anat·2000
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
- 327 MEDICAL PARK DR
BRIDGEPORT, WV 26330 - Phone
- (681) 342-1000
Quick Facts
- NPI
- 1689061343
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 11
- Publications
- 18
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