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TEJAL SHAIKH, D.O.
D.O.
Family Medicine Physician
NPI: 1508312893IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
66749(CT)
Education
OTHER
Class of 2017
Research & Publications (20)
A partial atomic structure for the flagellar hook of Salmonella typhimurium.
PMID 15657146·Proc Natl Acad Sci U S A·2005
8-other
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
PMID 19546859·Mol Psychiatry·2010
8-other
Ribosome-induced changes in elongation factor Tu conformation control GTP hydrolysis.
PMID 19122150·Proc Natl Acad Sci U S A·2009
8-other
The twitch interpolation technique is not useful for determining whether a contraction is maximal.
PMID 19670481·J Appl Physiol (1985)·2009
8-other
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.
PMID 19500772·Am J Hum Genet·2009
8-other
Human papillomavirus is detected in transitional cell carcinoma arising in renal transplant recipients.
PMID 19291536·Pathology·2009
8-other
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.
PMID 19592680·Genome Res·2009
8-other
Implementation of a flash-photolysis system for time-resolved cryo-electron microscopy.
PMID 19114106·J Struct Biol·2009
8-other
Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors.
PMID 19276269·Clin Cancer Res·2009
8-other
Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.
PMID 19193630·Hum Mol Genet·2009
8-other
Duplication of 7q34 in pediatric low-grade astrocytomas detected by high-density single-nucleotide polymorphism-based genotype arrays results in a novel BRAF fusion gene.
PMID 19016743·Brain Pathol·2009
8-other
Transitional cell carcinoma of the urinary tract in renal transplant recipients.
PMID 19404862·Pathology·2009
8-other
A 781-kb deletion of 13q12.3 in a patient with Peters plus syndrome.
PMID 19610101·Am J Med Genet A·2009
5-case
SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation.
PMID 19058200·Hum Mutat·2009
8-other
Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.
PMID 18997000·Genome Res·2009
8-other
A training model for suprapubic catheter insertion: the UroEmerge suprapubic catheter model.
PMID 18513785·Urology·2008
8-other
Exploration of parameters in cryo-EM leading to an improved density map of the E. coli ribosome.
PMID 18606549·J Struct Biol·2008
8-other
Particle-verification for single-particle, reference-based reconstruction using multivariate data analysis and classification.
PMID 18619547·J Struct Biol·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 13 CHURCH RD
EAST GRANBY, CT 06026 - Phone
- (860) 653-4526
Quick Facts
- NPI
- 1508312893
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 9
- Publications
- 20
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