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JACOB ROTTER, MD
MD
Pediatrics Physician
NPI: 1720547821Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
315541-01(NY)
Research & Publications (20)
The HMG-CoA reductase gene and lipid and lipoprotein levels: the multi-ethnic study of atherosclerosis.
PMID 19554360·Lipids·2009
8-other
MAGI2 genetic variation and inflammatory bowel disease.
PMID 18720471·Inflamm Bowel Dis·2009
4-observational
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.
PMID 19557197·PLoS Genet·2009
8-other
IBD-associated TL1A gene (TNFSF15) haplotypes determine increased expression of TL1A protein.
PMID 19262684·PLoS One·2009
8-other
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.
PMID 19584346·JAMA·2009
1-meta
Correlates and heritability of nonalcoholic fatty liver disease in a minority cohort.
PMID 19584882·Obesity (Silver Spring)·2009
4-observational
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
PMID 19597492·Nat Genet·2009
8-other
A genome-wide association scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS).
PMID 19430760·Diabetologia·2009
8-other
Genetic epistasis of IL23/IL17 pathway genes in Crohn's disease.
PMID 19235914·Inflamm Bowel Dis·2009
8-other
Replication of calpain-10 genetic association with carotid intima-media thickness.
PMID 19193380·Atherosclerosis·2009
8-other
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.
PMID 19122664·Nat Genet·2009
8-other
Genome-wide association study of blood pressure and hypertension.
PMID 19430479·Nat Genet·2009
8-other
High-frequency haplotypes in the X chromosome locus TLR8 are associated with both CD and UC in females.
PMID 18942751·Inflamm Bowel Dis·2009
4-observational
Linkage of Crohn's disease-related serological phenotypes: NFKB1 haplotypes are associated with anti-CBir1 and ASCA, and show reduced NF-kappaB activation.
PMID 18832525·Gut·2009
8-other
Common variants at ten loci influence QT interval duration in the QTGEN Study.
PMID 19305408·Nat Genet·2009
8-other
Genes associated with risk of type 2 diabetes identified by a candidate-wide association scan: as a trickle becomes a flood.
PMID 18971440·Diabetes·2008
8-other
Association of the Kir6.2 E23K variant with reduced acute insulin response in African-Americans.
PMID 18796522·J Clin Endocrinol Metab·2008
8-other
Heritability of the severity of diabetic retinopathy: the FIND-Eye study.
PMID 18765632·Invest Ophthalmol Vis Sci·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
- 300 COMMUNITY DR
MANHASSET, NY 11030 - Phone
- (516) 562-0100
Quick Facts
- NPI
- 1720547821
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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