Dr. Swapan Kumar Nath D.D.S.
Dentist | General Practice
637 Sutter Ave Brooklyn NY, 11207About
Dr. Swapan Nath is a Dentist practicing in Brooklyn, NY. Dr. Nath specializes in preventing, diagnosing, and treating diseases and conditions associated with the mouth and overall dental health. Dentists are trained to carry out such treatment as professional cleaning, restorative, prosthodontic, and endodontic procedures, and performing examinations, among many others.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Segregation analysis of blood pressure and body mass index in a rural US community.
- Genetic admixture of European FRDA genes is the cause of Friedreich ataxia in the Mexican population.
- CTLA-4 polymorphisms and systemic lupus erythematosus (SLE): a meta-analysis.
- Systemic lupus erythematosus susceptibility loci defined by genome scan meta-analysis.
- Meta-analysis of TNF-alpha promoter -308 A/G polymorphism and SLE susceptibility.
- Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis.
- Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34.
- Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1.
- Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.
- Osteopontin and systemic lupus erythematosus association: a probable gene-gender interaction.
- A genome-wide ordered-subset linkage analysis for rheumatoid arthritis.
- Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk.
- Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.
- Evaluation of imputation-based association in and around the integrin-alpha-M (ITGAM) gene and replication of robust association between a non-synonymous functional variant within ITGAM and systemic lupus erythematosus (SLE).
- ITGAM coding variant (rs1143679) influences the risk of renal disease, discoid rash and immunological manifestations in patients with systemic lupus erythematosus with European ancestry.
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