Sarkar B - Search Results

1

Role of HLA class II loci polymorphism in the manifestation of type 1 diabetes in a Bengali Indian patient population.

Raha O, Sarkar B, Veerraju P, Sudhakar G, Raychaudhuri P, Mukhopadhyay S, Rao VR. Raha O, et al. Among authors: sarkar b. Genet Test Mol Biomarkers. 2013 Jan;17(1):52-61. doi: 10.1089/gtmb.2012.0221. Epub 2012 Nov 2. Genet Test Mol Biomarkers. 2013. PMID: 23121162

2

HLA class II SNP interactions and the association with type 1 diabetes mellitus in Bengali speaking patients of Eastern India.

Raha O, Sarkar B, Lakkakula BV, Pasumarthy V, Godi S, Chowdhury S, Raychaudhuri P, Vadlamudi RR. Raha O, et al. Among authors: sarkar b. J Biomed Sci. 2013 Feb 27;20(1):12. doi: 10.1186/1423-0127-20-12. J Biomed Sci. 2013. PMID: 23441825 Free PMC article.

3

Menarcheal age of type 1 diabetic Bengali Indian females.

Raha O, Sarkar B, Godi S, GhoshRoy A, Pasumarthy V, Chowdhury S; JDRF-India; Vadlamudi RR. Raha O, et al. Among authors: sarkar b. Gynecol Endocrinol. 2013 Nov;29(11):963-6. doi: 10.3109/09513590.2013.819080. Epub 2013 Aug 19. Gynecol Endocrinol. 2013. PMID: 23952104 Free article.

4

A novel polymorphism in codon 25 of the KRAS gene associated with gallbladder carcinoma patients of the eastern part of India.

Pramanik V, Sarkar BN, Kar M, Das G, Malay BK, Sufia KK, Lakkakula BV, Vadlamudi RR. Pramanik V, et al. Genet Test Mol Biomarkers. 2011 Jun;15(6):431-4. doi: 10.1089/gtmb.2010.0194. Epub 2011 Mar 4. Genet Test Mol Biomarkers. 2011. PMID: 21375404

5

Environmental and familial risk factors of Parkinsons disease: case-control study.

Sanyal J, Chakraborty DP, Sarkar B, Banerjee TK, Mukherjee SC, Ray BC, Rao VR. Sanyal J, et al. Among authors: sarkar b. Can J Neurol Sci. 2010 Sep;37(5):637-42. doi: 10.1017/s0317167100010829. Can J Neurol Sci. 2010. PMID: 21059511

6

Absence of commonly reported leucine-rich repeat kinase 2 mutations in Eastern Indian Parkinson's disease patients.

Sanyal J, Sarkar B, Ojha S, Banerjee TK, Ray BC, Rao VR. Sanyal J, et al. Among authors: sarkar b. Genet Test Mol Biomarkers. 2010 Oct;14(5):691-4. doi: 10.1089/gtmb.2010.0054. Epub 2010 Aug 19. Genet Test Mol Biomarkers. 2010. PMID: 20722494

7

The promise of discovering population-specific disease-associated genes in South Asia.

Nakatsuka N, Moorjani P, Rai N, Sarkar B, Tandon A, Patterson N, Bhavani GS, Girisha KM, Mustak MS, Srinivasan S, Kaushik A, Vahab SA, Jagadeesh SM, Satyamoorthy K, Singh L, Reich D, Thangaraj K. Nakatsuka N, et al. Among authors: sarkar b. Nat Genet. 2017 Sep;49(9):1403-1407. doi: 10.1038/ng.3917. Epub 2017 Jul 17. Nat Genet. 2017. PMID: 28714977 Free PMC article.

8

Polymorphic haplotypes of CRELD1 differentially predispose Down syndrome and euploids individuals to atrioventricular septal defect.

Ghosh P, Bhaumik P, Ghosh S, Ozbek U, Feingold E, Maslen C, Sarkar B, Pramanik V, Biswas P, Bandyopadhyay B, Dey SK. Ghosh P, et al. Among authors: sarkar b. Am J Med Genet A. 2012 Nov;158A(11):2843-8. doi: 10.1002/ajmg.a.35626. Epub 2012 Sep 14. Am J Med Genet A. 2012. PMID: 22987595

9

Evaluating intra-genetic variants of DJ-1 among Parkinson's disease patients of eastern India.

Sanyal J, Sarkar B, Banerjee TK, Mukherjee SC, Ray BC, Raghavendra Rao V. Sanyal J, et al. Among authors: sarkar b. Neurol Res. 2011 May;33(4):349-53. doi: 10.1179/016164110X12767786356679. Neurol Res. 2011. PMID: 21535932

10

Hb Tianshui (HBB: C.119A > G) in Compound Heterozygosity with Hb S (HBB: C.20A > T) from Odisha, India.

Meher S, Dehury S, Mohanty PK, Patel S, Pattanayak C, Bhattacharya S, Das K, Sarkar B. Meher S, et al. Among authors: sarkar b. Hemoglobin. 2016 Aug;40(4):270-2. doi: 10.1080/03630269.2016.1174873. Epub 2016 Jun 2. Hemoglobin. 2016. PMID: 27254408

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