Majumder P - Search Results

1

LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population.

Azmanov DN, Dimitrova S, Florez L, Cherninkova S, Draganov D, Morar B, Saat R, Juan M, Arostegui JI, Ganguly S, Soodyall H, Chakrabarti S, Padh H, López-Nevot MA, Chernodrinska V, Anguelov B, Majumder P, Angelova L, Kaneva R, Mackey DA, Tournev I, Kalaydjieva L. Azmanov DN, et al. Among authors: majumder p. Eur J Hum Genet. 2011 Mar;19(3):326-33. doi: 10.1038/ejhg.2010.181. Epub 2010 Nov 17. Eur J Hum Genet. 2011. PMID: 21081970 Free PMC article.

2

Genomic diversities and affinities among four endogamous groups of Punjab (India) based on autosomal and mitochondrial DNA polymorphisms.

Kaur I, Roy S, Chakrabarti S, Sarhadi VK, Majumder PP, Bhanwer AJ, Singh JR. Kaur I, et al. Among authors: majumder pp. Hum Biol. 2002 Dec;74(6):819-36. doi: 10.1353/hub.2003.0007. Hum Biol. 2002. PMID: 12617491

3

Globally, CYP1B1 mutations in primary congenital glaucoma are strongly structured by geographic and haplotype backgrounds.

Chakrabarti S, Kaur K, Kaur I, Mandal AK, Parikh RS, Thomas R, Majumder PP. Chakrabarti S, et al. Among authors: majumder pp. Invest Ophthalmol Vis Sci. 2006 Jan;47(1):43-7. doi: 10.1167/iovs.05-0912. Invest Ophthalmol Vis Sci. 2006. PMID: 16384942

4

A polymorphism in the CYP1B1 promoter is functionally associated with primary congenital glaucoma.

Chakrabarti S, Ghanekar Y, Kaur K, Kaur I, Mandal AK, Rao KN, Parikh RS, Thomas R, Majumder PP. Chakrabarti S, et al. Among authors: majumder pp. Hum Mol Genet. 2010 Oct 15;19(20):4083-90. doi: 10.1093/hmg/ddq309. Epub 2010 Jul 21. Hum Mol Genet. 2010. PMID: 20660114

5

Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India.

Pramanik S, Basu P, Gangopadhaya PK, Sinha KK, Jha DK, Sinha S, Das SK, Maity BK, Mukherjee SC, Roychoudhuri S, Majumder PP, Bhattacharyya NP. Pramanik S, et al. Among authors: majumder pp. Eur J Hum Genet. 2000 Sep;8(9):678-82. doi: 10.1038/sj.ejhg.5200515. Eur J Hum Genet. 2000. PMID: 10980573

6

OCA1 in different ethnic groups of india is primarily due to founder mutations in the tyrosinase gene.

Chaki M, Sengupta M, Mukhopadhyay A, Subba Rao I, Majumder PP, Das M, Samanta S, Ray K. Chaki M, et al. Among authors: majumder pp. Ann Hum Genet. 2006 Sep;70(Pt 5):623-30. doi: 10.1111/j.1469-1809.2006.00247.x. Ann Hum Genet. 2006. PMID: 16907708

7

Using HapMap data: a cautionary note.

Biswas NK, Dey B, Majumder PP. Biswas NK, et al. Among authors: majumder pp. Eur J Hum Genet. 2007 Feb;15(2):246-9. doi: 10.1038/sj.ejhg.5201743. Epub 2006 Nov 29. Eur J Hum Genet. 2007. PMID: 17133257

8

Human-specific insertion/deletion polymorphisms in Indian populations and their possible evolutionary implications.

Majumder PP, Roy B, Banerjee S, Chakraborty M, Dey B, Mukherjee N, Roy M, Thakurta PG, Sil SK. Majumder PP, et al. Eur J Hum Genet. 1999 May-Jun;7(4):435-46. doi: 10.1038/sj.ejhg.5200317. Eur J Hum Genet. 1999. PMID: 10352934

9

Genomic structures and population histories of linguistically distinct tribal groups of India.

Roychoudhury S, Roy S, Basu A, Banerjee R, Vishwanathan H, Usha Rani MV, Sil SK, Mitra M, Majumder PP. Roychoudhury S, et al. Among authors: majumder pp. Hum Genet. 2001 Sep;109(3):339-50. doi: 10.1007/s004390100577. Hum Genet. 2001. PMID: 11702215

10

Exome sequencing reveals the likely involvement of SOX10 in uveal melanoma.

Das D, Kaur I, Ali MJ, Biswas NK, Das S, Kumar S, Honavar SG, Maitra A, Chakrabarti S, Majumder PP. Das D, et al. Among authors: majumder pp. Optom Vis Sci. 2014 Jul;91(7):e185-92. doi: 10.1097/OPX.0000000000000309. Optom Vis Sci. 2014. PMID: 24927141

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