Colah R - Search Results

1

A genome-wide search for non-UGT1A1 markers associated with unconjugated bilirubin level reveals significant association with a polymorphic marker near a gene of the nucleoporin family.

Datta S, Chowdhury A, Ghosh M, Das K, Jha P, Colah R, Mukerji M, Majumder PP. Datta S, et al. Among authors: colah r. Ann Hum Genet. 2012 Jan;76(1):33-41. doi: 10.1111/j.1469-1809.2011.00688.x. Epub 2011 Nov 28. Ann Hum Genet. 2012. PMID: 22118420

2

Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study.

Mohanty D, Colah RB, Gorakshakar AC, Patel RZ, Master DC, Mahanta J, Sharma SK, Chaudhari U, Ghosh M, Das S, Britt RP, Singh S, Ross C, Jagannathan L, Kaul R, Shukla DK, Muthuswamy V. Mohanty D, et al. Among authors: colah rb. J Community Genet. 2013 Jan;4(1):33-42. doi: 10.1007/s12687-012-0114-0. Epub 2012 Oct 21. J Community Genet. 2013. PMID: 23086467 Free PMC article.

3

Interaction of iron deficiency anemia and hemoglobinopathies among college students and pregnant women: a multi center evaluation in India.

Mohanty D, Gorakshakar AC, Colah RB, Patel RZ, Master DC, Mahanta J, Sharma SK, Chaudhari U, Ghosh M, Das S, Britt RP, Singh S, Ross C, Jagannathan L, Kaul R, Shukla DK, Muthuswamy V. Mohanty D, et al. Among authors: colah rb. Hemoglobin. 2014;38(4):252-7. doi: 10.3109/03630269.2014.913517. Hemoglobin. 2014. PMID: 25023086

4

Guidelines for screening, diagnosis and management of hemoglobinopathies.

Ghosh K, Colah R, Manglani M, Choudhry VP, Verma I, Madan N, Saxena R, Jain D, Marwaha N, Das R, Mohanty D, Choudhary R, Agarwal S, Ghosh M, Ross C. Ghosh K, et al. Among authors: colah r. Indian J Hum Genet. 2014 Apr;20(2):101-19. doi: 10.4103/0971-6866.142841. Indian J Hum Genet. 2014. PMID: 25400338 Free PMC article. Review.

5

Genetic Variations in Bilirubin Metabolism Genes and Their Association with Unconjugated Hyperbilirubinemia in Adults.

Chiddarwar AS, D'Silva SZ, Colah RB, Ghosh K, Mukherjee MB. Chiddarwar AS, et al. Ann Hum Genet. 2017 Jan;81(1):11-19. doi: 10.1111/ahg.12179. Epub 2016 Dec 12. Ann Hum Genet. 2017. PMID: 27943244

6

A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India.

Chalvam R, Kedar PS, Colah RB, Ghosh K, Mukherjee MB. Chalvam R, et al. Among authors: colah rb. J Hum Genet. 2008;53(2):181-184. doi: 10.1007/s10038-007-0225-3. Epub 2007 Nov 28. J Hum Genet. 2008. PMID: 18043863

7

The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies.

Italia KY, Jijina FF, Jain D, Merchant R, Nadkarni AH, Mukherjee M, Ghosh K, Colah RB. Italia KY, et al. Among authors: colah rb. Clin Biochem. 2010 Nov;43(16-17):1329-32. doi: 10.1016/j.clinbiochem.2010.08.006. Epub 2010 Aug 13. Clin Biochem. 2010. PMID: 20709051

8

UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults.

D'Silva S, Colah RB, Ghosh K, Mukherjee MB. D'Silva S, et al. Gene. 2013 Jan 15;513(1):36-9. doi: 10.1016/j.gene.2012.10.081. Epub 2012 Nov 9. Gene. 2013. PMID: 23147267

9

Clinical and molecular characterization of Hb Hofu in eastern India.

Purohit P, Mashon RS, Patel S, Dehury S, Pattanayak C, Das K, Nair S, Italia K, Bag S, Colah R, Patel DK. Purohit P, et al. Among authors: colah r. Int J Lab Hematol. 2014 Feb;36(1):71-6. doi: 10.1111/ijlh.12128. Epub 2013 Jul 25. Int J Lab Hematol. 2014. PMID: 23889802

10

Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates.

D'Silva S, Colah RB, Ghosh K, Mukherjee MB. D'Silva S, et al. Gene. 2014 Aug 15;547(1):18-22. doi: 10.1016/j.gene.2014.05.047. Epub 2014 May 24. Gene. 2014. PMID: 24865931

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