Jayandharan GR - Search Results

1

Mutations in coagulation factor XIII A gene in eight unrelated Indians. Five novel mutations identified by a novel PCR-CSGE approach.

Jayandharan GR, Viswabandya A, Baidya S, Nair SC, George B, Mathews V, Chandy M, Srivastava A. Jayandharan GR, et al. Thromb Haemost. 2006 Mar;95(3):551-6. doi: 10.1160/TH05-09-0617. Thromb Haemost. 2006. PMID: 16525586

2

Molecular basis of Bernard-Soulier syndrome in 27 patients from India.

Sumitha E, Jayandharan GR, David S, Jacob RR, Sankari Devi G, Bargavi B, Shenbagapriya S, Nair SC, Abraham A, George B, Viswabandya A, Mathews V, Chandy M, Srivastava A. Sumitha E, et al. Among authors: jayandharan gr. J Thromb Haemost. 2011 Aug;9(8):1590-8. doi: 10.1111/j.1538-7836.2011.04417.x. J Thromb Haemost. 2011. PMID: 21699652 Free article.

3

Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India.

Jayandharan GR, Shaji RV, Baidya S, Nair SC, Chandy M, Srivastava A. Jayandharan GR, et al. Thromb Haemost. 2005 Oct;94(4):883-6. Thromb Haemost. 2005. PMID: 16270648 No abstract available.

4

Molecular basis of hereditary factor VII deficiency in India: five novel mutations including a double missense mutation (Ala191Glu; Trp364Cys) in 11 unrelated patients.

Jayandharan GR, Viswabandya A, Nair SC, Chandy M, Srivastava A. Jayandharan GR, et al. Haematologica. 2007 Jul;92(7):1002-3. doi: 10.3324/haematol.10835. Haematologica. 2007. PMID: 17606459 Free article.

5

Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.

Jayandharan G, Viswabandya A, Baidya S, Nair SC, Shaji RV, Chandy M, Srivastava A. Jayandharan G, et al. J Thromb Haemost. 2005 Jul;3(7):1446-53. doi: 10.1111/j.1538-7836.2005.01402.x. J Thromb Haemost. 2005. PMID: 15892853 Free article.

6

Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin.

Jayandharan G, Viswabandya A, Baidya S, Nair SC, Shaji RV, George B, Chandy M, Srivastava A. Jayandharan G, et al. J Thromb Haemost. 2005 Jul;3(7):1482-7. doi: 10.1111/j.1538-7836.2005.01339.x. Epub 2005 May 9. J Thromb Haemost. 2005. PMID: 15892863 Free article.

7

Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.

Jayandharan G, Shaji RV, Baidya S, Nair SC, Chandy M, Srivastava A. Jayandharan G, et al. Haemophilia. 2005 Sep;11(5):481-91. doi: 10.1111/j.1365-2516.2005.01121.x. Haemophilia. 2005. PMID: 16128892

8

Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India.

Jayandharan G, Spreafico M, Viswabandya A, Chandy M, Srivastava A, Peyvandi F. Jayandharan G, et al. Haemophilia. 2007 Jul;13(4):413-9. doi: 10.1111/j.1365-2516.2007.01477.x. Haemophilia. 2007. PMID: 17610559

9

Polymorphism in factor VII gene modifies phenotype of severe haemophilia.

Jayandharan GR, Nair SC, Poonnoose PM, Thomas R, John J, Keshav SK, Cherian RS, Devadarishini M, Lakshmi KM, Shaji RV, Viswabandya A, George B, Mathews V, Chandy M, Srivastava A. Jayandharan GR, et al. Haemophilia. 2009 Nov;15(6):1228-36. doi: 10.1111/j.1365-2516.2009.02080.x. Epub 2009 Aug 16. Haemophilia. 2009. PMID: 19686262

10

Molecular basis of hereditary factor V deficiency in India: identification of four novel mutations and their genotype-phenotype correlation.

Chapla A, Jayandharan GR, Sumitha E, Sankari Devi G, Shenbagapriya P, Nair SC, Viswabandya A, George B, Mathews V, Srivastava A. Chapla A, et al. Among authors: jayandharan gr. Thromb Haemost. 2011 Jun;105(6):1120-3. doi: 10.1160/TH10-11-0767. Epub 2011 Apr 20. Thromb Haemost. 2011. PMID: 21647534 No abstract available.

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