Kakar N - Search Results

1

Missense mutations (p.H371Y, p.D438Y) in gene CHEK2 are associated with breast cancer risk in women of Balochistan origin.

Baloch AH, Daud S, Raheem N, Luqman M, Ahmad A, Rehman A, Shuja J, Rasheed S, Ali A, Kakar N, Naseeb HK, Mengal MA, Awan MA, Wasim M, Baloch DM, Ahmad J. Baloch AH, et al. Among authors: kakar n. Mol Biol Rep. 2014 Feb;41(2):1103-7. doi: 10.1007/s11033-013-2956-x. Epub 2014 Jan 4. Mol Biol Rep. 2014. PMID: 24390236

2

Prevalence of hepatitis C virus (HCV) genotypes in Balochistan.

Afridi S, Naeem M, Hussain A, Kakar N, Babar ME, Ahmad J. Afridi S, et al. Among authors: kakar n. Mol Biol Rep. 2009 Jul;36(6):1511-4. doi: 10.1007/s11033-008-9342-0. Epub 2008 Sep 3. Mol Biol Rep. 2009. PMID: 18766467

3

A novel HSF4 gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan.

Sajjad N, Goebel I, Kakar N, Cheema AM, Kubisch C, Ahmad J. Sajjad N, et al. Among authors: kakar n. BMC Med Genet. 2008 Nov 11;9:99. doi: 10.1186/1471-2350-9-99. BMC Med Genet. 2008. PMID: 19014451 Free PMC article.

4

Epidemiology of Van der Woude syndrome from mutational analyses in affected patients from Pakistan.

Malik S, Kakar N, Hasnain S, Ahmad J, Wilcox ER, Naz S. Malik S, et al. Among authors: kakar n. Clin Genet. 2010 Sep;78(3):247-56. doi: 10.1111/j.1399-0004.2010.01375.x. Epub 2010 Feb 10. Clin Genet. 2010. PMID: 20184620

5

An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group.

Borck G, Kakar N, Hoch J, Friedrich K, Freudenberg J, Nürnberg G, Yilmaz R, Daud S, Baloch DM, Nürnberg P, Oldenburg J, Ahmad J, Kubisch C. Borck G, et al. Among authors: kakar n. Hum Genet. 2012 Feb;131(2):209-16. doi: 10.1007/s00439-011-1062-1. Epub 2011 Jul 15. Hum Genet. 2012. PMID: 21761136

6

Identification of a novel LCA5 mutation in a Pakistani family with Leber congenital amaurosis and cataracts.

Ahmad A, Daud S, Kakar N, Nürnberg G, Nürnberg P, Babar ME, Thoenes M, Kubisch C, Ahmad J, Bolz HJ. Ahmad A, et al. Among authors: kakar n. Mol Vis. 2011;17:1940-5. Epub 2011 Jul 16. Mol Vis. 2011. PMID: 21850168 Free PMC article.

7

A missense mutation (p.G274R) in gene ASPA causes Canavan disease in a Pakistani family.

Hussain R, Daud S, Kakar N, Ahmad A, Baloch AH, Tareen AM, Kakar MA, Ahmad J. Hussain R, et al. Among authors: kakar ma, kakar n. Mol Biol Rep. 2012 May;39(5):6197-201. doi: 10.1007/s11033-011-1438-2. Epub 2012 Jan 5. Mol Biol Rep. 2012. PMID: 22219087

8

Detection of BRCA1/2 mutations in breast cancer patients from Thailand and Pakistan.

Ahmad J, Le Calvez-Kelm F, Daud S, Voegele C, Vallée M, Ahmad A, Kakar N, McKay JD, Gaborieau V, Léoné M, Sinilnikova O, Sangrajrang S, Tavtigian SV, Lesueur F. Ahmad J, et al. Among authors: kakar n. Clin Genet. 2012 Dec;82(6):594-8. doi: 10.1111/j.1399-0004.2012.01869.x. Epub 2012 Apr 8. Clin Genet. 2012. PMID: 22486713 No abstract available.

9

A homozygous splice site mutation in TRAPPC9 causes intellectual disability and microcephaly.

Kakar N, Goebel I, Daud S, Nürnberg G, Agha N, Ahmad A, Nürnberg P, Kubisch C, Ahmad J, Borck G. Kakar N, et al. Eur J Med Genet. 2012 Dec;55(12):727-31. doi: 10.1016/j.ejmg.2012.08.010. Epub 2012 Aug 30. Eur J Med Genet. 2012. PMID: 22989526

10

Various aspects, patterns and risk factors in breast cancer patients of Balochistan.

Baloch AH, Shuja J, Daud S, Ahmed M, Ahmad A, Tareen M, Khan F, Kakar MA, Baloch DM, Kakar N, Naseeb HK, Ahmad J. Baloch AH, et al. Among authors: kakar ma, kakar n. Asian Pac J Cancer Prev. 2012;13(8):4013-6. doi: 10.7314/apjcp.2012.13.8.4013. Asian Pac J Cancer Prev. 2012. PMID: 23098509 Free article.

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