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Jamil Ahmad

Research Profile

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Recessive Genes

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Publications

TOP 3
Sarwat Afridi; Muhammad Naeem; Abid Hussain; Naseebullah Kakar; Masroor Ellahi Babar; Jamil Ahmad
Prevalence of hepatitis C virus (HCV) genotypes in Balochistan.
M E Babar; A Farid; B F Benkel; Jamil Ahmad; A Nadeem; M Imran
Frequencies of PrP genotypes and their implication for breeding against scrapie susceptibility in nine Pakistani sheep breeds.
M E Babar; A Farid; B F Benkel; Jamil Ahmad; I A Sajid; M Imran; T Hussain; A Nadeem
Genetic variability at seven codons of the prion protein gene in nine Pakistani sheep breeds.

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All Publications

2009: Sarwat Afridi; Muhammad Naeem; Abid Hussain; Naseebullah Kakar; Masroor Ellahi Babar; Jamil Ahmad
Prevalence of hepatitis C virus (HCV) genotypes in Balochistan.
Molecular biology reports 2009;36(6):1511-4.
2009: M E Babar; A Farid; B F Benkel; Jamil Ahmad; A Nadeem; M Imran
Frequencies of PrP genotypes and their implication for breeding against scrapie susceptibility in nine Pakistani sheep breeds.
Molecular biology reports 2009;36(3):561-5.
2008: M E Babar; A Farid; B F Benkel; Jamil Ahmad; I A Sajid; M Imran; T Hussain; A Nadeem
Genetic variability at seven codons of the prion protein gene in nine Pakistani sheep breeds.
Journal of genetics 2008;87(2):187-90.
2008: Naheed Sajjad; Ingrid Goebel; Naseebullah Kakar; Abdul Majeed Cheema; Christian Kubisch; Jamil Ahmad
A novel HSF4 gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan.
BMC medical genetics 2008;9():99.
2005: Naveeda Riaz; Stacy Steinberg; Jamil Ahmad; Anna Pluzhnikov; Sheikh Amer Riazuddin; Nancy J Cox; Dennis Drayna
Genomewide significant linkage to stuttering on chromosome 12.
American journal of human genetics 2005;76(4):647-51.
2005: Jamil Ahmad; Shaheen N Khan; Shahid Y Khan; Khushnooda Ramzan; Sheikh Amer Riazuddin; Zubair M Ahmed; Edward R Wilcox; Thomas B Friedman; Sheikh Riazuddin
DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1.
Human genetics 2005;116(5):407-12.
2005: Khushnooda Ramzan; Rehan S Shaikh; Jamil Ahmad; Shaheen N Khan; Sheikh Amer Riazuddin; Zubair M Ahmed; Thomas B Friedman; Edward R Wilcox; Sheikh Riazuddin
A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1.
Human genetics 2005;116(1-2):17-22.
2003: Zubair M Ahmed; Sheikh Amer Riazuddin; Jamil Ahmad; Steven L Bernstein; Yan Guo; Muhammad F Sabar; Paul Sieving; Sheikh Riazuddin; Andrew J Griffith; Thomas B Friedman; Inna A Belyantseva; Edward R Wilcox
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23.
Human molecular genetics 2003;12(24):3215-23.