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Fareeha Zulfiqar

Research Profile

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Pakistan

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Publications

TOP 3
Mounira Hmani-Aifa; Zeineb Benzina; Fareeha Zulfiqar; Houria Dhouib; Amber Shahzadi; Ali Ghorbel; Ahmed Rebaï; Peter Söderkvist; Sheikh Amer Riazuddin; William J Kimberling; Hammadi Ayadi
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.
Sheikh Amer Riazuddin; Sabiha Nazli; Zubair M Ahmed; Yi Yang; Fareeha Zulfiqar; Rehan S Shaikh; Ahmed U Zafar; Shaheen N Khan; Farooq Sabar; Fouzia T Javid; Edward R Wilcox; Ekaterini Tsilou; Erich T Boger; James R Sellers; Inna A Belyantseva; Sheikh Riazuddin; Thomas B Friedman
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; Sheikh Amer Riazuddin; Zahoor Ahmad; Raphael Caruso; Ian MacDonald; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene.

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All Publications

2009: Mounira Hmani-Aifa; Zeineb Benzina; Fareeha Zulfiqar; Houria Dhouib; Amber Shahzadi; Ali Ghorbel; Ahmed Rebaï; Peter Söderkvist; Sheikh Amer Riazuddin; William J Kimberling; Hammadi Ayadi
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.
European journal of human genetics : EJHG 2009;17(4):474-82.
2008: Sheikh Amer Riazuddin; Sabiha Nazli; Zubair M Ahmed; Yi Yang; Fareeha Zulfiqar; Rehan S Shaikh; Ahmed U Zafar; Shaheen N Khan; Farooq Sabar; Fouzia T Javid; Edward R Wilcox; Ekaterini Tsilou; Erich T Boger; James R Sellers; Inna A Belyantseva; Sheikh Riazuddin; Thomas B Friedman
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
Human mutation 2008;29(4):502-11.
2007: Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; Sheikh Amer Riazuddin; Zahoor Ahmad; Raphael Caruso; Ian MacDonald; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene.
Human genetics 2007;122(3-4):293-9.
2006: Sheikh Amer Riazuddin; Fareeha Zulfiqar; Qingjiong Zhang; Wenliang Yao; Shouling Li; Xiaodong Jiao; Amber Shahzadi; MUHAMMAD AMER; Muhammad Iqbal; Tayyab Hussnain; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Mutations in the gene encoding the alpha-subunit of rod phosphodiesterase in consanguineous Pakistani families.
Molecular vision 2006;12():1283-91.
2005: Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; Sheikh Amer Riazuddin; Radha Ayyagari; Farooq Sabar; Raphael Caruso; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4.
Human genetics 2005;118(3-4):356-65.
2005: Sheikh Amer Riazuddin; Fareeha Zulfiqar; Qingjiong Zhang; Yuri V Sergeev; Zaheeruddin A Qazi; Tayyab Husnain; Raphael Caruso; Sheikh Riazuddin; Paul Sieving; J Fielding Hejtmancik
Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
Investigative ophthalmology & visual science 2005;46(7):2264-70.
2005: Sheikh Amer Riazuddin; Afshan Yasmeen; Wenliang Yao; Yuri V Sergeev; Qingjiong Zhang; Fareeha Zulfiqar; Assad Riaz; Sheikh Riazuddin; J Fielding Hejtmancik
Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families.
Investigative ophthalmology & visual science 2005;46(6):2100-6.
2005: Qingjiong Zhang; Fareeha Zulfiqar; Sheikh Amer Riazuddin; Xueshan Xiao; Afshan Yasmeen; Peter K Rogan; Raphael Caruso; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.
Molecular vision 2005;11():977-85.
2004: Qingjiong Zhang; Fareeha Zulfiqar; Sheikh Amer Riazuddin; Xueshan Xiao; Zahoor Ahmad; Sheikh Riazuddin; J Fielding Hejtmancik
Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.
Molecular vision 2004;10():884-9.