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Shahid Khan

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Atteeq Ur Rehman; Robert J Morell; Inna A Belyantseva; Shahid Y Khan; Erich T Boger; Mohsin Shahzad; Zubair M Ahmed; Saima Riazuddin; Shaheen N Khan; Sheikh Amer Riazuddin; Thomas B Friedman
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79.
A M Waryah; A Rehman; Zubair M Ahmed; Z-H Bashir; Shahid Y Khan; A U Zafar; Sheikh Amer Riazuddin; Thomas B Friedman; S Riazuddin
DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.
Sheikh Amer Riazuddin; Saima Anwar; Martin Fischer; Zubair M Ahmed; Shahid Y Khan; Audrey G H Janssen; Ahmad U Zafar; Ute Scholl; Tayyab Husnain; Inna A Belyantseva; Penelope L Friedman; Sheikh Riazuddin; Thomas B Friedman; Christoph Fahlke
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.

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All Publications

2010: Atteeq Ur Rehman; Robert J Morell; Inna A Belyantseva; Shahid Y Khan; Erich T Boger; Mohsin Shahzad; Zubair M Ahmed; Saima Riazuddin; Shaheen N Khan; Sheikh Amer Riazuddin; Thomas B Friedman
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79.
American journal of human genetics 2010;86(3):378-88.
2009: A M Waryah; A Rehman; Zubair M Ahmed; Z-H Bashir; Shahid Y Khan; A U Zafar; Sheikh Amer Riazuddin; Thomas B Friedman; S Riazuddin
DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.
Clinical genetics 2009;76(3):270-5.
2009: Sheikh Amer Riazuddin; Saima Anwar; Martin Fischer; Zubair M Ahmed; Shahid Y Khan; Audrey G H Janssen; Ahmad U Zafar; Ute Scholl; Tayyab Husnain; Inna A Belyantseva; Penelope L Friedman; Sheikh Riazuddin; Thomas B Friedman; Christoph Fahlke
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.
American journal of human genetics 2009;85(2):273-80.
2009: Saima Anwar; Saima Riazuddin; Zubair M Ahmed; Saba Tasneem; Shahid Y Khan; Andrew J Griffith; Thomas B Friedman; Sheikh Amer Riazuddin
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.
Journal of human genetics 2009;54(5):266-70.
2008: Zubair M Ahmed; Saber Masmoudi; Ersan Kalay; Inna A Belyantseva; Mohamed Ali Mosrati; Rob W J Collin; Saima Riazuddin; Mounira Hmani-Aifa; Hanka Venselaar; Mayya N Kawar; Abdelaziz Tlili; Bert van der Zwaag; Shahid Y Khan; Leila Ayadi; Sheikh Amer Riazuddin; Robert J Morell; Andrew J Griffith; Ilhem Charfedine; Refik Caylan; Jaap Oostrik; Ahmet Karaguzel; Abdelmonem Ghorbel; Sheikh Riazuddin; Thomas B Friedman; Hammadi Ayadi; Hannie Kremer
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
Nature genetics 2008;40(11):1335-40.
2007: Shahid Y Khan; Zubair M Ahmed; Muhammad I Shabbir; Shin-ichiro Kitajiri; Saeeda Kalsoom; Saba Tasneem; Sara Shayiq; Arabandi Ramesh; Srikumari Srisailpathy; Shaheen N Khan; Richard J H Smith; Sheikh Amer Riazuddin; Thomas B Friedman; Sheikh Riazuddin
Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus.
Human mutation 2007;28(5):417-23.
2007: Shahid Y Khan; Saima Riazuddin; Muhammad Tariq; Saima Anwar; Muhammad I Shabbir; Sheikh Amer Riazuddin; Shaheen N Khan; Tayyab Husnain; Zubair M Ahmed; Thomas B Friedman; Sheikh Riazuddin
Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3.
Human genetics 2007;120(6):789-93.
2006: Muhammad I Shabbir; Zubair M Ahmed; Shahid Y Khan; Sheikh Amer Riazuddin; A M Waryah; Shaheen N Khan; R D Camps; M Ghosh; M Kabra; Inna A Belyantseva; Thomas B Friedman; Sheikh Riazuddin
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
Journal of medical genetics 2006;43(8):634-40.
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.