FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Zubair Ahmed

Research Profile

Concepts & Ideas

Disorders

Genes & Molecular Sequences

Physiology

Living Beings

Geographic Areas

Pakistan

Chemicals & Drugs

Procedures

Co-author Network

Publications

TOP 3
Tasleem Kausar; Sobia Sadia; Rehan S Shaikh; Nabeela Tariq; Muhammad Ali; Thomas J Jaworek; Zubair M Ahmed
Genetic studies of TYRP1 and SLC45A2 in Pakistani patients with nonsyndromic oculocutaneous albinism.
Thomas J Jaworek; Shaheen N Khan; Noreen Latief; Saima Riazuddin; Rashid Bhatti; Zubair M Ahmed
USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.
Robert B Hufnagel; Zubair M Ahmed; Zélia M Corrêa; Robert A Sisk
Gene therapy for Leber congenital amaurosis: advances and future directions.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Zubair Ahmed (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Tasleem Kausar; Sobia Sadia; Rehan S Shaikh; Nabeela Tariq; Muhammad Ali; Thomas J Jaworek; Zubair M Ahmed
Genetic studies of TYRP1 and SLC45A2 in Pakistani patients with nonsyndromic oculocutaneous albinism.
The Journal of investigative dermatology 2013;133(4):1099-102.
2012: Thomas J Jaworek; Shaheen N Khan; Noreen Latief; Saima Riazuddin; Rashid Bhatti; Zubair M Ahmed
USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.
Journal of human genetics 2012;57(10):633-7.
2012: Robert B Hufnagel; Zubair M Ahmed; Zélia M Corrêa; Robert A Sisk
Gene therapy for Leber congenital amaurosis: advances and future directions.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 2012;250(8):1117-28.
2012: Thomas J Jaworek; Tasleem Kausar; Muhammad Imran Maqsood; Shafqat Rasool; Saima Riazuddin; Rehan S Shaikh; Asma Sohail; Nabeela Tariq; Muhmmmad Ali; Shannon M Bell; Furhan Iqbal; Zubair M Ahmed
Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population.
Orphanet journal of rare diseases 2012;7():44.
2011: Atteeq U Rehman; Saima Riazuddin; Sheikh Amer Riazuddin; Mohsin Shahzad; Wasim Ahmad; Zubair M Ahmed; Rana A Ali; Paula B Andrade; Carmen C Brewer; Khitab Gul; Ateeq-Ul Jaleel; Saadullah Khan; Shaheen N Khan; Suzanne M Leal; Kwanghyuk Lee; Robert J Morell; Thomas B Friedman
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p.
Human genetics 2011;130(6):759-65.
2011: Julie M Schultz; Ekaterini T Tsilou; Amy Turriff; Christopher K Zalewski; Wadih M Zein; Nazir Ahmad; Zubair M Ahmed; Rashid Bhatti; Carmen C Brewer; Manju Ghosh; Andrew J Griffith; Zawar Hussain; Shaheen N Kahn; Kelly A King; Xue Zhong Liu; Anne C Madeo; Meira R Meltzer; Murali Munisamy; Julie A Muskett; Muhammad Qasim; Heidi L Rehm; Sheikh Amer Riazuddin; Saima Riazuddin; Thomas B Friedman
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.
Journal of medical genetics 2011;48(11):767-75.
2011: Ali M Waryah; Munir A Bhinder; Mohsin Shahzad; Robert A Sisk; Zubair M Ahmed; Munir A Binder; Daniel I Choo; Thomas B Friedman; Shaheen N Khan; Sheikh Amer Riazuddin; Saima Riazuddin
Molecular and clinical studies of X-linked deafness among Pakistani families.
Journal of human genetics 2011;56(7):534-40.
2011: Zubair M Ahmed; Rizwan Yousaf; Byung Cheon Lee; Shaheen N Khan; Sue Lee; Kwanghyuk Lee; Tayyab Husnain; Atteeq Ur Rehman; Sarah Bonneux; Muhammad Ansar; Wasim Ahmad; Suzanne M Leal; Vadim N Gladyshev; Inna A Belyantseva; Guy Van Camp; Sheikh Amer Riazuddin; Thomas B Friedman; Saima Riazuddin
Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.
American journal of human genetics 2011;88(1):19-29.
2011: Thomas B Friedman; Julie M Schultz; Zubair M Ahmed; Ekaterini T Tsilou; Carmen C Brewer
Usher syndrome: hearing loss with vision loss.
Advances in oto-rhino-laryngology 2011;70():56-65.
2011: Saima Riazuddin; Zubair M Ahmed; Rashmi S Hegde; Shaheen N Khan; Idrees Nasir; Uzma Shaukat; Sheikh Amer Riazuddin; John A Butman; Andrew J Griffith; Thomas B Friedman; Byung Yoon Choi
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome.
BMC medical genetics 2011;12():21.
2010: Sheikh Amer Riazuddin; Amber Shahzadi; Christina Zeitz; Zubair M Ahmed; Radha Ayyagari; Venkata R M Chavali; Virgilio G Ponferrada; Isabelle Audo; Christelle Michiels; Marie-Elise Lancelot; Idrees A Nasir; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Xiaodong Jiao; Ian M MacDonald; Sheikh Riazuddin; Paul Sieving; Nicholas Katsanis; J Fielding Hejtmancik
A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.
American journal of human genetics 2010;87(4):523-31.
2010: Shin-ichiro Kitajiri; Takeshi Sakamoto; Inna A Belyantseva; Richard J Goodyear; Ruben Stepanyan; Ikuko Fujiwara; Jonathan E Bird; Sheikh Amer Riazuddin; Sheikh Riazuddin; Zubair M Ahmed; Jenny E Hinshaw; James Sellers; James R Bartles; John A Hammer; Guy P Richardson; Andrew J Griffith; Gregory I Frolenkov; Thomas B Friedman
Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearing.
Cell 2010;141(5):786-98.
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.
2010: Shahid Yar Khan; Sheikh Amer Riazuddin; Mohsin Shahzad; Nazir Ahmed; Ahmad Usman Zafar; Atteeq Ur Rehman; Robert J Morell; Andrew J Griffith; Zubair M Ahmed; Sheikh Riazuddin; Thomas B Friedman
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3.
European journal of human genetics : EJHG 2010;18(1):125-9.
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: Julie M Schultz; Shaheen N Khan; Zubair M Ahmed; Saima Riazuddin; Ali M Waryah; Dhananjay Chhatre; Matthew F Starost; Barbara Ploplis; Stephanie Buckley; David Velásquez; Madhulika Kabra; Kwanghyuk Lee; Muhammad J Hassan; Ghazanfar Ali; Muhammad Ansar; Manju Ghosh; Edward R Wilcox; Wasim Ahmad; Glenn Merlino; Suzanne M Leal; Sheikh Amer Riazuddin; Thomas B Friedman; Robert J Morell
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
American journal of human genetics 2009;85(1):25-39.
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.
2009: Zubair M Ahmed; Sheikh Amer Riazuddin; Shaheen N Khan; P L Friedman; S Riazuddin; Thomas B Friedman
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
Clinical genetics 2009;75(1):86-91.
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.
2008: Zubair M Ahmed; Saima Riazuddin; Sandar Aye; Rana A Ali; Hanka Venselaar; Saima Anwar; Polina P Belyantseva; Muhammad Qasim; Sheikh Amer Riazuddin; Thomas B Friedman
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.
Human genetics 2008;124(3):215-23.
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.
2008: Zubair M Ahmed; Sten Kjellstrom; Ricky J L Haywood-Watson; Ronald A Bush; Lori L Hampton; James F Battey; Saima Riazuddin; Gregory Frolenkov; Paul Sieving; Thomas B Friedman
Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration.
Molecular vision 2008;14():2227-36.
2008: Rob W J Collin; Ersan Kalay; Muhammad Tariq; Theo Peters; Bert van der Zwaag; Hanka Venselaar; Jaap Oostrik; Kwanghyuk Lee; Zubair M Ahmed; Refik Caylan; Yun Li; Henk A Spierenburg; Erol Eyupoglu; Angelien Heister; Saima Riazuddin; Elif Bahat; Muhammad Ansar; Selcuk Arslan; Bernd Wollnik; Han G Brunner; Cor W R J Cremers; Ahmet Karaguzel; Wasim Ahmad; Frans P M Cremers; Gert Vriend; Thomas B Friedman; Sheikh Amer Riazuddin; Suzanne M Leal; Hannie Kremer
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.
American journal of human genetics 2008;82(1):125-38.
2007: Shin-ichiro Kitajiri; R McNamara; Tomoko Makishima; Tayyab Husnain; A U Zafar; Rick Kittles; Zubair M Ahmed; Thomas B Friedman; Sheikh Amer Riazuddin; Andrew J Griffith
Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan.
Clinical genetics 2007;72(6):546-50.
2007: Quratul Ain; Sabiha Nazli; Saima Riazuddin; Ateeq-ul Jaleel; Sheikh Amer Riazuddin; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Andrew J Griffith; Zubair M Ahmed; Thomas B Friedman; Sheikh Riazuddin
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3.
Human genetics 2007;122(5):445-50.
2007: Annie Rebibo-Sabbah; Igor Nudelman; Zubair M Ahmed; Timor Baasov; Tamar Ben-Yosef
In vitro and ex vivo suppression by aminoglycosides of PCDH15 nonsense mutations underlying type 1 Usher syndrome.
Human genetics 2007;122(3-4):373-81.
2007: Nevra Nal; Zubair M Ahmed; Engin Erkal; Özgül M Alper; Güven Lüleci; Oktay Dinç; Ali Muhammad Waryah; Quratul Ain; Saba Tasneem; Tayyab Husnain; Parna Chattaraj; Sheikh Amer Riazuddin; Erich T Boger; Manju Ghosh; Madhulika Kabra; Sheikh Riazuddin; Robert J Morell; Thomas B Friedman
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.
Human mutation 2007;28(10):1014-9.
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: Ronna Hertzano; Amiel A Dror; Mireille Montcouquiol; Zubair M Ahmed; Buffy Ellsworth; Sally A Camper; Thomas B Friedman; Matthew W Kelley; Karen B Avraham
Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system.
The European journal of neuroscience 2007;25(4):999-1005.
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: Sheikh Amer Riazuddin; Zubair M Ahmed; Alan S Fanning; Ayala Lagziel; Shin-ichiro Kitajiri; Khushnooda Ramzan; Shaheen N Khan; Parna Chattaraj; Penelope L Friedman; James M Anderson; Inna A Belyantseva; Andrew Forge; Sheikh Riazuddin; Thomas B Friedman
Tricellulin is a tight-junction protein necessary for hearing.
American journal of human genetics 2006;79(6):1040-51.
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.
2006: Ricky J L Haywood-Watson; Zubair M Ahmed; Sten Kjellstrom; Ronald A Bush; Yuichiro Takada; Lori L Hampton; James F Battey; Paul Sieving; Thomas B Friedman
Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts.
Investigative ophthalmology & visual science 2006;47(7):3074-84.
2006: Zubair M Ahmed; Richard J Goodyear; Sheikh Amer Riazuddin; Ayala Lagziel; P Kevin Legan; Martine Behra; Shawn M Burgess; Kathryn S Lilley; Edward R Wilcox; Sheikh Riazuddin; Andrew J Griffith; Gregory I Frolenkov; Inna A Belyantseva; Guy P Richardson; Thomas B Friedman
The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2006;26(26):7022-34.
2006: Sheikh Amer Riazuddin; Shaheen N Khan; Zubair M Ahmed; Manju Ghosh; Kyle Caution; Sabiha Nazli; Madhulika Kabra; Ahmad U Zafar; Kevin Chen; Sadaf Naz; Anthony Antonellis; William J Pavan; Eric Green; Edward R Wilcox; Penelope L Friedman; Robert J Morell; Sheikh Riazuddin; Thomas B Friedman
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness.
American journal of human genetics 2006;78(1):137-43.
2005: Thomas B Friedman; Julie M Schultz; Zubair M Ahmed
Usher syndrome type 1: genotype-phenotype relationships.
Retina (Philadelphia, Pa.) 2005;25(8 Suppl):S40-S42.
2005: Rehan Sadiq Shaikh; Khushnooda Ramzan; Sabiha Nazli; Sameera Sattar; Shaheen N Khan; Sheikh Amer Riazuddin; Zubair M Ahmed; Thomas B Friedman; Sheikh Riazuddin
A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12.
American journal of medical genetics. Part A 2005;138(4):392-5.
2005: Ayala Lagziel; Zubair M Ahmed; Julie M Schultz; Robert J Morell; Inna A Belyantseva; Thomas B Friedman
Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development.
Developmental biology 2005;280(2):295-306.
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: Inna A Belyantseva; Erich T Boger; Sadaf Naz; Gregory I Frolenkov; James R Sellers; Zubair M Ahmed; Andrew J Griffith; Thomas B Friedman
Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia.
Nature cell biology 2005;7(2):148-56.
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.
2004: Zubair M Ahmed; Xiaoyan Cindy Li; Shontell D Powell; Sheikh Amer Riazuddin; Terry-Lynn Young; Khushnooda Ramzan; Zahoor Ahmad; Sandra Luscombe; Kiran Dhillon; Linda MacLaren; Barbara Ploplis; Lawrence I Shotland; Elizabeth Ives; Sheikh Riazuddin; Thomas B Friedman; Robert J Morell; Edward R Wilcox
Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan.
BMC medical genetics 2004;5():24.
2004: Saidi Mohiddin; Zubair M Ahmed; Andrew J Griffith; Dorothy J Tripodi; Thomas B Friedman; Lameh Fananapazir; Robert J Morell
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6).
Journal of medical genetics 2004;41(4):309-14.
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.
2003: Thomas B Friedman; Julie M Schultz; Tamar Ben-Yosef; Shannon P Pryor; Ayala Lagziel; Rachel A Fisher; Edward R Wilcox; Sheikh Amer Riazuddin; Zubair M Ahmed; Inna A Belyantseva; Andrew J Griffith
Recent advances in the understanding of syndromic forms of hearing loss.
Ear and hearing 2003;24(4):289-302.
2003: Zubair M Ahmed; Sheikh Amer Riazuddin; S Riazuddin; Edward R Wilcox
The molecular genetics of Usher syndrome.
Clinical genetics 2003;63(6):431-44.
2003: Zubair M Ahmed; Robert J Morell; Sheikh Amer Riazuddin; Andrea Gropman; Shahzad Shaukat; Mussaber M Ahmad; Saidi Mohiddin; Lameh Fananapazir; Rafael C Caruso; Tayyab Husnain; Shaheen N Khan; Sheikh Riazuddin; Andrew J Griffith; Thomas B Friedman; Edward R Wilcox
Mutations of MYO6 are associated with recessive deafness, DFNB37.
American journal of human genetics 2003;72(5):1315-22.
2003: Tamar Ben-Yosef; Seth L Ness; Anne C Madeo; Adi Bar-Lev; Jessica H Wolfman; Zubair M Ahmed; Robert J Desnick; Judith P Willner; Karen B Avraham; Harry Ostrer; Carole Oddoux; Andrew J Griffith; Thomas B Friedman
A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome.
The New England journal of medicine 2003;348(17):1664-70.
2002: Zubair M Ahmed; Tenesha N Smith; Sheikh Amer Riazuddin; Tomoko Makishima; Manju Ghosh; Sirosh Bokhari; P S N Menon; Dilip Deshmukh; Andrew J Griffith; Sheikh Riazuddin; Thomas B Friedman; Edward R Wilcox
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.
Human genetics 2002;110(6):527-31.
2002: Kiyoto Kurima; Linda M Peters; Yandan Yang; Sheikh Amer Riazuddin; Zubair M Ahmed; Sadaf Naz; Deidre Arnaud; Stacy Drury; Jianhong Mo; Tomoko Makishima; Manju Ghosh; P S N Menon; Dilip Deshmukh; Carole Oddoux; Harry Ostrer; Shaheen Khan; Sheikh Riazuddin; Prescott L Deininger; Lori L Hampton; Susan L Sullivan; James F Battey; Bronya J B Keats; Edward R Wilcox; Thomas B Friedman; Andrew J Griffith
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Nature genetics 2002;30(3):277-84.
2002: Sheikh Amer Riazuddin; Zubair M Ahmed; Thomas B Friedman; Andrew J Griffith; Sheikh Riazuddin; Edward R Wilcox
Genetic modifiers of hereditary hearing loss.
Advances in oto-rhino-laryngology 2002;61():224-9.
2002: Zubair M Ahmed; Sheikh Amer Riazuddin; Thomas B Friedman; Sheikh Riazuddin; Edward R Wilcox; Andrew J Griffith
Clinical manifestations of DFNB29 deafness.
Advances in oto-rhino-laryngology 2002;61():156-60.
2001: NA Liburd; Manju Ghosh; S Riazuddin; Sadaf Naz; S Khan; Zubair M Ahmed; Sheikh Amer Riazuddin; Y Liang; P S N Menon; T Smith; A C Smith; Ken-Shiung Chen; James R Lupski; Edward R Wilcox; L Potocki; Thomas B Friedman
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.
Human genetics 2001;109(5):535-41.
2001: Z M Ahmed; Sheikh Amer Riazuddin; Steven L Bernstein; Zubair M Ahmed; Shaheen Khan; Andrew J Griffith; Robert J Morell; Thomas B Friedman; S Riazuddin; Edward R Wilcox
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
American journal of human genetics 2001;69(1):25-34.
2001: Tamar Ben-Yosef; Marie Wattenhofer; S Riazuddin; Z M Ahmed; Hamish Scott; Jun Kudoh; Kazunori Shibuya; Stylianos E Antonarakis; Batsheva Bonne-Tamir; Uppala Radhakrishna; Sadaf Naz; Zubair M Ahmed; Sheikh Amer Riazuddin; Arti Pandya; Walter E Nance; Edward R Wilcox; Thomas B Friedman; Robert J Morell
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness.
Journal of medical genetics 2001;38(6):396-400.
2001: Julie M Bork; Linda M Peters; S Riazuddin; Steven L Bernstein; Z M Ahmed; Seth L Ness; R Polomeno; Arabandi Ramesh; M Schloss; C R Srisailpathy; S Wayne; S Bellman; D Desmukh; Zubair M Ahmed; Shaheen N Khan; V M Kaloustian; XC Li; Anil K Lalwani; Sheikh Amer Riazuddin; Maria Bitner-Glindzicz; Walter E Nance; Xue Zhong Liu; G Wistow; Richard J H Smith; Andrew J Griffith; Edward R Wilcox; Thomas B Friedman; Robert J Morell
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
American journal of human genetics 2001;68(1):26-37.
2000: Sheikh Amer Riazuddin; Caley M Castelein; Zubair M Ahmed; Anil K Lalwani; Mary Ann Mastroianni; Sadaf Naz; Tenesha N Smith; NA Liburd; Thomas B Friedman; Andrew J Griffith; S Riazuddin; Edward R Wilcox
Dominant modifier DFNM1 suppresses recessive deafness DFNB26.
Nature genetics 2000;26(4):431-4.