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Edward Wilcox

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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.
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.
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.

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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.
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.
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: 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.
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: Sadaf Naz; Andrew J Griffith; S Riazuddin; Lori L Hampton; James F Battey; Shaheen N Khan; Sheikh Amer Riazuddin; Edward R Wilcox; Thomas B Friedman
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction.
Journal of medical genetics 2004;41(8):591-5.
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: Tamar Ben-Yosef; Inna A Belyantseva; Thomas L Saunders; Elizabeth D Hughes; Kohei Kawamoto; Christina M Van Itallie; Lisa A Beyer; Kärin Halsey; Donald J Gardner; Edward R Wilcox; Julia Rasmussen; James M Anderson; David F Dolan; Andrew Forge; Yehoash Raphael; Sally A Camper; Thomas B Friedman
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.
Human molecular genetics 2003;12(16):2049-61.
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: Sadaf Naz; F Alasti; Alireza Mowjoodi; Sheikh Amer Riazuddin; Mohammad Hossein Sanati; Thomas B Friedman; Andrew J Griffith; Edward R Wilcox; S Riazuddin
Distinctive audiometric profile associated with DFNB21 alleles of TECTA.
Journal of medical genetics 2003;40(5):360-3.
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: H-J Park; S Shaukat; Xue Zhong Liu; S H Hahn; Sadaf Naz; M Ghosh; H-N Kim; S-K Moon; S Abe; K Tukamoto; S Riazuddin; M Kabra; Raadnabazar Erdenetungalag; J Radnaabazar; S Khan; Arti Pandya; S-I Usami; Walter E Nance; Edward R Wilcox; Sheikh Amer Riazuddin; Andrew J Griffith
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.
Journal of medical genetics 2003;40(4):242-8.
2002: Sadaf Naz; Chantal M Giguere; David C Kohrman; Kristina L Mitchem; Sheikh Amer Riazuddin; Robert J Morell; Arabandi Ramesh; Srikumari Srisailpathy; Dilip Deshmukh; Sheikh Riazuddin; Andrew J Griffith; Thomas B Friedman; Richard J H Smith; Edward R Wilcox
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.
American journal of human genetics 2002;71(3):632-6.
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: Sarah Vreugde; Alexandra Erven; Corné J Kros; Walter Marcotti; Helmut Fuchs; Kiyoto Kurima; Edward R Wilcox; Thomas B Friedman; Andrew J Griffith; Rudi Balling; Martin Hrabé De Angelis; Karen B Avraham; Karen P Steel
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.
Nature genetics 2002;30(3):257-8.
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.
2002: Julie M Bork; Robert J Morell; Shaheen Khan; Sheikh Amer Riazuddin; Edward R Wilcox; Thomas B Friedman; Andrew J Griffith
Clinical presentation of DFNB12 and Usher syndrome type 1D.
Advances in oto-rhino-laryngology 2002;61():145-52.
2002: Thomas B Friedman; John T Hinnant; Manju Ghosh; Erich T Boger; Sheikh Amer Riazuddin; James R Lupski; Lorraine Potocki; Edward R Wilcox
DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlation.
Advances in oto-rhino-laryngology 2002;61():124-30.
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: Edward R Wilcox; Quianna Burton; Sadaf Naz; Sheikh Amer Riazuddin; Tenesha N Smith; B Ploplis; Inna A Belyantseva; Tamar Ben-Yosef; NA Liburd; Robert J Morell; Anne E White-Olson; Doris K Wu; Andrew J Griffith; S Riazuddin; Thomas B Friedman
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.
Cell 2001;104(1):165-72.
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.
2000: S Yasunaga; M'hamed Grati; Sébastien Chardenoux; Tenesha N Smith; Thomas B Friedman; Anil K Lalwani; Edward R Wilcox; Christine Petit
OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.
American journal of human genetics 2000;67(3):591-600.
2000: T Friedman; James F Battey; Anne E White-Olson; Sheikh Amer Riazuddin; Konrad Noben-Trauth; Andrew J Griffith; Edward R Wilcox
Modifier genes of hereditary hearing loss.
Current opinion in neurobiology 2000;10(4):487-93.
2000: Edward R Wilcox; L A Everett; X C Li; Anil K Lalwani; Eric Green
The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4.
Advances in oto-rhino-laryngology 2000;56():145-51.
2000: Thomas B Friedman; John T Hinnant; RA Fridell; Edward R Wilcox; Yehoash Raphael; Sally A Camper
DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15.
Advances in oto-rhino-laryngology 2000;56():131-44.
1999: Anil K Lalwani; William M Luxford; Anand N Mhatre; A Attaie; Edward R Wilcox; Caley M Castelein
A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration.
American journal of human genetics 1999;64(1):318-23.
1998: Anil K Lalwani; A Attaie; F T Randolph; D Deshmukh; C Wang; Anand N Mhatre; Edward R Wilcox
Point mutation in the MITF gene causing Waardenburg syndrome type II in a three-generation Indian family.
American journal of medical genetics 1998;80(4):406-9.
1998: P K Jain; Anil K Lalwani; XC Li; T L Singleton; Tenesha N Smith; A Chen; Dilip Deshmukh; I C Verma; Richard J H Smith; Edward R Wilcox
A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene.
Genomics 1998;50(2):290-2.
1998: A Wang; Y Liang; RA Fridell; Frank J Probst; Edward R Wilcox; JW Touchman; C C Morton; Robert J Morell; Konrad Noben-Trauth; Sally A Camper; Thomas B Friedman
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.
Science (New York, N.Y.) 1998;280(5368):1447-51.
1998: Anita L DeStefano; L A Cupples; Kathleen S Arnos; JH Asher; Clinton T Baldwin; S Blanton; ML Carey; E O da Silva; Thomas B Friedman; J Greenberg; A K Lalwani; Aubrey Milunsky; Walter E Nance; Arti Pandya; Rajkumar Ramesar; A P Read; M Tassabejhi; Edward R Wilcox; Lindsay A Farrer
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations.
Human genetics 1998;102(5):499-506.
1998: Y Liang; A Wang; Frank J Probst; I N Arhya; T D Barber; Ken-Shiung Chen; Dilip Deshmukh; David F Dolan; John T Hinnant; L E Carter; P K Jain; Anil K Lalwani; XC Li; James R Lupski; S Moeljopawiro; Robert J Morell; C Negrini; Edward R Wilcox; S Winata; Sally A Camper; Thomas B Friedman
Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.
American journal of human genetics 1998;62(4):904-15.
1998: T L Singleton; Edward R Wilcox
The largest subunit of mouse RNA polymerase II (RPB1) functionally substituted for its yeast counterpart in vivo.
Gene 1998;209(1-2):131-8.
1998: X C Li; L A Everett; A K Lalwani; D Desmukh; T B Friedman; Eric Green; Edward R Wilcox
A mutation in PDS causes non-syndromic recessive deafness.
Nature genetics 1998;18(3):215-7.
1998: C Wang; E Kim; A Attaie; Tenesha N Smith; Edward R Wilcox; Anil K Lalwani
A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome type 2.
Molecular and cellular probes 1998;12(1):55-7.
1997: A Attaie; E Kim; Edward R Wilcox; Anil K Lalwani
A splice-site mutation affecting the paired box of PAX3 in a three generation family with Waardenburg syndrome type I (WS1).
Molecular and cellular probes 1997;11(3):233-6.
1997: Anil K Lalwani; Fred H Linthicum; Edward R Wilcox; J K Moore; F C Walters; T B San Agustin; J Mislinski; M R Miller; Y Sinninger; A Attaie; William M Luxford
A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration.
Audiology & neuro-otology 1997;2(3):139-54.
1996: Anil K Lalwani; Anand N Mhatre; T B San Agustin; Edward R Wilcox
Genotype-phenotype correlations in type 1 Waardenburg syndrome.
The Laryngoscope 1996;106(7):895-902.
1996: Marsha E O'Neill; J Marietta; Darryl Nishimura; Sigrid Wayne; Guy Van Camp; L Van Laer; C Negrini; Edward R Wilcox; A Chen; Kunihiro Fukushima; L Ni; Val C Sheffield; Richard J H Smith
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6.
Human molecular genetics 1996;5(6):853-6.
1996: M N Rivolta; C Negrini; Edward R Wilcox
A novel zinc finger gene preferentially expressed in the retina and the organ of Corti localizes to human chromosome 12q24.3.
Biochimica et biophysica acta 1996;1306(2-3):127-32.
1995: M N Rivolta; Edward R Wilcox
A novel and simple methodology to generate subtracted cDNA libraries.
Nucleic acids research 1995;23(13):2565-6.
1995: Anil K Lalwani; J. Rodney Brister; J Fex; K M Grundfast; B Ploplis; T B San Agustin; Edward R Wilcox
Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two families.
American journal of human genetics 1995;56(1):75-83.
1994: Anil K Lalwani; J. Rodney Brister; J Fex; K M Grundfast; A T Pikus; B Ploplis; T San Agustin; H Skarka; Edward R Wilcox
A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.
American journal of human genetics 1994;55(4):685-94.
1994: M Tachibana; T Asano; Edward R Wilcox; N Yokotani; M N Rivolta; J Fex
G protein Gi2 alpha in the cochlea: cloning and selective occurrence in receptor cells.
Brain research. Molecular brain research 1994;21(3-4):355-8.
1994: Edward R Wilcox; J Fex
Construction of a cDNA library from microdissected guinea pig crista ampullaris.
Hearing research 1994;73(1):65-6.
1992: Edward R Wilcox
Strategies for constructing a guinea pig organ of Corti cDNA library and its potential use.
Otolaryngologic clinics of North America 1992;25(5):1011-6.
1992: M Tachibana; Edward R Wilcox; N Yokotani; M Schneider; J Fex
Selective amplification and partial sequencing of cDNAs encoding G protein alpha subunits from cochlear tissues.
Hearing research 1992;62(1):82-8.
1992: Edward R Wilcox; J Fex
Construction of a cDNA library from microdissected guinea pig organ of Corti.
Hearing research 1992;62(1):124-6.
1992: Dennis G Drescher; S Upadhyay; Edward R Wilcox; J Fex
Analysis of muscarinic receptor subtypes in the mouse cochlea by means of the polymerase chain reaction.
Journal of neurochemistry 1992;59(2):765-7.
1992: Edward R Wilcox; M N Rivolta; B Ploplis; S B Potterf; J Fex
The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat.
Human molecular genetics 1992;1(3):215.