Zubair M. Ahmed

Overview

Best Publications

• Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

  Daniel J. Klionsky;Amal Kamal Abdel-Aziz;Sara Abdelfatah;Mahmoud Abdellatif

  10661
  Citations

• Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

  Julie M. Bork;Linda M. Peters;Saima Riazuddin;Saima Riazuddin;Steve L. Bernstein

  642
  Citations

• Dominant and recessive deafness caused by mutations of a novel gene, TMC1 , required for cochlear hair-cell function

  Kiyoto Kurima;Linda M. Peters;Yandan Yang;Saima Riazuddin

  503
  Citations

• Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.

  Zubair M. Ahmed;Saima Riazuddin;Steve L. Bernstein;Zahoor Ahmed

  479
  Citations

• Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia.

  Inna A. Belyantseva;Erich T. Boger;Erich T. Boger;Sadaf Naz;Gregory I. Frolenkov

  403
  Citations

• Tricellulin Is a Tight-Junction Protein Necessary for Hearing

  Saima Riazuddin;Saima Riazuddin;Zubair M. Ahmed;Alan S. Fanning;Ayala Lagziel

  352
  Citations

• PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

  Zubair M. Ahmed;Saima Riazuddin;Jamil Ahmad;Steve L. Bernstein

  342
  Citations

• The Tip-Link Antigen, a Protein Associated with the Transduction Complex of Sensory Hair Cells, Is Protocadherin-15

  Zubair M. Ahmed;Richard Goodyear;Saima Riazuddin;Ayala Lagziel

  325
  Citations

• Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48

  Saima Riazuddin;Inna A Belyantseva;Arnaud P J Giese;Kwanghyuk Lee

  283
  Citations

• Increasing the complexity: new genes and new types of albinism

  Lluís Montoliu;Karen Grønskov;Karen Grønskov;Ai-Hua Wei;Mónica Martínez-García

  242
  Citations

• Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79

  Atteeq Ur Rehman;Atteeq Ur Rehman;Robert J. Morell;Inna A. Belyantseva;Shahid Y. Khan

  240
  Citations

• Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37

  Zubair M. Ahmed;Robert J. Morell;Saima Riazuddin;Andrea Gropman

  233
  Citations

• Mutations in SLC25A46 , encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

  Alexander J Abrams;Robert B Hufnagel;Adriana Rebelo;Claudia Zanna

  222
  Citations

• Actin-Bundling Protein TRIOBP Forms Resilient Rootlets of Hair Cell Stereocilia Essential for Hearing

  Shin Ichiro Kitajiri;Takeshi Sakamoto;Inna A. Belyantseva;Richard J. Goodyear

  217
  Citations

• The molecular genetics of Usher syndrome.

  ZM Ahmed;S Riazuddin;ER Wilcox;ER Wilcox

  200
  Citations

• Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.

  Zubair M. Ahmed;Tenesha N. Smith;Saima Riazuddin;Tomoko Makishima

  189
  Citations

• Loss-of-function mutations in RAB18 cause Warburg micro syndrome.

  Danai Bem;Shin Ichiro Yoshimura;Ricardo Nunes-Bastos;Frances F. Bond

  188
  Citations

• Dominant modifier DFNM1 suppresses recessive deafness DFNB26

  Saima Riazuddin;Saima Riazuddin;Caley M. Castelein;Zubair M. Ahmed;Zubair M. Ahmed;Anil K. Lalwani

  176
  Citations

• CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells.

  Arnaud P. J. Giese;Yi-Quan Tang;Ghanshyam P. Sinha;Michael R. Bowl

  165
  Citations

• Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development.

  Ayala Lagziel;Zubair M. Ahmed;Julie M. Schultz;Robert J. Morell

  160
  Citations