Wasim Ahmad

Research.com Recognitions

• 2015 - Fellow, The World Academy of Sciences
• 2010 - Fellow of Pakistan Academy of Sciences

Overview

Best Publications

• Alopecia Universalis Associated with a Mutation in the Human hairless Gene

  Wasim Ahmad;Muhammad Faiyaz ul Haque;Valeria Brancolini;Hui C. Tsou

  408
  Citations

• Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion: Evidence from Inherited Hypotrichosis and Acquired Pemphigus Vulgaris

  Ana Kljuic;Hisham Bazzi;John P Sundberg;Amalia Martinez-Mir

  406
  Citations

• WDR62 is associated with the spindle pole and is mutated in human microcephaly

  Adeline K. Nicholas;Maryam Khurshid;Julie Désir;Ofélia P. Carvalho

  343
  Citations

• Exposing the human nude phenotype

  Jorge Frank;Claudio Pignata;Andrei A. Panteleyev;David M. Prowse

  304
  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

• Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

  Emma M. Jenkinson;Atteeq U. Rehman;Tom Walsh;Jill Clayton-Smith

  245
  Citations

• Autosomal recessive primary microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum

  Saqib Mahmood;Wasim Ahmad;Muhammad J Hassan

  233
  Citations

• Mutations in Orthologous Genes in Human Spondyloepimetaphyseal Dysplasia and the Brachymorphic Mouse

  Faiyaz ul Haque M;King Lm;Krakow D;Krakow D;Cantor Rm

  197
  Citations

• Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humans.

  A. A. Panteleyev;R. Paus;W. Ahmad;J. P. Sundberg

  170
  Citations

• Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35

  Rob W.J. Collin;Ersan Kalay;Ersan Kalay;Muhammad Tariq;Theo Peters

  135
  Citations

• Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

  Guntram Borck;Atteeq Ur Rehman;Atteeq Ur Rehman;Kwanghyuk Lee;Hans Martin Pogoda

  134
  Citations

• Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74

  Zubair M. Ahmed;Rizwan Yousaf;Rizwan Yousaf;Byung Cheon Lee;Shaheen N. Khan

  132
  Citations

• Mutations in KARS, Encoding Lysyl-tRNA Synthetase, Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB89

  Regie Lyn P. Santos-Cortez;Kwanghyuk Lee;Zahid Azeem;Patrick J. Antonellis

  127
  Citations

• Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family.

  Wasim Ahmad;Abraham Zlotogorski;Andrei A. Panteleyev;HaMut Lam

  124
  Citations

• Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

  Julie M. Schultz;Shaheen N. Khan;Zubair M. Ahmed;Saima Riazuddin

  118
  Citations

• Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome).

  M Faiyaz-Ul-Haque;W Ahmad;S H E Zaidi;S Haque

  115
  Citations

• A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers

  W Ahmad;Alan D Irvine;H Lam;C Buckley

  114
  Citations

• Congenital atrichia in five Arab Palestinian families resulting from a deletion mutation in the human hairless gene

  Abraham Zlotogorski;Wasim Ahmad;Angela M. Christiano

  107
  Citations

• Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment.

  Regie Santos;Regie Santos;M. Wajid;Thanh Pham;J. Hussan

  106
  Citations

• A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.

  Wasim Ahmad;Valeria Brancolini;Muhammad Faiyaz ul Haque;HaMut Lam

  103
  Citations