M. Chishti

发表

Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)

W. Ahmad, M. Amin-ud-din, M. Jelani, 2008, Human Genetics.

Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33–q27.3

S. Leal, P. John, W. Ahmad, 2005, Human Genetics.

Synthesis and biological activities of 2-aminophenol-based Schiff bases and their structure–activity relationship

S. Iqbal, S. Perveen, I. Khan, 2015, Medicinal Chemistry Research.

A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families

W. Ahmad, D. Muhammad, M. Chishti, 2006, Journal of Human Genetics.

Synthesis and biological activities of 2-aminophenol-based Schiff bases and their structure–activity relationship

S. Iqbal, S. Perveen, I. Khan, 2015, Medicinal Chemistry Research.

A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2)

W. Ahmad, M. Jelani, G. Ali, 2008, Clinical genetics.

A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis

P. John, W. Ahmad, S. I. Raza, 2007, Human Genetics.

Mutation in the HPGD gene encoding NAD+ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC)

W. Ahmad, G. Ali, Z. Azeem, 2008, Journal of Medical Genetics.

Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families

S. Leal, A. Bhatti, W. Ahmad, 2008, Journal of Human Genetics.

A Novel Locus for Ectodermal Dysplasia of Hairs, Nails and Teeth Type Maps to Chromosome 18q22.1–22.3

W. Ahmad, G. Ali, M. Chishti, 2007, Annals of human genetics.

A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22–q11.2

W. Ahmad, M. Tariq, S. M. Jamal, 2008, Human Genetics.

Mapping of a Gene for Alopecia with Mental Retardation Syndrome (APMR3) on Chromosome 18q11.2‐q12.2

P. John, W. Ahmad, G. Ali, 2007, Annals of human genetics.

Previously described sequence variant in CDK5RAP2 gene in a Pakistani family with autosomal recessive primary microcephaly

P. John, W. Ahmad, G. Ali, 2007, BMC Medical Genetics.

Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11–q21.32

P. John, W. Ahmad, M. Ayub, 2007, Clinical genetics.

Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12–q21.2

P. John, M. Naeem, W. Ahmad, 2006, The British journal of dermatology.

A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2‐q26.31

P. John, W. Ahmad, G. Ali, 2006, Clinical genetics.

A novel missense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a consanguineous Pakistani family

W. Ahmad, N. Kausar, M. Rafiq, 2007, The British journal of dermatology.

Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families

S. Basit, W. Ahmad, S. I. Raza, 2009, British Journal of Dermatology.

Mitral regurgitation as a phenotypic manifestation of nonphotosensitive trichothiodystrophy due to a splice variant in MPLKIP

J. Shendure, D. Nickerson, S. Leal, 2016, BMC Medical Genetics.

Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families

D. Nickerson, S. Leal, M. Bamshad, 2017, International journal of dermatology.

Mutation in PVRL4 gene encoding nectin-4 underlies ectodermal-dysplasia-syndactyly syndrome (EDSS1)

W. Ahmad, M. Jelani, M. Chishti, 2011, Journal of Human Genetics.

Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: novel sequence variants in ASPM gene

T. Siddique, M. Rafiq, S. Mahmood, 2006, Neurogenetics.

A novel deletion mutation in CENPJ gene in a Pakistani family with autosomal recessive primary microcephaly

W. Ahmad, A. Gul, S. I. Raza, 2006, Journal of Human Genetics.

Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3

S. Leal, W. Ahmad, M. Ansar, 2009, Journal of Human Genetics.

Previously described sequence variant in CDK5RAP2 gene in a Pakistani family with autosomal recessive primary microcephaly

P. John, W. Ahmad, G. Ali, 2007, BMC Medical Genetics.