Muhammad Salman Chishti
Overview
Explore the profile of Muhammad Salman Chishti including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
138
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Recent Articles
1.
Shah K, Ali R, Ansar M, Lee K, Chishti M, Abbe I, et al.
BMC Med Genet
. 2016 Feb;
17:13.
PMID: 26880286
Background: Nonphotosensitive trichothiodystrophy (TTDN) is a rare autosomal recessive disorder of neuroectodermal origin. The condition is marked by hair abnormalities, intellectual impairment, nail dystrophies and susceptibility to infections but with...
2.
Jelani M, Chishti M, Ahmad W
J Hum Genet
. 2011 Feb;
56(5):352-7.
PMID: 21346770
Ectodermal-dysplasia-syndactyly syndrome (EDSS1) is a rare form of ectodermal dysplasia (ED), affecting skin and its appendages mainly hair, teeth and nails. In the present study, we have investigated a large...
3.
Chishti M, Lee K, McDonald M, Hassan M, Ansar M, Ahmad W, et al.
J Hum Genet
. 2009 Feb;
54(3):141-4.
PMID: 19229252
A novel ARNSHI (autosomal recessive non-syndromic hearing impairment) locus, DFNB71, was localized to 8p22-21.3. To map the locus, a whole-genome scan was carried out using DNA samples from a consanguineous...
4.
Azeem Z, Jelani M, Naz G, Tariq M, Wasif N, Naqvi S, et al.
Hum Genet
. 2008 May;
123(5):515-9.
PMID: 18461368
Autosomal recessive hypotrichosis (LAH3) is a rare hair disorder characterized by sparse hair on scalp and the rest of the body of affected individuals. Recently mutations in a G protein-coupled...
5.
Hassan M, Chishti M, Jamal S, Tariq M, Ahmad W
Hum Genet
. 2007 Dec;
123(1):77-82.
PMID: 18071751
We report a consanguineous Pakistani family with seven affected individuals showing a syndromic form of congenital microcephaly. Clinical features of affected individuals include congenital microcephaly with sharply slopping forehead, moderate...
6.
Hassan M, Khurshid M, Azeem Z, John P, Ali G, Chishti M, et al.
BMC Med Genet
. 2007 Sep;
8:58.
PMID: 17764569
Background: Autosomal Recessive Primary Microcephaly (MCPH) is a disorder of neurogenic mitosis. MCPH leads to reduced cerebral cortical volume and hence, reduced head circumference associated with mental retardation of variable...
7.
Ali G, Chishti M, Raza S, John P, Ahmad W
Hum Genet
. 2007 Mar;
121(3-4):319-25.
PMID: 17333281
Hereditary hypotrichosis is a rare autosomal recessive disorder characterized by sparse hair on scalp and rest of the body of affected individuals. Two forms of such hypotrichosis LAH and AH...
8.
Gul A, Hassan M, Hussain S, Raza S, Chishti M, Ahmad W
J Hum Genet
. 2006 Aug;
51(9):760-764.
PMID: 16900296
Autosomal recessive primary microcephaly (MCPH) is a rare human genetic disorder in which the head circumference is reduced because of abnormality in fetal brain growth. To date, six loci and...
9.
Gul A, Hassan M, Mahmood S, Chen W, Rahmani S, Naseer M, et al.
Neurogenetics
. 2006 May;
7(2):105-10.
PMID: 16673149
Human autosomal recessive primary microcephaly (MCPH) is a rare genetic disorder in which affected individuals are born with reduced brain size. MCPH is genetically heterogeneous, with six loci and four...