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Niamatullah Khan

Observed names: Khan, Niamatullah, Sher Alam Khan
ORCID: 0000-0003-2374-665X
Observed ORCID: 0000-0003-2374-665X
OpenAlex ID: A5065169907
Pakistan Genetic Mutation Database (PGMD); A centralized Pakistani mutome data source
2017 · Iqbal Qasim, Bilal Ahmad, et al. · European Journal of Medical Genetics · 29
Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet–Biedl Syndrome
2023 · Hamed Nawaz, Mujahid, et al. · Genes · 11
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Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms
2023 · Nazif Muhammad, Syeda Iqra Hussain, et al. · Frontiers in Neurology · 10
Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability
2023 · Syeda Iqra Hussain, Nazif Muhammad, et al. · BMC Neurology · 7
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Biallelic mutations in the LPAR 6 gene causing autosomal recessive wooly hair/hypotrichosis phenotype in five Pakistani families
2019 · Ghulam M. Khan, Noor Hassan, et al. · International Journal of Dermatology · 6
Molecular insight into CREBBP and TANGO2 variants causing intellectual disability
2023 · Syeda Iqra Hussain, Nazif Muhammad, et al. · The Journal of Gene Medicine · 4
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Biallelic mutations in FLG , TGM1 , and STS genes segregated with different types of ichthyoses in eight families of Pakistani origin
2023 · Niamatullah Khan, Khadim Shah, et al. · International Journal of Dermatology · 2
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Works count: 13
Citation count: 76
H-index: 6
I10-index: 3
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