Author

Syeda Iqra Hussain

Observed name: Hussain, Syeda Iqra

Institution: Kohat University of Science and Technology

Observed institutions: Kohat University of Science and Technology, Ziauddin University

ORCID: 0000-0003-1589-7626

Observed ORCID: 0000-0003-1589-7626

OpenAlex ID: A5063351895

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

Molecular insight into CREBBP and TANGO2 variants causing intellectual disability

2023 · Syeda Iqra Hussain, Nazif Muhammad, et al. · The Journal of Gene Medicine · 4

Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani families

2024 · Syeda Iqra Hussain, Nazif Muhammad, et al. · BMC Medical Genomics · 3

Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)

2024 · Seda Susgun, Afif Ben-Mahmoud, et al. · Human Mutation · 1

The Genetic Basis of Neurological Disorders: Missense and Nonsense Variants in Three Pakistani Families With Syndromic Intellectual Disability

2025 · Kenza Javed, Nazif Muhammad, et al. · Annals of Human Genetics

Design of a device for the assessment of dyspnea patients

2022 · Mehwish Faiz, Taha Mushtaq Shaikh, et al. · Mehran University Research Journal of Engineering and Technology

Works count: 15

Citation count: 25

H-index: 3

I10-index: 1