M. Hussain

发表

Novel Loss-of-Function Mutations in COCH Cause Autosomal Recessive Nonsyndromic Deafness

S. Riazuddin, Z. Ahmed, M. Shahzad, 2020, bioRxiv.

Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay

D. Misceo, S. Antonarakis, S. Riazuddin, 2017, Genetics in Medicine.

TULP3 NLS inhibition: an in silico study to hamper cargo transport to nucleus

M. Afzal, A. Tariq, M. Hussain, 2022, Journal of biomolecular structure & dynamics.

Pathogenicity Prediction of Potential Variants of Iba57 Gene Causing Heredity Spastic Paraplegia Through Mitochondrial Dysfunction by using Computational Tools

M. Hussain, R. Mateen, D. Azeem, 2021, THE JOURNAL OF MICROBIOLOGY AND MOLECULAR GENETICS.

Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder

J. Schuurs-Hoeijmakers, S. Antonarakis, R. Płoski, 2021, Genetics in Medicine.

Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

D. Grozeva, J. Veltman, T. O’Connor, 2016, Molecular Psychiatry.

Role of post translational modifications and novel crosstalk between phosphorylation and O-beta-GlcNAc modifications in human claudin-1, -3 and -4

A. Butt, Jun Lu, Y. Tong, 2011, Molecular Biology Reports.

Variants in PUS7 Cause Intellectual Disability with Speech Delay, Microcephaly, Short Stature, and Aggressive Behavior.

R. Pfundt, Pedro Rebelo-Guiomar, M. Minczuk, 2018, American journal of human genetics.

De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy.

W. Chung, E. Puffenberger, Z. Niu, 2021, American journal of human genetics.

Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing loss

S. Riazuddin, Z. Ahmed, M. Shahzad, 2020, Human Genetics.

Genetics A Comprehensive In Silico Analysis of Deleterious SNPs of Paraplegin Protein Associated with Hereditary Spastic Paraplegia through Mitochondrial Dysfunction

A. Akhtar, M. Hussain, R. Mateen, 2020 .

In silico identification of potential drug-like molecules against G glycoprotein of Nipah virus by molecular docking, DFT studies, and molecular dynamic simulation

M. Afzal, Asma Tariq, Iqra Naeem, 2022, Journal of biomolecular structure & dynamics.

The Insight of In Silico and In Vitro evaluation of Beta vulgaris phytochemicals against Alzheimer’s disease targeting acetylcholinesterase

I. Shahid, M. Sufyan, Sidra Rehman, 2022, PloS one.

Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay

D. Misceo, S. Antonarakis, S. Riazuddin, 2018, Genetics in Medicine.

Current Trends in OMICS (CTO)

H. Sadia, Misbah Hussain, M. Hussain, 2023 .

In silico computation of functional SNPs of CYP2U1 protein leading to hereditary spastic paraplegia

A. Akhtar, M. Hussain, S. Ch, 2021 .

In Silico Analysis of MARS1 Gene to Elucidate Low- Frequency Variants Associated with Interstitial Lung and Liver Disease

M. Hussain, R. M. Mateen, Aamna Syed, 2023, Lahore Garrison University Journal of Life Sciences.

Current Trends in OMICS (CTO)

M. Hussain, M. I. Fareed, R. M. Mateen, 2023 .

In-silico analysis of potential anticancer drug for NEK7 and PPP1CA proteins overexpressed in pancreatic ductal adenocarcinoma.

Asma Tariq, M. Hussain, R. Mateen, 2024, Journal of biomolecular structure & dynamics.