A. Mir

发表

Identification of bioflavonoid as fusion inhibitor of dengue virus using molecular docking approach

A. Mir, Humaira Ismatullah, S. Rauf, 2016 .

Structural, phylogenetic and docking studies of D-amino acid oxidase activator (DAOA), a candidate schizophrenia gene

A. Mir, S. A. Sehgal, N. Khattak, 2013, Theoretical Biology and Medical Modelling.

Evaluation of inhibitory potential of some selective methanolic plants extracts on biological characteristics of Acanthamoeba castellanii using human corneal epithelial cells in vitro

Suk-Yul Jung, A. Mir, A. Matin, 2013, Parasitology Research.

Causal variants in Maturity Onset Diabetes of the Young (MODY) – A systematic review

C. Polychronakos, L. Marchand, A. Mir, 2021, BMC Endocrine Disorders.

Identification of Missense Mutation (I12T) in the BSND Gene and Bioinformatics Analysis

A. Mir, H. Iqbal, Tayyba Sarfaraz, 2011, Journal of biomedicine & biotechnology.

Phylogenetic analysis of human Tp53 gene using computational approach

A. Mir, H. Rashid, Mohammad Haroon Khan, 2011 .

Computational analysis of benzofuran-2-carboxlic acids as potent Pim-1 kinase inhibitors

A. Mir, S. B. Jamal, A. Wadood, 2014, Pharmaceutical biology.

Pharmacoinformatics and molecular docking reveal potential drug candidates against Schizophrenia to target TAAR6

H. Qing, G. Ashraf, A. Mir, 2018, Journal of cellular physiology.

In Silico Studies of C3 Metabolic Pathway Proteins of Wheat (Triticum aestivum)

A. Mir, S. Rauf, H. Iqbal, 2012, BioMed research international.

Maturity Onset Diabetes of the Young – An Overview of Common Types. A Review

A. Mir, M. Naeem, I. Rafique, 2018, Romanian Journal of Diabetes Nutrition and Metabolic Diseases.

Comparative Modeling and Molecular Docking Study of P53 and AKT1, Genes of Lung Cancer Pathways

A. Mir, S. Rauf, Syeda Naqsh e Zahra, 2017 .

Identification of novel mutation in the HR gene responsible for atrichia with papular lesions in a Pakistani family

A. Mir, S. Rauf, Muhammad Saad Ahmed, Ph.D., 2013, The Journal of dermatology.

Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family

J. Vincent, M. Rafiq, J. So, 2014, Human Genetics.

Molecular variants of Bardet-Biedl Syndrome

A. Mir, F. Hafeez, H. M. Wahedi, 2010 .

Comprehensive genetic screening reveals wide spectrum of genetic variants in monogenic forms of diabetes among Pakistani population

C. Polychronakos, L. Marchand, A. Mir, 2021, World journal of diabetes.

Genetic characterization of suspected MODY patients in Pakistan by next generation sequencing—a pilot study

A. Mir, A. Basit, Prof. Dr. Asher. Fawwad, 2021, International Journal of Diabetes in Developing Countries.

Insight to FBXO31 Novel Mutation p.Cys283Asn causing Non‑Syndromic Autosomal Recessive Intellectual Disability using Computational Methods

A. Mir, S. Rauf, Asif Mir, 2016 .

Exploring evolution of brain genes involved in microcephaly through phylogeny and synteny analysis

A. Mir, S. Rauf, Asif Mir, 2013, Theoretical Biology and Medical Modelling.

Whole-exome sequencing identifies a novel mutation in spermine synthase gene (SMS) associated with Snyder-Robinson Syndrome

H. Qing, Ailikemu Aierken, D. Lu, 2020, BMC Medical Genetics.

Immunoinformatics and Molecular Docking Studies Predicted Potential Multiepitope-Based Peptide Vaccine and Novel Compounds against Novel SARS-CoV-2 through Virtual Screening

Hafiza Nisha Akram, M. Sufyan, A. Mir, 2021, BioMed research international.

Seed Coat Morphology and Sculpturing of Selected Invasive Alien Plants from Lesser Himalaya Pakistan and Their Systematic Implications

S. Sultana, M. Ameen, A. Mir, 2022, BioMed research international.

EFFECT OF SINGLE ORAL DOSE OF MELATONIN ON PLASMA CONCENTRATION OF PROLACTIN AND CORTISOL IN MALE RHESUS MONKEYS

A. Mir, S. Jahan, Z. Agha, 2010 .

Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

C. Khor, A. Mir, S. Siddiqi, 2018, Journal of Biomedical Science.

In silico modeling of lipase H

N. Riaz, J. Khattak, A. Mir, 2013 .

Mapping of Genes Involved in Bardet-Biedl Syndrome (BBS) in Pakistani Population

A. Mir, H. M. Wahedi, Shiraz Ahmad, 2012 .

Novel variants underlying autosomal recessive intellectual disability in Pakistani consanguineous families

S. Efthymiou, H. Houlden, V. Salpietro, 2020, BMC Medical Genetics.

HUNTINGTON GENE ONTOLOGICAL STUDY AND ORTHOLOGICAL ANALYSIS

S. Nazir, A. Mir, S. Rauf, 2016 .

Generation of a 3D model for human cereblon using comparative modelling

A. Mir, S. Fazal, S. Bilal, 2013 .

Molecular modeling of mutant kinase domain of Btk, a Tec family member, for structure prediction

A. Mir, R. Faryal, H. Iqbal, 2011 .

Mutation Screening of MEFV and TNF Gene in Pakistani Patients with Rheumatic Heart Disease: A Case Control-Study

A. Mohyuddin, A. Mir, A. Khanum, 2015 .

Novel Hemizygous Missense Variation in AFF2 Gene Underlies Fragile XE Syndrome

A. Mir, G. Harlalka, M. Ilyas, 2020 .

The C-Terminal Region of G72 Increases D-Amino Acid

C. Hsieh, H. Lane, G. Tsai, 2014 .

The C-Terminal Region of G72 Increases d-Amino Acid Oxidase Activity

C. Hsieh, H. Lane, G. Tsai, 2013, International journal of molecular sciences.

Diversity of invasive alien plants species of lesser Himalayas-Pakistan

Mushtaq Ahmad, S. Sultana, A. Mir, 2022, Pakistan journal of botany.

Evaluation of inhibitory potential of some selective methanolic plants extracts on biological characteristics of Acanthamoeba castellanii using human corneal epithelial cells in vitro

A. Mir, A. Matin, Hafiz Muhammad Shoaib, 2013, Parasitology Research.

Molecular Docking Studies

A. Mir, S. A. Sehgal, R. Tahir, 2018 .

Hutchinson–Gilford Progeria Syndrome: A Premature Aging Disease

Muhammad Saad Ahmed, Asif Mir, Nousheen Bibi, 2017, Molecular Neurobiology.

Identification and in silico characterization of p.G380R substitution in FGFR3, associated with achondroplasia in a non-consanguineous Pakistani family

M. Shoaib, S. Malik, A. Mir, 2017, Diagnostic Pathology.

Haplotype Analysis for DFNB4/PDS Locus in Hearing Impaired Families of Punjab (Pakistan)

J. Khattak, A. Mir, S. B. Jamal, 2012 .

Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairment

S. Leal, A. Bhatti, M. Chahrour, 2005, Human mutation.

Epigenetics in Alzheimer’s Disease: Perspective of DNA Methylation

Hong Qing, Zhenzhen Quan, Talal Jamil Qazi, 2018, Molecular Neurobiology.

The genetics of intellectual disability: advancing technology and gene editing

S. Efthymiou, H. Houlden, A. Mir, 2020, F1000Research.

Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan

J. Vincent, M. Rafiq, E. Schaftingen, 2015, Clinical genetics.

Comparative modeling and docking studies of p16ink4/Cyclin D1/Rb pathway genes in lung cancer revealed functionally interactive residue of RB1 and its functional partner E2F1

Naureen Aslam Khattak, A. Mir, N. A. Khattak, 2013, Theoretical Biology and Medical Modelling.

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

A. Noor, J. Vincent, M. Rafiq, 2017, Molecular Psychiatry.

Application of proteomics to investigate stress-induced proteins for improvement in crop protection

S. Komatsu, A. Afroz, A. Mir, 2011, Plant Cell Reports.

GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates

J. Vincent, Judy S. H. Liu, E. Morrow, 2019, Human Genetics.

Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family

J. Vincent, M. Rafiq, J. So, 2014, Human Genetics.

Pathogenic variants in PIDD1 lead to an autosomal recessive neurodevelopmental disorder with pachygyria and psychiatric features

Gloria L. Porras-Hurtado, J. Vincent, Hiba Mohammed, 2021, European Journal of Human Genetics.

Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disability

J. Vincent, C. Schwarzer, K. Girisha, 2021, Translational Psychiatry.

Bioinformatics evaluation of NPHS2 deletion mutation associated with congenital nephrotic syndrome in a consanguineous Pakistani family

A. Mir, M. Ajmal, A. Hameed, 2015, Clinical genetics.

Identification of recurrent c.742G>T nonsense mutation in ECM1 in Pakistani families suffering from lipoid proteinosis

S. Malik, A. Mir, N. Ahmad, 2014, Molecular Biology Reports.

Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family

C. Khor, S. Malik, A. Mir, 2017, BMC Medical Genetics.

Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation.

A. Noor, J. Vincent, R. Weksberg, 2009, American journal of human genetics.

Structural, phylogenetic and docking studies of D-amino acid oxidase activator (DAOA), a candidate schizophrenia gene

A. Mir, S. A. Sehgal, N. A. Khattak, 2013, Theoretical Biology and Medical Modelling.

A novel single base pair duplication in WDR62 causes primary microcephaly

A. Mir, S. Rauf, Ishrat Naveed, 2014, BMC Medical Genetics.

An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan

A. Noegel, S. Baig, P. Nürnberg, 2020, Molecular genetics & genomic medicine.

Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly

S. Basit, S. Mahmood, A. Mir, 2011, BMC neurology.

Computational analysis of TRAPPC9: candidate gene for autosomal recessive non-syndromic mental retardation.

A. Mir, N. A. Khattak, 2014, CNS & neurological disorders drug targets.

CatSper ion channels: Bioinformatics analysis in Homo sapiens

A. Mir, S. Kanwal, H. Iqbal, 2011 .

Adaptive evolution and elucidating the potential inhibitor against schizophrenia to target DAOA (G72) isoforms

A. Mir, S. A. Sehgal, S. Kanwal, 2015, Drug design, development and therapy.

Tumor necrosis factor receptor superfamily 10B (TNFRSF10B): an insight from structure modeling to virtual screening for designing drug against head and neck cancer

A. Mir, S. A. Sehgal, Jabar Zaman Khan Khattak, 2013, Theoretical Biology and Medical Modelling.

Quick Guideline for Computational Drug Design

Asif Mir, Sheikh Arslan Sehgal, Rana Adnan Tahir, 2018 .

Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

C. Khor, A. Mir, S. Siddiqi, 2019, Journal of Biomedical Science.

Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

C. Khor, A. Mir, S. Siddiqi, 2018, Journal of Biomedical Science.

A Novel Variant in VPS13B Underlying Cohen Syndrome

S. Leal, A. Mir, I. Schrauwen, 2023, BioMed research international.

Development and Characterization of Clotrimazole Loaded Electrospun Nanofibers for the Management of Oral Candidiasis

T. Garg, A. Goyal, G. Rath, 2014 .

Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32‐p11.31

S. Leal, M. Chahrour, A. Mir, 2005, American journal of medical genetics. Part A.

Susceptibility pattern of pseudomonas aeruginosa against various antibiotics

A. Mir, F. Anjum, Asif Mir, 2010 .

Structure modeling and mutational analysis of gap junction beta 2 (GJB2)

S. A. Ch, J. Khattak, A. Mir, 2012 .