Asif Mir

发表

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.

Susceptibility pattern of pseudomonas aeruginosa against various antibiotics

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

Epigenetics in Alzheimer’s Disease: Perspective of DNA Methylation

Hong Qing, Zhenzhen Quan, Talal Jamil Qazi, 2017, Molecular Neurobiology.

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.

Novel Hemizygous Missense Variation in AFF2 Gene Underlies Fragile XE Syndrome

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

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

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

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.

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.

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 .

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.

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

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

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

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

Concept of Halal Food and Biotechnology

Zubair Anwar, Humaira Ismatullah, Asif Mir, 2011 .

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

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

Identification and association of recurrent ALOXE3 mutation with non‐bullous congenital ichthyosiform erythroderma in two ethnically distinct Pakistani families

S. Malik, N. Ahmad, M. Nasir, 2018, Congenital anomalies.

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.

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

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

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.

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.

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.

A Novel Variant in VPS13B Underlying Cohen Syndrome

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

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.

Bioinformatics and phylogenetic analysis of human Tp73 gene

Naureen Aslam Khattak, A. Sehgal, Asif Mir, 2013 .

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.

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.

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.

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

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

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

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

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.

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.

The genetics of intellectual disability: advancing technology and gene editing

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

Hutchinson–Gilford Progeria Syndrome: A Premature Aging Disease

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

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.

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

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

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

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

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

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

A novel single base pair duplication in WDR62 causes primary microcephaly

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

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

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

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

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

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

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