Muhammad ASIF Naeem

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“Muhammad Asif Naeem” have done PhD in Molecular Biology specifically in Ophthalmic Genetic Diseases from National Centre of Excellence in Molecular Biology (CEMB), University of the Punjab, Lahore – Pakistan. Expertise is Genetic Mapping by Genotyping & Sequencing of reported/candidate genes in Vision Impairment Laboratory, CEMB, PU, Lahore & Discovered novel genes & novel mutations. I have twenty publications of ophthalmic genetic disorders in peer reviewed international journals.

Research Interests

Papers共 51 篇Author StatisticsCo-AuthorSimilar Experts

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Substitution of a Single Non-Coding Nucleotide Upstream of TMEM216 Causes Non-Syndromic Retinitis Pigmentosa and is Associated with Reduced TMEM216 Expression

AMERICAN JOURNAL OF HUMAN GENETICSno. 9 (2024)

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Analysis of a Homozygous TGFBI Variant in a Pakistani Family with Granular Corneal Dystrophy Type 2: Implications for Genotype-Phenotype Correlation and Inheritance Patterns

Ayesha Khush Bakht,Shagufta Naz,Muhammad Asif Naeem,Saima Sharif,Muhammad Qasim,Haiba Kaul,Sabika Firasat,Khajista Jabeen,Afia Iqbal

Research Square (Research Square) (2023)

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CLCC1 C. 75C>A Mutation in Pakistani Derived Retinitis Pigmentosa Families Likely Originated with a Single Founder Mutation 2,000-5,000 Years Ago

Yan Ma,Xun Wang,Nadav Shoshany,Xiaodong Jiao,Adrian Lee,Gregory Ku,Emma L. Baple,James Fasham,Raheela Nadeem,Muhammad Asif Naeem,Sheikh Riazuddin,S. Amer Riazuddin,Andrew H. Crosby,J. Fielding Hejtmancik

Frontiers in Genetics（2022）

Cited3Views0WOSBibtex

A Genomic Deletion Encompassing CRYBB2-CRYBB2P1 is Responsible for Autosomal Recessive Congenital Cataracts

Bushra Irum,Firoz Kabir,Nadav Shoshany,Shahid Y. Khan,Bushra Rauf,Muhammad Asif Naeem,Tanveer A. Qaiser,Sheikh Riazuddin,J. Fielding Hejtmancik,S. Amer Riazuddin

Human Genome Variation（2022）

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Next-generation Whole Exome Sequencing to Delineate the Genetic Basis of Primary Congenital Glaucoma

Bushra Rauf,Shahid Y. Khan,Xiaodong Jiao,Bushra Irum,Ramla Ashfaq,Mubashra Zehra,Asma A. Khan,Muhammad Asif Naeem,Mohsin Shahzad,Sheikh Riazuddin,J. Fielding Hejtmancik,S. Amer Riazuddin

Scientific Reports（2022）

Cited6Views0WOSNATUREBibtex

Mutational Analysis in Sodium-Borate Cotransporter SLC4A11 in Consanguineous Families from Punjab, Pakistan

Afia Iqbal,Shagufta Naz,Haiba Kaul,Saima Sharif,Aysha Khushbakht,Muhammad Asif Naeem,Mehwish Iqtedar,Afshan Kaleem,Sabika Firasat,Farkhanda Manzoor

PLoS ONE（2022）

Cited3Views0WOSBibtex

A Missense Allele of PEX5 is Responsible for the Defective Import of PTS2 Cargo Proteins into Peroxisomes

Ali Muhammad,Khan Shahid Y., Instituto de Ciências Biomédicas Abel Salazar, Universidade Do Porto,Jiao Xiaodong, Qi Hang, University of the Punjab,Khan Asma A.,Mehmood Azra,Naeem Muhammad Asif,Assir Muhammad Zaman,Ali Muhammad Hassaan, Shaheed Zulfiqar Ali Bhutto Medical University,Abu-Amero Khaled K.,Akram Shehla Javed,Akram Javed,Riazuddin Saima,Robinson Michael L.,Baes Myriam,Hejtmancik J. Fielding,Riazuddin S. Amer

Human Genetics（2021）

Cited5Views0WOSBibtex

Genetic Analysis of Consanguineous Pakistani Families with Congenital Stationary Night Blindness

Hafiz Muhammad Azhar Baig,Muhammad Ansar,Afia Iqbal,Muhammad Asif Naeem,Mathieu Quinodoz,Giacomo Calzetti,Muhammad Iqbal,Carlo Rivolta

Ophthalmic Research（2021）

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A founder RDH5 splice site mutation leads to retinitis punctata albescens in two inbred Pakistani kindreds (vol 124, pg 87, 2019)

R. Khan,R. M. K. Shabbir, I Raza,U. Abdullah,M. A. Naeem,A. Ahmed,S. Malik, Z. Hu, K. Xia

OPHTHALMIC GENETICS（2020）

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Novel Mutations in LTBP2 Identified in Familial Cases of Primary Congenital Glaucoma

Bushra Rauf,Bushra Irum,Shahid Y. Khan,Firoz Kabir,Muhammad Asif Naeem,Sheikh Riazuddin,Radha Ayyagari,S. Amer Riazuddin

Molecular vision (2020): 14-25

Cited29Views0WOSBibtex

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Assistant Professor

Papers共 51 篇Author StatisticsCo-AuthorSimilar Experts