Personal information

Human Genetics, Neuroscience, Next Generation Sequencing, Molecular Biology

Biography

I completed my PhD. and one year Post Doc. from prestigious Gyeongsang National University, South Korea in 2011. I have 16 year of teaching and research experience. My area of expertise are human genetics, includes gene structure and organization, gene expression, mutation detection and analysis, bioinformatics, gene therapy and gene editing, cellular and developmental neuroscience etc. My PhD work was based on the effect of ethanol on siRNA-Mediated GABAB1 receptor expression for downstream signaling pathways, apoptotic neurodegeneration, maternal epileptic seizure and role of GABABR1 receptor expression in early development of pre/postnatal rat brain.
Currently I am actively involved in Neurogenetic research program at CEGMR, working on rare, ulta rare and common neurologic disorders including Epilepsy, Autism, Mental retardation, Microcephaly and other neurodegenerative and neurodevelopmental disorders of Saudi Arabia. I am using microarray platform for array CGH, CNV/SNP analysis and Next generation technology for expression and whole exome/whole genome and Sanger sequencing analysis for identification of novel genes and mutations from rare genetic disorders in the Saudi Arabia. I have more than 16 years of research experience with more than 150 international peer reviewed article published reputed journals.
My aim of the research is to find novel genes and mutations specially the role of different KIFs genes in neurodegenerative disorders in the Saudi Arabia including Epilepsy, Autism, Alzheimer's intellectual disabilities and mental retardations. In addition, I use Knock-in/Knock-out animal models based on the identification of novel mutations/findings related to epileptic patients, rare genetics disorders for known as well as novel genetic aberrations to utilize them for testing novel therapeutic agents in a targeted therapeutic approach for rare, ultra rare genetic disorder, autism, epilepsy and microcephaly.

Activities

Employment (1)

King Abdulaziz University: Jeddah, Makkah, SA

2011-02-23 to present (CEGMR)
Employment
Source: Self-asserted source
Naseer MI

Education and qualifications (3)

Gyeongsang National University: Jinju, KR

2010-02-10 to 2011-02-10 | Post Doc. (Applied Life Science)
Education
Source: Self-asserted source
Naseer MI

Gyeongsang National University: Jinju, KR

2006-09-01 to 2010-02-15 | Ph.D (Applied Life Science)
Education
Source: Self-asserted source
Naseer MI

Quaid-i-Azam University: Islamabad, PK

2003-09-01 to 2005-06-31 | M.phil (Biochemistry/Molecularbiology)
Education
Source: Self-asserted source
Naseer MI

Professional activities (1)

Center of Excellence in Genomic Medicine Research: Jeddah, SA

2024-04-24 | Best Senior Researcher 2023 (Center of Excellence in Genomic Medicine Research King Abdulaziz University Jeddah)
Distinction
Source: Self-asserted source
Naseer MI

Funding (18)

Application of advanced high-density array technology for mutational analysis to detect genome-wide copy number variations and single nucleotide polymorphisms in Juvenile Myoclonic Epilepsy from Western Saudi Arabia

Grant
King Abdulaziz City for Science and Technology (KACST) (Riyadh, SA)
Source: Self-asserted source
Naseer MI

Association of SNPs in GC and CYP2R1 with total and directly measured free 25-hydroxyvitamin D in multi-ethnic postmenopausal women in Saudi Arabia

Grant
Deanship of Scientific Research (DSR), King Abdulaziz University(KAU) (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Comprehensive molecular analysis of Kinesin superfamily proteins (KIFs) and their role in neurodegenerative disease model in Saudi Arabia

Grant
KAU HiCi grant 1432/6-1 (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Deciphering the therapeutic importance of IL-33/ST2 axis in colonic inflammation and colon carcinoma using cellular, molecular and systems immunological strategies

Grant
IFPRC-012-141-2020 DSR KAU Institutional (National Challenge Grant) (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Developing Strategies to Dissect the Role of IL-33-ST2-Mast Cell Axis in Allergic Disorders: In Vitro, In Vivo and In Silico Approaches

Grant
King Abdulaziz City for Science and Technology (KACST) (Riyadh, SA)
Source: Self-asserted source
Naseer MI

Exome Analysis Identified Novel Homozygous Splice Site Donor Alteration in NT5C2 Gene in a Saudi Family Associated With Spastic Diplegia Cerebral Palsy, Developmental Delay, and Intellectual Disability

Grant
KiDeanship of Scientific Research (DSR), King Abdulaziz Universityng Abdulaziz University (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Exome sequencing reveled a compound heterozygous mutations in RTTN gene causing developmental delay and primary microcephaly

Grant
King Abdulaziz University- Deanship of Scientific Research (DSR) (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Gene Mapping and Molecular Analysis of Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome) in Saudi Arabian population

Grant
King Abdulaziz City for Science and Technology (KACST) (Riyadh, SA)
Source: Self-asserted source
Naseer MI

Identification of novel gene and mutations from Epileptic patients

Grant
KiDeanship of Scientific Research (DSR), King Abdulaziz Universityng Abdulaziz University (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Identification of Novel Genes and mutation in the families having Rare Genetics disorders

Grant
Deanship of scientific research (DSR), King Abdulaziz University (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Innovative Gene Therapy for Primary Microcephaly in Saudi Arabia

Grant
Research and Development Office, Ministry of Education RDO-902 (Riyadh, SA)
Source: Self-asserted source
Naseer MI

Neurogenetics Research Program

Grant
King Salman Center for Disability Research (Riyadh, SA)
Source: Self-asserted source
Naseer MI

Next generation sequencing reveals novel homozygous frameshift in PUS7 and splice acceptor variants in AASS gene leading to intellectual disability, developmental delay, dysmorphic feature and microcephaly

Grant
Deanship of Scientific Research (DSR), King Abdulaziz University(KAU) (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Novel Missense Variant in Heterozygous State in the BRPF1 Gene Leading to Intellectual Developmental Disorder With Dysmorphic Facies and Ptosis

Grant
Deanship of Scientific Research (DSR), King Abdulaziz University(KAU) (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Study of novel gene and mutations from primary Microcephaly in Saudi Arabia using advanced high-density array technology to detect genome-wide copy number variations and single nucleotide polymorphisms

Grant
King Abdulaziz City for Science and Technology` (Riyadh, SA)
Source: Self-asserted source
Naseer MI

Use of Whole Exome Sequencing for Identification of Genetic Variants Related to Growth Hormone Deficiency and Short Stature: Family-Based Study

Grant
KiDeanship of Scientific Research (DSR), King Abdulaziz Universityng Abdulaziz University (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Whole exome sequencing reveals a homozygous nonsense mutation in HEXA gene leading to Tay-Sachs disease in Saudi Family

Grant
King Abdulaziz University- Deanship of Scientific Research (DSR) (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Whole exome sequencing technique to identify of novel genes and mutation from Primary Microcephaly families in Saudi Arabia

Grant
Deanship of Scientific Research (DSR), King Abdulaziz University(KAU) (Jeddah, SA)
Source: Self-asserted source
Naseer MI

Works (50 of 153)

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Page 1 of 4

Evaluating the Therapeutic Efficacy of<i> Swertia</i><i> Chirayita</i> in Liver Cancer Management

Journal of Biological Regulators and Homeostatic Agents
2024 | Journal article
Contributors: Arshad, Fatima; Altaf, Awais; Lodhi, Madeeha Shahzad; Malik, Arif; Sattar, Huma; Zahid, Sara; Naseer, Muhammad Imran; Abojamel, Torki S.; Haque, Absarul; Ali, Qurban
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Neuroprotective profile of pyruvate against ethanol-induced neurodegeneration in developing mice brain (vol 34, pg 2137, 2024)

Neurological Sciences
2024 | Journal article
Contributors: Ullah, Najeeb; Naseer, Muhammad Imran; Ullah, Ikram; Kim, Tae Hyun; Lee, Hae Young; Kim, Myeong Ok
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Unveiling genetics of non-syndromic albinism using whole exome sequencing: A comprehensive study of<i> TYR,</i><i> TYRP1,</i><i> OCA2</i> and<i> MC1R</i> genes in 17 families

Gene
2024 | Journal article
Contributors: Zaman, Qaiser; Khan, Jamshid; Ahmad, Mashal; Khan, Hamza; Chaudhary, Hammad Tufail; Rehman, Gauhar; Rahman, Obaid Ur; Shah, Muhammad M.; Hussain, Javeria; Jamal, Qaisar et al.
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Whole exome sequencing of a novel homozygous missense variant in <i>PALB2</i> gene leading to Fanconi anaemia complementation group

Biomedical Reports
2024 | Journal article
Contributors: Abdulkareem, Angham Abdulrhman; Shirah, Bader H.; Bagabir, Hala Abubaker; Haque, Absarul; Naseer, Muhammad Imran
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Childhood-related neural genotype–phenotype in ATP1A3 mutations: comprehensive analysis

Genes & Genomics
2024-04 | Journal article
Contributors: Osama Y. Muthaffar; Asma Alqarni; Jumana A. Shafei; Sarah Y. Bahowarth; Anas S. Alyazidi; Muhammad Imran Naseer
Source: check_circle
Crossref

A Novel Homozygous Abnormal Splice Variant in the Myoferlin Gene Leading to Floppy Infant Syndrome in a Saudi Family

Journal of Disability Research
2023 | Journal article
Contributors: Angham Abdulrahman Abdulkareem; Bader H. Shirah; Osama Yousef Muthaffar; Hala Abubaker Bagabir; Muhammad Imran Naseer
Source: check_circle
Crossref

A Novel Homozygous Nonsense Variant in the <i>DYM</i> Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family

Genes
2023 | Journal article
Contributors: Bakar, Abu; Shams, Sulaiman; Bibi, Nousheen; Ullah, Asmat; Ahmad, Wasim; Jelani, Musharraf; Muthaffar, Osama Yousef; Abdulkareem, Angham Abdulrhman; Abujamel, Turki S. S.; Haque, Absarul et al.
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A novel homozygous splice donor variant in the LRPPRC gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case report

Frontiers in Pediatrics
2023 | Journal article
Contributors: Muthaffar, Osama Y.; Abdulkareem, Angham Abdulrhman; Ashi, Abrar; Naseer, Muhammad Imran
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Combinatorial Therapeutic Potential of Stem Cells and Benzimidazol Derivatives for the Reduction of Liver Fibrosis

Pharmaceuticals
2023 | Journal article
Contributors: Iqbal, Maryam; Shams, Sulaiman; Rafiq, Huma; Khan, Momin; Khan, Shahid; Sadique Khattak, Umer; Afridi, Sahib Gul; Bibi, Fehmida; Abdulkareem, Angham Abdulrhman; Naseer, Muhammad Imran
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Defining the role of the antineoplastic drug bleomycin based on toxicogenomic-DNA damage inducing (TGx-DDI) genomic biomarkers data: A meta-analysis using next-generation knowledge discovery method

Pakistan Journal of Medical Sciences
2023 | Journal article
Contributors: Pushparaj, Peter Natesan; Rasool, Mahmood; Naseer, Muhammad Imran; Gauthaman, Kalamegam
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Exploration of potential molecular mechanisms and genotoxicity of anti-cancer drugs using next generation knowledge discovery methods

Pakistan Journal of Medical Sciences
2023 | Journal article
Contributors: Pushparaj, Peter Natesan; Rasool, Mahmood; Naseer, Muhammad Imran; Gauthaman, Kalamegam
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Exploring bioactive compounds from a symbiotic bacterial strain of<i> Spongiobacter</i> sp

Bioinformation
2023 | Journal article
Contributors: Bibi, Fehmida; Naseer, Muhammad Imran; Azhar, Esam Ibraheem
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Leber hereditary optic neuropathy presenting as bilateral visual loss and white matter disease

Bioinformation
2023 | Journal article
Contributors: Algahtani, Hussein; Shirah, Bader; Abdulkareem, Angham Abdulrhman; Bibi, Fehmida; Pushparaj, Peter Natesan; Naseer, Muhammad Imran
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Novel Variants in <i>MPV17, PRX, GJB1</i>, and <i>SACS</i> Cause Charcot-Marie-Tooth and Spastic Ataxia of Charlevoix-Saguenay Type Diseases

Genes
2023 | Journal article
Contributors: Zaman, Qaiser; Khan, Muhammad Abbas; Sahar, Kalsoom; Rehman, Gauhar; Khan, Hamza; Rehman, Mehwish; Najumuddin; Ahmad, Ilyas; Tariq, Muhmmad; Muthaffar, Osama Yousef et al.
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Phenotypic Classification of Eye Colour and Developmental Validation of the Irisplex System on Population Living in Malakand Division, Pakistan

Biomedicines
2023 | Journal article
Contributors: Rahat, Murad Ali; Akbar, Fazal; Rasool, Akhtar; Ilyas, Muhammad; Rakha, Allah; Shams, Sulaiman; Jelani, Musharraf; Bibi, Fehmida; Shirah, Bader H.; Abdulkareem, Angham Abdulrhman et al.
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Pretreatment with troxerutin protects/improves neurological deficits in a mouse model of traumatic brain injury

Heliyon
2023 | Journal article
Contributors: Malik, Ashfaq Ahmed Khan; Ahmad, Waqas; Younas, Farhan; Badshah, Haroon; Alharazy, Shatha; Rehman, Shafiq Ur; Naseer, Muhammad Imran; Muthaffar, Osama Yousef; Achakzai, Rehmatullah; Ullah, Ikram
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Report of Hermansky-Pudlak Syndrome in Two Families with Novel Variants in <i>HPS3</i> and <i>HPS4</i> Genes

Genes
2023 | Journal article
Contributors: Zaman, Qaiser; Sadeeda; Anas, Muhammad; Rehman, Gauhar; Khan, Qadeem; Iftikhar, Aiman; Ahmad, Mashal; Owais, Muhammad; Ahmad, Ilyas; Muthaffar, Osama Yousef et al.
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Two novel homozygous variants of <i>ATP6V0A2</i> and <i>ALDH18A1</i> lead to autosomal recessive cutis laxa type 2 and 3 in two Pakistani families

Journal of Gene Medicine
2023 | Journal article
Contributors: Zaman, Qaiser; Iftikhar, Aiman; Rehman, Gauhar; Khan, Qadeem; Najumuddin, Amin; Jan, Amin; Khan, Jamshid; Anas, Muhammad; Liba, Osama Yousef; Umair, Muhammad et al.
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Use of whole exome sequencing for identification of genetic variants related to Growth Hormone Deficiency and Short Stature: A Family-Based Study

Pakistan Journal of Medical Sciences
2023 | Journal article
Contributors: Alharazy, Shatha; Naseer, Muhammad Imran
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Whole Exome Sequencing Reveals a Novel Homozygous Variant in the Ganglioside Biosynthetic Enzyme, <i>ST3GAL5</i> Gene in a Saudi Family Causing Salt and Pepper Syndrome

Genes
2023 | Journal article
Contributors: Abdulkareem, Angham Abdulrhman; Shirah, Bader H.; Naseer, Muhammad Imran
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Whole Exome Sequencing Reveals Two Novel Homozygous Variants in the TRAPPC9 and PLOD3 Genes Leading to Intellectual Disability and Bone Fragility with Contractures

Journal of Disability Research
2023 | Journal article
Contributors: Angham Abdulrahman Abdulkareem; Bader H. Shirah; Osama Yousef Muthaffar; Muhammad Imran Naseer
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Crossref

Whole-Exome Sequencing Reveals a Missense Variant c.1612C&gt;T (p.Arg538Cys) in the <i>BTD</i> Gene Leading to Neuromyelitis Optica Spectrum Disorder in Saudi Families

Frontiers in Pediatrics
2022 | Journal article
Contributors: Naseer, Muhammad Imran; Pushparaj, Peter Natesan; Abdulkareem, Angham Abdulrahman; Muthaffar, Osama Y.
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KIF4 regulates neuronal morphology and seizure susceptibility via the PARP1 signaling pathway

2022-11-10 | Other
Contributors: Yuansong Wan; Momo Morikawa; Manatsu Morikawa; Suguru Iwata; Muhammad Imran Naseer; Adeel Chaudhary; Yosuke Tanaka; Nobutaka Hirokawa
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Crossref

Exome sequencing reveled a compound heterozygous mutations in RTTN gene causing developmental delay and primary microcephaly

Saudi Journal of Biological Sciences
2021 | Journal article
Contributors: Naseer, Muhammad Imran; Abdulkareem, Angham Abdulrahman; Muthaffar, Osama Yousef; Chaudhary, Adeel G.
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Chronic progressive external ophthalmoplegia in a Saudi patient with a mutation in the POLG gene successfully managed with bilateral frontalis sling

Journal of Genetic Medicine
2021-12-31 | Journal article
Contributors: Hussein Algahtani; Bader Shirah; Khalid Alsaggaf; Mohammad H. Al-Qahtani; Angham Abdulrahman Abdulkareem; Muhammad Imran Naseer; Ahmad R. Abuzinadah
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Crossref

Identification of Novel Gene Signatures using Next-Generation Sequencing Data from COVID-19 Infection Models: Focus on Neuro-COVID and Potential Therapeutics.

Frontiers in pharmacology
2021-08-31 | Journal article
Source: Self-asserted source
Naseer MI

Association between vitamin D and glycaemic parameters in a multi-ethnic cohort of postmenopausal women with type 2 diabetes in Saudi Arabia.

BMC endocrine disorders
2021-08-12 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Whole-Exome Sequencing for Identification of Genetic Variants Involved in Vitamin D Metabolic Pathways in Families With Vitamin D Deficiency in Saudi Arabia.

Frontiers in genetics
2021-06-08 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Association of SNPs in GC and CYP2R1 with total and directly measured free 25-hydroxyvitamin D in multi-ethnic postmenopausal women in Saudi Arabia.

Saudi journal of biological sciences
2021-05-04 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Assessing the diversity of bacterial communities from marine sponges and their bioactive compounds.

Saudi journal of biological sciences
2021-03-23 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Array comparative genomic hybridization based identification of key genetic alterations at 2p21-p16.3 (MSH2, MSH6, EPCAM), 3p23-p14.2 (MLH1), 7p22.1 (PMS2) and 1p34.1-p33 (MUTYH) regions in hereditary non polyposis colorectal cancer (Lynch syndrome) in the Kingdom of Saudi Arabia

Saudi Journal of Biological Sciences
2020 | Journal article
Contributors: Rasool, Mahmood; Pushparaj, Peter Natesan; Mirza, Zeenat; Naseer, Muhammad Imran; Abusamra, Heba; Alquaiti, Maha; Shaabad, Manal; Sibiany, Abdulrahman Mohamed Saeed; Gauthaman, Kalamegam; Al-Qahtani, Mohammed Hussein et al.
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Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family.

The journal of gene medicine
2020-10-27 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 3)‎

A Novel Mutation in HERC2 Gene in a Patient with Global Developmental Delay, Intellectual Disability, and Refractory Seizures.

Neuropediatrics
2020-10-16 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

A Novel Variant in CWF19L1 Gene in a Family with Late-Onset Autosomal Recessive Cerebellar Ataxia 17.

Neurological research
2020-10-04 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Next generation sequencing reveals novel homozygous frameshift in <i>PUS7</i> and splice acceptor variants in <i>AASS</i> gene leading to intellectual disability, developmental delay, dysmorphic feature and microcephaly.

Saudi journal of biological sciences
2020-09-23 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Whole exome sequencing reveals a homozygous nonsense mutation in <i>HEXA</i> gene leading to Tay-Sachs disease in Saudi Family.

Pakistan journal of medical sciences
2020-09-01 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

A novel variant c.3706C>T p.(Avg 1236Cys) in the <i>ABCA7</i> gene in a Saudi patient with susceptibility to Alzheimer's disease 9.

Intractable & rare diseases research
2020-08-01 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

A Novel Intronic Variant in <i>SLC2A1</i> Gene in a Saudi Patient with Myoclonic Epilepsy.

Journal of epilepsy research
2020-06-30 | Journal article
Source: Self-asserted source
Naseer MI

A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
2020-05-13 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Novel Missense Variant in Heterozygous State in the BRPF1 Gene Leading to Intellectual Developmental Disorder With Dysmorphic Facies and Ptosis.

Frontiers in genetics
2020-05-07 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

A novel mutation in <i>ATM</i> gene in a Saudi female with ataxia telangiectasia.

The International journal of neuroscience
2020-03-16 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Exome Analysis Identified Novel Homozygous Splice Site Donor Alteration in NT5C2 Gene in a Saudi Family Associated With Spastic Diplegia Cerebral Palsy, Developmental Delay, and Intellectual Disability.

Frontiers in genetics
2020-02-21 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Antimicrobial activity of bacteria from marine sponge Suberea mollis and bioactive metabolites of Vibrio sp. EA348.

Saudi journal of biological sciences
2020-02-11 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Whole Exome Sequencing Identifies Three Novel Mutations in the <i>ASPM</i> Gene From Saudi Families Leading to Primary Microcephaly.

Frontiers in pediatrics
2020-01-01 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Hepato-protective effect of Allium sativum against immobilization stress in rats

Pakistan Journal of Pharmaceutical Sciences
2019 | Journal article
Contributors: Zaidi, Syed Kashif; Ansari, Shakeel Ahmed; Tabrez, Shams; Ashraf, Ghulam Md.; Shakil, Shazi; Jafri, Mohammad Alam; Naseer, Muhammad Imran; Abdulaal, Wesam H.; Banu, Naheed; Al-Qahtani, Muhammed
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Autosomal recessive cerebellar ataxia with spasticity due to a rare mutation in <i>GBA2</i> gene in a large consanguineous Saudi family.

Genes & diseases
2019-07-27 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Data mining analysis of human gut microbiota links Fusobacterium spp. with colorectal cancer onset.

Bioinformation
2019-05-30 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

Pyrosequencing reveals sponge specific bacterial communities in marine sponges of Red Sea, Saudi Arabia.

Saudi journal of biological sciences
2019-05-07 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

A novel mutation in <i>TTN</i> gene in a Saudi patient with bilateral facial weakness and scapular winging.

Intractable & rare diseases research
2019-05-01 | Journal article
Source: Self-asserted source
Naseer MI
grade
Preferred source (of 2)‎

A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 gene.

Seizure
2019-04-19 | Journal article
Source: Self-asserted source
Naseer MI
grade
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Peer review (8 reviews for 4 publications/grants)

Review activity for European journal of medical genetics. (1)
Review activity for Heliyon. (4)
Review activity for PloS one. (2)
Review activity for Progress in neuro-psychopharmacology & biological psychiatry. (1)