MOHAMMAD ATHAR

About

Dr Mohammad Athar is an Associate Professor of genomic medicine at the Department of Medical Genetics and Science and Technology Unit, Umm Al-Qura University, Makkah, Saudi Arabia. Dr Athar obtained his PhD in Bioscience from the Jamia Millia Islamia/INMAS-DRDO, Delhi, India, in 2012. Human Molecular Genetics, Functional Genomics and Molecular Medicine are the major disciplines of his area of research. His research interests focus on inherited disorders (Familial hypercholesterolemia, Polycystic Kidney Disease, Haemophilia, and Thrombophilia) using cutting-edge genetic and genomic technologies such as Next-generation sequencing (NGS). He has over ten years of experience in a clinical research laboratory as a PI, Co-I, and Research Scientist on several national-level research grants. Dr Athar contributed significantly to establishing the genetics spectrum of Familial hypercholesterolemia in Saudi populations, in addition to developing high throughput, cost-effective Next-generation Sequencing (NGS) based methods for the molecular diagnosis of inherited disorders.

Work

Umm al-Qura University

Associate Professor

Saudi Arabia

Jan 2022→ Present

Umm Al-Qura University

Assistant Professor

Saudi Arabia

Jan 2012→ Jan 2021

SMS Medical College and Hospital

Research Scientist

India

Oct 2011→ Apr 2012

Education

Jamia Millia Islamia

India

Oct 2011→ Apr 2012

PhD

Jamia Hamdard

India

Oct 2011→ Apr 2012

M.Sc.

Publications

Proton next generation DNA sequencing [version 1; peer review

journal-article

Deciphering the Structural and Functional Effects of the R1150W Non-Synonymous Variant in SCN9A Linked to Altered Pain Perception

NeuroSci

Jan 2025

journal-article

Characterising acute and chronic care needs: insights from the Global Burden of Disease Study 2019

Nature Communications

Jan 2025

journal-article

Characterising acute and chronic care needs: insights from the Global Burden of Disease Study 2019

Nature Communications

Jan 2025

journal-article

Deciphering the Structural and Functional Effects of the R1150W Non-Synonymous Variant in SCN9A Linked to Altered Pain Perception

NeuroSci

Jan 2025

journal-article

Global, regional, and national prevalence of kidney failure with replacement therapy and associated aetiologies, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023

The Lancet Global Health

Jan 2025

journal-article

Global, regional, and national prevalence of kidney failure with replacement therapy and associated aetiologies, 1990–2023: a systematic analysis for the Global Burden of Disease Study 2023

The Lancet Global Health

Jan 2025

journal-article

Global, Regional, and National Burden of Nontraumatic Subarachnoid Hemorrhage

JAMA Neurology

Jan 2025

journal-article

Potentials of artificial intelligence in familial hypercholesterolemia: Advances in screening, diagnosis, and risk stratification for early intervention and treatment

International Journal of Cardiology

Jan 2024

journal-article

Mortality and disability-adjusted life years in North Africa and Middle East attributed to kidney dysfunction: a systematic analysis for the Global Burden of Disease Study 2019

Clinical Kidney Journal

Jan 2024

journal-article

Temporal patterns of cancer burden in Asia, 1990–2019: a systematic examination for the Global Burden of Disease 2019 study

The Lancet Regional Health - Southeast Asia

Jan 2024

journal-article

Temporal patterns of cancer burden in Asia, 1990–2019: a systematic examination for the Global Burden of Disease 2019 study

The Lancet Regional Health - Southeast Asia

Jan 2024

journal-article

Global burden and strength of evidence for 88 risk factors in 204 countries and 811 subnational locations, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021

The Lancet

Jan 2024

journal-article

Global burden of 288 causes of death and life expectancy decomposition in 204 countries and territories and 811 subnational locations, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021

The Lancet

Jan 2024

journal-article

The burden of neurological conditions in north Africa and the Middle East, 1990–2019: a systematic analysis of the Global Burden of Disease Study 2019

The Lancet Global Health

Jan 2024

journal-article

Mortality and disability-adjusted life years in North Africa and Middle East attributed to kidney dysfunction: a systematic analysis for the Global Burden of Disease Study 2019

Clinical Kidney Journal

Jan 2024

journal-article

Correlation between platelet metrics and cardiovascular risk in prediabetes with coronary artery disease: A two-year cross-sectional study

Journal of King Saud University - Science

Jan 2024

journal-article

An insight into impact of nanomaterials toxicity on human health.

PeerJ

Jan 2024

journal-article

Substantial Changes in Selected Volatile Organic Compounds (VOCs) and Associations with Health Risk Assessments in Industrial Areas during the COVID-19 Pandemic

Toxics

Jan 2023

journal-article

Corrigendum to “Anti- E. coli immunoglobulin yolk (IgY): Reduction of pathogen receptors and inflammation factors could be caused by decrease in E. coli load” [Heliyon 9(3) (February 21, 2023) e13876]> (Heliyon (2023) 9(3), (S2405844023010836), (10.1016/j.heliyon.2023.e13876))

Heliyon

Jan 2023

journal-article

Global, regional, and national burden of diabetes from 1990 to 2021, with projections of prevalence to 2050: a systematic analysis for the Global Burden of Disease Study 2021

The Lancet

Jan 2023

journal-article

Global Burden of Cardiovascular Diseases and Risks, 1990-2022

Journal of the American College of Cardiology

Jan 2023

journal-article

SARS-CoV-2 vaccine breakthrough infections (VBI) by Omicron variant (B.1.1.529) and consequences in structural and functional impact

Cellular Signalling

Jan 2023

journal-article

SARS-CoV-2 vaccine breakthrough infections (VBI) by Omicron variant (B.1.1.529) and consequences in structural and functional impact

Cellular Signalling

Jan 2023

journal-article

Novel LDLR Variant in Familial Hypercholesterolemia: NGS-Based Identification, In Silico Characterization, and Pharmacogenetic Insights

Life

Jan 2023

journal-article

Novel LDLR Variant in Familial Hypercholesterolemia: NGS-Based Identification, In Silico Characterization, and Pharmacogenetic Insights

Life

Jan 2023

journal-article

Novel LDLR Variant in Familial Hypercholesterolemia: NGS-Based Identification, In Silico Characterization, and Pharmacogenetic Insights

Life

Jan 2023

journal-article

Protein structural insights into a rare PCSK9 gain-of-function variant (R496W) causing familial hypercholesterolemia in a Saudi family: whole exome sequencing and computational analysis

Frontiers in Physiology

Jan 2023

journal-article

Protein structural insights into a rare PCSK9 gain-of-function variant (R496W) causing familial hypercholesterolemia in a Saudi family: whole exome sequencing and computational analysis

Frontiers in Physiology

Jan 2023

journal-article

Role of single nucleotide polymorphism rs2383206 on coronary artery disease risk among Saudi Population: a case-control study

European Review for Medical and Pharmacological Sciences

Jan 2023

journal-article

Role of single nucleotide polymorphism rs2383206 on coronary artery disease risk among Saudi Population: a case-control study

European review for medical and pharmacological sciences

Jan 2023

journal-article

Global, regional, and national burden of diabetes from 1990 to 2021, with projections of prevalence to 2050: a systematic analysis for the Global Burden of Disease Study 2021

The Lancet

Jan 2023

journal-article

The burden of metabolic risk factors in North Africa and the Middle East, 1990–2019: findings from the Global Burden of Disease Study

eClinicalMedicine

Jan 2023

journal-article

The burden of metabolic risk factors in North Africa and the Middle East, 1990–2019: findings from the Global Burden of Disease Study

eClinicalMedicine

Jan 2023

journal-article

Anti-E. coli Immunoglobulin Yolk (IgY): Reduction of pathogen receptors and inflammation factors could be caused by decrease in E. coli load

Heliyon

Jan 2023

journal-article

Anti-E. coli Immunoglobulin Yolk (IgY): Reduction of pathogen receptors and inflammation factors could be caused by decrease in E. coli load

Heliyon

Jan 2023

journal-article

Substantial Changes in Selected Volatile Organic Compounds (VOCs) and Associations with Health Risk Assessments in Industrial Areas during the COVID-19 Pandemic

Toxics

Jan 2023

journal-article

Substantial Changes in Selected Volatile Organic Compounds (VOCs) and Associations with Health Risk Assessments in Industrial Areas during the COVID-19 Pandemic

Toxics

Jan 2023

journal-article

The global burden of cancer attributable to risk factors, 2010–19: a systematic analysis for the Global Burden of Disease Study 2019

The Lancet

Jan 2022

journal-article

Variations in the Yamuna River Water Quality During the COVID-19 Lockdowns

Frontiers in Environmental Science

Jan 2022

journal-article

Identification of Novel and Known LDLR Variants Triggering Severe Familial Hypercholesterolemia in Saudi Families

Current Vascular Pharmacology

Jan 2022

journal-article

The global burden of cancer attributable to risk factors, 2010–19: a systematic analysis for the Global Burden of Disease Study 2019

The Lancet

Jan 2022

journal-article

Identification of Novel and Known LDLR Variants Triggering Severe Familial Hypercholesterolemia in Saudi Families

Current Vascular Pharmacology

Jan 2022

journal-article

Design and optimization of 18-gene Ion AmpliSeq panel of Next-generation sequencing for gene mutation analysis causing pain insensitivity

Journal of Umm Al-Qura University for Medical Sciences

Jan 2022

journal-article

Variations in the Yamuna River Water Quality During the COVID-19 Lockdowns

Frontiers in Environmental Science

Jan 2022

journal-article

Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism

Clinica Chimica Acta

Jan 2021

journal-article

Compound A Increases Cell Infiltration in Target Organs of Acute Graft-versus-Host Disease (aGVHD) in a Mouse Model

Molecules

Jan 2021

journal-article

Compound a increases cell infiltration in target organs of acute graft-versus-host disease (Agvhd) in a mouse model

Molecules

Jan 2021

journal-article

Compound a increases cell infiltration in target organs of acute graft-versus-host disease (Agvhd) in a mouse model

Molecules

Jan 2021

journal-article

Genetic association of rs10757278 on chromosome 9p21 and coronary artery disease in a saudi population

International Journal of General Medicine

Jan 2021

journal-article

Genetic association of rs10757278 on chromosome 9p21 and coronary artery disease in a saudi population

International Journal of General Medicine

Jan 2021

journal-article

Mutation Profiling of Intracranial Myxopapillary Ependymoma by Next Generation DNA Sequencing

The Gulf journal of oncology

Jan 2021

journal-article

Prevalence of the Factor V Leiden Mutation Arg534Gln in Western Region of Saudi Arabia: Functional Alteration and Association Study With Different Populations

Clinical and Applied Thrombosis/Hemostasis

Jan 2021

journal-article

Prevalence of the Factor V Leiden Mutation Arg534Gln in Western Region of Saudi Arabia: Functional Alteration and Association Study With Different Populations

Clinical and Applied Thrombosis/Hemostasis

Jan 2021

journal-article

Prevalence of the Factor V Leiden Mutation Arg534Gln in Western Region of Saudi Arabia: Functional Alteration and Association Study With Different Populations

Clinical and Applied Thrombosis/Hemostasis

Jan 2021

journal-article

Genetic Association of rs10757278 on Chromosome 9p21 and Coronary Artery Disease in a Saudi Population

International Journal of General Medicine

Jan 2021

journal-article

Global, regional, and national burden of stroke and its risk factors, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019

The Lancet Neurology

Jan 2021

journal-article

Global, regional, and national burden of stroke and its risk factors, 1990-2019: A systematic analysis for the Global Burden of Disease Study 2019

The Lancet Neurology

Jan 2021

journal-article

Mutation Profiling of Intracranial Myxopapillary Ependymoma by Next Generation DNA Sequencing

Gulf Journal of Oncology

Jan 2021

journal-article

Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism

Clinica Chimica Acta

Jan 2021

journal-article

Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism

Clinica Chimica Acta

Jan 2021

journal-article

Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism

Clinica Chimica Acta

Jan 2021

journal-article

EGFRvIII expression and isocitrate dehydrogenase mutations in patients with glioma

Oncology Letters

Jan 2020

journal-article

EGFRvIII expression and isocitrate dehydrogenase mutations in patients with glioma

Oncology Letters

Jan 2020

journal-article

EGFRvIII expression and isocitrate dehydrogenase mutations in patients with glioma

Oncology Letters

Jan 2020

journal-article

Future appeal of comparative studies on putative binding sites of HIV-1 virus-encoded proteolytic enzyme inhibitor of different Food and Drug Administration-approved compounds

HIV AIDS Rev

Jan 2020

journal-article

Future appeal of comparative studies on putative binding sites of HIV-1 virus-encoded proteolytic enzyme inhibitor of different Food and Drug Administration-approved compounds

HIV and AIDS Review

Jan 2020

journal-article

Future appeal of comparative studies on putative binding sites of HIV-1 virus-encoded proteolytic enzyme inhibitor of different Food and Drug Administration-approved compounds

HIV and AIDS Review

Jan 2020

journal-article

Xanthomas Can Be Misdiagnosed and Mistreated in Homozygous Familial Hypercholesterolemia Patients: A Call for Increased Awareness Among Dermatologists and Health Care Practitioners

Global Heart

Jan 2020

journal-article

Xanthomas can be misdiagnosed and mistreated in homozygous familial hypercholesterolemia patients: A call for increased awareness among dermatologists and health care practitioners

Global Heart

Jan 2020

journal-article

Xanthomas can be misdiagnosed and mistreated in homozygous familial hypercholesterolemia patients: A call for increased awareness among dermatologists and health care practitioners

Global Heart

Jan 2020

journal-article

Mutation profiling of anaplastic ependymoma grade III by Ion Proton next generation DNA sequencing

F1000Research

Jan 2020

journal-article

Mutation profiling of anaplastic ependymoma grade III by Ion Proton next generation DNA sequencing

F1000Research

Jan 2020

journal-article

Whole exome sequencing reveals multiple mutations in uncommon genes of familial hypercholesterolaemia

Journal of Cardiovascular Disease Research

Jan 2019

journal-article

Identification of six novel factor VIII gene variants using next generation sequencing and molecular dynamics simulation

Acta Biochimica Polonica

Jan 2019

journal-article

Association of functional variants and protein-to-protein physical interactions of human MutY homolog linked with familial adenomatous polyposis and colorectal cancer syndrome

Non-coding RNA research

Jan 2019

journal-article

Association of functional variants and protein-to-protein physical interactions of human MutY homolog linked with familial adenomatous polyposis and colorectal cancer syndrome

Non-coding RNA Research

Jan 2019

journal-article

Association of functional variants and protein-to-protein physical interactions of human MutY homolog linked with familial adenomatous polyposis and colorectal cancer syndrome

Non-coding RNA Research

Jan 2019

journal-article

Identification of six novel factor VIII gene variants using next generation sequencing and molecular dynamics simulation

Acta Biochimica Polonica

Jan 2019

journal-article

Identification of six novel factor VIII gene variants using next generation sequencing and molecular dynamics simulation

Acta Biochimica Polonica

Jan 2019

journal-article

Modifying inter-cistronic sequence significantly enhances IRES dependent second gene expression in bicistronic vector: Construction of optimised cassette for gene therapy of familial hypercholesterolemia

Non-coding RNA research

Jan 2019

journal-article

Modifying inter-cistronic sequence significantly enhances IRES dependent second gene expression in bicistronic vector: Construction of optimised cassette for gene therapy of familial hypercholesterolemia

Non-coding RNA Research

Jan 2019

journal-article

Modifying inter-cistronic sequence significantly enhances IRES dependent second gene expression in bicistronic vector: Construction of optimised cassette for gene therapy of familial hypercholesterolemia

Non-coding RNA Research

Jan 2019

journal-article

Molecular Dynamics Simulation Reveals Exposed Residues in the Ligand-Binding Domain of the Low-Density Lipoprotein Receptor that Interacts with Vesicular Stomatitis Virus-G Envelope

Viruses

Jan 2019

journal-article

Molecular dynamics simulation reveals exposed residues in the ligand-binding domain of the low-density lipoprotein receptor that interacts with vesicular stomatitis virus-G envelope

Viruses

Jan 2019

journal-article

Molecular dynamics simulation reveals exposed residues in the ligand-binding domain of the low-density lipoprotein receptor that interacts with vesicular stomatitis virus-G envelope

Viruses

Jan 2019

journal-article

Mutation profiling of anaplastic ependymoma grade III by Ion Proton next generation DNA sequencing

F1000Research

Jan 2019

journal-article

Mutation profiling of anaplastic ependymoma grade III by Ion Proton next generation DNA sequencing [version 1; peer review: 1 approved with reservations]

F1000Research

Jan 2019

journal-article

Mutation profiling of anaplastic ependymoma grade III by Ion Proton next generation DNA sequencing [version 1; peer review: 1 approved with reservations]

F1000Research

Jan 2019

journal-article

Next generation DNA sequencing of atypical choroid plexus papilloma of brain: Identification of novel mutations in a female patient by Ion Proton

Oncology Letters

Jan 2019

journal-article

Next generation DNA sequencing of atypical choroid plexus papilloma of brain: Identification of novel mutations in a female patient by ion proton

Oncology Letters

Jan 2019

journal-article

Next generation DNA sequencing of atypical choroid plexus papilloma of brain: Identification of novel mutations in a female patient by ion proton

Oncology Letters

Jan 2019

journal-article

Whole exome sequencing reveals multiple mutations in uncommon genes of familial hypercholesterolaemia

J Cardiovasc Dis Res

Jan 2019

journal-article

Whole exome sequencing reveals multiple mutations in uncommon genes of familial hypercholesterolaemia

Journal of Cardiovascular Disease Research

Jan 2019

journal-article

In Silico Approach to Investigate the Structural and Functional Attributes of Familial Hypercholesterolemia Variants Reported in the Saudi Population

Journal of Computational Biology

Jan 2018

journal-article

In Silico Approach to Investigate the Structural and Functional Attributes of Familial Hypercholesterolemia Variants Reported in the Saudi Population

Journal of Computational Biology

Jan 2018

journal-article

Next Generation Sequencing on Ion Proton for Mutation Detection in Brain Tumors: Development of Molecular Pathology Assays in the Kingdom of Saudi Arabia

The Journal of Molecular Diagnostics

Jan 2018

journal-article

Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemia

Atherosclerosis

Jan 2018

journal-article

Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemia

Atherosclerosis

Jan 2018

journal-article

Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemia

Atherosclerosis

Jan 2018

journal-article

Identification of a Novel ATM Missense Mutation by Next Generation Sequencing in Choroid Plexus Papilloma 

The Journal of Molecular Diagnostics

Jan 2018

journal-article

In Silico Approach to Investigate the Structural and Functional Attributes of Familial Hypercholesterolemia Variants Reported in the Saudi Population

Journal of Computational Biology

Jan 2018

journal-article

Compound heterozygous LDLR variant in severely affected familial hypercholesterolemia patient

Acta Biochimica Polonica

Jan 2017

journal-article

Compound heterozygous LDLR variant in severely affected familial hypercholesterolemia patient

Acta Biochimica Polonica

Jan 2017

journal-article

Compound heterozygous LDLR variant in severely affected familial hypercholesterolemia patient.

Acta Biochimica Polonica

Jan 2017

journal-article

Identification of four novel factor VIII gene mutations and protein structure analysis using molecular dynamic simulation

J Genet Syndr Gene Ther

Jan 2017

journal-article

Molecular Analysis of Factor VIII and Factor IX Genes in Hemophilia Patients: Identification of Novel Mutations and Molecular Dynamics Studies

Journal of clinical medicine research

Jan 2017

journal-article

The spectrum of familial hypercholesterolemia (FH) in Saudi Arabia: Prime time for patient FH registry

Open Cardiovascular Medicine Journal

Jan 2017

journal-article

The Open Cardiovascular Medicine

Open Cardiovascular Medicine Journal

Jan 2017

journal-article

The spectrum of familial hypercholesterolemia (FH) in Saudi Arabia: prime time for patient FH registry

The open cardiovascular medicine journal

Jan 2017

journal-article

The spectrum of familial hypercholesterolemia (FH) in Saudi Arabia: Prime time for patient FH registry

Open Cardiovascular Medicine Journal

Jan 2017

journal-article

1. Founder mutation identified in the LDLR gene causing familial hypercholesterolemia associated with increased risk of coronary heart disease

Journal of the Saudi Heart Association

Jan 2017

journal-article

4. Identification of a novel nonsense variant C. 1332DUP, P.(D445*) in the LDLR gene that causes familial hypercholesterolemia

Journal of the Saudi Heart Association

Jan 2017

journal-article

Compound heterozygous mutation in the LDLR gene in Saudi patients suffering severe hypercholesterolemia

Human Genomics

Jan 2016

journal-article

Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015)

BMC Genomics

Jan 2016

conference-paper

Association of functional variants and protein physical interactions of human MUTY homolog linked with familial adenomatous polyposis and colorectal cancer syndrome

Human Genomics

Jan 2016

journal-article

Functional alterations due to amino acid changes and evolutionary comparative analysis of ARPKD and ADPKD genes

Genomics data

Jan 2016

journal-article

Functional alterations due to amino acid changes and evolutionary comparative analysis of ARPKD and ADPKD genes

Genomics Data

Jan 2016

journal-article

Functional alterations due to amino acid changes and evolutionary comparative analysis of ARPKD and ADPKD genes

Genomics Data

Jan 2016

journal-article

Identification of a recurrent frameshift mutation at the LDLR exon 14 (c. 2027delG, p.(G676Afs* 33)) causing familial hypercholesterolemia in Saudi Arab homozygous children

Genomics

Jan 2016

journal-article

Identification of a recurrent frameshift mutation at the LDLR exon 14 (c.2027delG, p.(G676Afs*33)) causing familial hypercholesterolemia in Saudi Arab homozygous children

Genomics

Jan 2016

journal-article

Identification of a recurrent frameshift mutation at the LDLR exon 14 (c.2027delG, p.(G676Afs*33)) causing familial hypercholesterolemia in Saudi Arab homozygous children

Genomics

Jan 2016

journal-article

Ion torrent next generation sequencing of recessive polycystic kidney disease in Saudi patients

Human Genomics

Jan 2016

journal-article

Mutation Screening of the Factor VIII Gene in Hemophilia A in Saudi Arabia: Two Novel Mutations and Genotype-Phenotype Correlation

Journal of Molecular and Genetic Medicine

Jan 2016

journal-article

Next-generation sequencing for molecular diagnosis of autosomal recessive polycystic kidney disease

Gene

Jan 2016

journal-article

Next-generation sequencing for molecular diagnosis of autosomal recessive polycystic kidney disease

Gene

Jan 2016

journal-article

Next-generation sequencing for molecular diagnosis of autosomal recessive polycystic kidney disease

Gene

Jan 2016

journal-article

Molecular genotyping of haemophilia A in Saudi Arabian population: report of novel mutations

JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Jan 2015

conference-paper

Next generation sequencing to identify novel genetic variants causative of autosomal dominant familial hypercholesterolemia associated with increased risk of coronary heart disease

Gene

Jan 2015

journal-article

Next generation sequencing to identify novel genetic variants causative of autosomal dominant familial hypercholesterolemia associated with increased risk of coronary heart disease

Gene

Jan 2015

journal-article

Next generation sequencing to identify novel genetic variants causative of autosomal dominant familial hypercholesterolemia associated with increased risk of coronary heart disease

Gene

Jan 2015

journal-article

Identification of novel genetic mutations in low-density lipoprotein receptor (LDLR) gene causing familial hypercholesterolemia in Saudi Arab homozygous children

JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Jan 2015

conference-paper

DNA mismatch repair MSH2 gene-based SNP associated with different populations

Molecular Genetics and Genomics

Jan 2014

journal-article

DNA mismatch repair MSH2 gene-based SNP associated with different populations

Molecular Genetics and Genomics

Jan 2014

journal-article

Evidence of Trem2 variant associated with triple risk of alzheimer's disease

PLoS ONE

Jan 2014

journal-article

Evidence of Trem2 variant associated with triple risk of alzheimer's disease

PLoS ONE

Jan 2014

journal-article

Evidence of trem2 variant associated with triple risk of Alzheimer’s disease

PloS one

Jan 2014

journal-article

Identification of a novel nonsense variant c. 1332dup, p.(D445*) in the LDLR gene that causes familial hypercholesterolemia

Human genome variation

Jan 2014

journal-article

Identification of a novel nonsense variant c.1332dup, p.(D445*) in the LDLR gene that causes familial hypercholesterolemia

Human Genome Variation

Jan 2014

journal-article

Identification of a novel nonsense variant c.1332dup, p.(D445*) in the LDLR gene that causes familial hypercholesterolemia

Human Genome Variation

Jan 2014

journal-article

DNA mismatch repair MSH2 gene-based SNP associated with different populations

Molecular Genetics and Genomics

Jan 2014

journal-article

Hoechst 33342 induced reactive oxygen species and impaired expression of cytochrome c oxidase subunit 1 leading to cell death in irradiated human cancer cells

Molecular and Cellular Biochemistry

Jan 2011

journal-article

Hoechst 33342 induced reactive oxygen species and impaired expression of cytochrome c oxidase subunit 1 leading to cell death in irradiated human cancer cells

Molecular and Cellular Biochemistry

Jan 2011

journal-article

Hoechst 33342 induced reactive oxygen species and impaired expression of cytochrome c oxidase subunit 1 leading to cell death in irradiated human cancer cells

Molecular and cellular biochemistry

Jan 2011

journal-article

Hoechst 33342 induces radiosensitization in malignant glioma cells via increase in mitochondrial reactive oxygen species

Free radical research

Jan 2010

journal-article

Hoechst 33342 induces radiosensitization in malignant glioma cells via increase in mitochondrial reactive oxygen species

Free Radical Research

Jan 2010

journal-article

Hoechst 33342 induces radiosensitization in malignant glioma cells via increase in mitochondrial reactive oxygen species

Free Radical Research

Jan 2010

journal-article