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Mohammad R. Toliat

Mohammad R. Toliat

D-Index & Metrics

Molecular Biology

D-Index
47
Citations
7556
World Ranking
2754
National Ranking
189

Overview

Mohammad R. Toliat is affiliated with the University of Cologne in Germany. Their research primarily spans the fields of Medicine and Biochemistry, Genetics, and Molecular Biology, with a focus on several subfields including Molecular Biology, Genetics, Cancer Research, Pathology and Forensic Medicine, and Immunology.

The scientist's work covers various main topics, highlighting Cancer Genomics and Diagnostics, Epigenetics and DNA Methylation, Single-cell and Spatial Transcriptomics, Hearing, Cochlea, Tinnitus, Genetics, Ear Surgery and Otitis Media, Vestibular and Auditory Disorders, and Autoimmune Bullous Skin Diseases.

Recent publications authored or co-authored by Mohammad R. Toliat include:

  • cfNOMe - A single assay for comprehensive epigenetic analyses of cell-free DNA (2020, Genome Medicine)
  • Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss (2020, Clinical Genetics)
  • Identification of two novel bullous pemphigoid-associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in Germans (2021, Orphanet Journal of Rare Diseases)
  • Unraveling Structural Rearrangements of the CFH Gene Cluster in Atypical Hemolytic Uremic Syndrome Patients Using Molecular Combing and Long-Fragment Targeted Sequencing (2022, Journal of Molecular Diagnostics)
  • Verification of immunology-related genetic associations in BPD supports ABCA3 and five other genes (2021, Pediatric Research)

Frequent co-authors collaborating with Mohammad R. Toliat include:

  • Peter Nürnberg
  • Janine Altmüller
  • Holger Thiele
  • Christian Becker
  • Birgit Budde

Publications by Mohammad R. Toliat have appeared repeatedly in notable venues such as Clinical Genetics, Genome Medicine, Orphanet Journal of Rare Diseases, Journal of Molecular Diagnostics, and Pediatric Research.

Best Publications

  • Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification

    Frank Rutsch;Nico Ruf;Sucheta Vaingankar;Mohammad R Toliat

  • NAD(P)H Oxidase and Multidrug Resistance Protein Genetic Polymorphisms Are Associated With Doxorubicin-Induced Cardiotoxicity

    Leszek Wojnowski;Bettina Kulle;Markus Schirmer;Gregor Schlüter

  • Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

    Johannes R Lemke;Dennis Lal;Eva M Reinthaler;Isabelle Steiner

  • tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia.

    Birgit S. Budde;Yasmin Namavar;Peter G. Barth;Bwee Tien Poll-The

  • Evaluation of a potential epigenetic biomarker by quantitative methyl-single nucleotide polymorphism analysis.

    Karen Uhlmann;Karen Uhlmann;Anja Brinckmann;Mohammad R. Toliat;Heide Ritter

  • Laminin-α4 and Integrin-Linked Kinase Mutations Cause Human Cardiomyopathy Via Simultaneous Defects in Cardiomyocytes and Endothelial Cells

    Ralph Knöll;Ruben Postel;Jianming Wang;Ralph Krätzner

  • Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes.

    Julian Schubert;Aleksandra Siekierska;Mélanie Langlois;Patrick May

  • Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism.

    Frank Rutsch;Susann Gailus;Isabelle R Miousse;Terttu Suormala

  • Mutations in PLK4 , encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy

    Carol Anne Martin;Ilyas Ahmad;Ilyas Ahmad;Anna Klingseisen;Muhammad Sajid Hussain

  • Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

    Michael Steffens;Costin Leu

  • SNP-Based Analysis of Genetic Substructure in the German Population

    Michael Steffens;Claudia Lamina;Thomas Illig;Thomas Bettecken

  • Induced pluripotent stem cell-derived neuronal cells from a sporadic Alzheimer’s disease donor as a model for investigating AD-associated gene regulatory networks

    Amir M Hossini;Matthias Megges;Matthias Megges;Matthias Megges;Alessandro Prigione;Alessandro Prigione;Bjoern Lichtner

  • Haplotypes and SNPs in 13 lipid-relevant genes explain most of the genetic variance in high-density lipoprotein and low-density lipoprotein cholesterol

    Hans Knoblauch;Anja Bauerfeind;Mohammad Reza Toliat;Christian Becker

  • RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy

    Dennis Lal;Eva M. Reinthaler;Janine Altmüller;Mohammad R. Toliat

  • Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome

    Stefanie Weber;Holger Thiele;Sevgi Mir;Mohammad Reza Toliat

  • GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

    P. Striano;Y.G. Weber;M.R. Toliat;J. Schubert

  • Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy

    Thomas Sander;Mohammad Reza Toliat;Armin Heils;Gundula Leschik

  • Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1.

    Laura Crisponi;Giangiorgio Crisponi;Alessandra Meloni;Mohammad Reza Toliat

  • New genetic evidence for involvement of the dopamine system in migraine with aura.

    Unda Todt;Christian Netzer;Mohammad Toliat;Axel Heinze

  • Association of the Serum and Glucocorticoid Regulated Kinase (sgk1) Gene with QT Interval

    Andreas Busjahn;Guiscard Seebohm;Gottlieb Maier;Mohammad Reza Toliat

Frequent Co-Authors

Peter Nürnberg
Peter Nürnberg University of Cologne
Thomas Sander
Thomas Sander University of Cologne
Holger Thiele
Holger Thiele Leipzig University
Janine Altmüller
Janine Altmüller University of Cologne
Holger Lerche
Holger Lerche University of Tübingen
Gudrun Nürnberg
Gudrun Nürnberg University of Cologne
Christian Becker
Christian Becker University of Cologne
Andre Franke
Andre Franke Kiel University
Thomas F. Wienker
Thomas F. Wienker Max Planck Society
Per Hoffmann
Per Hoffmann University of Bonn

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Related Online Degrees & Career Pathways

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