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Genetics

D-Index
69
Citations
30467
World Ranking
2316
National Ranking
288

Overview

Mina Ryten is affiliated with University College London in the United Kingdom. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, and Medicine, with a total of 238 publications in the former and 149 in the latter.

Their work focuses on several subfields, including Molecular Biology, Neurology, Cellular and Molecular Neuroscience, Genetics, and Physiology. The scientist's research topics of interest include:

  • Parkinson's Disease Mechanisms and Treatments
  • RNA Research and Splicing
  • Genetic Neurodegenerative Diseases
  • Bioinformatics and Genomic Networks
  • RNA regulation and disease
  • Mitochondrial Function and Pathology
  • Alzheimer's disease research and treatments

Mina Ryten has contributed to prominent scientific venues where they have frequently published. The most common publication venues include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Brain
  • Nature Communications
  • Movement Disorders
  • Brain Communications

They have collaborated extensively with other researchers, with frequent co-authors including John Hardy, Regina H. Reynolds, Emil K. Gustavsson, Sonia García-Ruiz, and Juan A. Botía.

Among their recent publications are:

  • "Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli" (2020) in Nature
  • "ggtranscript: an R package for the visualization and interpretation of transcript isoforms using ggplot2" (2022) in Bioinformatics
  • "Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome" (2021) in Nature Communications
  • "Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets" (2021) in JAMA Neurology
  • "Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans" (2021) in New England Journal of Medicine

Best Publications

  • A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

    Alan E. Renton;Elisa Majounie;Adrian James Waite;Javier Simón-Sánchez;Javier Simón-Sánchez

  • Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

    Mike A Nalls;Cornelis Blauwendraat;Costanza L Vallerga;Karl Heilbron

  • Analysis of shared heritability in common disorders of the brain

    Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters

  • Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli.

    Cayetano Pleguezuelos-Manzano;Jens Puschhof;Axel Rosendahl Huber;Arne van Hoeck

  • Common genetic variants influence human subcortical brain structures.

    Derrek P. Hibar;Jason L. Stein;Jason L. Stein;Miguel E. Renteria;Alejandro Arias-Vasquez

  • The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

    Paul M. Thompson;Jason L. Stein;Sarah E. Medland;Derrek P. Hibar

  • The transcriptional landscape of age in human peripheral blood

    Marjolein J. Peters;Roby Joehanes;Luke C. Pilling;Claudia Schurmann;Claudia Schurmann

  • Identification of common variants associated with human hippocampal and intracranial volumes

    Jason L Stein;Sarah E Medland;Sarah E Medland;Alejandro Arias Vasquez;Alejandro Arias Vasquez;Derrek P Hibar

  • Genetic variability in the regulation of gene expression in ten regions of the human brain

    Adaikalavan Ramasamy;Adaikalavan Ramasamy;Daniah Trabzuni;Sebastian Guelfi;Vibin Varghese

  • Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

    C Cruchaga;CM Karch;SC Jin;BA Benitez

  • Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus

    Michael J. Devine;Mina Ryten;Petr Vodicka;Alison J. Thomson

  • Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study.

    Christopher D Whelan;Christopher D Whelan;Andre Altmann;Juan A Botía;Neda Jahanshad

  • Evidence for 28 genetic disorders discovered by combining healthcare and research data

    J Kaplanis;K E Samocha;L Wiel;Z Zhang

  • Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease

    L.A. Robak;L.A. Robak;I.E. Jansen;I.E. Jansen;J van Rooij;A.G. Uitterlinden

  • Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

    Suzanne Lesage;Valérie Drouet;Elisa Majounie;Vincent Deramecourt

  • Genome-wide association study of obsessive-compulsive disorder.

    S. E. Stewart;D. Yu;J. M. Scharf;B. M. Neale

  • Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

    A. Beilina;I. N. Rudenko;A. Kaganovich;L. Civiero

  • A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease

    V. Plagnol;M.A. Nalls;J.M. Bras;D.G. Hernandez;D.G. Hernandez

  • Major Shifts in Glial Regional Identity Are a Transcriptional Hallmark of Human Brain Aging.

    Lilach Soreq;Lilach Soreq;Jamie Rose;Eyal Soreq;John Hardy

  • Novel genetic loci associated with hippocampal volume

    Derrek Hibar;Hieab H.H. Adams;Neda Jahanshad;Ganesh Chauhan

Frequent Co-Authors

John Hardy
John Hardy University College London
Adaikalavan Ramasamy
Adaikalavan Ramasamy A*STAR - Agency for Science, Technology and Research
Michael E. Weale
Michael E. Weale King's College London
Dena G. Hernandez
Dena G. Hernandez National Institutes of Health
Henry Houlden
Henry Houlden University College London
Andrew B. Singleton
Andrew B. Singleton National Institutes of Health
Colin Smith
Colin Smith University of Edinburgh
Nicholas W. Wood
Nicholas W. Wood University College London
Mike A. Nalls
Mike A. Nalls National Institutes of Health
Mark R. Cookson
Mark R. Cookson National Institutes of Health

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