2026 Michael John Owen: Genetics Researcher – H-Index, Publications & Awards

Discipline name	D-Index	World Ranking	Current World Ranking	National Ranking	Current National Ranking	Publications	Citations
Best Scientists	197	322	302	35	33	1529	210271
Genetics	199	23	23	3	3	1230	211584
Medicine	203	158	145	21	20	1361	219609

Research.com Recognitions

2026 - Research.com Genetics in United Kingdom Leader Award
2026 - Research.com Medicine in United Kingdom Leader Award
2025 - Research.com Best Scientists Award
2025 - Research.com Genetics in United Kingdom Leader Award
2025 - Research.com Medicine in United Kingdom Leader Award
2024 - Research.com Genetics in United Kingdom Leader Award
2024 - Research.com Genetics and Molecular Biology in United Kingdom Leader Award
2023 - Research.com Genetics in United Kingdom Leader Award
2023 - Research.com Medicine in United Kingdom Leader Award
2022 - Research.com Genetics and Molecular Biology in United Kingdom Leader Award
Member of the European Molecular Biology Organization (EMBO)
Member of the European Molecular Biology Organization (EMBO)
Member of the European Molecular Biology Organization (EMBO)
Member of the European Molecular Biology Organization (EMBO)
Member of the European Molecular Biology Organization (EMBO)

Overview

Michael John Owen is affiliated with Cardiff University in the United Kingdom. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, with significant contributions also in Medicine. Within these areas, they have focused notably on Genetics, Molecular Biology, Psychiatry and Mental Health, Cognitive Neuroscience, and Clinical Psychology.

The scientist's work covers a broad range of topics including Genetic Associations and Epidemiology, Genomic Variations and Chromosomal Abnormalities, Genetics and Neurodevelopmental Disorders, Congenital Heart Defects Research, Genomics and Rare Diseases, Schizophrenia Research and Treatment, and Autism Spectrum Disorder Research.

Michael John Owen has been published frequently in several scholarly venues, among which are bioRxiv (Cold Spring Harbor Laboratory), European Neuropsychopharmacology, Molecular Psychiatry, Translational Psychiatry, and UNC Libraries.

Recent notable papers include:

Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia, 2022, Nature Genetics
A Population-Based Cohort Study Examining the Incidence and Impact of Psychotic Experiences From Childhood to Adulthood, and Prediction of Psychotic Disorder, 2020, American Journal of Psychiatry
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome, 2020, Nature Medicine
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia, 2020, Nature Neuroscience
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion, 2020, Molecular Psychiatry

Collaboration is a significant aspect of their career, with frequent co-authors including Michael O'Donovan, James Walters, Marianne B. M. van den Bree, Peter Holmans, and Jérémy Hall.

Among the recognitions received, Michael John Owen is a Member of the European Molecular Biology Organization (EMBO).

Best Publications

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Paul R. Burton;David G. Clayton;Lon R. Cardon;Nick Craddock

9206
Citations
Biological insights from 108 schizophrenia-associated genetic loci

Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Aiden Corvin;James T. R. Walters

7722
Citations
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease.

Alison Goate;Marie-Christine Chartier-Harlin;Mike Mullan;Jeremy Brown

6236
Citations
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

Jean-Charles Lambert;Jean-Charles Lambert;Jean-Charles Lambert;Carla A Ibrahim-Verbaas;Denise Harold;Adam C Naj

4855
Citations
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

Shaun M. Purcell;Shaun M. Purcell;Naomi R. Wray;Jennifer L. Stone;Jennifer L. Stone;Peter M. Visscher

4724
Citations
Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development

Florian Otto;Anders P Thornell;Tessa Crompton;Angela Denzel

3450
Citations
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Denise Harold;Richard Abraham;Paul Hollingworth;Rebecca Sims

3441
Citations
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Naomi R. Wray;Stephan Ripke;Stephan Ripke;Stephan Ripke;Manuel Mattheisen;MacIej Trzaskowski

3191
Citations
Synaptic, transcriptional and chromatin genes disrupted in autism

Silvia De Rubeis;Xin-Xin He;Arthur P Goldberg;Christopher S. Poultney

3036
Citations
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (Nature Genetics (2009) 41 (1088-1093))

D Harold;R Abraham;P Hollingworth;R Sims

2859
Citations
Genome-wide association study identifies five new schizophrenia loci

Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson

2714
Citations
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone

2429
Citations
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Ditte Demontis;Ditte Demontis;Raymond K Walters;Raymond K Walters;Joanna Martin;Joanna Martin;Joanna Martin;Manuel Mattheisen

2363
Citations
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.

Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish

2310
Citations
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

1978
Citations
Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia

S Mundlos;S Mundlos;F Otto;C Mundlos;C Mundlos;J.B Mulliken

1852
Citations
De novo mutations in schizophrenia implicate synaptic networks

Menachem Fromer;Andrew Pocklington;David Kavanagh;Hywel John Williams

1849
Citations
Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Stephan Ripke;Stephan Ripke;Colm T. O'Dushlaine;Kimberly D. Chambert;Jennifer L. Moran

1788
Citations
The Genetic Basis of Complex Human Behaviors

Robert Plomin;Michael J. Owen;Peter McGuffin

1508
Citations
Rare chromosomal deletions and duplications increase risk of schizophrenia

Jennifer L. Stone;Jennifer L. Stone;Jennifer L. Stone;Michael C. O’Donovan;Hugh Gurling;George K. Kirov

1402
Citations

Frequent Co-Authors

Kaushik De The University of Texas at Arlington

P. M. Tuts Columbia University

J. T. Linnemann Michigan State University

External Links

Wikipedia of Michael John Owen Personal website of Michael John Owen

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