D-Index & Metrics Best Publications
Michael Conlon O'Donovan

Michael Conlon O'Donovan

Research.com 2022 Best Scientist Award Badge
Genetics
UK
2023

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Best Scientists D-index 158 Citations 133,072 848 World Ranking 891 National Ranking 85
Medicine D-index 160 Citations 139,728 826 World Ranking 409 National Ranking 46
Genetics D-index 160 Citations 137,713 745 World Ranking 55 National Ranking 9

Research.com Recognitions

Awards & Achievements

2023 - Research.com Medicine in United Kingdom Leader Award

2023 - Research.com Genetics in United Kingdom Leader Award

2022 - Research.com Best Scientist Award

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • Internal medicine

Michael Conlon O'Donovan mainly investigates Genetics, Genome-wide association study, Schizophrenia, Bipolar disorder and Single-nucleotide polymorphism. His Genetics study frequently draws connections between related disciplines such as Psychosis. His Genome-wide association study study integrates concerns from other disciplines, such as Linkage disequilibrium, Case-control study, Genomics, Genetic association and Candidate gene.

His research integrates issues of Meta-analysis, Autism, Autism spectrum disorder and Genetic architecture in his study of Schizophrenia. His studies deal with areas such as Major depressive disorder, ANK3 and Zinc finger protein 804A as well as Bipolar disorder. His Single-nucleotide polymorphism research is multidisciplinary, incorporating perspectives in Apolipoprotein E, Disease and Haplotype.

His most cited work include:

  • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (7922 citations)
  • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes (6309 citations)
  • Biological insights from 108 schizophrenia-associated genetic loci (4834 citations)

What are the main themes of his work throughout his whole career to date?

His primary areas of study are Genetics, Schizophrenia, Genome-wide association study, Psychiatry and Bipolar disorder. Single-nucleotide polymorphism, Genetic association, Allele, Gene and Copy-number variation are among the areas of Genetics where Michael Conlon O'Donovan concentrates his study. His Single-nucleotide polymorphism research incorporates themes from Allele frequency, Locus and Candidate gene.

The study incorporates disciplines such as Psychosis, Internal medicine, Autism spectrum disorder, Clinical psychology and Depression in addition to Schizophrenia. His biological study spans a wide range of topics, including Odds ratio, Case-control study, Disease, Genetic variation and Genetic architecture. As part of his studies on Bipolar disorder, Michael Conlon O'Donovan often connects relevant subjects like Major depressive disorder.

He most often published in these fields:

  • Genetics (51.19%)
  • Schizophrenia (29.78%)
  • Genome-wide association study (28.09%)

What were the highlights of his more recent work (between 2018-2021)?

  • Schizophrenia (29.78%)
  • Psychiatry (20.16%)
  • Bipolar disorder (19.82%)

In recent papers he was focusing on the following fields of study:

Michael Conlon O'Donovan focuses on Schizophrenia, Psychiatry, Bipolar disorder, Genome-wide association study and Clinical psychology. His Schizophrenia study combines topics from a wide range of disciplines, such as Genetics, Gene, Psychosis, Genetic association and Depression. His Genetics study frequently draws connections to other fields, such as Schizophrenia.

His study on Bipolar disorder also encompasses disciplines like

  • Major depressive disorder which connect with Attention deficit hyperactivity disorder, Mood and Odds ratio,
  • Psychiatric interview which is related to area like Internal medicine. His Genome-wide association study study combines topics in areas such as Expression quantitative trait loci, Prefrontal cortex, Locus, Heritability and Genetic architecture. Michael Conlon O'Donovan combines subjects such as Longitudinal study, Cognition and Anxiety with his study of Clinical psychology.

Between 2018 and 2021, his most popular works were:

  • Genome-wide association study identifies 30 loci associated with bipolar disorder (518 citations)
  • Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (242 citations)
  • Comparative genetic architectures of schizophrenia in East Asian and European populations (117 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Genetics
  • Internal medicine

The scientist’s investigation covers issues in Schizophrenia, Genome-wide association study, Bipolar disorder, Psychiatry and Clinical psychology. His Schizophrenia research is multidisciplinary, incorporating elements of Genetics, Gene, Psychosis, Autism spectrum disorder and Depression. Michael Conlon O'Donovan regularly links together related areas like Schizophrenia in his Genetics studies.

His Genome-wide association study study contributes to a more complete understanding of Single-nucleotide polymorphism. His Bipolar disorder research incorporates elements of Insomnia, Psychiatric interview, Major depressive disorder, Genetic heterogeneity and Genetic variation. His study in Psychiatry is interdisciplinary in nature, drawing from both Pleiotropy, Incidence and Gene–environment interaction.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

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.
Nature (2007)

8473 Citations

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

Marcy E. MacDonald;Christine M. Ambrose;Mabel P. Duyao;Richard H. Myers.
Cell (1993)

6784 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.
Nature (2014)

6161 Citations

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group.

M Shah;N Datson;L Srinidhi;VP Stanton.
Cell (1993)

4881 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.
Nature (2009)

4024 Citations

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

Jordan W. Smoller;Kenneth Kendler;Nicholas John Craddock;Phil Hyoun Lee.
The Lancet (2013)

3879 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.
Nature Genetics (2013)

3630 Citations

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

Denise Harold;Richard Abraham;Paul Hollingworth;Rebecca Sims.
Nature Genetics (2009)

2992 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.
Nature Genetics (2013)

2857 Citations

Genome-wide association study identifies five new schizophrenia loci

Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson.
Nature Genetics (2011)

2508 Citations

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