D-Index & Metrics Best Publications

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
Genetics D-index 62 Citations 30,988 191 World Ranking 2122 National Ranking 954

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • Mutation

His primary areas of study are Genetics, Genome-wide association study, Schizophrenia, Bipolar disorder and Locus. His Genetics study often links to related topics such as Psychosis. His studies deal with areas such as Copy-number variation, Psychiatry, Case-control study, Linkage disequilibrium and Genetic association as well as Genome-wide association study.

His research integrates issues of Schizoaffective disorder, Genetic variation and ANK3 in his study of Genetic association. His work carried out in the field of Schizophrenia brings together such families of science as Major depressive disorder, Disease, Allele and Genetic architecture. His Locus research is multidisciplinary, incorporating perspectives in Founder effect and Spinocerebellar ataxia.

His most cited work include:

  • Biological insights from 108 schizophrenia-associated genetic loci (4834 citations)
  • Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis (2059 citations)
  • Genome-wide association study identifies five new schizophrenia loci (1474 citations)

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

The scientist’s investigation covers issues in Genetics, Genome-wide association study, Gene, Schizophrenia and Genetic association. His study in Single-nucleotide polymorphism, Locus, Genetic linkage, Candidate gene and Haplotype is done as part of Genetics. The concepts of his Genetic linkage study are interwoven with issues in Genetic marker and Linkage.

His work in Genome-wide association study tackles topics such as Psychiatry which are related to areas like Neuroticism. Brien P. Riley works mostly in the field of Schizophrenia, limiting it down to concerns involving Psychosis and, occasionally, Genetic determinism. His Genetic association research incorporates themes from Odds ratio, Meta-analysis, Disease, Imputation and Summary statistics.

He most often published in these fields:

  • Genetics (60.00%)
  • Genome-wide association study (31.58%)
  • Gene (25.26%)

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

  • Genome-wide association study (31.58%)
  • Gene (25.26%)
  • Genetics (60.00%)

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

Brien P. Riley mainly focuses on Genome-wide association study, Gene, Genetics, Computational biology and Genetic association. His Genome-wide association study research is multidisciplinary, incorporating elements of Eating disorders and Psychiatry. His study ties his expertise on Schizophrenia together with the subject of Genetics.

His study in Computational biology is interdisciplinary in nature, drawing from both Cell, Gene expression, Expression data and Identity by descent. His Genetic association study combines topics from a wide range of disciplines, such as Odds ratio, DNA sequencing and Haplotype. Brien P. Riley has included themes like Schizophrenia, Biological pathway, Bipolar disorder, Neuropsychiatric disorder and De novo mutations in his Genetic architecture study.

Between 2018 and 2021, his most popular works were:

  • Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (242 citations)
  • Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium (21 citations)
  • A large-scale genome-wide association study meta-analysis of cannabis use disorder. (13 citations)

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

  • Gene
  • Genetics
  • Mutation

Brien P. Riley focuses on Genetic architecture, Gene, Genome-wide association study, Schizophrenia and Psychiatry. His Genetic architecture study is concerned with Genetics in general. Brien P. Riley works in the field of Genetics, focusing on Phenotype in particular.

His work deals with themes such as Major histocompatibility complex, Genetic association and Depression, which intersect with Genome-wide association study. His Genetic association study combines topics in areas such as Gene expression, Haplotype and Human genome. His Schizophrenia research includes themes of Eating disorders, Anorexia nervosa, Clinical psychology and Binge eating.

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

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

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

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

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.
Nature Genetics (2018)

1759 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.
Nature Genetics (2013)

1605 Citations

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Bjarni J. Vilhjálmsson;Jian Yang;Hilary K. Finucane;Alexander Gusev.
American Journal of Human Genetics (2015)

960 Citations

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy.

J Buxton;P Shelbourne;J Davies;C Jones.
Nature (1992)

766 Citations

Childhood adversity, monoamine oxidase a genotype, and risk for conduct disorder.

Debra L. Foley;Lindon J. Eaves;Brandon Wormley;Judy L. Silberg.
Archives of General Psychiatry (2004)

755 Citations

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Christian R Marshall;Daniel P Howrigan;Daniel P Howrigan;Daniele Merico;Bhooma Thiruvahindrapuram.
Nature Genetics (2017)

658 Citations

Sparse whole-genome sequencing identifies two loci for major depressive disorder

Na Cai;Tim B. Bigdeli;Warren Kretzschmar;Yihan Li.
Nature (2015)

654 Citations

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