D-Index & Metrics Best Publications

D-Index & Metrics

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 and Molecular Biology D-index 125 Citations 76,391 592 World Ranking 156 National Ranking 5
Medicine D-index 110 Citations 54,163 564 World Ranking 2374 National Ranking 87

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • Mutation

The scientist’s investigation covers issues in Genetics, Genome-wide association study, Single-nucleotide polymorphism, Genetic association and Internal medicine. His study in Genetics is interdisciplinary in nature, drawing from both Bipolar disorder and Psychosis. His Psychosis study combines topics in areas such as Zinc finger protein 804A, Schizophrenia and Copy-number variation.

His biological study spans a wide range of topics, including Odds ratio, Polymorphism, Bioinformatics, Case-control study and Genetic architecture. The various areas that Markus M. Nöthen examines in his Single-nucleotide polymorphism study include Apolipoprotein E, Disease and Heritability. His Internal medicine research includes themes of Endocrinology and Oncology.

His most cited work include:

  • Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease (2614 citations)
  • Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2556 citations)
  • Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (1570 citations)

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

Markus M. Nöthen focuses on Genetics, Genome-wide association study, Single-nucleotide polymorphism, Internal medicine and Gene. His Genetics study typically links adjacent topics like Bipolar disorder. His Bipolar disorder research focuses on Schizophrenia and how it connects with Psychosis and Neuroscience.

His Genome-wide association study research includes elements of Odds ratio, Case-control study, Genetic predisposition and Linkage disequilibrium. Markus M. Nöthen is studying SNP, which is a component of Single-nucleotide polymorphism. His Internal medicine study incorporates themes from Gastroenterology, Endocrinology and Oncology.

He most often published in these fields:

  • Genetics (60.19%)
  • Genome-wide association study (32.77%)
  • Single-nucleotide polymorphism (22.07%)

What were the highlights of his more recent work (between 2017-2021)?

  • Genome-wide association study (32.77%)
  • Genetics (60.19%)
  • Internal medicine (22.54%)

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

Markus M. Nöthen mostly deals with Genome-wide association study, Genetics, Internal medicine, Bipolar disorder and Schizophrenia. His Genome-wide association study study is concerned with Single-nucleotide polymorphism in general. His research in Gene, Locus, Candidate gene, Allele and Expression quantitative trait loci are components of Genetics.

Markus M. Nöthen usually deals with Internal medicine and limits it to topics linked to Oncology and Risk factor. The Bipolar disorder study combines topics in areas such as Multiple comparisons problem, Lithium, Mood, Schizoaffective disorder and Genetic heterogeneity. His Schizophrenia research incorporates themes from Major depressive disorder, Depression, Psychosis and Disease.

Between 2017 and 2021, his most popular works were:

  • Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (1131 citations)
  • Genome-wide association study identifies 30 loci associated with bipolar disorder (518 citations)
  • Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (328 citations)

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

  • Gene
  • Mutation
  • Internal medicine

Genome-wide association study, Schizophrenia, Bipolar disorder, Genetics and Internal medicine are his primary areas of study. Markus M. Nöthen has included themes like Alcohol dependence, Genetic predisposition, Case-control study, Genetic association and Genetic architecture in his Genome-wide association study study. His Schizophrenia research integrates issues from Major depressive disorder, Depression, Multifactorial Inheritance and Genetic correlation.

His Bipolar disorder research incorporates elements of Multiple comparisons problem, Psychosis, Brain Structure and Function, Disease and Genetic heterogeneity. His study involves Gene, SNP, Locus, Linkage disequilibrium and Expression quantitative trait loci, a branch of Genetics. His Internal medicine research is multidisciplinary, incorporating perspectives in Neuroticism, Endocrinology, Oncology, Single-nucleotide polymorphism and Genetic load.

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

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)

2605 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)

2573 Citations

Large recurrent microdeletions associated with schizophrenia

Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen.
Nature (2008)

1816 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.
Nature Genetics (2013)

1708 Citations

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

Heribert Schunkert;Inke R. König;Sekar Kathiresan;Muredach P. Reilly.
Nature Genetics (2011)

1700 Citations

Common variants conferring risk of schizophrenia

Hreinn Stefansson;Hreinn Stefansson;Roel A. Ophoff;Roel A. Ophoff;Roel A. Ophoff;Stacy Steinberg;Stacy Steinberg;Ole A. Andreassen.
Nature (2009)

1685 Citations

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Andrew P Morris;Benjamin F Voight;Benjamin F Voight;Tanya M Teslovich;Teresa Ferreira.
Nature Genetics (2012)

1642 Citations

Genome-wide association study identifies five new schizophrenia loci

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

1603 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.
Nature Genetics (2011)

1570 Citations

Defining the role of common variation in the genomic and biological architecture of adult human height

Andrew R. Wood;Tonu Esko;Jian Yang;Sailaja Vedantam.
Nature Genetics (2014)

1508 Citations

If you think any of the details on this page are incorrect, let us know.

Contact us

Best Scientists Citing Markus M. Nöthen

Ole A. Andreassen

Ole A. Andreassen

Oslo University Hospital

Publications: 422

Michael Conlon O'Donovan

Michael Conlon O'Donovan

Cardiff University

Publications: 342

Michael John Owen

Michael John Owen

Cardiff University

Publications: 327

Patrick F. Sullivan

Patrick F. Sullivan

University of North Carolina at Chapel Hill

Publications: 281

James L. Kennedy

James L. Kennedy

Centre for Addiction and Mental Health

Publications: 280

Nicholas G. Martin

Nicholas G. Martin

QIMR Berghofer Medical Research Institute

Publications: 264

Mark I. McCarthy

Mark I. McCarthy

University of Oxford

Publications: 255

Benjamin M. Neale

Benjamin M. Neale

Harvard University

Publications: 242

Dorret I. Boomsma

Dorret I. Boomsma

Vrije Universiteit Amsterdam

Publications: 238

Andrew M. McIntosh

Andrew M. McIntosh

University of Edinburgh

Publications: 235

Gerome Breen

Gerome Breen

King's College London

Publications: 233

Kari Stefansson

Kari Stefansson

deCODE Genetics (Iceland)

Publications: 230

Thomas Werge

Thomas Werge

University of Copenhagen

Publications: 228

Anders D. Børglum

Anders D. Børglum

Lundbeck (Denmark)

Publications: 221

Paul M. Thompson

Paul M. Thompson

University of Southern California

Publications: 220

Hakon Hakonarson

Hakon Hakonarson

Children's Hospital of Philadelphia

Publications: 219

Something went wrong. Please try again later.