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 58 Citations 30,259 127 World Ranking 2477 National Ranking 39

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • Internal medicine

His primary areas of study are Genome-wide association study, Genetics, Single-nucleotide polymorphism, Schizophrenia and Bioinformatics. His Genome-wide association study research includes elements of Linkage disequilibrium, Genomics, Allele, Genetic association and Genetic architecture. His studies in Genetic association integrate themes in fields like Case-control study and Type 2 diabetes.

His work on Epigenetics, Human genetics and CpG site as part of general Genetics research is frequently linked to Cell aging and Induced pluripotent stem cell, thereby connecting diverse disciplines of science. His Single-nucleotide polymorphism research incorporates themes from Apolipoprotein E and Disease. The study incorporates disciplines such as Bipolar disorder, Psychosis, Brain mapping and Attention deficit hyperactivity disorder in addition to Schizophrenia.

His most cited work include:

  • 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)
  • Large recurrent microdeletions associated with schizophrenia (1516 citations)

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

His main research concerns Genetics, Genome-wide association study, Bipolar disorder, Single-nucleotide polymorphism and Schizophrenia. His study in Genetics concentrates on Locus, Gene, Genetic variation, Genetic determinism and Genomics. His work carried out in the field of Genome-wide association study brings together such families of science as Odds ratio, Bioinformatics, Case-control study, Allele and Genetic association.

Thomas W. Mühleisen focuses mostly in the field of Bipolar disorder, narrowing it down to matters related to Clinical psychology and, in some cases, Phenotype. His Single-nucleotide polymorphism study incorporates themes from Disease, Genetic predisposition and Haplotype. His Schizophrenia research is multidisciplinary, incorporating perspectives in Psychosis, Neuroscience, Brain mapping and Internal medicine.

He most often published in these fields:

  • Genetics (57.26%)
  • Genome-wide association study (48.39%)
  • Bipolar disorder (37.10%)

What were the highlights of his more recent work (between 2017-2020)?

  • Genome-wide association study (48.39%)
  • Genetics (57.26%)
  • Bipolar disorder (37.10%)

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

His primary areas of investigation include Genome-wide association study, Genetics, Bipolar disorder, Computational biology and Schizophrenia. Thomas W. Mühleisen regularly links together related areas like Heritability in his Genome-wide association study studies. His Heritability research is multidisciplinary, incorporating elements of Single-nucleotide polymorphism, 1000 Genomes Project, Genetic correlation and Brain size.

His Genetics research focuses on Genotype-Phenotype Association in particular. His research investigates the connection with Computational biology and areas like Multiple comparisons problem which intersect with concerns in Genetic association, Genotype, Neurodevelopmental disorder and RNA. His Schizophrenia research includes themes of Copy-number variation, Multifactorial Inheritance, Psychosis and Disease, Age of onset.

Between 2017 and 2020, his most popular works were:

  • Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (328 citations)
  • Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder (8 citations)
  • Dynamics of Brain Structure and its Genetic Architecture over the Lifespan (4 citations)

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

  • Gene
  • Genetics
  • Internal medicine

Thomas W. Mühleisen mainly focuses on Schizophrenia, Gene, Genetic association, Bipolar disorder and Genome-wide association study. Thomas W. Mühleisen has researched Schizophrenia in several fields, including Genetics, Atrophy, Brain morphometry, Human brain and Depression. His study in Gene is interdisciplinary in nature, drawing from both Evolutionary biology and Multiple comparisons problem.

His Genetic association research includes elements of Neurodevelopmental disorder, Computational biology and Neuroscience. His research in Bipolar disorder intersects with topics in Copy-number variation, Multifactorial Inheritance, Psychosis and Disease, Age of onset.

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 identifies variants at CLU and PICALM associated with Alzheimer's disease

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

2992 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)

2097 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)

1965 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)

1960 Citations

Large recurrent microdeletions associated with schizophrenia

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

1907 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)

1904 Citations

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Pamela Sklar;Pamela Sklar;Stephan Ripke;Stephan Ripke;Laura J. Scott;Ole A. Andreassen.
Nature Genetics (2011)

1409 Citations

Genetic associations with valvular calcification and aortic stenosis.

George Thanassoulis;George Thanassoulis;Catherine Y. Campbell;David S. Owens;J. Gustav Smith;J. Gustav Smith.
The New England Journal of Medicine (2013)

855 Citations

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease.

Lesley Jones;Peter A. Holmans;Marian L. Hamshere;Denise Harold.
PLOS ONE (2010)

779 Citations

Common genetic variants influence human subcortical brain structures.

Derrek P. Hibar;Jason L. Stein;Jason L. Stein;Miguel E. Renteria;Alejandro Arias-Vasquez.
Nature (2015)

738 Citations

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