World's Best Scientists 2026 revealed!
Thomas W. Mühleisen

Thomas W. Mühleisen

D-Index & Metrics

Genetics

D-Index
68
Citations
45277
World Ranking
2381
National Ranking
38

Thomas W. Mühleisen publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Thomas W. Mühleisen sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 157 publications — 33rd percentile

33% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Thomas W. Mühleisen D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Thomas W. Mühleisen sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 68 D-Index — 45th percentile

45% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Overview

Thomas W. Mühleisen is affiliated with the University of Basel in Switzerland. Their research spans multiple fields with a primary focus on biochemistry, genetics, and molecular biology, complemented by work in medicine. The scientist has published extensively in various subfields, including genetics, molecular biology, cardiology and cardiovascular medicine, cognitive neuroscience, and developmental and educational psychology.

The main topics of research covered by Mühleisen include genetic associations and epidemiology, epigenetics and DNA methylation, genomic variations and chromosomal abnormalities, congenital heart defects research, genetics and neurodevelopmental disorders, heart rate variability and autonomic control, as well as cardiac electrophysiology and arrhythmias.

Mühleisen's recent publications highlight their involvement in brain structure genetics, psychiatric illness, and cognitive alterations linked to genetic variations. Selected recent works include:

  • "Genetic variants associated with longitudinal changes in brain structure across the lifespan," 2022, published in Nature Neuroscience
  • "Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs," 2021, Human Brain Mapping
  • "1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans," 2021, Translational Psychiatry
  • "A common variation in HCN1 is associated with heart rate variability in schizophrenia," 2020, Schizophrenia Research
  • "Identification of Phonology-Related Genes and Functional Characterization of Broca's and Wernicke's Regions in Language and Learning Disorders," 2021, Frontiers in Neuroscience

The venues where Mühleisen frequently publishes reflect the thematic focus of the research, including Translational Psychiatry, bioRxiv (Cold Spring Harbor Laboratory), NeuroImage, Nature Neuroscience, and Human Brain Mapping.

Collaborations with other researchers play a significant role in Mühleisen's work. Frequent co-authors include Sven Cichon, Andreas J. Forstner, Robin Bülow, Christiane Jockwitz, and Katrin Amunts, with each contributing to multiple publications together.

Overall, Thomas W. Mühleisen's scholarly output centers around the genetic and molecular bases of brain structure, psychiatric and neurodevelopmental disorders, and cardiovascular genetics, integrating epidemiological genetics with molecular and clinical approaches.

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

  • 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

  • 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

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

    Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish

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

    Heribert Schunkert;Inke R. König;Sekar Kathiresan;Muredach P. Reilly

  • 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

  • Large recurrent microdeletions associated with schizophrenia

    Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen

  • 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

  • Genome-wide association study identifies 30 loci associated with bipolar disorder

    Eli A. Stahl;Eli A. Stahl;Gerome Breen;Andreas J. Forstner;Andrew McQuillin

  • 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

  • Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

    Niamh Mullins;Andreas J. Forstner;Andreas J. Forstner;Andreas J. Forstner;Kevin S. O'Connell;Kevin S. O'Connell;Brandon Coombes

  • Genetic associations with valvular calcification and aortic stenosis.

    George Thanassoulis;George Thanassoulis;Catherine Y. Campbell;David S. Owens;J. Gustav Smith;J. Gustav Smith

  • Common genetic variants influence human subcortical brain structures.

    Derrek P. Hibar;Jason L. Stein;Jason L. Stein;Miguel E. Renteria;Alejandro Arias-Vasquez

  • Aging of blood can be tracked by DNA methylation changes at just three CpG sites.

    Carola Ingrid Weidner;Qiong Lin;Carmen Maike Koch;Lewin Eisele

  • 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

  • The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

    Paul M. Thompson;Jason L. Stein;Sarah E. Medland;Derrek P. Hibar

  • Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

    Sonja I Berndt;Stefan Gustafsson;Stefan Gustafsson;Reedik Mägi;Reedik Mägi;Andrea Ganna

  • An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

    Robert A. Scott;Laura J. Scott;Reedik Mägi;Letizia Marullo

  • Identification of common variants associated with human hippocampal and intracranial volumes

    Jason L Stein;Sarah E Medland;Sarah E Medland;Alejandro Arias Vasquez;Alejandro Arias Vasquez;Derrek P Hibar

  • Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimertextquotesingles disease

    Denise Harold;Richard Abraham;Paul Hollingworth;Rebecca Sims

Frequent Co-Authors

Markus M. Nöthen
Markus M. Nöthen University Hospital Bonn
Sven Cichon
Sven Cichon University of Basel
Marcella Rietschel
Marcella Rietschel Heidelberg University
Manuel Mattheisen
Manuel Mattheisen Dalhousie University
Thomas G. Schulze
Thomas G. Schulze Ludwig-Maximilians-Universität München
Jana Strohmaier
Jana Strohmaier Heidelberg University
Stefan Herms
Stefan Herms University of Basel
Susanne Moebus
Susanne Moebus University of Duisburg-Essen
Stephanie H. Witt
Stephanie H. Witt Heidelberg University
Roel A. Ophoff
Roel A. Ophoff University of California, Los Angeles

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