World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
68
Citations
13956
World Ranking
2451
National Ranking
26

Hans Eiberg 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 Hans Eiberg 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: 236 publications — 62nd percentile

62% of scientists in this discipline score the same or lower.

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

Hans Eiberg 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 Hans Eiberg 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

Hans Eiberg is affiliated with the University of Copenhagen in Denmark. Their research spans multiple disciplines within medicine and biochemistry, genetics, and molecular biology, focusing on genetics, molecular biology, and pharmacology as primary subfields. Their work also intersects with cognitive neuroscience and ophthalmology.

The researcher's recent scholarly contributions include studies on neurodevelopmental disorders, major depression treatment, and molecular mechanisms linked to brain function. Their publications cover topics such as treatment approaches for major depressive disorder, genetics and neurodevelopmental disorders, functional brain connectivity, tryptophan-related brain disorders, RNA modifications in cancer, epigenetics and DNA methylation, and the influence of neurotransmitter receptors on behavior.

Hans Eiberg has authored or co-authored papers in recognized scientific venues, including the following recent publications:

  • RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis, 2020, Nature Communications
  • Serotonin 4 Receptor Brain Binding in Major Depressive Disorder and Association With Memory Dysfunction, 2023, JAMA Psychiatry
  • Evidence for a serotonergic subtype of major depressive disorder: A NeuroPharm-1 study, 2021, bioRxiv (Cold Spring Harbor Laboratory)
  • A family with ulcerative colitis maps to 7p21.1 and comprises a region with regulatory activity for the aryl hydrocarbon receptor gene, 2023, European Journal of Human Genetics
  • Paroxysmal Cranial Dyskinesia and Nail-Patella Syndrome Caused by a Novel Variant in the LMX1B Gene, 2020, Movement Disorders

Frequent collaborators in their research include Lars Hestbjerg Hansen, Kristin Köhler-Forsberg, Vibeke H. Dam, Brice Ozenne, and Søren Vinther Larsen. These collaborations contribute to the multidisciplinary nature of their scholarly output.

The primary publication venues where Hans Eiberg has shared research findings are:

  • JAMA Psychiatry
  • Nature Communications
  • bioRxiv (Cold Spring Harbor Laboratory)
  • European Journal of Human Genetics
  • Movement Disorders

The scientist's research focus integrates investigations into neurogenetic mechanisms and disorders alongside psychiatric conditions, with attention to molecular pathways and receptor-mediated brain processes. Their profile demonstrates a consistent emphasis on exploring the genetic and biochemical foundations of neurological and psychiatric diseases.

Best Publications

  • Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker

    Lap-Chee Tsui;Manuel Buchwald;David Barker;Jeffrey C. Braman

  • Localization of cystic fibrosis locus to human chromosome 7cen–q22

    Brandon J. Wainwright;Peter J. Scambler;Jorg Schmidtke;Eila A. Watson

  • Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression.

    Hans Eiberg;Jesper Troelsen;Mette Nielsen;Annemette Mikkelsen

  • Linkage Studies of Cholestasis Familiaris Groenlandica/Byler-Like Disease with Polymorphic Protein and Blood Group Markers

    Hans Eiberg;Inge-Merete Nielsen

  • Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract.

    Lei Bu;Yiping Jin;Yuefeng Shi;Renyuan Chu

  • Cloning of a human UDP-N-acetyl-alpha-D-Galactosamine:polypeptide N-acetylgalactosaminyltransferase that complements other GalNAc-transferases in complete O-glycosylation of the MUC1 tandem repeat.

    Eric Paul Bennett;Helle Hassan;Ulla Mandel;Ekatarina Mirgorodskaya

  • A degradation-sensitive anionic trypsinogen ( PRSS2 ) variant protects against chronic pancreatitis

    Heiko Witt;Miklós Sahin-Tóth;Olfert Landt;Jian Min Chen

  • Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q

    Hans Eiberg;Ida Berendt;Jan Mohr

  • THE GENETICS OF ENURESIS: A REVIEW

    Alexander von Gontard;Henritte Schaumburg;Elke Hollmann;Hans Eiberg

  • Blood-based biomarkers of age-associated epigenetic changes in human islets associate with insulin secretion and diabetes

    Karl Bacos;Linn Gillberg;Petr Volkov;Anders H Olsson

  • Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter

    Jens J Hansen;Peter Bross;Majken Westergaard;Marit Nyholm Nielsen

  • Dominant optic atrophy mapped to chromosome 3q region. II. Clinical and epidemiological aspects.

    Birgit Kjer;Hans Eiberg;Poul Kjer;Thomas Rosenberg

  • Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation

    Elena Gardella;Felicitas Becker;Rikke S. Møller;Julian Schubert

  • Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis

    Hans Eiberg;Birgit Kjer;Poul Kjer;Thomas Rosenberg

  • Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios

    Søren Besenbacher;Siyang Liu;José M. G. Izarzugaza;Jakob Grove

  • Identification of Four New Mutations in the Short-Chain Acyl-CoA Dehydrogenase (SCAD) Gene in Two Patients: One of the Variant Alleles, 511C→T, is Present at an Unexpectedly High Frequency in the General Population, as Was the Case for 625G→A, Together Conferring Susceptibility to Ethylmalonic Aciduria

    Niels Gregersen;Vibeke S. Winter;Morten J. Corydon;Thomas J. Corydon

  • Loss of the retinoblastoma protein-related p130 protein in small cell lung carcinoma

    Kristian Helin;Karin Holm;Anita Niebuhr;Hans Eiberg

  • Linkage relationships of paraoxonase (PON) with other markers: indication of PON-cystic fibrosis synteny.

    H. Eiberg;J. Mohr;K. Schmiegelow;L. S. Nielsen

  • Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8.

    Lars Hansen;Wenliang Yao;Hans Eiberg;Klaus Wilbrandt Kjaer

  • Sequencing and de novo assembly of 150 genomes from Denmark as a population reference

    Lasse Maretty;Jacob Malte Jensen;Bent Petersen;Jonas Andreas Sibbesen

Frequent Co-Authors

Oluf Pedersen
Oluf Pedersen University of Copenhagen
Torben Hansen
Torben Hansen University of Copenhagen
Niels Tommerup
Niels Tommerup University of Copenhagen
Lap-Chee Tsui
Lap-Chee Tsui University of Toronto
Thomas Rosenberg
Thomas Rosenberg University of Copenhagen
Kenneth K. Kidd
Kenneth K. Kidd Yale University
Ole Mors
Ole Mors Aarhus University
Knut Borch-Johnsen
Knut Borch-Johnsen Aarhus University
Lars Bolund
Lars Bolund Aarhus University

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