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Genetics

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

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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