Hans Eiberg

11.0k total citations · 1 hit paper
196 papers, 7.4k citations indexed

About

Hans Eiberg is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Hans Eiberg has authored 196 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 96 papers in Molecular Biology, 63 papers in Genetics and 31 papers in Surgery. Recurrent topics in Hans Eiberg's work include Genetics and Neurodevelopmental Disorders (21 papers), Pancreatic function and diabetes (17 papers) and Connexins and lens biology (16 papers). Hans Eiberg is often cited by papers focused on Genetics and Neurodevelopmental Disorders (21 papers), Pancreatic function and diabetes (17 papers) and Connexins and lens biology (16 papers). Hans Eiberg collaborates with scholars based in Denmark, Germany and Hungary. Hans Eiberg's co-authors include Jan Mohr, Thomas Rosenberg, Lars Hestbjerg Hansen, Inge-Merete Nielsen, Klaus Kjaer, Torben Hansen, Oluf Pedersen, P Kjer, Birgit Kjer and Niels Tommerup and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Hans Eiberg

192 papers receiving 7.0k citations

Hit Papers

Cystic Fibrosis Locus Defined by a Genetically Linked Pol... 1985 2026 1998 2012 1985 100 200 300
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic DNA Marker
    1985 356 citations Hans Eiberg, Jan Mohr et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Hans Eiberg Denmark 48 3.9k 2.0k 835 787 672 196 7.4k
Didier Lacombe France 48 4.0k 1.0× 2.7k 1.3× 1.1k 1.4× 632 0.8× 791 1.2× 322 7.8k
Niklas Dahl Sweden 50 5.9k 1.5× 2.9k 1.4× 957 1.1× 1.3k 1.7× 262 0.4× 245 9.8k
Nicholas D. Hastie United Kingdom 54 9.7k 2.5× 3.0k 1.5× 1.0k 1.2× 703 0.9× 1.4k 2.1× 128 12.1k
Vincent Goffin France 49 3.0k 0.8× 1.9k 0.9× 535 0.6× 311 0.4× 454 0.7× 167 8.5k
Naomi Nakagata Japan 46 3.6k 0.9× 1.7k 0.9× 559 0.7× 408 0.5× 225 0.3× 236 7.4k
Cynthia J. Curry United States 54 4.4k 1.1× 2.5k 1.2× 2.2k 2.7× 434 0.6× 625 0.9× 126 9.8k
André Mégarbané Lebanon 43 4.1k 1.1× 2.1k 1.1× 440 0.5× 723 0.9× 370 0.6× 276 7.0k
Manfred Gessler Germany 53 8.6k 2.2× 1.7k 0.9× 600 0.7× 820 1.0× 1.4k 2.1× 165 10.8k
James F. Reynolds United States 48 4.7k 1.2× 3.3k 1.6× 1.5k 1.8× 630 0.8× 400 0.6× 294 9.1k
Gösta Holmgren Sweden 44 4.3k 1.1× 1.7k 0.9× 501 0.6× 918 1.2× 226 0.3× 165 6.6k

Countries citing papers authored by Hans Eiberg

Since Specialization
Citations

This map shows the geographic impact of Hans Eiberg's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hans Eiberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hans Eiberg more than expected).

Fields of papers citing papers by Hans Eiberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hans Eiberg. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hans Eiberg. The network helps show where Hans Eiberg may publish in the future.

Co-authorship network of co-authors of Hans Eiberg

This figure shows the co-authorship network connecting the top 25 collaborators of Hans Eiberg. A scholar is included among the top collaborators of Hans Eiberg based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hans Eiberg. Hans Eiberg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Homøe, Preben, Anders Koch, Nanna Dahl Rendtorff, et al.. (2012). GJB2(Connexin-26) mutations are not frequent among hearing impaired patients in East Greenland. International Journal of Audiology. 51(6). 433–436. 8 indexed citations
2.
Gjesing, Anette P., Claus Thorn Ekstrøm, Hans Eiberg, et al.. (2012). Fasting and oral glucose-stimulated levels of glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) are highly familial traits. Diabetologia. 55(5). 1338–1345. 22 indexed citations
3.
Farooq, Muhammad, Jesper T. Troelsen, Mette Boyd, et al.. (2010). Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS. European Journal of Human Genetics. 18(6). 733–736. 37 indexed citations
4.
Průhová, Štěpánka, Ondřej Cinek, Jakob Ek, et al.. (2008). Autosomal inheritance of diabetes in two families characterized by obesity and a novel H241Q mutation inNEUROD1. Pediatric Diabetes. 9(4pt2). 367–372. 37 indexed citations
5.
Rendtorff, Nanna Dahl, Klaus Kjaer, Hans Eiberg, et al.. (2007). Branchio-Oto-Renal Syndrome: Detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, sequencing and MLPA analyses. European Journal of Human Genetics. 1 indexed citations
6.
Rendtorff, Nanna Dahl, Klaus Kjaer, Hans Eiberg, et al.. (2007). Branchio–oto–renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses. European Journal of Human Genetics. 15(11). 1121–1131. 56 indexed citations
7.
Kjaer, Klaus, Lars Hestbjerg Hansen, Hans Eiberg, et al.. (2005). Male‐to‐male transmission in Laurin–Sandrow syndrome and exclusion of RARB and RARG. American Journal of Medical Genetics Part A. 137A(2). 148–152. 5 indexed citations
8.
Eiberg, Hans, Lars Hestbjerg Hansen, Claus Thustrup Hansen, et al.. (2005). Mapping of hereditary trichilemmal cyst(TRICY1)to chromosome 3p24-p21.2 and exclusion of β-CATENINandMLH1. American Journal of Medical Genetics Part A. 133A(1). 44–47. 11 indexed citations
9.
Hansen, Sara K., Marcelina Párrizas, Štěpánka Průhová, et al.. (2002). Genetic evidence that HNF-1α–dependent transcriptional control of HNF-4α is essential for human pancreatic β cell function. Journal of Clinical Investigation. 110(6). 827–833. 77 indexed citations
10.
Hansen, Sara K., Marcelina Párrizas, Štěpánka Průhová, et al.. (2002). Genetic evidence that HNF-1α–dependent transcriptional control of HNF-4α is essential for human pancreatic β cell function. Journal of Clinical Investigation. 110(6). 827–833. 4 indexed citations
11.
Thiselton, Dawn L., Christiane Alexander, Simon P. Brooks, et al.. (2001). A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect. Human Genetics. 109(5). 498–502. 50 indexed citations
12.
13.
Sørensen, Charlotte Brandt, A.-S. Ladekjær-Mikkelsen, Brage Storstein Andresen, et al.. (1999). Identification of Novel and Known Mutations in the Genes for Keratin 5 and 14 in Danish Patients with Epidermolysis Bullosa Simplex: Correlation Between Genotype and Phenotype. Journal of Investigative Dermatology. 112(2). 184–190. 46 indexed citations
14.
Ewald, H., Ole Mors, Karen Koed, Hans Eiberg, & Thomas Kruse. (1997). Susceptibility loci for bipolar affective disorder on chromosome 18? A review and a study of Danish families. Psychiatric Genetics. 7(1). 1–12. 27 indexed citations
15.
Jónasdóttir, Aðalbjörg, Hans Eiberg, Birgit Kjer, P Kjer, & Thomas Rosenberg. (1996). Refinement of the dominant optic atrophy locus (OPA1) to a 1.4-cM interval on chromosome 3q28-3q29, within a 3-Mb YAC contig. Human Genetics. 99(1). 115–120. 28 indexed citations
16.
Eiberg, Hans, Birgit Kjer, P Kjer, & Thomas Rosenberg. (1994). Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis. Human Molecular Genetics. 3(6). 977–980. 115 indexed citations
17.
Rosenberg, Thomas, et al.. (1989). Autosomal dominant congenital cataract Morphology and genetic mapping. Acta Ophthalmologica. 67(2). 151–158. 50 indexed citations
18.
Møller, Hans Ulrik, Hans Eiberg, & Torben A. Kruse. (1989). Linkage relations of the locus for granular corneal dystrophy Groenouw type I with 35 polymorphic systems. Acta Ophthalmologica. 67(6). 721–723. 3 indexed citations
19.
Eiberg, Hans, et al.. (1988). Marner's cataract (CAM) assigned to chromosome 16: linkage to haptoglobin. Clinical Genetics. 34(4). 272–275. 52 indexed citations
20.
Mohr, Jan, et al.. (1976). Some lod scores concerning chromosome 1. Cytogenetic and Genome Research. 16(1-5). 340–340. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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