Søren Nørby

3.9k total citations
31 papers, 1.2k citations indexed

About

Søren Nørby is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Søren Nørby has authored 31 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Clinical Biochemistry. Recurrent topics in Søren Nørby's work include Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (6 papers) and Forensic and Genetic Research (5 papers). Søren Nørby is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (6 papers) and Forensic and Genetic Research (5 papers). Søren Nørby collaborates with scholars based in Denmark, United Kingdom and Netherlands. Søren Nørby's co-authors include Niels Lynnerup, Juliette Saillard, Peter Forster, Hans‐Jürgen Bandelt, Thomas Rosenberg, Ragnheiður Fossdal, Dorien J.M. Peters, David Ravine, Jasper J. Saris and Ronald van Eijk and has published in prestigious journals such as Nature, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Søren Nørby

30 papers receiving 1.1k citations

Peers

Søren Nørby
Alla G. Reddy India
K Omoto Japan
Chiara Rengo Italy
Ramiro Barrantes Costa Rica
Spitsyn Va Russia
Xianyun Mao United States
Lotte Henke Germany
Daniele Sellitto Italy
G. David Poznik United States
Alla G. Reddy India
Søren Nørby
Citations per year, relative to Søren Nørby Søren Nørby (= 1×) peers Alla G. Reddy

Countries citing papers authored by Søren Nørby

Since Specialization
Citations

This map shows the geographic impact of Søren Nørby'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 Søren Nørby with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Søren Nørby more than expected).

Fields of papers citing papers by Søren Nørby

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Søren Nørby. 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 Søren Nørby. The network helps show where Søren Nørby may publish in the future.

Co-authorship network of co-authors of Søren Nørby

This figure shows the co-authorship network connecting the top 25 collaborators of Søren Nørby. A scholar is included among the top collaborators of Søren Nørby 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 Søren Nørby. Søren Nørby 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.
Strøman, Per, Erik Bahn, Søren Nørby, & KNUD SICK. (2009). 6-azauracil induced phenocopies of rudimentary wing mutants and their suppression by a suppressor mutant of rudimentary in Drosophila melanogaster. Hereditas. 73(2). 239–245. 4 indexed citations
2.
Nørby, Søren. (2009). The biochemical genetics of rudimentary mutants of Drosophila melanogaster. Hereditas. 73(1). 11–16. 4 indexed citations
3.
Bahn, Erik, Søren Nørby, & KNUD SICK. (2009). Interallelic complementation for pyrimidine requirement in rudimentary mutants of Drosophila melanogaster. Hereditas. 69(2). 187–192. 2 indexed citations
4.
Nørby, Søren. (2009). A specific nutritional requirement for pyrimidines in rudimentary mutants of Drosophila melanogaster. Hereditas. 66(2). 205–214. 12 indexed citations
5.
Lynnerup, Niels & Søren Nørby. (2004). The Greenland Norse: bones, graves, computers, and DNA. Polar Record. 40(2). 107–111. 7 indexed citations
6.
Bosch, Elena, Zoë H. Rosser, Søren Nørby, Niels Lynnerup, & Mark A. Jobling. (2003). Y-chromosomal STR haplotypes in Inuit and Danish population samples. Forensic Science International. 132(3). 228–232. 8 indexed citations
7.
Bosch, Elena, Francesc Calafell, Zoë H. Rosser, et al.. (2003). High level of male-biased Scandinavian admixture in Greenlandic Inuit shown by Y-chromosomal analysis. Human Genetics. 112(4). 353–363. 53 indexed citations
8.
Saillard, Juliette, Peter Forster, Niels Lynnerup, Hans‐Jürgen Bandelt, & Søren Nørby. (2000). mtDNA Variation among Greenland Eskimos: The Edge of the Beringian Expansion. The American Journal of Human Genetics. 67(3). 718–726. 393 indexed citations
9.
Saillard, Juliette, et al.. (2000). Mitochondrial DNA variant 11719G is a marker for the mtDNA haplogroup cluster HV.. PubMed. 72(6). 1065–8. 18 indexed citations
10.
Veldhuisen, Barbera, Jasper J. Saris, Simone de Haij, et al.. (1997). A Spectrum of Mutations in the Second Gene for Autosomal Dominant Polycystic Kidney Disease (PKD2). The American Journal of Human Genetics. 61(3). 547–555. 77 indexed citations
11.
Magalhães, Paulo, O. Sjö, & Søren Nørby. (1996). Ocular myopathy and mitochondrial DNA deletion. A presentation of seven identified Danish patients.. PubMed. 29–32. 3 indexed citations
12.
13.
Black, Graeme C., Ian Craig, Roelof‐Jan Oostra, et al.. (1995). Leber's hereditary optic neuropathy: Implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation. Eye. 9(4). 513–516. 18 indexed citations
14.
Peters, Dorien J.M., Lia Spruit, Jasper J. Saris, et al.. (1993). Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease. Nature Genetics. 5(4). 359–362. 192 indexed citations
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Yang, Huanming, Torben Lund, E. Niebuhr, et al.. (1990). Exclusion mapping of 12 X‐linked disease loci and 10 DNA probes from the long arm of the X‐chromosome. Clinical Genetics. 38(2). 94–104. 7 indexed citations
18.
Nørby, Søren, et al.. (1989). Non-allelic genetic heterogeneity of autosomal dominant polycystic kidney disease?. PubMed. 305. 83–8. 7 indexed citations
19.
Nørby, Søren, et al.. (1989). Autosomal dominant polycystic kidney disease in the 1980's. Clinical Genetics. 36(5). 320–325. 17 indexed citations
20.
Nørby, Søren. (1973). The biochemical genetics of rudimentary mutants of Drosophila melanogaster. I. Aspartate carbamoyltransferase levels in complementing and non-complementing strains.. PubMed. 73(1). 11–6. 74 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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