F Skovby

483 total citations
10 papers, 366 citations indexed

About

F Skovby is a scholar working on Rheumatology, Genetics and Molecular Biology. According to data from OpenAlex, F Skovby has authored 10 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Rheumatology, 3 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in F Skovby's work include Connective tissue disorders research (2 papers), Bartonella species infections research (1 paper) and Glycogen Storage Diseases and Myoclonus (1 paper). F Skovby is often cited by papers focused on Connective tissue disorders research (2 papers), Bartonella species infections research (1 paper) and Glycogen Storage Diseases and Myoclonus (1 paper). F Skovby collaborates with scholars based in Denmark, United States and Poland. F Skovby's co-authors include Nurten Akarsu, Wim Brussel, Sevim Balcı, E. Ferda Perçin, Jacopo Celli, Han G. Brunner, Hans van Bokhoven, Ellen van Beusekom, Hülya Kayserili and Henrik Toft Simonsen and has published in prestigious journals such as Nature Genetics, Human Mutation and Acta Paediatrica.

In The Last Decade

F Skovby

10 papers receiving 360 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F Skovby Denmark	7	195	100	80	47	32	10	366
Kazuso Iinuma Japan	13	144 0.7×	183 1.8×	28 0.3×	38 0.8×	22 0.7×	33	467
Antonio González‐Meneses Spain	11	225 1.2×	106 1.1×	48 0.6×	21 0.4×	41 1.3×	34	393
Koumudi Godbole India	10	102 0.5×	36 0.4×	77 1.0×	19 0.4×	69 2.2×	22	295
Riccardo De Marco Italy	9	144 0.7×	63 0.6×	79 1.0×	49 1.0×	22 0.7×	19	502
J. M. Costello New Zealand	7	149 0.8×	45 0.5×	48 0.6×	9 0.2×	12 0.4×	11	279
Jadranka Popović United States	10	245 1.3×	144 1.4×	29 0.4×	47 1.0×	24 0.8×	12	522
Luíza Ferreira de Araújo Brazil	14	287 1.5×	54 0.5×	15 0.2×	43 0.9×	23 0.7×	25	478
Anton Mlikotic United States	11	66 0.3×	80 0.8×	42 0.5×	41 0.9×	157 4.9×	19	371
Vanda Boshnjaku United States	8	140 0.7×	49 0.5×	81 1.0×	86 1.8×	16 0.5×	8	346
G. Bourrouillou France	14	279 1.4×	398 4.0×	21 0.3×	71 1.5×	23 0.7×	40	587

Countries citing papers authored by F Skovby

Since Specialization

Citations

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

Fields of papers citing papers by F Skovby

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F Skovby

This figure shows the co-authorship network connecting the top 25 collaborators of F Skovby. A scholar is included among the top collaborators of F Skovby 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 F Skovby. F Skovby is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

1.

Santer, René, Martina Kinner, Ulrike Steuerwald, et al.. (2001). Molecular genetic basis and prevalence of glycogen storage disease type IIIA in the Faroe Islands. European Journal of Human Genetics. 9(5). 388–391. 64 indexed citations

2.

Bokhoven, Hans van, Jacopo Celli, Hülya Kayserili, et al.. (2000). Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome. Nature Genetics. 25(4). 423–426. 195 indexed citations

3.

Lund, Allan M., F Skovby, & F Knudsen. (2000). [Child abuse and osteogenesis imperfecta. How do we distinguish?].. PubMed. 162(11). 1528–33. 4 indexed citations

4.

Lund, Allan M., et al.. (1999). Osteogenesis imperfecta: Mosaicism and refinement of the genotype-phenotype map in OI type III. Human Mutation. 13(6). 503–503. 15 indexed citations

5.

Skovby, F, et al.. (1999). Oral manifestations of Schimmelpenning syndrome: case report and review of literature.. PubMed. 28(5). 744–8. 7 indexed citations

6.

Rasmussen, Lone Banke, Niels Lyhne Andersen, Göran Andersson, et al.. (1998). Folate and neural tube defects. Recommendations from a Danish working group.. PubMed. 45(2). 213–7. 32 indexed citations

7.

Schwartz, M., et al.. (1996). [A follow-up study of carriers of cystic fibrosis].. PubMed. 158(33). 4623–7. 4 indexed citations

8.

Stender, Steen, et al.. (1993). Cholesterol-lowering diets may increase the food costs for Danish children. A cross-sectional study of food costs for Danish children with and without familial hypercholesterolaemia.. PubMed. 47(11). 776–86. 32 indexed citations

9.

Dyerberg, J., Stefan Stender, Ole Færgeman, et al.. (1990). [Recommendations for clinical-chemical departments: lipid-lipoprotein analysis].. PubMed. 152(20). 1434–7. 8 indexed citations

10.

Skovby, F & M. P. Sullivan. (1982). HERPES ZOSTER AND VARICELLA IN CHILDREN WITH HODGKIN'S DISEASE. Acta Paediatrica. 71(2). 269–273. 5 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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