J. Gulcher

572 total citations
7 papers, 418 citations indexed

About

J. Gulcher is a scholar working on Pathology and Forensic Medicine, Genetics and Immunology. According to data from OpenAlex, J. Gulcher has authored 7 papers receiving a total of 418 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Pathology and Forensic Medicine, 2 papers in Genetics and 2 papers in Immunology. Recurrent topics in J. Gulcher's work include Genetic Associations and Epidemiology (2 papers), Migraine and Headache Studies (2 papers) and Trigeminal Neuralgia and Treatments (2 papers). J. Gulcher is often cited by papers focused on Genetic Associations and Epidemiology (2 papers), Migraine and Headache Studies (2 papers) and Trigeminal Neuralgia and Treatments (2 papers). J. Gulcher collaborates with scholars based in Iceland and Denmark. J. Gulcher's co-authors include Kāri Stefánsson, Hreinn Stefánsson, Augustine Kong, Valgerður Steinthórsdóttir, Helgi Jónsson, Reynir Tómas Geirsson, Andrei Manolescu, Jes Olesen, Ásgeir Björnsson and Ari Kárason and has published in prestigious journals such as Journal of Clinical Oncology, Brain and Human Reproduction.

In The Last Decade

J. Gulcher

6 papers receiving 403 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. Gulcher Iceland	5	180	167	116	114	56	7	418
Bénédicte Paindaveine United States	5	60 0.3×	175 1.0×	10 0.1×	152 1.3×	4 0.1×	7	412
Ahmed Talaat United Kingdom	7	8 0.0×	99 0.6×	43 0.4×	42 0.4×	157 2.8×	11	366
Berthold Jeßberger Germany	5	58 0.3×	150 0.9×	10 0.1×	4 0.0×	5 0.1×	11	245
Barry J. Lewis United Kingdom	6	141 0.8×	9 0.1×	31 0.3×	1 0.0×	69 1.2×	8	377
Mary Hanna United States	6	61 0.3×	19 0.1×	10 0.1×	4 0.0×	12 0.2×	10	360
Igor Medica Slovenia	11	70 0.4×	29 0.2×	1 0.0×	77 0.7×	7 0.1×	28	359
Chanond A. Nasamran United States	10	31 0.2×	25 0.1×	8 0.1×	5 0.0×	9 0.2×	25	243
Johanna Vendelin Finland	8	70 0.4×	35 0.2×	4 0.0×	3 0.0×	3 0.1×	10	298
Patrick Meyer Switzerland	11	18 0.1×	22 0.1×	8 0.1×	3 0.0×	22 0.4×	26	310
Rachel Sayuri Honjo Brazil	13	59 0.3×	15 0.1×	10 0.1×	4 0.0×	22 0.4×	60	460

Countries citing papers authored by J. Gulcher

Since Specialization

Citations

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

Fields of papers citing papers by J. Gulcher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Gulcher

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

All Works

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7 of 7 papers shown

1.

Bailey, Shannon T., et al.. (2018). High-quality whole-genome sequencing of FFPE samples.. Journal of Clinical Oncology. 36(15_suppl). e13500–e13500. 1 indexed citations

2.

Thomsen, LL, Ásgeir Björnsson, Hreinn Stefánsson, et al.. (2008). Screen for CACNA1A and ATP1A2 Mutations in Sporadic Hemiplegic Migraine Patients. Cephalalgia. 28(9). 914–921. 30 indexed citations

3.

Gulcher, J. & Kāri Stefánsson. (2006). Positional Cloning: Complex Cardiovascular Traits. Humana Press eBooks. 128. 137–152. 1 indexed citations

4.

Thomsen, L. L., Malene Kirchmann, Ásgeir Björnsson, et al.. (2006). The genetic spectrum of a population-based sample of familial hemiplegic migraine. Brain. 130(2). 346–356. 104 indexed citations

5.

Guðjónsson, Jóhann E., Ari Kárason, Valdimar B. Hauksson, et al.. (2003). Psoriasis patients who are homozygous for the HLA-Cw*0602 allele have a 2.5-fold increased risk of developing psoriasis compared with Cw6 heterozygotes. British Journal of Dermatology. 148(2). 233–235. 83 indexed citations

6.

Stefánsson, Hreinn, Reynir Tómas Geirsson, Valgerður Steinthórsdóttir, et al.. (2002). Genetic factors contribute to the risk of developing endometriosis. Human Reproduction. 17(3). 555–559. 178 indexed citations

7.

Gulcher, J.. (2001). The role of linkage studies for common diseases. Current Opinion in Genetics & Development. 11(3). 264–267. 21 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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