R.R. Frants

1.5k total citations
33 papers, 1.1k citations indexed

About

R.R. Frants is a scholar working on Psychiatry and Mental health, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, R.R. Frants has authored 33 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Psychiatry and Mental health, 9 papers in Molecular Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in R.R. Frants's work include Migraine and Headache Studies (12 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological diseases and metabolism (3 papers). R.R. Frants is often cited by papers focused on Migraine and Headache Studies (12 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological diseases and metabolism (3 papers). R.R. Frants collaborates with scholars based in Netherlands, Hungary and Finland. R.R. Frants's co-authors include Nelleke A. Gruis, W. Bergman, Pieter A. van der Velden, Michel D. Ferrari, Hans F. A. Vasen, E.T.M. Hille, GM Terwindt, J. Haan, Lodewijk A. Sandkuijl and AMJM van den Maagdenberg and has published in prestigious journals such as Blood, Gastroenterology and Biochemical and Biophysical Research Communications.

In The Last Decade

R.R. Frants

33 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R.R. Frants Netherlands 19 396 349 336 229 211 33 1.1k
Ivan Selak Bosnia and Herzegovina 19 527 1.3× 162 0.5× 214 0.6× 203 0.9× 73 0.3× 52 1.4k
Kazuo Washiyama Japan 23 791 2.0× 187 0.5× 75 0.2× 189 0.8× 137 0.6× 60 1.5k
Dora Stauffer United States 12 1.2k 3.1× 355 1.0× 464 1.4× 209 0.9× 499 2.4× 15 2.2k
Alonso Martínez Colombia 10 965 2.4× 138 0.4× 95 0.3× 202 0.9× 57 0.3× 22 1.4k
S Staddon United Kingdom 10 293 0.7× 347 1.0× 95 0.3× 96 0.4× 63 0.3× 14 770
Ken Opeskin Australia 11 355 0.9× 201 0.6× 112 0.3× 175 0.8× 57 0.3× 20 742
Glenda Hendson Canada 19 288 0.7× 70 0.2× 178 0.5× 67 0.3× 50 0.2× 45 1.3k
Katherine Holland United States 13 307 0.8× 181 0.5× 259 0.8× 45 0.2× 51 0.2× 25 1.1k
Sara Rollinson United Kingdom 28 847 2.1× 121 0.3× 125 0.4× 95 0.4× 94 0.4× 50 2.3k
Maria Maryanovich United States 11 755 1.9× 216 0.6× 343 1.0× 178 0.8× 27 0.1× 31 1.7k

Countries citing papers authored by R.R. Frants

Since Specialization
Citations

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

Fields of papers citing papers by R.R. Frants

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R.R. Frants

This figure shows the co-authorship network connecting the top 25 collaborators of R.R. Frants. A scholar is included among the top collaborators of R.R. Frants 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 R.R. Frants. R.R. Frants 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.
Lemos, Carolina, Boukje de Vries, José Barros, et al.. (2008). First Mutation in the Voltage-Gated Nav1.1 Subunit Gene SCN1A with Co-Occurring Familial Hemiplegic Migraine and Epilepsy. Cephalalgia. 29(3). 308–313. 74 indexed citations
2.
Callenbach, Petra M.C., I.F.M. de Coo, R. ten Houten, et al.. (2005). Refinement of the chromosome 16 locus for benign familial infantile convulsions. Clinical Genetics. 67(6). 517–525. 20 indexed citations
3.
Kia, Sima Kheradmand, et al.. (2005). The 3p21.1-p21.3 Hereditary Vascular Retinopathy Locus Increases the Risk for Raynaud's Phenomenon and Migraine. Cephalalgia. 25(12). 1168–1172. 15 indexed citations
4.
Putter, Hein, Marian Beekman, Nico Lakenberg, et al.. (2004). Mapping QTLs for HDL-C, LDL-C and Associated Proteins and Identification of Underlying Genetic Variation: A Meta-analysis of Four Genome Scans. Twin Research and Human Genetics. 7(6). 683. 1 indexed citations
5.
Terwindt, G.M., et al.. (2003). Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine.. Headache The Journal of Head and Face Pain. 43(3). 303–303. 3 indexed citations
6.
Haan, J., et al.. (2001). No Involvement of the Calcium Channel Gene (CACNA1A) in a Family with Cluster Headache. Cephalalgia. 21(10). 959–962. 29 indexed citations
7.
Sandkuijl, L., et al.. (1999). オランダの家族性異型多発母斑黒色腫(FAMMM)症候群の家族における黒色腫のリスクを変化させるP16にリンクされた遺伝子座. Genome Research. 9(6). 575–580. 2 indexed citations
8.
Frants, R.R.. (1999). The Use of Isolates in Migraine Genetic Research. Cephalalgia. 19(24 suppl). 19–24. 3 indexed citations
9.
Terwindt, G.M., et al.. (1998). Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. European Journal of Human Genetics. 6(4). 297–307. 66 indexed citations
10.
Vergouwe, Monique N., Marina A.J. Tijssen, Rita Shiang, et al.. (1997). Hyperekplexia-like syndromes without mutations in the GLRA1 gene. Clinical Neurology and Neurosurgery. 99(3). 172–178. 30 indexed citations
11.
Boomsma, Dorret I., H.J.M. Kempen, J.A. Gevers Leuven, et al.. (1996). Genetic analysis of sex and generation differences in plasma lipid, lipoprotein, and apolipoprotein levels in adolescent twins and their parents. Genetic Epidemiology. 13(1). 49–60. 51 indexed citations
12.
Gruis, Nelleke A., Lodewijk A. Sandkuijl, Pieter A. van der Velden, W. Bergman, & R.R. Frants. (1995). CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families. Melanoma Research. 5(3). 169–178. 80 indexed citations
13.
Petrij, Fred, et al.. (1993). The Mouse Low-Density Lipoprotein Receptor Gene: cDNA Sequence and Exon-Intron Structure. Biochemical and Biophysical Research Communications. 191(3). 880–886. 32 indexed citations
14.
Bergman, W., Nelleke A. Gruis, & R.R. Frants. (1992). The Dutch FAMMM family material: Clinical and genetic data. Cytogenetic and Genome Research. 59(2-3). 161–164. 17 indexed citations
15.
Scheffer, Hans, et al.. (1991). LINKAGE ANALYSIS IN FAMILIES WITH PROXIMAL SPINAL MUSCULAR-ATROPHY FROM THE NETHERLANDS. The American Journal of Human Genetics. 49(4). 203–203. 22 indexed citations
16.
Mannens, M., E. M. Bleeker‐Wagemakers, Jet Bliek, et al.. (1989). Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family. Cytogenetic and Genome Research. 52(1-2). 32–36. 27 indexed citations
17.
Smit, M., Peter de Knijff, Alice J.A.M. Sijts, et al.. (1988). Rare Apolipoprotein E Variant Cosegregating with a Unique APOE-C1-C2 Haplotype in a Normolipidemic Family. Human Heredity. 38(5). 277–282. 8 indexed citations
18.
Frants, R.R., et al.. (1983). Genetic evidence for fetal origin of transcobalamin II in human cord blood. Blood. 62(1). 234–237. 14 indexed citations
19.
Frants, R.R. & Aldur W. Eriksson. (1979). 7.4. Application of the Pi system for identification purposes. Forensic Science International. 14(2). 134–135. 1 indexed citations
20.
Frants, R.R., et al.. (1976). &alpha;<sub>1</sub>-Antitrypsin: Common Subtypes of Pi M. Human Heredity. 26(6). 435–440. 49 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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