R.A. Ophoff

700 total citations
6 papers, 449 citations indexed

About

R.A. Ophoff is a scholar working on Cellular and Molecular Neuroscience, Neurology and Psychiatry and Mental health. According to data from OpenAlex, R.A. Ophoff has authored 6 papers receiving a total of 449 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Cellular and Molecular Neuroscience, 2 papers in Neurology and 2 papers in Psychiatry and Mental health. Recurrent topics in R.A. Ophoff's work include Neurological disorders and treatments (2 papers), Migraine and Headache Studies (2 papers) and Genetic Neurodegenerative Diseases (2 papers). R.A. Ophoff is often cited by papers focused on Neurological disorders and treatments (2 papers), Migraine and Headache Studies (2 papers) and Genetic Neurodegenerative Diseases (2 papers). R.A. Ophoff collaborates with scholars based in Netherlands, United States and Italy. R.A. Ophoff's co-authors include Rune R. Frants, Francesco Pierelli, Elide Mantuano, Fabrizio Salvi, Marina Frontali, Flavia Trettel, L. Calandriello, M. Spadaro, Carla Jodice and Liana Veneziano and has published in prestigious journals such as Human Molecular Genetics, Epilepsia and Cephalalgia.

In The Last Decade

R.A. Ophoff

6 papers receiving 437 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R.A. Ophoff Netherlands	6	319	268	118	111	84	6	449
Paul J. Adams Canada	8	287 0.9×	194 0.7×	74 0.6×	40 0.4×	115 1.4×	14	377
G. Sabbadini Italy	8	315 1.0×	317 1.2×	43 0.4×	202 1.8×	23 0.3×	9	417
Stephan Grueninger Switzerland	10	473 1.5×	479 1.8×	44 0.4×	127 1.1×	71 0.8×	11	600
Hafsa Mamsa United States	7	206 0.6×	137 0.5×	73 0.6×	52 0.5×	13 0.2×	8	336
Stephanie Nadine Reichel Germany	4	173 0.5×	130 0.5×	108 0.9×	46 0.4×	71 0.8×	5	326
J. Jay Gargus United States	10	209 0.7×	69 0.3×	144 1.2×	23 0.2×	26 0.3×	14	420
Monika Jeub Germany	11	189 0.6×	217 0.8×	100 0.8×	145 1.3×	23 0.3×	16	463
Susan E Tomlinson Australia	8	134 0.4×	147 0.5×	42 0.4×	94 0.8×	35 0.4×	13	251
Fabio Aglieco United States	5	361 1.1×	243 0.9×	16 0.1×	39 0.4×	45 0.5×	7	472
Fatima Jaffer United Kingdom	6	138 0.4×	86 0.3×	47 0.4×	55 0.5×	42 0.5×	12	264

Countries citing papers authored by R.A. Ophoff

Since Specialization

Citations

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

Fields of papers citing papers by R.A. Ophoff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R.A. Ophoff

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

All Works

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6 of 6 papers shown

1.

Rao, P. Nagesh, et al.. (2010). Recurrent Inversion Events at 17q21.31 Microdeletion Locus Are Linked to the <i>MAPT</i> H2 Haplotype. Cytogenetic and Genome Research. 129(4). 275–279. 21 indexed citations

2.

Jodice, Carla, Elide Mantuano, Liana Veneziano, et al.. (1997). Episodic Ataxia Type 2 (EA2) and Spinocerebellar Ataxia Type 6 (SCA6) Due to CAG Repeat Expansion in the CACNA1A Gene on Chromosome 19p. Human Molecular Genetics. 6(11). 1973–1978. 215 indexed citations

3.

Terwindt, G.M., R.A. Ophoff, Dick Lindhout, et al.. (1997). Partial Cosegregation of Familial Hemiplegic Migraine and a Benign Familial Infantile Epileptic Syndrome. Epilepsia. 38(8). 915–921. 44 indexed citations

4.

Terwindt, GM, et al.. (1996). Familial Hemiplegic Migraine: A Clinical Comparison of Families Linked and Unlinked to Chromosome 19. Cephalalgia. 16(3). 153–155. 60 indexed citations

5.

Elbaz, Alexis, Karin Jurkat‐Rott, P. Lapie, et al.. (1995). Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families.. PubMed. 56(2). 374–80. 88 indexed citations

6.

Fijneman, Remond J.A., R.A. Ophoff, Andrew Hart, & Peter Démant. (1994). Kras-2 alleles, mutations, and lung tumor susceptibility in the mouse--an evaluation.. PubMed. 9(5). 1417–21. 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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