JP Fryns

1.0k total citations
14 papers, 563 citations indexed

About

JP Fryns is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, JP Fryns has authored 14 papers receiving a total of 563 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 4 papers in Plant Science. Recurrent topics in JP Fryns's work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (4 papers) and Congenital heart defects research (4 papers). JP Fryns is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (4 papers) and Congenital heart defects research (4 papers). JP Fryns collaborates with scholars based in Belgium, United States and Netherlands. JP Fryns's co-authors include Koenraad Devriendt, Joris Vermeesch, Femke Hannes, Griet Van Buggenhout, Peter Marynen, Regina Regan, Annick Vogels, Helen Stewart, Thomy de Ravel and Heather C. Mefford and has published in prestigious journals such as Journal of Medical Genetics, European Journal of Human Genetics and Clinical Genetics.

In The Last Decade

JP Fryns

13 papers receiving 538 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
JP Fryns Belgium	11	427	284	108	107	80	14	563
Aimee S. Spikes United States	9	452 1.1×	326 1.1×	79 0.7×	94 0.9×	102 1.3×	11	598
Anna Capalbo Italy	16	389 0.9×	244 0.9×	112 1.0×	77 0.7×	41 0.5×	29	579
Monika Cohen Germany	11	488 1.1×	551 1.9×	98 0.9×	84 0.8×	113 1.4×	13	859
Shino Shimada Japan	15	318 0.7×	315 1.1×	62 0.6×	45 0.4×	68 0.8×	36	545
Nicole Maas Belgium	7	351 0.8×	191 0.7×	101 0.9×	120 1.1×	29 0.4×	13	455
Melissa T. Carter Canada	16	326 0.8×	320 1.1×	75 0.7×	34 0.3×	94 1.2×	34	616
Naohiro Kurotaki Japan	12	312 0.7×	223 0.8×	76 0.7×	59 0.6×	67 0.8×	20	446
Barbara Utermann Austria	13	177 0.4×	128 0.5×	100 0.9×	62 0.6×	46 0.6×	18	336
C E de Die-Smulders Netherlands	13	266 0.6×	272 1.0×	90 0.8×	19 0.2×	89 1.1×	21	516
Tiziana Filippi Italy	9	374 0.9×	207 0.7×	157 1.5×	71 0.7×	41 0.5×	10	539

Countries citing papers authored by JP Fryns

Since Specialization

Citations

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

Fields of papers citing papers by JP Fryns

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of JP Fryns

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

All Works

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14 of 14 papers shown

Chabchoub, Elyes, et al.. (2011). Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineated. Clinical Genetics. 81(6). 584–589. 3 indexed citations

Vogels, Annick & JP Fryns. (2011). Microdeletions and molecular genetics. Atlas of Genetics and Cytogenetics in Oncology and Haematology.

Breckpot, Jeroen, et al.. (2009). DISC1 duplication in two brothers with autism and mild mental retardation. Clinical Genetics. 77(4). 389–394. 23 indexed citations

Froyen, Guy, Karen Govaerts, Hilde Van Esch, et al.. (2009). Novel PORCN mutations in focal dermal hypoplasia. Clinical Genetics. 76(6). 535–543. 17 indexed citations

Hannes, Femke, Andrew J. Sharp, Heather C. Mefford, et al.. (2008). Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant. Journal of Medical Genetics. 46(4). 223–232. 207 indexed citations

Maas, Nicole, Griet Van Buggenhout, Femke Hannes, et al.. (2007). Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH). Journal of Medical Genetics. 45(2). 71–80. 99 indexed citations

Decruyenaere, Marleen, Gerry Evers‐Kiebooms, T Cloostermans, et al.. (2003). Predictive testing for Huntington's disease: relationship with partners after testing. Clinical Genetics. 65(1). 24–31. 25 indexed citations

Mols, Raf, et al.. (2002). Involvement of a palindromic chromosome 22‐specific low‐copy repeat in a constitutional t(X; 22)(q27;q11). Clinical Genetics. 62(5). 410–414. 16 indexed citations

Frints, Suzanna G.M., et al.. (2002). X‐linked mental retardation: vanishing boundaries between non‐specific (MRX) and syndromic (MRXS) forms. Clinical Genetics. 62(6). 423–432. 49 indexed citations

10.

Vermeesch, Joris, Emiel Baten, JP Fryns, & Koenraad Devriendt. (2002). Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequences. Clinical Genetics. 62(5). 415–417. 32 indexed citations

11.

Thoelen, Ronald, et al.. (2000). Physical map of a 1.5 Mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint. European Journal of Human Genetics. 8(8). 561–570. 10 indexed citations

12.

Lammens, Martin, et al.. (1998). Neuropathological findings in Moebius syndrome. Clinical Genetics. 54(2). 136–141. 25 indexed citations

13.

Lukusa, T., Koenraad Devriendt, Maureen Holvoet, & JP Fryns. (1998). Severe mental retardation ‐ distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a lOq25→qter deletion. Clinical Genetics. 54(3). 224–230. 2 indexed citations

14.

Steyaert, Jean, et al.. (1997). A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy. Clinical Genetics. 52(3). 135–141. 55 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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