Frederik J. Hes

11.2k total citations
136 papers, 4.1k citations indexed

About

Frederik J. Hes is a scholar working on Cancer Research, Pathology and Forensic Medicine and Surgery. According to data from OpenAlex, Frederik J. Hes has authored 136 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Cancer Research, 52 papers in Pathology and Forensic Medicine and 46 papers in Surgery. Recurrent topics in Frederik J. Hes's work include Genetic factors in colorectal cancer (51 papers), Cancer Genomics and Diagnostics (39 papers) and Adrenal and Paraganglionic Tumors (29 papers). Frederik J. Hes is often cited by papers focused on Genetic factors in colorectal cancer (51 papers), Cancer Genomics and Diagnostics (39 papers) and Adrenal and Paraganglionic Tumors (29 papers). Frederik J. Hes collaborates with scholars based in Netherlands, Belgium and Germany. Frederik J. Hes's co-authors include Hans F. A. Vasen, Maartje Nielsen, Hans Morreau, Carli M.J. Tops, Stefan Aretz, Eleonora P.M. Corssmit, Juul Wijnen, Tom van Wezel, Julian R. Sampson and Stefanie Vogt and has published in prestigious journals such as Gastroenterology, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Frederik J. Hes

131 papers receiving 4.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Frederik J. Hes Netherlands	38	1.8k	1.7k	1.3k	1.2k	1.2k	136	4.1k
Carli M.J. Tops Netherlands	35	2.3k 1.2×	1.3k 0.8×	1.4k 1.1×	891 0.8×	690 0.6×	93	3.3k
Rob B. van der Luijt Netherlands	28	804 0.4×	782 0.5×	931 0.7×	802 0.7×	445 0.4×	64	2.7k
Anne C. Tersmette United States	23	2.0k 1.1×	1.1k 0.6×	2.3k 1.7×	833 0.7×	1.4k 1.2×	32	4.3k
Patrick Treseler United States	31	1.3k 0.7×	475 0.3×	870 0.6×	524 0.4×	597 0.5×	66	3.4k
Stefan Aretz Germany	31	2.1k 1.1×	827 0.5×	1.1k 0.8×	876 0.7×	624 0.5×	92	3.0k
Ian M. Frayling United Kingdom	31	1.9k 1.0×	789 0.5×	1.4k 1.1×	998 0.8×	405 0.4×	72	3.3k
Judith Dierlamm Germany	33	1.8k 1.0×	599 0.3×	1.3k 0.9×	1.0k 0.9×	466 0.4×	111	4.1k
Christian Bastard France	46	3.1k 1.7×	527 0.3×	2.3k 1.7×	2.5k 2.1×	206 0.2×	152	6.4k
Manoj Gandhi United States	21	602 0.3×	323 0.2×	1.2k 0.9×	1.2k 1.1×	446 0.4×	32	3.4k
Juul Wijnen Netherlands	40	3.4k 1.9×	1.8k 1.0×	2.4k 1.8×	1.3k 1.1×	547 0.5×	109	4.8k

Countries citing papers authored by Frederik J. Hes

Since Specialization

Citations

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

Fields of papers citing papers by Frederik J. Hes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frederik J. Hes

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

All Works

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20 of 20 papers shown

Segers, Ingrid, Philippe Giron, Antonio Capalbo, et al.. (2025). Oocyte/zygote/embryo maturation arrest: a clinical study expanding the phenotype of NOBOX variants. Journal of Assisted Reproduction and Genetics. 42(3). 763–771.

Joris, Sofie, Philippe Giron, Catharina Olsen, et al.. (2024). Identification of RAD17 as a candidate cancer predisposition gene in families with histories of pancreatic and breast cancers. BMC Cancer. 24(1). 723–723. 1 indexed citations

Crabben, Saskia N. van der, et al.. (2024). Development of a novel Patient-Reported Outcome Measure (PROM) for adults with an Inherited Cardiac Condition (ICC). European Heart Journal. 45(Supplement_1).

Belva, Florence, Christophe Blockeel, Kathelijn Keymolen, et al.. (2023). Impact of embryo vitrification on children’s health, including growth up to two years of age, in comparison with results following a fresh embryo transfer. Fertility and Sterility. 119(6). 932–941. 6 indexed citations

Kupper, Nina, Esther Scheirlynck, Ahmad S. Amin, et al.. (2023). Are disease-specific patient-reported outcomes measures (PROMs) used in cardiogenetics? A systematic review. European Journal of Human Genetics. 32(6). 607–618. 3 indexed citations

Okutman, Özlem, Münevver Serdarogullari, Ingrid Segers, et al.. (2022). A systematic review and evidence assessment of monogenic gene–disease relationships in human female infertility and differences in sex development. Human Reproduction Update. 29(2). 218–232. 18 indexed citations

Aretz, Stefan, Inge Bernstein, Chrystelle Colas, et al.. (2020). Disease expression in juvenile polyposis syndrome: a retrospective survey on a cohort of 221 European patients and comparison with a literature-derived cohort of 473 SMAD4/BMPR1A pathogenic variant carriers. Genetics in Medicine. 22(9). 1524–1532. 47 indexed citations

Belva, Florence, M Bonduelle, Andrea Buysse, et al.. (2020). Chromosomal abnormalities after ICSI in relation to semen parameters: results in 1114 fetuses and 1391 neonates from a single center. Human Reproduction. 35(9). 2149–2162. 14 indexed citations

Buffet, Alexandre, Heggert Rebel, Eleonora P.M. Corssmit, et al.. (2020). Germline DLST Variants Promote Epigenetic Modifications in Pheochromocytoma-Paraganglioma. The Journal of Clinical Endocrinology & Metabolism. 106(2). 459–471. 8 indexed citations

10.

Belva, Florence, Mathieu Roelants, S. Desmyttere, et al.. (2019). OUP accepted manuscript. Human Reproduction Open. 2020(1). hoz043–hoz043. 9 indexed citations

11.

Bakker, Egbert, Maarten H. Vermeer, Tjalling Bosse, et al.. (2017). A novel keratin 13 variant in a four‐generation family with white sponge nevus. Clinical Case Reports. 5(9). 1503–1509. 11 indexed citations

12.

Rijken, Johannes A., Nicolasine D. Niemeijer, Marianne A. Jonker, et al.. (2017). The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers. Clinical Genetics. 93(1). 60–66. 51 indexed citations

13.

Hoekstra, Attje S., Erik F. Hensen, Ekaterina S. Jordanova, et al.. (2017). Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas. Oncotarget. 8(9). 14525–14536. 17 indexed citations

14.

Nieuwenhuis, Marry H., Jeanine J. Houwing‐Duistermaat, Frederik J. Hes, et al.. (2016). Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers. Familial Cancer. 15(4). 563–570. 7 indexed citations

15.

Adank, Muriel A., Frederik J. Hes, Wendy A.G. van Zelst–Stams, et al.. (2015). CHEK2-mutatie in Nederlandse borstkankerfamilies: uitbreiding van de genetische diagnostiek op borstkanker.. Nederlandsch tijdschrift voor geneeskunde/Nederlands tijdschrift voor geneeskunde/NTvG-databank. 159(45). 1 indexed citations

16.

Hes, Frederik J., et al.. (2015). [CHEK2-mutation in Dutch breast cancer families: expanding genetic testing for breast cancer].. PubMed. 159. A8910–A8910. 7 indexed citations

17.

Miranda, Noel F.C.C. de, Ekaterina S. Jordanova, Carli M.J. Tops, et al.. (2012). Infiltration of Lynch Colorectal Cancers by Activated Immune Cells Associates with Early Staging of the Primary Tumor and Absence of Lymph Node Metastases. Clinical Cancer Research. 18(5). 1237–1245. 28 indexed citations

18.

Aaronson, Neil K., Frederik J. Hes, Thera P. Links, et al.. (2011). Compliance with periodic surveillance for Von-Hippel-Lindau disease. Genetics in Medicine. 13(6). 519–527. 12 indexed citations

19.

Middeldorp, Anneke, Shantie Jagmohan–Changur, Ronald van Eijk, et al.. (2009). Enrichment of Low Penetrance Susceptibility Loci in a Dutch Familial Colorectal Cancer Cohort. Cancer Epidemiology Biomarkers & Prevention. 18(11). 3062–3067. 53 indexed citations

20.

Hes, Frederik J., Tom P.V.M. de Jong, N. M. A. Bax, & R. H. J. Houwen. (1995). Urinary Tract Infections and Cholelithiasis in Early Childhood. Journal of Pediatric Gastroenterology and Nutrition. 21(3). 319–321. 1 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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