Frederik J. Hes

11.2k citations

136 papers · 4.1k indexed · h-index 38

Pathology and Forensic Medicine top 0.5%
Cancer Research top 0.5%
Oncology top 2%
Molecular Biology top 10%
Surgery top 2%

Co-authors: Hans F. A. Vasen Maartje Nielsen Hans Morreau Carli M.J. Tops Stefan Aretz Eleonora P.M. Corssmit Juul Wijnen Tom van Wezel
Topics: Genetic factors in colorectal cancer (51 papers)Cancer Genomics and Diagnostics (39 papers)Adrenal and Paraganglionic Tumors (29 papers)
Cited by: Cancer Research Pathology and Forensic Medicine Oncology
Journals: Gastroenterology PLoS ONE The Journal of Clinical Endocrinology & Metabolism
Partner nations: Netherlands Belgium Germany

In The Last Decade

Frederik J. Hes

131 papers receiving 4.0k citations

Peers

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

#	Work	Indexed citations
1	Oocyte/zygote/embryo maturation arrest: a clinical study expanding the phenotype of NOBOX variants 2025 ·Journal of Assisted Reproduction and Genetics ·(unknown),(unknown),(unknown),(unknown),Ingrid Segers,(unknown),(unknown),Philippe Giron,Antonio Capalbo,Willem Verpoest,Frederik J. Hes,Pieter Verdyck,Alexander Gheldof	0
2	Development of a novel Patient-Reported Outcome Measure (PROM) for adults with an Inherited Cardiac Condition (ICC) 2024 ·European Heart Journal ·(unknown),Saskia N. van der Crabben,(unknown),(unknown),Esther Scheirlynck,Julie Nekkebroeck,Frederik J. Hes,Nina Kupper	0
3	Identification of RAD17 as a candidate cancer predisposition gene in families with histories of pancreatic and breast cancers 2024 ·BMC Cancer ·Sofie Joris,Philippe Giron,Catharina Olsen,Sara Seneca,Alexander Gheldof,(unknown),(unknown),Sylvia De Brakeleer,Erik Teugels,Jacques De Grève,Frederik J. Hes	1
4	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 2023 ·Fertility and Sterility ·Florence Belva,Christophe Blockeel,Kathelijn Keymolen,Andrea Buysse,M Bonduelle,Greta Verheyen,Mathieu Roelants,Herman Tournaye,Frederik J. Hes,L. Van Landuyt	6
5	A systematic review and evidence assessment of monogenic gene–disease relationships in human female infertility and differences in sex development 2022 ·Human Reproduction Update ·(unknown),Özlem Okutman,(unknown),Münevver Serdarogullari,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Ingrid Segers,Alexander Gheldof,Frederik J. Hes,Karen Sermon,Willem Verpoest,Stéphane Viville	18
6	Barriers and facilitators for the implementation of patient-centered care in cardiogenetics: a Delphi study among ERN GUARD-heart members 2022 ·European Journal of Human Genetics ·(unknown),(unknown),Sonia Van Dooren,Frederik J. Hes,(unknown)	1
7	Chromosomal abnormalities after ICSI in relation to semen parameters: results in 1114 fetuses and 1391 neonates from a single center 2020 ·Human Reproduction ·Florence Belva,M Bonduelle,Andrea Buysse,Ann Van Den Bogaert,Frederik J. Hes,Mathieu Roelants,Greta Verheyen,Herman Tournaye,Kathelijn Keymolen	14
8	Germline DLST Variants Promote Epigenetic Modifications in Pheochromocytoma-Paraganglioma 2020 ·The Journal of Clinical Endocrinology & Metabolism ·Alexandre Buffet,(unknown),Heggert Rebel,Eleonora P.M. Corssmit,Jeroen C. Jansen,Erik F. Hensen,Judith V.M.G. Bovée,(unknown),Anne‐Paule Gimenez‐Roqueplo,Frederik J. Hes,Peter Devilee,Judith Favier,Jean‐Pierre Bayley	8
9	Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas 2017 ·Oncotarget ·Attje S. Hoekstra,Erik F. Hensen,Ekaterina S. Jordanova,Esther Korpershoek,Anouk N.A. van der Horst‐Schrivers,Cees J. Cornelisse,Eleonora P.M. Corssmit,Frederik J. Hes,Jeroen C. Jansen,Henricus P. M. Kunst,Henri Timmers,Adrian C Bateman,Diana Eccles,Judith V.M.G. Bovée,Peter Devilee,Jean‐Pierre Bayley	17
10	The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers 2017 ·Clinical Genetics ·Johannes A. Rijken,Nicolasine D. Niemeijer,Marianne A. Jonker,(unknown),Jeroen C. Jansen,Anouk van Berkel,Henri Timmers,Henricus P. M. Kunst,Peter H. Bisschop,M. N. Kerstens,Koen M.A. Dreijerink,M. F. van Dooren,Anouk N.A. van der Horst‐Schrivers,Frederik J. Hes,C. René Leemans,Eleonora P.M. Corssmit,Erik F. Hensen	51
11	A novel keratin 13 variant in a four‐generation family with white sponge nevus 2017 ·Clinical Case Reports ·(unknown),Egbert Bakker,Maarten H. Vermeer,(unknown),Tjalling Bosse,Vincent T.H.B.M. Smit,(unknown),W.H. Irwin McLean,Alexander A.W. Peters,Frederik J. Hes	11
12	Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers 2016 ·Familial Cancer ·(unknown),Marry H. Nieuwenhuis,Jeanine J. Houwing‐Duistermaat,(unknown),Frederik J. Hes,Carli M.J. Tops,Anja Wagner,Cora M. Aalfs,Senno Verhoef,E. Gómez,Rolf H. Sijmons,Fred H. Menko,Tom G.W. Letteboer,Nicoline Hoogerbrugge,Tom van Wezel,Hans F. A. Vasen,Juul Wijnen	7
13	[CHEK2-mutation in Dutch breast cancer families: expanding genetic testing for breast cancer]. 2015 ·PubMed ·(unknown),Frederik J. Hes,(unknown),M. Petrousjka van den Tol,Caroline Seynaeve,Jan C. Oosterwijk	7
14	CHEK2-mutatie in Nederlandse borstkankerfamilies: uitbreiding van de genetische diagnostiek op borstkanker. 2015 ·Nederlandsch tijdschrift voor geneeskunde/Nederlands tijdschrift voor geneeskunde/NTvG-databank ·Muriel A. Adank,Frederik J. Hes,Wendy A.G. van Zelst–Stams,M. Petrousjka van den Tol,Caroline Seynaeve,Jan C. Oosterwijk	1
15	Infiltration of Lynch Colorectal Cancers by Activated Immune Cells Associates with Early Staging of the Primary Tumor and Absence of Lymph Node Metastases 2012 ·Clinical Cancer Research ·Noel F.C.C. de Miranda,(unknown),Ekaterina S. Jordanova,Carli M.J. Tops,Frederik J. Hes,Hans F. A. Vasen,Tom van Wezel,Hans Morreau	28
16	Insertion of an SVA element, a nonautonomous retrotransposon, inPMS2intron 7 as a novel cause of lynch syndrome 2012 ·Human Mutation ·Heleen M. van der Klift,Carli M.J. Tops,Frederik J. Hes,Peter Devilee,Juul Wijnen	39
17	Low penetrance of a SDHB mutation in a large Dutch paraganglioma family 2010 ·BMC Medical Genetics ·Frederik J. Hes,Marjan M. Weiss,(unknown),Noel F.C.C. de Miranda,(unknown),Bert A. Bonsing,Marcel P. M. Stokkel,Hans Morreau,Johannes A. Romijn,Jeroen C. Jansen,A. H. J. T. Vriends,Jean‐Pierre Bayley,Eleonora P.M. Corssmit	38
18	Enrichment of Low Penetrance Susceptibility Loci in a Dutch Familial Colorectal Cancer Cohort 2009 ·Cancer Epidemiology Biomarkers & Prevention ·Anneke Middeldorp,Shantie Jagmohan–Changur,Ronald van Eijk,Carli Tops,Peter Devilee,Hans F. A. Vasen,Frederik J. Hes,Richard S. Houlston,Ian Tomlinson,Jeanine J. Houwing‐Duistermaat,Juul Wijnen,Hans Morreau,Tom van Wezel	53
19	Colorectal carcinomas in MUTYH-associated polyposis display histopathological similarities to microsatellite unstable carcinomas 2009 ·BMC Cancer ·Maartje Nielsen,Noel F.C.C. de Miranda,Marjo van Puijenbroek,Ekaterina S. Jordanova,Anneke Middeldorp,Tom van Wezel,Ronald van Eijk,Carli M.J. Tops,Hans F. A. Vasen,Frederik J. Hes,Hans Morreau	47
20	Urinary Tract Infections and Cholelithiasis in Early Childhood 1995 ·Journal of Pediatric Gastroenterology and Nutrition ·Frederik J. Hes,Tom P.V.M. de Jong,N. M. A. Bax,R. H. J. Houwen	1

About Frederik J. Hes

Frederik J. Hes is a scholar working on Cancer Research, Pathology and Forensic Medicine and Endocrinology, Diabetes and Metabolism, having authored 136 papers that have together received 4.1k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (51 papers), Cancer Genomics and Diagnostics (39 papers) and Adrenal and Paraganglionic Tumors (29 papers). The work is most often cited by research in Cancer Research (1.7k citations), Pathology and Forensic Medicine (1.8k citations) and Oncology (1.3k citations). Frederik J. Hes has collaborated with scholars based in Netherlands, Belgium and Germany. Frequent 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. Their work appears in journals such as Gastroenterology, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

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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