Jeroen Knijnenburg

2.5k citations

47 papers · 1.4k indexed · h-index 22

Dermatology top 2%
- Cutaneous lymphoproliferative disorders research 3
Genetics top 5%
- Genomic variations and chromosomal abnormalities 27
- Genomics and Rare Diseases 5
- Genetics and Neurodevelopmental Disorders 5
Pathology and Forensic Medicine top 5%
Genetics top 10%
- Genomic variations and chromosomal abnormalities 27
- Genomics and Rare Diseases 5
- Genetics and Neurodevelopmental Disorders 5
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 8
Molecular Biology
- Congenital heart defects research 10
Plant Science
- Chromosomal and Genetic Variations 10
Pulmonary and Respiratory Medicine
- Sarcoma Diagnosis and Treatment 4

Co-authors: Károly Szuhai Carla Rosenberg Hans J. Tanke Remco Dijkman Maarten H. Vermeer Cornelis P. Tensen Rein Willemze Remco van Doorn
Cited by: Dermatology Genetics Pathology and Forensic Medicine
Journals: European Journal of Human Genetics (4 papers)European Journal of Medical Genetics (4 papers)Cytogenetic and Genome Research (3 papers)
Partner nations: Netherlands Brazil United States

In The Last Decade

Jeroen Knijnenburg

47 papers receiving 1.4k citations

Peers

Countries citing papers authored by Jeroen Knijnenburg

Since Specialization

Citations

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

Fields of papers citing papers by Jeroen Knijnenburg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Jeroen Knijnenburg, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jeroen Knijnenburg Line = papers co-authored together Jeroen Knijnenburg links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Acquisition of a glycosylated B-cell receptor drives follicular lymphoma toward a dark zone phenotype Blood Advances ·Cornelis A.M. van Bergen,Susan L. Kloet,Edwin Quinten,Ung-Sik Jin,Roberta Menafra,Marieke Griffioen,Patty M. Jansen,Marvyn T. Koning,Jeroen Knijnenburg,Marcelo A. Navarrete,Szymon M. Kiełbasa,Hendrik Veelken	2023	3
2	Hearing loss, cleft palate, and congenital hip dysplasia in female carriers of an intragenic deletion of AMMECR1 American Journal of Medical Genetics Part A ·Saskia Koene,Jeroen Knijnenburg,Mariëtte J.V. Hoffer,Nurhussen Mossa Ahmed,Monique C. Haak,Heiko Locher,Min Jeung 김민정Kim,Gijs W.E. Santen,Liselotte J. C. Rotteveel	2022	2
3	Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance Human Molecular Genetics ·A. A. Vercheba,Marianne Bootsma,Chai‐Ann Ng,Arthur A.M. Wilde,MARIA ROSENDO BRANDÃO,Hennie Bikker,Imke Christiaans,Saskia N. van der Crabben,Janna A. Hol,Tamara T. Koopmann,Jeroen Knijnenburg,H. Srinivasan,Jasper J. van der Smagt,Connie R. Bezzina,Jamie I. Vandenberg,Arie O. Verkerk,Daniela Q.C.M. Barge‐Schaapveld,Elisabeth M. Lodder	2022	2
4	Intracerebral hemorrhage in a neonate with an intragenic COL4A2 duplication American Journal of Medical Genetics Part A ·Saskia Koene,Cacha Peeters‐Scholte,Jeroen Knijnenburg,Linda S. de Vries,P. N. Adama van Scheltema,Marije Meuwissen,Sylke J. Steggerda,Gijs W.E. Santen	2020	3
5	The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies Human Mutation ·Malgorzata I. Srebniak,Maarten F. C. M. Knapen,Marike Polak,Marieke Joosten,Karin E. M. Diderich,Lutgarde Govaerts,Marjan Boter,Liu Xiaotian,Michael Beadle,Randall Williams,Wilfred F. J. van IJcken,R. Heydanus,Anneke Dijkman,Xuyang Liao,Femke A.T. de Vries,Jeroen Knijnenburg,Attie T. J. I. Go,Robert‐Jan H. Galjaard,Diane Van Opstal	2017	18
6	A 600 kb triplication in the cat eye syndrome critical region causes anorectal, renal and preauricular anomalies in a three-generation family European Journal of Human Genetics ·Jeroen Knijnenburg,Yolande van Bever,Lorette O. M. Hulsman,N. Rejeb,JinHwa Oh,Rosa Laura E. van Loon,H. Berna Beverloo,Laura J. C. M. van Zutven	2012	33
7	Two distinct regions in 2q24.2‐q24.3 associated with idiopathic epilepsy Epilepsia ·Ana Cristina Victorino Krepischi,Jeroen Knijnenburg,Débora Romeo Bertola,Chong Ae Kim,P. Pearson,Emilia Bijlsma,Károly Szuhai,Fernando Kok,Angela Maria Vianna‐Morgante,Carla Rosenberg	2010	41
8	Split hand‐foot malformation, tetralogy of Fallot, mental retardation and a 1 Mb 19p deletion—evidence for further heterogeneity? American Journal of Medical Genetics Part A ·Emmelien Aten,Nicolette S. den Hollander,Claudia Ruivenkamp,Jeroen Knijnenburg,Hans van Bokhoven,Johan T. den Dunnen,Martijn H. Breuning	2009	17
9	Molecular characterization of two patients with de novo interstitial deletions in 4q22–q24 American Journal of Medical Genetics Part A ·Yvonne Hilhorst‐Hofstee,Zeynep Tümer,Peter Born,Jeroen Knijnenburg,Kerstin Hansson,和彦野崎,Shoichi Yamasita,Reinhard Ullmann,Ger J. A. Arkesteijn,Niels Tommerup,Lars Allan Larsen	2009	3
10	Novel gene rearrangements in transformed breast cells identified by high-resolution breakpoint analysis of chromosomal aberrations Endocrine Related Cancer ·Kristian Unger,Johannes Wienberg,Andrew Riches,Ludwig Hieber,Axel Walch,Jeanne Stierman,Patricia C. O’Brien,S Ben Abdallah,Dewi Rinanda,Elke Rodríguez,SpAn Calcarina Fitriani R.W.,Jeroen Knijnenburg,Giovanni Tallini,Malcolm Ferguson-Smith,Horst Zitzelsberger	2009	29
11	Novel and Highly Recurrent Chromosomal Alterations in Sezary Syndrome Cancer Research ·Maarten H. Vermeer,Remco van Doorn,Remco Dijkman,Xin Mao,Sean Whittaker,Pieter C. van Voorst Vader,Marie‐Jeanne P. Gerritsen,Marie‐Louise Geerts,Sylke Gellrich,Ola Söderberg,Karl‐Johan Leuchowius,Ulf Landegren,Jacoba J. Out‐Luiting,Jeroen Knijnenburg,Marije IJszenga,Károly Szuhai,Rein Willemze,Cornelis P. Tensen	2008	133
12	Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting Cytogenetic and Genome Research ·Sharan Goobie,Jeroen Knijnenburg,David Fitzpatrick,Freddie H. Sharkey,Anath C. Lionel,Christian R. Marshall,Jean M. Drulis,Mary Shago,Kelly K. Chong,Roberto Mendoza‐Londono,Nicolette S. den Hollander,Claudia Ruivenkamp,E.R. Maher,Hans J. Tanke,Károly Szuhai,Richard F. Wintle,Stephen W. Scherer	2008	30
13	Interstitial deletion of 6q without phenotypic effect American Journal of Medical Genetics Part A ·Kerstin Hansson,Károly Szuhai,Jeroen Knijnenburg,Arie van Haeringen,G. Cuccia	2007	11
14	The Role of EXT1 in Nonhereditary Osteochondroma: Identification of Homozygous Deletions JNCI Journal of the National Cancer Institute ·Liesbeth Hameetman,Károly Szuhai,Arzu Yavaş,Jeroen Knijnenburg,Mark van Duin,Herman van Dekken,A. H. M. Taminiau,A.M. Cleton-Jansen,Judith V.M.G. Bovée,Pancras C.W. Hogendoorn	2007	77
15	Diagnosis of genetic abnormalities in developmentally delayed patients: A new strategy combining MLPA and array‐CGH American Journal of Medical Genetics Part A ·Marjolein Kriek,Jeroen Knijnenburg,Stefan J. White,Carla Rosenberg,Johan T. den Dunnen,Gert‐Jan B. van Ommen,Hans J. Tanke,Martijn H. Breuning,Károly Szuhai	2007	19
16	Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion European Journal of Human Genetics ·Jeroen Knijnenburg,Arie van Haeringen,Kerstin Hansson,Arjan C. Lankester,Mochammad Triansyah Noor,Carissa Slone,Egbert Bakker,Carla Rosenberg,Hans J. Tanke,Károly Szuhai	2007	63
17	Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome American Journal of Medical Genetics Part A ·Juliana F. Mazzeu,Ana Cristina Victorino Krepischi,Carla Rosenberg,Károly Szuhai,Jeroen Knijnenburg,Viky Julieta Arias Delgado,Irina Kerkis,Zan Mustacchi,A M Karsznicka,APL Bento,Rita de Cássia M. Pavanello,Paulo Alberto Otto,Angela Maria Vianna‐Morgante	2007	8
18	Rapid detection of genomic imbalances using micro-arrays consisting of pooled BACs covering all human chromosome arms Nucleic Acids Research ·Jeroen Knijnenburg	2005	14
19	Multicolor fluorescence in situ hybridization analysis of a synovial sarcoma of the larynx with a t(X;18)(p11.2;q11.2) and trisomies 2 and 8 Cancer Genetics and Cytogenetics ·Károly Szuhai,Jeroen Knijnenburg,Marije IJszenga,Hans J. Tanke,Robert J. Baatenburg de Jong,Karla Miletić,Carla Rosenberg,Pancras C.W. Hogendoorn	2004	12
20	Insights from genomic microarrays into structural chromosome rearrangements American Journal of Medical Genetics Part A ·Jeroen Knijnenburg,Károly Szuhai,Jacques C. Giltay,Farid Amin Fuleihan,Willem C.R. Sloos,Martin Poot,Hans J. Tanke,Carla Rosenberg	2004	50

About Jeroen Knijnenburg

Jeroen Knijnenburg is a scholar working on Genetics, Developmental Biology, Dermatology, Sensory Systems and Pediatrics, Perinatology and Child Health, having authored 47 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (27 papers), Congenital heart defects research (10 papers), Chromosomal and Genetic Variations (10 papers), Prenatal Screening and Diagnostics (8 papers), Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Sarcoma Diagnosis and Treatment (4 papers) and Cutaneous lymphoproliferative disorders research (3 papers). The work is most often cited by research in Dermatology (277 citations), Genetics (578 citations), Pathology and Forensic Medicine (287 citations), Genetics (109 citations) and Pediatrics, Perinatology and Child Health (201 citations). Jeroen Knijnenburg has collaborated with scholars based in Netherlands, Brazil and United States. Frequent co-authors include Károly Szuhai, Carla Rosenberg, Hans J. Tanke, Remco Dijkman, Maarten H. Vermeer, Cornelis P. Tensen, Rein Willemze, Remco van Doorn, Aat A. Mulder and Ana Cristina Victorino Krepischi. Their work appears in journals such as European Journal of Human Genetics, European Journal of Medical Genetics, Cytogenetic and Genome Research, Human Genetics and Prenatal Diagnosis.

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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