Trijnie Dijkhuizen

2.6k citations

62 papers · 1.6k indexed · h-index 24

Molecular Biology top 10%
Genetics top 5%
Pulmonary and Respiratory Medicine top 10%
Cancer Research top 10%
Pediatrics, Perinatology and Child Health top 5%

Co-authors: Conny M.A. van Ravenswaaij‐Arts Bauke M. de Jong Anke van den Berg Birgit Sikkema‐Raddatz Stephan Störkel Klaas Kok Eva van den Berg J. Wolter Oosterhuis
Topics: Genomic variations and chromosomal abnormalities (22 papers)Congenital heart defects research (11 papers)Renal cell carcinoma treatment (10 papers)
Cited by: Genetics Cancer Research Developmental Biology
Journals: Journal of Biological Chemistry International Journal of Cancer Human Reproduction
Partner nations: Netherlands Germany United Kingdom

In The Last Decade

Trijnie Dijkhuizen

60 papers receiving 1.5k citations

Peers

Countries citing papers authored by Trijnie Dijkhuizen

Since Specialization

Citations

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

Fields of papers citing papers by Trijnie Dijkhuizen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Trijnie Dijkhuizen

This figure shows the co-authorship network connecting the top 25 collaborators of Trijnie Dijkhuizen. A scholar is included among the top collaborators of Trijnie Dijkhuizen 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 Trijnie Dijkhuizen. Trijnie Dijkhuizen 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	Contiguous Gene Deletion of Chromosome 15q25.2q25.3 in Biallelic ALPK3 -Related Cardiomyopathy: Novel Insights Into Phenotypic Presentation and Variant Spectrum 2023 ·Circulation Genomic and Precision Medicine ·(unknown),Jolien S. Klein Wassink‐Ruiter,Trijnie Dijkhuizen,(unknown),Jan D.H. Jongbloed,Johanna C. Herkert	1
2	Novel GAA Variants and Mosaicism in Pompe Disease Identified by Extended Analyses of Patients with an Incomplete DNA Diagnosis 2020 ·Molecular Therapy — Methods & Clinical Development ·Stijn L.M. in ‘t Groen,(unknown),(unknown),Johanna M. P. van den Hout,Hannie Douben,Trijnie Dijkhuizen,David Cassiman,Peter Witters,(unknown),Annelies de Klein,(unknown),Jasper J. Saris,Lies H. Hoefsloot,Ans T. van der Ploeg,Atze J. Bergsma,W.W.M. Pim Pijnappel	13
3	Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays 2019 ·European Journal of Human Genetics ·(unknown),(unknown),(unknown),Marianne Hoogeveen‐Westerveld,Marian A. Kroos,Sirpa Ala‐Mello,Olga Amaral,Clara Sá-Miranda,Irene Mavridou,Helen Michelakakis,K Naess,Frans W. Verheijen,Lies H. Hoefsloot,Trijnie Dijkhuizen,(unknown),(unknown),Ans T. van der Ploeg,W.W.M. Pim Pijnappel,Jasper J. Saris,Dicky Halley	8
4	The phenotypic spectrum of proximal 6q deletions based on a large cohort derived from social media and literature reports 2018 ·European Journal of Human Genetics ·(unknown),(unknown),A. Lya den Ouden,Boudien Flapper,Morris A. Swertz,Erica H. Gerkes,Mirjam Plantinga,Trijnie Dijkhuizen,Conny M.A. van Ravenswaaij‐Arts	28
5	Identification of prognostic relevant chromosomal abnormalities in chronic lymphocytic leukemia using microarray-based genomic profiling 2014 ·Molecular Cytogenetics ·Marian Stevens‐Kroef,Eva van den Berg,Daniël Olde Weghuis,Ad Geurts van Kessel,Rolph Pfundt,(unknown),(unknown),Trijnie Dijkhuizen,Patricia J.T.A. Groenen,Annet Simons	17
6	Central 22q11.2 deletions 2014 ·American Journal of Medical Genetics Part A ·Patrick Rump,Nicole de Leeuw,Anthonie J. van Essen,Corien C. Verschuuren‐Bemelmans,Hermine E. Veenstra‐Knol,Mariëlle E.M. Swinkels,Wilma Oostdijk,Claudia Ruivenkamp,William Reardon,Sonja de Munnik,(unknown),Ayala Frumkin,Dorit Lev,Christina Evers,Birgit Sikkema‐Raddatz,Trijnie Dijkhuizen,Conny M.A. van Ravenswaaij‐Arts	43
7	Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of <b><i>OTX2</i></b> 2013 ·Molecular Syndromology ·(unknown),Conny M.A. van Ravenswaaij‐Arts,Julia Tantau,Nicole Corsten‐Janssen,J. Peter van Tintelen,Trijnie Dijkhuizen,Josseline Kaplan,Nicolas Chassaing	27
8	Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome 2009 ·Genes Chromosomes and Cancer ·Renée C. Niessen,Robert M.W. Hofstra,Helga Westers,Marjolijn J. L. Ligtenberg,Krista Kooi,(unknown),(unknown),Trijnie Dijkhuizen,Maran J.W. Olderode-Berends,Harry Hollema,Jan H. Kleibeuker,Rolf H. Sijmons	139
9	Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation 2005 ·European Journal of Medical Genetics ·Klaas Kok,Trijnie Dijkhuizen,(unknown),(unknown),Pieter van der Vlies,Rudolf S.N. Fehrmann,Gerard J. te Meerman,Klasien B.J. Gerssen‐Schoorl,Ton van Essen,Birgit Sikkema‐Raddatz,Charles H.C.M. Buys	26
10	Structural and Functional Genomics of the CPT1B Gene for Muscle-type Carnitine Palmitoyltransferase I in Mammals 2002 ·Journal of Biological Chemistry ·Feike R. van der Leij,(unknown),Vicky N. Jackson,Nicolette Huijkman,Beatrijs Bartelds,Jaap R. G. Kuipers,Trijnie Dijkhuizen,P. Terpstra,Philip A. Wood,Victor A. Zammit,Nigel T. Price	42
11	Genetics as a diagnostic tool in sarcomatoid renal-cell cancer 1997 ·International Journal of Cancer ·Trijnie Dijkhuizen,Eva van den Berg,Anke van den Berg,(unknown),Anke Dam,(unknown),Charles H.C.M. Buys,Stephan Störkel,Bauke M. de Jong	18
12	Involvement of the chromosomal region 11q13 in renal oncocytoma: Case report and literature review 1997 ·Cancer Genetics and Cytogenetics ·Christine Neuhaus,Trijnie Dijkhuizen,Anke van den Berg,Stephan Störkel,Michael Stöckle,(unknown),Christoph Huber,(unknown)	32
13	Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation 1996 ·Human Genetics ·Marian A. J. Weterman,M. Wilbrink,Trijnie Dijkhuizen,Anke van den Berg,Ad Geurts van Kessel	26
14	Cytogenetic analysis of a case of myxoid liposarcoma with cartilaginous differentiation 1996 ·Cancer Genetics and Cytogenetics ·Trijnie Dijkhuizen,Willemina M. Molenaar,H.J. Hoekstra,Janneke Wiersema,Anke van den Berg	14
15	Intracranial teratoma with multiple fetuses: Pre- and post-natal appearance 1995 ·Human Pathology ·(unknown),Christl Vermeij‐Keers,(unknown),(unknown),Klasien B.J. Gerssen‐Schoorl,Trijnie Dijkhuizen	15
16	Carcinoid in a horseshoe kidney 1995 ·Cancer Genetics and Cytogenetics ·Anke van den Berg,Annette Gouw,J. Wolter Oosterhuis,Stephan Störkel,Trijnie Dijkhuizen,H.J.A. Mensink,Bauke M. de Jong	25
17	Rearrangements involving 12p12 in two cases of cardiac myxoma 1995 ·Cancer Genetics and Cytogenetics ·Trijnie Dijkhuizen,Eva van den Berg,Willemina M. Molenaar,J. J. Meuzelaar,Bauke M. de Jong	12
18	Tumor progression in a giant cell type malignant fibrous histiocytoma of bone: Clinical, radiologic, histologic, and cytogenetic evidence 1994 ·Genes Chromosomes and Cancer ·Willemina M. Molenaar,Eva van den Berg,R.P.H. Veth,Trijnie Dijkhuizen,Elisabeth G.E. de Vries	8
19	Cytogenetics of a case of cardiac myxoma 1992 ·Cancer Genetics and Cytogenetics ·Trijnie Dijkhuizen,Eva van den Berg,Willemina M. Molenaar,J. J. Meuzelaar,Bauke M. de Jong	19
20	CYTOGENETIC CLASSIFICATION OF RENAL-CELL CARCINOMAS 1991 ·Data Archiving and Networked Services (DANS) ·(unknown),(unknown),Bauke M. de Jong,Trijnie Dijkhuizen,Janneke Wiersema,(unknown),Anke Dam	2

About Trijnie Dijkhuizen

Trijnie Dijkhuizen is a scholar working on Genetics, Developmental Biology and Cancer Research, having authored 62 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Congenital heart defects research (11 papers) and Renal cell carcinoma treatment (10 papers). The work is most often cited by research in Genetics (677 citations), Cancer Research (306 citations) and Developmental Biology (27 citations). Trijnie Dijkhuizen has collaborated with scholars based in Netherlands, Germany and United Kingdom. Frequent co-authors include Conny M.A. van Ravenswaaij‐Arts, Bauke M. de Jong, Anke van den Berg, Birgit Sikkema‐Raddatz, Stephan Störkel, Klaas Kok, Eva van den Berg, J. Wolter Oosterhuis, Willemina M. Molenaar and Joanne Verheij. Their work appears in journals such as Journal of Biological Chemistry, International Journal of Cancer and Human Reproduction.

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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