Trijnie Dijkhuizen

2.6k total citations
62 papers, 1.6k citations indexed

About

Trijnie Dijkhuizen is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Trijnie Dijkhuizen has authored 62 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 28 papers in Genetics and 18 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Trijnie Dijkhuizen's work include Genomic variations and chromosomal abnormalities (22 papers), Congenital heart defects research (11 papers) and Renal cell carcinoma treatment (10 papers). Trijnie Dijkhuizen is often cited by papers focused on Genomic variations and chromosomal abnormalities (22 papers), Congenital heart defects research (11 papers) and Renal cell carcinoma treatment (10 papers). Trijnie Dijkhuizen collaborates with scholars based in Netherlands, Germany and United Kingdom. Trijnie Dijkhuizen's 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 and has published in prestigious journals such as Journal of Biological Chemistry, International Journal of Cancer and Human Reproduction.

In The Last Decade

Trijnie Dijkhuizen

60 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Trijnie Dijkhuizen Netherlands	24	801	677	382	306	201	62	1.6k
Hermann‐Josef Lüdecke Germany	19	937 1.2×	864 1.3×	255 0.7×	149 0.5×	117 0.6×	39	1.8k
Luitgard M. Neumann Germany	20	708 0.9×	1.0k 1.5×	208 0.5×	170 0.6×	110 0.5×	46	1.7k
David J. Bunyan United Kingdom	23	991 1.2×	979 1.4×	153 0.4×	139 0.5×	113 0.6×	60	2.0k
Paolo Simi Italy	22	633 0.8×	571 0.8×	201 0.5×	73 0.2×	138 0.7×	82	1.4k
Jeroen Knijnenburg Netherlands	22	473 0.6×	578 0.9×	151 0.4×	111 0.4×	201 1.0×	47	1.4k
Lesley C. Adès Australia	23	915 1.1×	1.3k 1.9×	396 1.0×	184 0.6×	240 1.2×	58	2.2k
Shirley Soukup United States	23	774 1.0×	556 0.8×	366 1.0×	197 0.6×	304 1.5×	66	1.7k
Daniel Pineda‐Alvarez United States	21	921 1.1×	1.3k 1.9×	220 0.6×	219 0.7×	503 2.5×	45	2.2k
Elisabeth Flori France	20	1.0k 1.3×	920 1.4×	178 0.5×	85 0.3×	344 1.7×	44	1.9k
Heinz‐Ulrich G. Weier United States	17	712 0.9×	507 0.7×	155 0.4×	125 0.4×	153 0.8×	47	1.3k

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

Wassink‐Ruiter, Jolien S. Klein, et al.. (2023). Contiguous Gene Deletion of Chromosome 15q25.2q25.3 in Biallelic ALPK3 -Related Cardiomyopathy: Novel Insights Into Phenotypic Presentation and Variant Spectrum. Circulation Genomic and Precision Medicine. 16(5). 493–495. 1 indexed citations

Groen, Stijn L.M. in ‘t, Johanna M. P. van den Hout, Hannie Douben, et al.. (2020). Novel GAA Variants and Mosaicism in Pompe Disease Identified by Extended Analyses of Patients with an Incomplete DNA Diagnosis. Molecular Therapy — Methods & Clinical Development. 17. 337–348. 13 indexed citations

Hoogeveen‐Westerveld, Marianne, Marian A. Kroos, Sirpa Ala‐Mello, et al.. (2019). Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays. European Journal of Human Genetics. 27(6). 919–927. 8 indexed citations

Johansson, Lennart, Mirjam Plantinga, Angela Fenwick, et al.. (2019). Reinterpretation, reclassification, and its downstream effects: challenges for clinical laboratory geneticists. BMC Medical Genomics. 12(1). 170–170. 35 indexed citations

Stevens‐Kroef, Marian, Eva van den Berg, Daniël Olde Weghuis, et al.. (2014). Identification of prognostic relevant chromosomal abnormalities in chronic lymphocytic leukemia using microarray-based genomic profiling. Molecular Cytogenetics. 7(1). 3–3. 17 indexed citations

Ravenswaaij‐Arts, Conny M.A. van, Julia Tantau, Nicole Corsten‐Janssen, et al.. (2013). Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of <b><i>OTX2</i></b>. Molecular Syndromology. 4(6). 302–305. 27 indexed citations

Leeuw, Nicole de, Trijnie Dijkhuizen, Jayne Y. Hehir‐Kwa, et al.. (2012). Diagnostic interpretation of array data using public databases and internet sources. Human Mutation. 33(6). 930–940. 83 indexed citations

Feenstra, Ilse, Birgit Sikkema‐Raddatz, Helger G. Yntema, et al.. (2011). Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis. European Journal of Human Genetics. 19(11). 1152–1160. 41 indexed citations

Akker, Peter C. van den, Trijnie Dijkhuizen, Joanne Verheij, et al.. (2009). Split hand/foot malformation due to chromosome 7q aberrations(SHFM1): additional support for functional haploinsufficiency as the causative mechanism. European Journal of Human Genetics. 17(11). 1432–1438. 41 indexed citations

10.

Zwaag, Paul A. van der, Trijnie Dijkhuizen, Klasien B.J. Gerssen‐Schoorl, et al.. (2009). An interstitial duplication of chromosome 13q31.3q32.1 further delineates the critical region for postaxial polydactyly type A2. European Journal of Medical Genetics. 53(1). 45–49. 18 indexed citations

11.

Raas‐Rothschild, Annick, et al.. (2009). The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: Report on two patients and review of the literature. European Journal of Medical Genetics. 52(2-3). 140–144. 14 indexed citations

12.

Kok, Klaas, Trijnie Dijkhuizen, Pieter van der Vlies, et al.. (2005). Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation. European Journal of Medical Genetics. 48(3). 250–262. 26 indexed citations

13.

Westra, Jantine L., Ludolf G. Boven, Pieter van der Vlies, et al.. (2005). A substantial proportion of microsatellite‐unstable colon tumors carry TP53 mutations while not showing chromosomal instability. Genes Chromosomes and Cancer. 43(2). 194–201. 5 indexed citations

14.

Leij, Feike R. van der, Vicky N. Jackson, Nicolette Huijkman, et al.. (2002). Structural and Functional Genomics of the CPT1B Gene for Muscle-type Carnitine Palmitoyltransferase I in Mammals. Journal of Biological Chemistry. 277(30). 26994–27005. 42 indexed citations

15.

Berg, Anke van den & Trijnie Dijkhuizen. (1999). Classification of Renal Cell Cancer Based on (Cyto)genetic Analysis. Contributions to nephrology. 128. 51–61. 13 indexed citations

16.

Weterman, Marian A. J., M. Wilbrink, Trijnie Dijkhuizen, Anke van den Berg, & Ad Geurts van Kessel. (1996). Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation. Human Genetics. 98(1). 16–21. 26 indexed citations

17.

Vermeij‐Keers, Christl, et al.. (1995). Intracranial teratoma with multiple fetuses: Pre- and post-natal appearance. Human Pathology. 26(7). 804–807. 15 indexed citations

18.

Berg, Anke van den, Annette Gouw, J. Wolter Oosterhuis, et al.. (1995). Carcinoid in a horseshoe kidney. Cancer Genetics and Cytogenetics. 84(2). 95–98. 25 indexed citations

19.

Berg, Anke van den, Trijnie Dijkhuizen, Stephan Störkel, et al.. (1995). Chromosomal changes in renal oncocytomas Evidence that t(5;11)(q35;q13) may characterize a second subgroup of oncocytomas. Cancer Genetics and Cytogenetics. 79(2). 164–168. 54 indexed citations

20.

Jong, Bauke M. de, et al.. (1991). CYTOGENETIC CLASSIFICATION OF RENAL-CELL CARCINOMAS. Data Archiving and Networked Services (DANS). 2 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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