Roel Hordijk

1.6k total citations
22 papers, 739 citations indexed

About

Roel Hordijk is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Roel Hordijk has authored 22 papers receiving a total of 739 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 7 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Roel Hordijk's work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (6 papers) and Genomics and Rare Diseases (3 papers). Roel Hordijk is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (6 papers) and Genomics and Rare Diseases (3 papers). Roel Hordijk collaborates with scholars based in Netherlands, Germany and United Kingdom. Roel Hordijk's co-authors include Klaas Kok, Birgit Sikkema‐Raddatz, Conny M.A. van Ravenswaaij‐Arts, Trijnie Dijkhuizen, Ton van Essen, Wilhelmina S. Kerstjens‐Frederikse, Beike Leegte, Anthonie J. van Essen, Hans Scheffer and Kerstin Hansson and has published in prestigious journals such as Nature Genetics, Human Reproduction and Cardiovascular Research.

In The Last Decade

Roel Hordijk

20 papers receiving 697 citations

Peers

Roel Hordijk

GENET

PPCH

SURGE

Michela Barbaro Sweden

Cathy M. Tuck‐Müller United States

Ewa Bocian Poland

Simona Cavani Italy

Fortunato Lonardo Italy

R. Williamson United Kingdom

Sophie Brisset France

Hiba Risheg United States

Julien Thévenon France

Nathalie Collot France

Michela Barbaro Sweden

Roel Hordijk

596 ×1.1

GENET

885 ×2.2

139 ×0.8

PPCH

50 ×0.5

52 ×0.7

SURGE

Citations per year, relative to Roel Hordijk Roel Hordijk (= 1×) peers Michela Barbaro

Countries citing papers authored by Roel Hordijk

Since Specialization

Citations

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

Fields of papers citing papers by Roel Hordijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roel Hordijk

This figure shows the co-authorship network connecting the top 25 collaborators of Roel Hordijk. A scholar is included among the top collaborators of Roel Hordijk 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 Roel Hordijk. Roel Hordijk 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

Heinen, Charlotte A., Aldo Jongejan, Peter J. Watson, et al.. (2016). A specific mutation in TBL1XR1 causes Pierpont syndrome. Journal of Medical Genetics. 53(5). 330–337. 44 indexed citations

Brouwer, Arjan Pm de, Sander B. Nabuurs, Ingrid E.C. Verhaart, et al.. (2013). A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy. European Journal of Human Genetics. 22(4). 480–485. 29 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

Boogerd, Cornelis J., Dennis Dooijes, Aho Ilgun, et al.. (2011). Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome (vol 88, pg 130, 2010). Cardiovascular Research. 89(1).

Sikkema‐Raddatz, Birgit, Gerben van der Vries, Trijnie Dijkhuizen, et al.. (2011). Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnostics. European Journal of Human Genetics. 20(2). 161–165. 52 indexed citations

Rump, Patrick, et al.. (2010). A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome). Clinical Genetics. 79(2). 183–188. 24 indexed citations

Boogerd, Cornelis J., Dennis Dooijes, Aho Ilgun, et al.. (2010). Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome. Cardiovascular Research. 88(1). 130–139. 34 indexed citations

Gerkes, Erica H., Roel Hordijk, Trijnie Dijkhuizen, et al.. (2010). Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion. European Journal of Medical Genetics. 53(5). 344–346. 11 indexed citations

Dijkhuizen, Trijnie, M.L. Haadsma, Maartje Boon, et al.. (2009). A 649 kb microduplication in 1p34.1, including POMGNT1, in a patient with microcephaly, coloboma and laryngomalacia; and a review of the literature. European Journal of Medical Genetics. 52(2-3). 116–119. 6 indexed citations

10.

Sikkema‐Raddatz, Birgit, Trijnie Dijkhuizen, Emilia K. Bijlsma, et al.. (2009). Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances. European Journal of Medical Genetics. 52(2-3). 108–115. 116 indexed citations

11.

Maas, Nicole, Griet Van Buggenhout, Femke Hannes, et al.. (2007). Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH). Journal of Medical Genetics. 45(2). 71–80. 99 indexed citations

12.

Hordijk, Roel, et al.. (2005). Plantar lipomatosis, unusual facies, and developmental delay: Confirmation of Pierpont syndrome. American Journal of Medical Genetics Part A. 137A(1). 77–80. 16 indexed citations

13.

Niessen, Renée C., et al.. (2005). Pigmentary mosaicism following the lines of Blaschko in a girl with a double aneuploidy mosaicism: (47,XX,+7/45,X). American Journal of Medical Genetics Part A. 137A(3). 313–322. 26 indexed citations

14.

Leegte, Beike, et al.. (2001). Two unbalanced segregation products due to a maternal t(7;16)inv(16). Prenatal Diagnosis. 21(7). 550–552.

15.

Hamers, A.J.H., Roel Hordijk, Kerstin Hansson, et al.. (1998). Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience. European Journal of Human Genetics. 6(3). 194–200. 82 indexed citations

16.

Rust, Stephan, Michael Walter, Harald Funke, et al.. (1998). Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy. Nature Genetics. 20(1). 96–98. 49 indexed citations

17.

Leegte, Beike, Birgit Sikkema‐Raddatz, Roel Hordijk, et al.. (1998). Three cases of mosaicism for balanced reciprocal translocations. American Journal of Medical Genetics. 79(5). 362–365. 10 indexed citations

18.

Hordijk, Roel, et al.. (1996). Chorioretinal dysplasia-microcephaly-mental retardation syndrome: another family with autosomal dominant inheritance.. PubMed. 7(2). 113–22. 9 indexed citations

19.

Tuerlings, J.H.A.M., et al.. (1994). Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32).. Journal of Medical Genetics. 31(2). 156–158. 21 indexed citations

20.

Hordijk, Roel, et al.. (1993). [Late diagnosis of classical galactosemia. An adult with special biochemistry].. PubMed. 61(5). 188–90. 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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