Roel Hordijk

1.6k citations

22 papers · 739 indexed · h-index 15

Genetics top 5%
Molecular Biology
Pediatrics, Perinatology and Child Health top 10%
Plant Science
Surgery

Co-authors: 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
Topics: Genomic variations and chromosomal abnormalities (11 papers)Prenatal Screening and Diagnostics (6 papers)Genomics and Rare Diseases (3 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Reproductive Medicine
Journals: Nature Genetics Human Reproduction Cardiovascular Research
Partner nations: Netherlands Germany United Kingdom

In The Last Decade

Roel Hordijk

20 papers receiving 697 citations

Peers

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

#	Work	Indexed citations
1	A specific mutation in TBL1XR1 causes Pierpont syndrome 2016 ·Journal of Medical Genetics ·Charlotte A. Heinen,Aldo Jongejan,Peter J. Watson,B. Redeker,Anita Boelen,(unknown),Francesca Forzano,Roel Hordijk,Richard I. Kelley,Ann Haskins Olney,Mary Ella Pierpont,G. Bradley Schaefer,Fiona Stewart,A S Paul van Trotsenburg,Eric Fliers,John W. R. Schwabe,Raoul C. M. Hennekam	44
2	A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy 2013 ·European Journal of Human Genetics ·Arjan Pm de Brouwer,Sander B. Nabuurs,Ingrid E.C. Verhaart,Astrid Oudakker,Roel Hordijk,Helger G. Yntema,(unknown),Krysta Voesenek,(unknown),Ton van Essen,Wei Chen,Hao Hu,Jamel Chelly,Johan T. den Dunnen,Vera M. Kalscheuer,Annemieke Aartsma‐Rus,Ben C.J. Hamel,Hans van Bokhoven,Tjitske Kleefstra	29
3	Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis 2011 ·European Journal of Human Genetics ·Ilse Feenstra,(unknown),Birgit Sikkema‐Raddatz,Helger G. Yntema,Trijnie Dijkhuizen,Dorien Lugtenberg,Joanne Verheij,Andrew Green,Roel Hordijk,William Reardon,Bert de Vries,Han G. Brunner,Ernie M.H.F. Bongers,Nicole de Leeuw,Conny M.A. van Ravenswaaij‐Arts	41
4	Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome (vol 88, pg 130, 2010) 2011 ·Cardiovascular Research ·Cornelis J. Boogerd,Dennis Dooijes,Aho Ilgun,Inge B. Mathijssen,Roel Hordijk,Ingrid M.B.H. van de Laar,Patrick Rump,Hermine E. Veenstra‐Knol,Antoon F.M. Moorman,Phil Barnett,Alex V. Postma	0
5	Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnostics 2011 ·European Journal of Human Genetics ·(unknown),Birgit Sikkema‐Raddatz,Gerben van der Vries,Trijnie Dijkhuizen,Roel Hordijk,Anthonie J. van Essen,Hermine E. Veenstra‐Knol,Wilhelmina S. Kerstjens‐Frederikse,Johanna C. Herkert,Erica H. Gerkes,(unknown),Klaas Kok,Richard J. Sinke,Conny M.A. van Ravenswaaij‐Arts	52
6	A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome) 2010 ·Clinical Genetics ·Patrick Rump,(unknown),(unknown),O.F. Brouwer,(unknown),Roel Hordijk	24
7	Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome 2010 ·Cardiovascular Research ·Cornelis J. Boogerd,Dennis Dooijes,Aho Ilgun,Inge B. Mathijssen,Roel Hordijk,Ingrid M.B.H. van de Laar,(unknown),Hermine E. Veenstra‐Knol,Antoon F.M. Moorman,Phil Barnett,Alex V. Postma	34
8	Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion 2010 ·European Journal of Medical Genetics ·Erica H. Gerkes,Roel Hordijk,Trijnie Dijkhuizen,Deborah A. Sival,Linda C. Meiners,Birgit Sikkema‐Raddatz,Conny M.A. van Ravenswaaij‐Arts	11
9	A 649 kb microduplication in 1p34.1, including POMGNT1, in a patient with microcephaly, coloboma and laryngomalacia; and a review of the literature 2009 ·European Journal of Medical Genetics ·(unknown),Trijnie Dijkhuizen,M.L. Haadsma,(unknown),Maartje Boon,Roel Hordijk,Klaas Kok,Birgit Sikkema‐Raddatz,Conny M.A. van Ravenswaaij‐Arts	6
10	Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances 2009 ·European Journal of Medical Genetics ·(unknown),Birgit Sikkema‐Raddatz,(unknown),Trijnie Dijkhuizen,Emilia K. Bijlsma,Antoinet C.J. Gijsbers,Yvonne Hilhorst‐Hofstee,Roel Hordijk,K. T. Verbruggen,Wilhelmina S. Kerstjens‐Frederikse,Ton van Essen,Klaas Kok,(unknown),Martijn H. Breuning,Conny M.A. van Ravenswaaij‐Arts	116
11	Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH) 2007 ·Journal of Medical Genetics ·Nicole Maas,Griet Van Buggenhout,Femke Hannes,Bernard Thienpont,Damien Sanlaville,Klaas Kok,Alina T. Midro,Joris Andrieux,(unknown),Jacqueline Schoumans,Roel Hordijk,Koenraad Devriendt,JP Fryns,Joris Vermeesch	99
12	Plantar lipomatosis, unusual facies, and developmental delay: Confirmation of Pierpont syndrome 2005 ·American Journal of Medical Genetics Part A ·(unknown),Roel Hordijk,Maartje Boon,Paul E. Sijens,Raoul C. M. Hennekam	16
13	Pigmentary mosaicism following the lines of Blaschko in a girl with a double aneuploidy mosaicism: (47,XX,+7/45,X) 2005 ·American Journal of Medical Genetics Part A ·Renée C. Niessen,Marcel F. Jonkman,(unknown),Roel Hordijk,Anthonie J. van Essen	26
14	Two unbalanced segregation products due to a maternal t(7;16)inv(16) 2001 ·Prenatal Diagnosis ·Beike Leegte,Birgit Sikkema‐Raddatz,Roel Hordijk,(unknown),Anneke van Veen,Jan-Maarten Cobben	0
15	Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience 1998 ·European Journal of Human Genetics ·(unknown),(unknown),A.J.H. Hamers,Roel Hordijk,(unknown),Kerstin Hansson,(unknown),K. Madan,(unknown),(unknown),J.A.M. Kremer,D F Smeets	82
16	Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy 1998 ·Nature Genetics ·Stephan Rust,Michael Walter,Harald Funke,Arnold von Eckardstein,Paul Cullen,Hester Y. Kroes,Roel Hordijk,Jürgen Geisel,J. Kastelein,Henri O.F. Molhuizen,(unknown),(unknown),Harry Hahmann,Gerd Assmann	49
17	Three cases of mosaicism for balanced reciprocal translocations 1998 ·American Journal of Medical Genetics ·Beike Leegte,Birgit Sikkema‐Raddatz,Roel Hordijk,Katelijne Bouman,Ton van Essen,Sérgio Castedo,Bauke M. de Jong	10
18	Chorioretinal dysplasia-microcephaly-mental retardation syndrome: another family with autosomal dominant inheritance. 1996 ·PubMed ·Roel Hordijk,(unknown),(unknown),(unknown)	9
19	Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32). 1994 ·Journal of Medical Genetics ·(unknown),J.H.A.M. Tuerlings,Roel Hordijk,(unknown),Leo P. ten Kate	21
20	[Late diagnosis of classical galactosemia. An adult with special biochemistry]. 1993 ·PubMed ·(unknown),Roel Hordijk,(unknown),(unknown),Dirk‐Jan Reijngoud,R. Berger	1

About Roel Hordijk

Roel Hordijk is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Biochemistry, having authored 22 papers that have together received 739 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (6 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (520 citations), Pediatrics, Perinatology and Child Health (184 citations) and Reproductive Medicine (62 citations). Roel Hordijk has collaborated with scholars based in Netherlands, Germany and United Kingdom. Frequent 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. Their work appears in journals such as Nature Genetics, Human Reproduction and Cardiovascular Research.

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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