Inge B. Mathijssen

1.5k citations

30 papers · 740 · h-index 17

Impact in

Pediatrics, Perinatology and Child Health top 10%
- Prenatal Screening and Diagnostics
Genetics top 10%
- Genomic variations and chromosomal abnormalities

Papers in

Molecular Biology 13
- RNA modifications and cancer 4
- Congenital heart defects research 4
Pediatrics, Perinatology and Child Health 8
- Prenatal Screening and Diagnostics 7

Co-authors: Eva Pajkrt (6 shared papers)Alex V. Postma (4 shared papers)Phil Barnett (3 shared papers)Aho Ilgun (3 shared papers)Lidewij Henneman (6 shared papers)Phillis Lakeman (5 shared papers)Jan Lam (2 shared papers)Vincent M. Christoffels (1 shared paper)
Journals: European Journal of Human Genetics (7 papers)Prenatal Diagnosis (4 papers)Cardiovascular Research (2 papers)European Journal of Medical Genetics (2 papers)Circulation Research (1 paper)
Partner nations: Netherlands United Kingdom United States

In The Last Decade

Inge B. Mathijssen

27 papers receiving 716 citations

Peers

Countries citing papers authored by Inge B. Mathijssen

Since Specialization

Citations

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

Fields of papers citing papers by Inge B. Mathijssen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Inge B. Mathijssen. 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 Inge B. Mathijssen. The network helps show where Inge B. Mathijssen may publish in the future.

Co-authors

The 25 scholars most cited alongside Inge B. Mathijssen, 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 Inge B. Mathijssen Line = papers co-authored together Inge B. Mathijssen links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation Circulation Research ·Alex V. Postma, Judith B.A. van de Meerakker, Inge B. Mathijssen, Phil Barnett, Vincent M. Christoffels, Aho Ilgun, Jan Lam, Arthur A.M. Wilde, Ronald H. Lekanne Deprez, Antoon F.M. Moorman	2008	123
2	Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings European Journal of Human Genetics ·Ellen A. Croonen, Willy M. Nillesen, Kyra E. Stuurman, Grétel Oudesluijs, Ingrid M B M van de Laar, Liesbeth Martens, Charlotte W. Ockeloen, Inge B. Mathijssen, Marga Schepens, Martina Ruiterkamp‐Versteeg, Hans Scheffer, Brigitte H. W. Faas, Ineke van der Burgt, Helger G. Yntema	2013	93
3	Genotype-Phenotype Correlation in Patients Suspected of Having Sotos Syndrome Hormone Research in Paediatrics ·Lonneke de Boer, Sarina G. Kant, Marcel Karperien, Lotte van Beers, Jennifer M.L. Tjon, Geraldine R. Vink, Dewy van Tol, Hans G. Dauwerse, Saskia le Cessie, Frits A. Beemer, Ineke van der Burgt, Ben C.J. Hamel, Raoul C. M. Hennekam, Ursula Kuhnle, Inge B. Mathijssen, Hermine E. Veenstra‐Knol, Connie T. Schrander Stumpel, Martijn H. Breuning, Jan M. Wit	2004	43
4	Structural heart defects associated with an increased nuchal translucency: 9 years experience in a referral centre Prenatal Diagnosis ·Sally‐Ann B. Clur, Inge B. Mathijssen, Eva Pajkrt, Andrew C. Cook, Ricardo Laurini, Jaap Ottenkamp, C. M. Bilardo	2008	42
5	LONG-TERM FOLLOW-UP OF PATIENTS WITH RETINITIS PIGMENTOSA TYPE 12 CAUSED BY CRB1 MUTATIONS Retina ·Inge B. Mathijssen, Ralph J. Florijn, L. Ingeborgh van den Born, Renate C. Zekveld-Vroon, Jacoline B. ten Brink, Astrid S. Plomp, Frank Baas, Hanne Meijers‐Heijboer, Arthur A. Bergen, Mary J. van Schooneveld	2016	38
6	Targeted ultrasound examination and DNA testing for Noonan syndrome, in fetuses with increased nuchal translucency and normal karyotype Prenatal Diagnosis ·Marian K. Bakker, Eva Pajkrt, Inge B. Mathijssen, Caterina M. Bilardo	2011	37
7	Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome 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	2010	34
8	Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis European Journal of Human Genetics ·Tessa van Dijk, Sacha Ferdinandusse, Jos P.N. Ruiter, Mariëlle Alders, Inge B. Mathijssen, Jillian S. Parboosingh, A. Micheil Innes, Hanne Meijers-Heijboer, Bwee Tien Poll‐The, François P. Bernier, Ronald J. A. Wanders, Ryan E. Lamont, Frank Baas	2018	31
9	Characteristics and Outcome and the Omphalocele Circumference/Abdominal Circumference Ratio in Prenatally Diagnosed Fetal Omphalocele Fetal Diagnosis and Therapy ·C. Emily Kleinrouweler, Caroline F. Kuijper, M. M. van Zalen‐Sprock, Inge B. Mathijssen, C. M. Bilardo, Eva Pajkrt	2011	30
10	Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence European Journal of Human Genetics ·Maria B. Tan-Sindhunata, Inge B. Mathijssen, Margriet Smit, Frank Baas, Johanna I. de Vries, J. Patrick van der Voorn, Irma Kluijt, Marleen A. Hagen, Eveline W Blom, Erik A. Sistermans, Hanne Meijers‐Heijboer, Quinten Waisfisz, Marjan M. Weiss, Alexander J. Groffen	2014	29
11	Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes Human Reproduction ·Margot J. Wyrwoll, Eva S. van Walree, Geert Hamer, Nadja Rotte, M. Mahdi Motazacker, Hanne Meijers-Heijboer, Mariëlle Alders, Andreas Meißner, Elke Kaminsky, Marius Wöste, Claudia Krallmann, Sabine Kliesch, T. Hunt, Amander T. Clark, Sherman J. Silber, Birgit Stallmeyer, Corinna Friedrich, Ans M. M. van Pelt, Inge B. Mathijssen, Frank Tüttelmann	2021	29
12	Factors for successful implementation of population-based expanded carrier screening: learning from existing initiatives: Table 1 European Journal of Public Health ·Kim C. A. Holtkamp, Inge B. Mathijssen, Phillis Lakeman, Merel C. van Maarle, Wybo Dondorp, Lidewij Henneman, Martina C. Cornel	2016	25
13	Audit of 10 years of referrals for fetal echocardiography Prenatal Diagnosis ·S. A. Clur, Peter M. van Brussel, Inge B. Mathijssen, Eva Pajkrt, Jaap Ottenkamp, C. M. Bilardo	2011	24
14	Targeted carrier screening for four recessive disorders: High detection rate within a founder population European Journal of Medical Genetics ·Inge B. Mathijssen, Lidewij Henneman, Janneke M. C. van Eeten-Nijman, Phillis Lakeman, Cecile P. E. Ottenheim, E. Redeker, Winnie Ottenhof, Hanne Meijers‐Heijboer, Merel C. van Maarle	2015	23
15	Preconception carrier screening for multiple disorders: evaluation of a screening offer in a Dutch founder population European Journal of Human Genetics ·Inge B. Mathijssen, Kim C. A. Holtkamp, Cecile P. E. Ottenheim, Janneke M. C. van Eeten-Nijman, Phillis Lakeman, Hanne Meijers‐Heijboer, Merel C. van Maarle, Lidewij Henneman	2018	22
16	Couples’ experiences with expanded carrier screening: evaluation of a university hospital screening offer European Journal of Human Genetics ·Ivy van Dijke, Phillis Lakeman, Naoual Sabiri, Hanna Rusticus, Cecile P. E. Ottenheim, Inge B. Mathijssen, Martina C. Cornel, Lidewij Henneman	2021	19
17	Noninvasive prenatal diagnosis of Huntington disease: detection of the paternally inherited expanded CAG repeat in maternal plasma Prenatal Diagnosis ·Jessica M.E. van den Oever, Emilia K. Bijlsma, Ilse Feenstra, N. D. Muntjewerff, Inge B. Mathijssen, Egbert Bakker, Martine J. van Belzen, Elles M. J. Boon	2015	18
18	Testicular cancer in a patient with Primrose syndrome European Journal of Medical Genetics ·Inge B. Mathijssen, Jos van Hasselt-van der Velde, Raoul C. M. Hennekam	2005	13
19	Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: A recognizable syndrome American Journal of Medical Genetics Part A ·Inge B. Mathijssen, J.M.N. Hoovers, Adri N. Mul, Hai‐Yen Man, Jan Lucas Ket, Raoul C. M. Hennekam	2005	11
20	TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes SHILAP Revista de lepidopterología ·Julie C. Van De Weghe, Jessica L. Giordano, Inge B. Mathijssen, Majid Mojarrad, Dorien Lugtenberg, Caitlin V. Miller, Jennifer C. Dempsey, Mahsa Sadat Asl Mohajeri, Elisabeth van Leeuwen, Eva Pajkrt, Caroline C. W. Klaver, Henry Houlden, Atieh Eslahi, Aoife Waters, Michael J. Bamshad, Deborah A. Nickerson, Vimla S. Aggarwal, Bert B.A. de Vries, Reza Maroofian, Dan Doherty	2020	10

About Inge B. Mathijssen

Inge B. Mathijssen is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics, Epidemiology and Surgery, having authored 30 papers that have together received 740 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (7 papers), Congenital Heart Disease Studies (6 papers), Cystic Fibrosis Research Advances (4 papers), RNA modifications and cancer (4 papers), Congenital heart defects research (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (173 citations), Genetics (192 citations), Molecular Biology (379 citations), Urology (28 citations) and Cardiology and Cardiovascular Medicine (84 citations). Inge B. Mathijssen has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Eva Pajkrt, Alex V. Postma, Phil Barnett, Aho Ilgun, Lidewij Henneman, Phillis Lakeman, Jan Lam, Vincent M. Christoffels, Antoon F.M. Moorman and Ronald H. Lekanne Deprez. Their work appears in journals such as European Journal of Human Genetics, Prenatal Diagnosis, Cardiovascular Research, European Journal of Medical Genetics and Circulation 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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In The Last Decade

Inge B. Mathijssen

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Fields of papers citing papers by Inge B. Mathijssen

All Works

About Inge B. Mathijssen

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