Inge B. Mathijssen

1.5k citations

30 papers · 740 indexed · 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

Pediatrics, Perinatology and Child Health 8
- Prenatal Screening and Diagnostics 7
Genetics 8
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 3

Co-authors: Eva Pajkrt Alex V. Postma Aho Ilgun Phil Barnett Lidewij Henneman Jan Lam Phillis Lakeman Arthur A.M. Wilde
Journals: European Journal of Human Genetics (7 papers)Prenatal Diagnosis (4 papers)Cardiovascular Research (2 papers)European Journal of Medical Genetics (2 papers)European Journal of Public Health (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-authorship network

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

#	Work
1	Counseling couples at risk of having a child with homozygous familial hypercholesterolemia – Clinical experience and recommendations Journal of clinical lipidology ·Tycho R. Tromp, M. Doortje Reijman, Albert Wiegman, G. Kees Hovingh, Joep C. Defesche, Merel C. van Maarle, Inge B. Mathijssen	2022	2
2	Couples’ experiences with expanded carrier screening: evaluation of a university hospital screening offer European Journal of Human Genetics ·Liyuan Zhang, Phillis Lakeman, Pauline Sterling, Ruth I. Dowell, Sébastien Roland, Inge B. Mathijssen, Martina C. Cornel, Lidewij Henneman	2021	19
3	How will new genetic technologies, such as gene editing, change reproductive decision-making? Views of high-risk couples European Journal of Human Genetics ·Liyuan Zhang, Phillis Lakeman, Inge B. Mathijssen, Mariëtte Goddijn, Martina C. Cornel, Lidewij Henneman	2020	8
4	Preconception carrier screening for multiple disorders: evaluation of a screening offer in a Dutch founder population European Journal of Human Genetics ·Inge B. Mathijssen, R Wilson, Sébastien Roland, Sam Woodhouse, Phillis Lakeman, Hanne Meijers‐Heijboer, Merel C. van Maarle, Lidewij Henneman	2018	22
5	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
6	With expanded carrier screening, founder populations run the risk of being overlooked Journal of Community Genetics ·Inge B. Mathijssen, Merel C. van Maarle, Novi Ratna Sari, E. Redeker, Leo P. ten Kate, Lidewij Henneman, Hanne Meijers‐Heijboer	2017	9
7	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
8	Factors for successful implementation of population-based expanded carrier screening: learning from existing initiatives: Table 1 European Journal of Public Health ·R Wilson, Inge B. Mathijssen, Phillis Lakeman, Merel C. van Maarle, Wybo Dondorp, Lidewij Henneman, Martina C. Cornel	2016	25
9	Targeted carrier screening for four recessive disorders: High detection rate within a founder population European Journal of Medical Genetics ·Inge B. Mathijssen, Lidewij Henneman, Sam Woodhouse, Phillis Lakeman, Sébastien Roland, E. Redeker, G. Fabiani, Hanne Meijers‐Heijboer, Merel C. van Maarle	2015	23
10	Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence European Journal of Human Genetics ·Карпунина Антонина Вячеславовна, Inge B. Mathijssen, Hasbullah Hasbullah, Frank Baas, Johanna I. de Vries, J. Patrick van der Voorn, Irma Kluijt, La Maison Royale, Eveline W Blom, Erik A. Sistermans, Hanne Meijers‐Heijboer, Quinten Waisfisz, Marjan M. Weiss, Alexander J. Groffen	2014	29
11	Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings European Journal of Human Genetics ·Josep Martínez Simó, Willy M. Nillesen, Kyra E. Stuurman, Grétel Oudesluijs, 鈴木光, 白神達也, 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
12	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
13	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, José Alfredo Balderrama Rueda, Inge B. Mathijssen, C. M. Bilardo, Eva Pajkrt	2011	30
14	Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome (vol 88, pg 130, 2010) 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	2011	0
15	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, Yuan Hua, Hermine E. Veenstra‐Knol, Antoon F.M. Moorman, Phil Barnett, Alex V. Postma	2010	34
16	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
17	A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation Circulation Research ·Alex V. Postma, 雍容覃, 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
18	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, Camille Sun, DUDLEY S. TAFT, Raoul C. M. Hennekam	2005	11
19	Testicular cancer in a patient with Primrose syndrome European Journal of Medical Genetics ·Inge B. Mathijssen, Amir Schneider Kaufman, Raoul C. M. Hennekam	2005	13
20	Genotype-Phenotype Correlation in Patients Suspected of Having Sotos Syndrome Hormone Research in Paediatrics ·Lonneke de Boer, Sarina G. Kant, Marcel Karperien, W. Kim, Jennifer M.L. Tjon, Geraldine R. Vink, A Rogiewicz, 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, Karanvir S. Aulakh, Martijn H. Breuning, Jan M. Wit	2004	43

About Inge B. Mathijssen

Inge B. Mathijssen is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Rheumatology, Molecular Biology and Gastroenterology, 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), Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (4 papers), RNA modifications and cancer (4 papers), Cystic Fibrosis Research Advances (4 papers), Genomics and Rare Diseases (3 papers) and Congenital Anomalies and Fetal Surgery (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, Aho Ilgun, Phil Barnett, Lidewij Henneman, Jan Lam, Phillis Lakeman, Arthur A.M. Wilde, Hanne Meijers‐Heijboer and Vincent M. Christoffels. Their work appears in journals such as European Journal of Human Genetics, Prenatal Diagnosis, Cardiovascular Research, European Journal of Medical Genetics and European Journal of Public Health.

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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