Nicole Corsten‐Janssen

1.0k total citations
14 papers, 249 citations indexed

About

Nicole Corsten‐Janssen is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Nicole Corsten‐Janssen has authored 14 papers receiving a total of 249 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Nicole Corsten‐Janssen's work include Congenital heart defects research (6 papers), Tracheal and airway disorders (6 papers) and Congenital Ear and Nasal Anomalies (6 papers). Nicole Corsten‐Janssen is often cited by papers focused on Congenital heart defects research (6 papers), Tracheal and airway disorders (6 papers) and Congenital Ear and Nasal Anomalies (6 papers). Nicole Corsten‐Janssen collaborates with scholars based in Netherlands, United Kingdom and United States. Nicole Corsten‐Janssen's co-authors include Conny M.A. van Ravenswaaij‐Arts, Wilhelmina S. Kerstjens‐Frederikse, Lies H. Hoefsloot, Livia Kapusta, Peter Scambler, Gideon J. du Marchie Sarvaas, Joanne Verheij, Cecilie F. Rustad, Marian K. Bakker and Trijnie Dijkhuizen and has published in prestigious journals such as Human Mutation, Scandinavian Journal of Work Environment & Health and Orphanet Journal of Rare Diseases.

In The Last Decade

Nicole Corsten‐Janssen

14 papers receiving 246 citations

Peers

Countries citing papers authored by Nicole Corsten‐Janssen

Since Specialization

Citations

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

Fields of papers citing papers by Nicole Corsten‐Janssen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicole Corsten‐Janssen. 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 Nicole Corsten‐Janssen. The network helps show where Nicole Corsten‐Janssen may publish in the future.

Co-authorship network of co-authors of Nicole Corsten‐Janssen

This figure shows the co-authorship network connecting the top 25 collaborators of Nicole Corsten‐Janssen. A scholar is included among the top collaborators of Nicole Corsten‐Janssen 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 Nicole Corsten‐Janssen. Nicole Corsten‐Janssen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Limitations of Semi-Automated Immunomagnetic Separation of HLA-G-Positive Trophoblasts from Papanicolaou Smears for Prenatal Genetic Diagnostics 2025 ·Diagnostics ·Eddy N. de Boer, Nicole Corsten‐Janssen, (unknown), Theo Bijma, (unknown), Gerard J. te Meerman, G. T. R. Manten, N. Knoers, Katelijne Bouman, L. Duin, Cleo C. van Diemen	1
2	The phenotypic spectrum of terminal 6q deletions based on a large cohort derived from social media and literature: a prominent role for DLL1 2023 ·Orphanet Journal of Rare Diseases ·(unknown), Wilhelmina S. Kerstjens‐Frederikse, Nicole Corsten‐Janssen, Trijnie Dijkhuizen, Conny M.A. van Ravenswaaij‐Arts	4
3	The effects of an online decision aid to support the reproductive decision‐making process of genetically at risk couples—A pilot study 2022 ·Journal of Genetic Counseling ·(unknown), Monique Heijmans, Christine de Die‐Smulders, Emilia K. Bijlsma, Nicole Corsten‐Janssen, (unknown), Sander M. J. van Kuijk, Klaske D. Lichtenbelt, (unknown), Kyra E. Stuurman, Gita Tan-Sindhunata, Hein de Vries, Liesbeth van Osch	5
4	Parental experiences of rapid exome sequencing in cases with major ultrasound anomalies during pregnancy 2021 ·Prenatal Diagnosis ·Mirjam Plantinga, (unknown), (unknown), (unknown), (unknown), (unknown), Katelijne Bouman, Joanne Verheij, Erwin Birnie, Adelita V. Ranchor, Nicole Corsten‐Janssen, Irene M. van Langen	17
5	Maternal occupational exposure and congenital heart defects in offspring 2020 ·Scandinavian Journal of Work Environment & Health ·(unknown), Jorieke E. H. Bergman, Hans Kromhout, Roel Vermeulen, Nicole Corsten‐Janssen, H. Marike Boezen, Gideon J. du Marchie Sarvaas, (unknown)	6
6	A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound 2020 ·Prenatal Diagnosis ·Nicole Corsten‐Janssen, Katelijne Bouman, (unknown), (unknown), (unknown), (unknown), (unknown), Joanne Verheij, Ron F. Suijkerbuijk, L. Duin, G. T. R. Manten, Irene M. van Langen, Rolf H. Sijmons, Birgit Sikkema‐Raddatz, Helga Westers, Cleo C. van Diemen	34
7	Variable cardiovascular phenotypes associated with SMAD2 pathogenic variants 2018 ·Human Mutation ·Jorge L. Granadillo, Wendy K. Chung, Leah Hecht, Nicole Corsten‐Janssen, Daniel Wegner, (unknown), Tomi L. Toler, Daniel Pineda‐Alvarez, Ganka Douglas, Joshua Murphy, Joshua S. Shimony, Marwan Shinawi	26
8	Clinical and molecular effects of CHD7 in the heart 2017 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Nicole Corsten‐Janssen, Peter Scambler	14
9	Congenital arch vessel anomalies in CHARGE syndrome: A frequent feature with risk for co-morbidity 2016 ·IJC Heart & Vasculature ·Nicole Corsten‐Janssen, Conny M.A. van Ravenswaaij‐Arts, Livia Kapusta	12
10	Definition of 5q11.2 microdeletion syndrome reveals overlap with CHARGE syndrome and 22q11 deletion syndrome phenotypes 2014 ·American Journal of Medical Genetics Part A ·Lot Snijders Blok, Nicole Corsten‐Janssen, David Fitzpatrick, Corrado Romano, Marco Fichera, Girolamo Aurelio Vitello, Marjolein H. Willemsen, Jeroen Schoots, Rolph Pfundt, Conny M.A. van Ravenswaaij‐Arts, Lies H. Hoefsloot, Tjitske Kleefstra	6
11	CHD7 mutations are not a major cause of atrioventricular septal and conotruncal heart defects 2014 ·American Journal of Medical Genetics Part A ·Nicole Corsten‐Janssen, Gideon J. du Marchie Sarvaas, Wilhelmina S. Kerstjens‐Frederikse, Lies H. Hoefsloot, Ingrid M. van Beynum, Livia Kapusta, Conny M.A. van Ravenswaaij‐Arts	9
12	More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often Anticipated 2013 ·Molecular Syndromology ·Nicole Corsten‐Janssen, Sulagna C. Saitta, Lies H. Hoefsloot, Donna M. McDonald‐McGinn, D.A. Driscoll, Ronny Derks, (unknown), Wilhelmina S. Kerstjens‐Frederikse, Beverly S. Emanuel, Elaine H. Zackai, Conny M.A. van Ravenswaaij‐Arts	36
13	Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of <b><i>OTX2</i></b> 2013 ·Molecular Syndromology ·(unknown), Conny M.A. van Ravenswaaij‐Arts, Julia Tantau, Nicole Corsten‐Janssen, J. Peter van Tintelen, Trijnie Dijkhuizen, Josseline Kaplan, Nicolas Chassaing	27
14	The Cardiac Phenotype in Patients With a CHD7 Mutation 2013 ·Circulation Cardiovascular Genetics ·Nicole Corsten‐Janssen, Wilhelmina S. Kerstjens‐Frederikse, Gideon J. du Marchie Sarvaas, (unknown), Marian K. Bakker, Jorieke E. H. Bergman, Hanne Hove, Ketil Heimdal, Cecilie F. Rustad, Raoul C. M. Hennekam, Robert M.W. Hofstra, Lies H. Hoefsloot, Conny M.A. van Ravenswaaij‐Arts, Livia Kapusta	52

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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