Irene M. Janssen

6.9k citations

23 papers · 3.4k indexed · 2 hit papers · h-index 17

Genetics top 0.5%
- Genomic variations and chromosomal abnormalities 13
- Genetics and Neurodevelopmental Disorders 4
- Genomics and Rare Diseases 3
Genetics top 1%
- Genomic variations and chromosomal abnormalities 13
- Genetics and Neurodevelopmental Disorders 4
- Genomics and Rare Diseases 3
Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics 3
Molecular Biology top 5%
- Renal and related cancers 2
Cancer Research top 10%
- Cancer Genomics and Diagnostics 5
Plant Science
- Chromosomal and Genetic Variations 6
Pathology and Forensic Medicine
- Lymphoma Diagnosis and Treatment 3

Co-authors: Joris A. Veltman Ad Geurts van Kessel Lisenka E.L.M. Vissers Han G. Brunner Eric Schoenmakers Bert B.A. de Vries Erik Huys Dominique Smeets
Cited by: Genetics Pediatrics, Perinatology and Child Health
Journals: Nature Genetics (2 papers)Journal of Clinical Oncology (1 paper)Blood (1 paper)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Irene M. Janssen

23 papers receiving 3.3k citations

Hit Papers

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Peers

Countries citing papers authored by Irene M. Janssen

Since Specialization

Citations

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

Fields of papers citing papers by Irene M. Janssen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Irene M. 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 Irene M. Janssen. The network helps show where Irene M. Janssen may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Reliable noninvasive prenatal testing by massively parallel sequencing of circulating cell-free DNA from maternal plasma processed up to 24 h after venipuncture Clinical Biochemistry ·Karen Buysse,Lean Beulen,Ingrid Gomes,Christian Gilissen,Chantal Keesmaat,Irene M. Janssen,Judith J.H.T. Derks-Willemen,Joep de Ligt,Ilse Feenstra,Mireille N. Bekker,J. M. G. van Vugt,Ad Geurts van Kessel,Lisenka E.L.M. Vissers,Brigitte H. W. Faas	2013	14
2	Non-invasive prenatal diagnosis of fetal aneuploidies using massively parallel sequencing-by-ligation and evidence that cell-free fetal DNA in the maternal plasma originates from cytotrophoblastic cells Expert Opinion on Biological Therapy ·Brigitte H. W. Faas,Joep de Ligt,Irene M. Janssen,Alex J. Eggink,Lia D. E. Wijnberger,John MG van Vugt,Lisenka E.L.M. Vissers,Ad Geurts van Kessel	2012	104
3	A de novo paradigm for mental retardationbreakdown → Nature Genetics ·Lisenka E.L.M. Vissers,Joep de Ligt,Christian Gilissen,Irene M. Janssen,Marloes Steehouwer,Petra de Vries,Bart van Lier,Peer Arts,Nienke Wieskamp,Marisol del Rosario,Bregje W.M. van Bon,Alexander Hoischen,Bert B.A. de Vries,Han G. Brunner,Joris A. Veltman	2010	526
4	Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture Human Molecular Genetics ·Lisenka E.L.M. Vissers,Samarth Bhatt,Irene M. Janssen,Zhilian Xia,Seema R. Lalani,Rolph Pfundt,Katarzyna Derwińska,Bert B.A. de Vries,Christian Gilissen,Alexander Hoischen,Monika Nesteruk,Barbara Wiśniowiecka‐Kowalnik,Marta Smyk,Han G. Brunner,Sau Wai Cheung,Ad Geurts van Kessel,Joris A. Veltman,Paweł Stankiewicz	2009	114
5	Constitutional DNA copy number changes in ICSI children Human Reproduction ·G.H. Woldringh,Irene M. Janssen,Jayne Y. Hehir‐Kwa,Christa van den Elzen,J.A.M. Kremer,P. de Boer,Eric Schoenmakers	2008	7
6	CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy Molecular Psychiatry ·Joseph I. Friedman,Terry Vrijenhoek,Sander Markx,Irene M. Janssen,W A van der Vliet,Brigitte H. W. Faas,Nine V.A.M. Knoers,Wiepke Cahn,René S. Kahn,Lisa Edelmann,Keith L. Davis,Jeremy M. Silverman,Han G. Brunner,Ad Geurts van Kessel,Cisca Wijmenga,Roel A. Ophoff,Joris A. Veltman	2007	224
7	Genome-wide Copy Number Profiling on High-density Bacterial Artificial Chromosomes, Single-nucleotide Polymorphisms, and Oligonucleotide Microarrays: A Platform Comparison based on Statistical Power Analysis DNA Research ·Jayne Y. Hehir‐Kwa,M. Egmont‐Petersen,Irene M. Janssen,Dominique Smeets,Ad Geurts van Kessel,Joris A. Veltman	2007	80
8	Identification of Novel Mutations in Patients with Leber Congenital Amaurosis and Juvenile RP by Genome-wide Homozygosity Mapping with SNP Microarrays Investigative Ophthalmology & Visual Science ·Anneke I. den Hollander,Irma López,Suzanne Yzer,Marijke N. Zonneveld,Irene M. Janssen,Tim M. Strom,Jayne Y. Hehir‐Kwa,Joris A. Veltman,Maarten Arends,Thomas Meitinger,Maria A. Musarella,L. Ingeborgh van den Born,Gerald A. Fishman,Irene H. Maumenee,Klaus Rohrschneider,Frans P.M. Cremers,Robert K. Koenekoop	2007	76
9	Identification of recurrent chromosomal aberrations in germ cell tumors of neonates and infants using genomewide array‐based comparative genomic hybridization Genes Chromosomes and Cancer ·Imke M. Veltman,Joris A. Veltman,Irene M. Janssen,Christina Hulsbergen‐van de Kaa,Wolter Oosterhuis,Dominik T. Schneider,Hans Stoop,Ad Gillis,Susanne Zahn,Leendert H. J. Looijenga,U. Göbel,Ad Geurts van Kessel	2005	32
10	Diagnostic Genome Profiling in Mental Retardation The American Journal of Human Genetics ·Bert B.A. de Vries,Rolph Pfundt,M.A.R. Leisink,David A. Koolen,Lisenka E.L.M. Vissers,Irene M. Janssen,Simon V. van Reijmersdal,Willy M. Nillesen,Erik Huys,Nicole de Leeuw,Dominique Smeets,Erik A. Sistermans,Ton Feuth,Conny M.A. van Ravenswaaij‐Arts,Ad Geurts van Kessel,Eric Schoenmakers,Han G. Brunner,Joris A. Veltman	2005	413
11	Mutations in a new member of the chromodomain gene family cause CHARGE syndromebreakdown → Nature Genetics ·Lisenka E.L.M. Vissers,Conny M.A. van Ravenswaaij,R.J.C. Admiraal,Jane A. Hurst,Bert B.A. de Vries,Irene M. Janssen,W A van der Vliet,Erik Huys,Pieter J. de Jong,Ben C.J. Hamel,Eric Schoenmakers,Han G. Brunner,Joris A. Veltman,Ad Geurts van Kessel	2004	876
12	Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities The American Journal of Human Genetics ·Lisenka E.L.M. Vissers,Bert B.A. de Vries,Kazutoyo Osoegawa,Irene M. Janssen,Ton Feuth,Chik On Choy,Huub Straatman,Walter van der Vliet,Erik Huys,Anke van Rijk,Dominique Smeets,Conny M.A. van Ravenswaaij‐Arts,Nine V.A.M. Knoers,Ineke van der Burgt,Pieter J. de Jong,Han G. Brunner,Ad Geurts van Kessel,Eric Schoenmakers,Joris A. Veltman	2003	348
13	Definition of a Critical Region on Chromosome 18 for Congenital Aural Atresia by ArrayCGH The American Journal of Human Genetics ·Joris A. Veltman,Yvonne M.H. Versleijen‐Jonkers,Inge Nuijten,Irene M. Janssen,Walter van der Vliet,Erik Huys,Joris Vermeesch,Griet Van Buggenhout,Jean‐Pierre Fryns,R.J.C. Admiraal,Pauline Terhal,Didier Lacombe,Ad Geurts van Kessel,Dominique Smeets,Eric Schoenmakers,Conny M.A. van Ravenswaaij‐Arts	2003	83
14	Chromosomal breakpoint mapping by arrayCGH using flow-sorted chromosomes BioTechniques ·Imke M. Veltman,Joris A. Veltman,Ger J. A. Arkesteijn,Irene M. Janssen,Lisenka E.L.M. Vissers,Pieter J. de Jong,Ad Geurts van Kessel,Eric Schoenmakers	2003	33
15	High-Throughput Analysis of Subtelomeric Chromosome Rearrangements by Use of Array-Based Comparative Genomic Hybridization The American Journal of Human Genetics ·Joris A. Veltman,Eric Schoenmakers,Bert H.J. Eussen,Irene M. Janssen,Gerard Merkx,Brigitte van Cleef,Conny Ma van Ravenswaaij,Han G. Brunner,Dominique Smeets,Ad Geurts van Kessel	2002	167
16	Molecular cytogenetic analysis of clustered sporadic and familial renal cell carcinoma-associated 3q13∼q22 breakpoints Cancer Genetics and Cytogenetics ·Daniëlle Bodmer,Irene M. Janssen,Yvonne M.H. Versleijen‐Jonkers,Eva van den Berg,Trijnie Dijkhuizen,Maria Dêbiec‐Rychter,Eric Schoenmakers,Ad Geurts van Kessel	2002	6
17	Masked t(X;18)(p11;q11) in a biphasic synovial sarcoma revealed by FISH and RT‐PCR Genes Chromosomes and Cancer ·Ad Geurts van Kessel,D. de Bruijn,L. Hermsen,Irene M. Janssen,Nuno R. dos Santos,Riki W. Willems,L. Makkus,H.W.B. Schreuder,R. P. H. Veth	1998	17
18	Masked t(X;18)(p11;q11) in a biphasic synovial sarcoma revealed by FISH and RT-PCR Genes Chromosomes and Cancer ·Ad Geurts van Kessel,D. de Bruijn,L. Hermsen,Irene M. Janssen,Nuno R. dos Santos,Riki W. Willems,L. Makkus,H.W.B. Schreuder,R. P. H. Veth	1998	16
19	Isolation of osteosarcoma-associated amplified DNA sequences using representational difference analysis Genes Chromosomes and Cancer ·Annet Simons,Irene M. Janssen,Ron F. Suijkerbuijk,R.P.H. Veth,M Pruszczyński,Christina A. Hulsbergen‐van de Kaa,Stanislas du Manoir,Ad Geurts van Kessel	1997	16
20	Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint Cytogenetic and Genome Research ·Marian A. J. Weterman,M. Wilbrink,Irene M. Janssen,Hilde Janssen,Anke van den Berg,Simon E. Fisher,Ian Craig,Ad Geurts van Kessel	1996	26

About Irene M. Janssen

Irene M. Janssen is a scholar working on Genetics, Cancer Research and Pathology and Forensic Medicine, having authored 23 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (6 papers), Cancer Genomics and Diagnostics (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers), Prenatal Screening and Diagnostics (3 papers), Lymphoma Diagnosis and Treatment (3 papers) and Renal and related cancers (2 papers). The work is most often cited by research in Genetics (2.1k citations), Genetics (625 citations) and Pediatrics, Perinatology and Child Health (524 citations). Irene M. Janssen has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Joris A. Veltman, Ad Geurts van Kessel, Lisenka E.L.M. Vissers, Han G. Brunner, Eric Schoenmakers, Bert B.A. de Vries, Erik Huys, Dominique Smeets, R.J.C. Admiraal and Pieter J. de Jong. Their work appears in journals such as Nature Genetics, Journal of Clinical Oncology and Blood.

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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