Marieke Joosten

1.6k citations

49 papers · 890 indexed · h-index 18

Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics 35
- Fetal and Pediatric Neurological Disorders 18
Genetics top 5%
- Genomic variations and chromosomal abnormalities 21
- Genomics and Rare Diseases 4
- Virus-based gene therapy research 4
- Genetic Syndromes and Imprinting 3
- BRCA gene mutations in cancer 3
Infectious Diseases
- Parvovirus B19 Infection Studies 6
Hematology
Developmental Biology

Co-authors: Diane Van Opstal Malgorzata I. Srebniak Lutgarde Govaerts Karin E. M. Diderich Maarten F. C. M. Knapen Attie T. J. I. Go Robert‐Jan H. Galjaard Marjan Boter
Cited by: Pediatrics, Perinatology and Child Health Genetics Infectious Diseases
Journals: Nucleic Acids Research (1 paper)Journal of Biological Chemistry (1 paper)PLoS ONE (1 paper)
Partner nations: Netherlands United States Austria

In The Last Decade

Marieke Joosten

47 papers receiving 875 citations

Peers

Countries citing papers authored by Marieke Joosten

Since Specialization

Citations

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

Fields of papers citing papers by Marieke Joosten

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marieke Joosten. 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 Marieke Joosten. The network helps show where Marieke Joosten may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	The role of confined placental mosaicism in fetal growth restriction: A retrospective cohort study Prenatal Diagnosis ·Geerke M. Eggenhuizen,Attie T. J. I. Go,Zoë Sauter,Mariëtte J.V. Hoffer,Monique C. Haak,Geert Geeven,Karin E. M. Diderich,Marieke Joosten,Myrthe van den Born,Malgorzata I. Srebniak,Diane Van Opstal	2024	10
2	Confined placental mosaicism: Distribution of chromosomally abnormal cells over the term placenta Placenta ·Geerke M. Eggenhuizen,Suzanne van Veen,Nicole van Koetsveld,Attie T. J. I. Go,Karin E. M. Diderich,Marieke Joosten,Myrthe van den Born,Malgorzata I. Srebniak,Diane Van Opstal	2024	3
3	The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis European Journal of Medical Genetics ·Karin E. M. Diderich,Jasmijn E. Klapwijk,Vyne van der Schoot,Myrthe van den Born,Martina Wilke,Marieke Joosten,Kyra E. Stuurman,Lies H. Hoefsloot,Diane Van Opstal,Hennie T. Brüggenwirth,Malgorzata I. Srebniak	2023	6
4	Limited additional value of karyotyping cultured amniotic fluid cell colonies in addition to microarray on uncultured cells for confirmation of abnormal non‐invasive prenatal testing results Prenatal Diagnosis ·Stephany Donze,Malgorzata I. Srebniak,Karin E. M. Diderich,Myrthe van den Born,Robert‐Jan H. Galjaard,Lutgarde Govaerts,Vyne van der Schoot,Maarten F. C. M. Knapen,Marieke Joosten,Diane Van Opstal	2023	2
5	Challenges and Pragmatic Solutions in Pre-Test and Post-Test Genetic Counseling for Prenatal Exome Sequencing The Application of Clinical Genetics ·Karin E. M. Diderich,Jasmijn E. Klapwijk,Vyne van der Schoot,Hennie T. Brüggenwirth,Marieke Joosten,Malgorzata I. Srebniak	2023	1
6	What proportion of couples with a history of recurrent pregnancy loss and with a balanced rearrangement in one parent can potentially be identified through cell-free DNA genotyping? Molecular Cytogenetics ·Laura J. C. M. van Zutven,Jona Mijalkovic,Monique van Veghel‐Plandsoen,Margaret Goense,Marike Polak,Maarten F. C. M. Knapen,Sabina de Weerd,Marieke Joosten,Karin E. M. Diderich,Lies H. Hoefsloot,Diane Van Opstal,Malgorzata I. Srebniak	2023	1
7	The Effect of Written and Video Discharge Instructions After Mild Traumatic Brain Injury on Healthcare Costs and Productivity Costs Journal of Head Trauma Rehabilitation ·Amber E. Hoek,A. J. L. M. Geraerds,P.P.M. Rood,Marieke Joosten,Diederik W.J. Dippel,Ed F. van Beeck,Leandra van den Hengel,Björn Dijkstra,Dafni Papathanasiou,Daphne van Rijssel,Maaike van den Hamer,Stephanie C. E. Schuit,Alex Burdorf,Juanita A. Haagsma,Suzanne Polinder	2021	2
8	Patient-friendly integrated first trimester screening by NIPT and fetal anomaly scan Molecular Cytogenetics ·Malgorzata I. Srebniak,Maarten F. C. M. Knapen,Marieke Joosten,Karin E. M. Diderich,Sander Galjaard,Diane Van Opstal	2021	3
9	Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin Genetics in Medicine ·Ellen H. van den Bogaard,Michel van Geel,Ivonne M.J.J. van Vlijmen‐Willems,Patrick A.M. Jansen,Malou Peppelman,P.E.J. van Erp,Selma Atalay,Hanka Venselaar,Marleen Simon,Marieke Joosten,Joost Schalkwijk,Patrick L.J.M. Zeeuwen	2018	11
10	The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies Human Mutation ·Malgorzata I. Srebniak,Maarten F. C. M. Knapen,Marike Polak,Marieke Joosten,Karin E. M. Diderich,Lutgarde Govaerts,Marjan Boter,Joan N. R. Kromosoeto,Daniella A.C.M. van Hassel,Gido Huijbregts,Wilfred F. J. van IJcken,R. Heydanus,Anneke Dijkman,Toon Toolenaar,Femke A.T. de Vries,Jeroen Knijnenburg,Attie T. J. I. Go,Robert‐Jan H. Galjaard,Diane Van Opstal	2017	18
11	Enlarged NT (≥3.5 mm) in the first trimester – not all chromosome aberrations can be detected by NIPT Molecular Cytogenetics ·Malgorzata I. Srebniak,M. C. de Wit,Karin E. M. Diderich,Lutgarde Govaerts,Marieke Joosten,Maarten F. C. M. Knapen,Marnix J. Bos,Gerda A. G. Looye-Bruinsma,Mieke Koningen,Attie T. J. I. Go,R. J. H. Galjaard,Diane Van Opstal	2016	30
12	False Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature Review PLoS ONE ·Diane Van Opstal,Malgorzata I. Srebniak,Joke Polak,Femke de Vries,Lutgarde Govaerts,Marieke Joosten,Attie T. J. I. Go,Maarten F. C. M. Knapen,Cardi van den Berg,Karin E. M. Diderich,Robert-Jan H. Galjaard	2016	38
13	Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs European Journal of Human Genetics ·Malgorzata I. Srebniak,Karin E. M. Diderich,Marieke Joosten,Lutgarde Govaerts,Jeroen Knijnenburg,Femke At de Vries,Marjan Boter,Debora Lont,Maarten F. C. M. Knapen,M. C. de Wit,Attie T. J. I. Go,Robert‐Jan H. Galjaard,Diane Van Opstal	2015	55
14	Chorionic villous vascularization related to phenotype and genotype in first trimester miscarriages in a recurrent pregnancy loss cohort Human Reproduction ·A. D. Reus,Mary D. Stephenson,Frédérique M. van Dunné,Ronald R. de Krijger,Marieke Joosten,EAP Steegers,N. Exalto	2013	8
15	Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities Molecular Cytogenetics ·Malgorzata I. Srebniak,Marjan Boter,Grétel Oudesluijs,Titia E. Cohen‐Overbeek,Lutgarde Govaerts,Karin E. M. Diderich,Renske Oegema,Maarten F. C. M. Knapen,Ingrid M.B.H. van de Laar,Marieke Joosten,Diane Van Opstal,Robert‐Jan H. Galjaard	2012	55
16	Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy Netherlands Heart Journal ·E. Otten,Ronald H. Lekanne Deprez,Marjan M. Weiss,Marjon van Slegtenhorst,Marieke Joosten,Jasper J. van der Smagt,Nicolaas de Jonge,Wilhelmina S. Kerstjens‐Frederikse,M. T. R. Roofthooft,A. H. M. M. Balk,Maarten P. van den Berg,Jolien S. Ruiter,J. Peter van Tintelen	2010	10
17	Leukemic predisposition of pSca-1/Cb2 transgenic mice Experimental Hematology ·Marieke Joosten,Peter J.M. Valk,Meritxell Alberich-Jordà,Yolanda Vankan-Berkhoudt,Sandra Verbakel,M. van den Broek,Antoinette Beijen,Bob Löwenberg,Ruud Delwel	2002	26
18	Large-scale identification of novel potential disease loci in mouse leukemia applying an improved strategy for cloning common virus integration sites Oncogene ·Marieke Joosten,Yolanda Vankan-Berkhoudt,Marjolein Tas,Monja Lunghi,Y.M. Bastiaansen-Jenniskens,Evan Parganas,Peter J.M. Valk,Bob Löwenberg,Eric van den Akker,Ruud Delwel	2002	36
19	Erythroid defects and increased retrovirally-induced tumor formation in Evi1 transgenic mice Leukemia ·Derrick Louz,M. van den Broek,Sandra Verbakel,Yolanda Vankan,Kirsten van Lom,Marieke Joosten,Dies Meijer,Bob Löwenberg,R Delwel	2000	49
20	Phenotyping of Evi1, Evi11/Cb2, and Evi12 Transformed Leukemias Isolated from a Novel Panel of Cas-Br-M Murine Leukemia Virus-Infected Mice Virology ·Marieke Joosten,Peter J.M. Valk,Yolanda Vankan,Nico de Both,Bob Löwenberg,Ruud Delwel	2000	10

About Marieke Joosten

Marieke Joosten is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Developmental Biology, having authored 49 papers that have together received 890 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (35 papers), Genomic variations and chromosomal abnormalities (21 papers), Fetal and Pediatric Neurological Disorders (18 papers), Parvovirus B19 Infection Studies (6 papers), Genomics and Rare Diseases (4 papers), Virus-based gene therapy research (4 papers), Genetic Syndromes and Imprinting (3 papers) and BRCA gene mutations in cancer (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (605 citations), Genetics (471 citations) and Infectious Diseases (112 citations). Marieke Joosten has collaborated with scholars based in Netherlands, United States and Austria. Frequent co-authors include Diane Van Opstal, Malgorzata I. Srebniak, Lutgarde Govaerts, Karin E. M. Diderich, Maarten F. C. M. Knapen, Attie T. J. I. Go, Robert‐Jan H. Galjaard, Marjan Boter, Bob Löwenberg and Ruud Delwel. Their work appears in journals such as Nucleic Acids Research, Journal of Biological Chemistry and PLoS ONE.

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