Marjan Boter

2.2k citations

32 papers · 1.1k · 2 hit papers · h-index 16

Impact in

Virology top 5%
- Poxvirus research and outbreaks
Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders

Papers in

Pediatrics, Perinatology and Child Health 12
- Prenatal Screening and Diagnostics 12
- Fetal and Pediatric Neurological Disorders 3
Virology 6
- Poxvirus research and outbreaks 6

Co-authors: Diane Van Opstal (14 shared papers)Robert‐Jan H. Galjaard (10 shared papers)Malgorzata Ilona Srebniak (13 shared papers)Leendert H. J. Looijenga (3 shared papers)Lutgarde C. P. Govaerts (9 shared papers)Marieke Joosten (10 shared papers)J. Wolter Oosterhuis (2 shared papers)Katja P. Wolffenbuttel (2 shared papers)
Journals: Eurosurveillance (4 papers)European Journal of Human Genetics (4 papers)Prenatal Diagnosis (3 papers)Molecular Cytogenetics (3 papers)Human Mutation (2 papers)
Partner nations: Netherlands Denmark Rwanda

In The Last Decade

Marjan Boter

30 papers receiving 1.0k citations

Marjan Boter's Hit Papers

align trajectories log scale

Epidemiological and genomic evolution of the ongoing outbreak of clade Ib mpox virus in the eastern Democratic Republic of the Congo 2025 · 22 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2025 Nature Medicine
2024 Eurosurveillance

Peers

Countries citing papers authored by Marjan Boter

Since Specialization

Citations

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

Fields of papers citing papers by Marjan Boter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Marjan Boter, 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 Marjan Boter Line = papers co-authored together Marjan Boter 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 32 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Detection of West Nile virus in a common whitethroat (Curruca communis) and Culex mosquitoes in the Netherlands, 2020 Eurosurveillance ·Reina S. Sikkema, Maarten J. J. Schrama, Tijs van den Berg, Jolien Morren, Emmanuelle Münger, Louie Krol, Jordy G. van der Beek, Rody Blom, Irina Chestakova, Anne van der Linden, Marjan Boter, Tjomme van Mastrigt, Richard Molenkamp, Constantianus J. M. Koenraadt, Judith M. van den Brand, Bas B. Oude Munnink, Marion Koopmans, Henk P. van der Jeugd	2020	187
2	Morphological and Immunohistochemical Differences between Gonadal Maturation Delay and Early Germ Cell Neoplasia in Patients with Undervirilization Syndromes The Journal of Clinical Endocrinology & Metabolism ·M. Cools, Koen van Aerde, Anne‐Marie F. Kersemaekers, Marjan Boter, Stenvert L. S. Drop, Katja P. Wolffenbuttel, Ewout Willem Steyerberg, J. Wolter Oosterhuis, Leendert H. J. Looijenga	2005	161
3	Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow European Journal of Human Genetics ·Malgorzata Ilona Srebniak, Marjan Boter, Grétel Oudesluijs, Marieke Joosten, Lutgarde C. P. Govaerts, Diane Van Opstal, Robert‐Jan H. Galjaard	2011	85
4	Ongoing mpox outbreak in Kamituga, South Kivu province, associated with monkeypox virus of a novel Clade I sub-lineage, Democratic Republic of the Congo, 2024 Eurosurveillance ·Leandre Murhula Masirika, Jean Claude Udahemuka, Leonard Schuele, Pacifique Ndishimye, Saria Otani, Justin Bengehya Mbiribindi, Jean M. Marekani, Léandre Mutimbwa Mambo, Nadine Malyamungu Bubala, Marjan Boter, David F. Nieuwenhuijse, Trudie A. Lang, Ernest Balyahamwabo Kalalizi, Jean Pierre Musabyimana, Frank M. Aarestrup, Marion Koopmans, Bas B. Oude Munnink, Freddy Belesi Siangoli Hit paper breakdown →	2024	77
5	VASA Is a Specific Marker for Both Normal and Malignant Human Germ Cells Laboratory Investigation ·Anne‐Marie Zeeman, Hans Stoop, Marjan Boter, Ad Gillis, Diego H. Castrillón, J. Wolter Oosterhuis, Leendert H. J. Looijenga	2002	65
6	Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs European Journal of Human Genetics ·Malgorzata Ilona Srebniak, Karin E. M. Diderich, Marieke Joosten, Lutgarde C. P. 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	59
7	Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities Molecular Cytogenetics ·Malgorzata Ilona Srebniak, Marjan Boter, Grétel Oudesluijs, Titia E. Cohen‐Overbeek, Lutgarde C. P. 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	58
8	Rapid aneuploidy detection with multiplex ligation-dependent probe amplification: a prospective study of 4000 amniotic fluid samples European Journal of Human Genetics ·Diane Van Opstal, Marjan Boter, Daniëlle de Jong, Cardi van den Berg, Hennie T. Brüggenwirth, Hajo I. J. Wildschut, Annelies de Klein, Robert‐Jan H. Galjaard	2008	57
9	Benefits and Burdens of Using a SNP Array in Pregnancies at Increased Risk for the Common Aneuploidies Human Mutation ·Diane Van Opstal, Femke de Vries, Lutgarde C. P. Govaerts, Marjan Boter, Debora Lont, Stefanie van Veen, Marieke Joosten, Karin E. M. Diderich, Robert‐Jan Galjaard, Malgorzata Ilona Srebniak	2014	40
10	Stable X Chromosome Reactivation in Female Human Induced Pluripotent Stem Cells Stem Cell Reports ·Tahsin Stefan Barakat, Mehrnaz Ghazvini, Bas de Hoon, Tracy M.W.Y. Li, Bert Eussen, Hannie Douben, Reinier van der Linden, Nathalie van der Stap, Marjan Boter, Joop S.E. Laven, Robert‐Jan Galjaard, J. Anton Grootegoed, Annelies de Klein, Joost H. Gribnau	2015	35
11	Noninvasive prenatal testing as compared to chorionic villus sampling is more sensitive for the detection of confined placental mosaicism involving the cytotrophoblast Prenatal Diagnosis ·Diane Van Opstal, Geerke M. Eggenhuizen, Marieke Joosten, Karin E. M. Diderich, Lutgarde C. P. Govaerts, Robert‐Jan Galjaard, Attie T. J. I. Go, Maarten F. C. M. Knapen, Marjan Boter, Wai Y. Cheung, Nicole van Koetsveld, Stefanie van Veen, Walter G. de Valk, Fernanda Sarquis Jehee, Femke de Vries, Iris H.I.M. Hollink, Lies H. Hoefsloot, Malgorzata Ilona Srebniak	2020	32
12	Impact of the Y‐containing cell line on histological differentiation patterns in dysgenetic gonads Clinical Endocrinology ·M. Cools, Marjan Boter, R van Gurp, Hans Stoop, Pino J. Poddighe, Yun‐Fai Chris Lau, Stenvert L. S. Drop, Katja P. Wolffenbuttel, Leendert H. J. Looijenga	2007	30
13	Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts European Journal of Human Genetics ·Danielle C. M. Veenma, Erwin Brosens, Elisabeth de Jong, Cornelis P. van de Ven, Connie Meeussen, Titia E. Cohen‐Overbeek, Marjan Boter, Hubertus Eussen, Hannie Douben, Dick Tibboel, Annelies de Klein	2011	23
14	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 Ilona Srebniak, Maarten F. C. M. Knapen, MARIKE G. POLAK, Marieke Joosten, Karin E. M. Diderich, Lutgarde C. P. Govaerts, Marjan Boter, Joan N. R. Kromosoeto, Daniella A.C.M. van Hassel, Gido Huijbregts, Wilfred FJ van IJcken, Roger 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	22
15	Epidemiological and genomic evolution of the ongoing outbreak of clade Ib mpox virus in the eastern Democratic Republic of the Congo Nature Medicine ·Leandre Murhula Masirika, Jean Claude Udahemuka, Leonard Schuele, David F. Nieuwenhuijse, Pacifique Ndishimye, Marjan Boter, Justin Bengehya Mbiribindi, Cris Kacita, Trudie A. Lang, Christian Gortázar, Jean Pierre Musabyimana, Saria Otani, Frank M. Aarestrup, Freddy Belesi Siangoli, Bas B. Oude Munnink, Marion Koopmans Hit paper breakdown →	2025	22
16	Deletion of 14.7 Mb 2q32.3q33.3 with a marfanoid phenotype and hypothyroidism American Journal of Medical Genetics Part A ·Agnieszka Tomaszewska, Agnieszka Podbiol‐Palenta, Marjan Boter, Gabriela Geisler, Angelika Wawrzkiewicz‐Witkowska, Robert‐Jan H. Galjaard, Stanisław Zajączek, Malgorzata Ilona Srebniak	2013	20
17	Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis Molecular Cytogenetics ·Diane Van Opstal, Marjan Boter, Petra Noomen, Malgorzata Ilona Srebniak, Guus Hamers, Robert‐Jan H. Galjaard	2011	16
18	Unexpected finding of uniparental disomy mosaicism in term placentas: Is it a common feature in trisomic placentas? Prenatal Diagnosis ·Diane Van Opstal, Karin E. M. Diderich, Marieke Joosten, Lutgarde C. P. Govaerts, Joke Polak, Marjan Boter, Jasper J. Saris, Wai Y. Cheung, Stefanie van Veen, Robert van der Helm, Attie T. J. I. Go, Maarten F. C. M. Knapen, Dimitri N.M. Papatsonis, Anneke Dijkman, Femke de Vries, Robert‐Jan H. Galjaard, Lies H. Hoefsloot, Malgorzata Ilona Srebniak	2018	13
19	Placental studies elucidate discrepancies between NIPT showing a structural chromosome aberration and a differently abnormal fetal karyotype Prenatal Diagnosis ·Diane Van Opstal, Stefanie van Veen, Marieke Joosten, Karin E. M. Diderich, Lutgarde C. P. Govaerts, Joke Polak, Nicole van Koetsveld, Marjan Boter, Attie T. J. I. Go, Dimitri N.M. Papatsonis, Krista Prinsen, Lies H. Hoefsloot, Malgorzata Ilona Srebniak	2019	12
20	Mpox outbreak among men who have sex with men in Amsterdam and Rotterdam, the Netherlands: no evidence for undetected transmission prior to May 2022, a retrospective study Eurosurveillance ·Henry J.C. de Vries, Hannelore M Götz, Sylvia Maria Bruisten, Annemiek A. van der Eijk, Maria Prins, Bas B. Oude Munnink, Matthijs R. A. Welkers, Marcel Jonges, Richard Molenkamp, Brenda M. Westerhuis, Leonard Schuele, Arjen Stam, Marjan Boter, Elske Hoornenborg, Daphne G.J.C. Mulders, Mariken van der Lubben, Marion Koopmans	2023	12

About Marjan Boter

Marjan Boter is a scholar working on Pediatrics, Perinatology and Child Health, Virology, Genetics, Infectious Diseases and Epidemiology, having authored 32 papers that have together received 1.1k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (8 papers), Poxvirus research and outbreaks (6 papers), Fetal and Pediatric Neurological Disorders (3 papers), Herpesvirus Infections and Treatments (3 papers), SARS-CoV-2 and COVID-19 Research (2 papers), Mosquito-borne diseases and control (2 papers) and Virology and Viral Diseases (2 papers). The work is most often cited by research in Virology (111 citations), Pediatrics, Perinatology and Child Health (330 citations), Genetics (334 citations), Infectious Diseases (159 citations) and Modeling and Simulation (41 citations). Marjan Boter has collaborated with scholars based in Netherlands, Denmark and Rwanda. Frequent co-authors include Diane Van Opstal, Robert‐Jan H. Galjaard, Malgorzata Ilona Srebniak, Leendert H. J. Looijenga, Lutgarde C. P. Govaerts, Marieke Joosten, J. Wolter Oosterhuis, Katja P. Wolffenbuttel, Stenvert L. S. Drop and M. Cools. Their work appears in journals such as Eurosurveillance, European Journal of Human Genetics, Prenatal Diagnosis, Molecular Cytogenetics and Human Mutation.

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

Marjan Boter

Marjan Boter's Hit Papers

Peers

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Fields of papers citing papers by Marjan Boter

All Works

About Marjan Boter

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