Erik A. Sistermans

11.7k citations

123 papers · 5.6k indexed · 1 hit paper · h-index 37

Genetics top 0.5%
- Genomic variations and chromosomal abnormalities 30
- Genetics and Neurodevelopmental Disorders 17
- Genomics and Rare Diseases 12
Pediatrics, Perinatology and Child Health top 1%
- Prenatal Screening and Diagnostics 37
- Fetal and Pediatric Neurological Disorders 21
Molecular Biology top 2%
- Congenital heart defects research 9
Developmental Neuroscience top 5%
Cancer Research top 5%
- Cancer Genomics and Diagnostics 11
Infectious Diseases
- Parvovirus B19 Infection Studies 16

Co-authors: Bert B.A. de Vries Willy M. Nillesen Ilse J. de Wijs David A. Koolen Nicole de Leeuw Marjan M. Weiss Rolph Pfundt Marcel Reinders
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Nucleic Acids Research (1 paper)Nature Genetics (2 papers)SHILAP Revista de lepidopterología (1 paper)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Erik A. Sistermans

120 papers receiving 5.4k citations

Hit Papers

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Peers

Countries citing papers authored by Erik A. Sistermans

Since Specialization

Citations

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

Fields of papers citing papers by Erik A. Sistermans

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erik A. Sistermans. 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 Erik A. Sistermans. The network helps show where Erik A. Sistermans may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Evaluating the effectiveness of pre-operative diagnosis of ovarian cancer using minimally invasive liquid biopsies by combining serum human epididymis protein 4 and cell-free DNA in patients with an ovarian mass International Journal of Gynecological Cancer ·Duco Gaillard,Pien Lof,Erik A. Sistermans,Tom Mokveld,Hugo M. Horlings,Constantijne H. Mom,Marcel Reinders,Frédéric Amant,Daan van den Broek,Lodewyk F.A. Wessels,Christianne Lok,Marco van Gent,Majoie Hemelaar,WM van Baal,M.B. Verbruggen,F Rosier-van Dunné,BBJ Hermse	2024	3
2	Implementing non-invasive prenatal testing in a national screening program: Lessons learned from the TRIDENT studies Best Practice & Research Clinical Obstetrics & Gynaecology ·Matea Skojo,Malgorzata I. Srebniak,Lidewij Henneman,Erik A. Sistermans,Karuna R. M. van der Meij	2024	1
3	In Vitro CRISPR-Cas12a-Based Detection of Cancer-Associated TP53 Hotspot Mutations Beyond the crRNA Seed Region The CRISPR Journal ·Kavish A.V. Kohabir,Lars O. Nooi,Arjen Brink,Ruud H. Brakenhoff,Erik A. Sistermans,Rob M.F. Wolthuis	2023	12
4	Fetal fraction of cell-free DNA in noninvasive prenatal testing and adverse pregnancy outcomes: a nationwide retrospective cohort study of 56,110 pregnant women American Journal of Obstetrics and Gynecology ·Ellis C. Becking,P Scheffer,Jens Henrichs,Caroline J. Bax,Neeltje Crombag,Marjan M. Weiss,Merryn Macville,Diane Van Opstal,Elles M. J. Boon,Erik A. Sistermans,Lidewij Henneman,Ewoud Schuit,Mireille N. Bekker	2023	10
5	Association between low fetal fraction in cell‐free DNA screening and fetal chromosomal aberrations: A systematic review and meta‐analysis Prenatal Diagnosis ·Ellis C. Becking,Ewoud Schuit,Sophie M. E. van Baar de Knegt,Erik A. Sistermans,Lidewij Henneman,Mireille N. Bekker,P Scheffer	2023	4
6	Non‐invasive prenatal testing for everybody or contingent screening? Prenatal Diagnosis ·Karuna R. M. van der Meij,Lidewij Henneman,Erik A. Sistermans	2022	5
7	The cell‐free DNA virome of 108,349 Dutch pregnant women Prenatal Diagnosis ·Jasper Linthorst,Moezammin M. M. Baksi,Matthijs R. A. Welkers,Erik A. Sistermans	2022	16
8	Uptake of fetal aneuploidy screening after the introduction of the non‐invasive prenatal test: A national population‐based register study Acta Obstetricia Et Gynecologica Scandinavica ·Karuna R. M. van der Meij,Maurike Dorothea de Groot-van der Mooren,Ellen W. S. Carbo,Mijntje J. Pieters,Wendy Rodenburg,Erik A. Sistermans,Martina C. Cornel,Lidewij Henneman	2021	30
9	International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies Prenatal Diagnosis ·Glenn E. Palomaki,Rossa W. K. Chiu,Mark D. Pertile,Erik A. Sistermans,Yuval Yaron,Joris Vermeesch,Neeta L. Vora,Robert G. Best,Louise Wilkins‐Haug	2020	41
10	The bivariate NRIP1/ZEB2 RNA marker permits non-invasive presymptomatic screening of pre-eclampsia Scientific Reports ·Vera Manders,Allerdien Visser,Remco Keijser,Naomi Min,Ankie Poutsma,Joyce Mulders,Tarah van den Berkmortel,Marjolein Hortensius,Aldo Jongejan,Eva Pajkrt,Erik A. Sistermans,Daoud Sie,Myron G. Best,Tom Würdinger,Marjon A. de Boer,Gijs Afink,Cees B.M. Oudejans	2020	5
11	A novel CCM2 variant in a family with non‐progressive cognitive complaints and cerebral microbleeds American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Petra E. Cohn‐Hokke,Henne Holstege,Marjan M. Weiss,Wiesje M. van der Flier,Frederik Barkhof,Erik A. Sistermans,Yolande A.L. Pijnenburg,John C. van Swieten,Hanne Meijers‐Heijboer,Philip Scheltens	2016	4
12	Trial by Dutch laboratories for evaluation of non‐invasive prenatal testing. Part I—clinical impact Prenatal Diagnosis ·Dick Oepkes,Godelieve C.M.L. Page‐Christiaens,Caroline J. Bax,Mireille N. Bekker,Catia M. Bilardo,Elles M. J. Boon,G. Heleen Schuring‐Blom,A. Coumans,Brigitte H. W. Faas,Robert‐Jan H. Galjaard,Attie T. J. I. Go,Lidewij Henneman,Merryn Macville,Eva Pajkrt,Ron F. Suijkerbuijk,Karin Huijsdens–van Amsterdam,Diane Van Opstal,E. J. T. Verweij,Marjan M. Weiss,Erik A. Sistermans	2016	110
13	A novel homozygous 5 bp deletion in FKBP10 causes clinically Bruck syndrome in an Indonesian patient European Journal of Medical Genetics ·Eva D. Setijowati,Fleur S. van Dijk,Jan M. Cobben,Rick R. van Rijn,Erik A. Sistermans,Sultana MH Faradz,S. Kawiyana,Gerard Pals	2011	23
14	Monitoring Standards for Molecular Genetic Testing in the United Kingdom, The Netherlands, and Ireland Genetic Testing ·Simon Ramsden,Zandra C. Deans,David Robinson,Roger Mountford,Erik A. Sistermans,Wayne W. Grody,Shirley McQuaid,Simon Patton,S Stenhouse	2006	27
15	A novel 2.3 Mb microduplication of 12q24.21q24.23 detected by genome-wide tiling-path resolution array comparative genomic hybridization in a girl with syndromic mental retardation Clinical Dysmorphology ·Mariken Ruiter,David A. Koolen,Rolph Pfundt,Nicole de Leeuw,Harry M.J. Klinkers,Erik A. Sistermans,Joris A. Veltman,Bert B.A. de Vries	2006	7
16	Interstitial 2.2 Mb deletion at 9q34 in a patient with mental retardation but without classical features of the 9q subtelomeric deletion syndrome American Journal of Medical Genetics Part A ·Tjitske Kleefstra,David A. Koolen,Willy M. Nillesen,Nicole de Leeuw,Ben C.J. Hamel,Joris A. Veltman,Erik A. Sistermans,Hans van Bokhoven,Conny van Ravenswaay,Bert B.A. de Vries	2006	16
17	Cerebrotendinous xanthomatosis: report of two Brazilian brothers Arquivos de Neuro-Psiquiatria ·Marcos Christiano Lange,Viviane Flumignan Zétola,Hélio Afonso Ghizoni Teive,Rosana Hermínia Scola,Ana Paula Trentin,Jorge A. Zavala,Eduardo Rafael Pereira,Salmo Raskin,Lineu César Werneck,Erik A. Sistermans	2004	8
18	Mutation detection in the aspartoacylase gene in 17 patients with Canavan disease: four new mutations in the non-Jewish population European Journal of Human Genetics ·Erik A. Sistermans,I.F.M. de Coo,Hetty M. van Beerendonk,Bwee Tien Poll‐The,Wim J. Kleijer,Bernard A. van Oost	2000	33
19	Gene symbol: PLP. Disease: Pelizaeus-Merzbacher disease. Human Genetics ·Erik A. Sistermans,Ilse J. de Wijs,F. Elmslie,K. Woodward	1999	2
20	Tissue- and cell-specific distribution of creatine kinase B: A new and highly specific monoclonal antibody for use in immunohistochemistry Cell and Tissue Research ·Erik A. Sistermans,Yvette J.M. de Kok,Wilma Peters,Leo A. Ginsel,P. H. K. Jap,B. Wieringa	1995	53

About Erik A. Sistermans

Erik A. Sistermans is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Cancer Research, having authored 123 papers that have together received 5.6k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (37 papers), Genomic variations and chromosomal abnormalities (30 papers), Fetal and Pediatric Neurological Disorders (21 papers), Genetics and Neurodevelopmental Disorders (17 papers), Parvovirus B19 Infection Studies (16 papers), Genomics and Rare Diseases (12 papers), Cancer Genomics and Diagnostics (11 papers) and Congenital heart defects research (9 papers). The work is most often cited by research in Genetics (2.7k citations), Pediatrics, Perinatology and Child Health (1.0k citations) and Molecular Biology (2.9k citations). Erik A. Sistermans has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Bert B.A. de Vries, Willy M. Nillesen, Ilse J. de Wijs, David A. Koolen, Nicole de Leeuw, Marjan M. Weiss, Rolph Pfundt, Marcel Reinders, Roy Straver and Cees B.M. Oudejans. Their work appears in journals such as Nucleic Acids Research, Nature Genetics and SHILAP Revista de lepidopterología.

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