基本信息
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职业迁徙
个人简介
Specialization
Erik Sistermans is a Clinical Laboratory Geneticist, with both a national (VKGL) and a European (EBMG) registration. He is head of the Genome analysis laboratory of AmsterdamUMC, which involves the Genome Diagnostics laboratory, the NIPT screening laboratory and the Core Facility Genomics (CFG).
Focus of research
Erik Sistermans is professor of human genetics, at the dept. of Human Genetics, Amsterdam UMC. He is member of the research board of the Amsterdam Reproduction & Development research institute.
Research interests focus on the improvement of prenatal screening and diagnostics. Based on the results obtained with the Dutch TRIDENT studies (Trial by Dutch laboratories for Evaluation of Non-Invasive Prenatal Testing), we are investigating genetic factors involved in clinical problems that can occur during and after pregnancy, such as growth restriction, early fetal demise and preeclampsia. Another interest is widening the scope of NIPT, what is technologically feasible and how can this be implemented in a responsible way.
Areas of interest: Genome diagnostics, prenatal screening and diagnostics, bioinformatics.
Erik Sistermans is board member of the Dutch non-invasive prenatal test (NIPT) Consortium and project leader of the TRIDENT studies. He is board member of the VKGL (Vereniging Klinisch Genetische Laboratoriumdiagnostiek), chair of the advisory board of Genomic Quality Assessment (GenQA) and associate editor of Extracellular Vesicles and Circulating Nucleic Acids (EVCNA).
He (co-)published over 135 international articles (H-index 45).
研究兴趣
论文共 216 篇作者统计合作学者相似作者
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Matthew Jensen,Corrine Smolen,Anastasia Tyryshkina,Lucilla Pizzo,Deepro Banerjee, Matthew Oetjens,Hermela Shimelis,Cora M Taylor,Vijay Kumar Pounraja,Hyebin Song, Laura Rohan,Emily Huber,Laila El Khattabi,Ingrid van de Laar,Rafik Tadros,Connie Bezzina, Marjon van Slegtenhorst,Janneke Kammeraad,Paolo Prontera,Jean-Hubert Caberg, Harry Fraser, Siddhartha Banka,Anke Van Dijck,Charles Schwartz,Els Voorhoeve,Patrick Callier,Anne-Laure Mosca-Boidron,Nathalie Marle,Mathilde Lefebvre,Kate Pope,Penny Snell,Amber Boys,Paul J Lockhart,Myla Ashfaq,Elizabeth McCready, Margaret Nowacyzk,Lucia Castiglia,Ornella Galesi,Emanuela Avola,Teresa Mattina,Marco Fichera, Maria Grazia Bruccheri, Giuseppa Maria Luana Mandarà,Francesca Mari,Flavia Privitera,Ilaria Longo,Aurora Curró,Alessandra Renieri,Boris Keren,Perrine Charles,Silvestre Cuinat,Mathilde Nizon,Olivier Pichon,Claire Bénéteau,Radka Stoeva,Dominique Martin-Coignard, Sophia Blesson,Cedric Le Caignec,Sandra Mercier,Marie Vincent,Christa Martin,Katrin Mannik,Alexandre Reymond,Laurence Faivre,Erik Sistermans,R Frank Kooy,David J Amor,Corrado Romano, Joris Andrieux,Santhosh Girirajan
medRxiv the preprint server for health sciences (2024)
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 769-769
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Best Practice & Research Clinical Obstetrics & Gynaecologypp.102543, (2024)
International journal of gynecological cancer : official journal of the International Gynecological Cancer Societyno. 5 (2024): 713-721
Brigitte H. W. Faas,Galuh Astuti,Willem J. G. Melchers, Annette Reuss,Christian Gilissen,Merryn V. E. Macville, Stijn A. I. Ghesquiere, Leonieke M. H. Houben,Malgorzata Ilona Srebniak, Geert Geeven,Janette C. Rahamat-Langendoen,Erik A. Sistermans,Jasper Linthorst
EBioMedicine (2024): 104983-104983
American journal of obstetrics and gynecologyno. 2 (2023): 244.e1-244.e18
PloS oneno. 4 (2023): e0284493-e0284493
Prenatal diagnosisno. 4 (2023): 381-388
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作者统计
#Papers: 216
#Citation: 8775
H-Index: 48
G-Index: 90
Sociability: 7
Diversity: 0
Activity: 2
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