Lutgarde Govaerts

1.4k citations

32 papers · 723 indexed · h-index 16

Pediatrics, Perinatology and Child Health top 2%
Genetics top 5%
Molecular Biology
Surgery
Infectious Diseases

Co-authors: Diane Van Opstal Malgorzata I. Srebniak Marieke Joosten Karin E. M. Diderich Robert‐Jan H. Galjaard Marjan Boter Maarten F. C. M. Knapen Attie T. J. I. Go
Topics: Prenatal Screening and Diagnostics (20 papers)Genomic variations and chromosomal abnormalities (18 papers)Fetal and Pediatric Neurological Disorders (10 papers)
Cited by: Pediatrics, Perinatology and Child Health Genetics Developmental Biology
Journals: PLoS ONE The Journal of Clinical Endocrinology & Metabolism Journal of Autism and Developmental Disorders
Partner nations: Netherlands Belgium United Kingdom

In The Last Decade

Lutgarde Govaerts

32 papers receiving 709 citations

Peers

Countries citing papers authored by Lutgarde Govaerts

Since Specialization

Citations

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

Fields of papers citing papers by Lutgarde Govaerts

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lutgarde Govaerts

This figure shows the co-authorship network connecting the top 25 collaborators of Lutgarde Govaerts. A scholar is included among the top collaborators of Lutgarde Govaerts based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lutgarde Govaerts. Lutgarde Govaerts is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	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 2023 ·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	2
2	How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies 2021 ·Clinical Genetics ·(unknown),Malgorzata I. Srebniak,Attie T. J. I. Go,Lutgarde Govaerts,Celine Lewis,Jennifer Hammond,Melissa Hill,Stina Lou,Ida Vogel,Kelly E. Ormond,Karin E. M. Diderich,Hennie T. Brüggenwirth,Sam Riedijk	19
3	Social and medical need for whole genome high resolution NIPT 2019 ·Molecular Genetics & Genomic Medicine ·Malgorzata I. Srebniak,Maarten F. C. M. Knapen,Lutgarde Govaerts,Marike Polak,Marieke Joosten,Karin E. M. Diderich,Laura J. C. M. van Zutven,(unknown),Sam Riedijk,Attie T. J. I. Go,Robert‐Jan H. Galjaard,Lies H. Hoefsloot,Diane Van Opstal	9
4	Unexpected finding of uniparental disomy mosaicism in term placentas: Is it a common feature in trisomic placentas? 2018 ·Prenatal Diagnosis ·Diane Van Opstal,Karin E. M. Diderich,Marieke Joosten,Lutgarde Govaerts,(unknown),Marjan Boter,Jasper J. Saris,(unknown),(unknown),(unknown),Attie T. J. I. Go,Maarten F. C. M. Knapen,Dimitri N.M. Papatsonis,Anneke Dijkman,(unknown),Robert‐Jan H. Galjaard,Lies H. Hoefsloot,Malgorzata I. Srebniak	11
5	The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies 2017 ·Human Mutation ·Malgorzata I. Srebniak,Maarten F. C. M. Knapen,Marike Polak,Marieke Joosten,Karin E. M. Diderich,Lutgarde Govaerts,Marjan Boter,(unknown),(unknown),(unknown),Wilfred F. J. van IJcken,R. Heydanus,Anneke Dijkman,(unknown),Femke A.T. de Vries,Jeroen Knijnenburg,Attie T. J. I. Go,Robert‐Jan H. Galjaard,Diane Van Opstal	18
6	Enlarged NT (≥3.5 mm) in the first trimester – not all chromosome aberrations can be detected by NIPT 2016 ·Molecular Cytogenetics ·Malgorzata I. Srebniak,(unknown),Karin E. M. Diderich,Lutgarde Govaerts,Marieke Joosten,Maarten F. C. M. Knapen,(unknown),(unknown),(unknown),Attie T. J. I. Go,R. J. H. Galjaard,Diane Van Opstal	30
7	False Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature Review 2016 ·PLoS ONE ·Diane Van Opstal,Malgorzata I. Srebniak,(unknown),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,(unknown)	38
8	Prenatal diagnosis of susceptibility loci for neurodevelopmental disorders – genetic counseling and pregnancy outcome in 57 cases 2016 ·Prenatal Diagnosis ·Lutgarde Govaerts,Malgorzata I. Srebniak,Karin E. M. Diderich,Marieke Joosten,Sam Riedijk,Maarten F. C. M. Knapen,Attie T. J. I. Go,Dimitri Papatsonis,(unknown),(unknown),(unknown),(unknown),Jeroen Knijnenburg,(unknown),Diane Van Opstal,Robert‐Jan Galjaard	9
9	Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs 2015 ·European Journal of Human Genetics ·Malgorzata I. Srebniak,Karin E. M. Diderich,Marieke Joosten,Lutgarde Govaerts,Jeroen Knijnenburg,(unknown),Marjan Boter,(unknown),Maarten F. C. M. Knapen,(unknown),Attie T. J. I. Go,Robert‐Jan H. Galjaard,Diane Van Opstal	55
10	The Social Behavioral Phenotype in Boys and Girls with an Extra X Chromosome (Klinefelter Syndrome and Trisomy X): A Comparison with Autism Spectrum Disorder 2013 ·Journal of Autism and Developmental Disorders ·Sophie van Rijn,Lex Stockmann,Martine Borghgraef,Hilgo Bruining,Conny M.A. van Ravenswaaij‐Arts,Lutgarde Govaerts,Kerstin Hansson,Hanna Swaab	62
11	Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification 2013 ·European Journal of Human Genetics ·Malgorzata I. Srebniak,Karin E. M. Diderich,Lutgarde Govaerts,Marieke Joosten,Sam Riedijk,R. J. H. Galjaard,Diane Van Opstal	27
12	Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities 2012 ·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	55
13	Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow 2011 ·European Journal of Human Genetics ·Malgorzata I. Srebniak,Marjan Boter,Grétel Oudesluijs,Marieke Joosten,Lutgarde Govaerts,Diane Van Opstal,Robert‐Jan H. Galjaard	81
14	Comparable Low-Level Mosaicism in Affected and Non Affected Tissue of a Complex CDH Patient 2010 ·PLoS ONE ·Danielle Veenma,(unknown),Hannie Douben,Bert Eussen,(unknown),Lutgarde Govaerts,E. W. M. Grijseels,Maarten H. Lequin,Ronald R. de Krijger,Dick Tibboel,Annelies de Klein,Diane Van Opstal	10
15	The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer 2009 ·Cancer Genetics and Cytogenetics ·Roland P. Kuiper,Lilian Vreede,Ramprasath Venkatachalam,Chris Ricketts,Eveline J. Kamping,Eugène T.P. Verwiel,Lutgarde Govaerts,Maria Dêbiec‐Rychter,Evelyne Lerut,(unknown),Nicoline Hoogerbrugge,(unknown),Eric Schoenmakers,(unknown),Eamonn R. Maher,Ad Geurts van Kessel	22
16	Phenotypic consequences of a novel SCO2 gene mutation 2008 ·American Journal of Medical Genetics Part A ·Robert M. Verdijk,Ronald R. de Krijger,Kees Schoonderwoerd,Valeria Tiranti,Hubert J.M. Smeets,Lutgarde Govaerts,I.F.M. de Coo	20
17	An incomplete trisomy 3 rescue resulting in a marker chromosome and UPD(3)—difficulties in interpretation 2008 ·Prenatal Diagnosis ·Malgorzata I. Srebniak,(unknown),(unknown),Dicky Halley,Raoul van de Graaf,Lutgarde Govaerts,Carine Wouters,Robert‐Jan H. Galjaard,Diane Van Opstal	4
18	A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat 2002 ·Cancer Genetics and Cytogenetics ·Imke M. Veltman,Martien van Asseldonk,Marga Schepens,Hans Stoop,Leendert H. J. Looijenga,Carine Wouters,Lutgarde Govaerts,Ron F. Suijkerbuijk,Ad Geurts van Kessel	12
19	Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14) 1999 ·American Journal of Medical Genetics ·Bert B.A. de Vries,Bert H.J. Eussen,Otto P. van Diggelen,(unknown),(unknown),Lutgarde Govaerts,Dick Lindhout,Carine Wouters,J. O. Van Hemel	1
20	Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14) 1999 ·American Journal of Medical Genetics ·(unknown),Bert H.J. Eussen,Otto P. van Diggelen,(unknown),(unknown),Lutgarde Govaerts,Dick Lindhout,Carine Wouters,J. O. Van Hemel	12

About Lutgarde Govaerts

Lutgarde Govaerts is a scholar working on Pediatrics, Perinatology and Child Health, Developmental Biology and Genetics, having authored 32 papers that have together received 723 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (18 papers) and Fetal and Pediatric Neurological Disorders (10 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (459 citations), Genetics (441 citations) and Developmental Biology (12 citations). Lutgarde Govaerts has collaborated with scholars based in Netherlands, Belgium and United Kingdom. Frequent co-authors include Diane Van Opstal, Malgorzata I. Srebniak, Marieke Joosten, Karin E. M. Diderich, Robert‐Jan H. Galjaard, Marjan Boter, Maarten F. C. M. Knapen, Attie T. J. I. Go, Grétel Oudesluijs and Anita C. S. Hokken‐Koelega. Their work appears in journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Journal of Autism and Developmental Disorders.

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.

Explore authors with similar magnitude of impact