Lutgarde Govaerts

1.4k citations

32 papers · 723 indexed · h-index 16

Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics 20
- Fetal and Pediatric Neurological Disorders 10
Genetics top 5%
- Genomic variations and chromosomal abnormalities 18
- Genomics and Rare Diseases 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genetics and Neurodevelopmental Disorders 3
Developmental Biology
- Congenital limb and hand anomalies 2
Infectious Diseases
- Parvovirus B19 Infection Studies 4
Endocrinology, Diabetes and Metabolism

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
Cited by: Pediatrics, Perinatology and Child Health Genetics Developmental Biology
Journals: PLoS ONE (2 papers)The Journal of Clinical Endocrinology & Metabolism (1 paper)Journal of Autism and Developmental Disorders (1 paper)
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

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

All Works

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20 of 20 papers shown

#	Work
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 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
2	How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies Clinical Genetics ·Jasmijn E. Klapwijk,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	2021	19
3	Social and medical need for whole genome high resolution NIPT 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,Krista Prinsen,Sam Riedijk,Attie T. J. I. Go,Robert‐Jan H. Galjaard,Lies H. Hoefsloot,Diane Van Opstal	2019	9
4	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 Govaerts,Joke Polak,Marjan Boter,Jasper J. Saris,Wai Y. Cheung,Stefanie van Veen,Robert van de 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 I. Srebniak	2018	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 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
6	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
7	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
8	Prenatal diagnosis of susceptibility loci for neurodevelopmental disorders – genetic counseling and pregnancy outcome in 57 cases 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,Katja de Graaf,Toon Toolenaar,Sanne van der Steen,Gido Huijbregts,Jeroen Knijnenburg,Femke de Vries,Diane Van Opstal,Robert‐Jan Galjaard	2016	9
9	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
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 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	2013	62
11	Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification 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	2013	27
12	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
13	Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow European Journal of Human Genetics ·Malgorzata I. Srebniak,Marjan Boter,Grétel Oudesluijs,Marieke Joosten,Lutgarde Govaerts,Diane Van Opstal,Robert‐Jan H. Galjaard	2011	81
14	Comparable Low-Level Mosaicism in Affected and Non Affected Tissue of a Complex CDH Patient PLoS ONE ·Danielle Veenma,Niels Beurskens,Hannie Douben,Bert Eussen,Petra Noomen,Lutgarde Govaerts,E. W. M. Grijseels,Maarten H. Lequin,Ronald R. de Krijger,Dick Tibboel,Annelies de Klein,Diane Van Opstal	2010	10
15	The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer 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,Femke van Erp,Nicoline Hoogerbrugge,Lianne van Kempen,Eric Schoenmakers,Anita Bonné,Eamonn R. Maher,Ad Geurts van Kessel	2009	22
16	Phenotypic consequences of a novel SCO2 gene mutation 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	2008	20
17	An incomplete trisomy 3 rescue resulting in a marker chromosome and UPD(3)—difficulties in interpretation Prenatal Diagnosis ·Malgorzata I. Srebniak,Petra Noomen,Pedro dos Santos,Dicky Halley,Raoul van de Graaf,Lutgarde Govaerts,Carine Wouters,Robert‐Jan H. Galjaard,Diane Van Opstal	2008	4
18	A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat 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	2002	12
19	Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14) American Journal of Medical Genetics ·Bert B.A. de Vries,Bert H.J. Eussen,Otto P. van Diggelen,Annet van der Heide,Wouter H. Deelen,Lutgarde Govaerts,Dick Lindhout,Carine Wouters,J. O. Van Hemel	1999	1
20	Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14) American Journal of Medical Genetics ·Bert B.A. de Vries,Bert H.J. Eussen,Otto P. van Diggelen,Annet van der Heide,Wouter H. Deelen,Lutgarde Govaerts,Dick Lindhout,Carine Wouters,J. O. Van Hemel	1999	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), Fetal and Pediatric Neurological Disorders (10 papers), Parvovirus B19 Infection Studies (4 papers), Genomics and Rare Diseases (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Congenital limb and hand anomalies (2 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.

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