Anniek Corveleyn

3.3k citations

44 papers · 1.3k indexed · h-index 17

Genetics top 5%
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 5
Genetics top 10%
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 5
Cancer Research
Neurology top 10%
Hematology top 10%
Cardiology and Cardiovascular Medicine
- Cardiomyopathy and Myosin Studies 8
- Cardiac electrophysiology and arrhythmias 6
Molecular Biology
- RNA modifications and cancer 6
- Ion channel regulation and function 5
- Congenital heart defects research 4
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 5

Co-authors: Gert Matthijs Erika Souche Hans Scheffer Marjan M. Weiss Helger G. Yntema Mariëlle Alders Egbert Bakker Sebastian Eck
Cited by: Genetics Cancer Research
Journals: Proceedings of the National Academy of Sciences (1 paper)Blood (1 paper)Neurology (2 papers)
Partner nations: Belgium United States Netherlands

In The Last Decade

Anniek Corveleyn

43 papers receiving 1.3k citations

Peers

Countries citing papers authored by Anniek Corveleyn

Since Specialization

Citations

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

Fields of papers citing papers by Anniek Corveleyn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Clinical application of multigene panel testing for bleeding, thrombotic, and platelet disorders: a 3-year Belgian experience Journal of Thrombosis and Haemostasis ·Christine Van Laer,Marc Jacquemin,Sarissa Baert,Veerle Labarque,Chantal Thys,Thomas Vanassche,Chris Van Geet,Peter Verhamme,Karen Willekens,Anniek Corveleyn,Kathelijne Peerlinck,Kathleen Freson	2023	13
2	Tools to differentiate between Filamin C and Titin truncating variant carriers: value of MRI European Journal of Human Genetics ·J. Jacobs,Lucas Van Aelst,Jeroen Breckpot,Anniek Corveleyn,Cuno Kuipéri,Matthias Dupont,Ward Heggermont,Katrien De Vadder,Rik Willems,Johan Van Cleemput,Jan Bogaert,Tomas Robyns	2023	3
3	Frequency of Participation in External Quality Assessment Programs Focused on Rare Diseases: Belgian Guidelines for Human Genetics Centers JMIR Medical Informatics ·Joséphine Lantoine,Anne Brysse,Vinciane Dideberg,Kathleen Claes,Sofie Symoens,Wim Coucke,Valérie Benoît,S. Rombout,Martine De Rycke,Sara Seneca,Lut Van Laer,Wim Wuyts,Anniek Corveleyn,Kris Van Den Bogaert,Catherine Rydlewski,Françoise Wilkin,Marie Ravoet,Elodie Fastré,Arnaud Capron,N Vandevelde	2021	0
4	Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the Literature Frontiers in Immunology ·Frederik Staels,Albrecht Betrains,Peter Doubel,Mathijs Willemsen,Vincent Cleemput,Steven Vanderschueren,Anniek Corveleyn,Isabelle Meyts,Ben Sprangers,Yanick J. Crow,Stéphanie Humblet‐Baron,Adrian Liston,Rik Schrijvers	2020	31
5	Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype Proceedings of the National Academy of Sciences ·Eline Blommaert,Romain Péanne,Н. А. Черепанова,Daisy Rymen,Frederik Staels,Jaak Jaeken,Valérie Race,Liesbeth Keldermans,Erika Souche,Anniek Corveleyn,Rebecca Sparkes,Kaustuv Bhattacharya,Christine Devalck,Rik Schrijvers,François Foulquier,Reid Gilmore,Gert Matthijs	2019	61
6	BCAP31-related syndrome: The first de novo report European Journal of Medical Genetics ·Berardo Rinaldi,Evelien Van Hoof,Anniek Corveleyn,Annick Van Cauter,Thomy de Ravel	2019	8
7	Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings PLoS Genetics ·Jacoba Louw,Ricardo Bastos,Xiaowen Chen,C Verdood,Anniek Corveleyn,Yaojuan Jia,Jeroen Breckpot,Marc Gewillig,Hilde Peeters,Massimo Santoro,Francis A. Barr,Koenraad Devriendt	2018	16
8	Discordance for placental mesenchymal dysplasia in a monochorionic diamniotic twin pregnancy: A case report Clinical Case Reports ·Willem Gheysen,David Strybol,Philippe Moerman,An Steylemans,Anniek Corveleyn,Luc De Catte,Isabel Couck,Liesbeth Lewi	2018	9
9	Massive parallel sequencing identifies RAPSN and PDHA1 mutations causing fetal akinesia deformation sequence European Journal of Paediatric Neurology ·Lore Winters,Elke Van Hoof,Luc De Catte,Kris Van Den Bogaert,Thomy de Ravel,Liesbeth De Waele,Anniek Corveleyn,Jeroen Breckpot	2017	13
10	Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutation European Journal of Medical Genetics ·Aleksandra Nijak,Maaike Alaerts,Cuno Kuipéri,Anniek Corveleyn,Bert Suys,Bernard P. Paelinck,Johan Saenen,Emeline M. Van Craenenbroeck,Lut Van Laer,Bart Loeys,Aline Verstraeten	2017	17
11	MEIS2 involvement in cardiac development, cleft palate, and intellectual disability American Journal of Medical Genetics Part A ·Jacoba Louw,Anniek Corveleyn,Yaojuan Jia,Greet Hens,Marc Gewillig,Koenraad Devriendt	2015	40
12	The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects American Journal of Medical Genetics Part A ·Yaojuan Jia,Jacoba Louw,Jeroen Breckpot,Bert Callewaert,Catherine Barréa,Yves Sznajer,Marc Gewillig,Erika Souche,Luc Dehaspe,Joris Vermeesch,Diether Lambrechts,Koenraad Devriendt,Anniek Corveleyn	2015	36
13	EuroGentest guidelines for diagnostic next generation sequencing European Journal of Human Genetics ·Gert Matthijs,Mariëlle Alders,Peter Bauer,Anniek Corveleyn,Sebastian Eck,Ilse Feenstra,Valérie Race,Hans Scheffer,E Sistrmans,Erika Souche,Marc Sturm,Maximilian E. R. Weiss,Helger G. Yntema	2014	3
14	Reduced Penetrance and Variable Expression of SCN5A Mutations and the Importance of Co-inherited Genetic Variants: Case Report and Review of the Literature Indian Pacing and Electrophysiology Journal ·Tomas Robyns,Dieter Nuyens,Lieve Van Casteren,Anniek Corveleyn,Thomy de Ravel,Hein Heidbüchel,Rik Willems	2014	18
15	A novel heterozygous mutation of three consecutive nucleotides causing Apert syndrome in a Congolese family European Journal of Medical Genetics ·Aimé Lumaka,Gerrye Mubungu,Papino Mukaba,Pierre Mutantu,Gertrude Luyeye,Anniek Corveleyn,Bruno‐Paul Tady,Prosper Lukusa-Tshilobo,Koenraad Devriendt	2014	5
16	Massive parallel Sequencing in non-syndromic familial CHD European Journal of Human Genetics ·Yaojuan Jia,Jacoba Louw,Jeroen Breckpot,Marc Gewillig,Koenraad Devriendt,Anniek Corveleyn	2013	1
17	Heterozygous α1-antitrypsin Z allele mutation in presumed healthy donor livers used for transplantation European Journal of Gastroenterology & Hepatology ·Philip Roelandt,Pieter Dobbels,Mina Komuta,Anniek Corveleyn,Marie‐Paule Emonds,Tania Roskams,Raymond Aerts,Diethard Monbaliu,Louis Libbrecht,Wim Laleman,Chris Verslype,Werner Van Steenbergen,Van der Merwe,Jacques Pirenne,Frederik Nevens,David Cassiman	2013	13
18	Cellular transformation of NIH3T3 fibroblasts by CIZ/NMP4 fusions Journal of Cellular Biochemistry ·Anniek Corveleyn,Hilde Janssen,Alessandra Cadete Martini,Riet Somers,Jan Cools,Peter Marynen	2005	9
19	The TET RNA-binding proteins, EWSR1 and TAF15, are involved in acute lymphoblastic leukemia, through fusion with a new transcription factor, CIZ/NMP4 Blood ·Alessandra Cadete Martini,Hilde Janssen,C Bilhou‐Nabera,R La Starza,Anniek Corveleyn,C Mecucci,Anne Hagemeijer‐Hausman,Peter Marynen	2002	2
20	A Physical, Transcript, and Deletion Map of Chromosome Region 12p12.3 Flanked byETV6andCDKN1B:Hypermethylation of theLRP6CpG Island in Two Leukemia Patients with Hemizygous del(12p) Genomics ·Mathijs Baens,Iwona Włodarska,Anniek Corveleyn,Inge Hoornaert,Anne Hagemeijer,Peter Marynen	1999	29

About Anniek Corveleyn

Anniek Corveleyn is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Genetics, having authored 44 papers that have together received 1.3k indexed citations. Recurring topics across this work include Cardiomyopathy and Myosin Studies (8 papers), Genomics and Rare Diseases (7 papers), Cardiac electrophysiology and arrhythmias (6 papers), RNA modifications and cancer (6 papers), Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Ion channel regulation and function (5 papers) and Congenital heart defects research (4 papers). The work is most often cited by research in Genetics (430 citations), Genetics (133 citations) and Cancer Research (157 citations). Anniek Corveleyn has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Gert Matthijs, Erika Souche, Hans Scheffer, Marjan M. Weiss, Helger G. Yntema, Mariëlle Alders, Egbert Bakker, Sebastian Eck, Marc Sturm and Erik A. Sistermans. Their work appears in journals such as Proceedings of the National Academy of Sciences, Blood and Neurology.

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