Concepedia

Author

Anniek Corveleyn

KU LeuvenORCID

Also Known As

A Corveleyn, A. Corveleyn, Anniek Corveleyn, CORVELEYN Anniek, Corveleyn, Anniek, Elfriede Swinnen, Pierre Corre

130

Publications

3.3K

Citations

24

H-Index

77

Concepts

All Affiliations

KU LeuvenInsermZiekenhuis Oost-LimburgCentre National de la Recherche ScientifiqueAssistance Publique – Hôpitaux de Paris
AC

About

Anniek Corveleyn is an author at KU Leuven specializing in medicine, genetics, and pathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

16

20

930

2

Public Health

3

3

119

3

Engineering

1

1

13

4

Allergy

1

1

22

5

Cell Biology

1

1

118

Anniek Corveleyn

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36

Publications

2K

Citations

21

H-Index

YearCitations

Guidelines for diagnostic next-generation sequencing

Gert Matthijs, Erika Souche, Mariëlle Alders,

European Journal of Human Genetics

2015

497

Disease-associated mutations identify a novel region in human STING necessary for the control of type I interferon signaling

Isabelle Melki, Y Rose, Carolina Uggenti,

Journal of Allergy and Clinical Immunology

2017

198

Inherited p40phox deficiency differs from classic chronic granulomatous disease

Annemarie van de Geer, Alejandro Nieto-Patlán, Douglas B. Kuhns,

Journal of Clinical Investigation

2018

129

Recurrent rearrangement of the Ewing's sarcoma gene, EWSR1, or its homologue, TAF15, with the transcription factor CIZ/NMP4 in acute leukemia.

Alessandra Cadete Martini, Roberta La Starza, Hilde Janssen,

PubMed

2002

118

Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

Judy Savige, Helen Storey, E. Watson,

European Journal of Human Genetics

2021

117

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Roddy Walsh, Najim Lahrouchi, Florence Kyndt,

Genetics in Medicine

2020

100

Mutations in <i>MAGT1</i> lead to a glycosylation disorder with a variable phenotype

Eline Blommaert, Romain Péanne, Daisy Rymen,

Proceedings of the National Academy of Sciences

2019

88

Criteria for HNF1B analysis in patients with congenital abnormalities of kidney and urinary tract

Anke Raaijmakers, Anniek Corveleyn, Koenraad Devriendt,

Nephrology Dialysis Transplantation

2014

73

Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiency

Robin Lemmens, Alessandra Maugeri, Hans W.M. Niessen,

Human Molecular Genetics

2012

68

<i>MEIS2</i> involvement in cardiac development, cleft palate, and intellectual disability

Jacoba Louw, Anniek Corveleyn, Yaojuan Jia,

American Journal of Medical Genetics Part A

2015

66

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