Catheline Vilain

3.4k total citations
39 papers, 712 citations indexed

About

Catheline Vilain is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Catheline Vilain has authored 39 papers receiving a total of 712 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 15 papers in Genetics and 5 papers in Surgery. Recurrent topics in Catheline Vilain's work include RNA regulation and disease (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Metabolism and Genetic Disorders (4 papers). Catheline Vilain is often cited by papers focused on RNA regulation and disease (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Metabolism and Genetic Disorders (4 papers). Catheline Vilain collaborates with scholars based in Belgium, France and United States. Catheline Vilain's co-authors include Gilbert Vassart, Jasmine Parma, Marc Abramowicz, Guy Decaux, Claudine Heinrichs, Frédéric Vandergheynst, B. Renneboog, Laurence Duprez, Sabine Costagliola and P Malvaux and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Catheline Vilain

36 papers receiving 689 citations

Peers

Countries citing papers authored by Catheline Vilain

Since Specialization

Citations

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

Fields of papers citing papers by Catheline Vilain

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catheline Vilain

This figure shows the co-authorship network connecting the top 25 collaborators of Catheline Vilain. A scholar is included among the top collaborators of Catheline Vilain 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 Catheline Vilain. Catheline Vilain is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Solute Carrier 45A1: A New Cerebral Glucose Transporter Brain Disorder with Focal Refractory Epilepsy Responsive to Ketogenic Diet and Acetazolamide 2025 ·Neuropediatrics ·(unknown), (unknown), Catheline Vilain, Corinne De Laet, (unknown), Claudine Sculier, Simon Baijot, Alec Aeby	0
2	A milder form of NSRP1‐associated neurodevelopmental disorder, caused by a missense variant in the nuclear localization signal 2024 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Julie Soblet, Sonia Van Dooren, Catharina Olsen, Toon Janssen, (unknown), Chang‐Duk Jun, Guillaume Smits, Sandra Coppens, Catheline Vilain	0
3	Comprehensive evaluation of the implementation of episignatures for diagnosis of neurodevelopmental disorders (NDDs) 2023 ·Human Genetics ·(unknown), (unknown), (unknown), (unknown), Bruno Pichon, (unknown), Catheline Vilain, Catharina Olsen, Sonia Van Dooren, Guillaume Smits, Matthieu Defrance	3
4	A novel human iPSC model of COL4A1/A2 small vessel disease unveils a key pathogenic role of matrix metalloproteinases 2023 ·Stem Cell Reports ·(unknown), Mary Goodwin-Trotman, Steven Bell, (unknown), (unknown), Catheline Vilain, Marc Abramowicz, Stuart M. Allan, Tao Wang, M. Zameel Cader, Karen Horsburgh, Tom Van Agtmael, Sanjay Sinha, Hugh S. Markus, Alessandra Granata	11
5	Two siblings with Bosch-Boonstra-Schaaf optic atrophy syndrome due to parental gonadal mosaicism 2023 ·European Journal of Medical Genetics ·(unknown), Catheline Vilain, Koenraad Devriendt, Ingele Casteels, Guillaume Smits, Julie Soblet, Irina Balikova	1
6	Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations 2021 ·Orphanet Journal of Rare Diseases ·Pascal Brouillard, Matthieu J. Schlögel, (unknown), Raphaël Helaers, Angela Queisser, (unknown), (unknown), Sandra Schmitz, Philippe Clapuyt, Frank Hammer, A. Dompmartin, (unknown), Jussi Laranne, (unknown), Catheline Vilain, Laurence M. Boon, Miikka Vikkula	32
7	Congenital Arthrogryposis - Renal dysfunction-Cholestasis (ARC) syndrome : a case report 2021 ·(unknown), (unknown), Catheline Vilain, Julie Soblet, (unknown), (unknown)	0
8	A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene 2021 ·SHILAP Revista de lepidopterología ·(unknown), G. Garofalo, T. Cos, Julie Désir, Xin Kang, Kathelijn Keymolen, Julie Soblet, (unknown), Catheline Vilain, (unknown), Marie Cassart	2
9	Acquired Zinc Deficiency Mimicking Acrodermatitis Enteropathica in a Breast-Fed Premature Infant 2021 ·Pediatric Reports ·(unknown), Corinne De Laet, Guillaume Smits, (unknown), Guillaume Deprez, Catheline Vilain, (unknown), (unknown)	6
10	Digestive involvement in a severe form of Snyder-Robinson syndrome: Possible expansion of the phenotype 2020 ·European Journal of Medical Genetics ·(unknown), (unknown), Martine Dassonville, (unknown), Véronique Catros, Julie Soblet, (unknown), Catheline Vilain	3
11	Homozygous p.R31H GNRH1 mutation and normosmic congenital hypogonadotropic hypogonadism in a patient and self-limited delayed puberty in his relatives 2020 ·Journal of Pediatric Endocrinology and Metabolism ·Cécile Brachet, (unknown), (unknown), Julie Soblet, Catheline Vilain, Claudine Heinrichs	5
12	Truncating RAX Mutations: Anophthalmia, Hypopituitarism, Diabetes Insipidus, and Cleft Palate in Mice and Men 2019 ·The Journal of Clinical Endocrinology & Metabolism ·Cécile Brachet, Elena Kozhemyakina, (unknown), Claudine Heinrichs, Irina Balikova, Julie Soblet, Guillaume Smits, Catheline Vilain, Peter H. Mathers	8
13	First Report on Fetal Cerebral Polyglucosan Bodies in Mucopolysaccharidosis Type VII 2017 ·SHILAP Revista de lepidopterología ·Hazim Kadhim, Valérie Segers, Catheline Vilain, Julie Désir, Nicky D’Haene	1
14	Chemical chaperone treatment reduces intracellular accumulation of mutant collagen IV and ameliorates the cellular phenotype of a COL4A2 mutation that causes haemorrhagic stroke 2013 ·Human Molecular Genetics ·Lydia Murray, Yinhui Lu, Aislynn Taggart, Nicole Van Regemorter, Catheline Vilain, Marc Abramowicz, Karl E. Kadler, Tom Van Agtmael	50
15	IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign 2012 ·Data Archiving and Networked Services (DANS) ·(unknown), Michella Ghassibe‐Sabbagh, Nicole Revençu, Odile Boute, Melissa Lees, (unknown), C. Verellen‐Dumoulin, Yves Sznajer, Kathleen Claes, Koenraad Devriendt, (unknown), Geert Mortier, Catheline Vilain, Geneviève Pierquin, C. Vincent‐Delorme, Y. Gillerot, R Vanwijck, Bénédicte Bayet, Miikka Vikkula	1
16	Iodotyrosine Deiodinase Defect Identified via Genome-Wide Approach 2012 ·The Journal of Clinical Endocrinology & Metabolism ·Agnès Burniat, Isabelle Pirson, Catheline Vilain, Willem Kulik, Gijs Afink, Rodrigo Moreno‐Reyes, Bernard Corvilain, Marc Abramowicz	16
17	A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome 2011 ·Clinical Genetics ·Catheline Vilain, (unknown), Alec Aeby, (unknown), Patrick Van Bogaert, Gauthier Remiche, Joél Smet, Rudy Van Coster, Marc Abramowicz, Isabelle Pirson	21
18	Hartsfield holoprosencephaly–ectrodactyly syndrome in five male patients: Further delineation and review 2009 ·American Journal of Medical Genetics Part A ·Catheline Vilain, Geert Mortier, Guy Van Vliet, Christèle Dubourg, Claudine Heinrichs, (unknown), Alain Verloès, Clarisse Baumann	12
19	Catheline Vilain and Gilbert Vassar 2004 ·Humana Press eBooks ·Catheline Vilain, Gilbert Vassart	6
20	Small amplified RNA-SAGE: an alternative approach to study transcriptome from limiting amount of mRNA 2003 ·Nucleic Acids Research ·Catheline Vilain	25

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.

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