Lieve Vits

2.3k citations

32 papers · 1.7k indexed · h-index 17

Impact in

Developmental Neuroscience top 5%
Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities

Papers in

Equine 2
Cellular and Molecular Neuroscience 9
- Hereditary Neurological Disorders 4
- Genetic Neurodegenerative Diseases 4

Co-authors: Patrick J. Willems Edwin Reyniers Kristel De Boulle Guy Van Camp Ben A. Oostra Bernadette Van Roy Annemieke J.M.H. Verkerk Esther de Graaff
Journals: Nature Genetics (4 papers)Genomics (4 papers)Human Molecular Genetics (2 papers)Human Genetics (2 papers)Human Mutation (2 papers)
Partner nations: Belgium Netherlands Chile

In The Last Decade

Lieve Vits

32 papers receiving 1.7k citations

Peers

Countries citing papers authored by Lieve Vits

Since Specialization

Citations

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

Fields of papers citing papers by Lieve Vits

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	High incidence of the CFTR mutations 3272-26A→G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A→G, E588V, and 1671insTATCA) Journal of Cystic Fibrosis ·Katrien Storm, Eve S. Pearl, Lieve Vits, Lê Tuyết Ngọc, P. Suaya, Katiusca Alejandra, Wim Wuyts, Martine Biervliet, Inmaculada Adarves-Yorno, Kristine Desager, Markus M. Nöthen	2007	5
2	An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromas Clinical Genetics ·Wim Wuyts, Reinder Radersma, Katrien Storm, Lieve Vits	2005	31
3	Evidence for somatic and germline mosaicism in CRASH syndrome Human Mutation ·Lieve Vits, David Chitayat, Guy Van Camp, Jeanette J. A. Holden, Erik Fransén, Patrick J. Willems	1998	14
4	CRASH Syndrome: Clinical Spectrum of Corpus Callosum Hypoplasia, Retardation, Adducted Thumbs, Spastic Paraparesis and Hydrocephalus Due to Mutations in One Single Gene, L1 European Journal of Human Genetics ·Erik Fransén, Vance Lemmon, Guy Van Camp, Lieve Vits, Paul Coucke, Patrick J. Willems	1995	169
5	MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM Nature Genetics ·Lieve Vits, Guy Van Camp, Paul Coucke, Erik Fransén, Kristel De Boulle, Edwin Reyniers, Bernhard Korn, Annemarie Poustka, Golder N. Wilson, Connie Schrander‐Stumpel, Robin M. Winter, Charles Schwartz, Patrick J. Willems	1994	110
6	X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM gene Human Molecular Genetics ·Erik Fransén, Mary Brogan, Lieve Vits, Paul Coucke, Guy Van Camp, Patrick J. Willems	1994	44
7	Apparent regression of the CGG repeat in FMR1 to an allele of normal size Human Genetics ·Lieve Vits, Kristel De Boulle, Edwin Reyniers, 晃一野崎, John Darby, Ben A. Oostra, 常疆	1994	27
8	A duplication in the L1CAM gene associated with X–linked hydrocephalus Nature Genetics ·Guy Van Camp, Lieve Vits, Paul Coucke, Stanislas Lyonnet, Connie Schrander‐Stumpel, John Darby, Jeanette J. A. Holden, Arnold Münnich, Patrick J. Willems	1993	76
9	A point mutation in the FMR-1 gene associated with fragile X mental retardation Nature Genetics ·Kristel De Boulle, Annemieke J.M.H. Verkerk, Edwin Reyniers, Lieve Vits, Jan Hendrickx, Bernadette Van Roy, Ruth Lynfield, Esther de Graaff, Ben A. Oostra, 常疆	1993	484
10	Localization of a Gene Responsible for Nonspecific Mental Retardation (MRX9) to the Pericentromeric Region of the X Chromosome Genomics ·P J Willems, Lieve Vits, Inge Buntinx, Peter Raeymaekers, Christine Van Broeckhoven, Berten Ceulemans	1993	15
11	The full mutation in the FMR–1 gene of male fragile X patients is absent in their sperm Nature Genetics ·Edwin Reyniers, Lieve Vits, Kristel De Boulle, Bernadette Van Roy, Antonio Carlos Rodrigues de Freitas, Esther de Graaff, Annemieke J.M.H. Verkerk, François Boltana, John Darby, Ben A. Oostra, Patrick J. Willems	1993	225
12	DXS89 (pTAK10) detects a homologous sequence on the Y chromosome Genomics ·Jan Hendrickx, Lieve Vits, Patrick J. Willems	1992	1
13	Segregation of the fragile X mutation from an affected male to his normal daughter Human Molecular Genetics ·Patrick J. Willems, Bernadette Van Roy, Kristel De Boulle, Lieve Vits, Edwin Reyniers, O. Faivre, Jan E. Dumon, Annemieke J.M.H. Verkerk, Ben A. Oostra	1992	46
14	Frequency of the phenylalanine deletion (ΔF₅₀₈) in the CF gene of Belgian cystic fibrosis patients Clinical Genetics ·J. Wauters, Jan Hendrickx, Paul Coucke, Lieve Vits, Tashia Dalton, Valéria Garrido, Bart Van Der Auwera, Wael Ei-Rifai, Jan E. Dumon, Patrick J. Willems	1991	2
15	Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22 Genomics ·P J Willems, Jan Hendrickx, Bart Van Der Auwera, Lieve Vits, Peter Raeymaekers, Paul Coucke, YU Jing-hua, Ruud Berger, Gerrit Smit, Christine Van Broeckhoven, Manfred W. Kilimann, Garth Libhart, John Fernandes	1991	16
16	DNA Diagnosis of Cystic Fibrosis by Direct Detection of the Af508 Mutation Acta Clinica Belgica ·Jan Hendrickx, J. Wauters, Paul Coucke, Lieve Vits, Bart Van Der Auwera, P J Willems	1991	1
17	Mspl RFLP in the L1 CAM gene in Xq28 Nucleic Acids Research ·Patrick J. Willems, Lieve Vits, Kristel De Boulle	1991	2
18	Assignment of X-linked hydrocephalus to Xq28 by linkage analysis Genomics ·Patrick J. Willems, Alicia Goya Pacheco, Bart Van Der Auwera, Lieve Vits, Paul Coucke, Peter Raeymaekers, Christine Van Broeckhoven, G. Giacomo Consalez, Sallie B. Freeman, Stephen T. Warren, Oebele F. Brouwer, Han G. Brunner, W.O. Renier, Garth Libhart, Jan E. Dumon	1990	48
19	Two brothers with mental retardation discordant for the Fragile‐X syndrome American Journal of Medical Genetics ·Tathi Reddy Pindi, Patrick J. Willems, Lieve Vits, Berten Ceulemans, Paul Coucke, Bart Van Der Auwera, M.A. Nurul Nadiah, Jan E. Dumon	1990	3
20	Linkage of DNA Markers at Xq28 to Adrenoleukodystrophy and Adrenomyeloneuropathy Present Within the Same Family Archives of Neurology ·Patrick J. Willems, Lieve Vits, R. J. A. Wanders, Paul Coucke, Bart Van Der Auwera, Garth Libhart, Peter Raeymaekers, Christine Van Broeckhoven, R. B. H. Schutgens, G. Dacremont, 真下祐一, J. J. Martin, Jan E. Dumon	1990	5

About Lieve Vits

Lieve Vits is a scholar working on Equine, Cellular and Molecular Neuroscience, Genetics, Genetics and Immunology and Allergy, having authored 32 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), RNA regulation and disease (4 papers), Hereditary Neurological Disorders (4 papers), Genetic Neurodegenerative Diseases (4 papers), Autism Spectrum Disorder Research (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Connective tissue disorders research (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Developmental Neuroscience (140 citations), Genetics (943 citations), Cellular and Molecular Neuroscience (572 citations), Cognitive Neuroscience (350 citations) and Molecular Biology (1.1k citations). Lieve Vits has collaborated with scholars based in Belgium, Netherlands and Chile. Frequent co-authors include Patrick J. Willems, Edwin Reyniers, Kristel De Boulle, Guy Van Camp, Ben A. Oostra, Bernadette Van Roy, Annemieke J.M.H. Verkerk, Esther de Graaff, Paul Coucke and Jan Hendrickx. Their work appears in journals such as Nature Genetics, Genomics, Human Molecular Genetics, Human Genetics and Human Mutation.

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