R. Vervoort

1.3k total citations
19 papers, 910 citations indexed

About

R. Vervoort is a scholar working on Molecular Biology, Organic Chemistry and Physiology. According to data from OpenAlex, R. Vervoort has authored 19 papers receiving a total of 910 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Organic Chemistry and 6 papers in Physiology. Recurrent topics in R. Vervoort's work include Carbohydrate Chemistry and Synthesis (7 papers), Retinal Development and Disorders (6 papers) and Glycosylation and Glycoproteins Research (5 papers). R. Vervoort is often cited by papers focused on Carbohydrate Chemistry and Synthesis (7 papers), Retinal Development and Disorders (6 papers) and Glycosylation and Glycoproteins Research (5 papers). R. Vervoort collaborates with scholars based in Belgium, United Kingdom and United States. R. Vervoort's co-authors include Alan F. Wright, Willy Lissens, Alan Lennon, B. Tulloch, Maria Giuseppina Miano, Alfons Meindl, Alan C. Bird, Thomas Meitinger, Richard A Axton and Alfredo Ciccodicola and has published in prestigious journals such as Nature Genetics, Blood and Biochemical and Biophysical Research Communications.

In The Last Decade

R. Vervoort

19 papers receiving 893 citations

Peers

Countries citing papers authored by R. Vervoort

Since Specialization

Citations

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

Fields of papers citing papers by R. Vervoort

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Vervoort

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Genetic modification of the inner ear lateral semicircular canal phenotype of the Bmp4 haplo-insufficient mouse 2010 ·Biochemical and Biophysical Research Communications ·R. Vervoort, (unknown), (unknown), Rudi D’Hooge, Guido David	10
2	RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosmin 2005 ·Human Molecular Genetics ·Xinhua Shu, Andrew M. Fry, B. Tulloch, Forbes Manson, John W. Crabb, (unknown), Alison J. Faragher, Alan Lennon, Shenghui He, (unknown), Andreas Gießl, Uwe Wolfrum, R. Vervoort, Anand Swaroop, Alan F. Wright	93
3	Novel deletion spanning RCC1-like domain of RPGR in Japanese X-linked retinitis pigmentosa family. 2005 ·PubMed ·Zi‐Bing Jin, Xiaoqiang Liu, (unknown), R. Vervoort, Kazuhiro Morishita, Mutsuko Hayakawa, Akira Murakami, Naomichi Matsumoto, Norio Niikawa, Nobuhisa Nao‐i	6
4	Mutations ofRPGR in X-linked retinitis pigmentosa (RP3) 2002 ·Human Mutation ·R. Vervoort, Alan F. Wright	74
5	Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X‐linked retinitis pigmentosa 2001 ·American Journal of Medical Genetics ·Akiko Yokoyama, (unknown), Mutsuko Hayakawa, Atsushi Kanai, R. Vervoort, Alan F. Wright, Koki Yamada, Norio Niikawa, Nobuhisa Nao‐i	5
6	Three novel mutations of theRPGR gene exon ORF15 in three Japanese families with X-linked retinitis pigmentosa 2001 ·American Journal of Medical Genetics ·Akiko Yokoyama, (unknown), Mutsuko Hayakawa, Atsushi Kanai, R. Vervoort, Alan F. Wright, Koki Yamada, Norio Niikawa, (unknown)	32
7	Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa 2000 ·Nature Genetics ·R. Vervoort, Alan Lennon, Alan C. Bird, B. Tulloch, Richard A Axton, Maria Giuseppina Miano, Alfons Meindl, Thomas Meitinger, Alfredo Ciccodicola, Alan F. Wright	365
8	Remapping of the RP15 Locus for X-Linked Cone-Rod Degeneration to Xp11.4-p21.1, and Identification of a De Novo Insertion in the RPGR Exon ORF15 2000 ·The American Journal of Human Genetics ·Alan J. Mears, Suja Hiriyanna, R. Vervoort, Beverly M. Yashar, Linn Gieser, (unknown), Stephen P. Daiger, John R. Heckenlively, Paul A. Sieving, Alan F. Wright, Anand Swaroop	55
9	Low β-glucuronidase enzyme activity and mutations in the human β-glucuronidase gene in mild mucopolysaccharidosis type VII, pseudodeficiency and a heterozygote 1998 ·Human Genetics ·R. Vervoort, R Gitzelmann, N. U. Bosshard, Irène Maire, Inge Liebaers, Willy Lissens	26
10	A mutation (IVS8+0.6kbdelTC) creating a new donor splice site activates a cryptic exon in an Alu-element in intron 8 of the human β-glucuronidase gene 1998 ·Human Genetics ·R. Vervoort, R Gitzelmann, Willy Lissens, I. Liebaers	63
11	A mutation (IVS8+0.6kbdelTC) creating a new donor splice site activates a cryptic exon in an 1998 ·Human Genetics ·R. Vervoort, R Gitzelmann, Willy Lissens, Inge Liebaers	3
12	Molecular analysis of the ß-glucuronidase gene: novel mutations in mucopolysaccharidosis type VII and heterogeneity of the polyadenylation region 1997 ·Human Genetics ·R. Vervoort, Neil R.M. Buist, Wim J. Kleijer, Ron A. Wevers, Jean‐Pierre Fryns, Inge Liebaers, Willy Lissens	16
13	β-Glucuronidase P408S, P415L mutations: evidence that both mutations combine to produce an MPS VII allele in certain Mexican patients 1996 ·Human Genetics ·Mohammed Rafiqul Islam, R. Vervoort, Willy Lissens, Joe J. Hoo, (unknown), William S. Sly	18
14	Localization by fluorescence in situ hybridization of the human functional β-glucuronidase gene (GUSB) to 7q11.21→q11.22 and two pseudogenes to 5p13 and 5q13 1996 ·Cytogenetic and Genome Research ·Frank Speleman, R. Vervoort, Nadine Van Roy, I. Liebærs, W S Sly, Willy Lissens	9
15	Molecular analysis of patients with beta-glucuronidase deficiency presenting as hydrops fetalis or as early mucopolysaccharidosis VII. 1996 ·PubMed ·R. Vervoort, M R Islam, William S. Sly, M. T. Zabot, W. J. Kleijer, Amparo Chabás, A. H. Fensom, Elisabeth Young, I. Liebærs, Willy Lissens	50
16	A D255H substitution in the arylsulphatase A gene of two unrelated Belgian patients with late‐infantile metachromatic leukodystrophy 1996 ·Journal of Inherited Metabolic Disease ·Willy Lissens, R. Vervoort, Nicole Van Regemorter, Patrick Van Bogaert, (unknown), C. Verellen‐Dumoulin, Sara Seneca, I. Liebærs	10
17	A pseudodeficiency allele (D152N) of the human beta-glucuronidase gene. 1995 ·PubMed ·R. Vervoort, M R Islam, William S. Sly, Amparo Chabás, Ron A. Wevers, J. de Jong, I. Liebærs, Willy Lissens	21
18	Antithrombin-Gly 424 Arg: a novel point mutation responsible for type 1 antithrombin deficiency and neonatal thrombosis 1994 ·Blood ·Kristin Jochmans, Willy Lissens, R. Vervoort, Stefaan Peeters, M. De Waele, I. Liebærs	32
19	Molecular analysis of a patient with hydrops fetalis caused by β-glucuronidase deficiency, and evidence for additional pseudogenes 1993 ·Human Mutation ·R. Vervoort, Willy Lissens, I. Liebaers	22

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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