V. Volpini

1.5k citations

33 papers · 996 indexed · h-index 17

Impact in

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders

Papers in

Cellular and Molecular Neuroscience 16
- Genetic Neurodegenerative Diseases 15
- Hereditary Neurological Disorders 5
Neurology 6
- Neurological diseases and metabolism 6

Co-authors: Xavier Estivill Jordi Corral Isidró Ferrer D. E. Genis Isabel Banchs Onofre Combarros Célia Bádenas A Darnell
Journals: Neurology (5 papers)Journal of Medical Genetics (4 papers)Transplant International (2 papers)Human Genetics (2 papers)Acta Neurologica Scandinavica (2 papers)
Partner nations: Spain United States Canada

In The Last Decade

V. Volpini

33 papers receiving 972 citations

Peers

Countries citing papers authored by V. Volpini

Since Specialization

Citations

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

Fields of papers citing papers by V. Volpini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing Case Reports in Neurology ·Beatriz Quintáns, José Ruiz Pardo, Berta Campos, Francisco Barros, V. Volpini, Ãngel Carracedo, María‐Jesús Sobrido	2011	12
2	Phenotypic spectrum of MFN2 mutations in the Spanish population Journal of Medical Genetics ·Carlos Casasnovas, Isabel Banchs, Julien Cassereau, Naïg Guéguen, Arnaud Chevrollier, Antonia Reitter, Dominique Bonneau, V. Volpini	2009	48
3	Two Spanish families with Charcot–Marie–Tooth type 2A: Clinical, electrophysiological and molecular findings Neuromuscular Disorders ·Isabel Banchs, Carlos Casasnovas, J. Montero, Antonia Reitter, V. Volpini	2008	15
4	A kindred with cerebellar ataxia and thermoanalgesia Journal of Neurology Neurosurgery & Psychiatry ·D. E. Genis, Isidró Ferrer, M Messana, Jordi Corral, V. Volpini, Zaruwa M. Zira, Jordi Gich, Lluís Ramió‐Torrentà, (unknown), Kaiyang Luo, (unknown)	2008	2
5	Genetic Analysis of 27 Spanish Patients with Hemiplegic Migraine, Basilar-Type Migraine and Childhood Periodic Syndromes Cephalalgia ·Ester Cuenca-León, Roser Corominas, Noèlia Fernàndez‐Castillo, V. Volpini, Mireia del Toro, Manuel G. Roig, Alfons Macaya, Bru Cormand	2008	52
6	Spinocerebellar ataxia type 2 (SCA2) with white matter involvement Neuroscience Letters ·Judith Armstrong, I Bonaventura, Ana I. Rojo, Guadalupe González, Jordi Corral, Nathalie Nadal, V. Volpini, Isidró Ferrer	2005	16
7	Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis Acta Neurologica Scandinavica ·Jon Infante, Onofre Combarros, V. Volpini, Jordi Corral, Javier Llorca, José Berciano	2005	38
8	Expanded GAA repeats and clinical variation in Friedreich's ataxia Acta Neurologica Scandinavica ·Ignacio Mateo, Javier Llorca, V. Volpini, Jordi Corral, José Berciano, Onofre Combarros	2003	24
9	Understanding the dynamics of Spinocerebellar Ataxia 8 (SCA8) locus through a comparative genetic approach in humans and apes Neuroscience Letters ·Aida M. Andrés, И. Шираз, Naruya Saitou, V. Volpini, Francesc Calafell, Jaume Bertranpetit	2003	11
10	Spinocerebellar ataxia type 10 is rare in populations other than Mexicans Neurology ·Taeko Matsuura, Laura P.W. Ranum, V. Volpini, Massimo Pandolfo, Hidenao Sasaki, K Tashiro, Kei Watase, Huda Y. Zoghbi, Tetsuo Ashizawa	2002	41
11	Identification of seven novel SNPS (five nucleotide and two amino acid substitutions) in the connexin31 (GJB3) gene Human Mutation ·Núria López-Bigas, Raquel Rabionet, Yating Luo, Isabel Banchs, V. Volpini, Jeffery M. Vance, Yiqing Fan, Xavier Estivill	2000	18
12	Celiac disease and idiopathic cerebellar ataxia Neurology ·Onofre Combarros, Jon Infante, Marcos López‐Hoyos, María José Luesma Bartolomé, José Berciano, Javier Corral, V. Volpini	2000	33
13	Anticipation is not associated with CAG repeat expansion in parent-offspring pairs of patients affected with schizophrenia American Journal of Medical Genetics ·Lourdes Martorell, Miguel Ángel Pujana, Paru Ramadhan, Jorge Joven, V. Volpini, Antonio Labad, Xavier Estivill, Elisabet Vilella	1999	13
14	Analysis of amino-acid and nucleotide variants in the spinocerebellar ataxia type 1 ( SCA1 ) gene in schizophrenic patients Human Genetics ·Miguel Ángel Pujana, Lourdes Martorell, V. Volpini, Shruthi Jayaprakash, Antonio Labad, Elisabet Vilella, Xavier Estivill	1997	5
15	A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome. Journal of Clinical Investigation ·Antoni Barrientos, V. Volpini, Jordi Casademont, D. E. Genis, José María Manzanares, Isidró Ferrer, Jordi Corral, Francesc Cardellach, Á Urbano-Márquez, Xavier Estivill, Virginia Nunes	1996	66
16	Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred Neurology ·D. E. Genis, T. Matilla, V. Volpini, Jordi Rosell, Antonio Dávalos, Isidró Ferrer, A. Barnadas Molins, Xavier Estivill	1995	99
17	WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia Human Molecular Genetics ·Jonathan M.J. Derry, Andrew Wu, Kenneth I. Weinberg, HD Ochs, V. Volpini, Xavier Estivill, Ann P. Walker, Uta Francke	1995	123
18	Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families Human Genetics ·Liss Dyah Dewi Arini, H. Kruyer, G. Glóver, Jane R. Hull, Pablo Carbonell, 宋瑞霞, V. Volpini, Jordi Rosell, Karine Zai, Hiroyuki Uenohara, bolivar cadena, F Ballesta, Xavier Estivill	1994	21
19	Prenatal diagnosis of werdnig‐hoffmann disease: DNA analysis of a mummified umbilical cord using closely linked microsatellite markers Prenatal Diagnosis ·T. Matilla, Javier Corral, Merce Miranda, Juan Troyano, Karen Morrison, V. Volpini, Xavier Estivill	1994	3
20	DMD carrier detection in a female with mosaic Turner's syndrome. Journal of Medical Genetics ·Montserrat Baiget, Eduardo F. Tizzano, V. Volpini, E. del Rı́o, Emmanuel L Puplampu, P. Gallano	1991	6

About V. Volpini

V. Volpini is a scholar working on Cellular and Molecular Neuroscience, Neurology, Molecular Biology, Cell Biology and Virology, having authored 33 papers that have together received 996 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (15 papers), Mitochondrial Function and Pathology (13 papers), Neurological diseases and metabolism (6 papers), Hereditary Neurological Disorders (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Endoplasmic Reticulum Stress and Disease (3 papers), Neuroendocrine Tumor Research Advances (2 papers) and Connexins and lens biology (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (369 citations), Clinical Biochemistry (105 citations), Neurology (91 citations), Neurology (167 citations) and Cell Biology (167 citations). V. Volpini has collaborated with scholars based in Spain, United States and Canada. Frequent co-authors include Xavier Estivill, Jordi Corral, Isidró Ferrer, D. E. Genis, Isabel Banchs, Onofre Combarros, Célia Bádenas, A Darnell, Carlos Nicolau and Roser Torrá. Their work appears in journals such as Neurology, Journal of Medical Genetics, Transplant International, Human Genetics and Acta Neurologica Scandinavica.

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