Concepedia

Author

Victoria Campuzano

Centre for Biomedical Network Research on Rare DiseasesORCID

Also Known As

Campuzano, V., Campuzano, Victoria, V. Campuzano, Victoria Campuzano

55

Publications

6.9K

Citations

22

H-Index

60

Concepts

All Affiliations

Centre for Biomedical Network Research on Rare DiseasesUniversitat Pompeu FabraCentro de Investigación Biomédica en RedInstituto de Salud Carlos IIIUniversidad de Salamanca
VC

About

Victoria Campuzano is an author at Centre for Biomedical Network Research on Rare Diseases specializing in medicine, molecular biology, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

9

9

2K

2

Natural Sciences

5

5

652

3

Health Sciences

4

4

660

4

Engineering

1

1

18

5

Social Sciences

1

1

22

Victoria Campuzano

×

29

Publications

6.7K

Citations

21

H-Index

YearCitations

Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

Victoria Campuzano, Laura Montermini, María Dolores Moltó,

Science

1996

2.7K

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia

Alexandra Dürr, Mireille Cossée, Yves Agid,

New England Journal of Medicine

1996

1.1K

Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes

Victoria Campuzano, Laura Montermini, Yves Lutz,

Human Molecular Genetics

1997

734

Tumor induction by an endogenous K-ras oncogene is highly dependent on cellular context

Carmen Guerra, Nieves Mijimolle, Alma Dhawahir,

Cancer Cell

2003

570

Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin

Hana Koutníková, Victoria Campuzano, Françoise Foury,

Nature Genetics

1997

470

Evolution of the Friedreich’s ataxia trinucleotide repeat expansion: Founder effect and premutations

Mireille Cossée, M. Schmitt, Victoria Campuzano,

Proceedings of the National Academy of Sciences

1997

327

Protein farnesyltransferase in embryogenesis, adult homeostasis, and tumor development

Nieves Mijimolle, Juan A. Velasco, Pierre Dubus,

Cancer Cell

2005

96

Heterozygous deletion of the Williams–Beuren syndrome critical interval in mice recapitulates most features of the human disorder

María Segura‐Puimedon, Ignasi Sahún, Émilie Velot,

Human Molecular Genetics

2014

76

Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion

Ivon Cuscó, Roser Corominas, Mónica Bayés,

Genome Research

2008

69

Cloning and sequence analysis of the Mucor circinelloides pyrG gene encoding orotidine-5′-monophosphate decar☐ylase: use of pyrG for homologous transformation

Ernesto P. Benito, José María Díaz-Mínguez, Enrique A. Iturriaga,

Gene

1992

62

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