Patricia Blanco - Concepedia

Author

Patricia Blanco

Fundación Pública Galega de Medicina Xenómica ORCID

Also Known As

Fernando Botto, P Blanco, P. Blanco, P. Blanco-Arias, P. Blanco‐Arias, Patricia Blanco, Patricia Blanco Arias, Patricia Blanco-Arias, Patricia Blanco‐Arias

102

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Fundación Pública Galega de Medicina Xenómica University of Cambridge Centre for Biomedical Network Research on Rare Diseases Universidade de Santiago de Compostela University Hospital Complex Of Vigo

About

Patricia Blanco is an author at Fundación Pública Galega de Medicina Xenómica specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	16	583
2	Public Health	2	2	28
3	Health Sciences	1	1	23
4	Natural Sciences	1	1	30
5	Biochemistry	1	1	92

Patricia Blanco

Publications

Citations

H-Index

Page 1

	Year	Citations
Divergent outcomes of intrachromosomal recombination on the human Y chromosome: male infertility and recurrent polymorphism Patricia Blanco Journal of Medical Genetics	2000	180
Conservation of PCDHX in mammals; expression of human X/Y genes predominantly in brain Patricia Blanco, Carole A. Sargent, Catherine Boucher, Mammalian Genome Knockout MouseDevelopmental BiologyGeneticsHuman X/y GenesNeuroscience	2000	124
‘Costa da Morte’ ataxia is spinocerebellar ataxia 36: clinical and genetic characterization María García-Murias, Beatriz Quintáns, Manuel Arias, Brain	2012	93
Imbalance of antioxidant enzymes in tumor cells and inhibition of proliferation and malignant features by scavenging hydrogen peroxide Lucı́a Policastro, Beatriz L. Molinari, Fernando Larcher, Molecular Carcinogenesis Chemoprevention StrategyLipid PeroxidationTumor CellsCell ProliferationAntioxidant Enzymes	2004	92
A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism Patricia Blanco, Anja P. Einholm, Hafsa Mamsa, Human Molecular Genetics	2009	65
A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy Saida Ortolano, Rosa Tarrı́o, Patricia Blanco, Neuromuscular Disorders Mendelian DisorderGenetic DisorderGeneticsPathologyMyosin Storage Myopathy	2011	51
Association study of the serotoninergic system in migraine in the spanish population Roser Corominas, María‐Jesús Sobrido, Marta Ribasès, American Journal of Medical Genetics Part B Neuropsychiatric Genetics GeneticsGenetic EpidemiologyHuman PolymorphismMigraine PhenotypeNeurology	2009	50
A Novel Poly(A)-Binding Protein Gene (PABPC5) Maps to an X-Specific Subinterval in the Xq21.3/Yp11.2 Homology Block of the Human Sex Chromosomes Patricia Blanco, Carole A. Sargent, Catherine Boucher, Genomics ChromatinCytogeneticsGeneticsGenomic MechanismMolecular Biology	2001	42
The human-specific Yp11.2/Xq21.3 homology block encodes a potentially functional testis-specific TGIF-like retroposon Patricia Blanco, Carole A. Sargent, Nabeel A. Affara Mammalian Genome Developmental BiologyGenetic DisorderGeneticsLinkage AnalysisGenomic Mechanism	2002	42
Distribution and genotype-phenotype correlation of GDAP1 mutations in Spain Rafael Sivera, Marina Frasquet, Vincenzo Lupo, Scientific Reports	2017	31

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