Raquel Rabionet - Concepedia

Author

Raquel Rabionet

Also Known As

Alfredo Ramirez, Colin A. Purdie, Dalila Pinto, Erika L. Nurmi, Gulietta M. Pupo, Joanna Pera, Kelly Rabionet, Kirstin Purves, Laura Domènech Salgado, Markus Perola

192

Publications

28.8K

Citations

H-Index

116

Concepts

All Affiliations

Centre for Genomic Regulation Universitat Pompeu Fabra Universitat de Barcelona Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública Inserm

About

Raquel Rabionet is an author at Centre for Genomic Regulation specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	30	7K
2	Arts	6	6	839
3	Public Health	6	6	2.8K
4	Natural Sciences	3	3	295
5	Health Sciences	1	1	13

Raquel Rabionet

Publications

13.2K

Citations

H-Index

Page 1

	Year	Citations
Pan-cancer analysis of whole genomes Lauri A. Aaltonen, Federico Abascal, Adam Abeshouse, Nature	2020	3.1K
Analysis of shared heritability in common disorders of the brain Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Science Brain FunctionPsychiatric DisordersGeneticsGenetic EpidemiologyNeuropsychiatry	2018	2K
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders Phil H. Lee, Verneri Anttila, Hyejung Won, Cell PsychiatryPsychiatric DisordersGenetic DisorderGeneticsPsychiatric Genetics	2019	1.4K
Connexin-26 mutations in sporadic and inherited sensorineural deafness Xavier Estivill, Paolo Fortina, Saul Surrey, The Lancet	1998	642
Comprehensive molecular characterization of mitochondrial genomes in human cancers Yuan Yuan, Young Seok Ju, Young-Wook Kim, Nature Genetics	2020	489
MicroRNA profiling of Parkinson's disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function Elena Miñones-Moyano, Sílvia Porta, Geòrgia Escaramís, Human Molecular Genetics Brain DevelopmentMitochondrial DysfunctionNeurochemical BiomarkersClinical NeuroscienceSynaptic Signaling	2011	480
Genetic Structure of Europeans: A View from the North–East Mari Nelis, Tōnu Esko, Reedik Mägi, PLoS ONE Genotype-phenotype AssociationMolecular EcologyHuman VariationMedicineGenetics	2009	432
High carrier frequency of the 35delG deafness mutation in European populations Paolo Gasparini, Raquel Rabionet, Guido Barbujani, European Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsEvolutionary BiologyAudiology	2000	389
A genome-wide association study of anorexia nervosa Christopher S. Franklin, J A B Floyd, Laura M. Thornton, Molecular Psychiatry Genome-wide Association StudyPsychiatryEating DisordersGeneticsAnorexia Nervosa	2014	331
Variants at APOE influence risk of deep and lobar intracerebral hemorrhage Alessandro Biffi, Akshata Sonni, Christopher D. Anderson, Annals of Neurology	2010	265

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