Amets Sáenz - Concepedia

Author

Amets Sáenz

Biogipuzkoa Health Research Institute ORCID

Also Known As

A Saenz, A Saénz, A Sáenz, A. Saenz, A. Saenz Pena, A. Sáenz, A.S. Peña, Amets Saenz, Amets Saénz Peňa, Amets Sàenz

Publications

4.6K

Citations

H-Index

Concepts

All Affiliations

Biogipuzkoa Health Research Institute Instituto de Biomedicina de Valencia University of the Basque Country Instituto de Salud Carlos III Matia Fundazioa

About

Amets Sáenz is an author at Biogipuzkoa Health Research Institute specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	16	3.3K
2	Cell Biology	5	5	2.5K
3	Public Health	4	4	155
4	Health Sciences	2	2	44
5	Natural Sciences	1	1	65

Amets Sáenz

Publications

4.4K

Citations

H-Index

Page 1

	Year	Citations
Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease Coro Paisán‐Ruíz, Shushant Jain, E. Whitney Evans, Neuron Neurodegenerative DiseasesGenetic DisorderParkinson DiseaseGeneticsGene Containing Mutations	2004	2.4K
Effect of COVID-19 pandemic lockdowns on planned cancer surgery for 15 tumour types in 61 countries: an international, prospective, cohort study James Glasbey, Adesoji Ademuyiwa, Adewale Adisa, The Lancet Oncology	2021	280
Calpainopathy—A Survey of Mutations and Polymorphisms Isabelle Richard, Carinne Roudaut, Amets Sáenz, The American Journal of Human Genetics Genetic DisorderGeneticsGenetic EpidemiologyPathologyGenetic Variation	1999	206
LGMD2A: genotype–phenotype correlations based on a large mutational survey on the calpain 3 gene Amets Sáenz, France Leturcq, A.M. Cobo, Brain	2005	179
Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures Eugenio Mercuri, Kate Bushby, Enzo Ricci, Neuromuscular Disorders Calpain 3Early ContracturesSkeletal MuscleMedicineMuscle Mri Findings	2004	162
The effectiveness of glucocorticoids in treating croup: meta-analysis Monica Ausejo, Amets Sáenz, B Pham, BMJ	1999	153
Parkinson's disease due to the R1441G mutation in Dardarin: A founder effect in the basques Javier Simón‐Sánchez, J.F. Martí-Massó, José V. Sánchez‐Mut, Movement Disorders	2006	94
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in a Spanish Family With a Ser252Phe Mutation in the CHRNA4 Gene Amets Sáenz, Juan Carlos Galán, Christophe Caloustian, Archives of Neurology	1999	84
Genotype–phenotype correlations in recessive titinopathies Marco Savarese, Anna Vihola, Emily C. Oates, Genetics in Medicine Genotype-phenotype AssociationGeneticsGenotype–phenotype CorrelationsGenetic VariationMedicine	2020	74
Mutations in Progranulin Gene: Clinical, Pathological, and Ribonucleic Acid Expression Findings Adolfo López de Munaín, Ainhoa Alzualde, Ana Gorostidi, Biological Psychiatry Mendelian DisorderGenetic DisorderMedicineGeneticsProteomics	2008	65

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