Rebecca R. Valentino

Author

Mayo Clinic in Florida ORCID

Also Known As

Rebecca R Valentino, Rebecca R. Valentino, Rebecca Valentino

Publications

301

Citations

H-Index

Concepts

All Affiliations

Mayo Clinic in Florida Jacksonville College WinnMed Johns Hopkins University National Hospital for Neurology and Neurosurgery

About

Rebecca R. Valentino is an author at Mayo Clinic in Florida specializing in genetics, medicine, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	128
2	Molecular Biology	1	1	17
3	Neurology	1	1	13
4	Neuroscience	1	1	13
5	Rehabilitation	1	1	115

Rebecca R. Valentino

Publications

267

Citations

H-Index

Page 1

	Year	Citations
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study Edwin Jabbari, Shunsuke Koga, Rebecca R. Valentino, The Lancet Neurology Genome-wide Association StudyGenetic DisorderGeneticsGenetic EpidemiologyProgressive Supranuclear Palsy	2020	115
Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease Jon‐Anders Tunold, Manuela Tan, Shunsuke Koga, Brain	2023	26
Mitochondrial haplogroups and cognitive progression in Parkinson’s disease Ganqiang Liu, Chunming Ni, Jiamin Zhan, Brain	2022	23
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study Rebecca R. Valentino, William J. Scotton, Shanu F. Roemer, The Lancet Neurology	2024	22
MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical features Rebecca R. Valentino, Shunsuke Koga, Ronald L. Walton, Acta Neuropathologica Communications	2020	20
Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's disease Alexandra I. Soto‐Beasley, Ronald L. Walton, Rebecca R. Valentino, Parkinsonism & Related Disorders Mendelian DisorderGenetic DisorderGeneticsMolecular BiologyDisease Gene Identification	2020	17
Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy Anna I. Wernick, Ronald L. Walton, Alexandra I. Soto‐Beasley, Clinical Autonomic Research Mendelian DisorderNeurological DisorderGenetic DisorderMultiple System AtrophySpinocerebellar Ataxia Mutations	2021	13
Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measures Rebecca R. Valentino, Nikoleta Tamvaka, Michael G. Heckman, Acta Neuropathologica Communications	2020	11
Association of <i>Tripartite Motif Containing 11</i> rs564309 With Tau Pathology in Progressive Supranuclear Palsy Rebecca R. Valentino, Shunsuke Koga, Michael G. Heckman, Movement Disorders	2020	10
Fine-mapping of the non-coding variation driving the Caucasian LRRK2 GWAS signal in Parkinson's disease Michael G. Heckman, Catherine Labbé, Ana Kolicheski, Parkinsonism & Related Disorders	2021	10

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