Carles Vilariño‐Güell

MedicineNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 9 papers. Top paper: “Large-scale replication and heterogeneity in Parkinson disease genetic loci”.

Large-scale replication and heterogeneity in Parkinson disease genetic loci

Neurology(2012)10.1212/wnl.0b013e318264e353

N/A

6.6DataRank · unranked

132 citations

Grazia Annesi, Alexis Brice, Christine Van Broeckhoven, Muin J. Khoury, Maria Bozi +160 more

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

Journal of Medical Genetics(2012)10.1136/jmedgenet-2012-101155

N/A

3.1DataRank · unranked

108 citations

John P. A. Ioannidis, Grazia Annesi, Alexis Brice, Muin J. Khoury, Maria Bozi +67 more

The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants

Neurobiology of Aging(2014)10.1016/j.neurobiolaging.2013.07.013

N/A

1.6DataRank · unranked

41 citations

Alexis Elbaz, Daniel J. Serie, Grazia Annesi, Georg Auburger, Justin A. Bacon +55 more

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

The Lancet Neurology(2011)10.1016/s1474-4422(11)70175-2

N/A

0.876DataRank · unranked

343 citations

Michael G. Heckman, Nadine Abahuni, Grazia Annesi, Justin A. Bacon, Soraya Bardien +60 more

RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses

The Lancet Neurology(2024)10.1016/s1474-4422(24)00121-2

N/A

0.706DataRank · unranked

110 citations

Jordan Follett, Joanne Trinh, Sandeep Kumar Barodia, Raquel Real, Zhiyong Liu +31 more

Independent and joint effects of the MAPT and SNCA genes in Parkinson disease

Annals of Neurology(2011)10.1002/ana.22321

N/A

0.663DataRank · unranked

82 citations

Owen A. Ross, John P. A. Ioannidis, Alexandra I. Soto‐Ortolaza, Frédéric Moisan, Jan Aasly +40 more

Population‐specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO‐PD) consortium

Movement Disorders(2013)10.1002/mds.25600

N/A

0.538DataRank · unranked

35 citations

Alexandra I. Soto‐Ortolaza, Nadine Abahuni, Grazia Annesi, Justin A. Bacon, Soraya Bardien +65 more

A pathogenic variant in RAB32 causes autosomal dominant Parkinson’s disease and activates LRRK2 kinase

medRxiv(2024)10.1101/2024.01.17.24300927

N/A

0.208DataRank · unranked

3 citations

Jordan Follett, Joanne Trinh, Sandeep Kumar Barodia, Raquel Real, Zhiyong Liu +32 more

Exome-wide rare variant analysis in familial essential tremor

Parkinsonism & Related Disorders(2020)10.1016/j.parkreldis.2020.11.021

N/A

0DataRank · unranked

15 citations

Gabrielle Houle, Sara Ortega‐Cubero, Sara Bandrés‐Ciga, Ignacio Álvarez, María Cárcel +28 more