🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Christine Van Broeckhoven

VIB-UAntwerp Center for Molecular Neurology

ORCID: 0000-0003-0183-7665
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 2%percentile
3.9Author DataRank

Indexed papers

3in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 3 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

Nature Communications(2021)10.1038/s41467-021-22491-8
Top 6%
3.9DataRank
Top 6%339 citations

Sonia Moreno–Grau, Niccoló Tesi, Benjamin Grenier‐Boley, Víctor Andrade, Iris E. Jansen +95 more

Papers

Driven by 14 papers — median percentile 0. 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

Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

Nature Communications(2021)10.1038/s41467-021-22491-8
Top 6%
3.9DataRank
Top 6%339 citations

Sonia Moreno–Grau, Niccoló Tesi, Benjamin Grenier‐Boley, Víctor Andrade, Iris E. Jansen +95 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

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

Neurobiology of Aging(2011)10.1016/j.neurobiolaging.2011.05.024
N/A
1.8DataRank · unranked
33 citations

Demetrius M. Maraganore, Peter Nuernberg, Grazia Annesi, Nadine Abahuni, Anna Rita Bentivoglio +42 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

C9orf72 , age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

Neurology(2020)10.1212/wnl.0000000000010914
N/A
0.632DataRank · unranked
10 citations

Claudia Manzoni, Manuel Bernal-Quirós, Demis A. Kia, Miquel Aguilar, Ignacio Álvarez +95 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

Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

Nature Communications(2023)10.1038/s41467-023-36192-x
Top 100%
0DataRank
Top 100%0 citations

Sonia Moreno–Grau, Niccoló Tesi, Benjamin Grenier‐Boley, Víctor Andrade, Iris E. Jansen +95 more

Genome-wide association study of Alzheimer’s disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset

Translational Psychiatry(2020)10.1038/s41398-020-01074-z
N/A
0DataRank · unranked
76 citations

Dmitry Prokopenko, Valerija Dobričić, Fabian Kilpert, Isabelle Bos, Stephanie J. B. Vos +41 more

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

WOS(2020)10.17863/cam.70957
Top 100%
0DataRank
Top 100%0 citations

Sonia Moreno–Grau, Niccoló Tesi, Benjamin Grenier‐Boley, Víctor Andrade, Iris E. Jansen +95 more

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

UNC Libraries(2020)10.17615/pbds-w495
N/A
0DataRank · unranked
0 citations

David Craig, Liming Qu, Jonathan L. Haines, Taniesha Morgan, Mark A. Sager +95 more

SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration

Brain(2021)10.1093/brain/awab171
N/A
0DataRank · unranked
26 citations

Agnès Camuzat, Khalid El Hachimi, Justine Guégan, Daisy Rinaldi, Serena Lattante +40 more

Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer’s disease CSF profile of neuronal injury and inflammation

Molecular Psychiatry(2022)10.1038/s41380-022-01437-6
N/A
0DataRank · unranked
25 citations

Fahri Küçükali, Isabelle Bos, Stephanie J. B. Vos, Sebastiaan Engelborghs, Tim De Pooter +35 more

Multivariate GWAS of Alzheimer’s disease CSF biomarker profiles implies GRIN2D in synaptic functioning

medRxiv(2022)10.1101/2022.08.02.22278185
N/A
0DataRank · unranked
4 citations

Olena Ohlei, Fahri Küçükali, Isabelle Bos, Stephanie J. B. Vos, Dmitry Prokopenko +33 more