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

Annette M. Hartmann

Lundbeck Foundation

ORCID: 0000-0003-0689-4335
Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicine

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

4in 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 4 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: “Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores”.

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

Genome-wide association study identifies 48 common genetic variants associated with handedness

Nature Human Behaviour(2020)10.1038/s41562-020-00956-y
N/A
3.7DataRank · unranked
157 citations

Joyce Y. Tung, Nicholas Eriksson, Eva Albrecht, Fazil Alıev, Ole A. Andreassen +95 more

Biological insights from 108 schizophrenia-associated genetic loci

Nature(2014)10.1038/nature13595
N/A
1.3DataRank · unranked
8042 citations

Stephan Ripke, Aiden Corvin, Jesse R. Dixon, Kai-How Farh, Peter Holmans +284 more

Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

Molecular Psychiatry(2022)10.1038/s41380-022-01793-3
N/A
1.1DataRank · unranked
66 citations

Emil Uffelmann, Benjamin Williams, Lucía Colodro‐Conde, Éloi Gagnon, Travis T. Mallard +95 more

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Nature Genetics(2016)10.1038/ng.3725
N/A
1.1DataRank · unranked
1129 citations

Daniel P. Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S. Greer +267 more

The alternative splicing of tau exon 10 and its regulatory proteins CLK2 and TRA2‐BETA1 changes in sporadic Alzheimer's disease

Journal of Neurochemistry(2006)10.1111/j.1471-4159.2005.03552.x
N/A
0.748DataRank · unranked
145 citations

Dan Rujescu, Yesheng Tang, Frank J. Berendt, Annette M. Hartmann, Frank Faltraco +10 more

GAA-FGF14 disease: defining its frequency, molecular basis, and 4-aminopyridine response in a large downbeat nystagmus cohort

EBioMedicine(2024)10.1016/j.ebiom.2024.105076
N/A
0.633DataRank · unranked
67 citations

Felix Heindl, Carlo Wilke, Matt C. Danzi, Andreas Traschütz, Catherine Ashton +12 more

Identifying nootropic drug targets via large-scale cognitive GWAS and transcriptomics

Neuropsychopharmacology(2021)10.1038/s41386-021-01023-4
N/A
0.489DataRank · unranked
25 citations

Chia‐Yen Chen, Tian Ge, Yan Xia, David W. Hill, Joey W. Trampush +66 more

Genome-wide association studies of binge-eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes

medRxiv(2025)10.1101/2025.01.31.25321397
N/A
0.395DataRank · unranked
11 citations

Helena L. Davies, Sang Hyuck Lee, Jessica Dennis, Christopher Hübel, Jessica Johnson +95 more

Identifying Nootropic Drug Targets via Large-Scale Cognitive GWAS and Transcriptomics

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.06.934752
N/A
0.312DataRank · unranked
7 citations

Chen Chia-Yen, Xia Yan, W. David Hill, Joey W. Trampush, Jin Yu +64 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

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

Intronic FGF14 GAA repeat expansions are a common cause of downbeat nystagmus syndromes: frequency, phenotypic profile, and 4-aminopyridine treatment response

medRxiv(2023)10.1101/2023.07.30.23293380
N/A
0DataRank · unranked
10 citations

Felix Heindl, Carlo Wilke, Matt C. Danzi, Andreas Traschütz, Catherine Ashton +12 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