Jan H. Veldink

MedicineNeuroscienceBiochemistry, Genetics and Molecular Biology

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

2.4Author DataRank

Indexed papers

2in 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 2 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 →

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

Brain expression quantitative trait locus and network analysis reveals downstream effects and putative drivers for brain-related diseases

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.01.433439

Top 14%

1.5DataRank

Top 14%51 citations

Ellen Tsai, Martijn Vochteloo, Denis Baird, Yunfeng Huang, Chia‐Yen Chen +15 more

Papers

Driven by 29 papers — median percentile 81. Top paper: “Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression”.

Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

Nature Genetics(2021)10.1038/s41588-021-00913-z

N/A

11.2DataRank · unranked

2226 citations

Annique Claringbould, Harm-Jan Westra, Marc Jan Bonder, Patrick Deelen, Biao Zeng +89 more

Brain expression quantitative trait locus and network analysis reveals downstream effects and putative drivers for brain-related diseases

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.01.433439

Top 14%

1.5DataRank

Top 14%51 citations

Ellen Tsai, Martijn Vochteloo, Denis Baird, Yunfeng Huang, Chia‐Yen Chen +15 more

OTTERS: a powerful TWAS framework leveraging summary-level reference data

Nature Communications(2023)10.1038/s41467-023-36862-w

N/A

1.1DataRank · unranked

56 citations

Geyu Zhou, Luca Pinello, Urmo Võsa, Lude Franke, Alexis Battle +81 more

Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1

Genome Medicine(2022)10.1186/s13073-021-01006-6

N/A

1.0DataRank · unranked

40 citations

Frederik J. Steyn, Edor Kabashi, Shyuan T. Ngo, Feifei Cheng, Marta F. Nabais +25 more

Comprehensive evaluation of smoking exposures and their interactions on DNA methylation

EBioMedicine(2024)10.1016/j.ebiom.2023.104956

Top 24%

0.830DataRank

Top 24%42 citations

Yunsung Lee, Daniel L. McCartney, Elin T.G. Kersten, Christian M. Page, Paige M. Hulls +70 more

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Nature Genetics(2021)10.1038/s41588-020-00762-2

N/A

0DataRank · unranked

296 citations

Catherine Francis, Xiao Yun Xu, Alexa M.C. Vermeer, Andrew R. Harper, Roy Huurman +65 more

Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

Genome biology(2021)10.1186/s13059-021-02275-5

N/A

0DataRank · unranked

108 citations

Marta F. Nabais, the Alzheimer’s Disease Neuroimaging Initiative, Simon M. Laws, Tian Lin, Costanza L. Vallerga +67 more

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

JAMA Neurology(2021)10.1001/jamaneurol.2021.2598

N/A

0DataRank · unranked

85 citations

Ruth Chia, Danny E. Miller, Rachel Li, Ravindran Kumaran, Yevgeniya Abramzon +87 more

Non-Coding Genetic Analysis Implicates Interleukin 18 Receptor Accessory Protein 3′UTR in Amyotrophic Lateral Sclerosis

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.03.446863

N/A

0DataRank · unranked

2 citations

Aviad Siany, Elad Barkan, Tsviya Olender, Kristel R. van Eijk, Matthieu Moisse +39 more

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

Nature Genetics(2022)10.1038/s41588-021-01007-6

N/A

0DataRank · unranked

143 citations

Rafik Tadros, Charlotte Glinge, David Y. Chiang, Mariam Jouni, Floriane Simonet +95 more

Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis

Neuron(2022)10.1016/j.neuron.2021.12.019

N/A

0DataRank · unranked

124 citations

Johnathan Cooper‐Knock, Annika K. Weimer, Minyi Shi, Tobias Moll, Jack N.G. Marshall +48 more

Functional genomics analysis identifies T and NK cell activation as a driver of epigenetic clock progression

Genome biology(2022)10.1186/s13059-021-02585-8

N/A

0DataRank · unranked

78 citations

Koen F. Dekkers, Roderick C. Slieker, Crystal D. Grant, M Arfan Ikram, Marleen M. J. van Greevenbroek +6 more

The impact of age on genetic testing decisions in amyotrophic lateral sclerosis

Brain(2022)10.1093/brain/awac279

N/A

0DataRank · unranked

50 citations

Alfredo Iacoangeli, Sarah Opie-Martin, Joke J.F.A. van Vugt, Ahmad Al Khleifat, Andrea Bredin +29 more

Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke

Neurology(2022)10.1212/wnl.0000000000201006

N/A

0DataRank · unranked

37 citations

Huichun Xu, Brady Gaynor, John W. Cole, Kristiina Rannikmäe, Tara M. Stanne +95 more

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

npj Genomic Medicine(2022)10.1038/s41525-021-00267-9

N/A

0DataRank · unranked

44 citations

Alfredo Iacoangeli, Joke J.F.A. van Vugt, Harry Bowles, Matthieu Moisse, Ramona A.J. Zwamborn +42 more

Genetic risk score for intracranial aneurysms to predict aneurysmal subarachnoid hemorrhage and identify associations with patient characteristics

medRxiv(2022)10.1101/2022.04.29.22274404

N/A

0DataRank · unranked

0 citations

Jos P. Kanning, Gad Abraham, Amy E. Martinsen, Bendik S Winsvold, John‐Anker Zwart +19 more

Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

Stroke(2023)10.1161/strokeaha.122.040715

N/A

0DataRank · unranked

31 citations

Jos P. Kanning, Gad Abraham, Amy E. Martinsen, Bendik Slagsvold Winsvold, John‐Anker Zwart +95 more

Clinical testing panels for ALS: global distribution, consistency, and challenges

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration(2023)10.1080/21678421.2023.2173015

N/A

0DataRank · unranked

17 citations

Ahmad Al Nasser, Marwa Elnagheeb, Jennifer A. Fifita, Lyndal Henden, Ingrid M. Keseler +33 more

A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 as a significant cause of intellectual disability

medRxiv(2023)10.1101/2023.05.03.23289461

N/A

0DataRank · unranked

7 citations

Paras Garg, Joke J.F.A. van Vugt, Kristina Ibáñez, Delia Gagliardi, William Lee +16 more

Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

Nature Genetics(2024)10.1038/s41588-024-01787-7

N/A

0DataRank · unranked

70 citations

Dongbing Lai, Pamela Keagle, Desiree M. Baron, Brendan Kenna, Maarten Kooyman +17 more

A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disability

Nature Genetics(2024)10.1038/s41588-024-01917-1

N/A

0DataRank · unranked

11 citations

Paras Garg, Joke J.F.A. van Vugt, Kristina Ibáñez, Delia Gagliardi, William Lee +19 more

Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis

Heliyon(2024)10.1016/j.heliyon.2024.e24975

N/A

0DataRank · unranked

11 citations

Marcel Weinreich, James Lee, Allan C. Shaw, Laura Ferraiuolo, Heather Mortiboys +20 more

An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2

Research Square(2024)10.21203/rs.3.rs-5419198/v1

N/A

0DataRank · unranked

0 citations

Koen C. Demaegd, Aoife Kernan, Joke J.F.A. van Vugt, Calum Harvey, Tobias Moll +25 more

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Neuron(2020)10.1016/j.neuron.2020.11.005

N/A

0DataRank · unranked

83 citations

Ruth Chia, Jinhui Ding, Richard A. Hickman, Thor D. Stein, Yevgeniya Abramzon +95 more

An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2

European Journal of Human Genetics(2025)10.1038/s41431-025-01811-2

N/A

0DataRank · unranked

8 citations

Aoife Kernan, Johnathan Cooper‐Knock, Joke J.F.A. van Vugt, Calum Harvey, Tobias Moll +25 more

ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization

Brain Communications(2020)10.1093/braincomms/fcaa064

N/A

0DataRank · unranked

56 citations

Steven Boeynaems, Mathias De Decker, Joke J.F.A. van Vugt, Lindy Kool, H. Stephan Goedee +81 more

Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

Neurobiology of Aging(2020)10.1016/j.neurobiolaging.2020.04.011

N/A

0DataRank · unranked

12 citations

Remi Stevelink, Mark McCormack, Wouter van Rheenen, Jurjen J. Luykx, Bobby P.C. Koeleman +2 more

Facial Onset Sensory and Motor Neuronopathy

Neurology Clinical Practice(2020)10.1212/cpj.0000000000000834

N/A

0DataRank · unranked

31 citations

Andrew W. Barritt, Marwa Elamin, Stuart Anderson, Rebecca Broad, Angus Nisbet +22 more

Genome-wide Identification of the Genetic Basis of Amyotrophic Lateral Sclerosis

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.14.382606

N/A

0DataRank · unranked

12 citations

Johnathan Cooper‐Knock, Annika K. Weimer, Minyi Shi, Tobias Moll, Calum Harvey +14 more

Jan H. Veldink

Indexed papers

Top data-sharing exemplar

Papers