Jaana Suvisaari

Finnish Institute for Health and Welfare

MedicineBiochemistry, Genetics and Molecular BiologyPsychologyNeuroscience

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 1%percentile

13.4Author 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 →

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

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Nature Communications(2015)10.1038/ncomms9111

Top 3%

6.7DataRank

Top 3%386 citations

Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min +234 more

Papers

Driven by 18 papers — median percentile 97. Top paper: “Rare coding variants in ten genes confer substantial risk for schizophrenia”.

Rare coding variants in ten genes confer substantial risk for schizophrenia

Nature(2022)10.1038/s41586-022-04556-w

N/A

7.2DataRank · unranked

900 citations

Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas +95 more

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Nature Communications(2015)10.1038/ncomms9111

Top 3%

6.7DataRank

Top 3%386 citations

Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min +234 more

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Nature Communications(2020)10.1038/s41467-019-12438-5

N/A

5.6DataRank · unranked

143 citations

James Zou, Beryl B. Cummings, Jessica Alföldi, Laurent C. Francioli, Laura D. Gauthier +174 more

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Nature Communications(2020)10.1038/s41467-019-10717-9

N/A

5.2DataRank · unranked

191 citations

Konrad J. Karczewski, Xiaolei Zhang, Sonia Chothani, Miriam J. Smith, D. Gareth Evans +181 more

The effect of LRRK2 loss-of-function variants in humans

Nature Medicine(2020)10.1038/s41591-020-0893-5

N/A

4.9DataRank · unranked

114 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric V. Minikel, Julia K. Goodrich +214 more

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

Nature Neuroscience(2016)10.1038/nn.4404

N/A

3.3DataRank · unranked

113 citations

Giulio Genovese, Daniel P. Howrigan, Andrea Byrnes, Mitja I Kurki, Seyedeh M. Zekavat +31 more

The mutational constraint spectrum quantified from variation in 141,456 humans

Nature(2020)10.1038/s41586-020-2308-7

N/A

1.4DataRank · unranked

9958 citations

Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi, Qingbo S. Wang +187 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

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 contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

Nature Genetics(2017)10.1038/ng.3903

N/A

0.826DataRank · unranked

246 citations

David M. Hougaard, Mandy Johnstone, Nicholas Bass, Jaana Suvisaari, Minna Torniainen +21 more

Transcript expression-aware annotation improves rare variant interpretation

Nature(2020)10.1038/s41586-020-2329-2

N/A

0.796DataRank · unranked

201 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +177 more

Evaluating drug targets through human loss-of-function genetic variation

Nature(2020)10.1038/s41586-020-2267-z

N/A

0.779DataRank · unranked

179 citations

Konrad J. Karczewski, Hilary C. Martin, Beryl B. Cummings, Nicola Whiffin, Daniel R. Rhodes +150 more

The impact of rare protein coding genetic variation on adult cognitive function

Nature Genetics(2023)10.1038/s41588-023-01398-8

N/A

0.628DataRank · unranked

65 citations

Ruoyu Tian, Tian Ge, Max Lam, Gabriela Sánchez-Andrade, Tarjinder Singh +76 more

Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders

Molecular Psychiatry(2024)10.1038/s41380-024-02516-6

N/A

0.360DataRank · unranked

10 citations

Jaana Suvisaari, Markku Lähteenvuo, Tarjinder Singh, Ari Ahola‐Olli, Lea Urpa +33 more

Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty

Nature Aging(2025)10.1038/s43587-025-00925-y

N/A

0.269DataRank · unranked

5 citations

Chenxi Qin, Moritz Krüger, Anna Kuukka, Aarno Palotie, Mark Daly +322 more

Genome-wide association study of borderline personality disorder identifies 11 loci and highlights shared risk with mental and somatic disorders

medRxiv(2024)10.1101/2024.11.12.24316957

N/A

0.241DataRank · unranked

4 citations

Swapnil Awasthi, Alisha S. M. Hall, Alice Braun, Maria Niarchou, Eirini Marouli +95 more

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

UNC Libraries(2024)10.17615/4nb8-at41

N/A

0DataRank · unranked

0 citations

David Curtis, Jennifer Sambrook, Robin Murray, David St Clair, Trevor Cole +54 more

Jaana Suvisaari

Indexed papers

Top data-sharing exemplar

Papers