Mitja Kurki

Also affiliated with Massachusetts General Hospital

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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

13.0Author DataRank

Indexed papers

1in 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 1 indexed paper 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.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

Papers

Driven by 34 papers — median percentile 100. Top paper: “Analysis of protein-coding genetic variation in 60,706 humans”.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses

Nature Medicine(2023)10.1038/s41591-023-02352-1

N/A

3.6DataRank · unranked

313 citations

Mitja Kurki, Jakob Grove, Georgios Voloudakis, Karen Therrien, Elisa Tasanko +38 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

A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

Nature Communications(2020)10.1038/s41467-020-17002-0

N/A

2.1DataRank · unranked

76 citations

Pamela M. Rist, Iyas Daghlas, Franco Giulianini, Padhraig Gormley, Verneri Anttila +95 more

The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

Nature Communications(2022)10.1038/s41467-022-31436-8

N/A

1.4DataRank · unranked

61 citations

Olli Pietiläinen, Mykyta Artomov, Matthew Tegtmeyer, Vera Valakh, Leevi Lehtonen +40 more

Recessive Genome-Wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes

Diabetes(2021)10.2337/db21-0545

N/A

0.952DataRank · unranked

26 citations

Philip Schroeder, Alicia Huerta‐Chagoya, Paula Cortés-Sánchez, Sílvia Bonàs‐Guarch, Marta Guindo-Martínez +15 more

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

The American Journal of Human Genetics(2018)10.1016/j.ajhg.2018.05.002

N/A

0.713DataRank · unranked

115 citations

F. Kyle Satterstrom, Seyedeh M. Zekavat, Indraniel Das, Mitja I Kurki, Claire Churchhouse +45 more

Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

Cell Genomics(2022)10.1016/j.xgen.2022.100210

N/A

0.670DataRank · unranked

86 citations

Roy Elzur, Wei Zhou, Kuan-Han Wu, Humaira Rasheed, Kristin Tsuo +91 more

Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

International Journal of Epidemiology(2020)10.1093/ije/dyaa050

N/A

0.665DataRank · unranked

83 citations

Derek Klarin, Scott M. Damrauer, Kyong-Mi Chang, Philip S. Tsao, Themistocles L. Assimes +93 more

Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes

Nature Genetics(2024)10.1038/s41588-023-01607-4

N/A

0.663DataRank · unranked

82 citations

Raymond K. Walters, Matti Pirinen, Mitja Kurki, Nella Junna, Jacqueline I. Goldstein +23 more

Identification of 64 new risk loci for major depression, refinement of the genetic architecture and risk prediction of recurrence and comorbidities

medRxiv(2022)10.1101/2022.08.24.22279149

N/A

0.648DataRank · unranked

12 citations

Mitja Kurki, Jakob Grove, Georgios Voloudakis, Karen Therrien, Elisa Tasanko +38 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

Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks

Nature Communications(2022)10.1038/s41467-022-32885-x

N/A

0.578DataRank · unranked

46 citations

Wei Zhou, Tuomo Kiiskinen, Aki S. Havulinna, Amanda Elliott, Juha Karjalainen +9 more

High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene

Nature Communications(2024)10.1038/s41467-024-53634-2

N/A

0.477DataRank · unranked

23 citations

Pekka Nieminen, Priyanka Kumari, Emma Juuri, Tiit Nikopensius, Kitt Paraiso +24 more

Diagnosing migraine from genome-wide genotype data: a machine learning analysis

Brain(2025)10.1093/brain/awaf172

N/A

0.269DataRank · unranked

5 citations

Tjaša Kumelj, Bendik S Winsvold, Marte‐Helene Bjørk, Parashkev Nachev, Manjit Matharu +70 more

Proteomic prediction of disease largely reflects environmental risk exposure

medRxiv(2025)10.1101/2025.08.27.25334571

N/A

0.208DataRank · unranked

3 citations

M. Austin Argentieri, Danni A. Gadd, Mitja Kurki, Zhili Zheng, Denis Baird +8 more

Genetic association of preeclampsia to von Willebrand factor and its size-regulator ADAMTS13

Research Square(2025)10.21203/rs.3.rs-5685318/v1

N/A

0.104DataRank · unranked

1 citations

Michael Triebwasser, Emma Daly, Mitja Kurki, Markus Perola, Kirsi Auro +11 more

Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure

medRxiv(2020)10.1101/2020.11.15.20227868

N/A

0DataRank · unranked

4 citations

Tuomo Kiiskinen, Juha Karjalainen, Kristi Krebs, Mitja Kurki, Aki S. Havulinna +17 more

A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development

European Journal of Human Genetics(2022)10.1038/s41431-022-01046-5

N/A

0DataRank · unranked

16 citations

Lea Urpa, Bishwa Ghimire, Hande Topa, Mitja Kurki, Maryna Koskela +15 more

An efficient and accurate frailty model approach for genome-wide survival association analysis controlling for population structure and relatedness in large-scale biobanks

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.31.358234

N/A

0DataRank · unranked

12 citations

Wei Zhou, Tuomo Kiiskinen, Aki S. Havulinna, Amanda Elliott, Juha Karjalainen +9 more

The impact of non-additive genetic associations on age-related complex diseases

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.12.084608

N/A

0DataRank · unranked

14 citations

Ramon Amela, Sílvia Bonàs‐Guarch, Montserrat Puiggròs, Cecilia Salvoro, Irene Miguel-Escalada +16 more

Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

Cell Genomics(2023)10.1016/j.xgen.2022.100241

N/A

0DataRank · unranked

113 citations

Shinichi Namba, Esteban A. Lopera-Maya, Sini Kerminen, Kristin Tsuo, Kristi Läll +83 more

GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer

Nature Communications(2020)10.1038/s41467-020-17718-z

N/A

0DataRank · unranked

141 citations

Ben Brumpton, Ömer Kabil, Jūlı́us Guðmundsson, Guðmar Þorleifsson, Joshua S. Weinstock +51 more

Distinct and shared genetic architectures of Gestational diabetes mellitus and Type 2 Diabetes Mellitus

medRxiv(2023)10.1101/2023.02.16.23286014

N/A

0DataRank · unranked

10 citations

Raymond K. Walters, Matti Pirinen, Mitja Kurki, Nella Junna, Jonathan T. Goldstein +9 more

The role of polygenic risk and susceptibility genes in breast cancer over the course of life

Nature Communications(2020)10.1038/s41467-020-19966-5

N/A

0DataRank · unranked

176 citations

Elisabeth Widén, Sini Kerminen, Tuomo J Meretoja, Matti Pirinen, Pietro Della Briotta Parolo +94 more

Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia

Genes and Immunity(2024)10.1038/s41435-024-00310-6

N/A

0DataRank · unranked

7 citations

Michael Triebwasser, Emma Daly, The FINNPEC Core Investigator Group, Seppo Heinonen, Eero Kajantie +13 more

High incidence and geographic distribution of cleft palate cases in Finland are associated with a regulatory variant in IRF6

medRxiv(2024)10.1101/2024.07.09.24310146

N/A

0DataRank · unranked

1 citations

Pekka Nieminen, Priyanka Kumari, Emma Juuri, Tiit Nikopensius, Kitt Paraiso +23 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

Loss of CFHR5 function reduces the risk for age-related macular degeneration

Nature Communications(2025)10.1038/s41467-025-61193-3

N/A

0DataRank · unranked

6 citations

Stephanie Loomis, Eija Nissilä, Thomas W. Soare, Tobias Rausch, Zhili Zheng +16 more

Recessive Genome-wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes

(2021)10.2337/figshare.17099780

N/A

0DataRank · unranked

0 citations

Philip Schroeder, Alicia Huerta‐Chagoya, Paula Cortés-Sánchez, Sílvia Bonàs‐Guarch, Marta Guindo-Martínez +15 more

Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variants

medRxiv(2025)10.1101/2025.11.24.25340878

N/A

0DataRank · unranked

1 citations

Alicia Huerta‐Chagoya, Xiaoyu Wang, Maheak Vora, Jiang Li, Lehte Türk +18 more

Recessive Genome-wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes

Figshare(2021)10.2337/figshare.17099780.v1

N/A

0DataRank · unranked

0 citations

Philip Schroeder, Alicia Huerta‐Chagoya, Paula Cortés-Sánchez, Sílvia Bonàs‐Guarch, Marta Guindo-Martínez +15 more

Genome-Wide Association Meta-Analysis Using a Recessive Model Illuminates Genetic Architecture of Type 2 Diabetes

medRxiv(2021)10.1101/2021.07.08.21258700

N/A

0DataRank · unranked

0 citations

Alicia Huerta‐Chagoya, Paula Cortés-Sánchez, Sílvia Bonàs‐Guarch, Marta Guindo-Martínez, Joanne B. Cole +13 more

The impact of non-additive genetic associations on age-related complex diseases

Nature Communications(2021)10.1038/s41467-021-21952-4

N/A

0DataRank · unranked

130 citations

Ramon Amela, Sílvia Bonàs‐Guarch, Montserrat Puiggròs, Cecilia Salvoro, Irene Miguel-Escalada +16 more

Mitja Kurki

Indexed papers

Top data-sharing exemplar

Papers