Markus Perola

Finnish Institute for Health and Welfare

Biochemistry, Genetics and Molecular BiologyMedicine

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 100%percentile

0Author DataRank

Indexed papers

7in 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 7 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.

Data from IgG Glycome in Colorectal Cancer

10.1158/1078-0432.c.6524025.v1

Top 100%

0DataRank

Top 100%0 citations

Evropi Theodoratou, Kujtim Thaçi, Maria Timofeeva, Aleksandar Vojta, Jerko Štambuk +12 more

Papers

Driven by 34 papers — median percentile 0. 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

Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells

Nature(2020)10.1038/s41586-020-2786-7

N/A

4.1DataRank · unranked

151 citations

Satish K. Nandakumar, Xiaotian Liao, Alexander G. Bick, Juha Karjalainen, Marcin Tabaka +79 more

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Nature Genetics(2020)10.1038/s41588-020-00713-x

N/A

3.7DataRank · unranked

242 citations

Elena V. Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, James P. Cook +94 more

Taxonomic signatures of cause-specific mortality risk in human gut microbiome

Nature Communications(2021)10.1038/s41467-021-22962-y

N/A

3.4DataRank · unranked

173 citations

Ville Laitinen, Aki S. Havulinna, Guillaume Méric, Susan Cheng, Markus Perola +17 more

The Use of Genome-Wide eQTL Associations in Lymphoblastoid Cell Lines to Identify Novel Genetic Pathways Involved in Complex Traits

PLoS ONE(2011)10.1371/journal.pone.0022070

N/A

2.0DataRank · unranked

38 citations

Jennifer M. Taylor, J. Brent Richards, Tim Watts, Fredrik H. Pettersson, John Broxholme +15 more

Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma

PLoS Genetics(2020)10.1371/journal.pgen.1008682

N/A

1.7DataRank · unranked

53 citations

Michael Wainberg, Juha Karjalainen, Tuomo Kiiskinen, Guhan Venkataraman, Susanna Lemmelä +9 more

Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure

Hypertension(2020)10.1161/hypertensionaha.120.14973

N/A

1.4DataRank · unranked

87 citations

Miina Ollikainen, Maheswary Muniandy, Tao Zhang, Jenny van Dongen, Guang Hao +47 more

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Nature Genetics(2010)10.1038/ng.520

N/A

1.2DataRank · unranked

2239 citations

Josée Dupuis, Claudia Langenberg, Inga Prokopenko, Richa Saxena, Nicole Soranzo +257 more

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics(2014)10.1038/ng.3097

N/A

1.1DataRank · unranked

2093 citations

Emilio Rodríguez-Ruiz, The PAGE Consortium, Diana O. Perkins, Tonu Esko, Jian Yang +479 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

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

Nature Genetics(2012)10.1038/ng.2274

N/A

1.0DataRank · unranked

897 citations

Marie-France Hivert, Robert A Scott, Jonna L Grimsby, Nabila Bouatia-Naji, Han Chen +211 more

The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections

EBioMedicine(2023)10.1016/j.ebiom.2023.104630

N/A

1.0DataRank · unranked

28 citations

Fahrisa I. Maisha, Satu Strausz, Vilma Lammi, Brian E. Cade, Anniina Tervi +88 more

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

Nature Genetics(2012)10.1038/ng.2385

N/A

1.0DataRank · unranked

862 citations

Vasiliki Lagou, Ryan P Welch, Eleanor Wheeler, May E Montasser, Jian'an Luan +209 more

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

Nature Communications(2021)10.1038/s41467-020-19366-9

N/A

0.771DataRank · unranked

170 citations

Reedik Mägi, Jouke‐Jan Hottenga, Harald Grallert, John R. B. Perry, Nabila Bouatia‐Naji +95 more

Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

Stroke(2023)10.1161/strokeaha.123.043052

N/A

0.706DataRank · unranked

27 citations

Anni Kauko, Sarah E. Tom, Hannele Laivuori, Teemu Niiranen, Natalie A. Bello +86 more

Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata

Nature Communications(2023)10.1038/s41467-023-35974-7

N/A

0.680DataRank · unranked

22 citations

Jaakko Tyrmi, Nilüfer Rahmioğlu, Krina T. Zondervan, Christian M. Becker, FinnGen +95 more

Genome-Wide Association Study of Peripheral Artery Disease

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.119.002862

N/A

0.670DataRank · unranked

86 citations

Alexander Stiby, Moustafa Abdalla, Erin Austin, Stela McLachlan, Efthymia Vlachopoulou +50 more

Development and validation of a model to predict incident chronic liver disease in the general population: The CLivD score

Journal of Hepatology(2022)10.1016/j.jhep.2022.02.021

N/A

0.641DataRank · unranked

71 citations

Panu K. Luukkonen, Anna But, Veikko Salomaa, Annie Britton, K. Petersen +10 more

Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

Nature Genetics(2024)10.1038/s41588-024-01763-1

N/A

0.609DataRank · unranked

57 citations

Chen Zhao, Steven Bell, Maria Didriksen, Muhammad Sulaman Nawaz, Nathalie Schandra +65 more

Taxonomic Signatures of Long-Term Mortality Risk in Human Gut Microbiota

medRxiv(2020)10.1101/2019.12.30.19015842

N/A

0.500DataRank · unranked

27 citations

Ville Laitinen, Aki S. Havulinna, Guillaume Méric, Susan Cheng, Markus Perola +17 more

Identification of complement factor H variants that predispose to pre‐eclampsia: A genetic and functional study

BJOG An International Journal of Obstetrics & Gynaecology(2023)10.1111/1471-0528.17529

N/A

0.464DataRank · unranked

21 citations

Zhen Ren, Michael Triebwasser, Emma Daly, Finnpec, Markus Perola +9 more

Metabolomic and genomic prediction of common diseases in 477,706 participants in three national biobanks

10.1101/2023.06.09.23291213

N/A

0.464DataRank · unranked

21 citations

Jeffrey C. Barrett, Tõnu Esko, Krista Fischer, Luke Jostins-Dean, Pekka Jousilahti +19 more

Dysfunction of complement receptors CR3 (CD11b/18) and CR4 (CD11c/18) in pre‐eclampsia: a genetic and functional study

BJOG An International Journal of Obstetrics & Gynaecology(2021)10.1111/1471-0528.16660

N/A

0.449DataRank · unranked

19 citations

Laura Teirilä, Michael Triebwasser, Eoin Daly, Arnab Bhattacharjee, Liisa M. Uotila +12 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

0.336DataRank · unranked

7 citations

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

Substantial Fat Loss in Physique Competitors Is Characterized by Increased Levels of Bile Acids, Very-Long Chain Fatty Acids, and Oxylipins

Metabolites(2022)10.3390/metabo12100928

N/A

0.269DataRank · unranked

5 citations

Juha J. Hulmi, Youwen Qin, Michael Inouye, Scott C. Ritchie, Susan Cheng +15 more

Narcolepsy as a potential risk factor for Schizophrenia

Translational Psychiatry(2025)10.1038/s41398-025-03259-w

N/A

0.248DataRank · unranked

3 citations

Anniina Tervi, Samuel E. Jones, FinnGen, Aarno Palotie, Mark Daly +95 more

Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsia

Research Square(2024)10.21203/rs.3.rs-4121735/v1

N/A

0.129DataRank · unranked

1 citations

Michael Triebwasser, Emma Daly, FINNPEC COHORT, M. Kurki, Markus Perola +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

Taxonomic signatures of cause-specific mortality risk in human gut microbiome

Figshare(2020)10.17863/cam.69735

N/A

0.104DataRank · unranked

1 citations

Ville Laitinen, Aki S. Havulinna, Guillaume Méric, Susan Cheng, Markus Perola +17 more

Data from IgG Glycome in Colorectal Cancer

10.1158/1078-0432.c.6524025.v1

Top 100%

0DataRank

Top 100%0 citations

Evropi Theodoratou, Kujtim Thaçi, Maria Timofeeva, Aleksandar Vojta, Jerko Štambuk +12 more

Attribution of diabetes to the development of severe liver disease in the general population

Liver International(2022)10.1111/liv.15296

N/A

0DataRank · unranked

3 citations

Ville Männistö, Veikko Salomaa, Annie Britton, Antti Jula, Satu Männistö +4 more

Identification of healthspan-promoting genes in Caenorhabditis elegans based on a human GWAS study

Biogerontology(2022)10.1007/s10522-022-09969-8

N/A

0DataRank · unranked

9 citations

Ineke Dhondt, Mikko Kuokkanen, Markus Perola, Clara Verschuuren, Brecht Wouters +9 more

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

UNC Libraries(2020)10.17615/qy4d-rv77

N/A

0DataRank · unranked

0 citations

Albert V. Smith, Stefan Gustafsson, Laura J. Rasmussen‐Torvik, J. Wouter Jukema, P. Johnson +27 more

Markus Perola

Indexed papers

Top data-sharing exemplar

Papers