Sisse Rye Ostrowski

Also affiliated with deCODE Genetics (Iceland), Aalborg University Hospital, Copenhagen University Hospital, Rigshospitalet, University College Copenhagen, Capital Region of Denmark, IT University of Copenhagen

MedicineBiochemistry, 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 3%percentile

1.4Author DataRank

Indexed papers

5in 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 5 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.

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

Nature Genetics(2024)10.1038/s41588-024-01720-y

Top 15%

1.4DataRank

Top 15%63 citations

Garðar Sveinbjörnsson, Marijana Vujković, Anne-Sofie Seidelin, Helene Gellert‐Kristensen, Gustav Ahlberg +47 more

Papers

Driven by 28 papers — median percentile 85. Top paper: “Acute COVID-19 severity and mental health morbidity trajectories in patient populations of six nations: an observational study”.

Acute COVID-19 severity and mental health morbidity trajectories in patient populations of six nations: an observational study

The Lancet Public Health(2022)10.1016/s2468-2667(22)00042-1

N/A

4.6DataRank · unranked

169 citations

Anikó Lovik, Anna Bára Unnarsdóttir, Daniel L. McCartney, Helga Ask, Kadri Kõiv +44 more

Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study

European Heart Journal(2023)10.1093/eurheartj/ehad142

N/A

2.9DataRank · unranked

113 citations

Christian Dina, Aeron Small, Christian M. Shaffer, Rebecca T. Levinson, Anna Helgadóttir +52 more

Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

Nature Genetics(2023)10.1038/s41588-023-01510-y

N/A

1.6DataRank · unranked

100 citations

Derek Klarin, Michael G. Levin, Joshua M. Spin, Yae Hyun Rhee, Alicia Deng +92 more

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

Nature Genetics(2024)10.1038/s41588-024-01720-y

Top 15%

1.4DataRank

Top 15%63 citations

Garðar Sveinbjörnsson, Marijana Vujković, Anne-Sofie Seidelin, Helene Gellert‐Kristensen, Gustav Ahlberg +47 more

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Nature Genetics(2025)10.1038/s41588-024-02072-3

N/A

0.821DataRank · unranked

50 citations

Ida Surakka, Morten S. Olesen, Garðar Sveinbjörnsson, Nicholas Marston, Seung Hoan Choi +95 more

Genetic effects on the timing of parturition and links to fetal birth weight

Nature Genetics(2023)10.1038/s41588-023-01343-9

N/A

0.695DataRank · unranked

102 citations

Christopher Flatley, Valgerður Steinthórsdóttir, Marc Vaudel, Julius Juodakis, Jing Chen +80 more

Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis

Journal of Clinical Investigation(2022)10.1172/jci158788

N/A

0.650DataRank · unranked

75 citations

Daniel J. Tyrrell, Alexi Vasbinder, Changli Wei, Feriel Presswalla, Hui Wang +37 more

High Plasma Levels of Intact and Cleaved Soluble Urokinase Receptor Reflect Immune Activation and Are Independent Predictors of Mortality in HIV-1-Infected Patients

JAIDS Journal of Acquired Immune Deficiency Syndromes(2005)10.1097/01.qai.0000157950.02076.a6

N/A

0.619DataRank · unranked

61 citations

Timo Piironen, Gunilla Høyer-Hansen, Jan Gerstoft, Bente Klarlund Pedersen, Henrik Ullum +1 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

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

Nature Genetics(2023)10.1038/s41588-023-01538-0

N/A

0.606DataRank · unranked

56 citations

Mona Ameri Chalmer, Lilja Stefánsdóttir, Ástrós Skúladóttir, Guðmundur Einarsson, Margrét B. Andrésdóttir +88 more

Time trends in per- and polyfluoroalkyl substances (PFAS) concentrations in the Danish population: A review based on published and newly analyzed data

Environmental Research(2023)10.1016/j.envres.2023.117036

N/A

0.557DataRank · unranked

40 citations

Laura Deen, Kajsa Ugelvig Petersen, Tina Kold Jensen, Paula Hammer, Regitze Sølling Wils +4 more

Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum

Nature Genetics(2025)10.1038/s41588-025-02156-8

N/A

0.464DataRank · unranked

21 citations

Laura B. L. Wittemans, Duncan S. Palmer, Nikolas Baya, Teresa Ferreira, Barney Hill +57 more

Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrum

medRxiv(2024)10.1101/2024.03.19.24304530

N/A

0.447DataRank · unranked

15 citations

Laura B. L. Wittemans, Duncan S. Palmer, Nikolas Baya, Teresa Ferreira, Barney Hill +46 more

Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci

European Heart Journal(2022)10.1093/eurheartj/ehac322

N/A

0.434DataRank · unranked

17 citations

Vinicius Tragante, Ayesha Muhammad, Gustav Ahlberg, Morten W. Skov, Dan M. Roden +22 more

Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development

JHEP Reports(2025)10.1016/j.jhepr.2025.101485

N/A

0.410DataRank · unranked

11 citations

Helene Gellert‐Kristensen, Colm J. O’Rourke, Anne-Sofie Seidelin, Gudmar Thorleifsson, Garðar Sveinbjörnsson +43 more

Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage

Nature Genetics(2024)10.1038/s41588-024-01839-y

N/A

0.360DataRank · unranked

10 citations

Valgerður Steinthórsdóttir, Lilja Stefánsdóttir, Palle Duun Rohde, Xiaoping Wu, Frank Geller +37 more

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.016

N/A

0.355DataRank · unranked

3 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +66 more

Pretransplantation Plasma ST2 Level as a Prognostic Biomarker of 1-Year Nonrelapse Mortality in Allogeneic Hematopoietic Cell Transplantation

Transplantation and Cellular Therapy(2023)10.1016/j.jtct.2022.11.009

N/A

0.330DataRank · unranked

8 citations

Sisse Rye Ostrowski, Frederikke Schierbeck, Niels Smedegaard Andersen, Lone Smidstrup Friis, Brian Kornblit +4 more

Inflammatory and endothelial host responses in community-acquired pneumonia: exploring the relationships with HbA1c, admission plasma glucose, and glycaemic gap—a cross-sectional study

Frontiers in Immunology(2024)10.3389/fimmu.2024.1372300

N/A

0.269DataRank · unranked

5 citations

Agnete Troen Lundgaard, Camilla Koch Ryrsø, Maria Hein Hegelund, Andreas Vestergaard Jensen, Peter Lommer Kristensen +6 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

Pregnancy-Associated Bleeding and Genetics: Five Sequence Variants in the Myometrium and Progesterone Signaling Pathway are associated with postpartum hemorrhage

medRxiv(2023)10.1101/2023.08.10.23293932

N/A

0.104DataRank · unranked

1 citations

Valgerður Steinthórsdóttir, Lilja Stefánsdóttir, Palle Duun Rohde, Xiaoping Wu, Frank Geller +37 more

Soluble urokinase receptor is a kidney-specific vasoconstrictor

EBioMedicine(2025)10.1016/j.ebiom.2025.106012

N/A

0.104DataRank · unranked

1 citations

Rasmus Bo Lindhardt, Georgina Gyarmati, Kirsten Madsen, Claus Bistrup, Lars Lund +7 more

Genome-wide study of somatic symptom and related disorders identifies novel genomic loci and map genetic architecture

medRxiv(2025)10.1101/2025.07.16.25331639

N/A

0.104DataRank · unranked

1 citations

Piotr Jahołkowski, Alexey Shadrin, Elise Koch, Laura Birgit Luitva, Dorte Helenius Mikkelsen +27 more

Germline Variants Influence Chronic Liver Disease Progression through Distinct Pathways

medRxiv(2025)10.1101/2025.09.16.25335186

N/A

0.104DataRank · unranked

1 citations

David E. Kaplan, Jonas Ghouse, Bao‐Li Loza, Joseph Brancale, Adam Lewis +68 more

The genetic architecture of fibromyalgia across 2.5 million individuals

medRxiv(2025)10.1101/2025.09.18.25335914

N/A

0.104DataRank · unranked

1 citations

Gyða Björnsdóttir, Keon Arbabi, Lea Urpa, Hele Haapaniemi, Gudmar Thorleifsson +46 more

Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children

The Journal of Experimental Medicine(2024)10.1084/jem.20231353

N/A

0DataRank · unranked

39 citations

Adrian Gervais, Maki Taniguchi, Liisa Saare, Karita Särekannu, Tom Le Voyer +95 more

Central role of glycosylation processes in human genetic susceptibility to SARS-CoV-2 infections with Omicron variants

medRxiv(2024)10.1101/2024.11.21.24317689

N/A

0DataRank · unranked

2 citations

Xiaoping Wu, Vilma Lammi, Erik Abner, Jesse Valliere, Katerina Nastou +36 more

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

medRxiv(2024)10.1101/2024.07.04.24309755

N/A

0DataRank · unranked

0 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +65 more

Sisse Rye Ostrowski

Indexed papers

Top data-sharing exemplar

Papers