Ida Surakka - Dissemin

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Papers authored by Ida Surakka

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2021 Pyry Helkkula, Scott M. Damrauer, Tuomo Kiiskinen, Havulinna As, Aki S. Havulinna, Juha Karjalainen, Seppo Koskinen

ORCID

, Veikko Salomaa, Daly Mj, Mark J. Daly, Aarno Palotie, Ida Surakka

ORCID

, Samuli Ripatti, FinnGen

ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease

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Bradley Crone, Amelia M. Krause, Whitney E. Hornsby, Cristen J. Willer, Ida Surakka

ORCID

Translating genetic association of lipid levels for biological and clinical application

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2020 Jonas B. Nielsen

ORCID

, Oren Rom, Ida Surakka

ORCID

, Sarah E. Graham

ORCID

, Wei Zhou

ORCID

, Tanmoy Roychowdhury, Lars G. Fritsche

ORCID

, Sarah A. Gagliano Taliun

ORCID

ORCID

, Yuhao Liu, Maiken E. Gabrielsen, Anne Heidi Skogholt, Brooke Wolford

ORCID

, William Overton, Ying Zhao and 92 other authors

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

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Shabbeer Hassan

ORCID

, Ida Surakka

ORCID

, Marja-Riitta Taskinen, Veikko Salomaa

ORCID

, Aarno Palotie, Maija Wessman, Taru Tukiainen, Matti Pirinen

ORCID

ORCID

, Samuli Ripatti

ORCID

High-resolution population-specific recombination rates and their effect on phasing and genotype imputation

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J. J. Partanen, Petri Virolainen, Sanni E. Ruotsalainen, Seppo Vainio, Outi Tuovila, Dawn Waterworth, Jeff Waring, Howard Jacob, Athena Matakidou, Juulia J. Partanen, Mark McCarthy, Anna Cichonska, Heiko Runz, Ruotsalainen Se, Kathy Klinger and 294 other authors

An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

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Bjørn O. Åsvold, Lars G. Fritsche, Ida Surakka

ORCID

, Jack A. Kosmicki, Wei Zhou, Fritsche Lg, Jonas B. Nielsen, Maiken E. Gabrielsen, Joshua Backman, Anne Heidi Skogholt, Sarah E. Graham, Y. Eugene Chen, Haocheng Lu, Seunggeun Lee, Hyun Min Kang and 43 other authors

MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

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Moksnes Mr, H. Røsjø, A. Richmond, Lyngbakken Mn, Graham Se, Hansen Af, Wolford Bn, Taliun Sag, J. LeFaive, H. Rasheed, Thomas Lf, W. Zhou, I. Surakka

ORCID

, T. Omland

Using human genetics to understand the causes and consequences of circulating cardiac troponin I in the general population

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

E. Widén, N. Junna, S. Ruotsalainen, I. Surakka

ORCID

, N. Mars, P. Ripatti, Partanen Jj, J. Aro, P. Mustonen, T. Tuomi, A. Palotie, V. Salomaa, J. Kaprio, J. Partanen, S. Ripatti

Communicating polygenic and non-genetic risk for atherosclerotic cardiovascular disease - An observational follow-up study

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Wei Zhou

ORCID

ORCID

, Omer Kabil, Julius Gudmundsson, Gudmar Thorleifsson, Josh Weinstock

ORCID

, Matthew Zawistowski

ORCID

, Jonas B. Nielsen

ORCID

, Layal Chaker, Marco Medici, Alexander Teumer

ORCID

, Silvia Naitza, Serena Sanna

ORCID

, Ulla T. Schultheiss, Anne Cappola and 41 other authors

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

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Nicholas J. Douville

ORCID

, Ida Surakka

ORCID

ORCID

, Christopher B. Douville

ORCID

, Whitney E. Hornsby

ORCID

, Chad M. Brummett, Sachin Kheterpal, Cristen J. Willer

ORCID

ORCID

, Michael R. Mathis

ORCID

Use of a Polygenic Risk Score Improves Prediction of Myocardial Injury after Non-cardiac Surgery

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P. Helkkula, T. Kiiskinen, Havulinna As, J. Karjalainen, S. Koskinen, V. Salomaa, FinnGen, Daly Mj, A. Palotie, I. Surakka

ORCID

, S. Ripatti

ANGPTL8 protein-truncating variant and the risk of coronary disease, type 2 diabetes and adverse effects

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Ida Surakka

ORCID

, Whitney E. Hornsby, Linda Farhat, Melvyn Rubenfire, Lars G. Fritsche, Kristian Hveem, Y. Eugene Chen, Robert D. Brook, Cristen J. Willer, Richard L. Weinberg

A Novel Variant in APOB Gene Causes Extremely Low LDL-C Without Known Adverse Effects

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Chen Li, Svetlana Stoma, Luca A. Lotta, Sophie Warner, Eva Albrecht, Alessandra Allione, Pascal P. Arp, Linda Broer

ORCID

, Jessica L. Buxton, Alexessander Da Silva Couto Alves

ORCID

, Joris Deelen, Iryna O. Fedko

ORCID

, Scott D. Gordon, Tao Jiang, Robert Karlsson and 84 other authors

Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length

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Sigrid Børte

ORCID

, John-Anker Zwart, Anne Heidi Skogholt, Maiken Elvestad Gabrielsen, Laurent F. Thomas, Lars G. Fritsche, Ida Surakka

ORCID

, Jonas B. Nielsen, Wei Zhou, Brooke N. Wolford, Magnus D. Vigeland, Knut Hagen, Espen Saxhaug Kristoffersen

ORCID

, Dale R. Nyholt, Daniel I. Chasman

ORCID

and 3 other authors

Mitochondrial genome-wide association study of migraine – the HUNT Study

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2019 Sini Kerminen

ORCID

, Alicia R. Martin, Jukka Koskela, Sanni E. Ruotsalainen, Aki S. Havulinna, Ida Surakka

ORCID

, Aarno Palotie, Markus Perola, Veikko Salomaa, Mark J. Daly, Samuli Ripatti, Matti Pirinen

Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Nielsen Jb, O. Rom, I. Surakka

ORCID

, Graham Se, W. Zhou, Fritsche Lg, Gagliano Taliun Sa, C. Sidore, Y. Liu, Gabrielsen Me, Skogholt Ah, B. Wolford, W. Overton, K. Hveem

Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

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Pietari Ripatti, Elisabeth Widen, Taru Tukiainen, Marja-Riitta Taskinen, Joel T. Rämö, Ramo Jt, Nina J. Mars, Mars Nj, Yu Fu, Joel T. Ramo, Sanni Soderlund, Jake Lin, Sanni Söderlund, Lin Jk, Christian Benner and 15 other authors

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

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Ben M. Brumpton, John-Anker Zwart, Brumpton Bm, Ferdinand M. van’t Hooft, Lars G. Fritsche, Bjørn Olav Åsvold, Fritsche Lg, Jonas Bille Nielsen, Jie Zheng, Maria Mannila, Nielsen Jb, Gunnhild Åberge Vie, Ida Surakka

ORCID

, Sarah E. Graham, Humaira Rasheed

ORCID

and 18 other authors

Variation in Serum PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9), Cardiovascular Disease Risk, and an Investigation of Potential Unanticipated Effects of PCSK9 Inhibition

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2018 S. Kerminen, Martin Ar, J. Koskela, Ruotsalainen Se, Havulinna As, I. Surakka

ORCID

, A. Palotie, M. Perola, V. Salomaa, Daly Mj, S. Ripatti, M. Pirinen

Geographic variation and bias in polygenic scores of complex diseases and traits in Finland

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Reetta Kivioja, Arto Pietilä, Nicolas Martinez‐Majander, Daniel Gordin, Aki S. Havulinna, Veikko Salomaa, Karoliina Aarnio, Sami Curtze, Jaana Leiviskä, Jorge Rodríguez‐Pardo

ORCID

, Ida Surakka

ORCID

, Markku Kaste, Turgut Tatlisumak, Jukka Putaala

Risk Factors for Early‐Onset Ischemic Stroke: A Case‐Control Study

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