Integrating lipidomics and genomics: emerging tools to understand cardiovascular diseases

por Tabassum, Rubina, Ripatti, Samuli
Publicado 2021

From genetic discovery to future personalized health research

por Palotie, Aarno, Widén, Elisabeth, Ripatti, Samuli
Publicado 2013

MetaPhat: Detecting and Decomposing Multivariate Associations From Univariate Genome-Wide Association Statistics

por Lin, Jake, Tabassum, Rubina, Ripatti, Samuli, Pirinen, Matti
Publicado 2020

Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes

por Tamlander, Max, Mars, Nina, Pirinen, Matti, Widén, Elisabeth, Ripatti, Samuli
Publicado 2022

Polygenic Score for Physical Activity Is Associated with Multiple Common Diseases

por SILLANPÄÄ, ELINA, PALVIAINEN, TEEMU, RIPATTI, SAMULI, KUJALA, URHO M., KAPRIO, JAAKKO
Publicado 2022

Regularized Machine Learning in the Genetic Prediction of Complex Traits

por Okser, Sebastian, Pahikkala, Tapio, Airola, Antti, Salakoski, Tapio, Ripatti, Samuli, Aittokallio, Tero
Publicado 2014

The relation of severe malocclusion to patients’ mental and behavioral disorders, growth, and speech problems

por Koskela, Anu, Neittaanmäki, Anneli, Rönnberg, Kaj, Palotie, Aarno, Ripatti, Samuli, Palotie, Tuula
Publicado 2020

Work-Related Exhaustion and Telomere Length: A Population-Based Study

por Ahola, Kirsi, Sirén, Ilari, Kivimäki, Mika, Ripatti, Samuli, Aromaa, Arpo, Lönnqvist, Jouko, Hovatta, Iiris
Publicado 2012

Towards a Molecular Systems Model of Coronary Artery Disease

por Abraham, Gad, Bhalala, Oneil G., de Bakker, Paul I. W., Ripatti, Samuli, Inouye, Michael
Publicado 2014

FINEMAP: efficient variable selection using summary data from genome-wide association studies

por Benner, Christian, Spencer, Chris C.A., Havulinna, Aki S., Salomaa, Veikko, Ripatti, Samuli, Pirinen, Matti
Publicado 2016

biMM: efficient estimation of genetic variances and covariances for cohorts with high-dimensional phenotype measurements

por Pirinen, Matti, Benner, Christian, Marttinen, Pekka, Järvelin, Marjo-Riitta, Rivas, Manuel A, Ripatti, Samuli
Publicado 2017

Childhood Adversities Are Associated with Shorter Telomere Length at Adult Age both in Individuals with an Anxiety Disorder and Controls

por Kananen, Laura, Surakka, Ida, Pirkola, Sami, Suvisaari, Jaana, Lönnqvist, Jouko, Peltonen, Leena, Ripatti, Samuli, Hovatta, Iiris
Publicado 2010

Does expecting more pain make it more intense? Factors associated with the first week pain trajectories after breast cancer surgery

por Sipilä, Reetta M., Haasio, Lassi, Meretoja, Tuomo J., Ripatti, Samuli, Estlander, Ann-Mari, Kalso, Eija A.
Publicado 2017

Lifetime risk of rheumatoid arthritis-associated interstitial lung disease in MUC5B mutation carriers

por Palomäki, Antti, Palotie, Aarno, Koskela, Jukka, Eklund, Kari K, Pirinen, Matti, Ripatti, Samuli, Laitinen, Tarja, Mars, Nina
Publicado 2021

Systematic comparison of family history and polygenic risk across 24 common diseases

por Mars, Nina, Lindbohm, Joni V., della Briotta Parolo, Pietro, Widén, Elisabeth, Kaprio, Jaakko, Palotie, Aarno, Ripatti, Samuli
Publicado 2022

Genetic Loci Associated with Allergic Sensitization in Lithuanians

por Šaulienė, Ingrida, Greičiuvienė, Jūratė, Šukienė, Laura, Juškevičiūtė, Neringa, Benner, Christian, Zinkevičienė, Auksė, Ripatti, Samuli, Donner, Kati, Kainov, Denis
Publicado 2015

Adipose tissue gene expression analysis reveals changes in inflammatory, mitochondrial respiratory and lipid metabolic pathways in obese insulin-resistant subjects

por Soronen, Jarkko, Laurila, Pirkka-Pekka, Naukkarinen, Jussi, Surakka, Ida, Ripatti, Samuli, Jauhiainen, Matti, Olkkonen, Vesa M, Yki-Järvinen, Hannele
Publicado 2012

Genome-wide association analysis of plasma lipidome identifies 495 genetic associations

por Ottensmann, Linda, Tabassum, Rubina, Ruotsalainen, Sanni E., Gerl, Mathias J., Klose, Christian, Widén, Elisabeth, Simons, Kai, Ripatti, Samuli, Pirinen, Matti
Publicado 2023

Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy

por Byars, Sean G., Huang, Qin Qin, Gray, Lesley-Ann, Bakshi, Andrew, Ripatti, Samuli, Abraham, Gad, Stearns, Stephen C., Inouye, Michael
Publicado 2017

SAIL—a software system for sample and phenotype availability across biobanks and cohorts

por Gostev, Mikhail, Fernandez-Banet, Julio, Rung, Johan, Dietrich, Joern, Prokopenko, Inga, Ripatti, Samuli, McCarthy, Mark I., Brazma, Alvis, Krestyaninova, Maria
Publicado 2011