Association of LIN28B with Adult Adiposity-Related Traits in Females

por Leinonen, Jaakko T., Surakka, Ida, Havulinna, Aki S., Kettunen, Johannes, Luoto, Riitta, Salomaa, Veikko, Widén, Elisabeth
Publicado 2012

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

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

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

por Helkkula, Pyry, Kiiskinen, Tuomo, Havulinna, Aki S., Karjalainen, Juha, Koskinen, Seppo, Salomaa, Veikko, Daly, Mark J., Palotie, Aarno, Surakka, Ida, Ripatti, Samuli
Publicado 2021

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

por Hassan, Shabbeer, Surakka, Ida, Taskinen, Marja-Riitta, Salomaa, Veikko, Palotie, Aarno, Wessman, Maija, Tukiainen, Taru, Pirinen, Matti, Palta, Priit, Ripatti, Samuli
Publicado 2020

Targeted Resequencing of the Pericentromere of Chromosome 2 Linked to Constitutional Delay of Growth and Puberty

por Cousminer, Diana L., Leinonen, Jaakko T., Sarin, Antti-Pekka, Chheda, Himanshu, Surakka, Ida, Wehkalampi, Karoliina, Ellonen, Pekka, Ripatti, Samuli, Dunkel, Leo, Palotie, Aarno, Widén, Elisabeth
Publicado 2015

Genome‐wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway

por Hällfors, Jenni, Palviainen, Teemu, Surakka, Ida, Gupta, Richa, Buchwald, Jadwiga, Raevuori, Anu, Ripatti, Samuli, Korhonen, Tellervo, Jousilahti, Pekka, Madden, Pamela A.F., Kaprio, Jaakko, Loukola, Anu
Publicado 2018

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

por Surakka, Ida, Hornsby, Whitney E., Farhat, Linda, Rubenfire, Melvyn, Fritsche, Lars G., Hveem, Kristian, Chen, Y. Eugene, Brook, Robert D., Willer, Cristen J., Weinberg, Richard L.
Publicado 2020

Genetic, sociodemographic, lifestyle, and clinical risk factors of recurrent coronary artery disease events: a population-based cohort study

por Cho, So Mi Jemma, Koyama, Satoshi, Honigberg, Michael C, Surakka, Ida, Haidermota, Sara, Ganesh, Shriienidhie, Patel, Aniruddh P, Bhattacharya, Romit, Lee, Hokyou, Kim, Hyeon Chang, Natarajan, Pradeep
Publicado 2023

Genetic predisposition may not improve prediction of cardiac surgery-associated acute kidney injury

por Douville, Nicholas J., Larach, Daniel B., Lewis, Adam, Bastarache, Lisa, Pandit, Anita, He, Jing, Heung, Michael, Mathis, Michael, Wanderer, Jonathan P., Kheterpal, Sachin, Surakka, Ida, Kertai, Miklos D.
Publicado 2023

Genetic variants in HFE are associated with non-alcoholic fatty liver disease in lean individuals

por Sun, Zewen, Pan, Xingchen, Tian, Aowen, Surakka, Ida, Wang, Tao, Jiao, Xu, He, Shanshan, Song, Jinfang, Tian, Xin, Tong, Dan, Wen, Jianping, Zhang, Yonggang, Liu, Wanqing, Chen, Peng
Publicado 2023

Use of Genome-Wide Expression Data to Mine the “Gray Zone” of GWA Studies Leads to Novel Candidate Obesity Genes

por Naukkarinen, Jussi, Surakka, Ida, Pietiläinen, Kirsi H., Rissanen, Aila, Salomaa, Veikko, Ripatti, Samuli, Yki-Järvinen, Hannele, van Duijn, Cornelia M., Wichmann, H.-Erich, Kaprio, Jaakko, Taskinen, Marja-Riitta, Peltonen, Leena
Publicado 2010

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

por Kivioja, Reetta, Pietilä, Arto, Martinez‐Majander, Nicolas, Gordin, Daniel, Havulinna, Aki S., Salomaa, Veikko, Aarnio, Karoliina, Curtze, Sami, Leiviskä, Jaana, Rodríguez‐Pardo, Jorge, Surakka, Ida, Kaste, Markku, Tatlisumak, Turgut, Putaala, Jukka
Publicado 2018

OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism

por Perttilä, Julia, Merikanto, Krista, Naukkarinen, Jussi, Surakka, Ida, Martin, Nicolas W., Tanhuanpää, Kimmo, Grimard, Vinciane, Taskinen, Marja-Riitta, Thiele, Christoph, Salomaa, Veikko, Jula, Antti, Perola, Markus, Virtanen, Ismo, Peltonen, Leena, Olkkonen, Vesa M.
Publicado 2009

Partial Sleep Restriction Activates Immune Response-Related Gene Expression Pathways: Experimental and Epidemiological Studies in Humans

por Aho, Vilma, Ollila, Hanna M., Rantanen, Ville, Kronholm, Erkki, Surakka, Ida, van Leeuwen, Wessel M. A., Lehto, Maili, Matikainen, Sampsa, Ripatti, Samuli, Härmä, Mikko, Sallinen, Mikael, Salomaa, Veikko, Jauhiainen, Matti, Alenius, Harri, Paunio, Tiina, Porkka-Heiskanen, Tarja
Publicado 2013

Assessing multivariate gene-metabolome associations with rare variants using Bayesian reduced rank regression

por Marttinen, Pekka, Pirinen, Matti, Sarin, Antti-Pekka, Gillberg, Jussi, Kettunen, Johannes, Surakka, Ida, Kangas, Antti J., Soininen, Pasi, O’Reilly, Paul, Kaakinen, Marika, Kähönen, Mika, Lehtimäki, Terho, Ala-Korpela, Mika, Raitakari, Olli T., Salomaa, Veikko, Järvelin, Marjo-Riitta, Ripatti, Samuli, Kaski, Samuel
Publicado 2014

The Contribution of GWAS Loci in Familial Dyslipidemias

por Ripatti, Pietari, Rämö, Joel T., Söderlund, Sanni, Surakka, Ida, Matikainen, Niina, Pirinen, Matti, Pajukanta, Päivi, Sarin, Antti-Pekka, Service, Susan K., Laurila, Pirkka-Pekka, Ehnholm, Christian, Salomaa, Veikko, Wilson, Richard K., Palotie, Aarno, Freimer, Nelson B., Taskinen, Marja-Riitta, Ripatti, Samuli
Publicado 2016

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

por Ripatti, Pietari, Rämö, Joel T., Mars, Nina J., Fu, Yu, Lin, Jake, Söderlund, Sanni, Benner, Christian, Surakka, Ida, Kiiskinen, Tuomo, Havulinna, Aki S., Palta, Priit, Freimer, Nelson B., Widén, Elisabeth, Salomaa, Veikko, Tukiainen, Taru, Pirinen, Matti, Palotie, Aarno, Taskinen, Marja-Riitta, Ripatti, Samuli
Publicado 2020

Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis

por Ruotsalainen, Sanni E., Surakka, Ida, Mars, Nina, Karjalainen, Juha, Kurki, Mitja, Kanai, Masahiro, Krebs, Kristi, Graham, Sarah, Mishra, Pashupati P., Mishra, Binisha H., Sinisalo, Juha, Palta, Priit, Lehtimäki, Terho, Raitakari, Olli, Milani, Lili, Okada, Yukinori, Palotie, Aarno, Widen, Elisabeth, Daly, Mark J., Ripatti, Samuli
Publicado 2022

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

por Børte, Sigrid, Zwart, John-Anker, Skogholt, Anne Heidi, Gabrielsen, Maiken Elvestad, Thomas, Laurent F, Fritsche, Lars G, Surakka, Ida, Nielsen, Jonas B, Zhou, Wei, Wolford, Brooke N, Vigeland, Magnus D, Hagen, Knut, Kristoffersen, Espen Saxhaug, Nyholt, Dale R, Chasman, Daniel I, Brumpton, Ben M, Willer, Cristen J, Winsvold, Bendik S
Publicado 2020