From genetic discovery to future personalized health research

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

High divergence in primate-specific duplicated regions: Human and chimpanzee Chorionic Gonadotropin Beta genes

por Hallast, Pille, Saarela, Janna, Palotie, Aarno, Laan, Maris
Publicado 2008

Towards an understanding of genetic predisposition to migraine

por Anttila, Verneri, Wessman, Maija, Kallela, Mikko, Palotie, Aarno
Publicado 2011

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

Migraine genetics: from genome-wide association studies to translational insights

por Gormley, Padhraig, Winsvold, Bendik S., Nyholt, Dale R., Kallela, Mikko, Chasman, Daniel I., Palotie, Aarno
Publicado 2016

Serum calcium and risk of migraine: a Mendelian randomization study

por Yin, Peter, Anttila, Verneri, Siewert, Katherine M., Palotie, Aarno, Davey Smith, George, Voight, Benjamin F.
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

An Evaluation of Different Target Enrichment Methods in Pooled Sequencing Designs for Complex Disease Association Studies

por Day-Williams, Aaron G., McLay, Kirsten, Drury, Eleanor, Edkins, Sarah, Coffey, Alison J., Palotie, Aarno, Zeggini, Eleftheria
Publicado 2011

A Comparison of the Whole Genome Approach of MeDIP-Seq to the Targeted Approach of the Infinium HumanMethylation450 BeadChip(®) for Methylome Profiling

por Clark, Christine, Palta, Priit, Joyce, Christopher J., Scott, Carol, Grundberg, Elin, Deloukas, Panos, Palotie, Aarno, Coffey, Alison J.
Publicado 2012

Describing the genetic architecture of epilepsy through heritability analysis

por Speed, Doug, O’Brien, Terence J., Palotie, Aarno, Shkura, Kirill, Marson, Anthony G., Balding, David J., Johnson, Michael R.
Publicado 2014

Finding disease candidate genes by liquid association

por Li, Ker-Chau, Palotie, Aarno, Yuan, Shinsheng, Bronnikov, Denis, Chen, Daniel, Wei, Xuelian, Choi, Oi-Wa, Saarela, Janna, Peltonen, Leena
Publicado 2007

Sleep apnoea is a risk factor for severe COVID-19

por Strausz, Satu, Kiiskinen, Tuomo, Broberg, Martin, Ruotsalainen, Sanni, Koskela, Jukka, Bachour, Adel, Palotie, Aarno, Palotie, Tuula, Ripatti, Samuli, Ollila, Hanna M.
Publicado 2021

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

The relative proportion of comorbidities among rhinitis and rhinosinusitis patients and their impact on visit burden

por Nuutinen, Mikko, Lyly, Annina, Virkkula, Paula, Hytönen, Maija, Saarentaus, Elmo, Mäkitie, Antti, Palotie, Aarno, Torkki, Paulus, Haukka, Jari, Toppila‐Salmi, Sanna
Publicado 2022

Use of electronic health record data mining for heart failure subtyping

por Vuori, Matti A., Kiiskinen, Tuomo, Pitkänen, Niina, Kurki, Samu, Laivuori, Hannele, Laitinen, Tarja, Mäntylahti, Sampo, Palotie, Aarno, FinnGen, Niiranen, Teemu J.
Publicado 2023

Obstructive sleep apnoea and the risk for coronary heart disease and type 2 diabetes: a longitudinal population-based study in Finland

por Strausz, Satu, Havulinna, Aki S., Tuomi, Tiinamaija, Bachour, Adel, Groop, Leif, Mäkitie, Antti, Koskinen, Seppo, Salomaa, Veikko, Palotie, Aarno, Ripatti, Samuli, Palotie, Tuula
Publicado 2018

Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population

por Helkkula, Pyry, Hassan, Shabbeer, Saarentaus, Elmo, Vartiainen, Emilia, Ruotsalainen, Sanni, Leinonen, Jaakko T., Palotie, Aarno, Karjalainen, Juha, Kurki, Mitja, Ripatti, Samuli, Tukiainen, Taru
Publicado 2023

Association of APOE Haplotypes With Common Age-Related Ocular Diseases in 412,171 Individuals

por Liuska, Perttu J., Rämö, Joel T., Lemmelä, Susanna, Kaarniranta, Kai, Uusitalo, Hannu, Lahtela, Elisa, Daly, Mark J., Harju, Mika, Palotie, Aarno, Turunen, Joni A.
Publicado 2023