Isolated populations and complex disease gene identification

Por Kristiansson, Kati, Naukkarinen, Jussi, Peltonen, Leena
Publicado em 2008

Genetics in an isolated population like Finland: a different basis for genomic medicine?

Por Kääriäinen, Helena, Muilu, Juha, Perola, Markus, Kristiansson, Kati
Publicado no J Community Genet (2017)

Association Analysis of Allelic Variants of USF1 in Coronary Atherosclerosis

Por Kristiansson, Kati, Ilveskoski, Erkki, Lehtimäki, Terho, Peltonen, Leena, Perola, Markus, Karhunen, Pekka J.
Publicado em 2008

Combined Effects of Thrombosis Pathway Gene Variants Predict Cardiovascular Events

Por Auro, Kirsi, Alanne, Mervi, Kristiansson, Kati, Silander, Kaisa, Kuulasmaa, Kari, Salomaa, Veikko, Peltonen, Leena, Perola, Markus
Publicado em 2007

Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging

Por Surakka, Ida, Kristiansson, Kati, Anttila, Verneri, Inouye, Michael, Barnes, Chris, Moutsianas, Loukas, Salomaa, Veikko, Daly, Mark, Palotie, Aarno, Peltonen, Leena, Ripatti, Samuli
Publicado em 2010

Genetic Association and Interaction Analysis of USF1 and APOA5 on Lipid Levels and Atherosclerosis

Por Laurila, Pirkka-Pekka, Naukkarinen, Jussi, Kristiansson, Kati, Ripatti, Samuli, Kauttu, Tuuli, Silander, Kaisa, Salomaa, Veikko, Perola, Markus, Karhunen, Pekka J., Barter, Philip J., Ehnholm, Christian, Peltonen, Leena
Publicado em 2009

Erratum to: high-resolution SNP array analysis of patients with developmental disorder and normal array CGH result

Por Siggberg, Linda, Ala-Mello, Sirpa, Linnankivi, Tarja, Avela, Kristiina, Scheinin, Ilari, Kristiansson, Kati, Lahermo, Päivi, Hietala, Marja, Metsähonkala, Liisa, Kuusinen, Esa, Laaksonen, Maarit, Saarela, Janna, Knuutila, Sakari
Publicado no BMC Med Genet (2014)

An epigenome-wide association study of metabolic syndrome and its components

Por Nuotio, Marja-Liisa, Pervjakova, Natalia, Joensuu, Anni, Karhunen, Ville, Hiekkalinna, Tero, Milani, Lili, Kettunen, Johannes, Järvelin, Marjo-Riitta, Jousilahti, Pekka, Metspalu, Andres, Salomaa, Veikko, Kristiansson, Kati, Perola, Markus
Publicado no Sci Rep (2020)

Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population

Por Salo, Perttu P., Havulinna, Aki S., Tukiainen, Taru, Raitakari, Olli, Lehtimäki, Terho, Kähönen, Mika, Kettunen, Johannes, Männikkö, Minna, Eriksson, Johan G., Jula, Antti, Blankenberg, Stefan, Zeller, Tanja, Salomaa, Veikko, Kristiansson, Kati, Perola, Markus
Publicado no Circ Cardiovasc Genet (2017)

Gender Differences in Genetic Risk Profiles for Cardiovascular Disease

Por Silander, Kaisa, Alanne, Mervi, Kristiansson, Kati, Saarela, Olli, Ripatti, Samuli, Auro, Kirsi, Karvanen, Juha, Kulathinal, Sangita, Niemelä, Matti, Ellonen, Pekka, Vartiainen, Erkki, Jousilahti, Pekka, Saarela, Janna, Kuulasmaa, Kari, Evans, Alun, Perola, Markus, Salomaa, Veikko, Peltonen, Leena
Publicado em 2008

Molecular Pathways Mediating Immunosuppression in Response to Prolonged Intensive Physical Training, Low-Energy Availability, and Intensive Weight Loss

Por Sarin, Heikki V., Gudelj, Ivan, Honkanen, Jarno, Ihalainen, Johanna K., Vuorela, Arja, Lee, Joseph H., Jin, Zhenzhen, Terwilliger, Joseph D., Isola, Ville, Ahtiainen, Juha P., Häkkinen, Keijo, Jurić, Julija, Lauc, Gordan, Kristiansson, Kati, Hulmi, Juha J., Perola, Markus
Publicado no Front Immunol (2019)

Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure

Por Gaál, Emília Ilona, Salo, Perttu, Kristiansson, Kati, Rehnström, Karola, Kettunen, Johannes, Sarin, Antti-Pekka, Niemelä, Mika, Jula, Antti, Raitakari, Olli T., Lehtimäki, Terho, Eriksson, Johan G., Widen, Elisabeth, Günel, Murat, Kurki, Mitja, von und zu Fraunberg, Mikael, Jääskeläinen, Juha E., Hernesniemi, Juha, Järvelin, Marjo-Riitta, Pouta, Anneli, Newton-Cheh, Christopher, Salomaa, Veikko, Palotie, Aarno, Perola, Markus
Publicado em 2012

Origins and functional impact of copy number variation in the human genome

Por Conrad, Donald F., Pinto, Dalila, Redon, Richard, Feuk, Lars, Gokcumen, Omer, Zhang, Yujun, Aerts, Jan, Andrews, T. Daniel, Barnes, Chris, Campbell, Peter, Fitzgerald, Tomas, Hu, Min, Ihm, Chun Hwa, Kristiansson, Kati, MacArthur, Daniel G., MacDonald, Jeffrey R., Onyiah, Ifejinelo, Pang, Andy Wing Chun, Robson, Sam, Stirrups, Kathy, Valsesia, Armand, Walter, Klaudia, Wei, John, Tyler-Smith, Chris, Carter, Nigel P., Lee, Charles, Scherer, Stephen W., Hurles, Matthew E.
Publicado em 2009

Genome-Wide Screen for Metabolic Syndrome Susceptibility Loci Reveals Strong Lipid Gene Contribution but No Evidence for Common Genetic Basis for Clustering of Metabolic Syndrome T...

Por Kristiansson, Kati, Perola, Markus, Tikkanen, Emmi, Kettunen, Johannes, Surakka, Ida, Havulinna, Aki S., Stančáková, Alena, Barnes, Chris, Widen, Elisabeth, Kajantie, Eero, Eriksson, Johan G., Viikari, Jorma, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T., Hartikainen, Anna-Liisa, Ruokonen, Aimo, Pouta, Anneli, Jula, Antti, Kangas, Antti J., Soininen, Pasi, Ala-Korpela, Mika, Männistö, Satu, Jousilahti, Pekka, Bonnycastle, Lori L., Järvelin, Marjo-Riitta, Kuusisto, Johanna, Collins, Francis S., Laakso, Markku, Hurles, Matthew E., Palotie, Aarno, Peltonen, Leena, Ripatti, Samuli, Salomaa, Veikko
Publicado em 2012

Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

Por Stoll, Georg, Pietiläinen, Olli P. H., Linder, Bastian, Suvisaari, Jaana, Brosi, Cornelia, Hennah, William, Leppä, Virpi, Torniainen, Minna, Ripatti, Samuli, Ala-Mello, Sirpa, Plöttner, Oliver, Rehnström, Karola, Tuulio-Henriksson, Annamari, Varilo, Teppo, Tallila, Jonna, Kristiansson, Kati, Isohanni, Matti, Kaprio, Jaakko, Eriksson, Johan G., Raitakari, Olli T., Lehtimäki, Terho, Jarvelin, Marjo-Riitta, Salomaa, Veikko, Hurles, Matthew, Stefansson, Hreinn, Peltonen, Leena, Sullivan, Patrick F., Paunio, Tiina, Lönnqvist, Jouko, Daly, Mark J., Fischer, Utz, Freimer, Nelson B., Palotie, Aarno
Publicado em 2013

Genetic Determinants of Circulating Interleukin-1 Receptor Antagonist Levels and Their Association With Glycemic Traits

Por Herder, Christian, Nuotio, Marja-Liisa, Shah, Sonia, Blankenberg, Stefan, Brunner, Eric J., Carstensen, Maren, Gieger, Christian, Grallert, Harald, Jula, Antti, Kähönen, Mika, Kettunen, Johannes, Kivimäki, Mika, Koenig, Wolfgang, Kristiansson, Kati, Langenberg, Claudia, Lehtimäki, Terho, Luotola, Kari, Marzi, Carola, Müller, Christian, Peters, Annette, Prokisch, Holger, Raitakari, Olli, Rathmann, Wolfgang, Roden, Michael, Salmi, Marko, Schramm, Katharina, Swerdlow, Daniel, Tabak, Adam G., Thorand, Barbara, Wareham, Nick, Wild, Philipp S., Zeller, Tanja, Hingorani, Aroon D., Witte, Daniel R., Kumari, Meena, Perola, Markus, Salomaa, Veikko
Publicado no Diabetes (2014)

Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis

Por Kiryluk, Krzysztof, Li, Yifu, Sanna-Cherchi, Simone, Rohanizadegan, Mersedeh, Suzuki, Hitoshi, Eitner, Frank, Snyder, Holly J., Choi, Murim, Hou, Ping, Scolari, Francesco, Izzi, Claudia, Gigante, Maddalena, Gesualdo, Loreto, Savoldi, Silvana, Amoroso, Antonio, Cusi, Daniele, Zamboli, Pasquale, Julian, Bruce A., Novak, Jan, Wyatt, Robert J., Mucha, Krzysztof, Perola, Markus, Kristiansson, Kati, Viktorin, Alexander, Magnusson, Patrik K., Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Stefansson, Kari, Boland, Anne, Metzger, Marie, Thibaudin, Lise, Wanner, Christoph, Jager, Kitty J., Goto, Shin, Maixnerova, Dita, Karnib, Hussein H., Nagy, Judit, Panzer, Ulf, Xie, Jingyuan, Chen, Nan, Tesar, Vladimir, Narita, Ichiei, Berthoux, Francois, Floege, Jürgen, Stengel, Benedicte, Zhang, Hong, Lifton, Richard P., Gharavi, Ali G.
Publicado em 2012

Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes

Por Wang, Heming, Lane, Jacqueline M., Jones, Samuel E., Dashti, Hassan S., Ollila, Hanna M., Wood, Andrew R., van Hees, Vincent T., Brumpton, Ben, Winsvold, Bendik S., Kantojärvi, Katri, Palviainen, Teemu, Cade, Brian E., Sofer, Tamar, Song, Yanwei, Patel, Krunal, Anderson, Simon G., Bechtold, David A., Bowden, Jack, Emsley, Richard, Kyle, Simon D., Little, Max A., Loudon, Andrew S., Scheer, Frank A. J. L., Purcell, Shaun M., Richmond, Rebecca C., Spiegelhalder, Kai, Tyrrell, Jessica, Zhu, Xiaofeng, Hublin, Christer, Kaprio, Jaakko A., Kristiansson, Kati, Sulkava, Sonja, Paunio, Tiina, Hveem, Kristian, Nielsen, Jonas B., Willer, Cristen J., Zwart, John-Anker, Strand, Linn B., Frayling, Timothy M., Ray, David, Lawlor, Deborah A., Rutter, Martin K., Weedon, Michael N., Redline, Susan, Saxena, Richa
Publicado no Nat Commun (2019)

Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval

Por Avery, Christy L., Sitlani, Colleen M., Arking, Dan E., Arnett, Donna K., Bis, Joshua C., Boerwinkle, Eric, Buckley, Brendan M., Chen, Y.-D. Ida, de Craen, Anton JM, Eijgelsheim, Mark, Enquobahrie, Daniel, Evans, Daniel S., Ford, Ian, Garcia, Melissa E., Gudnason, Vilmundur, Harris, Tamara B., Heckbert, Susan R., Hochner, Hagit, Hofman, Albert, Hsueh, Wen-Chi, Isaacs, Aaron, Jukema, J. Wouter, Knekt, Paul, Kors, Jan A., Krijthe, Bouwe P., Kristiansson, Kati, Laaksonen, Maarit, Liu, Yongmei, Li, Xiaohui, MacFarlane, Peter W., Newton-Cheh, Christopher, Nieminen, Markku S., Oostra, Ben A., Peloso, Gina M., Porthan, Kimmo, Rice, Kenneth, Rivadeneira, Fernando F., Rotter, Jerome I., Salomaa, Veikko, Sattar, Naveed, Siscovick, David S., Slagboom, P. Eline, Smith, Albert V., Sotoodehnia, Nona, Stott, David J., Stricker, Bruno H., Stürmer, Til, Trompet, Stella, Uitterlinden, Andre G., van Duijn, Cornelia M., Westendorp, Rudi GJ, Witteman, Jacqueline C., Whitsel, Eric A., Psaty, Bruce M.
Publicado em 2013

Adiposity as a cause of cardiovascular disease: a Mendelian randomization study

Por Hägg, Sara, Fall, Tove, Ploner, Alexander, Mägi, Reedik, Fischer, Krista, Draisma, Harmen HM, Kals, Mart, de Vries, Paul S, Dehghan, Abbas, Willems, Sara M, Sarin, Antti-Pekka, Kristiansson, Kati, Nuotio, Marja-Liisa, Havulinna, Aki S, de Bruijn, Renée FAG, Ikram, M Arfan, Kuningas, Maris, Stricker, Bruno H, Franco, Oscar H, Benyamin, Beben, Gieger, Christian, Hall, Alistair S, Huikari, Ville, Jula, Antti, Järvelin, Marjo-Riitta, Kaakinen, Marika, Kaprio, Jaakko, Kobl, Michael, Mangino, Massimo, Nelson, Christopher P, Palotie, Aarno, Samani, Nilesh J, Spector, Tim D, Strachan, David P, Tobin, Martin D, Whitfield, John B, Uitterlinden, André G, Salomaa, Veikko, Syvänen, Ann-Christine, Kuulasmaa, Kari, Magnusson, Patrik K, Esko, Tõnu, Hofman, Albert, de Geus, Eco JC, Lind, Lars, Giedraitis, Vilmantas, Perola, Markus, Evans, Alun, Ferrières, Jean, Virtamo, Jarmo, Kee, Frank, Tregouet, David-Alexandre, Arveiler, Dominique, Amouyel, Philippe, Gianfagna, Francesco, Brambilla, Paolo, Ripatti, Samuli, van Duijn, Cornelia M, Metspalu, Andres, Prokopenko, Inga, McCarthy, Mark I, Pedersen, Nancy L, Ingelsson, Erik
Publicado no Int J Epidemiol (2015)