Improved production of human type II procollagen in the yeast Pichia pastoris in shake flasks by a wireless-controlled fed-batch system

por Ruottinen, Maria, Bollok, Monika, Kögler, Martin, Neubauer, Antje, Krause, Mirja, Hämäläinen, Eija-Riitta, Myllyharju, Johanna, Vasala, Antti, Neubauer, Peter
Publicado 2008

The Collagen V Homotrimer [α1(V)](3) Production Is Unexpectedly Favored over the Heterotrimer [α1(V)](2)α2(V) in Recombinant Expression Systems

por Roulet, Muriel, Välkkilä, Merja, Chanut-Delalande, Hélène, Hämäläinen, Eija-Riitta, Kessler, Efrat, Ala-Kokko, Leena, Männikkö, Minna, Bonod-Bidaud, Christelle, Ruggiero, Florence
Publicado 2010

Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families

por Häppölä, Paavo, Gormley, Padhraig, Nuottamo, Marjo E, Artto, Ville, Sumelahti, Marja-Liisa, Nissilä, Markku, Keski-Säntti, Petra, Ilmavirta, Matti, Kaunisto, Mari A, Hämäläinen, Eija I, Ripatti, Samuli, Pirinen, Matti, Wessman, Maija, Palotie, Aarno, Kallela, Mikko
Publicado 2021

An Immune Response Network Associated with Blood Lipid Levels

por Inouye, Michael, Silander, Kaisa, Hamalainen, Eija, Salomaa, Veikko, Harald, Kennet, Jousilahti, Pekka, Männistö, Satu, Eriksson, Johan G., Saarela, Janna, Ripatti, Samuli, Perola, Markus, van Ommen, Gert-Jan B., Taskinen, Marja-Riitta, Palotie, Aarno, Dermitzakis, Emmanouil T., Peltonen, Leena
Publicado 2010

Metabonomic, transcriptomic, and genomic variation of a population cohort

por Inouye, Michael, Kettunen, Johannes, Soininen, Pasi, Silander, Kaisa, Ripatti, Samuli, Kumpula, Linda S, Hämäläinen, Eija, Jousilahti, Pekka, Kangas, Antti J, Männistö, Satu, Savolainen, Markku J, Jula, Antti, Leiviskä, Jaana, Palotie, Aarno, Salomaa, Veikko, Perola, Markus, Ala-Korpela, Mika, Peltonen, Leena
Publicado 2010

A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development

por Rahikkala, Elisa, Urpa, Lea, Ghimire, Bishwa, Topa, Hande, Kurki, Mitja I., Koskela, Maryna, Airavaara, Mikko, Hämäläinen, Eija, Pylkäs, Katri, Körkkö, Jarmo, Savolainen, Helena, Suoranta, Anu, Bertoli-Avella, Aida, Rolfs, Arndt, Mattila, Pirkko, Daly, Mark, Palotie, Aarno, Pietiläinen, Olli, Moilanen, Jukka, Kuismin, Outi
Publicado 2022

Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure

por Rämö, Joel T., Kiiskinen, Tuomo, Seist, Richard, Krebs, Kristi, Kanai, Masahiro, Karjalainen, Juha, Kurki, Mitja, Hämäläinen, Eija, Häppölä, Paavo, Havulinna, Aki S., Hautakangas, Heidi, Mägi, Reedik, Palta, Priit, Esko, Tõnu, Metspalu, Andres, Pirinen, Matti, Karczewski, Konrad J., Ripatti, Samuli, Milani, Lili, Stankovic, Konstantina M., Mäkitie, Antti, Daly, Mark J., Palotie, Aarno
Publicado 2023

Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland

por Kurki, Mitja I., Saarentaus, Elmo, Pietiläinen, Olli, Gormley, Padhraig, Lal, Dennis, Kerminen, Sini, Torniainen-Holm, Minna, Hämäläinen, Eija, Rahikkala, Elisa, Keski-Filppula, Riikka, Rauhala, Merja, Korpi-Heikkilä, Satu, Komulainen–Ebrahim, Jonna, Helander, Heli, Vieira, Päivi, Männikkö, Minna, Peltonen, Markku, Havulinna, Aki S., Salomaa, Veikko, Pirinen, Matti, Suvisaari, Jaana, Moilanen, Jukka S., Körkkö, Jarmo, Kuismin, Outi, Daly, Mark J., Palotie, Aarno
Publicado 2019

Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy

por Leu, Costin, Balestrini, Simona, Maher, Bridget, Hernández-Hernández, Laura, Gormley, Padhraig, Hämäläinen, Eija, Heggeli, Kristin, Schoeler, Natasha, Novy, Jan, Willis, Joseph, Plagnol, Vincent, Ellis, Rachael, Reavey, Eleanor, O'Regan, Mary, Pickrell, William O., Thomas, Rhys H., Chung, Seo-Kyung, Delanty, Norman, McMahon, Jacinta M., Malone, Stephen, Sadleir, Lynette G., Berkovic, Samuel F., Nashef, Lina, Zuberi, Sameer M., Rees, Mark I., Cavalleri, Gianpiero L., Sander, Josemir W., Hughes, Elaine, Helen Cross, J., Scheffer, Ingrid E., Palotie, Aarno, Sisodiya, Sanjay M.
Publicado 2015

The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

por Nehme, Ralda, Pietiläinen, Olli, Artomov, Mykyta, Tegtmeyer, Matthew, Valakh, Vera, Lehtonen, Leevi, Bell, Christina, Singh, Tarjinder, Trehan, Aditi, Sherwood, John, Manning, Danielle, Peirent, Emily, Malik, Rhea, Guss, Ellen J., Hawes, Derek, Beccard, Amanda, Bara, Anne M., Hazelbaker, Dane Z., Zuccaro, Emanuela, Genovese, Giulio, Loboda, Alexander A., Neumann, Anna, Lilliehook, Christina, Kuismin, Outi, Hamalainen, Eija, Kurki, Mitja, Hultman, Christina M., Kähler, Anna K., Paulo, Joao A., Ganna, Andrea, Madison, Jon, Cohen, Bruce, McPhie, Donna, Adolfsson, Rolf, Perlis, Roy, Dolmetsch, Ricardo, Farhi, Samouil, McCarroll, Steven, Hyman, Steven, Neale, Ben, Barrett, Lindy E., Harper, Wade, Palotie, Aarno, Daly, Mark, Eggan, Kevin
Publicado 2022

Migraine without aura: genome-wide association analysis identifies several novel susceptibility

por de Vries, Boukje, Freilinger, Tobias, Anttila, Verneri, Malik, Rainer, Kallela, Mikko, Terwindt, Gisela M, Pozo-Rosich, Patricia, Winsvold, Bendik, Nyholt, Dale R, van Oosterhout, Willebrordus PJ, Artto, Ville, Todt, Unda, Hämäläinen, Eija, Fernández-Morales, Jèssica, Louter, Mark A, Kaunisto, Mari A, Schoenen, Jean, Raitakari, Olli, Lehtimäki, Terho, Vila-Pueyo, Marta, Göbel, Hartmut, Wichmann, Erich, Sintas, Cèlia, Uitterlinden, Andre G, Hofman, Albert, Rivadeneira, Fernando, Heinze, Axel, Tronvik, Erling, van Duijn, Cornelia M, Kaprio, Jaakko, Cormand, Bru, Wessman, Maija, Frants, Rune R, Meitinger, Thomas, Müller-Myhsok, Bertram, Zwart, John-Anker, Färkkilä, Markus, Macaya, Alfons, Ferrari, Michel D, Kubisch, Christian, Palotie, Aarno, Dichgans, Martin, van den Maagdenberg, Arn MJM
Publicado 2013

Pitfalls in genetic testing: the story of missed SCN1A mutations

por Djémié, Tania, Weckhuysen, Sarah, von Spiczak, Sarah, Carvill, Gemma L., Jaehn, Johanna, Anttonen, Anna‐Kaisa, Brilstra, Eva, Caglayan, Hande S., de Kovel, Carolien G., Depienne, Christel, Gaily, Eija, Gennaro, Elena, Giraldez, Beatriz G., Gormley, Padhraig, Guerrero‐López, Rosa, Guerrini, Renzo, Hämäläinen, Eija, Hartmann, Corinna, Hernandez‐Hernandez, Laura, Hjalgrim, Helle, Koeleman, Bobby P. C., Leguern, Eric, Lehesjoki, Anna‐Elina, Lemke, Johannes R., Leu, Costin, Marini, Carla, McMahon, Jacinta M., Mei, Davide, Møller, Rikke S., Muhle, Hiltrud, Myers, Candace T., Nava, Caroline, Serratosa, Jose M., Sisodiya, Sanjay M., Stephani, Ulrich, Striano, Pasquale, van Kempen, Marjan J. A., Verbeek, Nienke E., Usluer, Sunay, Zara, Federico, Palotie, Aarno, Mefford, Heather C., Scheffer, Ingrid E., De Jonghe, Peter, Helbig, Ingo, Suls, Arvid
Publicado 2016

Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population

por Lim, Elaine T., Würtz, Peter, Havulinna, Aki S., Palta, Priit, Tukiainen, Taru, Rehnström, Karola, Esko, Tõnu, Mägi, Reedik, Inouye, Michael, Lappalainen, Tuuli, Chan, Yingleong, Salem, Rany M., Lek, Monkol, Flannick, Jason, Sim, Xueling, Manning, Alisa, Ladenvall, Claes, Bumpstead, Suzannah, Hämäläinen, Eija, Aalto, Kristiina, Maksimow, Mikael, Salmi, Marko, Blankenberg, Stefan, Ardissino, Diego, Shah, Svati, Horne, Benjamin, McPherson, Ruth, Hovingh, Gerald K., Reilly, Muredach P., Watkins, Hugh, Goel, Anuj, Farrall, Martin, Girelli, Domenico, Reiner, Alex P., Stitziel, Nathan O., Kathiresan, Sekar, Gabriel, Stacey, Barrett, Jeffrey C., Lehtimäki, Terho, Laakso, Markku, Groop, Leif, Kaprio, Jaakko, Perola, Markus, McCarthy, Mark I., Boehnke, Michael, Altshuler, David M., Lindgren, Cecilia M., Hirschhorn, Joel N., Metspalu, Andres, Freimer, Nelson B., Zeller, Tanja, Jalkanen, Sirpa, Koskinen, Seppo, Raitakari, Olli, Durbin, Richard, MacArthur, Daniel G., Salomaa, Veikko, Ripatti, Samuli, Daly, Mark J., Palotie, Aarno
Publicado 2014

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

por Anttila, Verneri, Stefansson, Hreinn, Kallela, Mikko, Todt, Unda, Terwindt, Gisela M, Calafato, M Stella, Nyholt, Dale R, Dimas, Antigone S, Freilinger, Tobias, Müller-Myhsok, Bertram, Artto, Ville, Inouye, Michael, Alakurtti, Kirsi, Kaunisto, Mari A, Hämäläinen, Eija, de Vries, Boukje, Stam, Anine H, Weller, Claudia M, Heinze, Axel, Heinze-Kuhn, Katja, Goebel, Ingrid, Borck, Guntram, Göbel, Hartmut, Steinberg, Stacy, Wolf, Christiane, Björnsson, Asgeir, Gudmundsson, Gretar, Kirchmann, Malene, Hauge, Anne, Werge, Thomas, Schoenen, Jean, Eriksson, Johan G, Hagen, Knut, Stovner, Lars, Wichmann, H-Erich, Meitinger, Thomas, Alexander, Michael, Moebus, Susanne, Schreiber, Stefan, Aulchenko, Yurii S, Breteler, Monique M B, Uitterlinden, Andre G, Hofman, Albert, van Duijn, Cornelia M, Tikka-Kleemola, Päivi, Vepsäläinen, Salli, Lucae, Susanne, Tozzi, Federica, Muglia, Pierandrea, Barrett, Jeffrey, Kaprio, Jaakko, Färkkilä, Markus, Peltonen, Leena, Stefansson, Kari, Zwart, John-Anker, Ferrari, Michel D, Olesen, Jes, Daly, Mark, Wessman, Maija, van den Maagdenberg, Arn M J M, Dichgans, Martin, Kubisch, Christian, Dermitzakis, Emmanouil T, Frants, Rune R, Palotie, Aarno
Publicado 2010

Genetic analysis for a shared biological basis between migraine and coronary artery disease

por Winsvold, Bendik S., Nelson, Christopher P., Malik, Rainer, Gormley, Padhraig, Anttila, Verneri, Vander Heiden, Jason, Elliott, Katherine S., Jacobsen, Line M., Palta, Priit, Amin, Najaf, de Vries, Boukje, Hämäläinen, Eija, Freilinger, Tobias, Ikram, M. Arfan, Kessler, Thorsten, Koiranen, Markku, Ligthart, Lannie, McMahon, George, Pedersen, Linda M., Willenborg, Christina, Won, Hong-Hee, Olesen, Jes, Artto, Ville, Assimes, Themistocles L., Blankenberg, Stefan, Boomsma, Dorret I., Cherkas, Lynn, Davey Smith, George, Epstein, Stephen E., Erdmann, Jeanette, Ferrari, Michel D., Göbel, Hartmut, Hall, Alistair S., Jarvelin, Marjo-Riitta, Kallela, Mikko, Kaprio, Jaakko, Kathiresan, Sekar, Lehtimäki, Terho, McPherson, Ruth, März, Winfried, Nyholt, Dale R., O'Donnell, Christopher J., Quaye, Lydia, Rader, Daniel J., Raitakari, Olli, Roberts, Robert, Schunkert, Heribert, Schürks, Markus, Stewart, Alexandre F.R., Terwindt, Gisela M., Thorsteinsdottir, Unnur, van den Maagdenberg, Arn M.J.M., van Duijn, Cornelia, Wessman, Maija, Kurth, Tobias, Kubisch, Christian, Dichgans, Martin, Chasman, Daniel I., Cotsapas, Chris, Zwart, John-Anker, Samani, Nilesh J., Palotie, Aarno
Publicado 2015

Genome-wide meta-analysis identifies new susceptibility loci for migraine

por Anttila, Verneri, Winsvold, Bendik S., Gormley, Padhraig, Kurth, Tobias, Bettella, Francesco, McMahon, George, Kallela, Mikko, Malik, Rainer, de Vries, Boukje, Terwindt, Gisela, Medland, Sarah E., Todt, Unda, McArdle, Wendy L., Quaye, Lydia, Koiranen, Markku, Ikram, M. Arfan, Lehtimäki, Terho, Stam, Anine H., Ligthart, Lannie, Wedenoja, Juho, Dunham, Ian, Neale, Benjamin M., Palta, Priit, Hamalainen, Eija, Schürks, Markus, Rose, Lynda M, Buring, Julie E., Ridker, Paul M., Steinberg, Stacy, Stefansson, Hreinn, Jakobsson, Finnbogi, Lawlor, Debbie A., Evans, David M., Ring, Susan M., Färkkilä, Markus, Artto, Ville, Kaunisto, Mari A, Freilinger, Tobias, Schoenen, Jean, Frants, Rune R., Pelzer, Nadine, Weller, Claudia M., Zielman, Ronald, Heath, Andrew C., Madden, Pamela A.F., Montgomery, Grant W., Martin, Nicholas G., Borck, Guntram, Göbel, Hartmut, Heinze, Axel, Heinze-Kuhn, Katja, Williams, Frances M.K., Hartikainen, Anna-Liisa, Pouta, Anneli, van den Ende, Joyce, Uitterlinden, Andre G., Hofman, Albert, Amin, Najaf, Hottenga, Jouke-Jan, Vink, Jacqueline M., Heikkilä, Kauko, Alexander, Michael, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Wichmann, Heinz Erich, Aromaa, Arpo, Eriksson, Johan G., Traynor, Bryan, Trabzuni, Daniah, Rossin, Elizabeth, Lage, Kasper, Jacobs, Suzanne B.R., Gibbs, J. Raphael, Birney, Ewan, Kaprio, Jaakko, Penninx, Brenda W., Boomsma, Dorret I., van Duijn, Cornelia, Raitakari, Olli, Jarvelin, Marjo-Riitta, Zwart, John-Anker, Cherkas, Lynn, Strachan, David P., Kubisch, Christian, Ferrari, Michel D., van den Maagdenberg, Arn M.J.M., Dichgans, Martin, Wessman, Maija, Smith, George Davey, Stefansson, Kari, Daly, Mark J., Nyholt, Dale R., Chasman, Daniel, Palotie, Aarno
Publicado 2013