Towards an understanding of genetic predisposition to migraine

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

Statistical power and utility of meta-analysis methods for cross-phenotype genome-wide association studies

por Zhu, Zhaozhong, Anttila, Verneri, Smoller, Jordan W., Lee, Phil H.
Publicado 2018

Novel hypotheses emerging from GWAS in migraine?

por van den Maagdenberg, Arn M. J. M., Nyholt, Dale R., Anttila, Verneri
Publicado 2019

Selectivity in Genetic Association with Sub-classified Migraine in Women

por Chasman, Daniel I., Anttila, Verneri, Buring, Julie E., Ridker, Paul M., Schürks, Markus, Kurth, Tobias
Publicado 2014

Correction: Selectivity in Genetic Association with Sub-classified Migraine in Women

por Chasman, Daniel I., Anttila, Verneri, Buring, Julie E., Ridker, Paul M., Schürks, Markus, Kurth, Tobias
Publicado 2015

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

In silico phenotyping via co-training for improved phenotype prediction from genotype

por Roqueiro, Damian, Witteveen, Menno J., Anttila, Verneri, Terwindt, Gisela M., van den Maagdenberg, Arn M.J.M., Borgwardt, Karsten
Publicado 2015

A Potential Novel Spontaneous Preterm Birth Gene, AR, Identified by Linkage and Association Analysis of X Chromosomal Markers

por Karjalainen, Minna K., Huusko, Johanna M., Ulvila, Johanna, Sotkasiira, Jenni, Luukkonen, Aino, Teramo, Kari, Plunkett, Jevon, Anttila, Verneri, Palotie, Aarno, Haataja, Ritva, Muglia, Louis J., Hallman, Mikko
Publicado 2012

The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort

por Robinson, Elise B., Kirby, Andrew, Ruparel, Kosha, Yang, Jian, McGrath, Lauren, Anttila, Verneri, Neale, Benjamin M., Merikangas, Kathleen, Lehner, Thomas, Sleiman, Patrick M.A., Daly, Mark J., Gur, Ruben, Gur, Raquel, Hakonarson, Hakon
Publicado 2014

An Atlas of Genetic Correlations across Human Diseases and Traits

por Bulik-Sullivan, Brendan, Finucane, Hilary K, Anttila, Verneri, Gusev, Alexander, Day, Felix R., Loh, Po-Ru, Duncan, Laramie, Perry, John R.B., Patterson, Nick, Robinson, Elise B., Daly, Mark J., Price, Alkes L., Neale, Benjamin M.
Publicado 2015

Genome-Wide Meta-Analysis of Sciatica in Finnish Population

por Lemmelä, Susanna, Solovieva, Svetlana, Shiri, Rahman, Benner, Christian, Heliövaara, Markku, Kettunen, Johannes, Anttila, Verneri, Ripatti, Samuli, Perola, Markus, Seppälä, Ilkka, Juonala, Markus, Kähönen, Mika, Salomaa, Veikko, Viikari, Jorma, Raitakari, Olli T., Lehtimäki, Terho, Palotie, Aarno, Viikari-Juntura, Eira, Husgafvel-Pursiainen, Kirsti
Publicado 2016

SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility—A Joint Analysis in Four European Populations

por Wolin, Annika, Lahtela, Elisa Laura, Anttila, Verneri, Petrek, Martin, Grunewald, Johan, van Moorsel, Coline H. M., Eklund, Anders, Grutters, Jan C., Kolek, Vitezslav, Mrazek, Frantisek, Kishore, Amit, Padyukov, Leonid, Pietinalho, Anne, Ronninger, Marcus, Seppänen, Mikko, Selroos, Olof, Lokki, Marja-Liisa
Publicado 2017

Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants

por Winsvold, Bendik S., Bettella, Francesco, Witoelar, Aree, Anttila, Verneri, Gormley, Padhraig, Kurth, Tobias, Terwindt, Gisela M., Freilinger, Tobias M., Frei, Oleksander, Shadrin, Alexey, Wang, Yunpeng, Dale, Anders M., van den Maagdenberg, Arn M. J. M., Chasman, Daniel I., Nyholt, Dale R., Palotie, Aarno, Andreassen, Ole A., Zwart, John-Anker
Publicado 2017

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation...

por Zheng, Jie, Erzurumluoglu, A Mesut, Elsworth, Benjamin L, Kemp, John P, Howe, Laurence, Haycock, Philip C, Hemani, Gibran, Tansey, Katherine, Laurin, Charles, Pourcain, Beate St, Warrington, Nicole M, Finucane, Hilary K, Price, Alkes L, Bulik-Sullivan, Brendan K, Anttila, Verneri, Paternoster, Lavinia, Gaunt, Tom R, Evans, David M, Neale, Benjamin M
Publicado 2017

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

por Finucane, Hilary K., Reshef, Yakir A., Anttila, Verneri, Slowikowski, Kamil, Gusev, Alexander, Byrnes, Andrea, Gazal, Steven, Loh, Po-Ru, Lareau, Caleb, Shoresh, Noam, Genovese, Giulio, Saunders, Arpiar, Macosko, Evan, Pollack, Samuela, Perry, John R.B., Buenrostro, Jason D., Bernstein, Bradley E., Raychaudhuri, Soumya, McCarroll, Steven, Neale, Benjamin M., Price, Alkes L.
Publicado 2018

Partitioning heritability by functional annotation using genome-wide association summary statistics

por Finucane, Hilary K., Bulik-Sullivan, Brendan, Gusev, Alexander, Trynka, Gosia, Reshef, Yakir, Loh, Po-Ru, Anttila, Verneri, Xu, Han, Zang, Chongzhi, Farh, Kyle, Ripke, Stephan, Day, Felix R., Consortium, ReproGen, Purcell, Shaun, Stahl, Eli, Lindstrom, Sara, Perry, John R. B., Okada, Yukinori, Raychaudhuri, Soumya, Daly, Mark, Patterson, Nick, Neale, Benjamin M., Price, Alkes L.
Publicado 2015

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

por Robinson, Elise B., St. Pourcain, Beate, Anttila, Verneri, Kosmicki, Jack A., Bulik-Sullivan, Brendan, Grove, Jakob, Maller, Julian, Samocha, Kaitlin E., Sanders, Stephan J., Ripke, Stephan, Martin, Joanna, Hollegaard, Mads V., Werge, Thomas, Hougaard, David M., Neale, Benjamin M., Evans, David M., Skuse, David, Mortensen, Preben Bo, Børglum, Anders D., Ronald, Angelica, Smith, George Davey, Daly, Mark J.
Publicado 2016

European lactase persistence genotype shows evidence of association with increase in body mass index

por Kettunen, Johannes, Silander, Kaisa, Saarela, Olli, Amin, Najaf, Müller, Martina, Timpson, Nicholas, Surakka, Ida, Ripatti, Samuli, Laitinen, Jaana, Hartikainen, Anna-Liisa, Pouta, Anneli, Lahermo, Päivi, Anttila, Verneri, Männistö, Satu, Jula, Antti, Virtamo, Jarmo, Salomaa, Veikko, Lehtimäki, Terho, Raitakari, Olli, Gieger, Christian, Wichmann, Erich H., Van Duijn, Cornelia M., Smith, George Davey, McCarthy, Mark I., Järvelin, Marjo-Riitta, Perola, Markus, Peltonen, Leena
Publicado 2010

Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies

por Pérez-Palma, Eduardo, Helbig, Ingo, Klein, Karl Martin, Anttila, Verneri, Horn, Heiko, Reinthaler, Eva Maria, Gormley, Padhraig, Ganna, Andrea, Byrnes, Andrea, Pernhorst, Katharina, Toliat, Mohammad R, Saarentaus, Elmo, Howrigan, Daniel P, Hoffman, Per, Miquel, Juan Francisco, De Ferrari, Giancarlo V, Nürnberg, Peter, Lerche, Holger, Zimprich, Fritz, Neubauer, Bern A, Becker, Albert J, Rosenow, Felix, Perucca, Emilio, Zara, Federico, Weber, Yvonne G, Lal, Dennis
Publicado 2017

IFITM3 restricts the morbidity and mortality associated with influenza

por Everitt, Aaron R., Clare, Simon, Pertel, Thomas, John, Sinu P., Wash, Rachael S., Smith, Sarah E., Chin, Christopher R., Feeley, Eric M., Sims, Jennifer S., Adams, David J., Wise, Helen M., Kane, Leanne, Goulding, David A., Digard, Paul, Anttila, Verneri, Baillie, J. Kenneth, Walsh, Tim S., Hume, David A., Palotie, Aarno, Xue, Yali, Colonna, Vincenza, Tyler-Smith, Chris, Dunning, Jake, Gordon, Stephen B., Smyth, Rosalind L., Openshaw, Peter, Dougan, Gordon, Brass, Abraham L., Kellam, Paul
Publicado 2012