Search Results - Verneri Anttila

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  1. 1
    Statistical power and utility of meta-analysis methods for cross-phenotype genome-wide association studies

    Statistical power and utility of meta-analysis methods for cross-phenotype genome-wide association studies by Zhaozhong Zhu, Verneri Anttila, Jordan W. Smoller, Phil H. Lee

    Published 2018
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  2. 2
    Selectivity in Genetic Association with Sub-classified Migraine in Women

    Selectivity in Genetic Association with Sub-classified Migraine in Women by Daniel I. Chasman, Verneri Anttila, Julie E. Buring, Paul M. Ridker, Markus Schürks, Tobias Kurth

    Published 2014
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  3. 3
    Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging

    Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging by Ida Surakka, Kati Kristiansson, Verneri Anttila, Michael Inouye, C. Barnes, Loukas Moutsianas, Veikko Salomaa, Mark J. Daly, Aarno Palotie, Leena Peltonen, Samuli Ripatti

    Published 2010
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  4. 4
    Trait Components Provide Tools to Dissect the Genetic Susceptibility of Migraine

    Trait Components Provide Tools to Dissect the Genetic Susceptibility of Migraine by Verneri Anttila, Mikko Kallela, G. Oswell, Mari Kaunisto, Dale R. Nyholt, Eija Hämäläinen, Hannele Havanka, Matti Ilmavirta, Joseph D. Terwilliger, Eric M. Sobel, Leena Peltonen, Jaakko Kaprio, Martti Färkkilâ, Maija Wessman, Aarno Palotie

    Published 2006
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  5. 5
    An Atlas of Genetic Correlations across Human Diseases and Traits

    An Atlas of Genetic Correlations across Human Diseases and Traits by Brendan Bulik‐Sullivan, Hilary K. Finucane, Verneri Anttila, Alexander Gusev, Felix R. Day, Laramie E. Duncan, John R. B. Perry, Nick Patterson, Elise Robinson, Mark J. Daly, Alkes L. Price, Benjamin M. Neale

    Published 2015
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  6. 6
    Novel mutations consolidate<i>KCTD7</i>as a progressive myoclonus epilepsy gene

    Novel mutations consolidate<i>KCTD7</i>as a progressive myoclonus epilepsy gene by Maria Kousi, Verneri Anttila, Angela Schulz, Stella Calafato, Eveliina Jakkula, Erik Riesch, Liisa Myllykangas, Hannu Kalimo, Meral Topçu, Sarenur Gökben, Füsun Alehan, Johannes R. Lemke, Michael Alber, Aarno Palotie, Outi Kopra, Anna‐Elina Lehesjoki

    Published 2012
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  7. 7
    The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort

    The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort by Elise Robinson, Andrew Kirby, Kosha Ruparel, Jian Yang, Lauren M. McGrath, Verneri Anttila, Benjamin M. Neale, Kathleen R. Merikangas, Thomas Lehner, Patrick Sleiman, Mark J. Daly, Raquel E. Gur, Raquel E. Gur, Hákon Hákonarson

    Published 2014
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  8. 8
    An atlas of genetic correlations across human diseases and traits

    An atlas of genetic correlations across human diseases and traits by Brendan Bulik‐Sullivan, Hilary K. Finucane, Verneri Anttila, Alexander Gusev, Felix R. Day, Po‐Ru Loh, Laramie E. Duncan, John R. B. Perry, Hon‐Cheong So, Elise Robinson, Mark J. Daly, Alkes L. Price, Benjamin M. Neale

    Published 2015
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  9. 9
    Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set

    Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set by Boukje de Vries, Verneri Anttila, Tobias Freilinger, Maija Wessman, Mari Kaunisto, Mikko Kallela, Ville Artto, Lisanne S. Vijfhuizen, Hartmut Göbel, Martin Dichgans, Christian Kubisch, Michel D. Ferrari, Aarno Palotie, Gisela M. Terwindt, Arn M. J. M. van den Maagdenberg

    Published 2015
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  10. 10
    Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants

    Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants by Bendik S. Winsvold, Francesco Bettella, Aree Witoelar, Verneri Anttila, Padhraig Gormley, Tobias Kurth, Gisela M. Terwindt, Tobias Freilinger, Oleksander Frei, Alexey Shadrin, Yunpeng Wang, Anders M. Dale, Arn M. J. M. van den Maagdenberg, Daniel I. Chasman, Dale R. Nyholt, Aarno Palotie, Ole A. Andreassen, John‐Anker Zwart

    Published 2017
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  11. 11
    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 analysis

    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... by Jie Zheng, A. Mesut Erzurumluoglu, Benjamin Elsworth, John P. Kemp, Laurence J Howe, Philip Haycock, Gibran Hemani, Katherine E. Tansey, Charles Laurin, Beaté St Pourcain, Nicole M. Warrington, Hilary K. Finucane, Alkes L. Price, Brendan Bulik‐Sullivan, Verneri Anttila, Lavinia Paternoster, Tom R. Gaunt, David M. Evans, Benjamin M. Neale

    Published 2016
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  12. 12
    Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

    Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types by Hilary K. Finucane, Yakir Reshef, Verneri Anttila, Kamil Slowikowski, Alexander Gusev, Andrea Byrnes, Steven Gazal, Po‐Ru Loh, Caleb A. Lareau, Noam Shoresh, Giulio Genovese, Arpiar Saunders, Evan Z. Macosko, Samuela Pollack, John R. B. Perry, Jason D. Buenrostro, B Bernstein, Soumya Raychaudhuri, Steven A. McCarroll, Benjamin M. Neale, Alkes L. Price

    Published 2018
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  13. 13
    Partitioning heritability by functional annotation using genome-wide association summary statistics

    Partitioning heritability by functional annotation using genome-wide association summary statistics by Hilary K. Finucane, Brendan Bulik‐Sullivan, Alexander Gusev, Gosia Trynka, Yakir Reshef, Po‐Ru Loh, Verneri Anttila, Han Xu, Chongzhi Zang, Kyle Kai-How Farh, Stephan Ripke, Felix R. Day, Shaun Purcell, Eli A. Stahl, Sara Lindström, John R. B. Perry, Yukinori Okada, Soumya Raychaudhuri, Mark J. Daly, Hon‐Cheong So, Benjamin M. Neale, Alkes L. Price

    Published 2015
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  14. 14
    Genome-wide association study reveals three susceptibility loci for common migraine in the general population

    Genome-wide association study reveals three susceptibility loci for common migraine in the general population by Daniel I. Chasman, Markus Schürks, Verneri Anttila, Boukje de Vries, Ulf Schminke, Lenore J. Launer, Gisela M. Terwindt, Arn M. J. M. van den Maagdenberg, Konstanze Fendrich, Henry Völzke, Florian Ernst, Lyn R. Griffiths, Julie E. Buring, Mikko Kallela, Tobias Freilinger, Christian Kubisch, Paul M. Ridker, Aarno Palotie, Michel D. Ferrari, Wolfgang Hoffmann, Robert Y.L. Zee, Tobias Kurth

    Published 2011
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  15. 15
    Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

    Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population by Elise Robinson, Beaté St Pourcain, Verneri Anttila, Jack A. Kosmicki, Brendan Bulik‐Sullivan, Jakob Grove, Julian Maller, Kaitlin E. Samocha, Stephan Sanders, Stephan Ripke, Joanna Martin, Mads V. Hollegaard, Thomas Werge, David M. Hougaard, Benjamin M. Neale, David M. Evans, David Skuse, Preben Bo Mortensen, Anders D. Børglum, Angelica Ronald, George Davey Smith, Mark J. Daly

    Published 2016
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  16. 16
    ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

    ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties by Beaté St Pourcain, Elise Robinson, Verneri Anttila, Bernard Sullivan, Julian Maller, Jean Golding, David Skuse, Susan M. Ring, David M. Evans, Stanley Zammit, Simon E. Fisher, Benjamin M. Neale, Richard Anney, Stephan Ripke, Mads V. Hollegaard, Thomas Werge, Angelica Ronald, Jakob Grove, David M. Hougaard, Anders D. Børglum, Preben Bo Mortensen, Mark J. Daly, George Davey Smith

    Published 2017
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  17. 17
    European lactase persistence genotype shows evidence of association with increase in body mass index

    European lactase persistence genotype shows evidence of association with increase in body mass index by Johannes Kettunen, Kaisa Silander, Olli Saarela, Najaf Amin, Martina Müller‐Nurasyid, Nicholas J. Timpson, Ida Surakka, Samuli Ripatti, Jaana Laitinen, Anna‐Liisa Hartikainen, Anneli Pouta, Päivi Lahermo, Verneri Anttila, Satu Männistö, Antti Jula, Jarmo Virtamo, Veikko Salomaa, Terho Lehtimäki, Olli Raitakari, Christian Gieger, E. Wichmann, Cornelia M. van Duijn, George Davey Smith, Mark I. McCarthy, Marjo‐Riitta Järvelin, Markus Perola, L. Peltonen

    Published 2009
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  18. 18
    IFITM3 restricts the morbidity and mortality associated with influenza

    IFITM3 restricts the morbidity and mortality associated with influenza by Aaron R. Everitt, Simon Clare, Thomas Pertel, Sinu P. John, R. Wash, Sarah E. Smith, Christopher R. Chin, Eric M. Feeley, Jennifer S. Sims, David J. Adams, Helen Wise, Leanne Kane, David Goulding, Paul Digard, Verneri Anttila, J. Kenneth Baillie, Timothy Walsh, David Hume, Aarno Palotie, Yali Xue, Vincenza Colonna, Chris Tyler‐Smith, Jake Dunning, Stephen B. Gordon, Rosalind L Smyth, Peter Openshaw, Gordon Dougan, Abraham L. Brass, Paul Kellam

    Published 2012
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  19. 19
    Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas

    Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas by Else Eising, Sjoerd M. H. Huisman, Ahmed Mahfouz, Lisanne S. Vijfhuizen, Verneri Anttila, Bendik S. Winsvold, Tobias Kurth, M. Arfan Ikram, Tobias Freilinger, Jaakko Kaprio, Dorret I. Boomsma, Cornelia M. van Duijn, Marjo‐Riitta Järvelin, John‐Anker Zwart, Lydia Quaye, David P. Strachan, Christian Kubisch, Martin Dichgans, George Davey Smith, Kāri Stefánsson, Aarno Palotie, Daniel I. Chasman, Michel D. Ferrari, Gisela M. Terwindt, Boukje de Vries, Dale R. Nyholt, Boudewijn P. F. Lelieveldt, Arn M. J. M. van den Maagdenberg, Marcel J. T. Reinders

    Published 2016
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  20. 20
    High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms

    High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms by Mitja Kurki, Emília Ilona Gaál, Johannes Kettunen, Tuuli Lappalainen, Androniki Menelaou, Verneri Anttila, Femke N. G. van ’t Hof, Mikael von und zu Fraunberg, Seppo Helisalmi, Mikko Hiltunen, Hanna Lehto, Aki Laakso, Riku Kivisaari, Timo Koivisto, Antti Ronkainen, Jaakko Rinne, Lambertus A. Kiemeney, Sita H. Vermeulen, Mari Kaunisto, Johan G. Eriksson, Arpo Aromaa, Markus Perola, Terho Lehtimäki, Olli T. Raitakari, Veikko Salomaa, Murat Günel, Emmanouil T. Dermitzakis, Ynte M. Ruigrok, Gabriël J.E. Rinkel, Mika Niemelä, Juha Hernesniemi, Samuli Ripatti, Paul I. W. de Bakker, Aarno Palotie, Juha E. Jääskeläinen

    Published 2014
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