Bilaketaren emaitzak - 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 nork Zhaozhong Zhu, Verneri Anttila, Jordan W. Smoller, Phil H. Lee

    Argitaratua 2018
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  2. 2
    Novel hypotheses emerging from GWAS in migraine?

    Novel hypotheses emerging from GWAS in migraine? nork Arn M. J. M. van den Maagdenberg, Dale R. Nyholt, Verneri Anttila

    Argitaratua 2019
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  3. 3
    Selectivity in Genetic Association with Sub-classified Migraine in Women

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

    Argitaratua 2014
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  4. 4
    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 nork Ida Surakka, Kati Kristiansson, Verneri Anttila, Michael Inouye, C. Barnes, Loukas Moutsianas, Veikko Salomaa, Mark J. Daly, Aarno Palotie, Leena Peltonen, Samuli Ripatti

    Argitaratua 2010
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  5. 5
    Trait Components Provide Tools to Dissect the Genetic Susceptibility of Migraine

    Trait Components Provide Tools to Dissect the Genetic Susceptibility of Migraine nork 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

    Argitaratua 2006
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  6. 6
    An Atlas of Genetic Correlations across Human Diseases and Traits

    An Atlas of Genetic Correlations across Human Diseases and Traits nork 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

    Argitaratua 2015
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  7. 7
    Novel mutations consolidate<i>KCTD7</i>as a progressive myoclonus epilepsy gene

    Novel mutations consolidate<i>KCTD7</i>as a progressive myoclonus epilepsy gene nork 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

    Argitaratua 2012
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  8. 8
    The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort

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

    Argitaratua 2014
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  9. 9
    An atlas of genetic correlations across human diseases and traits

    An atlas of genetic correlations across human diseases and traits nork 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

    Argitaratua 2015
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  10. 10
    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 nork 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

    Argitaratua 2015
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  11. 11
    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 nork 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

    Argitaratua 2017
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  12. 12
    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... nork 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

    Argitaratua 2016
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  13. 13
    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 nork 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

    Argitaratua 2018
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  14. 14
    Partitioning heritability by functional annotation using genome-wide association summary statistics

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

    Argitaratua 2015
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  15. 15
    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 nork 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

    Argitaratua 2011
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  16. 16
    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 nork 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

    Argitaratua 2016
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  17. 17
    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 nork 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

    Argitaratua 2017
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  18. 18
    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 nork 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

    Argitaratua 2009
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  19. 19
    IFITM3 restricts the morbidity and mortality associated with influenza

    IFITM3 restricts the morbidity and mortality associated with influenza nork 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

    Argitaratua 2012
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  20. 20
    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 nork 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

    Argitaratua 2016
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