Suchergebnisse - Pau Navarro

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  1. 1
    The genomic signature of trait-associated variants

    The genomic signature of trait-associated variants von Alida Kindt, Pau Navarro, Colin A. Semple, Chris Haley

    Veröffentlicht 2013
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  2. 2
    Recent human effective population size estimated from linkage disequilibrium

    Recent human effective population size estimated from linkage disequilibrium von Albert Tenesa, Pau Navarro, Ben J. Hayes, David L. Duffy, Geraldine M Clarke, Michael E. Goddard, Peter M. Visscher

    Veröffentlicht 2007
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  3. 3
    Recent genomic heritage in Scotland

    Recent genomic heritage in Scotland von Carmen Amador, Jennifer E. Huffman, Holly Trochet, Archie Campbell, David J. Porteous, James F. Wilson, Nick Hastie, Véronique Vitart, Caroline Hayward, Pau Navarro, Chris Haley

    Veröffentlicht 2015
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  4. 4
    Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation

    Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation von Charley Xia, Carmen Amador, Jennifer E. Huffman, Holly Trochet, Archie Campbell, David J. Porteous, N D Hastie, Caroline Hayward, Véronique Vitart, Pau Navarro, Chris Haley

    Veröffentlicht 2016
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  5. 5
    Uncovering Networks from Genome-Wide Association Studies via Circular Genomic Permutation

    Uncovering Networks from Genome-Wide Association Studies via Circular Genomic Permutation von Claudia Cabrera, Pau Navarro, Jennifer E. Huffman, Alan F. Wright, Caroline Hayward, Harry Campbell, James F. Wilson, Igor Rudan, Nicholas D. Hastie, Véronique Vitart, Chris Haley

    Veröffentlicht 2012
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  6. 6
    Application of high-dimensional feature selection: evaluation for genomic prediction in man

    Application of high-dimensional feature selection: evaluation for genomic prediction in man von Mairead L. Bermingham, Ricardo Pong‐Wong, Athina Spiliopoulou, Caroline Hayward, Igor Rudan, Harry Campbell, Alan F. Wright, James F. Wilson, Felix Agakov, Pau Navarro, Chris Haley

    Veröffentlicht 2015
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  7. 7
    Genetic regulation of post-translational modification of two distinct proteins

    Genetic regulation of post-translational modification of two distinct proteins von Arianna Landini, Irena Trbojević‐Akmačić, Pau Navarro, Yakov A. Tsepilov, Sodbo Sharapov, Frano Vučković, Ozren Polašek, Caroline Hayward, Tea Petrović, Marija Vilaj, Yurii S. Aulchenko, Gordan Lauc, James F. Wilson, Lucija Klarić

    Veröffentlicht 2022
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  8. 8
    Genomic analysis of family data reveals additional genetic effects on intelligence and personality

    Genomic analysis of family data reveals additional genetic effects on intelligence and personality von W. David Hill, Ruben C. Arslan, Charley Xia, Michelle Luciano, Carmen Amador, Pau Navarro, Caroline Hayward, Réka Nagy, David J. Porteous, Andrew M. McIntosh, Ian J. Deary, Chris Haley, Lars Penke

    Veröffentlicht 2018
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  9. 9
    Mapping the serum proteome to neurological diseases using whole genome sequencing

    Mapping the serum proteome to neurological diseases using whole genome sequencing von Grace Png, Andrei Barysenka, L. Repetto, Pau Navarro, Xia Shen, Maik Pietzner, Eleanor Wheeler, Nicholas J. Wareham, Claudia Langenberg, Emmanouil Tsafantakis, Maria Karaleftheri, George Dedoussis, Anders Mälarstig, James F. Wilson, Arthur Gilly, Eleftheria Zeggini

    Veröffentlicht 2021
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  10. 10
    Localising Loci underlying Complex Trait Variation Using Regional Genomic Relationship Mapping

    Localising Loci underlying Complex Trait Variation Using Regional Genomic Relationship Mapping von Yoshitaka NAGAMINE, Ricardo Pong‐Wong, Pau Navarro, Véronique Vitart, Caroline Hayward, Igor Rudan, Harry Campbell, James F. Wilson, Sarah H. Wild, Andrew A. Hicks, Peter P. Pramstaller, Nicholas D. Hastie, Alan F. Wright, Chris Haley

    Veröffentlicht 2012
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  11. 11
    A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder

    A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder von Yanni Zeng, Pau Navarro, Ana Maria Fernandez-Pujals, Lynsey S. Hall, Toni‐Kim Clarke, Pippa A. Thomson, Blair H. Smith, Lynne J. Hocking, Sandosh Padmanabhan, Caroline Hayward, Donald J. MacIntyre, Naomi R. Wray, Ian J. Deary, David J. Porteous, Chris Haley, Andrew M. McIntosh

    Veröffentlicht 2016
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  12. 12
    Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits

    Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits von Andrew D. Bretherick, Oriol Canela‐Xandri, Peter K. Joshi, David W. Clark, Konrad Rawlik, Thibaud Boutin, Yanni Zeng, Carmen Amador, Pau Navarro, Igor Rudan, Alan F. Wright, Harry Campbell, Véronique Vitart, Caroline Hayward, James F. Wilson, Albert Tenesa, Chris P. Ponting, J. Kenneth Baillie, Chris Haley

    Veröffentlicht 2020
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  13. 13
    New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8

    New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8 von Véronique Vitart, Goran Benčić, Caroline Hayward, Jelena Škunca Herman, Jennifer E. Huffman, Susan Campbell, Kajo Bućan, Pau Navarro, Grgo Gunjača, Josipa Marin Lovrić, Lina Zgaga, Ivana Kolčić, Ozren Polašek, Mirna Kirin, Nicholas D. Hastie, James F. Wilson, Igor Rudan, Harry Campbell, Zoran Vatavuk, Brian W. Fleck, Alan F. Wright

    Veröffentlicht 2010
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  14. 14
    Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

    Parent of origin genetic effects on methylation in humans are common and influence complex trait variation von Yanni Zeng, Carmen Amador, Charley Xia, Riccardo E. Marioni, Duncan Sproul, Rosie M. Walker, Stewart W. Morris, Andrew D. Bretherick, Oriol Canela‐Xandri, Thibaud Boutin, David W. Clark, Archie Campbell, Konrad Rawlik, Caroline Hayward, Réka Nagy, Albert Tenesa, David J. Porteous, James F. Wilson, Ian J. Deary, Kathryn L. Evans, Andrew M. McIntosh, Pau Navarro, Chris Haley

    Veröffentlicht 2019
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  15. 15
    A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness

    A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness von Jared O’Connell, Deepti Gurdasani, Olivier Delaneau, Nicola Pirastu, Sheila Ulivi, Massimiliano Cocca, Michela Traglia, Jie Huang, Jennifer E. Huffman, Igor Rudan, Ruth McQuillan, Ross M. Fraser, Harry Campbell, Ozren Polašek, Gershim Asiki, Kenneth Ekoru, Caroline Hayward, Alan F. Wright, Véronique Vitart, Pau Navarro, Jean-François Zagury, James F. Wilson, Daniela Toniolo, Paolo Gasparini, Nicole Soranzo, Manjinder S. Sandhu, Jonathan Marchini

    Veröffentlicht 2014
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  16. 16
    Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

    Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants von Réka Nagy, Thibaud Boutin, Jonathan Marten, Jennifer E. Huffman, Shona M. Kerr, Archie Campbell, Louise Evenden, Jude Gibson, Carmen Amador, David M. Howard, Pau Navarro, Andrew P. Morris, Ian J. Deary, Lynne J. Hocking, Sandosh Padmanabhan, Blair H. Smith, Peter K. Joshi, James F. Wilson, Nicholas D. Hastie, Alan F. Wright, Andrew M. McIntosh, David J. Porteous, Chris Haley, Véronique Vitart, Caroline Hayward

    Veröffentlicht 2017
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  17. 17
    A multi-tissue atlas of regulatory variants in cattle

    A multi-tissue atlas of regulatory variants in cattle von Shuli Liu, Yahui Gao, Oriol Canela‐Xandri, Sheng Wang, Ying Yu, Wentao Cai, Bingjie Li, Ruidong Xiang, Amanda J. Chamberlain, Erola Pairo‐Castineira, Kenton D’Mellow, Konrad Rawlik, Charley Xia, Yuelin Yao, Pau Navarro, Dominique Rocha, Xiujin Li, Ze Yan, Congjun Li, Benjamin D. Rosen, Curtis P. Van Tassell, P.M. VanRaden, Shengli Zhang, Li Ma, John B. Cole, George E. Liu, Albert Tenesa, Lingzhao Fang

    Veröffentlicht 2022
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  18. 18
    Clustered Coding Variants in the Glutamate Receptor Complexes of Individuals with Schizophrenia and Bipolar Disorder

    Clustered Coding Variants in the Glutamate Receptor Complexes of Individuals with Schizophrenia and Bipolar Disorder von René Frank, Allan F. McRae, Andrew Pocklington, Louie N. van de Lagemaat, Pau Navarro, Mike D. R. Croning, Noboru H. Komiyama, Sophie J. Bradley, R. A. John Challiss, J. Douglas Armstrong, ROBERT FINN, M. P. Malloy, Alan Maclean, Sarah E. Harris, John M. Starr, Sanjeev S. Bhaskar, Eleanor Howard, Sarah Hunt, Alison J. Coffey, Venkatesh Ranganath, Panos Deloukas, Jane Rogers, Walter Muir, Ian J. Deary, Douglas Blackwood, Peter M. Visscher, Seth G. N. Grant

    Veröffentlicht 2011
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  19. 19
    Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases

    Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases von John R. B. Perry, Benjamin F. Voight, Loïc Yengo, Najaf Amin, Josée Dupuis, Martha Ganser, Harald Grallert, Pau Navarro, Man Li, Lu Qi, Valgerður Steinthórsdóttir, Robert A. Scott, Peter Almgren, Dan E. Arking, Yurii S. Aulchenko, Beverley Balkau, Rafn Benediktsson, Richard N. Bergman, Eric Boerwinkle, Lori L. Bonnycastle, Noël P. Burtt, Harry Campbell, G. Charpentier, Francis S. Collins, Christian Gieger, Todd J. Green, Samy Hadjadj, Andrew T. Hattersley, Christian Herder, Albert Hofman, Andrew D. Johnson, Anna Köttgen, Peter Kraft, Yann Labrune, Claudia Langenberg, Alisa K. Manning, Karen L. Mohlke, Andrew P. Morris, Ben A. Oostra, James S. Pankow, Ann-Kristin Petersen, Peter P. Pramstaller, Inga Prokopenko, Wolfgang Rathmann, W Rayner, Michael Roden, Igor Rudan, Denis Rybin, Laura J. Scott, Gunnar Sigurðsson, Robert Sladek, Guðmar Þorleifsson, Unnur Þorsteinsdóttir, Jaakko Tuomilehto, André G. Uitterlinden, Sidonie Vivequin, Michael N. Weedon, Alan F. Wright, Frank B. Hu, Thomas Illig, Linda Kao, James B. Meigs, James F. Wilson, Kāri Stefánsson, Cornelia M. van Duijn, David M. Altschuler, Andrew D. Morris, Michael Boehnke, Mark I. McCarthy, Philippe Froguel, Colin N. A. Palmer, Nicholas J. Wareham, Leif Groop, Timothy M. Frayling, Stéphane Cauchi

    Veröffentlicht 2012
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  20. 20
    Genome-wide association analysis identifies multiple loci related to resting heart rate

    Genome-wide association analysis identifies multiple loci related to resting heart rate von M. Eijgelsheim, Chris Newton-Cheh, N. Sotoodehnia, Paul I. W. de Bakker, Martina Müller‐Nurasyid, Alanna C. Morrison, Albert V. Smith, Aaron Isaacs, Serena Sanna, Marcus Dörr, Pau Navarro, Christian Fuchsberger, I Nolte, Eco J. C. de Geus, Karol Estrada, Shih‐Jen Hwang, Josh Bis, I.-M. Ruckert, Álvaro Alonso, L. J. Launer, J. J. Hottenga, Fernando Rivadeneira, Peter A. Noseworthy, Kenneth Rice, Siegfried Perz, Dan E. Arking, T. D. Spector, Jan A. Kors, Yurii S. Aulchenko, Kirill V. Tarasov, Georg Homuth, SH Wild, Fabio Marroni, Christian Gieger, Carmilla M.M. Licht, Ronald J. Prineas, Albert Hofman, J. I. Rotter, Andrew A. Hicks, Florian Ernst, Samer S. Najjar, A.F. Wright, Annette Peters, Ervin R. Fox, Ben A. Oostra, H K Kroemer, David Couper, Henry Völzke, Harry Campbell, Thomas Meitinger, Manuela Uda, J. C. M. Witteman, Bruce M. Psaty, H-Erich Wichmann, T. B. Harris, Stefan Kääb, David S. Siscovick, Yalda Jamshidi, André G. Uitterlinden, A. R. Folsom, Martin G. Larson, James F. Wilson, Brenda W.J.H. Penninx, Harold Snieder, Peter P. Pramstaller, Cornelia M. van Duijn, Edward G. Lakatta, Stephan B. Felix, Vilmundur Guðnason, Arne Pfeufer, Susan R. Heckbert, Bruno H. Stricker, Eric Boerwinkle, Christopher J. O’Donnell

    Veröffentlicht 2010
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