Torthaí cuardaigh - Mark Lathrop

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  1. 1
    Control of fetal hemoglobin: new insights emerging from genomics and clinical implications

    Control of fetal hemoglobin: new insights emerging from genomics and clinical implications de réir Swee Lay Thein, Stephan Menzel, Mark Lathrop, C. Garner

    Foilsithe / Cruthaithe 2009
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  2. 2
    Mapping complex disease traits with global gene expression

    Mapping complex disease traits with global gene expression de réir William Cookson, Liming Liang, Gonçalo R. Abecasis, Miriam F. Moffatt, Mark Lathrop

    Foilsithe / Cruthaithe 2009
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  3. 3
    <i>CD14</i> and Toll-like Receptor Gene Polymorphisms, Country Living, and Asthma in Adults

    <i>CD14</i> and Toll-like Receptor Gene Polymorphisms, Country Living, and Asthma in Adults de réir Lidwien A.M. Smit, Valérie Siroux, Emmanuelle Bouzigon, Marie‐Pierre Oryszczyn, Mark Lathrop, Florence Démenais, F. Kauffmann

    Foilsithe / Cruthaithe 2008
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  4. 4
    No Impact of KIF6 Genotype on Vascular Risk and Statin Response Among 18,348 Randomized Patients in the Heart Protection Study

    No Impact of KIF6 Genotype on Vascular Risk and Statin Response Among 18,348 Randomized Patients in the Heart Protection Study de réir Jemma C. Hopewell, Sarah Parish, Robert Clarke, Jane Armitage, Louise Bowman, Jörg Hager, Mark Lathrop, Rory Collins

    Foilsithe / Cruthaithe 2011
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  5. 5
    Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study

    Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study de réir Jemma C. Hopewell, Sarah Parish, Alison Offer, Emma Link, Robert Clarke, Mark Lathrop, Jane Armitage, Rory Collins

    Foilsithe / Cruthaithe 2012
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  6. 6
    <i>SLCO1B1</i>Variants and Statin-Induced Myopathy — A Genomewide Study

    <i>SLCO1B1</i>Variants and Statin-Induced Myopathy — A Genomewide Study de réir Emma Link, Sarah Parish, Jane Armitage, Louise Bowman, Simon Heath, Fumihiko Matsuda, Marta Gut, Mark Lathrop, Rory Collins

    Foilsithe / Cruthaithe 2008
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  7. 7
    Class II HLA-DC beta-chain DNA restriction fragments differentiate among HLA-DR2 individuals in insulin-dependent diabetes and multiple sclerosis.

    Class II HLA-DC beta-chain DNA restriction fragments differentiate among HLA-DR2 individuals in insulin-dependent diabetes and multiple sclerosis. de réir Daniel Cohen, Oded Cohen, A. Marcadet, Catherine Massart, Mark Lathrop, I Deschamps, J Hors, E Schuller, J Dausset

    Foilsithe / Cruthaithe 1984
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  8. 8
    Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3

    Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3 de réir Caroline Lefèvre, B. Bouadjar, Véronique Ferrand, Gianluca Tadini, André Mégarbané, Mark Lathrop, Jean‐François Prud'homme, Judith Fischer

    Foilsithe / Cruthaithe 2006
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  9. 9
    The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells

    The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells de réir Karin Wahlberg, Jie Jiang, Helen Rooks, Kiran Jawaid, Fumihiko Matsuda, Masao Yamaguchi, Mark Lathrop, Swee Lay Thein, Steve Best

    Foilsithe / Cruthaithe 2009
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  10. 10
    Polymorphism discovery in 62 DNA repair genes and haplotype associations with risks for lung and head and neck cancers

    Polymorphism discovery in 62 DNA repair genes and haplotype associations with risks for lung and head and neck cancers de réir Stefan Michiels, Patrick Danoy, P Dessen, Asit Kumar Bera, Thomas Boulet, C Bouchardy, Mark Lathrop, Alain Sarasin, Simone Benhamou

    Foilsithe / Cruthaithe 2007
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  11. 11
    Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene.

    Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene. de réir Alain Hovnanian, Philippe Duquesnoy, C Blanchet‐Bardon, Robert G. Knowlton, Serge Amselem, Mark Lathrop, L Dubertret, Jouni Uitto, Michel Goossens

    Foilsithe / Cruthaithe 1992
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  12. 12
    Genetic analysis of an F2 intercross between two chicken lines divergently selected for body-weight

    Genetic analysis of an F2 intercross between two chicken lines divergently selected for body-weight de réir Per Wahlberg, Örjan Carlborg, Mario Foglio, Xavier Tordoir, Ann‐Christine Syvänen, Mark Lathrop, Marta Gut, P.B. Siegel, Leif Andersson

    Foilsithe / Cruthaithe 2009
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  13. 13
    Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis

    Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis de réir Caroline Lefèvre, B. Bouadjar, Ayşen Karaduman, Florence Jobard, Safa Saker, Meral Özgüç, Mark Lathrop, Jean-François Prud’homme, Judith Fischer

    Foilsithe / Cruthaithe 2004
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  14. 14
    Association of the CpG Methylation Pattern of the Proximal Insulin Gene Promoter with Type 1 Diabetes

    Association of the CpG Methylation Pattern of the Proximal Insulin Gene Promoter with Type 1 Diabetes de réir Delphine Fradin, Sophie Le Fur, Clémence Mille, Nadia Naoui, Chris Groves, Diana Zélénika, Mark I. McCarthy, Mark Lathrop, Pierre Bougnères

    Foilsithe / Cruthaithe 2012
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  15. 15
    True and False Positive Peaks in Genomewide Scans: Applications of Length-Biased Sampling to Linkage Mapping

    True and False Positive Peaks in Genomewide Scans: Applications of Length-Biased Sampling to Linkage Mapping de réir Joseph D. Terwilliger, William D. Shannon, G. Mark Lathrop, John P. Nolan, Lynn R. Goldin, Gary A. Chase, Daniel E. Weeks

    Foilsithe / Cruthaithe 1997
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  16. 16
    A Replicated, Genome-Wide Significant Association of Aortic Stenosis With a Genetic Variant for Lipoprotein(a)

    A Replicated, Genome-Wide Significant Association of Aortic Stenosis With a Genetic Variant for Lipoprotein(a) de réir Benjamin J. Cairns, Sean Coffey, Ruth C. Travis, Bernard Prendergast, Jane Green, James C. Engert, Mark Lathrop, George Thanassoulis, Robert Clarke

    Foilsithe / Cruthaithe 2017
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  17. 17
    Genetic Variants of<i>FOXP2</i>and<i>KIAA0319/TTRAP/THEM2</i>Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions

    Genetic Variants of<i>FOXP2</i>and<i>KIAA0319/TTRAP/THEM2</i>Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions de réir Philippe Pinel, Fabien Fauchereau, Antonio Moreno, Alexis Barbot, Mark Lathrop, Diana Zélénika, Denis Le Bihan, Jean-Baptiste Poline, Thomas Bourgeron, Stanislas Dehaene

    Foilsithe / Cruthaithe 2012
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  18. 18
    The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans

    The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans de réir Stephan Menzel, Jie Jiang, Nicholas Silver, Joy Gallagher, Juliette Cunningham, Gabriela Surdulescu, Mark Lathrop, Martin Farrall, Tim D. Spector, Swee Lay Thein

    Foilsithe / Cruthaithe 2007
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  19. 19
    Neuropeptide Y genotype, central obesity, and abdominal fat distribution: the POUNDS LOST trial

    Neuropeptide Y genotype, central obesity, and abdominal fat distribution: the POUNDS LOST trial de réir Xiaochen Lin, Qibin Qi, Yan Zheng, Tao Huang, Mark Lathrop, Diana Zélénika, George A. Bray, Frank M. Sacks, Liming Liang, Lu Qi

    Foilsithe / Cruthaithe 2015
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  20. 20
    Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans

    Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans de réir Lisa Heinz, Gwang-Jin Kim, Slaheddine Marrakchi, Julie Christiansen, H. Turki, Marc‐Alexander Rauschendorf, Mark Lathrop, Ingrid Haußer, Andreas Zimmer, Judith Fischer

    Foilsithe / Cruthaithe 2017
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