Hasil Pencarian - Mark J. Daly

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  1. 1
    Mosaic mutations in blood DNA sequence are associated with solid tumor cancers

    Mosaic mutations in blood DNA sequence are associated with solid tumor cancers oleh Mykyta Artomov, Manuel A. Rivas, Giulio Genovese, Mark J. Daly

    Diterbitkan 2017-07-01
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  2. 2
    Network Analysis of Genome-Wide Selective Constraint Reveals a Gene Network Active in Early Fetal Brain Intolerant of Mutation.

    Network Analysis of Genome-Wide Selective Constraint Reveals a Gene Network Active in Early Fetal Brain Intolerant of Mutation. oleh Jinmyung Choi, Parisa Shooshtari, Kaitlin E Samocha, Mark J Daly, Chris Cotsapas

    Diterbitkan 2016-06-01
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  3. 3
    Impaired autophagy of an intracellular pathogen induced by a Crohn's disease associated ATG16L1 variant.

    Impaired autophagy of an intracellular pathogen induced by a Crohn's disease associated ATG16L1 variant. oleh Petric Kuballa, Alan Huett, John D Rioux, Mark J Daly, Ramnik J Xavier

    Diterbitkan 2008-01-01
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  4. 4
    Genetic variants in cellular transport do not affect mesalamine response in ulcerative colitis.

    Genetic variants in cellular transport do not affect mesalamine response in ulcerative colitis. oleh Christopher J Moran, Hailiang Huang, Manuel Rivas, Jess L Kaplan, Mark J Daly, Harland S Winter

    Diterbitkan 2018-01-01
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  5. 5
    Mendelian Randomization Analysis reveals Inverse Genetic Risks between Skin Cancers and Vitiligo

    Mendelian Randomization Analysis reveals Inverse Genetic Risks between Skin Cancers and Vitiligo oleh Sarem Rashid, Ivan Molotkov, Nikolai Klebanov, Michael Shaughnessy, Mark J. Daly, Mykyta Artomov, Hensin Tsao

    Diterbitkan 2023-11-01
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  6. 6
    Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits.

    Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits. oleh Ayellet V Segrè, DIAGRAM Consortium, MAGIC investigators, Leif Groop, Vamsi K Mootha, Mark J Daly, David Altshuler

    Diterbitkan 2010-08-01
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  7. 7
    Profiling the inflammatory bowel diseases using genetics, serum biomarkers, and smoking information

    Profiling the inflammatory bowel diseases using genetics, serum biomarkers, and smoking information oleh Ruize Liu, Dalin Li, Talin Haritunians, Yunfeng Ruan, Mark J. Daly, Hailiang Huang, Dermot P.B. McGovern

    Diterbitkan 2023-10-01
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  8. 8
    Case Report: Supernormal Vascular Aging in Leningrad Siege Survivors

    Case Report: Supernormal Vascular Aging in Leningrad Siege Survivors oleh Oxana Rotar, Maria Boyarinova, Ekaterina Moguchaya, Kristina Tolkunova, Nikita Kolosov, Nikita Kolosov, Nikita Kolosov, Valeriia Rezapova, Valeriia Rezapova, Valeriia Rezapova, Olga Freylikhman, Dmitrii Usoltsev, Dmitrii Usoltsev, Dmitrii Usoltsev, Olesya Melnik, Alexey Sergushichev, Vladislav Solntsev, Anna Kostareva, Elena Dubinina, Elena Dubinina, Trudy Voortman, Trudy Voortman, Christine Stevens, Mark J. Daly, Mark J. Daly, Mark J. Daly, Alexandra Konradi, Alexandra Konradi, Evgeny Shlyakhto, Mykyta Artomov, Mykyta Artomov, Mykyta Artomov, Mykyta Artomov, Mykyta Artomov

    Diterbitkan 2022-05-01
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  9. 9
    Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.

    Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. oleh Soumya Raychaudhuri, Joshua M Korn, Steven A McCarroll, International Schizophrenia Consortium, David Altshuler, Pamela Sklar, Shaun Purcell, Mark J Daly

    Diterbitkan 2010-09-01
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  10. 10
    Host genetic variation and its microbiome interactions within the Human Microbiome Project

    Host genetic variation and its microbiome interactions within the Human Microbiome Project oleh Raivo Kolde, Eric A. Franzosa, Gholamali Rahnavard, Andrew Brantley Hall, Hera Vlamakis, Christine Stevens, Mark J. Daly, Ramnik J. Xavier, Curtis Huttenhower

    Diterbitkan 2018-01-01
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  11. 11
    Changes in the fine-scale genetic structure of Finland through the 20th century.

    Changes in the fine-scale genetic structure of Finland through the 20th century. oleh Sini Kerminen, Nicola Cerioli, Darius Pacauskas, Aki S Havulinna, Markus Perola, Pekka Jousilahti, Veikko Salomaa, Mark J Daly, Rupesh Vyas, Samuli Ripatti, Matti Pirinen

    Diterbitkan 2021-03-01
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  12. 12
    ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease.

    ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease. oleh Pyry Helkkula, Tuomo Kiiskinen, Aki S Havulinna, Juha Karjalainen, Seppo Koskinen, Veikko Salomaa, Mark J Daly, Aarno Palotie, Ida Surakka, Samuli Ripatti, FinnGen

    Diterbitkan 2021-04-01
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  13. 13
    Fine-Scale Genetic Structure in Finland

    Fine-Scale Genetic Structure in Finland oleh Sini Kerminen, Aki S. Havulinna, Garrett Hellenthal, Alicia R. Martin, Antti-Pekka Sarin, Markus Perola, Aarno Palotie, Veikko Salomaa, Mark J. Daly, Samuli Ripatti, Matti Pirinen

    Diterbitkan 2017-10-01
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  14. 14
    Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology.

    Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology. oleh Elizabeth J Rossin, Kasper Lage, Soumya Raychaudhuri, Ramnik J Xavier, Diana Tatar, Yair Benita, International Inflammatory Bowel Disease Genetics Constortium, Chris Cotsapas, Mark J Daly

    Diterbitkan 2011-01-01
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  15. 15
    Testing for an unusual distribution of rare variants.

    Testing for an unusual distribution of rare variants. oleh Benjamin M Neale, Manuel A Rivas, Benjamin F Voight, David Altshuler, Bernie Devlin, Marju Orho-Melander, Sekar Kathiresan, Shaun M Purcell, Kathryn Roeder, Mark J Daly

    Diterbitkan 2011-03-01
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  16. 16
    Genotype imputation and polygenic score estimation in northwestern Russian population.

    Genotype imputation and polygenic score estimation in northwestern Russian population. oleh Nikita Kolosov, Valeriia Rezapova, Oxana Rotar, Alexander Loboda, Olga Freylikhman, Olesya Melnik, Alexey Sergushichev, Christine Stevens, Trudy Voortman, Anna Kostareva, Alexandra Konradi, Mark J Daly, Mykyta Artomov

    Diterbitkan 2022-01-01
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  17. 17
    Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events

    Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events oleh Henrike O. Heyne, Fanny-Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie, FinnGen, Estonian Biobank research team, Reetta Kälviainen, Mark J. Daly

    Diterbitkan 2024-07-01
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  18. 18
    Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study

    Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study oleh Christopher DeBoever, Yosuke Tanigawa, Malene E. Lindholm, Greg McInnes, Adam Lavertu, Erik Ingelsson, Chris Chang, Euan A. Ashley, Carlos D. Bustamante, Mark J. Daly, Manuel A. Rivas

    Diterbitkan 2018-04-01
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  19. 19
    Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion

    Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion oleh Rossella Spataro, Maria Kousi, Sali M. K. Farhan, Jason R. Willer, Jay P. Ross, Patrick A. Dion, Guy A. Rouleau, Mark J. Daly, Benjamin M. Neale, Vincenzo La Bella, Nicholas Katsanis

    Diterbitkan 2019-04-01
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  20. 20
    Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.

    Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions. oleh Soumya Raychaudhuri, Robert M Plenge, Elizabeth J Rossin, Aylwin C Y Ng, International Schizophrenia Consortium, Shaun M Purcell, Pamela Sklar, Edward M Scolnick, Ramnik J Xavier, David Altshuler, Mark J Daly

    Diterbitkan 2009-06-01
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