Search Results - Mark J Daly
Mark Daly (scientist)
Mark Joseph Daly is Director of the Finnish Institute for Molecular Medicine (FIMM) at the University of Helsinki, a Professor of Genetics at Harvard Medical School, Chief of the Analytic and Translational Genetic Unit at Massachusetts General Hospital, and a member of the Broad Institute of MIT and Harvard. In the early days of the Human Genome Project, Daly helped develop the genetic model by which linkage disequilibrium could be used to map the haplotype structure of the human genome. In addition, he developed statistical methods to find associations between genes and disorders such as Crohn's disease, inflammatory bowel disease, autism and schizophrenia.Daly is considered a pioneer in the field of human genetics, and is amongst the most cited scientists in the field, and one of the top 100 most cited scientists of all time. He was elected to the National Academy of Medicine in 2017. Provided by Wikipedia
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Mosaic mutations in blood DNA sequence are associated with solid tumor cancers by Mykyta Artomov, Manuel A. Rivas, Giulio Genovese, Mark J. Daly
Published 2017-07-01
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Case Report: Supernormal Vascular Aging in Leningrad Siege Survivors by 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
Published 2022-05-01
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Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. by Soumya Raychaudhuri, Joshua M Korn, Steven A McCarroll, International Schizophrenia Consortium, David Altshuler, Pamela Sklar, Shaun Purcell, Mark J Daly
Published 2010-09-01
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ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease. by Pyry Helkkula, Tuomo Kiiskinen, Aki S Havulinna, Juha Karjalainen, Seppo Koskinen, Veikko Salomaa, Mark J Daly, Aarno Palotie, Ida Surakka, Samuli Ripatti, FinnGen
Published 2021-04-01
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Fine-Scale Genetic Structure in Finland by 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
Published 2017-10-01
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Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology. by 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
Published 2011-01-01
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Genotype imputation and polygenic score estimation in northwestern Russian population. by 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
Published 2022-01-01
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Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events by 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
Published 2024-07-01
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Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study by 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
Published 2018-04-01
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Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion by 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
Published 2019-04-01
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Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions. by 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
Published 2009-06-01
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