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1دورية أكاديمية
المؤلفون: David Jakubosky, Erin N. Smith, Matteo D’Antonio, Marc Jan Bonder, William W. Young Greenwald, Agnieszka D’Antonio-Chronowska, Hiroko Matsui, i2QTL Consortium, Oliver Stegle, Stephen B. Montgomery, Christopher DeBoever, Kelly A. Frazer
المصدر: Nature Communications, Vol 11, Iss 1, Pp 1-15 (2020)
مصطلحات موضوعية: Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2041-1723
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2دورية أكاديمية
المؤلفون: David Jakubosky, Matteo D’Antonio, Marc Jan Bonder, Craig Smail, Margaret K. R. Donovan, William W. Young Greenwald, Hiroko Matsui, i2QTL Consortium, Agnieszka D’Antonio-Chronowska, Oliver Stegle, Erin N. Smith, Stephen B. Montgomery, Christopher DeBoever, Kelly A. Frazer
المصدر: Nature Communications, Vol 11, Iss 1, Pp 1-15 (2020)
مصطلحات موضوعية: Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2041-1723
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3دورية أكاديمية
المؤلفون: Jakubosky, David, D'Antonio, Matteo, Bonder, Marc Jan, Smail, Craig, Donovan, Margaret KR, Young Greenwald, William W, Matsui, Hiroko, i2QTL Consortium, D'Antonio-Chronowska, Agnieszka, Stegle, Oliver, Smith, Erin N, Montgomery, Stephen B, DeBoever, Christopher, Frazer, Kelly A
المصدر: Nature communications. 11(1)
مصطلحات موضوعية: i2QTL Consortium, Cell Line, Humans, Microsatellite Repeats, Multifactorial Inheritance, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Genetic Variation, Genome-Wide Association Study, Genetics, Human Genome, Generic health relevance
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/70r233g6
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4دورية أكاديمية
المؤلفون: Jakubosky, David, Smith, Erin N, D'Antonio, Matteo, Jan Bonder, Marc, Young Greenwald, William W, D'Antonio-Chronowska, Agnieszka, Matsui, Hiroko, i2QTL Consortium, Stegle, Oliver, Montgomery, Stephen B, DeBoever, Christopher, Frazer, Kelly A
المصدر: Nature communications. 11(1)
مصطلحات موضوعية: i2QTL Consortium, Humans, Computational Biology, Microsatellite Repeats, Genotype, Haplotypes, Algorithms, High-Throughput Nucleotide Sequencing, Whole Genome Sequencing, Human Genome, Genetics
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/0xg9m5j5
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5دورية أكاديمية
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6دورية أكاديمية
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7
المؤلفون: Mahmoud Elansary, Knut Krohn, Eleonora Porcu, Julia Dmitrieva, Michel Georges, Harm-Jan Westra, Isabel Alves, Matthias Nauck, Jan H. Veldink, Joost Verlouw, Anette Kalnapenkis, Silva Kasela, Alex W. Hewitt, Roy Oelen, Willem H. Ouwehand, Frank Beutner, Ilkka Seppälä, Yukihide Momozawa, Samuli Ripatti, Brenda W.J.H. Penninx, Patrick Deelen, Michael Stumvoll, Jenny van Dongen, Jonathan K. Pritchard, Roman Kreuzhuber, Marie-Julie Favé, Bernett Lee, Hailang Mei, Biao Zeng, Philip Awadalla, Shuang Li, Kate Downes, Gibran Hemani, Urko M. Marigorta, Anke Tönjes, Morris Swertz, Robert Warmerdam, Joseph E. Powell, Mika Kähönen, Urmo Võsa, Brandon L. Pierce, Benjamin P. Fairfax, Anand Kumar Andiappan, Bastiaan T. Heijmans, Martina Müller-Nurasyid, Sven Bergmann, Katharina Schramm, Hanieh Yaghootkar, Sina Rüeger, Monique G. P. van der Wijst, Lude Franke, Ting Qi, Rick Jansen, Greg Gibson, Cisca Wijmenga, Marc Jan Bonder, Yungil Kim, Viktorija Kukushkina, Johannes Kettunen, Joachim Thiery, Peter A C 't Hoen, Zoltán Kutalik, Jian Yang, Dylan H. de Vries, Olaf Rötzschke, Maarten van Iterson, Peter Kovacs, Peter M. Visscher, Wibowo Arindrarto, Oliver Stegle, Natalia Pervjakova, Julian C. Knight, Tõnu Esko, Annique Claringbould, Lili Milani, Patrick F. Sullivan, Habibul Ahsan, Timothy M. Frayling, Lin Tong, Uwe Völker, Reyhan Sönmez Flitman, Eline Slagboom, Dorret I. Boomsma, Holger Prokisch, Michel G. Nivard, Mawusse Agbessi, Joyce B. J. van Meurs, Alexis Battle, Futao Zhang, Emmanouil T. Dermitzakis, Morris A. Swertz, Grant W. Montgomery, Terho Lehtimäki, Coen D.A. Stehouwer, Jaanika Kronberg, Holger Kirsten, Olli T. Raitakari, Sina A. Gharib, Bruce M. Psaty, Seyhan Yazar, Markus Loeffler, Harm Brugge, Jose Alquicira Hernandez, Mark W. Christiansen, Andrew A. Brown, Markus Perola, Markus Scholz, Ashis Saha, Alexander Teumer
المساهمون: Psychiatry, APH - Mental Health, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, APH - Digital Health, Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Stem Cell Aging Leukemia and Lymphoma (SALL), BIOS Consortium, i2QTL Consortium, 't Hoen, PAC, van Meurs, J., van Dongen, J., van Iterson, M., Swertz, M.A., Jan Bonder, M., Biological Psychology, APH - Personalized Medicine, APH - Methodology, Internal Medicine, Interne Geneeskunde, MUMC+: HVC Pieken Maastricht Studie (9), MUMC+: MA Interne Geneeskunde (3), MUMC+: MA Med Staf Artsass Interne Geneeskunde (9), RS: Carim - V01 Vascular complications of diabetes and metabolic syndrome
المصدر: Nature Genetics, 53(9), 1300-1310. Nature Publishing Group
Võsa, U, Jansen, R, Nivard, M G, van Dongen, J, Boomsma, D I, Franke, L, BIOS Consortium & i2QTL Consortium 2021, ' Large-scale cis-and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression ', Nature genetics, vol. 53, no. 9, pp. 1300-1310 . https://doi.org/10.1038/s41588-021-00913-z
Nature Genetics, 53(9), 1300-+. NATURE PORTFOLIO
BIOS Consortium & i2QTL Consortium 2021, ' Large-scale cis-and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression ', Nature Genetics, vol. 53, no. 9, pp. 1300-1310 . https://doi.org/10.1038/s41588-021-00913-z
Nature Genetics
Nature genetics, vol. 53, no. 9, pp. 1300-1310
Nature Genetics, 53, 1300-1310
Nature Genetics, 53, pp. 1300-1310
Nature genetics, 53(9), 1300-1310. Nature Publishing Groupمصطلحات موضوعية: DISORDER, Multifactorial Inheritance, Quantitative Trait Loci, Genome-wide association study, Quantitative trait locus, Biology, Polymorphism, Single Nucleotide, Gene Expression Regulation/genetics, DISEASE, LINKS, Transcriptome, 03 medical and health sciences, 0302 clinical medicine, All institutes and research themes of the Radboud University Medical Center, RELEVANCE, Blood Proteins/genetics, Gene expression, Genetics, Humans, GENOME-WIDE ASSOCIATION, Polymorphism, Gene, Multifactorial Inheritance/genetics, 030304 developmental biology, Regulation of gene expression, RISK, 0303 health sciences, ARCHITECTURE, Blood Proteins, Transcriptome/genetics, Polymorphism, Single Nucleotide/genetics, Phenotype, SERINE BIOSYNTHESIS, HUMAN TRANSCRIPTOME, DEFICIENCY, Gene Expression Regulation, Expression quantitative trait loci, genome-wide association studies, gene expression, gene regulation, Quantitative Trait Loci/genetics, Nanomedicine Radboud Institute for Molecular Life Sciences [Radboudumc 19], Single Nucleotide/genetics, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/pdf