المؤلفون: Temprano‐Sagrera, Gerard, Sitlani, Colleen M, Bone, William P, Martin‐Bornez, Miguel, Voight, Benjamin F, Morrison, Alanna C, Damrauer, Scott M, de Vries, Paul S, Smith, Nicholas L, Sabater‐Lleal, Maria, Dehghan, Abbas, Heath, Adam S, Reiner, Alex P, Johnson, Andrew, Richmond, Anne, Peters, Annette, van Hylckama Vlieg, Astrid, McKnight, Barbara, Psaty, Bruce M, Hayward, Caroline, Ward‐Caviness, Cavin, O’Donnell, Christopher, Chasman, Daniel, Strachan, David P, Tregouet, David A, Mook‐Kanamori, Dennis, Gill, Dipender, Thibord, Florian, Asselbergs, Folkert W, Leebeek, Frank WG, Rosendaal, Frits R, Davies, Gail, Homuth, Georg, Temprano, Gerard, Campbell, Harry, Taylor, Herman A, Bressler, Jan, Huffman, Jennifer E, Rotter, Jerome I, Yao, Jie, Wilson, James F, Bis, Joshua C, Hahn, Julie M, Desch, Karl C, Wiggins, Kerri L, Raffield, Laura M, Bielak, Lawrence F, Yanek, Lisa R, Kleber, Marcus E, Mueller, Martina, Kavousi, Maryam, Mangino, Massimo, Liu, Melissa, Brown, Michael R, Conomos, Matthew P, Jhun, Min‐A, Chen, Ming‐Huei, de Maat, Moniek PM, Pankratz, Nathan, Peyser, Patricia A, Elliot, Paul, Wei, Peng, Wild, Philipp S, Morange, Pierre E, van der Harst, Pim, Yang, Qiong, Le, Ngoc‐Quynh, Marioni, Riccardo, Li, Ruifang, Cox, Simon R, Trompet, Stella, Felix, Stephan B, Völker, Uwe, Tang, Weihong, Koenig, Wolfgang, Jukema, J Wouter, Guo, Xiuqing, Lindstrom, Sara, Wang, Lu, Smith, Erin N, Gordon, William, de Andrade, Mariza, Brody, Jennifer A, Pattee, Jack W, Haessler, Jeffrey, Brumpton, Ben M, Chasman, Daniel I, Suchon, Pierre, Turman, Constance, Germain, Marine, MacDonald, James, Braekkan, Sigrid K

المصدر: Journal of Thrombosis and Haemostasis. 20(6)

مصطلحات موضوعية: Genetics, Biotechnology, Human Genome, Atherosclerosis, Prevention, Cardiovascular, Hematology, 2.1 Biological and endogenous factors, Aetiology, Cardiovascular Diseases, Factor XI, Genetic Predisposition to Disease, Genome-Wide Association Study, Hemostasis, Hemostatics, Humans, Phenotype, Polymorphism, Single Nucleotide, Tissue Plasminogen Activator, blood coagulation, cardiovascular diseases, genetic pleiotropy, genome-wide association study, hemostasis, Cardiorespiratory Medicine and Haematology, Clinical Sciences, Cardiovascular System & Hematology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/2wd699zzTest

المؤلفون: Mahedy, Liam, Anderson, Emma L, Tilling, Kate M, Thornton, Zak, Elmore, Andrew, Szalma, Sandor, Simen, Arthur, Culp, Meredith, Zicha, Stephen, Harel, Brian, Davey Smith, George, Smith, Erin N, Paternoster, Lavinia

المصدر: Mahedy , L , Anderson , E L , Tilling , K M , Thornton , Z , Elmore , A , Szalma , S , Simen , A , Culp , M , Zicha , S , Harel , B , Davey Smith , G , Smith , E N & Paternoster , L 2024 , ' Investigation of genetic determinants of cognitive change in later life ' , Translational Psychiatry , vol. 14 , no. 1 , 31 . https://doi.org/10.1038/s41398-023-02726-6Test

مصطلحات موضوعية: /dk/atira/pure/core/keywords/population_health_SRI, name=Bristol Population Health Science Institute

العلاقة: https://research-information.bris.ac.uk/en/publications/0b0293f0-a328-45c2-a3d5-30bafc053f42Test

الإتاحة: https://doi.org/10.1038/s41398-023-02726-6Test
https://hdl.handle.net/1983/0b0293f0-a328-45c2-a3d5-30bafc053f42Test
https://research-information.bris.ac.uk/en/publications/0b0293f0-a328-45c2-a3d5-30bafc053f42Test

المؤلفون: Bonder, Marc Jan, Smail, Craig, Gloudemans, Michael J, Frésard, Laure, Jakubosky, David, D'Antonio, Matteo, Li, Xin, Ferraro, Nicole M, Carcamo-Orive, Ivan, Mirauta, Bogdan, Seaton, Daniel D, Cai, Na, Vakili, Dara, Horta, Danilo, Zhao, Chunli, Zastrow, Diane B, Bonner, Devon E, HipSci Consortium, iPSCORE consortium, Undiagnosed Diseases Network, PhLiPS consortium, Wheeler, Matthew T, Kilpinen, Helena, Knowles, Joshua W, Smith, Erin N, Frazer, Kelly A, Montgomery, Stephen B, Stegle, Oliver

المصدر: Nature genetics. 53(3)

مصطلحات موضوعية: HipSci Consortium, iPSCORE consortium, Undiagnosed Diseases Network, PhLiPS consortium, Cell Line, Humans, Bardet-Biedl Syndrome, Cerebellar Ataxia, Rare Diseases, Proteins, Calcium Channels, Sequence Analysis, RNA, DNA Methylation, Gene Expression, Regulatory Sequences, Nucleic Acid, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Genetic Variation, Induced Pluripotent Stem Cells, Whole Genome Sequencing, Stem Cell Research - Induced Pluripotent Stem Cell, Stem Cell Research - Induced Pluripotent Stem Cell - Human, Human Genome, Stem Cell Research - Embryonic - Human, Regenerative Medicine, Genetics, Stem Cell Research - Induced Pluripotent Stem Cell - Non-Human, Stem Cell Research, 2.1 Biological and endogenous factors, 1.1 Normal biological development and functioning, Generic health relevance, Developmental Biology, Biological Sciences, Medical and Health Sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/9rp1p30xTest

المؤلفون: Paulsen, Benedikte, Skille, Hanne, Smith, Erin N, Hveem, Kristian, Gabrielsen, Maiken E, Brækkan, Sigrid K, Rosendaal, Frits R, Frazer, Kelly A, Gran, Olga V, Hansen, John-Bjarne

المصدر: Haematologica. 105(7)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Oncology and Carcinogenesis, Genetics, Rare Diseases, Cancer, Hematology, Prevention, Clinical Research, Aetiology, 2.1 Biological and endogenous factors, Alleles, Fibrinogen, Humans, Incidence, Neoplasms, Risk Factors, Venous Thromboembolism, Cardiorespiratory Medicine and Haematology, Immunology, Cardiovascular medicine and haematology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/8xc274thTest

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

الوصول الحر: https://escholarship.org/uc/item/70r233g6Test

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

الوصول الحر: https://escholarship.org/uc/item/0xg9m5j5Test

المؤلفون: D'Antonio-Chronowska, Agnieszka, Donovan, Margaret KR, Greenwald, William W Young, Nguyen, Jennifer Phuong, Fujita, Kyohei, Hashem, Sherin, Matsui, Hiroko, Soncin, Francesca, Parast, Mana, Ward, Michelle C, Coulet, Florence, Smith, Erin N, Adler, Eric, D'Antonio, Matteo, Frazer, Kelly A

المصدر: Stem Cell Reports. 13(5)

مصطلحات موضوعية: Biological Sciences, Genetics, Biotechnology, Heart Disease, Stem Cell Research - Induced Pluripotent Stem Cell - Human, Stem Cell Research, Stem Cell Research - Induced Pluripotent Stem Cell, Cardiovascular, 1.1 Normal biological development and functioning, Underpinning research, Cell Differentiation, Cells, Cultured, Chromosomes, Human, X, Female, Humans, Induced Pluripotent Stem Cells, Male, Myocytes, Cardiac, Pericardium, Transcriptome, X Chromosome Inactivation, X chromosome erosion, X chromosome inactivation, iPSC, iPSC differentiation, iPSC-derived cardiomyocytes, iPSC-derived cardiovascular progenitor cells, iPSC-derived epicardium, scRNA-seq, single-cell transcriptomics, Biochemistry and Cell Biology, Clinical Sciences, Biochemistry and cell biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/8cw3w2nqTest

المؤلفون: Benaglio, Paola, D’Antonio-Chronowska, Agnieszka, Ma, Wubin, Yang, Feng, Young Greenwald, William W, Donovan, Margaret KR, DeBoever, Christopher, Li, He, Drees, Frauke, Singhal, Sanghamitra, Matsui, Hiroko, van Setten, Jessica, Sotoodehnia, Nona, Gaulton, Kyle J, Smith, Erin N, D’Antonio, Matteo, Rosenfeld, Michael G, Frazer, Kelly A

المصدر: Nature Genetics. 51(10)

مصطلحات موضوعية: Biological Sciences, Genetics, Heart Disease, Human Genome, Cardiovascular, Stem Cell Research, Aetiology, 2.1 Biological and endogenous factors, Adolescent, Adult, Aged, Aged, 80 and over, Alleles, Atrial Fibrillation, Child, Electrocardiography, Epigenomics, Female, Genetic Predisposition to Disease, Genome, Human, Genome-Wide Association Study, Homeobox Protein Nkx-2.5, Humans, Induced Pluripotent Stem Cells, Male, Middle Aged, Myocytes, Cardiac, Phenotype, Polymorphism, Single Nucleotide, Protein Binding, Quantitative Trait Loci, Regulatory Elements, Transcriptional, Transcriptome, Young Adult, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/8b61p2fbTest

المؤلفون: Smith, Erin N, D'Antonio-Chronowska, Agnieszka, Greenwald, William W, Borja, Victor, Aguiar, Lana R, Pogue, Robert, Matsui, Hiroko, Benaglio, Paola, Borooah, Shyamanga, D'Antonio, Matteo, Ayyagari, Radha, Frazer, Kelly A

المصدر: Stem Cell Reports. 12(6)

مصطلحات موضوعية: Biological Sciences, Genetics, Neurodegenerative, Aging, Human Genome, Stem Cell Research - Embryonic - Human, Eye Disease and Disorders of Vision, Macular Degeneration, Stem Cell Research, Stem Cell Research - Induced Pluripotent Stem Cell - Human, Neurosciences, Stem Cell Research - Induced Pluripotent Stem Cell, Human Fetal Tissue, Aetiology, 2.1 Biological and endogenous factors, Eye, Female, Genetic Loci, Humans, Induced Pluripotent Stem Cells, Retinal Pigment Epithelium, Sequence Analysis, RNA, Vascular Endothelial Growth Factor A, VEGFA, age-related macular degeneration, chromatin accessibility, fine mapping, genome-wide association, iPSC-RPE, induced pluripotent stem cells, regulatory variants, retinal pigment epithelium, Biochemistry and Cell Biology, Clinical Sciences, Biochemistry and cell biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/11b8t9p2Test

المؤلفون: Lindström, Sara, Brody, Jennifer A, Turman, Constance, Germain, Marine, Bartz, Traci M, Smith, Erin N, Chen, Ming‐Huei, Puurunen, Marja, Chasman, Daniel, Hassler, Jeffrey, Pankratz, Nathan, Basu, Saonli, Guan, Weihua, Gyorgy, Beata, Ibrahim, Manal, Empana, Jean‐Philippe, Olaso, Robert, Jackson, Rebecca, Brækkan, Sigrid K, McKnight, Barbara, Deleuze, Jean‐Francois, O’Donnell, Cristopher J, Jouven, Xavier, Frazer, Kelly A, Psaty, Bruce M, Wiggins, Kerri L, Taylor, Kent, Reiner, Alexander P, Heckbert, Susan R, Kooperberg, Charles, Ridker, Paul, Hansen, John‐Bjarne, Tang, Weihong, Johnson, Andrew D, Morange, Pierre‐Emmanuel, Trégouët, David A, Kraft, Peter, Smith, Nicholas L, Kabrhel, Christopher, Consortium, on behalf of the INVENT

المصدر: Genetic Epidemiology. 43(4)

مصطلحات موضوعية: Prevention, Clinical Research, Biotechnology, Human Genome, Genetics, 2.1 Biological and endogenous factors, Aetiology, Black or African American, Alleles, Case-Control Studies, Exome, Female, Gene Frequency, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, High-Throughput Nucleotide Sequencing, Humans, Male, Microarray Analysis, Odds Ratio, Polymorphism, Single Nucleotide, Sample Size, Venous Thromboembolism, exome, genetic association, venous thromboembolism, INVENT Consortium, Public Health and Health Services, Epidemiology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/7q72p65hTest