المؤلفون: Timing Liu, Alagu Sankareswaran, Gordon Paterson, Genes & Health Research Team, Diane P. Fraser, Sam Hodgson, Qin Qin Huang, Teng Hiang Heng, Meera Ladwa, Nick Thomas, David A. van Heel, Michael N. Weedon, Chittaranjan S. Yajnik, Richard A. Oram, Giriraj R. Chandak, Hilary C. Martin, Sarah Finer

المصدر: Scientific Reports, Vol 15, Iss 1, Pp 1-12 (2025)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2045-2322

URL الوصول: https://doaj.org/article/7a37f0f10e5b48e8a38e858c66b30058

المؤلفون: Benjamin M. Jacobs, Daniel Stow, Sam Hodgson, Julia Zöllner, Miriam Samuel, Stavroula Kanoni, Saeed Bidi, Genes & Health Research Team, Klaudia Walter, Claudia Langenberg, Ruth Dobson, Sarah Finer, Caroline Morton, Moneeza K. Siddiqui, Hilary C. Martin, Maik Pietzner, Rohini Mathur, David A. van Heel

المصدر: Nature Communications, Vol 15, Iss 1, Pp 1-12 (2024)

مصطلحات موضوعية: Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2041-1723

URL الوصول: https://doaj.org/article/a55af57d72a54cd593f54dfaf2d077e0

المؤلفون: Alexander T. Williams, Jing Chen, Kayesha Coley, Chiara Batini, Abril Izquierdo, Richard Packer, Erik Abner, Stavroula Kanoni, David J. Shepherd, Robert C. Free, Edward J. Hollox, Nigel J. Brunskill, Ioanna Ntalla, Nicola Reeve, Christopher E. Brightling, Laura Venn, Emma Adams, Catherine Bee, Susan E. Wallace, Manish Pareek, Anna L. Hansell, Tõnu Esko, Estonian Biobank Research Team, Daniel Stow, Benjamin M. Jacobs, David A. van Heel, Genes & Health Research Team, William Hennah, Balasubramanya S. Rao, Frank Dudbridge, Louise V. Wain, Nick Shrine, Martin D. Tobin, Catherine John

المصدر: Nature Communications, Vol 14, Iss 1, Pp 1-14 (2023)

مصطلحات موضوعية: Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2041-1723

URL الوصول: https://doaj.org/article/e621fa13197b48d594bb390c78b9b2c1

المؤلفون: Sylvia Hartmann, Summaira Yasmeen, Benjamin M. Jacobs, Spiros Denaxas, Munir Pirmohamed, Eric R. Gamazon, Mark J. Caulfield, Genes & Health Research Team, Harry Hemingway, Maik Pietzner, Claudia Langenberg

المصدر: Nature Communications, Vol 14, Iss 1, Pp 1-11 (2023)

مصطلحات موضوعية: Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2041-1723

URL الوصول: https://doaj.org/article/afa46f3656294092abb905cb5110852c

المؤلفون: Sam Hodgson, Qin Qin Huang, Neneh Sallah, Genes & Health Research Team, Chris J Griffiths, William G Newman, Richard C Trembath, John Wright, R Thomas Lumbers, Karoline Kuchenbaecker, David A van Heel, Rohini Mathur, Hilary C Martin, Sarah Finer

المصدر: PLoS Medicine, Vol 19, Iss 5, p e1003981 (2022)

مصطلحات موضوعية: Medicine

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1549-1277; https://doaj.org/toc/1549-1676

URL الوصول: https://doaj.org/article/62845c8652514e528a945b09500a0c31

المؤلفون: Xiangrui Meng, Georgina Navoly, Olga Giannakopoulou, Daniel F. Levey, Dora Koller, Gita A. Pathak, Koen, Nastassja, Lin, Kuang, Adams, Mark J., Rentería, Miguel E., Feng, Yanzhe, Gaziano, J. Michael, Stein, Dan J., Zar, Heather J., Campbell, Megan L., van Heel, David A., Trivedi, Bhavi, Finer, Sarah, McQuillin, Andrew, Bass, Nick, Chundru, V. Kartik, Martin, Hilary C., Huang, Qin Qin, Valkovskaya, Maria, Chu, Chia-Yi, Kanjira, Susan, Kuo, Po-Hsiu, Chen, Hsi-Chung, Tsai, Shih-Jen, Liu, Yu-Li, Kendler, Kenneth S., Peterson, Roseann E., Cai, Na, Fang, Yu, Sen, Srijan, Scott, Laura J., Burmeister, Margit, Loos, Ruth J. F., Preuss, Michael H., Actkins, Ky'Era V., Davis, Lea K., Uddin, Monica, Wani, Agaz H, Wildman, Derek E., Aiello, Allison E., Ursano, Robert J., Kessler, Ronald C., Kanai, Masahiro, Okada, Yukinori, Sakaue, Saori, Rabinowitz, Jill, Maher, Brion S., Uhl, George, Eaton, William, Cruz-Fuentes, Carlos S., Martinez-Levy, Gabriela A., Campos, Adrian I., Millwood, Iona Y., Chen, Zhengming, Li, Liming, Wassertheil-Smoller, Sylvia, Jiang, Yunxuan, Tian, Chao, Martin, Nicholas G., Mitchell, Brittany L., Byrne, Enda M., Awasthi, Swapnil, Coleman, Jonathan R. I., Ripke, Stephan, PGC MDD Working Group, China Kadoorie Biobank Collaborative Group, the 23andMe Research Team, Genes & Health Research Team, BioBank Japan Project, Sofer, Tamar, Walters, Robin G., McIntosh, Andrew M., Polimanti, Renato, Dunn, Erin C., Stein, Murray B., Gelernter, Joel, Lewis, Cathryn M., Kuchenbaecker, Karoline

المصدر: Nature Genetics, (2024-01-04)

مصطلحات موضوعية: GWAS, major depression, multi ancestry

Relation: https://doi.org/10.1101/2022.07.20.500802; https://doi.org/10.1038/s41588-023-01596-4; https://doi.org/10.6084/m9.figshare.24799299; https://zenodo.org/communities/eu; https://doi.org/10.5281/zenodo.8335658; https://doi.org/10.5281/zenodo.8335659; oai:zenodo.org:8335659

الاتاحة: https://doi.org/10.5281/zenodo.8335659

المؤلفون: Burley, K, Fitzgibbon, L, van Heel, D, Genes & Health Research Team@EastLondonGenes, Vuckovic, D, Mumford, AD, Genes & Health Research Team

مصطلحات موضوعية: Bangladesh, blood platelets, cardiovascular diseases, genome-wide association study, phosphatidylinositol 3-kinases

وصف الملف: 100175 - ?

Relation: Res Pract Thromb Haemost; https://qmro.qmul.ac.uk/xmlui/handle/123456789/89162

الاتاحة: https://qmro.qmul.ac.uk/xmlui/handle/123456789/89162
https://doi.org/10.1016/j.rpth.2023.100175

المؤلفون: deCODE Genetics, Estonian Biobank, FinnGen, Generation Scotland, Genes & Health Research Team, LifeLines, Mass General Brigham Biobank, Michigan Genomics Initiative, National Biobank of Korea, Penn Medicine BioBank, Qatar Biobank, The QSkin Sun and Health Study, Taiwan Biobank, The HUNT Study, UCLA ATLAS Community Health Initiative, Uganda Genome Resource, UK Biobank, Biobank of the Americas, BioBank Japan Project, BioMe, BioVU, CanPath - Ontario Health Study, China Kadoorie Biobank Collaborative Group, Colorado Center for Personalized Medicine, Zhou, Wei, Kanai, Masahiro, Wu, Kuan Han H., Surakka, Ida, Partanen, Juulia J., Karjalainen, Juha, Kurki, Mitja, Palta, Priit, Ganna, Andrea, Koskela, Jukka T., Palotie, Aarno V., Daly, Mark J., Neale, Benjamin M.

المساهمون: Samuli Olli Ripatti / Principal Investigator, Institute for Molecular Medicine Finland, Complex Disease Genetics, Genomics of Neurological and Neuropsychiatric Disorders, Data Science Genetic Epidemiology Lab, University of Helsinki, HUS Abdominal Center, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, HUS Helsinki and Uusimaa Hospital District

مصطلحات موضوعية: ancestry diversity, biobank, genetic association studies, GWAS, meta-analysis, phenotype harmonization, Biomedicine, Genetics, developmental biology, physiology

وصف الملف: application/pdf

Relation: The work of the contributing biobanks was supported by numerous grants from governmental and charitable bodies. Biobank-specific acknowledgments and more detailed acknowledgments are included in Data S2. Initiative management, S.B.C. J.C. N.J.C. M.J.D. E.E.K. A.R.M. B.M.N. Y.O. A.V.P. D.A.v.H. R.G.W. C.J.W. W.Z. and S.Z.; individual biobank analysis, A.B. Y.B. B.M.B. C.D.B. S.C. T.-T.C. K.C. S.M.D. M.D. G.H.d.B. Y.D. N.J.D. M.-J.F. Y.-C.A.F. S.F. V.L.F. L.G.F. E.R.G. T.R.G. D.H.G. C.R.G. G.G.-A. S.E.G. L.A.G. C.H. J.B.H. W.E.H. H.H. K.H. N.I. A.I. R.J. M. Kurki, J.K. N.K. E.E.K. J.T.K. M. Kanai, T.L. K.L. M.H.L. S.L. K.L. Y.-F.L. V.L.F. R.J.F.L. E.A.L.-M. A.R.-M. S.M.-G. R.M. R.E.M. H.C.M. A.R.M. Y.M. H.M. S.E.M. I.Y.M. B.M. S.M. K.N. S.N. M.A.N.-A. K.N. Y.O. P.P. A.L.-P. A.P. B.P. S.P. M.H.P. D.J.R. N.R. M.D.R. A.R. C.S. S.S. S.S.S. J.A.S. P.S. I.S. T.T. R.T. K.T. J.U. D.A.v.H. B.V. M.V. Y.V. J.M.V. R.G.W. Y.W. S.J.W. B.N.W. K.-H.H.W. M.Z. X.Z. and S.Z.; individual biobank management, N.A. A.A.T. K.M.A.-D. P.A. K.C.B. M. Boehnke, M. Boezen, C.D.B. A.C. Z.C. C.-Y.C. J.C. N.J.C. S.M.D. S.F. Y.-C.A.F. S.F. E.F. T.G. C.R.G. C.J.G. Y.G. H.H. K.A.H. K.H. S.I.I. N.M.J. N.K. E.E.K. J.T.K. C.L. M.H.L. M.T.M.L. L.L. K.L. Y.-F.L. R.J.F.L. J.L. S.M. Y.M. K.M. I.Y.M. Y.O. C.M.O. A.V.P. B.P. D.J.P. D.J.R. M.D.R. S.S. J.W.S. H.S. K.S. T.T. U.T. R.C.T. D.A.v.H. M.V. R.G.W. D.C.W. C.W. J.W. M.Z. X.Z. and S.Z.; study design and interpretation of results, A.B. M. Boehnke, M. Boezen, B.M.B. T.-T.C. C.-Y.C. M.J.D. G.D.S. N.J.D. S.F. M.-J.F. H.K.F. E.R.G. A.G. T.G. J.B.H. J.H. K.H. R.J. M.K. E.E.K. T.K. C.M.L. V.L.F. E.A.L.-M. A.R.M. S.N. B.M.N. C.M.O. J.J.P. B.P. N.R. H.R. J.A.S. I.S. K.T. D.A.v.H. R.G.W. Y.W. D.C.W. S.J.W. C.J.W. B.N.W. J.W. K.-H.H.W. M.Z. H.Z. J.Z. W.Z. X.Z. and S.Z.; drafted and edited the paper, A.B. M. Boehnke, M. Boezen, M.J.D. G.H.d.B. N.J.D. T.R.G. J.B.H. N.I. N.M.J. M.K. V.L.F. S.M. A.R.M. H.M. S.N. B.M.N. C.M.O. B.P. H.R. C.S. J.A.S. J.W.S. K.T. Y.W. D.C.W. C.J.W. K.-H.H.W. H.Z. J.Z. W.Z. and S.Z.; primary meta-analysis and quality control, M.J.D. H.K.F. M. Kanai, J.K. J.T.K. M. Kurki, M.M. B.M.N. C.J.W. K.-H.H.W. and W.Z.; drug discovery: S.N. T.K. K.-H.H.W. W.Z. and Y.O.; fine mapping, M. Kanai, W.Z. M.J.D. and H.K.F.; polygenic risk score, Y.W. S.N. E.A.L.-M. S.K. K.T. K.L. M. Kanai, W.Z. K.W. M.-J.F. L.B. P.A. P.D. V.L.F. R.M. Y.M. B.B. S.S. J.U. E.R.G. N.J.C. I.S. Y.O. A.R.M. and J.B.H.; proteome-wide Mendelian randomization, H.Z. H.R. A.B. G.H. G.D.S. B.M.B. W.Z. B.M.N. T.R.G. and J.Z.; transcriptome-wide association study, A.B. J.B.H. W.Z. J.Z. M. Kanai, B.P. E.R.G. and N.J.C.; asthma, K.T. W.Z. Y.W. M. Kanai, S.N. Y.O. B.M.N. M.J.D. and A.R.M.; heart failure, K.-H.H.W. N.J.D. B.N.W. I.S. S.E.G. J.B.H. N.J.C. M.P. R.J.F.L. M.J.D. B.M.N. W.Z. W.E.H. and C.J.W.; idiopathic pulmonary fibrosis, J.J.P. W.Z. M.J.D. J.T.K. N.J.C. and J.B.H.; primary open-angle glaucoma, V.L.F. A.B. W.Z. Y.W. K.L. M. Kanai, E.A.L.-M. P.S. R.T. X.Z. S.N. S.S. Y.O. N.I. S.M. H.S. I.S. C.W. A.R.M. E.R.G. N.M.J. N.J.C. and J.B.H.; stroke, I.S. K.-H.H.W. W.H. B.N.W. W.Z. J.E.H. A.P. B.B. A.H.S. M.E.G. R.G.W. K.H. C.K. S.Z. M.J.D. B.M.N. and C.J.W.; venous thromboembolism, B.N.W. I.S. K.-H.H.W. B.B. V.L.F. K.T. M.D. B.N. W.Z. J.A.S. and C.J.W. All authors reviewed the manuscript. M.J.D. is a founder of Maze Therapeutics. B.M.N. is a member of the scientific advisory board at Deep Genomics and a consultant for Camp4 Therapeutics, Takeda Pharmaceutical, and Biogen. The spouse of C.J.W. works at Regeneron Pharmaceuticals. C.-Y.C. is employed by Biogen. C.R.G. owns stock in 23andMe, Inc. T.R.G. has received research funding from various pharmaceutical companies to support the application of Mendelian randomization to drug target prioritization. E.E.K. has received speaker fees from Regeneron, Illumina, and 23andMe and is a member of the advisory board for Galateo Bio. R.E.M. has received speaker fees from Illumina and is a scientific advisor to the Epigenetic Clock Development Foundation. G.D.S. has received research funding from various pharmaceutical companies to support the application of Mendelian randomization to drug target prioritization. K.S. and U.T. are employed by deCODE Genetics/Amgen, Inc. J.Z. has received research funding from various pharmaceutical companies to support the application of Mendelian randomization to drug target prioritization. S.M. is a co-founder of and holds stock in Seonix Bio.; deCODE Genetics , Estonian Biobank , FinnGen , Generation Scotland , Genes & Health Research Team , LifeLines , Mass General Brigham Biobank , Michigan Genomics Initiative , National Biobank of Korea , Penn Medicine BioBank , Qatar Biobank , The QSkin Sun and Health Study , Taiwan Biobank , The HUNT Study , UCLA ATLAS Community Health Initiative , Uganda Genome Resource , UK Biobank , Biobank of the Americas , BioBank Japan Project , BioMe , BioVU , CanPath - Ontario Health Study , China Kadoorie Biobank Collaborative Group , Colorado Center for Personalized Medicine , Zhou , W , Kanai , M , Wu , K H H , Surakka , I , Partanen , J J , Karjalainen , J , Kurki , M , Palta , P , Ganna , A , Koskela , J T , Palotie , A V , Daly , M J & Neale , B M 2022 , ' Global Biobank Meta-analysis Initiative : Powering genetic discovery across human disease ' , Cell genomics , vol. 2 , no. 10 , 100192 . https://doi.org/10.1016/j.xgen.2022.100192; ORCID: /0000-0002-2527-5874/work/130142076; ORCID: /0000-0002-0154-7222/work/130151172; ORCID: /0000-0001-9320-7008/work/130151208; ORCID: /0000-0002-8147-240X/work/130152525; http://hdl.handle.net/10138/355244; 8a1d2d2d-17dc-45af-acb7-19729d6d7a8e; 85139994619

الاتاحة: http://hdl.handle.net/10138/355244

المؤلفون: Zhou, Wei, Kanai, Masahiro, Wu, Kuan-Han H, Rasheed, Humaira, Tsuo, Kristin, Hirbo, Jibril B, Wang, Ying, Bhattacharya, Arjun, Zhao, Huiling, Namba, Shinichi, Surakka, Ida, Wolford, Brooke N, Lo Faro, Valeria, Lopera-Maya, Esteban A, Läll, Kristi, Favé, Marie-Julie, Partanen, Juulia J, Chapman, Sinéad B, Karjalainen, Juha, Kurki, Mitja, Maasha, Mutaamba, Brumpton, Ben M, Chavan, Sameer, Chen, Tzu-Ting, Daya, Michelle, Ding, Yi, Feng, Yen-Chen A, Guare, Lindsay A, Gignoux, Christopher R, Graham, Sarah E, Hornsby, Whitney E, Ingold, Nathan, Ismail, Said I, Johnson, Ruth, Laisk, Triin, Lin, Kuang, Lv, Jun, Millwood, Iona Y, Moreno-Grau, Sonia, Nam, Kisung, Palta, Priit, Pandit, Anita, Preuss, Michael H, Saad, Chadi, Setia-Verma, Shefali, Thorsteinsdottir, Unnur, Uzunovic, Jasmina, Verma, Anurag, Zawistowski, Matthew, Zhong, Xue, Afifi, Nahla, Al-Dabhani, Kawthar M, Al Thani, Asma, Bradford, Yuki, Campbell, Archie, Crooks, Kristy, de Bock, Geertruida H, Damrauer, Scott M, Douville, Nicholas J, Finer, Sarah, Fritsche, Lars G, Fthenou, Eleni, Gonzalez-Arroyo, Gilberto, Griffiths, Christopher J, Guo, Yu, Hunt, Karen A, Ioannidis, Alexander, Jansonius, Nomdo M, Konuma, Takahiro, Lee, Ming Ta Michael, Lopez-Pineda, Arturo, Matsuda, Yuta, Marioni, Riccardo E, Moatamed, Babak, Nava-Aguilar, Marco A, Numakura, Kensuke, Patil, Snehal, Rafaels, Nicholas, Richmond, Anne, Rojas-Muñoz, Agustin, Shortt, Jonathan A, Straub, Peter, Tao, Ran, Vanderwerff, Brett, Vernekar, Manvi, Veturi, Yogasudha, Barnes, Kathleen C, Boezen, Marike, Chen, Zhengming, Chen, Chia-Yen, Cho, Judy, Smith, George Davey, Finucane, Hilary K, Franke, Lude, Gamazon, Eric R, Ganna, Andrea, Gaunt, Tom R, Ge, Tian, Huang, Hailiang, Huffman, Jennifer, Katsanis, Nicholas, Koskela, Jukka T, Lajonchere, Clara, Law, Matthew H, Li, Liming, Lindgren, Cecilia M, Loos, Ruth JF, MacGregor, Stuart, Matsuda, Koichi, Olsen, Catherine M, Porteous, David J, Shavit, Jordan A, Snieder, Harold, Takano, Tomohiro, Trembath, Richard C, Vonk, Judith M, Whiteman, David C, Wicks, Stephen J, Wijmenga, Cisca, Wright, John, Zheng, Jie, Zhou, Xiang, Awadalla, Philip, Boehnke, Michael, Bustamante, Carlos D, Cox, Nancy J, Fatumo, Segun, Geschwind, Daniel H, Hayward, Caroline, Hveem, Kristian, Kenny, Eimear E, Lee, Seunggeun, Lin, Yen-Feng, Mbarek, Hamdi, Mägi, Reedik, Martin, Hilary C, Medland, Sarah E, Okada, Yukinori, Palotie, Aarno V, Pasaniuc, Bogdan, Rader, Daniel J, Ritchie, Marylyn D, Sanna, Serena, Smoller, Jordan W, Stefansson, Kari, van Heel, David A, Walters, Robin G, Zöllner, Sebastian, Biobank of the Americas, Biobank Japan Project, BioMe, BioVU, CanPath - Ontario Health Study, China Kadoorie Biobank Collaborative Group, Colorado Center for Personalized Medicine, deCODE Genetics, Estonian Biobank, FinnGen, Generation Scotland, Genes & Health Research Team, LifeLines, Mass General Brigham Biobank, Michigan Genomics Initiative, National Biobank of Korea, Penn Medicine BioBank, Qatar Biobank, QSkin Sun and Health Study, Taiwan Biobank, HUNT Study, UCLA ATLAS Community Health Initiative, Uganda Genome Resource, UK Biobank, Martin, Alicia R, Willer, Cristen J, Daly, Mark J, Neale, Benjamin M

المصدر: nlmid: 9918284260106676 ; essn: 2666-979X

مصطلحات موضوعية: GWAS, ancestry diversity, biobank, genetic association studies, meta-analysis, phenotype harmonization

وصف الملف: application/pdf

Relation: https://www.repository.cam.ac.uk/handle/1810/347665

الاتاحة: https://www.repository.cam.ac.uk/handle/1810/347665
https://doi.org/10.17863/CAM.95080

المؤلفون: Patel, Aniruddh P, Wang, Minxian, Ruan, Yunfeng, Koyama, Satoshi, Clarke, Shoa L, Yang, Xiong, Tcheandjieu, Catherine, Agrawal, Saaket, Fahed, Akl C, Ellinor, Patrick T, Genes & Health Research Team, the Million Veteran Program, Tsao, Philip S, Sun, Yan V, Cho, Kelly, Wilson, Peter WF, Assimes, Themistocles L, van Heel, David A, Butterworth, Adam S, Aragam, Krishna G, Natarajan, Pradeep, Khera, Amit V

مصطلحات موضوعية: Humans, Coronary Artery Disease, Genome-Wide Association Study, Genetic Predisposition to Disease, Risk Factors, Phenotype

وصف الملف: application/pdf; text/xml; application/zip

Relation: https://www.repository.cam.ac.uk/handle/1810/355172

الاتاحة: https://www.repository.cam.ac.uk/handle/1810/355172

المؤلفون: Hartmann, Sylvia, Yasmeen, Summaira, Jacobs, Benjamin M, Denaxas, Spiros, Pirmohamed, Munir, Gamazon, Eric R, Caulfield, Mark J, Genes & Health Research Team, Hemingway, Harry, Pietzner, Maik, Langenberg, Claudia

المصدر: Nature Communications , 14 , Article 6156. (2023)

مصطلحات موضوعية: Genes & Health Research Team

وصف الملف: application/pdf

Relation: https://discovery.ucl.ac.uk/id/eprint/10179134/1/s41467-023-41876-5.pdf; https://discovery.ucl.ac.uk/id/eprint/10179134/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10179134/1/s41467-023-41876-5.pdf
https://discovery.ucl.ac.uk/id/eprint/10179134/

المؤلفون: Magavern, EF, Jacobs, B, Warren, H, Finocchiaro, G, Finer, S, van Heel, DA, Genes & Health Research Team, Smedley, D, Caulfield, MJ

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

Relation: https://openaccess.sgul.ac.uk/id/eprint/116036/1/1-s2.0-S2772963X23005173-main.pdf; https://openaccess.sgul.ac.uk/id/eprint/116036/6/1-s2.0-S2772963X23005173-mmc1.docx; Magavern, EF; Jacobs, B; Warren, H; Finocchiaro, G; Finer, S; van Heel, DA; Genes & Health Research Team; Smedley, D; Caulfield, MJ (2023) CYP2C19 Genotype Prevalence and Association With Recurrent Myocardial Infarction in British-South Asians Treated With Clopidogrel. JACC Adv, 2 (7). p. 100573. ISSN 2772-963X https://doi.org/10.1016/j.jacadv.2023.100573 SGUL Authors: Finocchiaro, Gherardo

الاتاحة: https://openaccess.sgul.ac.uk/id/eprint/116036/
https://openaccess.sgul.ac.uk/id/eprint/116036/1/1-s2.0-S2772963X23005173-main.pdf
https://openaccess.sgul.ac.uk/id/eprint/116036/6/1-s2.0-S2772963X23005173-mmc1.docx
https://doi.org/10.1016/j.jacadv.2023.100573

المؤلفون: Magavern, EF, Durrani, F, Raza, M, Lerner, R, Islam, MR, Genes & Health Research Team, Clinch, M, Caulfield, MJ

Relation: Pharmacogenomics J; https://qmro.qmul.ac.uk/xmlui/handle/123456789/91977

الاتاحة: https://qmro.qmul.ac.uk/xmlui/handle/123456789/91977
https://doi.org/10.1038/s41397-023-00317-8

المؤلفون: Malawsky, DS, van Walree, E, Jacobs, BM, Heng, TH, Huang, QQ, Sabir, AH, Rahman, S, Sharif, SM, Khan, A, Mirkov, MU, 23andMe Research Team, Genes & Health Research Team, Kuwahara, H, Gao, X, Alkuraya, FS, Posthuma, D, Newman, WG, Griffiths, CJ, Mathur, R, van Heel, DA, Finer, S, O'Connell, J, Martin, HC

مصطلحات موضوعية: autozygosity, common diseases, consanguinity, diverse cohorts, medical genetics, recessive

Relation: Cell; https://qmro.qmul.ac.uk/xmlui/handle/123456789/91435

الاتاحة: https://qmro.qmul.ac.uk/xmlui/handle/123456789/91435
https://doi.org/10.1016/j.cell.2023.08.028

المؤلفون: Hodgson, Sam, Huang, Qin Qin, Sallah, Neneh, Genes & Health Research Team, ., Griffiths, Chris J, Newman, William G, Trembath, Richard C, Wright, John, Lumbers, R Thomas, Kuchenbaecker, Karoline, van Heel, David A, Mathur, Rohini, Martin, Hilary C, Finer, Sarah

المصدر: PLoS Med , 19 (5) , Article e1003981. (2022)

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10149226/1/Lumbers_journal.pmed.1003981.pdf; https://discovery.ucl.ac.uk/id/eprint/10149226/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10149226/1/Lumbers_journal.pmed.1003981.pdf
https://discovery.ucl.ac.uk/id/eprint/10149226/

المؤلفون: Zhou, W, Kanai, M, Wu, K-HH, Rasheed, H, Tsuo, K, Hirbo, JB, Wang, Y, Bhattacharya, A, Zhao, H, Namba, S, Surakka, I, Wolford, BN, Lo Faro, V, Lopera-Maya, EA, Läll, K, Favé, M-J, Partanen, JJ, Chapman, SB, Karjalainen, J, Kurki, M, Maasha, M, Brumpton, BM, Chavan, S, Chen, T-T, Daya, M, Ding, Y, Feng, Y-CA, Guare, LA, Gignoux, CR, Graham, SE, Hornsby, WE, Ingold, N, Ismail, SI, Johnson, R, Laisk, T, Lin, K, Lv, J, Millwood, IY, Moreno-Grau, S, Nam, K, Palta, P, Pandit, A, Preuss, MH, Saad, C, Setia-Verma, S, Thorsteinsdottir, U, Uzunovic, J, Verma, A, Zawistowski, M, Zhong, X, Afifi, N, Al-Dabhani, KM, Al Thani, A, Bradford, Y, Campbell, A, Crooks, K, de Bock, GH, Damrauer, SM, Douville, NJ, Finer, S, Fritsche, LG, Fthenou, E, Gonzalez-Arroyo, G, Griffiths, CJ, Guo, Y, Hunt, KA, Ioannidis, A, Jansonius, NM, Konuma, T, Lee, MTM, Lopez-Pineda, A, Matsuda, Y, Marioni, RE, Moatamed, B, Nava-Aguilar, MA, Numakura, K, Patil, S, Rafaels, N, Richmond, A, Rojas-Muñoz, A, Shortt, JA, Straub, P, Tao, R, Vanderwerff, B, Vernekar, M, Veturi, Y, Barnes, KC, Boezen, M, Chen, Z, Chen, C-Y, Cho, J, Smith, GD, Finucane, HK, Franke, L, Gamazon, ER, Ganna, A, Gaunt, TR, Ge, T, Huang, H, Huffman, J, Katsanis, N, Koskela, JT, Lajonchere, C, Law, MH, Li, L, Lindgren, CM, Loos, RJF, MacGregor, S, Matsuda, K, Olsen, CM, Porteous, DJ, Shavit, JA, Snieder, H, Takano, T, Trembath, RC, Vonk, JM, Whiteman, DC, Wicks, SJ, Wijmenga, C, Wright, J, Zheng, J, Zhou, X, Awadalla, P, Boehnke, M, Bustamante, CD, Cox, NJ, Fatumo, S, Geschwind, DH, Hayward, C, Hveem, K, Kenny, EE, Lee, S, Lin, Y-F, Mbarek, H, Mägi, R, Martin, HC, Medland, SE, Okada, Y, Palotie, AV, Pasaniuc, B, Rader, DJ, Ritchie, MD, Sanna, S, Smoller, JW, Stefansson, K, van Heel, DA, Walters, RG, Zöllner, S, Biobank of the Americas, Biobank Japan Project, BioMe, BioVU, CanPath - Ontario Health Study, China Kadoorie Biobank Collaborative Group, Colorado Center for Personalized Medicine, deCODE Genetics, Estonian Biobank, FinnGen, Generation Scotland, Genes & Health Research Team, LifeLines, Mass General Brigham Biobank, Michigan Genomics Initiative, National Biobank of Korea, Penn Medicine BioBank, Qatar Biobank, QSkin Sun and Health Study, Taiwan Biobank, HUNT Study, UCLA ATLAS Community Health Initiative, Uganda Genome Resource, UK Biobank, Martin, AR, Willer, CJ, Daly, MJ, Neale, BM

مصطلحات موضوعية: GWAS, ancestry diversity, biobank, genetic association studies, meta-analysis, phenotype harmonization

وصف الملف: 100192 - ?

Relation: Cell Genom; https://qmro.qmul.ac.uk/xmlui/handle/123456789/82461

الاتاحة: https://qmro.qmul.ac.uk/xmlui/handle/123456789/82461
https://doi.org/10.1016/j.xgen.2022.100192

المؤلفون: Spreckley, Marie, Raza, Mehru, Islam, Kamrul, Russell, Jessry, Hunt, Karen, Durham, Ceri, Genes & Health Research Team, van Heel, David, Khan, Ahsan, Finer, Sarah, Siddiqui, Moneeza K.

المصدر: Trends in Endocrinology & Metabolism ; ISSN 1043-2760

الاتاحة: https://doi.org/10.1016/j.tem.2024.11.002
https://api.elsevier.com/content/article/PII:S1043276024002935?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1043276024002935?httpAccept=text/plain

المؤلفون: Hartmann, Sylvia, Yasmeen, Summaira, Jacobs, Benjamin M, Denaxas, Spiros, Pirmohamed, Munir, Gamazon, Eric R, Caulfield, Mark J, Genes & Health Research Team, Hemingway, Harry, Pietzner, Maik, Langenberg, Claudia

مصطلحات موضوعية: Humans, Genome-Wide Association Study, Ulcer, Raynaud Disease, Pain, Transcription Factors, Homeodomain Proteins, Receptors, Adrenergic, alpha-2

وصف الملف: text/xml; application/pdf; application/zip

Relation: https://www.repository.cam.ac.uk/handle/1810/363424

الاتاحة: https://www.repository.cam.ac.uk/handle/1810/363424

المؤلفون: Masahiro Kanai, Roy Elzur, Wei Zhou, Mark J. Daly, Hilary K. Finucane, Kuan-Han H. Wu, Humaira Rasheed, Kristin Tsuo, Jibril B. Hirbo, Ying Wang, Arjun Bhattacharya, Huiling Zhao, Shinichi Namba, Ida Surakka, Brooke N. Wolford, Valeria Lo Faro, Esteban A. Lopera-Maya, Kristi Läll, Marie-Julie Favé, Juulia J. Partanen, Sinéad B. Chapman, Juha Karjalainen, Mitja Kurki, Mutaamba Maasha, Ben M. Brumpton, Sameer Chavan, Tzu-Ting Chen, Michelle Daya, Yi Ding, Yen-Chen A. Feng, Lindsay A. Guare, Christopher R. Gignoux, Sarah E. Graham, Whitney E. Hornsby, Nathan Ingold, Said I. Ismail, Ruth Johnson, Triin Laisk, Kuang Lin, Jun Lv, Iona Y. Millwood, Sonia Moreno-Grau, Kisung Nam, Priit Palta, Anita Pandit, Michael H. Preuss, Chadi Saad, Shefali Setia-Verma, Unnur Thorsteinsdottir, Jasmina Uzunovic, Anurag Verma, Matthew Zawistowski, Xue Zhong, Nahla Afifi, Kawthar M. Al-Dabhani, Asma Al Thani, Yuki Bradford, Archie Campbell, Kristy Crooks, Geertruida H. de Bock, Scott M. Damrauer, Nicholas J. Douville, Sarah Finer, Lars G. Fritsche, Eleni Fthenou, Gilberto Gonzalez-Arroyo, Christopher J. Griffiths, Yu Guo, Karen A. Hunt, Alexander Ioannidis, Nomdo M. Jansonius, Takahiro Konuma, Ming Ta Michael Lee, Arturo Lopez-Pineda, Yuta Matsuda, Riccardo E. Marioni, Babak Moatamed, Marco A. Nava-Aguilar, Kensuke Numakura, Snehal Patil, Nicholas Rafaels, Anne Richmond, Agustin Rojas-Muñoz, Jonathan A. Shortt, Peter Straub, Ran Tao, Brett Vanderwerff, Manvi Vernekar, Yogasudha Veturi, Kathleen C. Barnes, Marike Boezen, Zhengming Chen, Chia-Yen Chen, Judy Cho, George Davey Smith, Lude Franke, Eric R. Gamazon, Andrea Ganna, Tom R. Gaunt, Tian Ge, Hailiang Huang, Jennifer Huffman, Nicholas Katsanis, Jukka T. Koskela, Clara Lajonchere, Matthew H. Law, Liming Li, Cecilia M. Lindgren, Ruth J.F. Loos, Stuart MacGregor, Koichi Matsuda, Catherine M. Olsen, David J. Porteous, Jordan A. Shavit, Harold Snieder, Tomohiro Takano, Richard C. Trembath, Judith M. Vonk, David C. Whiteman, Stephen J. Wicks, Cisca Wijmenga, John Wright, Jie Zheng, Xiang Zhou, Philip Awadalla, Michael Boehnke, Carlos D. Bustamante, Nancy J. Cox, Segun Fatumo, Daniel H. Geschwind, Caroline Hayward, Kristian Hveem, Eimear E. Kenny, Seunggeun Lee, Yen-Feng Lin, Hamdi Mbarek, Reedik Mägi, Hilary C. Martin, Sarah E. Medland, Yukinori Okada, Aarno V. Palotie, Bogdan Pasaniuc, Daniel J. Rader, Marylyn D. Ritchie, Serena Sanna, Jordan W. Smoller, Kari Stefansson, David A. van Heel, Robin G. Walters, Sebastian Zöllner, null Biobank of the Americas, null Biobank Japan Project, null BioMe, null BioVU, null CanPath - Ontario Health Study, null China Kadoorie Biobank Collaborative Group, null Colorado Center for Personalized Medicine, null deCODE Genetics, null Estonian Biobank, FinnGen, null Generation Scotland, null Genes & Health Research Team, null LifeLines, null Mass General Brigham Biobank, null Michigan Genomics Initiative, null National Biobank of Korea, null Penn Medicine BioBank, null Qatar Biobank, null The Qskin Sun and Health Study, null Taiwan Biobank, null The Hunt Study, null Ucla Atlas Community Health Initiative, null Uganda Genome Resource, null Uk Biobank, Alicia R. Martin, Cristen J. Willer, Benjamin M. Neale

المساهمون: Institute for Molecular Medicine Finland, Samuli Olli Ripatti / Principal Investigator, Complex Disease Genetics, Genomics of Neurological and Neuropsychiatric Disorders, Data Science Genetic Epidemiology Lab, Research Programs Unit, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, University of Helsinki

مصطلحات موضوعية: biobank, meta-analysis, genome-wide association study, fine-mapping, Genetics, 1184 Genetics, developmental biology, physiology, GWAS, 3111 Biomedicine, heterogeneity, summary statistics, Biochemistry, Genetics and Molecular Biology (miscellaneous), linkage disequilibrium, miscalibration

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26876d7b7cfd7d51f3112e7e7afb5a3a
http://hdl.handle.net/10138/355361

المؤلفون: Monti, Remo, Hudjashov, Georgi, Läll, Kristi, Eick, Lisa, Kanoni, Stavroula, Wolford, Brooke, Wingfield, Benjamin, Pain, Oliver, Wharrie, Sophie, Jermy, Bradley, McMahon, Aoife, Hartonen, Tuomo, Heyne, Henrike, Mars, Nina, Genes & Health Research Team, Hveem, Kristian, Inouye, Michael, A. van Heel, David, Mägi, Reedik, Marttinen, Pekka, Ripatti, Samuli, Ganna, Andrea, Lippert, Christoph

Relation: https://doi.org/10.5281/zenodo.10171072; https://doi.org/10.1101/2023.11.20.23298215v1; https://doi.org/10.5281/zenodo.10170951; https://zenodo.org/communities/eu; https://doi.org/10.5281/zenodo.10012995; https://doi.org/10.5281/zenodo.10012996; oai:zenodo.org:10012996

الاتاحة: https://doi.org/10.5281/zenodo.10012996