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1دورية أكاديمية
المؤلفون: Arturo Lopez-Pineda, Manvi Vernekar, Sonia Moreno-Grau, Agustin Rojas-Muñoz, Babak Moatamed, Ming Ta Michael Lee, Marco A. Nava-Aguilar, Gilberto Gonzalez-Arroyo, Kensuke Numakura, Yuta Matsuda, Alexander Ioannidis, Nicholas Katsanis, Tomohiro Takano, Carlos D. Bustamante
المصدر: Human Genomics, Vol 16, Iss 1, Pp 1-10 (2022)
مصطلحات موضوعية: Polygenic risk score, Genome-wide association study, Type 2 diabetes mellitus, Hypertension, Ancestry, Medicine, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1479-7364
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2دورية أكاديمية
المؤلفون: Alfonso R. Alvarez Paredes, Anel Gómez García, Martha Angélica Alvarez Paredes, Nely Velázquez, Diana Cindy Ojeda Bolaños, Miriam Sarai Padilla Sandoval, Juan M. Gallardo, Gerardo Muñoz Cortés, Seydhel Cristina Reyes Granados, Mario Felipe Rodríguez Morán, Joaquin Tripp, Arturo Lopez Pineda, Cleto Alvarez Aguilar
المصدر: PeerJ, Vol 12, p e17817 (2024)
مصطلحات موضوعية: Chronic kidney disease, Glomerular filtration rate, Overweight, Obesity, Dyslipidemia, Hyperuricemia, Medicine, Biology (General), QH301-705.5
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Christine G. Preston, Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L. Goldstein, Xi Luo, Hannah Wand, Bryan Wulf, Gloria Cheung, Mark E. Mandell, Howard Tong, Shaung Cheng, Michael A. Iacocca, Arturo Lopez Pineda, Alice B. Popejoy, Karen Dalton, Jimmy Zhen, Selina S. Dwight, Lawrence Babb, Marina DiStefano, Julianne M. O’Daniel, Kristy Lee, Erin R. Riggs, Diane B. Zastrow, Jessica L. Mester, Deborah I. Ritter, Ronak Y. Patel, Sai Lakshmi Subramanian, Aleksander Milosavljevic, Jonathan S. Berg, Heidi L. Rehm, Sharon E. Plon, J. Michael Cherry, Carlos D. Bustamante, Helio A. Costa, on behalf of the Clinical Genome Resource (ClinGen)
المصدر: Genome Medicine, Vol 14, Iss 1, Pp 1-12 (2022)
مصطلحات موضوعية: Variant curation, Precision medicine, Clinical genetics, Clinical Genome Resource Consortium, Medicine, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1756-994X
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4دورية أكاديمية
المؤلفون: Guhan Ram Venkataraman, Arturo Lopez Pineda, Oliver J Bear Don't Walk Iv, Ashley M Zehnder, Sandeep Ayyar, Rodney L Page, Carlos D Bustamante, Manuel A Rivas
المصدر: PLoS ONE, Vol 15, Iss 6, p e0234647 (2020)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1932-6203
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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 -
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المؤلفون: William B. Capra, Navdeep Pal, Ying Lu, James Zou, Samuel Whipple, Brandon Arnieri, Shemra Rizzo, Michael Lu, Ruishan Liu, Ryan Copping, Arturo Lopez Pineda
المصدر: Nature. 592:629-633
مصطلحات موضوعية: medicine.medical_specialty, Lung Neoplasms, MEDLINE, Datasets as Topic, Medical Oncology, 03 medical and health sciences, Patient safety, 0302 clinical medicine, Artificial Intelligence, Common Criteria, Carcinoma, Non-Small-Cell Lung, medicine, Electronic Health Records, Humans, Medical physics, 030212 general & internal medicine, Lung cancer, Proportional Hazards Models, Clinical Trials as Topic, Multidisciplinary, Clinical Laboratory Techniques, business.industry, Patient Selection, Hazard ratio, Reproducibility of Results, Cancer, medicine.disease, Clinical trial, 030220 oncology & carcinogenesis, Patient Safety, business, Real world data
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7دورية أكاديمية
المؤلفون: Ruishan Liu, Shemra Rizzo, Samuel Whipple, Navdeep Pal, Arturo Lopez Pineda, Michael Lu, Brandon Arnieri, Ying Lu, William Capra, Ryan Copping, James Zou
المصدر: Nature, Nature. 592(7855):629-633
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المؤلفون: Wei Zhou, Masahiro Kanai, 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, Hilary K. Finucane, 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, Alicia R. Martin, Cristen J. Willer, Mark J. Daly, Benjamin M. Neale
المساهمون: Samuli Olli Ripatti / Principal Investigator, University of Helsinki, Institute for Molecular Medicine Finland, Complex Disease Genetics, Genomics of Neurological and Neuropsychiatric Disorders, Data Science Genetic Epidemiology Lab, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, Basic and Translational Research and Imaging Methodology Development in Groningen (BRIDGE), Life Course Epidemiology (LCE), Damage and Repair in Cancer Development and Cancer Treatment (DARE), Perceptual and Cognitive Neuroscience (PCN), Groningen Research Institute for Asthma and COPD (GRIAC), Stem Cell Aging Leukemia and Lymphoma (SALL), Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI)
المصدر: Cell Genomics
Hayward, C, Campbell, A, Porteous, D J, Richmond, A & Marioni, R E 2022, ' Global Biobank Meta-analysis Initiative: powering genetic discovery across human disease ', Cell Genomics . https://doi.org/10.1016/j.xgen.2022.100192
Cell Genomics, 2(10):100192
Zhou, W, Kanai, M, Wu, K H H, Rasheed, H, Tsuo, K, Hirbo, J B, Wang, Y, Bhattacharya, A, Zhao, H, Namba, S, Surakka, I, Wolford, B N, Lo Faro, V, Lopera-Maya, E A, Läll, K, Favé, M J, Partanen, J J, Chapman, S B, Karjalainen, J, Kurki, M, Maasha, M, Brumpton, B M, Chavan, S, Chen, T T, Daya, M, Ding, Y, Feng, Y C A, Guare, L A, Gignoux, C R, Graham, S E, Hornsby, W E, Ingold, N, Ismail, S I, Johnson, R, Laisk, T, Lin, K, Lv, J, Millwood, I Y, Moreno-Grau, S, Nam, K, Palta, P, Pandit, A, Preuss, M H, Saad, C, Setia-Verma, S, Thorsteinsdottir, U, Uzunovic, J, Verma, A, Zawistowski, M, Loos, R J F, 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 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.2022.100192مصطلحات موضوعية: biobank, meta-analysis, genetic association studies, 1184 Genetics, developmental biology, physiology, GWAS, 3111 Biomedicine, biobank meta-analysis, ancestry diversity, phenotype harmonization
وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document
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المؤلفون: Arturo Lopez Pineda, Josue Abinadi Garrido-Sanchez, Gilberto Gonzalez-Arroyo, Cleto Alvarez-Aguilar
المصدر: Journal of Clinical Oncology. 40:e22513-e22513
مصطلحات موضوعية: Cancer Research, Oncology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::1f36df31148c3ec319bb338cefb4cec4
https://doi.org/10.1200/jco.2022.40.16_suppl.e22513 -
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المؤلفون: Dalton K, Preston Cg, Steven M. Harrison, Lawrence J. Babb, Bryan Wulf, Heidi L. Rehm, Selina S. Dwight, Jimmy Zhen, J. M. Cherry, Deborah I. Ritter, Kristy Lee, Erin Rooney Riggs, Madhavrao R, Cheng S, Jessica L. Mester, Ronak Y. Patel, Matthew Wright, Tong H, Jennifer L. Goldstein, Carlos Bustamante, Julianne M. O’Daniel, Xi Luo, Hannah Wand, Cheung G, Helio A. Costa, Zastrow Db, Jonathan S. Berg, Mandell Me, Sai Lakshmi Subramanian, Sharon E. Plon, Alice B. Popejoy, Arturo Lopez Pineda, Michael A. Iacocca, Marina T. DiStefano, Aleksandar Milosavljevic
المصدر: Genome Medicine
Genome Medicine, Vol 14, Iss 1, Pp 1-12 (2022)مصطلحات موضوعية: Process (engineering), Computer science, Interface (Java), Genomics, QH426-470, Variant curation, Resource (project management), Genetics, Humans, Genetic Testing, Clinical genetics, Molecular Biology, Genetics (clinical), Genome, Human, Suite, Precision medicine, Genetic Variation, Pathogenicity, Data science, Identification (information), Workflow, Clinical Genome Resource Consortium, Medicine, Molecular Medicine, Software