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by Stray-Pedersen, Asbjørg, MD, PhD and Sorte, Hanne Sørmo, MS and Samarakoon, Pubudu, MS and Gambin, Tomasz, PhD and Chinn, Ivan K., MD and Coban Akdemir, Zeynep H., PhD and Erichsen, Hans Christian, MD, PhD and Forbes, Lisa R., MD and Gu, Shen, PhD and Yuan, Bo, PhD and Jhangiani, Shalini N., MS and Muzny, Donna M., MS and Rødningen, Olaug Kristin, PhD and Sheng, Ying, PhD and Nicholas, Sarah K., MD, PhD and Noroski, Lenora M., MD, MPH and Seeborg, Filiz O., MD, MPH and Davis, Carla M., MD and Canter, Debra L., MS and Mace, Emily M., PhD and Vece, Timothy J., MD and Allen, Carl E., MD, PhD and Abhyankar, Harshal A., MS and Boone, Philip M., MD, PhD and Beck, Christine R., PhD and Wiszniewski, Wojciech, MD, PhD and Fevang, Børre, MD, PhD and Aukrust, Pål, MD, PhD and Tjønnfjord, Geir E., MD, PhD and Gedde-Dahl, Tobias, MD, PhD and Hjorth-Hansen, Henrik, MD, PhD and Dybedal, Ingunn, MD, PhD and Nordøy, Ingvild, MD, PhD and Jørgensen, Silje F., MD and Abrahamsen, Tore G., MD, PhD and Øverland, Torstein, MD and Bechensteen, Anne Grete, MD, PhD and Skogen, Vegard, MD, PhD and Osnes, Liv T.N., MD, PhD and Kulseth, Mari Ann, PhD and Prescott, Trine E., MD and Rustad, Cecilie F., MD and Heimdal, Ketil R., MD, PhD and Belmont, John W., MD, PhD and Rider, Nicholas L., DO and Chinen, Javier, MD, PhD and Cao, Tram N., MS and Smith, Eric A., BSc and Caldirola, Maria Soledad, BSc and Bezrodnik, Liliana, MD and Lugo Reyes, Saul Oswaldo, MD and Espinosa Rosales, Francisco J., MD and Guerrero-Cursaru, Nina Denisse, BSc and Pedroza, Luis Alberto, PhD and Poli, Cecilia M., MD and Franco, Jose L., MD, PhD and Trujillo Vargas, Claudia M., PhD and Aldave Becerra, Juan Carlos, MD and Wright, Nicola, MD and Issekutz, Thomas B., MD and Issekutz, Andrew C., MD and Abbott, Jordan, MD and Caldwell, Jason W., DO and Bayer, Diana K., DO and Chan, Alice Y., MD, PhD and Aiuti, Alessandro, MD, PhD and Cancrini, Caterina, MD, PhD and Holmberg, Eva, MD and West, Christina, MD, PhD and Burstedt, Magnus, MD, PhD and Karaca, Ender, MD and Yesil, Gözde, MD and Artac, Hasibe, MD and Bayram, Yavuz, MD and Atik, Mehmed Musa, BSc and Eldomery, Mohammad K., MD and Ehlayel, Mohammad S., MD, PhD and Jolles, Stephen, MD, PhD and Flatø, Berit, MD, PhD and Bertuch, Alison A., MD, PhD and Hanson, I. Celine, MD and Zhang, Victor W., PhD and Wong, Lee-Jun, PhD and Hu, Jianhong, PhD and Walkiewicz, Magdalena, PhD and Yang, Yaping, PhD and Eng, Christine M., MD and Boerwinkle, Eric, PhD and Gibbs, Richard A., PhD and Shearer, William T., MD, PhD and Lyle, Robert, PhD and Orange, Jordan S., MD, PhD and Lupski, James R., MD, PhD, DSc (Hon) and Medicinska fakulteten and Institutionen för klinisk vetenskap and Pediatrik and Umeå universitet
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 139, Issue 1, pp. 232 - 245
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 06/2019, Volume 380, Issue 23, pp. 2192 - 2195
Major advances leveraging large-scale genomic and phenotype data require not only contemporary analytics based on deep learning and artificial intelligence,... 
National Institutes of Health (U.S.) | Datasets as Topic | United States | Genomics | Humans | Databases, Genetic | Organizational Policy | Information Dissemination | Analysis | Big data | Datasets | Phenotypes | Agreements | Artificial intelligence | Collaboration | Innovations | Index Medicus | Abridged Index Medicus
Journal Article
by Postmus, Iris and Trompet, Stella and Deshmukh, Harshal A and Barnes, Michael R and Li, Xiaohui and Warren, Helen R and Chasman, Daniel I and Zhou, Kaixin and Arsenault, Benoit J and Donnelly, Louise A and Wiggins, Kerri L and Avery, Christy L and Griffin, Paula and Feng, QiPing and Taylor, Kent D and Li, Guo and Evans, Daniel S and Smith, Albert V and de Keyser, Catherine E and Johnson, Anew D and de Craen, Anton J. M and Stott, David J and Buckley, Brendan M and Ford, Ian and Westendorp, Rudi G. J and Slagboom, P. Eline and Sattar, Naveed and Munroe, Patricia B and Sever, Peter and Poulter, Neil and Stanton, Alice and Shields, Denis C and O'Brien, Eoin and Shaw-Hawkins, Sue and Chen, Y.-D. Ida and Nickerson, Deborah A and Smith, Joshua D and Dubé, Marie Pierre and Boekholdt, S. Matthijs and Hovingh, G. Kees and Kastelein, John J. P and McKeigue, Paul M and Betteridge, John and Neil, Anew and Durrington, Paul N and Doney, Alex and Carr, Fiona and Morris, Anew and McCarthy, Mark I and Groop, Leif and Ahlqvist, Emma and Bis, Joshua C and Rice, Kenneth and Smith, Nicholas L and Lumley, Thomas and Whitsel, Eric A and Stürmer, Til and Boerwinkle, Eric and Ngwa, Julius S and O'Donnell, Christopher J and Vasan, Ramachanan S and Wei, Wei-Qi and Wilke, Russell A and Liu, Ching-Ti and Sun, Fangui and Guo, Xiuqing and Heckbert, Susan R and Post, Wendy and Sotoodehnia, Nona and Arnold, Alice M and Stafford, Jeanette M and Ding, Jingzhong and Herrington, David M and Kritchevsky, Stephen B and Eiriksdottir, Gudny and Launer, Leonore J and Harris, Tamara B and Chu, Auey Y and Giulianini, Franco and Macfadyen, Jean G and Barratt, Bryan J and Nyberg, Freik and Stricker, Bruno H and Uitterlinden, Ané G and Hofman, Albert and Rivadeneira, Fernando and Emilsson, Valur and Franco, Oscar H and Ridker, Paul M and Gudnason, Vilmundur and Liu, Yongmei and Denny, Joshua C and Ballantyne, Christie M and Rotter, Jerome I and Aienne Cupples, L and Psaty, Bruce M and Palmer, Colin N. A and Tardif, Jean-Claude and Colhoun, Helen M and Hitman, Graham and ... and Welcome Trust Case Control Consort and Welcome Trust Case Control Consortium and Data and Analysis Group and DNA, Genotyping, Data QC and Informatics Group and Membership of Wellcome Trust Case Control Consortium and Publications Committee and Sahlgrenska akademin and Göteborgs universitet and Institutionen för medicin, avdelningen för samhällsmedicin och folkhälsa, enheten för arbets-och miljömedicin and Gothenburg University and Institute of Medicine, Department of Public Health and Community Medicine, Section of Occupational and environmental medicine and Sahlgrenska Academy
Nature communications, ISSN 2041-1723, 2014, Volume 5, Issue 1, pp. 5068 - 5068
Journal Article
Circulation, ISSN 0009-7322, 03/2019, Volume 139, Issue Suppl_1
Journal Article
Arteriosclerosis, thrombosis, and vascular biology, 07/2019, Volume 39, Issue 7, pp. 1475 - 1482
Objective- Alterations in the serum metabolome may be detectable in at-risk individuals before the onset of coronary heart disease (CHD). Identifying... 
Journal Article
New England Journal of Medicine, ISSN 0028-4793, 01/2015, Volume 372, Issue 3, pp. 295 - 296
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2014, Volume 95, Issue 1, pp. 96 - 107
Journal Article
Circulation, ISSN 0009-7322, 03/2019, Volume 139, Issue Suppl_1
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2009, Volume 84, Issue 5, pp. 617 - 627
Journal Article
Stroke, ISSN 0039-2499, 01/2018, Volume 49, Issue Suppl_1
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2014, Volume 111, Issue 2, pp. 757 - 762
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 03/2019, Volume 104, Issue 3, pp. 410 - 421
Set-based analysis that jointly tests the association of variants in a group has emerged as a popular tool for analyzing rare and low-frequency variants in... 
variant set test | omnibus test | rare-variant analysis | whole-genome sequencing | TESTS | LIPOPROTEIN | GENETICS & HEREDITY | MISSING HERITABILITY | ASSOCIATION | GENOME | HIGHER CRITICISM | Genetic variation | Atherosclerosis | Physiological aspects | Genetic aspects | Research | Nucleotide sequencing | Risk factors | Methods | DNA sequencing | Index Medicus
Journal Article
Medicine, ISSN 0025-7974, 08/2018, Volume 97, Issue 33, pp. e11865 - e11865
Rare variants, in particular renal salt handling genes, contribute to monogenic forms of hypertension and hypotension syndromes with electrolyte abnormalities.... 
hypotension | blood pressure | COMMON VARIANTS | METAANALYSIS | epidemiologic studies | LOCI | BARTTERS-SYNDROME | HEART | INDIVIDUALS | MEDICINE, GENERAL & INTERNAL | exome | genomics | MUTATIONS | HYPERTENSION | TRAITS | GENOME-WIDE ASSOCIATION | Usage | Genetic variation | Exome sequencing | Blood pressure | Genetic aspects | Research | Hypotension | Index Medicus | Abridged Index Medicus
Journal Article
Circulation, ISSN 0009-7322, 11/2018, Volume 138, Issue Suppl_1 Suppl 1, pp. A11421 - A11421
BackgroundMetabolic changes may be detectable in at-risk individuals prior to the onset of coronary heart disease (CHD). Identifying a pattern of metabolites... 
Journal Article