نتائج البحث - "DBDS Genomic Consortium"

المساهمون: Institute for Molecular Medicine Finland, Centre of Excellence in Complex Disease Genetics, HUS Abdominal Center, Tiinamaija Tuomi Research Group, Clinicum, CAMM - Research Program for Clinical and Molecular Metabolism, Research Programs Unit, Department of Medicine, Endokrinologian yksikkö, HUS Children and Adolescents, Doctoral Programme in Biomedicine, Lastentautien yksikkö, Children's Hospital

مصطلحات موضوعية: Bone-mineral density, Genome-wide association, Body-mass index, Mendelian randomization, Loci, Risk, Architecture, Metaanalysis, Women, Susceptibility, 1184 Genetics, developmental biology, physiology

وصف الملف: application/pdf

العلاقة: Nethander , M , Moverare-Skrtic , S , Kämpe , A , Coward , E , Reimann , E , Grahnemo , L , Borbely , E , Helyes , Z , Funck-Brentano , T , Cohen-Solal , M , Tuukkanen , J , Koskela , A , Wu , J , Li , L , Lu , T , Gabrielsen , M E , Estonian Biobank Res Team , R , Magi , R , Hoff , M , Lerner , U H , Henning , P , Ullum , H , Erikstrup , C , Brunak , S , DBDS Genomic Consortium , T , Langhammer , A , Tuomi , T , Oddsson , A , Stefansson , K , Pettersson-Kymmer , U , Ostrowski , S R , Pedersen , O B V , Styrkarsdottir , U , Mäkitie , O , Hveem , K , Richards , J B & Ohlsson , C 2023 , ' An atlas of genetic determinants of forearm fracture ' , Nature Genetics . https://doi.org/10.1038/s41588-023-01527-3Test; ORCID: /0000-0002-8306-6202/work/146906520; ORCID: /0000-0002-4547-001X/work/155652022; http://hdl.handle.net/10138/567283Test; e72b3bdf-c8c0-4e48-a034-79eb86da92e2; 001093262400002

الإتاحة: http://hdl.handle.net/10138/567283Test

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9

دورية أكاديمية

Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

المؤلفون: DBDS Genomic Consortium, Oddsson, Asmundur, Sulem, Patrick, Sveinbjornsson, Gardar, Karjalainen, Juha M., Daly, Mark

المساهمون: Institute for Molecular Medicine Finland

مصطلحات موضوعية: Mutations, Disease, Variants, Drosophila, Cohort, Risk, Rnai, Identification, Discovery, Spectrum, 1184 Genetics, developmental biology, physiology

وصف الملف: application/pdf

العلاقة: DBDS Genomic Consortium , Oddsson , A , Sulem , P , Sveinbjornsson , G , Karjalainen , J M & Daly , M 2023 , ' Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality ' , Nature Communications , vol. 14 , no. 1 , 3453 . https://doi.org/10.1038/s41467-023-38951-2Test; 65b252bb-e782-4394-8cc6-cee00a9365c1; http://hdl.handle.net/10138/563682Test; 001003866300016

الإتاحة: http://hdl.handle.net/10138/563682Test

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10

دورية أكاديمية

The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

المؤلفون: Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Møller, Peter L, Stefansdottir, Lilja, Galarneau, Geneviève, Turman, Constance, Danning, Rebecca, Law, Matthew H, Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Giri, Ayush, Banasik, Karina, Krassowski, Michal, Lepamets, Maarja, Marciniak, Błażej, Nõukas, Margit, Perro, Danielle, Sliz, Eeva, Sobalska-Kwapis, Marta, Thorleifsson, Gudmar, Topbas-Selcuki, Nura F, Vitonis, Allison, Westergaard, David, Arnadottir, Ragnheidur, Burgdorf, Kristoffer S, Campbell, Archie, Cheuk, Cecilia SK, Clementi, Caterina, Cook, James, De Vivo, Immaculata, DiVasta, Amy, Dorien, O, Donoghue, Jacqueline F, Edwards, Todd, Fontanillas, Pierre, Fung, Jenny N, Geirsson, Reynir T, Girling, Jane E, Harkki, Paivi, Harris, Holly R, Healey, Martin, Heikinheimo, Oskari, Holdsworth-Carson, Sarah, Hostettler, Isabel C, Houlden, Henry, Houshdaran, Sahar, Irwin, Juan C, Jarvelin, Marjo-Riitta, Kamatani, Yoichiro, Kennedy, Stephen H, Kepka, Ewa, Kettunen, Johannes, Kubo, Michiaki, Kulig, Bartosz, Kurra, Venla, Laivuori, Hannele, Laufer, Marc R, Lindgren, Cecilia M, MacGregor, Stuart, Mangino, Massimo, Martin, Nicholas G, Matalliotaki, Charoula, Matalliotakis, Michail, Murray, Alison D, Ndungu, Anne, Nezhat, Camran, Olsen, Catherine M, Opoku-Anane, Jessica, Padmanabhan, Sandosh, Paranjpe, Manish, Peters, Maire, Polak, Grzegorz, Porteous, David J, Rabban, Joseph, Rexrode, Kathyrn M, Romanowicz, Hanna, Saare, Merli, Saavalainen, Liisu, Schork, Andrew J, Sen, Sushmita, Shafrir, Amy L, Siewierska-Górska, Anna, Słomka, Marcin, Smith, Blair H, Smolarz, Beata, Szaflik, Tomasz, Szyłło, Krzysztof, Takahashi, Atsushi, Terry, Kathryn L, Tomassetti, Carla, Treloar, Susan A, Vanhie, Arne, Vincent, Katy, Vo, Kim C, Werring, David J, Zeggini, Eleftheria, Zervou, Maria I, DBDS Genomic Consortium, ., FinnGen Study, ., FinnGen Endometriosis Taskforce, ., Celmatix Research Team, ., 23andMe Research Team, ., Adachi, Sosuke, Buring, Julie E, Ridker, Paul M, D'Hooghe, Thomas, Goulielmos, George N, Hapangama, Dharani K, Hayward, Caroline, Horne, Andrew W, Low, Siew-Kee, Martikainen, Hannu, Chasman, Daniel I, Rogers, Peter AW, Saunders, Philippa T, Sirota, Marina, Spector, Tim, Strapagiel, Dominik, Tung, Joyce Y, Whiteman, David C, Giudice, Linda C, Velez-Edwards, Digna R, Uimari, Outi, Kraft, Peter, Salumets, Andres, Nyholt, Dale R, Mägi, Reedik, Stefansson, Kari, Becker, Christian M, Yurttas-Beim, Piraye, Steinthorsdottir, Valgerdur, Nyegaard, Mette, Missmer, Stacey A, Montgomery, Grant W, Morris, Andrew P, Zondervan, Krina T

المصدر: Nature Genetics , 55 (3) pp. 423-436. (2023)

مصطلحات موضوعية: Comorbidity, Endometriosis, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Pain

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10168216/1/nihms-1873427.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10168216Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10168216/1/nihms-1873427.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10168216Test/

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