المؤلفون: Gareth Hawkes, Loic Yengo, Sailaja Vedantam, Eirini Marouli, Robin N Beaumont, GIANT Consortium, Jessica Tyrrell, Michael N Weedon, Joel Hirschhorn, Timothy M Frayling, Andrew R Wood

المصدر: PLoS Genetics, Vol 19, Iss 9, p e1010934 (2023)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1010934&type=printableTest; https://doaj.org/toc/1553-7390Test; https://doaj.org/toc/1553-7404Test

الوصول الحر: https://doaj.org/article/de75353f177a495d861e3958357fc622Test

المؤلفون: Hawkes, G, Yengo, L, Vedantam, S, Marouli, E, Beaumont, RN, GIANT Consortium, Tyrrell, J, Weedon, MN, Hirschhorn, J, Frayling, TM, Wood, AR

المساهمون: Cordell, HJ

العلاقة: https://www.ncbi.nlm.nih.gov/pubmed/37733769Test; http://www.ukbiobank.ac.ukTest; https://csg.sph.umich.edu/willer/public/glgc-lipids2021Test/; orcid:0000-0002-3367-789X (Hawkes, Gareth); orcid:0000-0003-0750-8248 (Beaumont, Robin N); orcid:0000-0002-9256-6065 (Tyrrell, Jessica); orcid:0000-0002-6174-6135 (Weedon, Michael N); orcid:0000-0003-1726-948X (Wood, Andrew R); Vol. 19, No. 9, article e1010934; https://doi.org/10.1371/journal.pgen.1010934Test; 875534; SBF004\1079; SBF006\1134; MR/WO14548/1; MR/T002239/1; DE200100425; http://hdl.handle.net/10871/134955Test; PLoS Genetics

الإتاحة: https://doi.org/10.1371/journal.pgen.1010934Test
http://hdl.handle.net/10871/134955Test

المؤلفون: Baronas, JM, Bartell, E, Eliasen, A, Doench, JG, Yengo, L, Vedantam, S, Marouli, E, GIANT Consortium, Kronenberg, HM, Hirschhorn, JN, Renthal, NE

مصطلحات موضوعية: chondrocyte, epiphysis, genome-wide CRISPR screen, genome-wide association studies, growth plate, height, skeletal growth

وصف الملف: 100299 - ?

العلاقة: Cell Genom; https://qmro.qmul.ac.uk/xmlui/handle/123456789/93822Test

الإتاحة: https://doi.org/10.1016/j.xgen.2023.100299Test
https://qmro.qmul.ac.uk/xmlui/handle/123456789/93822Test

المؤلفون: Mahajan, Anubha, Wessel, Jennifer, Willems, Sara M, Zhao, Wei, Robertson, Neil R, Chu, Audrey Y, Gan, Wei, Kitajima, Hidetoshi, Taliun, Daniel, Rayner, N William, Guo, Xiuqing, Lu, Yingchang, Li, Man, Jensen, Richard A, Hu, Yao, Huo, Shaofeng, Lohman, Kurt K, Zhang, Weihua, Cook, James P, Prins, Bram Peter, Flannick, Jason, Grarup, Niels, Trubetskoy, Vassily Vladimirovich, Kravic, Jasmina, Kim, Young Jin, Rybin, Denis V, Yaghootkar, Hanieh, Müller-Nurasyid, Martina, Meidtner, Karina, Li-Gao, Ruifang, Varga, Tibor V, Marten, Jonathan, Li, Jin, Smith, Albert Vernon, An, Ping, Ligthart, Symen, Gustafsson, Stefan, Malerba, Giovanni, Demirkan, Ayse, Tajes, Juan Fernandez, Steinthorsdottir, Valgerdur, Wuttke, Matthias, Lecoeur, Cécile, Preuss, Michael, Bielak, Lawrence F, Graff, Marielisa, Highland, Heather M, Justice, Anne E, Liu, Dajiang J, Marouli, Eirini, Peloso, Gina Marie, Warren, Helen R, ExomeBP Consortium, MAGIC Consortium, GIANT Consortium, Afaq, Saima, Afzal, Shoaib, Ahlqvist, Emma, Almgren, Peter, Amin, Najaf, Bang, Lia B, Bertoni, Alain G, Bombieri, Cristina, Bork-Jensen, Jette, Brandslund, Ivan, Brody, Jennifer A, Burtt, Noël P, Canouil, Mickaël, Chen, Yii-Der Ida, Cho, Yoon Shin, Christensen, Cramer, Eastwood, Sophie V, Eckardt, Kai-Uwe, Fischer, Krista, Gambaro, Giovanni, Giedraitis, Vilmantas, Grove, Megan L, de Haan, Hugoline G, Hackinger, Sophie, Hai, Yang, Han, Sohee, Tybjærg-Hansen, Anne, Hivert, Marie-France, Isomaa, Bo, Jäger, Susanne, Jørgensen, Marit E, Jørgensen, Torben, Käräjämäki, Annemari, Kim, Bong-Jo, Kim, Sung Soo, Koistinen, Heikki A, Kovacs, Peter, Kriebel, Jennifer, Kronenberg, Florian, Läll, Kristi, Lange, Leslie A, Lee, Jung-Jin, Lehne, Benjamin, Li, Huaixing, Lin, Keng-Hung

المصدر: Nature genetics. 50(4)

مصطلحات موضوعية: ExomeBP Consortium, MAGIC Consortium, GIANT Consortium, Humans, Diabetes Mellitus, Type 2, Genetic Predisposition to Disease, Chromosome Mapping, Alleles, European Continental Ancestry Group, Female, Male, Genetic Variation, Genome-Wide Association Study, Whole Exome Sequencing, Diabetes Mellitus, Type 2, Developmental Biology, Biological Sciences, Medical and Health Sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/8xr3h10vTest

المؤلفون: Chan, Yingleong, Lim, Elaine T., Sandholm, Niina, Wang, Sophie R., McKnight, Amy Jayne, Ripke, Stephan, Daly, Mark J., Neale, Benjamin M., Salem, Rany M., Hirschhorn, Joel N., DIAGRAM Consortium, GENIE Consortium, GIANT Consortium, IIBDGC Consortium, PGC Consortium

المساهمون: Clinicum, Department of Medicine, Nefrologian yksikkö

مصطلحات موضوعية: GENOME-WIDE ASSOCIATION, INFLAMMATORY-BOWEL-DISEASE, GENETIC ARCHITECTURE, MISSING HERITABILITY, ULCERATIVE-COLITIS, PROVIDES INSIGHTS, COMMON SNPS, METAANALYSIS, LOCI, SUSCEPTIBILITY, General medicine, internal medicine and other clinical medicine

وصف الملف: application/pdf

العلاقة: Funding for this work was provided by NIH grants R01DK075787 and R01DK081923. R.M.S. was supported by a Juvenile Diabetes Research Foundation postdoctoral fellowship (JDRF #3-2011-70).; Chan , Y , Lim , E T , Sandholm , N , Wang , S R , McKnight , A J , Ripke , S , Daly , M J , Neale , B M , Salem , R M , Hirschhorn , J N , DIAGRAM Consortium , GENIE Consortium , GIANT Consortium , IIBDGC Consortium & PGC Consortium 2014 , ' An Excess of Risk-Increasing Low-Frequency Variants Can Be a Signal of Polygenic Inheritance in Complex Diseases ' , American Journal of Human Genetics , vol. 94 , no. 3 , pp. 437-452 . https://doi.org/10.1016/j.ajhg.2014.02.006Test; ORCID: /0000-0003-4322-6942/work/44577643; http://hdl.handle.net/10138/337093Test; e10271bf-9214-4532-abd4-e3aa14e3b23d; 84896780157; 000332611400017

الإتاحة: http://hdl.handle.net/10138/337093Test

المؤلفون: Turchin, Michael C, Chiang, Charleston WK, Palmer, Cameron D, Sankararaman, Sriram, Reich, David, Genetic Investigation of ANthropometric Traits (GIANT) Consortium, Hirschhorn, Joel N

المصدر: Nature genetics. 44(9)

مصطلحات موضوعية: Genetic Investigation of ANthropometric Traits (GIANT) Consortium, Humans, Body Height, Likelihood Functions, Cohort Studies, Genetics, Population, Gene Frequency, Multifactorial Inheritance, Polymorphism, Single Nucleotide, Adult, European Continental Ancestry Group, Europe, Female, Male, Genetic Variation, Genome-Wide Association Study, Selection, Genetic, Genetics, Population, Polymorphism, Single Nucleotide, Selection, Genetic, Developmental Biology, Biological Sciences, Medical and Health Sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/8r36h8krTest

المؤلفون: Strawbridge, Rona J, Dupuis, Josée, Prokopenko, Inga, Barker, Adam, Ahlqvist, Emma, Rybin, Denis, Petrie, John R, Travers, Mary E, Bouatia-Naji, Nabila, Dimas, Antigone S, Nica, Alexandra, Wheeler, Eleanor, Chen, Han, Voight, Benjamin F, Taneera, Jalal, Kanoni, Stavroula, Peden, John F, Turrini, Fabiola, Gustafsson, Stefan, Zabena, Carina, Almgren, Peter, Barker, David JP, Barnes, Daniel, Dennison, Elaine M, Eriksson, Johan G, Eriksson, Per, Eury, Elodie, Folkersen, Lasse, Fox, Caroline S, Frayling, Timothy M, Goel, Anuj, Gu, Harvest F, Horikoshi, Momoko, Isomaa, Bo, Jackson, Anne U, Jameson, Karen A, Kajantie, Eero, Kerr-Conte, Julie, Kuulasmaa, Teemu, Kuusisto, Johanna, Loos, Ruth JF, Luan, Jian'an, Makrilakis, Konstantinos, Manning, Alisa K, Martínez-Larrad, María Teresa, Narisu, Narisu, Nastase Mannila, Maria, Ohrvik, John, Osmond, Clive, Pascoe, Laura, Payne, Felicity, Sayer, Avan A, Sennblad, Bengt, Silveira, Angela, Stancáková, Alena, Stirrups, Kathy, Swift, Amy J, Syvänen, Ann-Christine, Tuomi, Tiinamaija, van 't Hooft, Ferdinand M, Walker, Mark, Weedon, Michael N, Xie, Weijia, Zethelius, Björn, DIAGRAM Consortium, GIANT Consortium, MuTHER Consortium, CARDIoGRAM Consortium, C4D Consortium, Ongen, Halit, Mälarstig, Anders, Hopewell, Jemma C, Saleheen, Danish, Chambers, John, Parish, Sarah, Danesh, John, Kooner, Jaspal, Ostenson, Claes-Göran, Lind, Lars, Cooper, Cyrus C, Serrano-Ríos, Manuel, Ferrannini, Ele, Forsen, Tom J, Clarke, Robert, Franzosi, Maria Grazia, Seedorf, Udo, Watkins, Hugh, Froguel, Philippe, Johnson, Paul, Deloukas, Panos, Collins, Francis S, Laakso, Markku, Dermitzakis, Emmanouil T, Boehnke, Michael, McCarthy, Mark I, Wareham, Nicholas J, Groop, Leif, Pattou, François, Gloyn, Anna L, Dedoussis, George V

المصدر: Diabetes. 60(10)

مصطلحات موضوعية: DIAGRAM Consortium, GIANT Consortium, MuTHER Consortium, CARDIoGRAM Consortium, C4D Consortium, Humans, Diabetes Mellitus, Type 2, Insulin, Proinsulin, Fasting, Genotype, Polymorphism, Single Nucleotide, Genome, Human, Adult, Female, Male, Genetic Variation, Diabetes Mellitus, Type 2, Polymorphism, Single Nucleotide, Genome, Human, Endocrinology & Metabolism, Medical and Health Sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/9354m27fTest

المؤلفون: Roopa Rajan, K. P. Divya, Rukmini Mridula Kandadai, Ravi Yadav, Venkata P. Satagopam, U. K. Madhusoodanan, Pankaj Agarwal, Niraj Kumar, Teresa Ferreira, Hrishikesh Kumar, A. V. Sreeram Prasad, Kuldeep Shetty, Sahil Mehta, Soaham Desai, Suresh Kumar, L. K. Prashanth, Mohit Bhatt, Pettarusp Wadia, Sudha Ramalingam, G. M. Wali, Sanjay Pandey, Felix Bartusch, Maximilian Hannussek, Jens Krüger, Ashwin Kumar-Sreelatha, Sandeep Grover, Peter Lichtner, Marc Sturm, Jochen Roeper, Volker Busskamp, Giriraj R. Chandak, Jens Schwamborn, Pankaj Seth, Thomas Gasser, Olaf Riess, Vinay Goyal, Pramod Kumar Pal, Rupam Borgohain, Rejko Krüger, Asha Kishore, Manu Sharma, The Lux-GIANT Consortium

المصدر: Frontiers in Neurology, Vol 11 (2020)

مصطلحات موضوعية: Parkinson's disease, genetic diversity, genome-wide association study, common genetic variation, biobank, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/article/10.3389/fneur.2020.00524/fullTest; https://doaj.org/toc/1664-2295Test

الوصول الحر: https://doaj.org/article/3268a466280148719c06966c967d7436Test

المؤلفون: Speliotes, Elizabeth K, Yerges-Armstrong, Laura M, Wu, Jun, Hernaez, Ruben, Kim, Lauren J, Palmer, Cameron D, Gudnason, Vilmundur, Eiriksdottir, Gudny, Garcia, Melissa E, Launer, Lenore J, Nalls, Michael A, Clark, Jeanne M, Mitchell, Braxton D, Shuldiner, Alan R, Butler, Johannah L, Tomas, Marta, Hoffmann, Udo, Hwang, Shih-Jen, Massaro, Joseph M, O'Donnell, Christopher J, Sahani, Dushyant V, Salomaa, Veikko, Schadt, Eric E, Schwartz, Stephen M, Siscovick, David S, NASH CRN, GIANT Consortium, MAGIC Investigators, Voight, Benjamin F, Carr, J Jeffrey, Feitosa, Mary F, Harris, Tamara B, Fox, Caroline S, Smith, Albert V, Kao, WH Linda, Hirschhorn, Joel N, Borecki, Ingrid B, GOLD Consortium

المصدر: PLoS genetics. 7(3)

مصطلحات موضوعية: NASH CRN, GIANT Consortium, MAGIC Investigators, GOLD Consortium, Humans, Fatty Liver, Insulin, Lipase, Blood Glucose, Adaptor Proteins, Signal Transducing, Lectins, C-Type, Membrane Proteins, Nerve Tissue Proteins, Tomography, X-Ray Computed, Case-Control Studies, Cohort Studies, Mutation, Missense, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Adult, Aged, Aged, 80 and over, Middle Aged, Male, Genome-Wide Association Study, Chondroitin Sulfate Proteoglycans, Non-alcoholic Fatty Liver Disease, Prevention, Human Genome, Digestive Diseases, Liver Disease, Hepatitis, Chronic Liver Disease and Cirrhosis, Genetics, Clinical Research, 2.1 Biological and endogenous factors, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5766v2gwTest

المؤلفون: Sung, YJ, Winkler, TW, de Las Fuentes, L, Bentley, AR, Brown, MR, Kraja, AT, Schwander, K, Ntalla, I, Guo, X, Franceschini, N, Lu, Y, Cheng, C-Y, Sim, X, Vojinovic, D, Marten, J, Musani, SK, Li, C, Feitosa, MF, Kilpeläinen, TO, Richard, MA, Noordam, R, Aslibekyan, S, Aschard, H, Bartz, TM, Dorajoo, R, Liu, Y, Manning, AK, Rankinen, T, Smith, AV, Tajuddin, SM, Tayo, BO, Warren, HR, Zhao, W, Zhou, Y, Matoba, N, Sofer, T, Alver, M, Amini, M, Boissel, M, Chai, JF, Chen, X, Divers, J, Gandin, I, Gao, C, Giulianini, F, Goel, A, Harris, SE, Hartwig, FP, Horimoto, ARVR, Hsu, F-C, Jackson, AU, Kähönen, M, Kasturiratne, A, Kühnel, B, Leander, K, Lee, W-J, Lin, K-H, 'an Luan, J, McKenzie, CA, Meian, H, Nelson, CP, Rauramaa, R, Schupf, N, Scott, RA, Sheu, WHH, Stančáková, A, Takeuchi, F, van der Most, PJ, Varga, TV, Wang, H, Wang, Y, Ware, EB, Weiss, S, Wen, W, Yanek, LR, Zhang, W, Zhao, JH, Afaq, S, Alfred, T, Amin, N, Arking, D, Aung, T, Barr, RG, Bielak, LF, Boerwinkle, E, Bottinger, EP, Braund, PS, Brody, JA, Broeckel, U, Cabrera, CP, Cade, B, Caizheng, Y, Campbell, A, Canouil, M, Chakravarti, A, CHARGE Neurology Working Group, Chauhan, G, Christensen, K, Cocca, M, COGENT-Kidney Consortium, Collins, FS, Connell, JM, de Mutsert, R, de Silva, HJ, Debette, S, Dörr, M, Duan, Q, Eaton, CB, Ehret, G, Evangelou, E, Faul, JD, Fisher, VA, Forouhi, NG, Franco, OH, Friedlander, Y, Gao, H, GIANT Consortium, Gigante, B, Graff, M, Gu, CC, Gu, D, Gupta, P, Hagenaars, SP, Harris, TB, He, J, Heikkinen, S, Heng, C-K, Hirata, M, Hofman, A, Howard, BV, Hunt, S, Irvin, MR, Jia, Y, Joehanes, R, Justice, AE, Katsuya, T, Kaufman, J, Kerrison, ND, Khor, CC, Koh, W-P, Koistinen, HA, Komulainen, P, Kooperberg, C, Krieger, JE, Kubo, M, Kuusisto, J, Langefeld, CD, Langenberg, C, Launer, LJ, Lehne, B, Lewis, CE, Li, Y, Lifelines Cohort Study, Lim, SH, Lin, S, Liu, C-T, Liu, J, Liu, K, Loh, M, Lohman, KK, Long, J, Louie, T, Mägi, R, Mahajan, A, Meitinger, T, Metspalu, A, Milani, L, Momozawa, Y, Morris, AP, Mosley, TH, Munson, P, Murray, AD, Nalls, MA, Nasri, U, Norris, JM, North, K, Ogunniyi, A, Padmanabhan, S, Palmas, WR, Palmer, ND, Pankow, JS, Pedersen, NL, Peters, A, Peyser, PA, Polasek, O, Raitakari, OT, Renström, F, Rice, TK, Ridker, PM, Robino, A, Robinson, JG, Rose, LM, Rudan, I, Sabanayagam, C, Salako, BL, Sandow, K, Schmidt, CO, Schreiner, PJ, Scott, WR, Seshadri, S, Sever, P, Sitlani, CM, Smith, JA, Snieder, H, Starr, JM, Strauch, K, Tang, H, Taylor, KD, Teo, YY, Tham, YC, Uitterlinden, AG, Waldenberger, M, Wang, L, Wang, YX, Wei, WB, Williams, C, Wilson, G, Wojczynski, MK, Yao, J, Yuan, J-M, Zonderman, AB, Becker, DM, Boehnke, M, Bowden, DW, Chambers, JC, Chen, Y-DI, de Faire, U, Deary, IJ, Esko, T, Farrall, M, Forrester, T, Franks, PW, Freedman, BI, Froguel, P, Gasparini, P, Gieger, C, Horta, BL, Hung, Y-J, Jonas, JB, Kato, N, Kooner, JS, Laakso, M, Lehtimäki, T, Liang, K-W, Magnusson, PKE, Newman, AB, Oldehinkel, AJ, Pereira, AC, Redline, S, Rettig, R, Samani, NJ, Scott, J, Shu, X-O, van der Harst, P, Wagenknecht, LE, Wareham, NJ, Watkins, H, Weir, DR, Wickremasinghe, AR, Wu, T, Zheng, W, Kamatani, Y, Laurie, CC, Bouchard, C, Cooper, RS, Evans, MK, Gudnason, V, Kardia, SLR, Kritchevsky, SB, Levy, D, O'Connell, JR, Psaty, BM, van Dam, RM, Sims, M, Arnett, DK, Mook-Kanamori, DO, Kelly, TN, Fox, ER, Hayward, C, Fornage, M, Rotimi, CN, Province, MA, van Duijn, CM, Tai, ES, Wong, TY, Loos, RJF, Reiner, AP, Rotter, JI, Zhu, X, Bierut, LJ, Gauderman, WJ, Caulfield, MJ, Elliott, P, Rice, K, Munroe, PB, Morrison, AC, Cupples, LA, Rao, DC, Chasman, DI

مصطلحات موضوعية: GWAS, GxE interactions, blood pressure, lifestyle, multi-ancestry, smoking, Cohort Studies, Continental Population Groups, Diastole, Epistasis, Genetic, Female, Genetic Loci, Genome-Wide Association Study, Humans, Male, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Reproducibility of Results, Systole

العلاقة: https://www.ncbi.nlm.nih.gov/pubmed/29455858Test; Am J Hum Genet, 2018, 102 (3), pp. 375-400; https://www.sciencedirect.com/science/article/pii/S000292971830017X?via%3DihubTest; http://hdl.handle.net/2381/43513Test; S0002-9297(18)30017-X

الإتاحة: https://doi.org/10.1016/j.ajhg.2018.01.015Test
https://www.sciencedirect.com/science/article/pii/S000292971830017X?via%3DihubTest
http://hdl.handle.net/2381/43513Test