Zobrazeno 1 - 10
of 115
pro vyhledávání: '"Verlouw J"'
Autor:
Kuiper LM; Genetic Laboratory, Department of Internal Medicine, Erasmus MC, Rotterdam, the Netherlands., Shi W; McKusick-Nathans Institute, Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA., Verlouw J; Genetic Laboratory, Department of Internal Medicine, Erasmus MC, Rotterdam, the Netherlands., Hong YS; McKusick-Nathans Institute, Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA., Arp P; Genetic Laboratory, Department of Internal Medicine, Erasmus MC, Rotterdam, the Netherlands., Puiu D; Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, USA., Broer L; Genetic Laboratory, Department of Internal Medicine, Erasmus MC, Rotterdam, the Netherlands., Xie J; McKusick-Nathans Institute, Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA., Newcomb C; McKusick-Nathans Institute, Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA., Rich SS; Center for Public Health Genomics, Department of Public Health Sciences, University of Virginia, Charlottesville, VA, USA., Taylor KD; The Institute for Translational Genomics and Population Sciences, Department of Pediatrics, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA., Rotter JI; The Institute for Translational Genomics and Population Sciences, Department of Pediatrics, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA., Bader JS; Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, USA., Guallar E; Department of Epidemiology and Medicine, and Welch Center for Prevention, Epidemiology, and Clinical Research, Johns Hopkins University Bloomberg School of Public Health. Baltimore, MD, USA., van Meurs JBJ; Genetic Laboratory, Department of Internal Medicine, Erasmus MC, Rotterdam, the Netherlands.; Department of Orthopeadics & Sports Medicine, Erasmus MC, Rotterdam, the Netherlands., Arking DE; McKusick-Nathans Institute, Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Publikováno v:
MedRxiv : the preprint server for health sciences [medRxiv] 2024 Apr 03. Date of Electronic Publication: 2024 Apr 03.
Autor:
Vosa, U. (Urmo), Claringbould, A. (Annique), Westra, H.-J. (Harm-Jan), Bonder, M. J. (Marc Jan), Deelen, P. (Patrick), Zeng, B. (Biao), Kirsten, H. (Holger), Saha, A. (Ashis), Kreuzhuber, R. (Roman), Yazar, S. (Seyhan), Brugge, H. (Harm), Oelen, R. (Roy), de Vries, D. H. (Dylan H.), van der Wijst, M. G. (Monique G. P.), Kasela, S. (Silva), Pervjakova, N. (Natalia), Alves, I. (Isabel), Fave, M.-J. (Marie-Julie), Agbessi, M. (Mawusse), Christiansen, M. W. (Mark W.), Jansen, R. (Rick), Seppala, I. (Ilkka), Tong, L. (Lin), Teumer, A. (Alexander), Schramm, K. (Katharina), Hemani, G. (Gibran), Verlouw, J. (Joost), Yaghootkar, H. (Hanieh), Flitman, R. S. (Reyhan Sonmez), Brown, A. (Andrew), Kukushkina, V. (Viktorija), Kalnapenkis, A. (Anette), Rueger, S. (Sina), Porcu, E. (Eleonora), Kronberg, J. (Jaanika), Kettunen, J. (Johannes), Lee, B. (Bernett), Zhang, F. (Futao), Qi, T. (Ting), Hernandez, J. A. (Jose Alquicira), Arindrarto, W. (Wibowo), Beutner, F. (Frank), Dmitrieva, J. (Julia), Elansary, M. (Mahmoud), Fairfax, B. P. (Benjamin P.), Georges, M. (Michel), Heijmans, B. T. (Bastiaan T.), Hewitt, A. W. (Alex W.), Kahonen, M. (Mika), Kim, Y. (Yungil), Knight, J. C. (Julian C.), Kovacs, P. (Peter), Krohn, K. (Knut), Li, S. (Shuang), Loeffler, M. (Markus), Marigorta, U. M. (Urko M.), Mei, H. (Hailang), Momozawa, Y. (Yukihide), Mueller-Nurasyid, M. (Martina), Nauck, M. (Matthias), Nivard, M. G. (Michel G.), Penninx, B. W. (Brenda W. J. H.), Pritchard, J. K. (Jonathan K.), Raitakari, O. T. (Olli T.), Rotzschke, O. (Olaf), Slagboom, E. P. (Eline P.), Stehouwer, C. D. (Coen D. A.), Stumvoll, M. (Michael), Sullivan, P. (Patrick), Thiery, J. (Joachim), Tonjes, A. (Anke), van Dongen, J. (Jenny), van Iterson, M. (Maarten), Veldink, J. H. (Jan H.), Voelker, U. (Uwe), Warmerdam, R. (Robert), Wijmenga, C. (Cisca), Swertz, M. (Morris), Andiappan, A. (Anand), Montgomery, G. W. (Grant W.), Ripatti, S. (Samuli), Perola, M. (Markus), Kutalik, Z. (Zoltan), Dermitzakis, E. (Emmanouil), Bergmann, S. (Sven), Frayling, T. (Timothy), van Meurs, J. (Joyce), Prokisch, H. (Holger), Ahsan, H. (Habibul), Pierce, B. L. (Brandon L.), Lehtimaki, T. (Terho), Boomsma, D. I. (Dorret, I), Psaty, B. M. (Bruce M.), Gharib, S. A. (Sina A.), Awadalla, P. (Philip), Milani, L. (Lili), Ouwehand, W. H. (Willem H.), Downes, K. (Kate), Stegle, O. (Oliver), Battle, A. (Alexis), Visscher, P. M. (Peter M.), Yang, J. (Jian), Scholz, M. (Markus), Powell, J. (Joseph), Gibson, G. (Greg), Esko, T. (Tonu), Franke, L. (Lude)
Trait-associated genetic variants affect complex phenotypes primarily via regulatory mechanisms on the transcriptome. To investigate the genetics of gene expression, we performed cis- and trans-expression quantitative trait locus (eQTL) analyses usin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2423::f87941627e153961d51c04d5bd95bb82
http://urn.fi/urn:nbn:fi-fe2022030422046
http://urn.fi/urn:nbn:fi-fe2022030422046
Autor:
Porcu, E., Rueger, S., Lepik, K., Agbessi, M., Ahsan, H., Alves, I., Andiappan, A., Arindrarto, W., Awadalla, P., Battle, A., Beutner, F., Bonder, M.J., Boomsma, D., Christiansen, M., Claringbould, A., Deelen, P., Esko, T., Fave, M.J., Franke, L., Frayling, T., Gharib, S.A., Gibson, G., Heijmans, B.T., Hemani, G., Jansen, R., Kahonen, M., Kalnapenkis, A., Kasela, S., Kettunen, J., Kim, Y., Kirsten, H., Kovacs, P., Krohn, K., Kronberg-Guzman, J., Kukushkina, V., Lee, B., Lehtimaki, T., Loeffler, M., Marigorta, U.M., Mei, H.L., Milani, L., Montgomery, G.W., Muller-Nurasyid, M., Nauck, M., Nivard, M., Penninx, B., Perola, M., Pervjakova, N., Pierce, B.L., Powell, J., Prokisch, H., Psaty, B.M., Raitakari, O.T., Ripatti, S., Rotzschke, O., Saha, A., Scholz, M., Schramm, K., Seppala, I., Slagboom, E.P., Stehouwer, C.D.A., Stumvoll, M., Sullivan, P., Hoen, P.A.C. 't, Teumer, A., Thiery, J., Tong, L., Tonjes, A., Dongen, J. van, Iterson, M. van, Meurs, J. van, Veldink, J.H., Verlouw, J., Visscher, P.M., Volker, U., Vosa, U., Westra, H.J., Wijmenga, C., Yaghootkar, H., Yang, J., Zeng, B., Zhang, F.T., Beekman, M., Boomsma, D.I., Bot, J., Deelen, J., Hofman, B.A., Hottenga, J.J., Isaacs, A., Jhamai, P.M., Kielbasa, S.M., Lakenberg, N., Luijk, R., Mei, H., Moed, M., Nooren, I., Pool, R., Schalkwijk, C.G., Slagboom, P.E., Suchiman, H.E.D., Swertz, M.A., Tigchelaar, E.F., Uitterlinden, A.G., Berg, L.H. van den, Breggen, R. van der, Kallen, C.J.H. van der, Dijk, F. van, Duijn, C.M. van, Galen, M. van, Greevenbroek, M.M.J. van, Heemst, D. van, Rooij, J. van, Van't Hof, P., Zwet, E.W. van, Vermaat, M., Verbiest, M., Verkerk, M., Zhernakova, D.V., Zhernakova, S., Santoni, F.A., Reymond, A., Kutalik, Z., eQTLGen Consortium, BIOS Consortium
Publikováno v:
Porcu, E, Rüeger, S, Lepik, K, eQTLGen Consortium, BIOS Consortium, Santoni, F, Reymond, A & Kutalik, Z 2019, ' Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ', Nature Communications, vol. 10, no. 1, 3300 . https://doi.org/10.1038/s41467-019-10936-0
Nature Communications, Vol 10, Iss 1, Pp 1-12 (2019)
Nature Communications
Nature Communications, 10:3300. Nature Publishing Group
eQTLGen Consortium & BIOS Consortium 2019, ' Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ', Nature Communications, vol. 10, no. 1, 3300 . https://doi.org/10.1038/s41467-019-10936-0
Nat. Commun. 10:3300 (2019)
Nature Communications, 10(1):3300. Nature Publishing Group
Nature Communications, 10(1):3300. Nature Publishing Group UK
Nature communications, vol. 10, no. 1, pp. 3300
Nature Communications, 10
Porcu, E, Kutalik, Z, eQTLGen Consortium, BIOS Consortium, Boomsma, D I, Nivard, M G, Hottenga, J J, Pool, R & van Dongen, J 2019, ' Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ', Nature Communications, vol. 10, no. 1, 3300 . https://doi.org/10.1038/s41467-019-10936-0
Nature Communications, Vol 10, Iss 1, Pp 1-12 (2019)
Nature Communications
Nature Communications, 10:3300. Nature Publishing Group
eQTLGen Consortium & BIOS Consortium 2019, ' Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ', Nature Communications, vol. 10, no. 1, 3300 . https://doi.org/10.1038/s41467-019-10936-0
Nat. Commun. 10:3300 (2019)
Nature Communications, 10(1):3300. Nature Publishing Group
Nature Communications, 10(1):3300. Nature Publishing Group UK
Nature communications, vol. 10, no. 1, pp. 3300
Nature Communications, 10
Porcu, E, Kutalik, Z, eQTLGen Consortium, BIOS Consortium, Boomsma, D I, Nivard, M G, Hottenga, J J, Pool, R & van Dongen, J 2019, ' Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ', Nature Communications, vol. 10, no. 1, 3300 . https://doi.org/10.1038/s41467-019-10936-0
Genome-wide association studies (GWAS) have identified thousands of variants associated with complex traits, but their biological interpretation often remains unclear. Most of these variants overlap with expression QTLs, indicating their potential in
Autor:
Timmers, P.R., Mounier, N., Lall, K., Fischer, K., Ning, Z., Feng, X., Bretherick, A.D., Clark, D.W., Agbessi, M., Ahsan, H., Alves, I., Andiappan, A., Awadalla, P., Battle, A., Bonder, M.J., Boomsma, D., Christiansen, M., Claringbould, A., Deelen, P., van Dongen, J., Esko, T., Favé, M., Franke, L., Frayling, T., Gharib, S.A., Gibson, G., Hemani, G., Jansen, R., Kalnapenkis, A., Kasela, S., Kettunen, J., Kim, Y., Kirsten, H., Kovacs, P., Krohn, K., Kronberg-Guzman, J., Kukushkina, V., Kutalik, Z., Kähönen, M., Lee, B., Lehtimäki, T., Loeffler, M., Marigorta, U., Metspalu, A., van Meurs, J., Milani, L., Müller-Nurasyid, M., Nauck, M., Nivard, M., Penninx, B., Perola, M., Pervjakova, N., Pierce, B., Powell, J., Prokisch, H., Psaty, B.M., Raitakari, O., Ring, S., Ripatti, S., Rotzschke, O., Ruëger, S., Saha, A., Scholz, M., Schramm, K., Seppälä, I., Stumvoll, M., Sullivan, P., Teumer, A., Thiery, J., Tong, L., Tönjes, A., Verlouw, J., Visscher, P.M., Võsa, U., Völker, U., Yaghootkar, H., Yang, J., Zeng, B., Zhang, F., Shen, X., Wilson, J.F., Joshi, P.K.
Publikováno v:
eLife, vol. 8, pp. e39856
eLife
eLife 8:e39856 (2019)
eLife, 8. eLife Sciences Publications Limited
eLife, Vol 8 (2019)
Timmers, P R, Mounier, N, Lall, K, Fischer, K, Ning, Z, Feng, X, Bretherick, A D, Clark, D W, Shen, X, Esko, T, Kutalik, Z, Wilson, J F, Joshi, P K & eQTLGen Consortium 2019, ' Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances ', eLife, vol. 8 . https://doi.org/10.7554/eLife.39856
eLife
eLife 8:e39856 (2019)
eLife, 8. eLife Sciences Publications Limited
eLife, Vol 8 (2019)
Timmers, P R, Mounier, N, Lall, K, Fischer, K, Ning, Z, Feng, X, Bretherick, A D, Clark, D W, Shen, X, Esko, T, Kutalik, Z, Wilson, J F, Joshi, P K & eQTLGen Consortium 2019, ' Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances ', eLife, vol. 8 . https://doi.org/10.7554/eLife.39856
We use a genome-wide association of 1 million parental lifespans of genotyped subjects and data on mortality risk factors to validate previously unreplicated findings near CDKN2B-AS1, ATXN2/BRAP, FURIN/FES, ZW10, PSORS1C3, and 13q21.31, and identify
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::48226c49150697a2cd359bc562fc0330
https://serval.unil.ch/notice/serval:BIB_771D2C9E3799
https://serval.unil.ch/notice/serval:BIB_771D2C9E3799
Autor:
Porcu, E. (Eleonora), Rueger, S. (Sina), Lepik, K. (Kaido), Agbessi, M. (Mawusse), Ahsan, H. (Habibul), Alves, I. (Isabel), Andiappan, A. (Anand), Arindrarto, W. (Wibowo), Awadalla, P. (Philip), Battle, A. (Alexis), Beutner, F. (Frank), Bonder, M. J. (Marc Jan), Boomsma, D. (Dorret), Christiansen, M. (Mark), Claringbould, A. (Annique), Deelen, P. (Patrick), Esko, T. (Tonu), Fave, M.-J. (Marie-Julie), Franke, L. (Lude), Frayling, T. (Timothy), Gharib, S. A. (Sina A.), Gibson, G. (Gregory), Heijmans, B. T. (Bastiaan T.), Hemani, G. (Gibran), Jansen, R. (Rick), Kahonen, M. (Mika), Kalnapenkis, A. (Anette), Kasela, S. (Silva), Kettunen, J. (Johannes), Kim, Y. (Yungil), Kirsten, H. (Holger), Kovacs, P. (Peter), Krohn, K. (Knut), Kronberg-Guzman, J. (Jaanika), Kukushkina, V. (Viktorija), Lee, B. (Bernett), Lehtimaki, T. (Terho), Loeffler, M. (Markus), Marigorta, U. M. (Urko M.), Mei, H. (Hailang), Milani, L. (Lili), Montgomery, G. W. (Grant W.), Mueler-Nurasyid, M. (Martina), Nauck, M. (Matthias), Nivard, M. (Michel), Penninx, B. (Brenda), Perola, M. (Markus), Pervjakova, N. (Natalia), Pierce, B. L. (Brandon L.), Powell, J. (Joseph), Prokisch, H. (Holger), Psaty, B. M. (Bruce M.), Raitakari, O. T. (Olli T.), Ripatti, S. (Samuli), Rotzschke, O. (Olaf), Saha, A. (Ashis), Scholz, M. (Markus), Schramm, K. (Katharina), Seppala, I. (Ilkka), Slagboom, E. P. (Eline P.), Stehouwer, C. D. (Coen D. A.), Stumvoll, M. (Michael), Sullivan, P. (Patrick), Teumer, A. (Alexander), Thiery, J. (Joachim), Tong, L. (Lin), Tonjes, A. (Anke), van Dongen, J. (Jenny), van Iterson, M. (Maarten), van Meurs, J. (Joyce), Veldink, J. H. (Jan H.), Verlouw, J. (Joost), Visscher, P. M. (Peter M.), Volker, U. (Uwe), Vosa, U. (Urmo), Westra, H.-J. (Harm-Jan), Wijmenga, C. (Cisca), Yaghootkar, H. (Hanieh), Yang, J. (Jian), Zeng, B. (Biao), Zhang, F. (Futao), Beekman, M. (Marian), Boomsma, D. I. (Dorret I.), Bot, J. (Jan), Deelen, J. (Joris), Hofman, B. A. (Bert A.), Hottenga, J. J. (Jouke J.), Isaacs, A. (Aaron), Jhamai, P. M. (P. Mila), Kielbasa, S. M. (Szymon M.), Lakenberg, N. (Nico), Luijk, R. (Rene), Mei, H. (Hailiang), Moed, M. (Matthijs), Nooren, I. (Irene), Pool, R. (Rene), Schalkwijk, C. G. (Casper G.), Slagboom, P. E. (P. Eline), Suchiman, H. E. (H. Eka D.), Swertz, M. A. (Morris A.), Tigchelaar, E. F. (Ettje F.), Uitterlinden, A. G. (Andre G.), van den Berg, L. H. (Leonard H.), van der Breggen, R. (Ruud), van der Kallen, C. J. (Carla J. H.), van Dijk, F. (Freerk), van Duijn, C. M. (Cornelia M.), van Galen, M. (Michiel), van Greevenbroek, M. M. (Marleen M. J.), van Heemst, D. (Diana), van Rooij, J. (Jeroen), Van't Hof, P. (Peter), van Zwet, E. W. (Erik. W.), Vermaat, M. (Martijn), Verbiest, M. (Michael), Verkerk, M. (Marijn), Zhernakova, D. V. (Dasha V.), Zhernakova, S. (Sasha), Santoni, F. A. (Federico A.), Reymond, A. (Alexandre), Kutalik, Z. (Zoltan)
Genome-wide association studies (GWAS) have identified thousands of variants associated with complex traits, but their biological interpretation often remains unclear. Most of these variants overlap with expression QTLs, indicating their potential in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2423::5d4f24d031228650820d283cc0d4fac4
http://urn.fi/urn:nbn:fi-fe202003117859
http://urn.fi/urn:nbn:fi-fe202003117859
Akademický článek
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Autor:
Battle SL; McKusick-Nathans Institute, Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA., Puiu D; Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, USA., Verlouw J; Department of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands., Broer L; Department of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands., Boerwinkle E; Human Genetics Center, Department of Epidemiology, Human Genetics, and Environmental Sciences, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA., Taylor KD; The Institute for Translational Genomics and Population Sciences, Department of Pediatrics, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA., Rotter JI; The Institute for Translational Genomics and Population Sciences, Department of Pediatrics, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA., Rich SS; Center for Public Health Genomics, University of Virginia, Charlottesville, VA, USA., Grove ML; Human Genetics Center, Department of Epidemiology, Human Genetics, and Environmental Sciences, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA., Pankratz N; Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, USA., Fetterman JL; Evans Department of Medicine and the Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, MA, USA., Liu C; Framingham Heart Study, Boston University School of Medicine, Boston, MA, USA., Arking DE; McKusick-Nathans Institute, Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Publikováno v:
NAR genomics and bioinformatics [NAR Genom Bioinform] 2022 May 17; Vol. 4 (2), pp. lqac034. Date of Electronic Publication: 2022 May 17 (Print Publication: 2022).
Autor:
Xue, A., Wu, Y., Zhu, Z., Zhang, F., Kemper, K.E., Zheng, Z., Yengo, L., Lloyd-Jones, L.R., Sidorenko, J., Agbessi, M., Ahsan, H., Alves, I., Andiappan, A., Awadalla, P., Battle, A., Beutner, F., Bonder, M.J., Boomsma, D., Christiansen, M., Claringbould, A., Deelen, P., Esko, T., Favé, M.-J., Franke, L., Frayling, T., Gharib, S., Gibson, G., Hemani, G., Jansen, R., Kähönen, M., Kalnapenkis, A., Kasela, S., Kettunen, J., Kim, Y., Kirsten, H., Kovacs, P., Krohn, K., Kronberg-Guzman, J., Kukushkina, V., Kutalik, Z., Lee, B., Lehtimäki, T., Loeffler, M., Marigorta, U.M., Metspalu, A., Milani, L., Müller-Nurasyid, M., Nauck, M., Nivard, M., Penninx, B., Perola, M., Pervjakova, N., Pierce, B., Powell, J., Prokisch, H., Psaty, B., Raitakari, O., Ring, S., Ripatti, S., Rotzschke, O., Ruëger, S., Saha, A., Scholz, M., Schramm, K., Seppälä, I., Stumvoll, M., Sullivan, P., Teumer, A., Thiery, J., Tong, L., Tönjes, A., van Dongen, J., van Meurs, J., Verlouw, J., Völker, U., Võsa, U., Yaghootkar, H., Zeng, B., McRae, A.F., Visscher, P.M., Zeng, J., Yang, J.
Publikováno v:
eQTLGen Consortium 2018, ' Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes ', Nature Communications, vol. 9, 2941 . https://doi.org/10.1038/s41467-018-04951-w
Nature Communications, 9(1):2941. Nature Publishing Group
Nature Communications
Nature Communications, 9(1):2941. Nature Publishing Group UK
Nat. Commun. 9:2941 (2018)
Nature Communications, Vol 9, Iss 1, Pp 1-14 (2018)
Boomsma, D, Nivard, M G & eQTLGen Consortium 2018, ' Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes ', Nature Communications, vol. 9, no. 1, 2941 . https://doi.org/10.1038/s41467-018-04951-w
eQTLGen Consortium 2018, ' Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes ', Nature Communications, vol. 9, no. 1, 2941 . https://doi.org/10.1038/s41467-018-04951-w
Nature Communications, 9(1):2941. Nature Publishing Group
Nature Communications
Nature Communications, 9(1):2941. Nature Publishing Group UK
Nat. Commun. 9:2941 (2018)
Nature Communications, Vol 9, Iss 1, Pp 1-14 (2018)
Boomsma, D, Nivard, M G & eQTLGen Consortium 2018, ' Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes ', Nature Communications, vol. 9, no. 1, 2941 . https://doi.org/10.1038/s41467-018-04951-w
eQTLGen Consortium 2018, ' Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes ', Nature Communications, vol. 9, no. 1, 2941 . https://doi.org/10.1038/s41467-018-04951-w
Type 2 diabetes (T2D) is a very common disease in humans. Here we conduct a meta-analysis of genome-wide association studies (GWAS) with ~16 million genetic variants in 62,892 T2D cases and 596,424 controls of European ancestry. We identify 139 commo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a40dc452315759bc81da37f76fd9422
https://hdl.handle.net/1983/fa34bfa6-7a44-421c-8f1a-fc5ee0e27bd9
https://hdl.handle.net/1983/fa34bfa6-7a44-421c-8f1a-fc5ee0e27bd9
Autor:
Võsa U; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands. urmo.vosa@gmail.com.; Estonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia. urmo.vosa@gmail.com., Claringbould A; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands. anniqueclaringbould@gmail.com.; Oncode Institute, Amsterdam, the Netherlands. anniqueclaringbould@gmail.com.; Structural & Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany. anniqueclaringbould@gmail.com., Westra HJ; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.; Oncode Institute, Amsterdam, the Netherlands., Bonder MJ; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.; Genome Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany., Deelen P; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.; Oncode Institute, Amsterdam, the Netherlands.; Genomics Coordination Center, University Medical Centre Groningen, Groningen, the Netherlands.; Department of Genetics, University Medical Centre Utrecht, Utrecht, the Netherlands., Zeng B; School of Biological Sciences, Georgia Tech, Atlanta, GA, USA., Kirsten H; Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.; LIFE Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany., Saha A; Department of Computer Science, Johns Hopkins University, Baltimore, MD, USA., Kreuzhuber R; Department of Haematology, University of Cambridge, Cambridge, United Kingdom.; NHS Blood and Transplant, Cambridge Biomedical Campus, Cambridge, United Kingdom.; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, United Kingdom., Yazar S; 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Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.; LIFE Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany., Marigorta UM; School of Biological Sciences, Georgia Tech, Atlanta, GA, USA.; Integrative Genomics Lab, CIC bioGUNE, Basque Research and Technology Alliance (BRTA), Bizkaia Science and Technology Park, Derio, Spain.; IKERBASQUE, Basque Foundation for Science, Bilbao, Spain., Mei H; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, the Netherlands., Momozawa Y; Unit of Animal Genomics, WELBIO, GIGA-R & Faculty of Veterinary Medicine, University of Liège, Liège, Belgium.; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan., Müller-Nurasyid M; Institute of Genetic Epidemiology, Helmholtz Zentrum München-German Research Center for Environmental Health, Neuherberg, Germany.; Department of Medicine I, University Hospital Munich, Ludwig Maximilian's University, Munich, Germany.; 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Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia., Ripatti S; Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.; Public Health, Faculty of Medicine, University of Helsinki, Helsinki, Finland.; Broad Institute of MIT and Harvard, Cambridge, MA, USA., Perola M; National Institute for Health and Welfare, University of Helsinki, Helsinki, Finland., Kutalik Z; Center for Primary Care and Public Health, University of Lausanne, Lausanne, Switzerland., Dermitzakis E; Swiss Institute of Bioinformatics, Lausanne, Switzerland.; Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland.; Institute of Genetics and Genomics in Geneva (iGE3), University of Geneva, Geneva, Switzerland., Bergmann S; Department of Computational Biology, University of Lausanne, Lausanne, Switzerland.; Swiss Institute of Bioinformatics, Lausanne, Switzerland., Frayling T; Genetics of Complex Traits, University of Exeter Medical School, Royal Devon & Exeter Hospital, Exeter, United Kingdom., van Meurs J; 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Division of Computational Genomics and Systems Genetics, German Cancer Research Center, Heidelberg, Germany., Battle A; Department of Computer Science, Johns Hopkins University, Baltimore, MD, USA.; Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, USA., Visscher PM; Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia., Yang J; Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia.; School of Life Sciences, Westlake University, Hangzhou, China.; Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, China., Scholz M; Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.; LIFE Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany., Powell J; Garvan Institute of Medical Research, Garvan-Weizmann Centre for Cellular Genomics, Sydney, New South Wales, Australia.; UNSW Cellular Genomics Futures Institute, University of New South Wales, Sydney, New South Wales, Australia., Gibson G; School of Biological Sciences, Georgia Tech, Atlanta, GA, USA., Esko T; Estonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia., Franke L; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands. lude@ludesign.nl.; Oncode Institute, Amsterdam, the Netherlands. lude@ludesign.nl.
Publikováno v:
Nature genetics [Nat Genet] 2021 Sep; Vol. 53 (9), pp. 1300-1310. Date of Electronic Publication: 2021 Sep 02.
Autor:
Sanders MGH; Department of Dermatology, Erasmus Medical Centre, Rotterdam, The Netherlands., Nijsten T; Department of Dermatology, Erasmus Medical Centre, Rotterdam, The Netherlands., Verlouw J; Department of Internal Medicine, Erasmus Medical Centre, Rotterdam, The Netherlands., Kraaij R; Department of Internal Medicine, Erasmus Medical Centre, Rotterdam, The Netherlands., Pardo LM; Department of Dermatology, Erasmus Medical Centre, Rotterdam, The Netherlands.
Publikováno v:
PloS one [PLoS One] 2021 May 24; Vol. 16 (5), pp. e0251136. Date of Electronic Publication: 2021 May 24 (Print Publication: 2021).