Zobrazeno 1 - 10
of 325
pro vyhledávání: '"Kukushkina, V."'
Autor:
Bui BN; Department of Gynecology and Reproductive Medicine, University Medical Center Utrecht, Utrecht, The Netherlands., Kukushkina V; Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia., Meltsov A; Competence Center on Health Technologies, Tartu, Estonia.; Department of Obstetrics and Gynecology, GROW, School for Oncology and Reproduction, Maastricht University Medical Center, Maastricht, The Netherlands., Olsen C; Center for Medical Genetics, Research Group Reproduction and Genetics, Vrije Universiteit Brussel, Brussels, Belgium.; Brussels Interuniversity Genomics High Throughput Core (BRIGHTcore), VUB-ULB, Brussels, Belgium.; Interuniversity Institute of Bioinformatics in Brussels (IB), Brussels, Belgium., van Hoogenhuijze N; Department of Gynecology and Reproductive Medicine, University Medical Center Utrecht, Utrecht, The Netherlands., Altmäe S; Department of Biochemistry and Molecular Biology, Faculty of Sciences, University of Granada, Granada, Spain.; Instituto de Investigación Biosanitaria, ibs.GRANADA, Granada, Spain.; Division of Obstetrics and Gynecology, Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institute and Karolinska University Hospital, Stockholm, Sweden., Mol F; Center for Reproductive Medicine, Reproduction and Development, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands., Teklenburg G; Isala Fertility Clinic, Isala Hospital, Zwolle, The Netherlands., de Bruin JP; Department of Obstetrics and Gynecology, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands., Besselink D; Department of Obstetrics and Gynecology, Radboud University Medical Center, Nijmegen, The Netherlands., Stevens Brentjens L; Department of Obstetrics and Gynecology, GROW, School for Oncology and Reproduction, Maastricht University Medical Center, Maastricht, The Netherlands., Obukhova D; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Department of Genetics and Cell Biology, GROW School for Oncology and Reproduction, Maastricht University, Maastricht, The Netherlands., Zamani Esteki M; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Department of Genetics and Cell Biology, GROW School for Oncology and Reproduction, Maastricht University, Maastricht, The Netherlands., van Golde R; Department of Obstetrics and Gynecology, GROW, School for Oncology and Reproduction, Maastricht University Medical Center, Maastricht, The Netherlands., Romano A; Department of Obstetrics and Gynecology, GROW, School for Oncology and Reproduction, Maastricht University Medical Center, Maastricht, The Netherlands., Laisk T; Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia., Steba G; Department of Gynecology and Reproductive Medicine, University Medical Center Utrecht, Utrecht, The Netherlands., Mackens S; Brussels IVF, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel, Brussels, Belgium., Salumets A; Competence Center on Health Technologies, Tartu, Estonia.; Division of Obstetrics and Gynecology, Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institute and Karolinska University Hospital, Stockholm, Sweden.; Department of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia., Broekmans F; Department of Gynecology and Reproductive Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.; Center for Infertility Care, Dijklander Hospital, Purmerend, The Netherlands.
Publikováno v:
Acta obstetricia et gynecologica Scandinavica [Acta Obstet Gynecol Scand] 2024 Jul; Vol. 103 (7), pp. 1348-1365. Date of Electronic Publication: 2024 Mar 22.
Autor:
Stevens Brentjens LBPM; Department of Obstetrics and Gynecology, Maastricht University Medical Center+, Maastricht, the Netherlands; GROW School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands. Electronic address: linda.brentjens@mumc.nl., Obukhova D; GROW School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands; Department of Clinical Genetics, Maastricht University, Maastricht, the Netherlands., den Hartog JE; Department of Obstetrics and Gynecology, Maastricht University Medical Center+, Maastricht, the Netherlands; GROW School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands., Delvoux B; Department of Obstetrics and Gynecology, Maastricht University Medical Center+, Maastricht, the Netherlands; GROW School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands., Koskivuori J; University of Eastern Finland, School of Pharmacy, Kuopio, Finland., Auriola S; University of Eastern Finland, School of Pharmacy, Kuopio, Finland., Häkkinen MR; Department of Health Security, Finnish Institute for Health and Welfare (THL), Kuopio, Finland., Bui BN; Department of Gynecology and Reproductive Medicine, University Medical Centre Utrecht, Utrecht, the Netherlands., van Hoogenhuijze NE; Department of Gynecology and Reproductive Medicine, University Medical Centre Utrecht, Utrecht, the Netherlands., Mackens S; Center for Reproductive Medicine, UZ Brussel, Jette, Belgium., Mol F; Center for Reproductive Medicine, Reproduction and Development, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, the Netherlands., de Bruin JP; Department of Obstetrics and Gynecology, Jeroen Bosch Hospital-Hertogenbosch, the Netherlands., Besselink D; Department of Obstetrics and Gynecology, Radboud University Medical Centre, Nijmegen, the Netherlands., Teklenburg G; Isala Fertility Clinic, Isala Hospital, Zwolle, the Netherlands., Kukushkina V; Competence Centre on Health Technologies, Tartu, Estonia., Salumets A; Competence Centre on Health Technologies, Tartu, Estonia; Department of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia; Division of Obstetrics and Gynecology, Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden., Broekmans FJM; Department of Gynecology and Reproductive Medicine, University Medical Centre Utrecht, Utrecht, the Netherlands., van Golde RJT; Department of Obstetrics and Gynecology, Maastricht University Medical Center+, Maastricht, the Netherlands; GROW School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands., Esteki MZ; GROW School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands; Department of Clinical Genetics, Maastricht University, Maastricht, the Netherlands., Romano A; Department of Obstetrics and Gynecology, Maastricht University Medical Center+, Maastricht, the Netherlands; GROW School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands.
Publikováno v:
F&S science [F S Sci] 2023 Aug; Vol. 4 (3), pp. 219-228. Date of Electronic Publication: 2023 May 02.
Autor:
Pathare ADS; Department of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia., Saare M; Department of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.; Competence Centre on Health Technologies, Tartu, Estonia., Meltsov A; Competence Centre on Health Technologies, Tartu, Estonia.; Department of Genetics and Cell Biology, GROW School for Oncology and Developmental Biology, Maastricht University, Maastricht, Netherlands., Lawarde A; Competence Centre on Health Technologies, Tartu, Estonia.; Institute of Clinical Medicine, University of Tartu, Tartu, Estonia., Modhukur V; Department of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.; Competence Centre on Health Technologies, Tartu, Estonia., Kalinina A; South Estonia Hospital, Võru, Estonia., Sekavin A; Women's Clinic, Tartu University Hospital, Tartu, Estonia., Kukushkina V; Institute of Genomics, University of Tartu, Tartu, Estonia., Karro H; Department of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.; Women's Clinic, Tartu University Hospital, Tartu, Estonia., Salumets A; Department of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.; Competence Centre on Health Technologies, Tartu, Estonia.; Institute of Genomics, University of Tartu, Tartu, Estonia.; Division of Obstetrics and Gynecology, Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institutet, and Karolinska University Hospital, Stockholm, Sweden., Peters M; Department of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.; Competence Centre on Health Technologies, Tartu, Estonia.
Publikováno v:
Frontiers in reproductive health [Front Reprod Health] 2023 Jul 14; Vol. 5, pp. 1224919. Date of Electronic Publication: 2023 Jul 14 (Print Publication: 2023).
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:
Orlov, Igor Ivanovich, Abdullah, L. S., Lavrentiev, Alexander Nikolaevich, Gantcheva, Anastasia Nikolaevna, Pavlova, O. S., Kukushkina, V. A.
Publikováno v:
Procedia-Environmental Science, Engineering & Management; 2022, Vol. 9 Issue 1, p117-125, 9p
Akademický článek
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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
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:
Suhorutshenko M, Kukushkina V, Velthut-Meikas A, Altmäe S, Peters M, Mägi R, Krjutškov K, Koel M, Codoñer FM, Martinez-Blanch JF, Vilella F, Simón C, Salumets A, Laisk T
Publikováno v:
HUMAN REPRODUCTION
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::a3d3d9324e3e3e09c681fbf8f9dfd8ec
https://www.fundanet.incliva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=1805
https://www.fundanet.incliva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=1805