Zobrazeno 1 - 10
of 113
pro vyhledávání: '"Richardson TG"'
Autor:
Richardson TG, Crouch DJM, Power GM, Morales-Berstein F, Hazelwood E, Fang S, Cho Y, Inshaw JRJ, Robertson CC, Sidore C, Cucca F, Rich SS, Todd JA, G Davey Smith
Publikováno v:
Yearbook of Paediatric Endocrinology.
Autor:
Sobczyk, MK, Richardson, TG, Zuber, V, Min, JL, Gaunt, TR, Paternoster, L, EQTLGen Consortium, BIOS Consortium, GoDMC
Publikováno v:
The Journal of Investigative Dermatology
Sobczyk-Barad, M K, Richardson, T G, Zuber, V, Min, J L, Gaunt, T R & Paternoster, L 2021, ' Triangulating molecular evidence to prioritize candidate causal genes at established atopic dermatitis loci ', Journal of Investigative Dermatology, vol. 141, no. 11, S0022-202X(21)01160-XDOI, pp. 2620-2629 . https://doi.org/10.1016/j.jid.2021.03.027
J Invest Dermatol
Sobczyk-Barad, M K, Richardson, T G, Zuber, V, Min, J L, Gaunt, T R & Paternoster, L 2021, ' Triangulating molecular evidence to prioritize candidate causal genes at established atopic dermatitis loci ', Journal of Investigative Dermatology, vol. 141, no. 11, S0022-202X(21)01160-XDOI, pp. 2620-2629 . https://doi.org/10.1016/j.jid.2021.03.027
J Invest Dermatol
BackgroundGenome-wide association studies for atopic dermatitis (AD, eczema) have identified 25 reproducible loci associated in populations of European descent. We attempt to prioritise candidate causal genes at these loci using a multifaceted bioinf
It is unclear if body weight in early life affects cancer risk independently of adult body weight. To investigate this question for 6 obesity-related cancers, we performed univariable and multivariable analyses using 1) Mendelian randomization (MR) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1064::2b36c5705a2a4962611b7838663131c7
https://ora.ox.ac.uk/objects/uuid:935aff75-2841-47a8-8b93-61daac01172c
https://ora.ox.ac.uk/objects/uuid:935aff75-2841-47a8-8b93-61daac01172c
Autor:
Morales Berstein, F, McCartney, DL, Lu, AT, Tsilidis, KK, Bouras, E, Haycock, P, Burrows, K, Phipps, AI, Buchanan, DD, Cheng, I, PRACTICAL consortium, Martin, RM, Davey Smith, G, Relton, CL, Horvath, S, Marioni, RE, Richardson, TG, Richmond, RC
Publikováno v:
Morales-Berstein, F, McCartney, D L, Lu, A T, Tsilidis, K K, Bouras, E, Haycock, P, Burrows, K, Phipps, A I, Buchanan, D D, Cheng, I, Martin, R M, Smith, G D, Relton, C L, Horvath, S, Marioni, R E, Richardson, T G & Richmond, R C 2022, ' Assessing the causal role of epigenetic clocks in the development of multiple cancers : a Mendelian randomization study ', eLife, vol. 11, e75374 . https://doi.org/10.7554/eLife.75374
Morales Berstein, F, McCartney, D L, Lu, A T, Tsilidis, K K, Bouras, E, Haycock, P, Burrows, K, Phipps, A I, Buchanan, D D, Cheng, I, Martin, R M, Davey Smith, G, Relton, C L, Horvath, S, Marioni, R E, Richardson, T G, Richmond, R C & The PRACTICAL Consortium 2022, ' Assessing the causal role of epigenetic clocks in the development of multiple cancers : a Mendelian randomization study ', eLife, vol. 11, e75374 . https://doi.org/10.7554/eLife.75374
eLife, 11:e75374. eLife Sciences Publications
Morales Berstein, F, McCartney, D L, Lu, A T, Tsilidis, K K, Bouras, E, Haycock, P, Burrows, K, Phipps, A I, Buchanan, D D, Cheng, I, Martin, R M, Davey Smith, G, Relton, C L, Horvath, S, Marioni, R E, Richardson, T G, Richmond, R C & The PRACTICAL Consortium 2022, ' Assessing the causal role of epigenetic clocks in the development of multiple cancers : a Mendelian randomization study ', eLife, vol. 11, e75374 . https://doi.org/10.7554/eLife.75374
eLife, 11:e75374. eLife Sciences Publications
Epigenetic clocks have been associated with cancer risk in several observational studies. Nevertheless, it is unclear whether they play a causal role in cancer risk or if they act as a non-causal biomarker.We conducted a two-sample Mendelian randomiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91d86c1c9a1c625fe7e789318a1c9c7d
https://hdl.handle.net/1983/6c17e445-590a-437a-8106-46a848a0dbf2
https://hdl.handle.net/1983/6c17e445-590a-437a-8106-46a848a0dbf2
Autor:
Surendran, P, Feofanova, EV, Lahrouchi, N, Ntalla, I, Karthikeyan, S, Cook, J, Chen, L, Mifsud, B, Yao, C, Kraja, AT, Cartwright, JH, Hellwege, JN, Giri, A, Tragante, V, Thorleifsson, G, Liu, DJ, Prins, BP, Stewart, ID, Cabrera, CP, Eales, JM, Akbarov, A, Auer, PL, Bielak, LF, Bis, JC, Braithwaite, VS, Brody, JA, Daw, EW, Warren, HR, Drenos, F, Nielsen, SF, Faul, JD, Fauman, EB, Fava, C, Ferreira, T, Foley, CN, Franceschini, N, Gao, H, Giannakopoulou, O, Giulianini, F, Gudbjartsson, DF, Guo, X, Harris, SE, Havulinna, AS, Helgadottir, A, Huffman, JE, Hwang, S-J, Kanoni, S, Kontto, J, Larson, MG, Li-Gao, R, Lindstrom, J, Lotta, LA, Lu, Y, Luan, J, Mahajan, A, Malerba, G, Masca, NGD, Mei, H, Menni, C, Mook-Kanamori, DO, Mosen-Ansorena, D, Muller-Nurasyid, M, Pare, G, Paul, DS, Perola, M, Poveda, A, Rauramaa, R, Richard, M, Richardson, TG, Sepulveda, N, Sim, X, Smith, AV, Smith, JA, Staley, JR, Stanakova, A, Sulem, P, Theriault, S, Thorsteinsdottir, U, Trompet, S, Varga, TV, Velez Edwards, DR, Veronesi, G, Weiss, S, Willems, SM, Yao, J, Young, R, Yu, B, Zhang, W, Zhao, J-H, Zhao, W, Evangelou, E, Aeschbacher, S, Asllanaj, E, Blankenberg, S, Bonnycastle, LL, Bork-Jensen, J, Brandslund, I, Braund, PS, Burgess, S, Cho, K, Christensen, C, Connell, J, De Mutsert, R, Dominiczak, AF, Dorr, M, Eiriksdottir, G, Farmaki, A-E, Gaziano, JM, Grarup, N, Grove, ML, Hallmans, G, Hansen, T, Have, CT, Heiss, G, Jorgensen, ME, Jousilahti, P, Kajantie, E, Kamat, M, Karajamaki, A, Karpe, F, Koistinen, HA, Kovesdy, CP, Kuulasmaa, K, Laatikainen, I, Lannfelt, L, Lee, I-T, Lee, W-J, Linneberg, A, Martin, LW, Moitry, M, Nadkarni, G, Neville, MJ, Palmer, CNA, Papanicolaou, GJ, Pedersen, O, Peters, J, Poulter, N, Rasheed, A, Rasmussen, KL, Rayner, NW, Magi, R, Renstrom, F, Rettig, R, Rossouw, J, Schreiner, PJ, Sever, PS, Sigurdsson, EL, Skaaby, T, Sun, YV, Sundstrom, J, Thorgeirsson, G, Esko, T, Trabetti, E, Tsao, PS, Tuomi, T, Turner, ST, Tzoulaki, I, Vaartjes, I, Vergnaud, A-C, Willer, CJ, Wilson, PWF, Witte, DR, Yonova-Doing, E, Zhang, H, Aliya, N, Almgren, P, Amouyel, P, Asselbergs, FW, Barnes, MR, Blakemore, AI, Boehnke, M, Bots, ML, Bottinger, EP, Buring, JE, Chambers, JC, Chen, Y-DI, Chowdhury, R, Conen, D, Correa, A, Davey Smith, G, Boer, RAD, Deary, IJ, Dedoussis, G, Deloukas, P, Di Angelantonio, E, Elliott, P, Felix, SB, Ferrieres, J, Ford, I, Fornage, M, Franks, PW, Franks, S, Frossard, P, Gambaro, G, Gaunt, TR, Groop, L, Gudnason, V, Harris, TB, Hayward, C, Hennig, BJ, Herzig, K-H, Ingelsson, E, Tuomilehto, J, Jarvelin, M-R, Jukema, JW, Kardia, SLR, Kee, F, Kooner, JS, Kooperberg, C, Launer, LJ, Lind, L, Loos, RJF, Majumder, AAS, Laakso, M, McCarthy, MI, Melander, O, Mohlke, KL, Murray, AD, Nordestgaard, BG, Orho-Melander, M, Packard, CJ, Padmanabhan, S, Palmas, W, Polasek, O, Porteous, DJ, Prentice, AM, Province, MA, Relton, CL, Rice, K, Ridker, PM, Rolandsson, O, Rosendaal, FR, Rotter, JI, Rudan, I, Salomaa, V, Samani, NJ, Sattar, N, Sheu, WH-H, Smith, BH, Soranzo, N, Spector, TD, Starr, JM, Sebert, S, Taylor, KD, Lakka, TA, Timpson, NJ, Tobin, MD, Van der Harst, P, Van der Meer, P, Ramachandran, VS, Verweij, N, Virtamo, J, Volker, U, Weir, DR, Zeggini, E, Charchar, FJ, Wareham, NJ, Langenberg, C, Tomaszewski, M, Butterworth, AS, Caulfield, MJ, Danesh, J, Edwards, TL, Holm, H, Hung, AM, Lindgren, CM, Liu, C, Manning, AK, Morris, AP, Morrison, AC, O'Donnell, CJ, Psaty, BM, Saleheen, D, Stefansson, K, Boerwinkle, E, Chasman, DI, Levy, D, Newton-Cheh, C, Munroe, PB, Howson, JMM
Publikováno v:
Lifelines Cohort Study, EPIC-CVD, EPIC-InterAct, Understanding Society Scientific Group & Million Veteran Program 2021, ' Publisher Correction : Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals ', Nature Genetics, vol. 53, no. 5, 762 . https://doi.org/10.1038/s41588-021-00832-z
In the version of this article originally published, the e-mail address of corresponding author Patricia B. Munroe was incorrect. The error has been corrected in the HTML and PDF versions of the article.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca24b467be4299d8e41d6ecf1e8f4f28
https://portal.findresearcher.sdu.dk/da/publications/45d317bb-a79e-419e-a69b-f5b60c70fd68
https://portal.findresearcher.sdu.dk/da/publications/45d317bb-a79e-419e-a69b-f5b60c70fd68
Autor:
Kazmi, N, Sharp, GC, Reese, SE, Vehmeijer, FO, Lahti, J, Page, CM, Zhang, WM, Rifas-Shiman, SL, Rezwan, FI, Simpkin, AJ, Burrows, K, Richardson, TG, Ferreira, D L S, Fraser, A, Harmon, QE, Zhao, SS, Jaddoe, Vincent, Czamara, D, Binder, EB, Magnus, MC, Haberg, SE, Nystad, W, Nohr, EA, Starling, AP, Kechris, KJ, Yang, IV, DeMeo, DL, Litonjua, AA, Baccarelli, A, Oken, E, Holloway, JW, Karmaus, W, Arshad, SH, Dabelea, D, Sorensen, TIA, Laivuori, H, Raikkonen, K, Felix, Janine, London, SJ, Hivert, MF, Gaunt, TR, Lawlor, DA, Relton, CL
Publikováno v:
Kazmi, N, Sharp, G C, Reese, S E, Vehmeijer, F O, Lahti, J, Page, C M, Zhang, W, Rifas-Shiman, S L, Rezwan, F I, Simpkin, A J, Burrows, K, Richardson, T G, Santos Ferreira, D L, Fraser, A, Harmon, Q E, Zhao, S, Jaddoe, V W V, Czamara, D, Binder, E B, Magnus, M C, Håberg, S E, Nystad, W, Nohr, E A, Starling, A P, Kechris, K J, Yang, I V, DeMeo, D L, Litonjua, A A, Baccarelli, A, Oken, E, Holloway, J W, Karmaus, W, Arshad, S H, Dabelea, D, Sørensen, T I A, Laivuori, H, Raikkonen, K, Felix, J F, London, S J, Hivert, M F, Gaunt, T R, Lawlor, D A & Relton, C L 2019, ' Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns : Findings From the Pregnancy and Childhood Epigenetics Consortium ', Hypertension, vol. 74, no. 2, pp. 375-383 . https://doi.org/10.1161/HYPERTENSIONAHA.119.12634
Kazmi, N, Sharp, G C, Reese, S E, Vehmeijer, F O, Lahti, J, Page, C M, Zhang, W, Rifas-Shiman, S L, Rezwan, F I, Simpkin, A J, Burrows, K, Richardson, T G, Santos Ferreira, D L, Fraser, A, Harmon, Q E, Zhao, S, Jaddoe, V W V, Czamara, D, Binder, E B, Magnus, M C, Håberg, S E, Nystad, W, Nohr, E A, Starling, A P, Kechris, K J, Yang, I V, DeMeo, D L, Litonjua, A A, Baccarelli, A, Oken, E, Holloway, J W, Karmaus, W, Arshad, S H, Dabelea, D, Sørensen, T I A, Laivuori, H, Raikkonen, K, Felix, J F, London, S J, Hivert, M-F, Gaunt, T R, Lawlor, D A & Relton, C L 2019, ' Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns : Findings from the Pregnancy and Childhood Epigenetics Consortium ', Hypertension, vol. 74, no. 2, pp. 375-383 . https://doi.org/10.1161/HYPERTENSIONAHA.119.12634
Kazmi, N, Sharp, G C, Reese, S E, Vehmeijer, F O, Lahti, J, Page, C M, Zhang, W, Rifas-Shiman, S L, Rezwan, F I, Simpkin, A J, Burrows, K, Richardson, T G, Ferreira, D L S, Fraser, A, Harmon, Q E, Zhao, S, Jaddoe, V W V, Czamara, D, Binder, E B, Magnus, M C, Haberg, S E, Nystad, W, Nohr, E A, Starling, A P, Kechris, K J, Yang, I V, DeMeo, D L, Litonjua, A A, Baccarelli, A, Oken, E, Holloway, J W, Karmaus, W, Arshad, S H, Dabelea, D, Sorensen, T I A, Laivuori, H, Raikkonen, K, Felix, J F, London, S J, Hivert, M-F, Gaunt, T R, Lawlor, D A & Relton, C L 2019, ' Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns Findings From the Pregnancy and Childhood Epigenetics Consortium ', Hypertension, vol. 74, no. 2, pp. 375-383 . https://doi.org/10.1161/HYPERTENSIONAHA.119.12634
Hypertension, 74(2), 375-383. Lippincott Williams & Wilkins
Kazmi, N, Sharp, G C, Reese, S E, Vehmeijer, F O, Lahti, J, Page, C M, Zhang, W, Rifas-Shiman, S L, Rezwan, F I, Simpkin, A J, Burrows, K, Richardson, T G, Santos Ferreira, D L, Fraser, A, Harmon, Q E, Zhao, S, Jaddoe, V W V, Czamara, D, Binder, E B, Magnus, M C, Håberg, S E, Nystad, W, Nohr, E A, Starling, A P, Kechris, K J, Yang, I V, DeMeo, D L, Litonjua, A A, Baccarelli, A, Oken, E, Holloway, J W, Karmaus, W, Arshad, S H, Dabelea, D, Sørensen, T I A, Laivuori, H, Raikkonen, K, Felix, J F, London, S J, Hivert, M-F, Gaunt, T R, Lawlor, D A & Relton, C L 2019, ' Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns : Findings from the Pregnancy and Childhood Epigenetics Consortium ', Hypertension, vol. 74, no. 2, pp. 375-383 . https://doi.org/10.1161/HYPERTENSIONAHA.119.12634
Kazmi, N, Sharp, G C, Reese, S E, Vehmeijer, F O, Lahti, J, Page, C M, Zhang, W, Rifas-Shiman, S L, Rezwan, F I, Simpkin, A J, Burrows, K, Richardson, T G, Ferreira, D L S, Fraser, A, Harmon, Q E, Zhao, S, Jaddoe, V W V, Czamara, D, Binder, E B, Magnus, M C, Haberg, S E, Nystad, W, Nohr, E A, Starling, A P, Kechris, K J, Yang, I V, DeMeo, D L, Litonjua, A A, Baccarelli, A, Oken, E, Holloway, J W, Karmaus, W, Arshad, S H, Dabelea, D, Sorensen, T I A, Laivuori, H, Raikkonen, K, Felix, J F, London, S J, Hivert, M-F, Gaunt, T R, Lawlor, D A & Relton, C L 2019, ' Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns Findings From the Pregnancy and Childhood Epigenetics Consortium ', Hypertension, vol. 74, no. 2, pp. 375-383 . https://doi.org/10.1161/HYPERTENSIONAHA.119.12634
Hypertension, 74(2), 375-383. Lippincott Williams & Wilkins
Hypertensive disorders of pregnancy (HDP) are associated with low birth weight, shorter gestational age, and increased risk of maternal and offspring cardiovascular diseases later in life. The mechanisms involved are poorly understood, but epigenetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d0f69e0963999a0ada775a2eb5de460f
http://www.scopus.com/inward/record.url?scp=85069621483&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85069621483&partnerID=8YFLogxK
Autor:
Power GM; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK. grace.power@bristol.ac.uk.; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK. grace.power@bristol.ac.uk.; Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia. grace.power@bristol.ac.uk., Warne N; Centre for Academic Mental Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK., Bould H; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.; Centre for Academic Mental Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.; Gloucestershire Health and Care NHS Foundation Trust, Gloucester, UK., Casanova F; Genetics of Complex Traits, College of Medicine and Health, University of Exeter, Exeter, UK., Jones SE; Institute for Molecular Medicine, University of Helsinki, Helsinki, Finland., Richardson TG; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK., Tyrrell J; Genetics of Complex Traits, College of Medicine and Health, University of Exeter, Exeter, UK., Davey Smith G; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.; NIHR Bristol Biomedical Research Centre Bristol, University Hospitals Bristol and Weston NHS Foundation Trust, University of Bristol, Bristol, UK., Heron J; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.; Centre for Academic Mental Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Publikováno v:
Molecular psychiatry [Mol Psychiatry] 2024 Aug 13. Date of Electronic Publication: 2024 Aug 13.
Autor:
Reed ZE; School of Psychological Science, University of Bristol, Bristol, UK.; MRC Integrative Epidemiology Unit, Bristol Medical School, University of Bristol, Bristol, UK., Wootton RE; School of Psychological Science, University of Bristol, Bristol, UK.; MRC Integrative Epidemiology Unit, Bristol Medical School, University of Bristol, Bristol, UK.; Nic Waals Institute, Lovisenberg Diaconal Hospital, Oslo, Norway., Khouja JN; School of Psychological Science, University of Bristol, Bristol, UK.; MRC Integrative Epidemiology Unit, Bristol Medical School, University of Bristol, Bristol, UK., Richardson TG; MRC Integrative Epidemiology Unit, Bristol Medical School, University of Bristol, Bristol, UK., Sanderson E; MRC Integrative Epidemiology Unit, Bristol Medical School, University of Bristol, Bristol, UK., Davey Smith G; MRC Integrative Epidemiology Unit, Bristol Medical School, University of Bristol, Bristol, UK., Munafò MR; School of Psychological Science, University of Bristol, Bristol, UK.; MRC Integrative Epidemiology Unit, Bristol Medical School, University of Bristol, Bristol, UK.; National Institute for Health Research Bristol Biomedical Research Centre, University Hospitals Bristol NHS Foundation Trust, University of Bristol, Bristol, UK.
Publikováno v:
Genetic epidemiology [Genet Epidemiol] 2024 Aug 04. Date of Electronic Publication: 2024 Aug 04.
Autor:
Chiesa ST; Medical Research Council Unit for Lifelong Health and Ageing at UCL, Institute of Cardiovascular Science, UCL, London WC1E 7HB, UK., Rader L; Institute for Behavioral Genetics, University of Colorado Boulder, Boulder, CO 80309, USA., Garfield V; Medical Research Council Unit for Lifelong Health and Ageing at UCL, Institute of Cardiovascular Science, UCL, London WC1E 7HB, UK., Foote I; Institute for Behavioral Genetics, University of Colorado Boulder, Boulder, CO 80309, USA., Suri S; Department of Psychiatry, University of Oxford, Oxford OX3 7JX, UK.; Oxford Centre for Human Brain Activity, Wellcome Centre for Integrative Neuroimaging, University of Oxford, Oxford OX3 9DU, UK., Davey Smith G; MRC Integrative Epidemiology Unit, University of Bristol, Oakfield House, Bristol, UK.; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK., Hughes AD; Medical Research Council Unit for Lifelong Health and Ageing at UCL, Institute of Cardiovascular Science, UCL, London WC1E 7HB, UK., Richardson TG; MRC Integrative Epidemiology Unit, University of Bristol, Oakfield House, Bristol, UK.
Publikováno v:
Brain : a journal of neurology [Brain] 2024 Jun 18. Date of Electronic Publication: 2024 Jun 18.
Autor:
Vabistsevits M; University of Bristol, MRC Integrative Epidemiology Unit, Bristol, UK. marina.vabistsevits@bristol.ac.uk.; University of Bristol, Population Health Sciences, Bristol, UK. marina.vabistsevits@bristol.ac.uk., Davey Smith G; University of Bristol, MRC Integrative Epidemiology Unit, Bristol, UK.; University of Bristol, Population Health Sciences, Bristol, UK., Richardson TG; University of Bristol, MRC Integrative Epidemiology Unit, Bristol, UK.; University of Bristol, Population Health Sciences, Bristol, UK., Richmond RC; University of Bristol, MRC Integrative Epidemiology Unit, Bristol, UK.; University of Bristol, Population Health Sciences, Bristol, UK., Sieh W; Icahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, Department of Population Health Science and Policy, New York, NY, USA.; University of Texas MD Anderson Cancer Center, Department of Epidemiology, Houston, TX, USA., Rothstein JH; Icahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, Department of Population Health Science and Policy, New York, NY, USA.; University of Texas MD Anderson Cancer Center, Department of Epidemiology, Houston, TX, USA., Habel LA; Kaiser Permanente Northern California, Division of Research, Oakland, CA, USA., Alexeeff SE; Kaiser Permanente Northern California, Division of Research, Oakland, CA, USA., Lloyd-Lewis B; University of Bristol, School of Cellular and Molecular Medicine, Bristol, UK., Sanderson E; University of Bristol, MRC Integrative Epidemiology Unit, Bristol, UK.; University of Bristol, Population Health Sciences, Bristol, UK.
Publikováno v:
Nature communications [Nat Commun] 2024 May 13; Vol. 15 (1), pp. 4021. Date of Electronic Publication: 2024 May 13.