Progress in genetics of type 2 diabetes and diabetic complications
Type 2 diabetes results from a complex interaction between genetic and environmental factors. Precision medicine for type 2 diabetes using genetic data is expected to predict the risk of developing diabetes and complications and to predict the effects of medications and life‐style intervention more...
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Published in | Journal of Diabetes Investigation Vol. 14; no. 4; pp. 503 - 515 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Japan
Wiley
01.04.2023
John Wiley & Sons, Inc John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
ISSN | 2040-1116 2040-1124 2040-1124 |
DOI | 10.1111/jdi.13970 |
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Abstract | Type 2 diabetes results from a complex interaction between genetic and environmental factors. Precision medicine for type 2 diabetes using genetic data is expected to predict the risk of developing diabetes and complications and to predict the effects of medications and life‐style intervention more accurately for individuals. Genome‐wide association studies (GWAS) have been conducted in European and Asian populations and new genetic loci have been identified that modulate the risk of developing type 2 diabetes. Novel loci were discovered by GWAS in diabetic complications with increasing sample sizes. Large‐scale genome‐wide association analysis and polygenic risk scores using biobank information is making it possible to predict the development of type 2 diabetes. In the ADVANCE clinical trial of type 2 diabetes, a multi‐polygenic risk score was useful to predict diabetic complications and their response to treatment. Proteomics and metabolomics studies have been conducted and have revealed the associations between type 2 diabetes and inflammatory signals and amino acid synthesis. Using multi‐omics analysis, comprehensive molecular mechanisms have been elucidated to guide the development of targeted therapy for type 2 diabetes and diabetic complications.
Genome‐wide association studies (GWAS) were conducted and new genetic loci were identified that modulate the risk of developing type 2 diabetes and diabetic complications. The polygenic risk score and multi‐omics analysis have begun to decipher the molecular mechanisms of diabetes and its complications. |
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AbstractList | Type 2 diabetes results from a complex interaction between genetic and environmental factors. Precision medicine for type 2 diabetes using genetic data is expected to predict the risk of developing diabetes and complications and to predict the effects of medications and life-style intervention more accurately for individuals. Genome-wide association studies (GWAS) have been conducted in European and Asian populations and new genetic loci have been identified that modulate the risk of developing type 2 diabetes. Novel loci were discovered by GWAS in diabetic complications with increasing sample sizes. Large-scale genome-wide association analysis and polygenic risk scores using biobank information is making it possible to predict the development of type 2 diabetes. In the ADVANCE clinical trial of type 2 diabetes, a multi-polygenic risk score was useful to predict diabetic complications and their response to treatment. Proteomics and metabolomics studies have been conducted and have revealed the associations between type 2 diabetes and inflammatory signals and amino acid synthesis. Using multi-omics analysis, comprehensive molecular mechanisms have been elucidated to guide the development of targeted therapy for type 2 diabetes and diabetic complications. Type 2 diabetes results from a complex interaction between genetic and environmental factors. Precision medicine for type 2 diabetes using genetic data is expected to predict the risk of developing diabetes and complications and to predict the effects of medications and life-style intervention more accurately for individuals. Genome-wide association studies (GWAS) have been conducted in European and Asian populations and new genetic loci have been identified that modulate the risk of developing type 2 diabetes. Novel loci were discovered by GWAS in diabetic complications with increasing sample sizes. Large-scale genome-wide association analysis and polygenic risk scores using biobank information is making it possible to predict the development of type 2 diabetes. In the ADVANCE clinical trial of type 2 diabetes, a multi-polygenic risk score was useful to predict diabetic complications and their response to treatment. Proteomics and metabolomics studies have been conducted and have revealed the associations between type 2 diabetes and inflammatory signals and amino acid synthesis. Using multi-omics analysis, comprehensive molecular mechanisms have been elucidated to guide the development of targeted therapy for type 2 diabetes and diabetic complications.Type 2 diabetes results from a complex interaction between genetic and environmental factors. Precision medicine for type 2 diabetes using genetic data is expected to predict the risk of developing diabetes and complications and to predict the effects of medications and life-style intervention more accurately for individuals. Genome-wide association studies (GWAS) have been conducted in European and Asian populations and new genetic loci have been identified that modulate the risk of developing type 2 diabetes. Novel loci were discovered by GWAS in diabetic complications with increasing sample sizes. Large-scale genome-wide association analysis and polygenic risk scores using biobank information is making it possible to predict the development of type 2 diabetes. In the ADVANCE clinical trial of type 2 diabetes, a multi-polygenic risk score was useful to predict diabetic complications and their response to treatment. Proteomics and metabolomics studies have been conducted and have revealed the associations between type 2 diabetes and inflammatory signals and amino acid synthesis. Using multi-omics analysis, comprehensive molecular mechanisms have been elucidated to guide the development of targeted therapy for type 2 diabetes and diabetic complications. Type 2 diabetes results from a complex interaction between genetic and environmental factors. Precision medicine for type 2 diabetes using genetic data is expected to predict the risk of developing diabetes and complications and to predict the effects of medications and life‐style intervention more accurately for individuals. Genome‐wide association studies (GWAS) have been conducted in European and Asian populations and new genetic loci have been identified that modulate the risk of developing type 2 diabetes. Novel loci were discovered by GWAS in diabetic complications with increasing sample sizes. Large‐scale genome‐wide association analysis and polygenic risk scores using biobank information is making it possible to predict the development of type 2 diabetes. In the ADVANCE clinical trial of type 2 diabetes, a multi‐polygenic risk score was useful to predict diabetic complications and their response to treatment. Proteomics and metabolomics studies have been conducted and have revealed the associations between type 2 diabetes and inflammatory signals and amino acid synthesis. Using multi‐omics analysis, comprehensive molecular mechanisms have been elucidated to guide the development of targeted therapy for type 2 diabetes and diabetic complications. Genome‐wide association studies (GWAS) were conducted and new genetic loci were identified that modulate the risk of developing type 2 diabetes and diabetic complications. The polygenic risk score and multi‐omics analysis have begun to decipher the molecular mechanisms of diabetes and its complications. Abstract Type 2 diabetes results from a complex interaction between genetic and environmental factors. Precision medicine for type 2 diabetes using genetic data is expected to predict the risk of developing diabetes and complications and to predict the effects of medications and life‐style intervention more accurately for individuals. Genome‐wide association studies (GWAS) have been conducted in European and Asian populations and new genetic loci have been identified that modulate the risk of developing type 2 diabetes. Novel loci were discovered by GWAS in diabetic complications with increasing sample sizes. Large‐scale genome‐wide association analysis and polygenic risk scores using biobank information is making it possible to predict the development of type 2 diabetes. In the ADVANCE clinical trial of type 2 diabetes, a multi‐polygenic risk score was useful to predict diabetic complications and their response to treatment. Proteomics and metabolomics studies have been conducted and have revealed the associations between type 2 diabetes and inflammatory signals and amino acid synthesis. Using multi‐omics analysis, comprehensive molecular mechanisms have been elucidated to guide the development of targeted therapy for type 2 diabetes and diabetic complications. |
Author | Nobuhiro Shojima Toshimasa Yamauchi |
AuthorAffiliation | 1 Department of Diabetes and Metabolic Diseases, Graduate School of Medicine The University of Tokyo Tokyo Japan |
AuthorAffiliation_xml | – name: 1 Department of Diabetes and Metabolic Diseases, Graduate School of Medicine The University of Tokyo Tokyo Japan |
Author_xml | – sequence: 1 givenname: Nobuhiro orcidid: 0000-0002-4078-3308 surname: Shojima fullname: Shojima, Nobuhiro organization: The University of Tokyo – sequence: 2 givenname: Toshimasa surname: Yamauchi fullname: Yamauchi, Toshimasa email: tyamau@m.u-tokyo.ac.jp organization: The University of Tokyo |
BackLink | https://cir.nii.ac.jp/crid/1872835442871241600$$DView record in CiNii https://www.ncbi.nlm.nih.gov/pubmed/36639962$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.2337/dc12-1235 10.1038/s41588-018-0332-4 10.2337/db06-1154 10.2337/db17-0914 10.1016/S2213-8587(20)30026-7 10.1038/s41588-018-0183-z 10.1038/ng.2383 10.1111/bjd.15787 10.1038/ng.208 10.1007/s12035-016-9823-4 10.1038/ng1732 10.1038/s42003-022-03448-z 10.1371/journal.pgen.1002921 10.1093/hmg/dds113 10.1007/s00125-014-3202-3 10.2337/diabetes.53.9.2449 10.1186/s40246-014-0019-6 10.1093/hmg/ddt399 10.1371/journal.pgen.1001127 10.1093/bioinformatics/btaa439 10.1093/molbev/msaa005 10.1016/j.chom.2019.03.006 10.1126/science.1142358 10.1038/s41588-020-0637-y 10.1038/nature05616 10.1159/000447954 10.1038/nrneph.2017.142 10.1152/ajpgi.00319.2013 10.1007/BF00275741 10.1038/s41586-020-2263-3 10.1089/omi.2011.0108 10.1038/ng.609 10.1038/s41588-018-0241-6 10.1038/ng0196-17 10.1038/s41467-018-03274-0 10.1038/s41576-020-0268-2 10.1038/ng.660 10.1007/s00125-013-2874-4 10.1371/journal.pone.0241365 10.1016/j.diabres.2019.107840 10.1016/j.cmet.2014.12.020 10.1038/ng.1053 10.1038/ng.207 10.1371/journal.pgen.1000842 10.1016/j.ophtha.2021.04.027 10.1038/s41574-022-00669-4 10.1001/jamanetworkopen.2019.1540 10.1099/jmm.0.000907 10.1001/jama.2014.6511 10.1371/journal.pgen.1005352 10.1038/nature12656 10.1038/s41588-018-0248-z 10.1038/nature13138 10.1038/s41576-021-00414-z 10.1038/s41591-021-01549-6 10.1371/journal.pone.0278764 10.1126/science.1142364 10.1210/clinem/dgz240 10.1038/ng.2915 10.1016/j.xgen.2022.100190 10.1016/j.kint.2021.10.039 10.1038/ncomms10531 10.1038/s41588-019-0379-x 10.1126/science.1142382 10.1093/hmg/ddab044 10.2337/dc20-2700 10.2337/dc10-0200 10.1038/ng0297-186 10.2337/db05-0450 10.1093/hmg/ddr121 10.2337/db16-1253 10.1186/s40246-019-0205-7 10.2337/db18-0567 10.1056/NEJMra1615439 10.1016/j.ophtha.2010.07.020 10.2337/db15-0661 10.1016/j.gde.2018.01.002 10.1038/ng.120 10.1371/journal.pone.0208654 10.1038/ncomms10023 10.1074/jbc.M112.385682 10.1111/aos.13769 10.1371/journal.pgen.1000847 10.1681/ASN.2012111122 10.1016/j.kint.2022.04.022 10.1210/er.2019-00088 10.1007/s00125-021-05491-7 10.2337/db19-1070 10.1038/ng.1019 10.1111/dom.12976 10.1371/journal.pone.0029202 10.1038/s41598-018-33507-7 10.1038/s41588-021-00931-x 10.1126/science.1193032 10.1038/s41576-022-00470-z 10.1007/s00125-022-05735-0 10.1007/s00125-015-3697-2 10.1038/ng.2882 10.1038/nature12828 10.1007/s00125-016-4024-2 10.2337/db12-1077 10.1038/s41591-019-0415-5 10.1038/ng.921 10.1038/ng.2897 10.1038/nrg.2016.56 10.1126/science.1109557 10.1038/s41586-021-04103-z 10.1681/ASN.2019030218 10.1038/s41746-022-00713-7 10.1038/s41581-020-0278-5 10.1038/ng2043 10.2337/db19-0109 10.1038/nm.2307 10.1126/scitranslmed.abd2699 |
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Copyright | 2023 The Authors. published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd. 2023 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd. 2023. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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References | 2021; 64 2011; 118 1987; 30 2013; 62 2006; 38 2019; 13 2022; 23 2020; 16 2020; 15 2004; 5 2012; 16 2009; 2010 2014; 23 2018; 9 2018; 8 2013; 56 2019; 25 2019; 157 2012; 21 2010; 6 2016; 44 2007; 445 2010; 33 2015; 58 2010; 329 2021; 44 2019; 30 2019; 2 2006; 55 2017; 66 2013; 503 2020; 37 2014; 46 2020; 36 2008; 50 2017; 376 2016; 17 1996; 12 2014; 311 2014; 306 2022; 101 2010; 42 2016; 7 2007; 316 2021; 53 2019; 40 2017; 54 2018; 96 2022; 2 2008; 40 2012; 44 2022; 17 2022; 18 2018; 14 2022; 223 2022; 102 2018; 13 2007; 39 2021; 27 2019; 51 2021; 22 2023; 5 2013; 24 2021; 128 2013; 288 2022; 65 2011; 17 2021; 30 2020; 8 2020; 5 2020; 52 2021; 599 1997; 15 2019; 68 2011; 20 2005; 308 2014; 57 2014; 8 2006; 12 2020; 582 2015; 11 2020; 105 2018; 67 2017; 177 2007; 56 2016; 59 2021; 13 2014; 507 2013; 36 2014; 506 2020 2015; 21 2016; 65 2011; 44 2011; 43 2020; 69 2017; 19 2018; 50 2012; 7 2012; 8 e_1_2_15_108_1 e_1_2_15_104_1 Hu C (e_1_2_15_97_1) 2021; 13 e_1_2_15_42_1 e_1_2_15_88_1 e_1_2_15_69_1 e_1_2_15_3_1 e_1_2_15_27_1 e_1_2_15_61_1 e_1_2_15_111_1 e_1_2_15_46_1 e_1_2_15_84_1 e_1_2_15_23_1 e_1_2_15_65_1 e_1_2_15_7_1 e_1_2_15_116_1 e_1_2_15_31_1 e_1_2_15_77_1 e_1_2_15_58_1 e_1_2_15_100_1 e_1_2_15_39_1 e_1_2_15_16_1 e_1_2_15_50_1 e_1_2_15_92_1 e_1_2_15_35_1 e_1_2_15_12_1 e_1_2_15_54_1 e_1_2_15_96_1 e_1_2_15_109_1 e_1_2_15_105_1 Devi RR (e_1_2_15_80_1) 2006; 12 e_1_2_15_20_1 e_1_2_15_43_1 e_1_2_15_66_1 e_1_2_15_89_1 e_1_2_15_28_1 e_1_2_15_81_1 e_1_2_15_112_1 e_1_2_15_2_1 e_1_2_15_24_1 e_1_2_15_47_1 e_1_2_15_62_1 e_1_2_15_85_1 e_1_2_15_6_1 e_1_2_15_117_1 Fu YP (e_1_2_15_73_1) 2009; 2010 e_1_2_15_32_1 e_1_2_15_55_1 e_1_2_15_78_1 e_1_2_15_59_1 e_1_2_15_17_1 e_1_2_15_70_1 e_1_2_15_93_1 e_1_2_15_101_1 e_1_2_15_13_1 e_1_2_15_36_1 e_1_2_15_51_1 e_1_2_15_74_1 e_1_2_15_106_1 e_1_2_15_21_1 e_1_2_15_67_1 e_1_2_15_40_1 e_1_2_15_29_1 e_1_2_15_113_1 e_1_2_15_48_1 e_1_2_15_82_1 e_1_2_15_25_1 e_1_2_15_63_1 e_1_2_15_44_1 e_1_2_15_86_1 e_1_2_15_9_1 e_1_2_15_118_1 e_1_2_15_90_1 e_1_2_15_5_1 e_1_2_15_114_1 e_1_2_15_10_1 e_1_2_15_56_1 e_1_2_15_79_1 e_1_2_15_18_1 e_1_2_15_94_1 e_1_2_15_102_1 e_1_2_15_37_1 e_1_2_15_71_1 e_1_2_15_14_1 e_1_2_15_52_1 e_1_2_15_98_1 e_1_2_15_33_1 e_1_2_15_75_1 e_1_2_15_107_1 e_1_2_15_103_1 e_1_2_15_19_1 e_1_2_15_41_1 e_1_2_15_68_1 e_1_2_15_110_1 e_1_2_15_26_1 e_1_2_15_49_1 e_1_2_15_60_1 e_1_2_15_83_1 e_1_2_15_22_1 e_1_2_15_45_1 e_1_2_15_64_1 e_1_2_15_87_1 e_1_2_15_8_1 e_1_2_15_119_1 e_1_2_15_4_1 e_1_2_15_115_1 e_1_2_15_30_1 e_1_2_15_57_1 e_1_2_15_99_1 e_1_2_15_15_1 e_1_2_15_38_1 e_1_2_15_72_1 e_1_2_15_91_1 e_1_2_15_11_1 e_1_2_15_34_1 e_1_2_15_53_1 e_1_2_15_76_1 e_1_2_15_95_1 |
References_xml | – volume: 27 start-page: 1876 year: 2021 end-page: 1884 article-title: Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps publication-title: Nat Med – volume: 2 year: 2019 article-title: Association of diabetic retinopathy and diabetic kidney disease with all‐cause and cardiovascular mortality in a multiethnic Asian population publication-title: JAMA Netw Open – volume: 62 start-page: 1746 year: 2013 end-page: 1755 article-title: Genome‐wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India publication-title: Diabetes – volume: 177 start-page: 1664 year: 2017 end-page: 1670 article-title: A genome‐wide association study suggests that MAPK14 is associated with diabetic foot ulcer publication-title: Br J Dermatol – volume: 316 start-page: 1341 year: 2007 end-page: 1345 article-title: A genome‐wide association study of type 2 diabetes in Finns detects multiple susceptibility variants publication-title: Science – volume: 15 start-page: 186 year: 1997 end-page: 189 article-title: A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange‐Nielsen cardioauditory syndrome publication-title: Nat Genet – volume: 66 start-page: 2888 year: 2017 end-page: 2902 article-title: An expanded genome‐wide association study of type 2 diabetes in Europeans publication-title: Diabetes – volume: 329 start-page: 841 year: 2010 end-page: 845 article-title: Association of trypanolytic ApoL1 variants with kidney disease in African Americans publication-title: Science – volume: 24 start-page: 1537 year: 2013 end-page: 1543 article-title: Chromosome 2q31.1 associate with ESRD in women with type 1 diabetes publication-title: J Am Soc Nephrol – volume: 15 year: 2020 article-title: Metabolomics profiles associated with diabetic retinopathy in type 2 diabetes patients publication-title: PLoS One – volume: 2010 year: 2009 article-title: Identification for diabetic retinopathy genes through a genome‐wide association study among Mexican‐Americans from Starr County, Texas publication-title: J Ophthalmol – volume: 68 start-page: 230 year: 2019 end-page: 240 article-title: Examining diabetic heel ulcers through an ecological lens: microbial community dynamics associated with healing and infection publication-title: J Med Microbiol – volume: 33 start-page: 2074 year: 2010 end-page: 2076 article-title: Common genetic variation in GLP1R and insulin secretion in response to exogenous GLP‐1 in nondiabetic subjects: a pilot study publication-title: Diabetes Care – volume: 40 start-page: 638 year: 2008 end-page: 645 article-title: Meta‐analysis of genome‐wide association data and large‐scale replication identifies additional susceptibility loci for type 2 diabetes publication-title: Nat Genet – volume: 56 start-page: 1577 year: 2007 end-page: 1585 article-title: Genome‐wide scans for diabetic nephropathy and albuminuria in multiethnic populations publication-title: Diabetes – volume: 128 start-page: 1580 year: 2021 end-page: 1591 article-title: Global prevalence of diabetic retinopathy and projection of burden through 2045: systematic review and meta‐analysis publication-title: Ophthalmology – volume: 118 start-page: 642 year: 2011 end-page: 648 article-title: Genome‐wide association study of diabetic retinopathy in a Taiwanese population publication-title: Ophthalmology – volume: 25 start-page: 641 year: 2019 end-page: 655 article-title: Strain‐ and species‐level variation in the microbiome of diabetic wounds is associated with clinical outcomes and therapeutic efficacy publication-title: Cell Host Microbe – volume: 25 start-page: 805 year: 2019 end-page: 813 article-title: A signature of circulating inflammatory proteins and development of end‐stage renal disease in diabetes publication-title: Nat Med – volume: 288 start-page: 3938 year: 2013 end-page: 3951 article-title: Regulation of glucagon secretion in normal and diabetic human islets by gamma‐hydroxybutyrate and glycine publication-title: J Biol Chem – volume: 44 start-page: 297 year: 2012 end-page: 301 article-title: Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes publication-title: Nat Genet – volume: 39 start-page: 770 year: 2007 end-page: 775 article-title: A variant in CDKAL1 influences insulin response and risk of type 2 diabetes publication-title: Nat Genet – volume: 105 start-page: 1000 year: 2020 end-page: 1008 article-title: Metabolomics signatures in type 2 diabetes: a systematic review and integrative analysis publication-title: J Clin Endocrinol Metab – volume: 21 start-page: 357 year: 2015 end-page: 368 article-title: Rare and common genetic events in type 2 diabetes: what should biologists know? publication-title: Cell Metab – volume: 22 start-page: 9 year: 2021 end-page: 37 article-title: Genetics meets proteomics: perspectives for large population‐based studies publication-title: Nat Rev Genet – volume: 54 start-page: 2435 year: 2017 end-page: 2444 article-title: Effects of common polymorphisms in the MTHER and ACE genes of diabetic peripheral neuropathy progression: a meta‐analysis publication-title: Mol Neurobiol – volume: 17 year: 2022 article-title: Polygenic risk scores for cardiovascular diseases and type 2 diabetes publication-title: PLoS One – volume: 9 start-page: 1631 year: 2018 article-title: Deep whole‐genome sequencing reveals recent selection signatures linked to evolution and disease risk of Japanese publication-title: Nat Commun – volume: 311 start-page: 2305 year: 2014 end-page: 2314 article-title: Association of a low‐frequency variant in HNF1A with type 2 diabetes in a Latino population publication-title: JAMA – volume: 57 start-page: 1143 year: 2014 end-page: 1153 article-title: Genome‐wide association study of urinary albumin excretion rate in patients with type 1 diabetes publication-title: Diabetologia – volume: 19 start-page: 1570 year: 2017 end-page: 1578 article-title: Variability in HbA1c, blood pressure, lipid parameters and serum uric acid and risk of development of chronic kidney disease in type 2 diabetes publication-title: Diabetes Obes Metab – volume: 2 year: 2022 article-title: A practical guideline of genomics‐driven drug discovery in the era of global biobank meta‐analysis publication-title: Cell Genomics – volume: 102 start-page: 370 year: 2022 end-page: 381 article-title: Results of untargeted analysis using the SOMAscan proteomics platform indicates novel association to kidney failure in diabetes publication-title: Kidney Int – volume: 17 start-page: 535 year: 2016 end-page: 549 article-title: Type 2 diabetes: genetic data sharing to advance complex disease research publication-title: Nat Rev Genet – volume: 8 start-page: 19 year: 2014 article-title: Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGD associated with inherited cataract publication-title: Hum Genomics – volume: 5 start-page: 580 year: 2023 article-title: Differential and shared genetic effects on kidney function between diabetic and non‐diabetic individuals publication-title: Commun Biol – volume: 13 year: 2018 article-title: A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes publication-title: PLoS One – volume: 8 year: 2018 article-title: Circulating metabolic biomarkers of renal function in diabetic and non‐diabetic populations publication-title: Sci Rep – volume: 14 start-page: 48 year: 2018 end-page: 56 article-title: Modelling diabetic nephropathy in mice publication-title: Nat Rev Nephrol – volume: 43 start-page: 984 year: 2011 end-page: 989 article-title: Genome‐wide association study in individuals of south Asian ancestry identifies six new type 2 diabetes susceptibility loci publication-title: Nat Genet – volume: 59 start-page: 1882 year: 2016 end-page: 1892 article-title: MASP1, THBS1, GPLD1 and ApoA‐IV are novel biomarkers associated with prediabetes: the KORA F4 study publication-title: Diabetologia – volume: 53 start-page: 1415 year: 2021 end-page: 1424 article-title: A cross‐population atlas of genetic associations for 220 human phenotypes publication-title: Nat Genet – volume: 55 start-page: 1223 year: 2006 end-page: 1231 article-title: Evidence for a role of the ubiquitin‐pproteasome pathway in pancreatic islets publication-title: Diabetes – volume: 44 start-page: 1410 year: 2021 end-page: 1418 article-title: A type 2 diabetes subtype responsive to ACCORD intensive glycemia treatment publication-title: Diabetes Care – volume: 506 start-page: 97 year: 2014 end-page: 101 article-title: Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico publication-title: Nature – volume: 44 start-page: 92 year: 2016 end-page: 103 article-title: Metabolomics in diabetic kidney disease: unraveling the biochemistry of a silent killer publication-title: Am J Nephrol – volume: 16 start-page: 377 year: 2020 end-page: 390 article-title: Genetics of diabetes and diabetic complications publication-title: Nat Rev Nephrol – volume: 40 start-page: 1098 year: 2008 end-page: 1102 article-title: SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations publication-title: Nat Genet – volume: 56 start-page: 1291 year: 2013 end-page: 1305 article-title: Genome‐wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4 publication-title: Diabetologia – volume: 51 start-page: 584 year: 2019 end-page: 591 article-title: Clinical use of current polygenic risk scores may exacerbate health disparities publication-title: Nat Genet – volume: 67 start-page: 1414 year: 2018 end-page: 1427 article-title: A genome‐wide association study of diabetic kidney disease in subjects with type 2 diabetes publication-title: Diabetes – volume: 7 year: 2012 article-title: A genome‐wide association search for type 2 diabetes genes in African Americans publication-title: PLoS One – volume: 13 start-page: 21 year: 2019 article-title: Genome‐wide association study identifies novel loci for type 2 diabetes‐attributed end‐stage kidney disease in African Americans publication-title: Hum Genomics – volume: 18 start-page: 413 year: 2022 end-page: 432 article-title: Pathophysiology, phenotypes and management of type 2 diabetes mellitus in Indian and Chinese populations publication-title: Nat Rev Endocrinol – volume: 42 start-page: 864 year: 2010 end-page: 868 article-title: A genome‐wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A‐C2CD4B publication-title: Nat Genet – volume: 50 start-page: 17 year: 2018 end-page: 24 article-title: Genetic basis of diabetic kidney disease and other diabetic complications publication-title: Curr Opin Genet Dev – volume: 36 start-page: i516 year: 2020 end-page: i524 article-title: Network‐based characterization of disease–disease relationships in terms of drugs and therapeutic targets publication-title: Bioinformatics – volume: 37 start-page: 1306 year: 2020 end-page: 1316 article-title: Genome‐wide natural selection signatures are linked to genetic risk of modern phenotypes in the Japanese population publication-title: Mol Biol Evol – volume: 50 start-page: 1593 year: 2008 end-page: 1599 article-title: An atlas of genetic associations in UK biobank publication-title: Nat Genet – volume: 68 start-page: 441 year: 2019 end-page: 456 article-title: Multiethnic genome‐wide association study of diabetic retinopathy using liability threshold modeling of duration of diabetes and glycemic control publication-title: Diabetes – volume: 445 start-page: 881 year: 2007 end-page: 885 article-title: A genome‐wide association study identifies novel risk loci for type 2 diabetes publication-title: Nature – volume: 44 start-page: 67 year: 2011 end-page: 72 article-title: Meta‐analysis of genome‐wide association studies identifies eight new loci for type 2 diabetes in east Asians publication-title: Nat Genet – volume: 21 start-page: 3042 year: 2012 end-page: 3049 article-title: A single‐nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations publication-title: Hum Mol Genet – volume: 50 start-page: 1505 year: 2018 end-page: 1513 article-title: Fine‐mapping type 2 diabetes loci to single‐variant resolution using high‐density imputation and islet‐specific epigenome maps publication-title: Nat Genet – volume: 58 start-page: 2288 year: 2015 end-page: 2297 article-title: Genome‐wide association study for sight‐threatening diabetic retinopathy reveals association with genetic variation near the GRB2 gene publication-title: Diabetologia – volume: 46 start-page: 294 year: 2014 end-page: 298 article-title: Identification of low frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes publication-title: Nat Genet – volume: 69 start-page: 1843 year: 2020 end-page: 1853 article-title: Circulating protein signatures and causal candidates for type 2 diabetes publication-title: Diabetes – volume: 40 start-page: 1500 year: 2019 end-page: 1520 article-title: Genetic risk scores for diabetes diagnosis and precision medicine publication-title: Endocr Rev – volume: 30 start-page: 716 year: 2021 end-page: 726 article-title: Genome‐wide association studies identify two novel conferring susceptibility to diabetic retinopathy in Japanese patients with type 2 diabetes publication-title: Hum Mol Genet – volume: 96 start-page: e811 year: 2018 end-page: e819 article-title: A genome‐wide association study suggests new evidence for an association of the NADPH oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes publication-title: Acta Ophthalmol – volume: 42 start-page: 579 year: 2010 end-page: 589 article-title: Twelve type 2 diabetes susceptibility loci identified through large‐scale association analysis publication-title: Nat Genet – volume: 23 start-page: 120 year: 2022 end-page: 133 article-title: The genetics of obesity: from discovery to biology publication-title: Nat Rev Genet – volume: 46 start-page: 234 year: 2014 end-page: 244 article-title: Genome‐wide trans‐ancestry meta‐analysis provides insight into the genetic architecture of type 2 diabetes susceptibility publication-title: Nat Genet – volume: 20 start-page: 2472 year: 2011 end-page: 2481 article-title: Genome‐wide meta‐analysis for severe diabetic retinopathy publication-title: Hum Mol Genet – volume: 316 start-page: 1336 year: 2007 end-page: 1341 article-title: Replication of genome‐wide association signals in UK samples reveals risk loci for type 2 diabetes publication-title: Science – volume: 507 start-page: 371 year: 2014 end-page: 375 article-title: Obesity‐zssociated variants with FTO form long‐range functional connections with IRX3 publication-title: Nature – volume: 7 start-page: 10531 year: 2016 article-title: Genome‐wide association studies in the Japanese population identify seven novel loci for type 2 diabetes publication-title: Nat Commun – volume: 5 start-page: 166 year: 2020 article-title: Discovering a trans‐omics biomarker signature that predisposes high risk diabetic patients to diabetic kidney disease publication-title: NPJ Digit Med – volume: 599 start-page: 628 year: 2021 end-page: 634 article-title: Exome sequencing and analysis of 454,787 UK biobank participants publication-title: Nature – volume: 64 start-page: 2012 year: 2021 end-page: 2025 article-title: Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control publication-title: Diabetologia – volume: 65 start-page: 1495 year: 2022 end-page: 1509 article-title: Genome‐wide meta‐analysis and omics integration identifies novel gene associated with diabetic kidney disease publication-title: Diabetologia – volume: 308 start-page: 385 year: 2005 end-page: 389 article-title: Complement factor H polymorphism in aggregated macular degeneration publication-title: Science – volume: 582 start-page: 240 year: 2020 end-page: 245 article-title: Identification of type 2 diabetes loci in 433,540 east Asian individuals publication-title: Nature – volume: 13 start-page: 576 year: 2021 end-page: 593 article-title: Multi‐omics profiling: the way towards precision medicine in metabolic diseases publication-title: J Mol Cell Biol – volume: 6 year: 2010 article-title: A single nucleotide polymorphism within the acetyl‐coenzyme a carboxylase beta gene is associated with proteinuria in patients with type 2 diabetes publication-title: PLoS Genet – volume: 12 start-page: 17 year: 1996 end-page: 23 article-title: Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias publication-title: Nat Genet – volume: 12 start-page: 190 year: 2006 end-page: 195 article-title: Novel mutation in GJA8 associated with autosomal dominant congenital cataract and microcornea publication-title: Mol Vis – volume: 376 start-page: 2367 year: 2017 end-page: 2375 article-title: Diabetic foot ulcers and their recurrence publication-title: N Engl J Med – volume: 101 start-page: 510 year: 2022 end-page: 526 article-title: Lysophosphatidylcholine mediates fast decline in kidney function in diabetic kidney disease publication-title: Kidney Int – volume: 23 start-page: 239 year: 2014 end-page: 246 article-title: Genome‐wide association study identifies three novel loci for type 2 diabetes publication-title: Hum Mol Genet – volume: 46 start-page: 357 year: 2014 end-page: 363 article-title: Loss‐of‐function mutations in SLC30A8 protect against type 2 diabetes publication-title: Nat Genet – volume: 11 year: 2015 article-title: Genome‐wide association and transethnic meta‐analysis for advanced diabetic kidney disease: family investigation of nephropathy and diabetes (FIND) publication-title: PLoS Genet – volume: 6 year: 2010 article-title: Identification of new genetic risk variants for type 2 diabetes publication-title: PLoS Genet – volume: 7 start-page: 10023 year: 2016 article-title: Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function publication-title: Nat Commun – volume: 36 start-page: 1789 year: 2013 end-page: 1796 article-title: Ethnic differences in the relationship between insulin sensitivity and insulin response publication-title: Diabetes Care – volume: 8 start-page: 301 year: 2020 end-page: 312 article-title: Early detection of diabetic kidney disease by urinary proteomics and subsequent intervention with spironolactone to delay progression (PRIORITY): a prospective observational study and embedded randomised placebo‐controlled trial publication-title: Lancet Diabetes Endocrinol – volume: 157 year: 2019 article-title: IDF diabetes atlas: a review of studies utilizing retinal photography on the global prevalence of diabetes related retinopathy between 2015 and 2018 publication-title: Diab Res Clin Pract – volume: 68 start-page: 1649 year: 2019 end-page: 1662 article-title: A genetic locus on chromosome 2q24 predicting peripheral neuropathy risk in type 2 diabetes: results from the ACCORD and BARI 2D studies publication-title: Diabetes – volume: 306 start-page: G906 year: 2014 end-page: G908 article-title: Alkaline sphingomyelinase (NPP7) promotes cholesterol absorption by affecting sphingomyelin levels in the gut: a study with NPP7 knockout mice publication-title: Am J Physiol Gastrointest Liver Physiol – volume: 51 start-page: 379 year: 2019 end-page: 386 article-title: Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population publication-title: Nat Genet – volume: 316 start-page: 1331 year: 2007 end-page: 1336 article-title: Genome‐wide association analysis identifies loci for type 2 diabetes and triglyceride levels publication-title: Science – volume: 65 start-page: 1099 year: 2016 end-page: 1108 article-title: Plasma metabolomic profiling of diabetic retinopathy publication-title: Diabetes – volume: 5 start-page: 2449 year: 2004 end-page: 2454 article-title: Population‐based assessment of familial clustering of diabetic nephropathy in type 1 diabetes publication-title: Diabetes – volume: 52 start-page: 680 year: 2020 end-page: 691 article-title: Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi‐ancestry meta‐analysis publication-title: Nat Genet – volume: 13 year: 2021 article-title: Circulating proteins protect against renal decline and progression to end‐stage renal disease in patients with diabetes publication-title: Sci Transl Med – volume: 40 start-page: 1092 year: 2008 end-page: 1097 article-title: Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus publication-title: Nat Genet – volume: 17 start-page: 448 year: 2011 end-page: 453 article-title: Metabolite profiles and the risk of developing diabetes publication-title: Nat Med – volume: 503 start-page: 493 year: 2013 end-page: 499 article-title: A small‐molecule AdipoR agonist for type 2 diabetes and short life in obesity publication-title: Nature – volume: 8 year: 2012 article-title: New susceptibility loci associated with kidney disease in type 1 diabetes publication-title: PLoS Genet – volume: 50 start-page: 1219 year: 2018 end-page: 1224 article-title: Genome‐wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations publication-title: Nat Genet – volume: 44 start-page: 981 year: 2012 end-page: 990 article-title: Large‐scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes publication-title: Nat Genet – year: 2020 – volume: 30 start-page: 763 year: 1987 end-page: 768 article-title: Concordance for type 2 (non‐insulin dependent) diabetes mellitus in male twins publication-title: Diabetologia – volume: 223 start-page: 524 year: 2022 end-page: 530 article-title: Polygenic scores in biomedical research publication-title: Nat Genet – volume: 38 start-page: 320 year: 2006 end-page: 323 article-title: Variant of transcription factor 7‐like 2 (TCF7L2) gene confers risk of type 2 diabetes publication-title: Nat Genet – volume: 6 year: 2010 article-title: A genome‐wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese publication-title: PLoS Genet – volume: 16 start-page: 231 year: 2012 end-page: 234 article-title: Diving through the omics the case for deep phenotyping and systems epidemiology publication-title: OMICS – volume: 30 start-page: 2000 year: 2019 end-page: 2016 article-title: Genome‐wide association study of diabetic kidney disease highlights biology involved in glomerular basement membrane collagen publication-title: J Am Soc Nephrol – ident: e_1_2_15_39_1 doi: 10.2337/dc12-1235 – ident: e_1_2_15_37_1 doi: 10.1038/s41588-018-0332-4 – ident: e_1_2_15_51_1 doi: 10.2337/db06-1154 – ident: e_1_2_15_62_1 doi: 10.2337/db17-0914 – ident: e_1_2_15_104_1 doi: 10.1016/S2213-8587(20)30026-7 – ident: e_1_2_15_90_1 doi: 10.1038/s41588-018-0183-z – ident: e_1_2_15_21_1 doi: 10.1038/ng.2383 – ident: e_1_2_15_84_1 doi: 10.1111/bjd.15787 – ident: e_1_2_15_12_1 doi: 10.1038/ng.208 – ident: e_1_2_15_83_1 doi: 10.1007/s12035-016-9823-4 – ident: e_1_2_15_41_1 doi: 10.1038/ng1732 – ident: e_1_2_15_69_1 doi: 10.1038/s42003-022-03448-z – ident: e_1_2_15_54_1 doi: 10.1371/journal.pgen.1002921 – ident: e_1_2_15_20_1 doi: 10.1093/hmg/dds113 – ident: e_1_2_15_56_1 doi: 10.1007/s00125-014-3202-3 – ident: e_1_2_15_50_1 doi: 10.2337/diabetes.53.9.2449 – ident: e_1_2_15_79_1 doi: 10.1186/s40246-014-0019-6 – ident: e_1_2_15_26_1 doi: 10.1093/hmg/ddt399 – ident: e_1_2_15_17_1 doi: 10.1371/journal.pgen.1001127 – ident: e_1_2_15_116_1 doi: 10.1093/bioinformatics/btaa439 – ident: e_1_2_15_49_1 doi: 10.1093/molbev/msaa005 – ident: e_1_2_15_87_1 doi: 10.1016/j.chom.2019.03.006 – ident: e_1_2_15_9_1 doi: 10.1126/science.1142358 – ident: e_1_2_15_35_1 doi: 10.1038/s41588-020-0637-y – ident: e_1_2_15_8_1 doi: 10.1038/nature05616 – ident: e_1_2_15_108_1 doi: 10.1159/000447954 – ident: e_1_2_15_52_1 doi: 10.1038/nrneph.2017.142 – ident: e_1_2_15_65_1 doi: 10.1152/ajpgi.00319.2013 – ident: e_1_2_15_4_1 doi: 10.1007/BF00275741 – ident: e_1_2_15_36_1 doi: 10.1038/s41586-020-2263-3 – ident: e_1_2_15_96_1 doi: 10.1089/omi.2011.0108 – ident: e_1_2_15_15_1 doi: 10.1038/ng.609 – ident: e_1_2_15_34_1 doi: 10.1038/s41588-018-0241-6 – ident: e_1_2_15_44_1 doi: 10.1038/ng0196-17 – ident: e_1_2_15_48_1 doi: 10.1038/s41467-018-03274-0 – ident: e_1_2_15_98_1 doi: 10.1038/s41576-020-0268-2 – ident: e_1_2_15_14_1 doi: 10.1038/ng.660 – ident: e_1_2_15_24_1 doi: 10.1007/s00125-013-2874-4 – ident: e_1_2_15_112_1 doi: 10.1371/journal.pone.0241365 – ident: e_1_2_15_72_1 doi: 10.1016/j.diabres.2019.107840 – ident: e_1_2_15_114_1 doi: 10.1016/j.cmet.2014.12.020 – ident: e_1_2_15_23_1 doi: 10.1038/ng.1053 – ident: e_1_2_15_11_1 doi: 10.1038/ng.207 – ident: e_1_2_15_53_1 doi: 10.1371/journal.pgen.1000842 – ident: e_1_2_15_71_1 doi: 10.1016/j.ophtha.2021.04.027 – ident: e_1_2_15_40_1 doi: 10.1038/s41574-022-00669-4 – ident: e_1_2_15_3_1 doi: 10.1001/jamanetworkopen.2019.1540 – ident: e_1_2_15_86_1 doi: 10.1099/jmm.0.000907 – volume: 2010 year: 2009 ident: e_1_2_15_73_1 article-title: Identification for diabetic retinopathy genes through a genome‐wide association study among Mexican‐Americans from Starr County, Texas publication-title: J Ophthalmol – ident: e_1_2_15_31_1 doi: 10.1001/jama.2014.6511 – ident: e_1_2_15_58_1 doi: 10.1371/journal.pgen.1005352 – ident: e_1_2_15_118_1 doi: 10.1038/nature12656 – ident: e_1_2_15_70_1 doi: 10.1038/s41588-018-0248-z – ident: e_1_2_15_61_1 doi: 10.1038/nature13138 – ident: e_1_2_15_38_1 doi: 10.1038/s41576-021-00414-z – ident: e_1_2_15_119_1 doi: 10.1038/s41591-021-01549-6 – ident: e_1_2_15_89_1 doi: 10.1371/journal.pone.0278764 – ident: e_1_2_15_43_1 doi: 10.1126/science.1142364 – ident: e_1_2_15_107_1 doi: 10.1210/clinem/dgz240 – ident: e_1_2_15_30_1 doi: 10.1038/ng.2915 – ident: e_1_2_15_115_1 doi: 10.1016/j.xgen.2022.100190 – ident: e_1_2_15_110_1 doi: 10.1016/j.kint.2021.10.039 – ident: e_1_2_15_32_1 doi: 10.1038/ncomms10531 – ident: e_1_2_15_91_1 doi: 10.1038/s41588-019-0379-x – ident: e_1_2_15_42_1 doi: 10.1126/science.1142382 – ident: e_1_2_15_81_1 doi: 10.1093/hmg/ddab044 – ident: e_1_2_15_94_1 doi: 10.2337/dc20-2700 – ident: e_1_2_15_47_1 doi: 10.2337/dc10-0200 – ident: e_1_2_15_45_1 doi: 10.1038/ng0297-186 – ident: e_1_2_15_46_1 doi: 10.2337/db05-0450 – ident: e_1_2_15_75_1 doi: 10.1093/hmg/ddr121 – ident: e_1_2_15_33_1 doi: 10.2337/db16-1253 – ident: e_1_2_15_63_1 doi: 10.1186/s40246-019-0205-7 – ident: e_1_2_15_78_1 doi: 10.2337/db18-0567 – ident: e_1_2_15_82_1 doi: 10.1056/NEJMra1615439 – ident: e_1_2_15_74_1 doi: 10.1016/j.ophtha.2010.07.020 – ident: e_1_2_15_111_1 doi: 10.2337/db15-0661 – ident: e_1_2_15_6_1 doi: 10.1016/j.gde.2018.01.002 – ident: e_1_2_15_13_1 doi: 10.1038/ng.120 – volume: 12 start-page: 190 year: 2006 ident: e_1_2_15_80_1 article-title: Novel mutation in GJA8 associated with autosomal dominant congenital cataract and microcornea publication-title: Mol Vis – ident: e_1_2_15_60_1 doi: 10.1371/journal.pone.0208654 – ident: e_1_2_15_59_1 doi: 10.1038/ncomms10023 – ident: e_1_2_15_57_1 doi: 10.1074/jbc.M112.385682 – ident: e_1_2_15_77_1 doi: 10.1111/aos.13769 – ident: e_1_2_15_16_1 doi: 10.1371/journal.pgen.1000847 – ident: e_1_2_15_55_1 doi: 10.1681/ASN.2012111122 – ident: e_1_2_15_102_1 doi: 10.1016/j.kint.2022.04.022 – ident: e_1_2_15_93_1 doi: 10.1210/er.2019-00088 – ident: e_1_2_15_95_1 doi: 10.1007/s00125-021-05491-7 – ident: e_1_2_15_99_1 doi: 10.2337/db19-1070 – ident: e_1_2_15_18_1 doi: 10.1038/ng.1019 – ident: e_1_2_15_66_1 doi: 10.1111/dom.12976 – ident: e_1_2_15_22_1 doi: 10.1371/journal.pone.0029202 – volume: 13 start-page: 576 year: 2021 ident: e_1_2_15_97_1 article-title: Multi‐omics profiling: the way towards precision medicine in metabolic diseases publication-title: J Mol Cell Biol – ident: e_1_2_15_109_1 doi: 10.1038/s41598-018-33507-7 – ident: e_1_2_15_117_1 doi: 10.1038/s41588-021-00931-x – ident: e_1_2_15_64_1 doi: 10.1126/science.1193032 – ident: e_1_2_15_88_1 doi: 10.1038/s41576-022-00470-z – ident: e_1_2_15_68_1 doi: 10.1007/s00125-022-05735-0 – ident: e_1_2_15_76_1 doi: 10.1007/s00125-015-3697-2 – ident: e_1_2_15_29_1 doi: 10.1038/ng.2882 – ident: e_1_2_15_28_1 doi: 10.1038/nature12828 – ident: e_1_2_15_2_1 – ident: e_1_2_15_100_1 doi: 10.1007/s00125-016-4024-2 – ident: e_1_2_15_25_1 doi: 10.2337/db12-1077 – ident: e_1_2_15_101_1 doi: 10.1038/s41591-019-0415-5 – ident: e_1_2_15_19_1 doi: 10.1038/ng.921 – ident: e_1_2_15_27_1 doi: 10.1038/ng.2897 – ident: e_1_2_15_92_1 doi: 10.1038/nrg.2016.56 – ident: e_1_2_15_7_1 doi: 10.1126/science.1109557 – ident: e_1_2_15_113_1 doi: 10.1038/s41586-021-04103-z – ident: e_1_2_15_67_1 doi: 10.1681/ASN.2019030218 – ident: e_1_2_15_105_1 doi: 10.1038/s41746-022-00713-7 – ident: e_1_2_15_5_1 doi: 10.1038/s41581-020-0278-5 – ident: e_1_2_15_10_1 doi: 10.1038/ng2043 – ident: e_1_2_15_85_1 doi: 10.2337/db19-0109 – ident: e_1_2_15_106_1 doi: 10.1038/nm.2307 – ident: e_1_2_15_103_1 doi: 10.1126/scitranslmed.abd2699 |
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Snippet | Type 2 diabetes results from a complex interaction between genetic and environmental factors. Precision medicine for type 2 diabetes using genetic data is... Abstract Type 2 diabetes results from a complex interaction between genetic and environmental factors. Precision medicine for type 2 diabetes using genetic... |
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SubjectTerms | Amino acids Asian people Association analysis Biobanks Diabetes Diabetes Complications Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - genetics Diabetic complications Disease Diseases of the endocrine glands. Clinical endocrinology Environmental factors Evolution & development Gene expression Gene loci Genetic Predisposition to Disease Genome-wide association studies Genome-Wide Association Study Genome-Wide Association Study - methods Genomes Genotype & phenotype Humans Inflammation Insulin resistance Meta-analysis Metabolomics Minority & ethnic groups Molecular modelling Polymorphism, Single Nucleotide Population genetics Precision medicine Proteomics RC648-665 Review Risk Factors Type 2 diabetes |
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Title | Progress in genetics of type 2 diabetes and diabetic complications |
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