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...

Full description

Saved in:
Bibliographic Details
Published inJournal of Diabetes Investigation Vol. 14; no. 4; pp. 503 - 515
Main Authors Shojima, Nobuhiro, Yamauchi, Toshimasa
Format Journal Article
LanguageEnglish
Published Japan Wiley 01.04.2023
John Wiley & Sons, Inc
John Wiley and Sons Inc
Subjects
Online AccessGet full text
ISSN2040-1116
2040-1124
2040-1124
DOI10.1111/jdi.13970

Cover

Loading…
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.
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
BookMark eNp9kstuEzEUhi3UipbSBS-ARoIFLNLaHo8vKwQF2qBKsIC15bGPg6OJHewJKG-Pc2lEKxUvfP3Pp9_nnGfoKKYICL0g-ILUcTl34YK0SuAn6JRihieEUHZ02BN-gs5LmeM6Wik5F0_RSct5qxSnp-jDt5xmGUppQmxmEGEMtjTJN-N6CQ1tXDA9jFAaE93-EGxj02I5BGvGkGJ5jo69GQqc79cz9OPzp-9XN5Pbr9fTq_e3E8upwhNObO8ZdtAS59rWOOUNU73FGIQnUmClGPTMO8Uo58o5AtJKI3sjKVOdaM_QdMd1ycz1MoeFyWudTNDbi5Rn2uTqbgDtoZOCWKI8GObBm45WaM-pddx4oyrr3Y61XPULcBbimM1wD3r_JYafepZ-a1KzWN3ISnizJ-T0awVl1ItQLAyDiZBWRVPBOyEEkV2VvnognadVjjVXVSUVZ4zJjaWX_1o6eLmrVRW83QlsTqVk8AcJwXrTCrq2gt62QtVePtDaMG7LVX8Thv9F_AkDrB9H6y8fp3cRr3cRMYSK38y1jFS2HWO0pp8ywmu2_gJoLM3b
CitedBy_id crossref_primary_10_1038_s41598_024_54769_4
crossref_primary_10_1007_s40200_024_01407_5
crossref_primary_10_1007_s42000_025_00644_4
crossref_primary_10_1007_s11030_025_11149_y
crossref_primary_10_1016_j_nutres_2024_08_004
crossref_primary_10_3390_ijms25179297
crossref_primary_10_1016_j_dsx_2023_102922
crossref_primary_10_1016_j_metop_2024_100333
crossref_primary_10_1002_ptr_8381
crossref_primary_10_1097_JCMA_0000000000001210
crossref_primary_10_3390_pharmaceutics15071995
crossref_primary_10_14341_DM13203
crossref_primary_10_1038_s41598_024_84160_2
crossref_primary_10_1016_j_amolm_2024_100046
crossref_primary_10_1093_labmed_lmae030
crossref_primary_10_2337_dc24_0022
crossref_primary_10_18699_vjgb_24_107
crossref_primary_10_3390_biology12111439
crossref_primary_10_1145_3719347
crossref_primary_10_1515_gps_2024_0203
crossref_primary_10_14341_DM13080
crossref_primary_10_1080_10837450_2024_2329763
crossref_primary_10_26442_00403660_2024_03_202651
crossref_primary_10_1016_j_gene_2024_149050
crossref_primary_10_1007_s11010_024_04999_x
crossref_primary_10_1097_CM9_0000000000003034
crossref_primary_10_1155_genr_6893109
crossref_primary_10_1038_s41467_024_48618_1
crossref_primary_10_1111_dom_15491
crossref_primary_10_1371_journal_pone_0318134
crossref_primary_10_3389_fendo_2024_1406382
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
ContentType Journal Article
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.
Copyright_xml – notice: 2023 The Authors. published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.
– notice: 2023 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.
– notice: 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.
DBID RYH
24P
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7T5
7TM
7X7
7XB
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
COVID
DWQXO
FYUFA
GHDGH
H94
K9.
M0S
PHGZM
PHGZT
PIMPY
PKEHL
PQEST
PQQKQ
PQUKI
PRINS
7X8
5PM
DOA
DOI 10.1111/jdi.13970
DatabaseName CiNii Complete
Wiley Online Library Open Access
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
Immunology Abstracts
Nucleic Acids Abstracts
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials - QC
ProQuest Central
ProQuest One Community College
Coronavirus Research Database
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
ProQuest Health & Medical Collection
ProQuest Central Premium
ProQuest One Academic (New)
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
Nucleic Acids Abstracts
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest Central China
ProQuest Central
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
AIDS and Cancer Research Abstracts
ProQuest Central (New)
ProQuest One Academic Eastern Edition
Coronavirus Research Database
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest One Academic UKI Edition
Immunology Abstracts
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList MEDLINE
MEDLINE - Academic


CrossRef

Publicly Available Content Database
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: 24P
  name: Wiley Online Library Open Access
  url: https://authorservices.wiley.com/open-science/open-access/browse-journals.html
  sourceTypes: Publisher
– sequence: 3
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 4
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 5
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
DocumentTitleAlternate Progress in genetics of diabetes
EISSN 2040-1124
EndPage 515
ExternalDocumentID oai_doaj_org_article_fe5871c19fea4fefa52426b62cd6afa9
PMC10034958
36639962
10_1111_jdi_13970
JDI13970
Genre reviewArticle
Journal Article
Review
GeographicLocations Japan
GeographicLocations_xml – name: Japan
GrantInformation_xml – fundername: Japan Agency for Medical Research and Development
  funderid: JP21tm0424218
– fundername: Japan Agency for Medical Research and Development
  grantid: JP21tm0424218
– fundername: ;
  grantid: JP21tm0424218
GroupedDBID ---
05W
0R~
1OC
24P
4.4
50Y
5DZ
5VS
7X7
8-0
8-1
8FI
8FJ
AAHHS
AAZKR
ABDBF
ABUWG
ACCFJ
ACCMX
ACGFO
ACPRK
ACUHS
ACXQS
ADBBV
ADKYN
ADPDF
ADZMN
AEEZP
AEGXH
AENEX
AEQDE
AFKRA
AHMBA
AIAGR
AIWBW
AJBDE
ALIPV
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AOIJS
AVUZU
BAWUL
BCNDV
BDRZF
BENPR
BPHCQ
BVXVI
CCPQU
DIK
EBD
EBS
FYUFA
GROUPED_DOAJ
GX1
HMCUK
HYE
HZ~
KQ8
LH4
M48
MY.
O9-
OK1
OVD
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
RPM
RX1
RYH
TEORI
UKHRP
31~
AANHP
ABJNI
ACBWZ
ACRPL
ACYXJ
ADNMO
ADRAZ
ASPBG
AVWKF
AZFZN
CAG
COF
EJD
GODZA
LW6
SUPJJ
WIN
AAYXX
AGQPQ
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7T5
7TM
7XB
8FK
AAMMB
AEFGJ
AGXDD
AIDQK
AIDYY
AZQEC
COVID
DWQXO
H94
K9.
PKEHL
PQEST
PQUKI
PRINS
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c6290-61cbf40de31dd33ad9fa49bc00e7f1870994eb4fd942669dd1e8c8a8ba8249573
IEDL.DBID M48
ISSN 2040-1116
2040-1124
IngestDate Wed Aug 27 01:31:48 EDT 2025
Thu Aug 21 18:38:36 EDT 2025
Fri Jul 11 08:04:21 EDT 2025
Fri Jul 25 03:53:50 EDT 2025
Wed Feb 19 02:24:54 EST 2025
Thu Apr 24 23:09:29 EDT 2025
Tue Jul 01 02:48:50 EDT 2025
Wed Jan 22 16:28:31 EST 2025
Thu Jun 26 23:50:23 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords Type 2 diabetes
Precision medicine
Diabetic complications
Language English
License Attribution-NonCommercial-NoDerivs
2023 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.
This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c6290-61cbf40de31dd33ad9fa49bc00e7f1870994eb4fd942669dd1e8c8a8ba8249573
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Review-3
content type line 23
ORCID 0000-0002-4078-3308
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.1111/jdi.13970
PMID 36639962
PQID 2789644489
PQPubID 1006415
PageCount 13
ParticipantIDs doaj_primary_oai_doaj_org_article_fe5871c19fea4fefa52426b62cd6afa9
pubmedcentral_primary_oai_pubmedcentral_nih_gov_10034958
proquest_miscellaneous_2765777185
proquest_journals_2789644489
pubmed_primary_36639962
crossref_primary_10_1111_jdi_13970
crossref_citationtrail_10_1111_jdi_13970
wiley_primary_10_1111_jdi_13970_JDI13970
nii_cinii_1872835442871241600
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate April 2023
PublicationDateYYYYMMDD 2023-04-01
PublicationDate_xml – month: 04
  year: 2023
  text: April 2023
PublicationDecade 2020
PublicationPlace Japan
PublicationPlace_xml – name: Japan
– name: Richmond
– name: Hoboken
PublicationTitle Journal of Diabetes Investigation
PublicationTitleAlternate J Diabetes Investig
PublicationYear 2023
Publisher Wiley
John Wiley & Sons, Inc
John Wiley and Sons Inc
Publisher_xml – name: Wiley
– name: John Wiley & Sons, Inc
– name: John Wiley and Sons Inc
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
SSID ssj0000388667
ssib027715943
ssib051604877
ssib058493193
Score 2.4501884
SecondaryResourceType review_article
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...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
wiley
nii
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 503
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
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1NT9wwEB0hDohLVSiUFLZyKw69BBLHcewjFFYUCcShSNwixx8iUpVFfPz_zjjZaCNAvfSy2k28kjOZ8XuTjN8AHKqC0mgrUq00T3H1k6kmLUJEYkyCMsyJDCWKV9fy4lZc3pV3K62-qCaslwfuDXccfImc3uY6eCOCD6YkUGkkt06aYOLWPcS8lWQqrsGFUjK2j-VUMocBLQdZoVjG49ojYj7ZBIyiZj9CTNe2b9HN11WTq2w2wtH8I3wYeCQ76ee_BWu-24aNq-FN-Sc4vaHCK1zGWNsxdBLaq_jEFoHRM1fG2fKZKzOdG360lk0KzHfgdn7---dFOvRLSK1E02IWaJsgMueL3LmiME4HI3Rjs8xXIcfA1Fr4RgSnCZa1c7lXVhnVGEUdqKtiF9a7Ref3gFW8Qe6VZUEaLqRFUFdR24z7wBujXQI_loar7SAmTj0t_tRjUuHaOto4ge_j0IdeQeOtQadk_XEAiV7HA-gK9eAK9b9cIYEZ3jucD33i9ZKUnIgpIdIUJHYJHCzvaj1E6lNNO4GREwqFf_82nsYYoxcnpvOLFxojy6pCFC8T-Nw7wTjTQhLHkzwBNXGPyaVMz3TtfdTxzqM4UKnQmNGT3jdPfXn2K3758j_stA-bHKlaX390AOvPjy9-htTqufkao-gvRGobSA
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwEB6VVkJcEJRXSosM4tBLIHEcxz4hClRtpSIOrbS3yPEDIqGkdNv_3xmvN21E4RJtNj7E4xnPN-PJNwDvVUVhtBW5VprnuPvJXBMXIXpiDIIKjIkMBYqn3-XRuThZ1IuUcFumssr1nhg3ajdaypF_pC820XcLpT9d_MmpaxSdrqYWGg9gi6jLqKSrWTRTjoWYTmRsIsupcA7NWiZyoVjM4_oPhH-KmUuKzP3oaIa-vw90_l07eRfTRqd0-AQeJzTJPq-W_yls-GEbHp6m8_JncPCDyq9wM2P9wFBV6IvFJRsDo8wr42ydeWVmcOmmt2xWZv4czg-_nX05ylPXhNxKFDDGgrYLonC-Kp2rKuN0MEJ3tih8E0o0T62F70Rwmpyzdq70yiqjOqOoD3VTvYDNYRz8K2AN7xCBFUWQhgtp0bWryHDGfeCd0S6D_bXgWpsoxamzxe92Ci1c30YZZ_BuGnqx4tG4b9ABSX8aQNTX8Y_x8mebLKkNvsYgz5Y6eCOCD6YmlNFJbp00wegM9nDt8H3oivMlQjkRA0MEKwjvMthdr2qb7HXZ3mpXBm-nx2hpdHxiBj9e0xhZNw368jqDlyslmN60koT0JM9AzdRjNpX5k6H_Fdm8y0gRVCsUZtSkf4unPfl6HH_s_H8Kr-ERRyi2qi_ahc2ry2u_h9DpqnsT7eMGPoYRSQ
  priority: 102
  providerName: ProQuest
– databaseName: Wiley Online Library Open Access
  dbid: 24P
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Na9wwEB1CCqGX0jZt4iYpSumhFwdblmWJnpq2IQmk5NBAbkafraF4Szb5_5mRP4hpAr0su-sR2CON5j159ATwUVVEo53ItdI8x9lP5pq0CDETIwkqkBMZIooXP-TplTi_rq834PO0F2bQh5gX3Cgy0nxNAW7s-mGQ--6I4Avy9We0tZaE87m4nBdYSOZEphNkOVXNYSM5KgulSp6p9SIfJdl-zDJ91z2GOP8tnHwIaFNGOnkJL0Yoyb4Mff8KNkL_GrYuxpfl23B8SbVXOJOxrmc4Tmi74pqtIqNlV8bZtOzKTO_HH51jixrzN3B18v3n19N8PDIhdxK9i0TQ2SgKH6rS-6oyXkcjtHVFEZpYYmxqLYIV0WvKzNr7MiinjLJG0SHUTfUWNvtVH3aBNdwi_CqKKA0X0mFeV0nejIfIrdE-g0-T41o36onTsRZ_2plX-K5NPs7gw2z6dxDReMzomLw_G5DudfpjdfOrHcOojaFGhudKHYMRMURTE8SwkjsvTTQ6gwPsO7wf-sTnJTU5kVghIhXEdhnsT73ajsG6bmkzMMJCobD54XwZw4zenZg-rO7IRtZNg4m8zmBnGATznVaSYJ7kGajF8Fg8yvJK3_1OUt5l0geqFTozjaSn3dOefztLX979v-kePOeIyYZCo33YvL25CweIoW7t-xQr9xebERo
  priority: 102
  providerName: Wiley-Blackwell
Title Progress in genetics of type 2 diabetes and diabetic complications
URI https://cir.nii.ac.jp/crid/1872835442871241600
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjdi.13970
https://www.ncbi.nlm.nih.gov/pubmed/36639962
https://www.proquest.com/docview/2789644489
https://www.proquest.com/docview/2765777185
https://pubmed.ncbi.nlm.nih.gov/PMC10034958
https://doaj.org/article/fe5871c19fea4fefa52426b62cd6afa9
Volume 14
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV3da9RAEB9qC-KL-G20PaL44EtKstlsdh9EPG2phSuHeHBvYbMfGik5vbag_70ze0nO4IkvIR8bkp2dyfxmM_sbgFcypzDa8ERJxRL8-olEERchemIMglKMiTQFirMLcbbg58tiuQd9jc1OgFc7QzuqJ7VYXx7__PHrLRr8myErxzbHBGQwcj9Ah1SSfc62KJ-VJfrsLetUkQlU2-3yS3TBChUxH6ZmiCBFhNqzjPLt8BGi4yQaPW3kyQLhP_qntml2YdW_Uy7_hMLBl53eg7sdCI3fbbTmPux90w_g9qz7zf4QpnPK2sJvYNy0MWoYLXS8ilc-pgnbmMX9hG2sW9sdNCYeZac_gsXpyef3Z0lXbCExAscFQ0hTe55al2fW5rm2ymuuapOmrvQZWrVS3NXcW0U-XVmbOWmklrWWVL66zB_Dfrtq3VOIS1YjcEtTLzTjwiAikIEYjTnPaq1sBK97wVWmYyKnghiX1RCR2KYKMo7g5dD0-4Z-Y1ejKUl_aECM2eHEav2l6gyw8q7A2NBkyjvNvfO6IHBSC2as0F6rCI5w7PB9aIv9JR46HuJJVClEhREc9qNa9Vpa0TJiBJRc4u0vhstooPTXRbdudUNtRFGiCsoigicbJRjeNBcEEAWLQI7UY9SV8ZW2-RpIwLPALFRIFGbQpH-Lpzr_8DHsPPtPF5_DHYYQbpOXdAj71-sbd4SQ67qewC3G57gtl-UEDqYnF_NPkzB9MQmm9hsO2yAW
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwED-NTgJeEN8ENjAIJF4CqeM48QNClG1qt7Wa0CbtLXP8AZFQOtZNiH-Kv5E7NwlUDN72UrWJVdnn893v7PPvAF4WKYXRRsSqUDxG6ydjRVyE6IkxCEowJtIUKE5ncnwkdo-z4zX42d2FobTKziYGQ23nhvbI39KNTfTdolDvT7_FVDWKTle7EhpLtdhzP75jyLZ4N9nC-X3F-c724cdx3FYViI3EDmCsZCovEuvSobVpqq3yWqjKJInL_RDVVynhKuGtIuelrB26whS6qHRBdZrzFP_3GqyLFEOZAayPtmcHn_pdHeJWkaFsLadUPTQksqUzCulDtn5DiCtZcYKhVgC6tqauL4O5f2dr_omigxvcuQ23WvzKPiwV7g6sueYuXJ-2J_T3YHRACV9oPlndMFROuiO5YHPPaK-Xcdbt9TLd2PZHbdhKYvt9OLoSiT6AQTNv3CNgOa8Q8yWJl5oLaRBMFIFTjTvPK61sBK87wZWmJTGnWhpfyz6YsXUZZBzBi77p6ZK547JGI5J-34DItsOD-dnnsl27pXcZhpVmqLzTwjuvM8I1leTGSu21imAT5w77Q584XqKwEyEURXiEgDKCjW5Wy9ZCLMrf-hzB8_41rm06sNGNm19QG5nlOaKHLIKHSyXoe5pKwpaSR1CsqMfKUFbfNPWXwB8-DKREWYHCDJr0b_GUu1uT8OXx_4fwDG6MD6f75f5ktvcEbnIEgsvspg0YnJ9duE0EbufV03a1MDi56gX6C-PjT7g
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Jb9UwEB6VIlVcEHsDLRgEEpfQxEmc-IAQ5fHU19KqByq9W3C8QCSUlL5WiL_Gr2PGWSCicOslymJF9niWb-zxDMDzIiE3WqehLCQPUfuJUFIuQrTE6ARF6BMpchQPj8TeSbq_zJZr8HM4C0NhlYNO9IratJrWyHfoxCba7rSQO64Piziezd-cfgupghTttA7lNDoWObA_vqP7tnq9mOFcv-B8_v7ju72wrzAQaoGdQb9JVy6NjE1iY5JEGelUKisdRTZ3MbKylKmtUmckGTJpTGwLXaiiUgXVbM4T_O81uJ4nWUwyli_zcX2HsqwIX8CWU9AeqhTRJzbygUSmfkXYK5qYQ181AI1cU9eXAd6_4zb_xNPeIM5vwc0eybK3HevdhjXb3IGNw36v_i7sHlPoFypSVjcM2ZROS65Y6xit-jLOhlVfphrTP9SaTULc78HJldDzPqw3bWM3geW8QvQXRU4ongqNsKLw2dW4dbxS0gTwciBcqft05lRV42s5ujWmLj2NA3g2Nj3tcnhc1miXqD82oLTb_kV79rnspbh0NkMHU8fSWZU661RGCKcSXBuhnJIBbOPcYX_oiuOlZHapd0oRKCG0DGBrmNWy1xWr8jdnB_B0_IxSTls3qrHtBbURWZ4jjsgCeNAxwdjTRBDKFDyAYsIek6FMvzT1F59JPPbpibICiek56d_kKfdnC3_z8P9DeAIbKJblh8XRwSO4wRERdmFOW7B-fnZhtxHBnVePvagw-HTVsvkL_jdSiA
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Progress+in+genetics+of+type+2+diabetes+and+diabetic+complications&rft.jtitle=Journal+of+Diabetes+Investigation&rft.au=Nobuhiro+Shojima&rft.au=Toshimasa+Yamauchi&rft.date=2023-04-01&rft.pub=Wiley&rft.issn=2040-1116&rft.eissn=2040-1124&rft.volume=14&rft.spage=503&rft.epage=515&rft_id=info:doi/10.1111%2Fjdi.13970
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2040-1116&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2040-1116&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2040-1116&client=summon