192 related articles for article (PubMed ID: 32531870)
1. Clinical and genetic analysis in a Chinese cohort of children and adolescents with diabetes/persistent hyperglycemia.
Ding Y; Li N; Lou D; Zhang Q; Chang G; Li J; Li X; Li Q; Huang X; Wang J; Jiang F; Wang X
J Diabetes Investig; 2021 Jan; 12(1):48-62. PubMed ID: 32531870
[TBL] [Abstract][Full Text] [Related]
2. Identification and functional analysis of GCK gene mutations in 12 Chinese families with hyperglycemia.
Wang Z; Diao C; Liu Y; Li M; Zheng J; Zhang Q; Yu M; Zhang H; Ping F; Li M; Xiao X
J Diabetes Investig; 2019 Jul; 10(4):963-971. PubMed ID: 30592380
[TBL] [Abstract][Full Text] [Related]
3. Delineation of the genetic and clinical spectrum, including candidate genes, of monogenic diabetes: a multicenter study in South Korea.
Cheon CK; Lee YJ; Yoo S; Lee JH; Lee JE; Kim HJ; Choi IJ; Choi Y; Lee S; Yoon JY
J Pediatr Endocrinol Metab; 2020 Dec; 33(12):1539-1550. PubMed ID: 33031055
[TBL] [Abstract][Full Text] [Related]
4. Maturity onset diabetes of the young (MODY) in Chinese children: genes and clinical phenotypes.
Ming-Qiang Z; Yang-Li D; Ke H; Wei W; Jun-Fen F; Chao-Chun Z; Guan-Ping D
J Pediatr Endocrinol Metab; 2019 Jul; 32(7):759-765. PubMed ID: 31216263
[TBL] [Abstract][Full Text] [Related]
5. [Hyperglycemia caused by mutation of GCK gene in 10 patients analysis of clinical and mutation characteristics].
Zhang J; Yuan K; Ding SX; Kong YM; Zhu JF; Fang YL; Liang L; Fu JF; Wang CL
Zhonghua Er Ke Za Zhi; 2019 Jun; 57(6):440-444. PubMed ID: 31216801
[No Abstract] [Full Text] [Related]
6. A preliminary study to evaluate the strategy of combining clinical criteria and next generation sequencing (NGS) for the identification of monogenic diabetes among multi-ethnic Asians.
Ang SF; Lim SC; Tan CSh; Fong JC; Kon WY; Lian JX; Subramanium T; Sum CF
Diabetes Res Clin Pract; 2016 Sep; 119():13-22. PubMed ID: 27420379
[TBL] [Abstract][Full Text] [Related]
7. Precision Therapy for a Chinese Family With Maturity-Onset Diabetes of the Young.
Li J; Shu M; Wang X; Deng A; Wen C; Wang J; Jin S; Zhang H
Front Endocrinol (Lausanne); 2021; 12():700342. PubMed ID: 34421822
[TBL] [Abstract][Full Text] [Related]
8. Genetic variants of ABCC8 and phenotypic features in Chinese early onset diabetes.
Li M; Gong S; Han X; Zhang S; Ren Q; Cai X; Luo Y; Zhou L; Zhang R; Liu W; Zhu Y; Zhou X; Sun Y; Li Y; Ma Y; Ji L
J Diabetes; 2021 Jul; 13(7):542-553. PubMed ID: 33300273
[TBL] [Abstract][Full Text] [Related]
9. Molecular diagnosis of maturity-onset diabetes of the young in a cohort of Chinese children.
Xu A; Lin Y; Sheng H; Cheng J; Mei H; Ting TH; Zeng C; Liang C; Zhang W; Li C; Li X; Liu L
Pediatr Diabetes; 2020 May; 21(3):431-440. PubMed ID: 31957151
[TBL] [Abstract][Full Text] [Related]
10. Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing.
Ağladıoğlu SY; Aycan Z; Çetinkaya S; Baş VN; Önder A; Peltek Kendirci HN; Doğan H; Ceylaner S
J Pediatr Endocrinol Metab; 2016 Apr; 29(4):487-96. PubMed ID: 26669242
[TBL] [Abstract][Full Text] [Related]
11. Next-generation sequencing identifies monogenic diabetes in 16% of patients with late adolescence/adult-onset diabetes selected on a clinical basis: a cross-sectional analysis.
Donath X; Saint-Martin C; Dubois-Laforgue D; Rajasingham R; Mifsud F; Ciangura C; Timsit J; Bellanné-Chantelot C;
BMC Med; 2019 Jul; 17(1):132. PubMed ID: 31291970
[TBL] [Abstract][Full Text] [Related]
12. Glucokinase gene mutations (MODY 2) in Asian Indians.
Kanthimathi S; Jahnavi S; Balamurugan K; Ranjani H; Sonya J; Goswami S; Chowdhury S; Mohan V; Radha V
Diabetes Technol Ther; 2014 Mar; 16(3):180-5. PubMed ID: 24405491
[TBL] [Abstract][Full Text] [Related]
13. Mild fasting hyperglycemia in children: high rate of glucokinase mutations and some risk of developing type 1 diabetes mellitus.
Codner E; Rocha A; Deng L; Martínez-Aguayo A; Godoy C; Mericq V; Chung WK
Pediatr Diabetes; 2009 Sep; 10(6):382-8. PubMed ID: 19309449
[TBL] [Abstract][Full Text] [Related]
14. Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population.
Huang M; Lu X; Dong G; Li J; Chen C; Yu Q; Li M; Su Y
Front Endocrinol (Lausanne); 2021; 12():695426. PubMed ID: 34276565
[TBL] [Abstract][Full Text] [Related]
15. Prevalence of gene mutations in a Chinese 46,XY disorders of sex development cohort detected by targeted next-generation sequencing.
Yu BQ; Liu ZX; Gao YJ; Wang X; Mao JF; Nie M; Wu XY
Asian J Androl; 2021; 23(1):69-73. PubMed ID: 32985417
[TBL] [Abstract][Full Text] [Related]
16. [Maturity-onset diabetes of the young 2 with a novel mutation of glucokinase gene in a Chinese boy and the clinical follow-up].
Li X; Liu L; Liang C; Sheng H; Zhao X
Zhonghua Er Ke Za Zhi; 2014 Nov; 52(11):867-71. PubMed ID: 25582477
[TBL] [Abstract][Full Text] [Related]
17. Clinical whole exome sequencing in early onset diabetes patients.
Kwak SH; Jung CH; Ahn CH; Park J; Chae J; Jung HS; Cho YM; Lee DH; Kim JI; Park KS
Diabetes Res Clin Pract; 2016 Dec; 122():71-77. PubMed ID: 27810688
[TBL] [Abstract][Full Text] [Related]
18. Genetic testing for monogenic diabetes using targeted next-generation sequencing in patients with maturity-onset diabetes of the young.
Szopa M; Ludwig-Gałęzowska A; Radkowski P; Skupień J; Zapała B; Płatek T; Klupa T; Kieć-Wilk B; Borowiec M; Młynarski W; Wołkow P; Małecki MT
Pol Arch Med Wewn; 2015; 125(11):845-51. PubMed ID: 26552609
[TBL] [Abstract][Full Text] [Related]
19. Frequency and characterization of mutations in genes in a large cohort of patients referred to MODY registry.
Breidbart E; Deng L; Lanzano P; Fan X; Guo J; Leibel RL; LeDuc CA; Chung WK
J Pediatr Endocrinol Metab; 2021 May; 34(5):633-638. PubMed ID: 33852230
[TBL] [Abstract][Full Text] [Related]
20. Identification of Five Novel Variants in Chinese Oculocutaneous Albinism by Targeted Next-Generation Sequencing.
Qiu B; Ma T; Peng C; Zheng X; Yang J
Genet Test Mol Biomarkers; 2018 Apr; 22(4):252-258. PubMed ID: 29437493
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
