日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Validation of an algorithm for selection of SGLT2 and DPP4 inhibitor therapies in people with type 2 diabetes across major UK ethnicity groups: a retrospective cohort study

一项针对英国主要族裔群体中2型糖尿病患者SGLT2和DPP4抑制剂治疗选择算法的验证:一项回顾性队列研究

Güdemann, Laura M; Young, Katherine G; Cardoso, Pedro; Mateen, Bilal A; Holman, Rury R; Sattar, Naveed; Pearson, Ewan R; Hattersley, Andrew T; Jones, Angus G; Shields, Beverley M; Dennis, John M

Type 2 diabetes risk alleles in peptidyl-glycine alpha-amidating monooxygenase influence GLP-1 levels and response to GLP-1 receptor agonists

肽基甘氨酸α-酰胺化单加氧酶中的2型糖尿病风险等位基因会影响GLP-1水平和对GLP-1受体激动剂的反应。

Umapathysivam, Mahesh M; Araldi, Elisa; Hastoy, Benoit; Dawed, Adem Y; Vatandaslar, Hasan; Mayrhofer, Johanna E; Lindquist, Peter; Silva, Pamuditha N; Goga, Algera; Trüllinger, Geraldine O; Godbersen, Svenja; Sengupta, Shahana; Kaufmann, Adrian; Thomsen, Søren Krogsgaard; Hartmann, Bolette; Chen, Yi-Chun; Jonsson, Anna E; Kabakci, Hasan; Thaman, Swaraj; Grarup, Niels; Have, Christian T; Pallo, Lindsay P; Faerch, Kristine; Gjesing, Anette P; Nawaz, Sameena; Cheeseman, Jane; Neville, Matthew J; Pedersen, Oluf; Walker, Mark; Sun, Han; Jennison, Christopher; Hattersley, Andrew T; Rehfeld, Jens F; Holman, Rury R; Verchere, Bruce C; Hansen, Torben; Karpe, Fredrik; Holst, Jens J; Rosenkilde, Mette M; Jones, Angus G; Ristow, Michael; McCarthy, Mark I; Pearson, Ewan R; Stoffel, Markus; Gloyn, Anna L

Genotype-first approach reveals monogenic lipodystrophy is underdiagnosed, with health and mortality risks

基因型优先检测方法揭示单基因脂肪营养不良症诊断不足,存在健康和死亡风险。

Sharp, Luke N; Colclough, Kevin; Murray Leech, Jacques; Evans, Amy V; Hattersley, Andrew T; Weedon, Michael N; Brown, Rebecca J; Patel, Kashyap A

Loss of function variants in the primate-specific gene ZNF808 cause neonatal, transient and adult-onset diabetes

灵长类特异性基因 ZNF808 的功能缺失变异会导致新生儿糖尿病、暂时性糖尿病和成人发病型糖尿病。

Russ-Silsby, James; Colclough, Kevin; Johnson, Matthew B; Wakeling, Matthew N; Owens, Nick D L; Amaratunga, Shenali A; Flanagan, Sarah E; Patel, Kashyap A; Hattersley, Andrew T; De Franco, Elisa

Precision medicine in type 2 diabetes: targeting SGLT2 inhibitor treatment for kidney protection

2型糖尿病精准医疗:靶向SGLT2抑制剂治疗以保护肾脏

Jansz, Thijs T; Young, Katherine G; Hopkins, Rhian; McGovern, Andrew P; Shields, Beverley M; Hattersley, Andrew T; Jones, Angus G; Pearson, Ewan R; Bingham, Coralie; Oram, Richard A; Dennis, John M

Bi-allelic variants in the non-protein-coding minor spliceosome components RNU6ATAC and RNU4ATAC cause syndromic monogenic autoimmune diabetes

非蛋白质编码的次要剪接体组分 RNU6ATAC 和 RNU4ATAC 的双等位基因变异会导致综合征型单基因自身免疫性糖尿病

Johnson, Matthew B; Russ-Silsby, James; Blair, Paul A; Govier, Molly; Bonfield, Georgia; Domingo-Vila, Clara; Wakeling, Matthew N; Oram, Richard A; Flanagan, Sarah E; Tree, Timothy I M; Patel, Kashyap A; Hattersley, Andrew T; De Franco, Elisa

Biallelic Pathogenic Variants in IL2RA Cause Neonatal-Onset Monogenic Autoimmune Diabetes

IL2RA基因的双等位致病变异导致新生儿期发病的单基因自身免疫性糖尿病

Bonfield, Georgia; Russ-Silsby, James; Ramchand, Suraj; Luckett, Amber M; Wakeling, Matthew N; Kulkarni, Abhishek; Nagesh, V Sri; Deeb, Asma; Ravikumar, K G; Nguyen, Phuong T K; Hattersley, Andrew T; Oram, Richard A; Flanagan, Sarah E; De Franco, Elisa; Johnson, Matthew B

MODY Is Prevalent in Later-Onset Diabetes and Has Potential for Targeted Therapy but Is Challenging to Identify

MODY在晚发型糖尿病中较为常见,具有靶向治疗的潜力,但识别难度较大。

Sharp, Luke N; Mirshahi, Uyenlinh L; Colclough, Kevin; Hall, Timothy S; Haley, Jeremy S; Cannon, Stuart J; Laver, Thomas W; Weedon, Michael N; Hattersley, Andrew T; Carey, David J; Patel, Kashyap A

The contribution of maternal glucose to birth weight is smaller in Uganda (sub-Saharan Africa) than in Afro-Caribbean or white ethnicity mother-child pairs from outside Africa

在乌干达(撒哈拉以南非洲),母体血糖对新生儿出生体重的贡献小于非洲以外地区的非裔加勒比人或白种人母婴。

Nakanga, Wisdom P; Sekitoleko, Isaac; Andrews, Rob C; Hughes, Alice E; Tino, Salome; Freathy, Rachel M; Shields, Beverley M; Lowe, William L; Jones, Angus; Hattersley, Andrew T; Nyirenda, Moffat J

Children With Diabetes and At Least One Non-Autoimmune Feature Should Be Considered for Monogenic Diabetes Testing

患有糖尿病且至少伴有一种非自身免疫特征的儿童应考虑进行单基因糖尿病检测。

Myers, Rebecca; Yildiz, Melek; Nuri Ozbek, Mehmet; Manzoor, Jaida; Ibrahim, Mohsina; Yajnik, Chittaranjan; Atar, Muge; Şiklar, Zeynep; Acar, Sezer; Globa, Evgenia; Magdy Omar, Omneya; Demirbilek, Huseyin; Hassan, Samar; Demir, Korcan; Hanif, Misbah; Guran, Tulay; Hatipoglu, Nihal; Koçyiğit, Cemil; Colclough, Kevin; Houghton, Jayne; Hattersley, Andrew; Van Heugten, Rachel; Patel, Kashyap