April 2024
1. ZHAO Y, Chukanova M, Kentistou KA, Fairhurst-Hunter Z, et al
   Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease.
   Nat Genet. 2024 Apr 4. doi: 10.1038/s41588-024-01694.
   

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   March 2024
2. LI W
   Genetic contribution to heterogeneity in type 2 diabetes.
   Nat Genet. 2024;56:357.
   

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   February 2024
3. CISSE AH, Freathy RM
   New insights into the genetics of diabetes in pregnancy.
   Nat Genet. 2024 Feb 27. doi: 10.1038/s41588-024-01675.
   

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   January 2024
4. ELLIOTT A, Walters RK, Pirinen M, Kurki M, et al
   Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes.
   Nat Genet. 2024 Jan 5. doi: 10.1038/s41588-023-01607.
   

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5. HOMILIUS M, Zhu W, Eddy SS, Thompson PC, et al
   Perturbational phenotyping of human blood cells reveals genetically determined latent traits associated with subsets of common diseases.
   Nat Genet. 2024;56:37-50.
   

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   September 2023
6. LAGOU V, Jiang L, Ulrich A, Zudina L, et al
   GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification.
   Nat Genet. 2023;55:1448-1461.
   

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   June 2023
7. WILLIAMSON A, Norris DM, Yin X, Broadaway KA, et al
   Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake.
   Nat Genet. 2023;55:973-983.
   

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   May 2023
8. WANG G, Chiou J, Zeng C, Miller M, et al
   Integrating genetics with single-cell multiomic measurements across disease states identifies mechanisms of beta cell dysfunction in type 2 diabetes.
   Nat Genet. 2023 May 25. doi: 10.1038/s41588-023-01397.
   

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   January 2023
9. WAGNER BK
   Identifying type 2 diabetes risk genes by beta-cell CRISPR screening.
   Nat Genet. 2023;55:4-5.
   

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   December 2022
10. ROTTNER AK, Ye Y, Navarro-Guerrero E, Rajesh V, et al
    A genome-wide CRISPR screen identifies CALCOCO2 as a regulator of beta cell function influencing type 2 diabetes risk.
    Nat Genet. 2022 Dec 21. doi: 10.1038/s41588-022-01261.
    

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    October 2022
11. DORNBOS P, Koesterer R, Ruttenburg A, Nguyen T, et al
    A combined polygenic score of 21,293 rare and 22 common variants improves diabetes diagnosis based on hemoglobin A1C levels.
    Nat Genet. 2022 Oct 24. pii: 10.1038/s41588-022-01200.
    

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    May 2022
12. MAHAJAN A, Spracklen CN, Zhang W, Ng MCY, et al
    Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
    Nat Genet. 2022;54:560-572.
    

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    March 2022
13. JURGENS SJ, Choi SH, Morrill VN, Chaffin M, et al
    Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank.
    Nat Genet. 2022;54:240-250.
    

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    November 2021
14. MANSOUR ALY D, Dwivedi OP, Prasad RB, Karajamaki A, et al
    Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes.
    Nat Genet. 2021 Nov 4. pii: 10.1038/s41588-021-00948.
    

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