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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 4 |
2022 | 2 |
2023 | 2 |
2024 | 1 |
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7 results
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Page 1
Proposed protocol for selection of living kidney donors with diabetes excludes >99% of people with diabetes.
Clin Transplant. 2024 Jan;38(1):e15179. doi: 10.1111/ctr.15179. Epub 2023 Nov 13.
Clin Transplant. 2024.
PMID: 37955617
Free PMC article.
No abstract available.
Genotype-stratified treatment for monogenic insulin resistance: a systematic review.
Semple RK, Patel KA, Auh S; ADA/EASD PMDI; Brown RJ.
Semple RK, et al.
Commun Med (Lond). 2023 Oct 5;3(1):134. doi: 10.1038/s43856-023-00368-9.
Commun Med (Lond). 2023.
PMID: 37794082
Free PMC article.
Item in Clipboard
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinism.
Wakeling MN, Owens NDL, Hopkinson JR, Johnson MB, Houghton JAL, Dastamani A, Flaxman CS, Wyatt RC, Hewat TI, Hopkins JJ, Laver TW, van Heugten R, Weedon MN, De Franco E, Patel KA, Ellard S, Morgan NG, Cheesman E, Banerjee I, Hattersley AT, Dunne MJ; International Congenital Hyperinsulinism Consortium; Richardson SJ, Flanagan SE.
Wakeling MN, et al.
Nat Genet. 2022 Nov;54(11):1615-1620. doi: 10.1038/s41588-022-01204-x. Epub 2022 Nov 4.
Nat Genet. 2022.
PMID: 36333503
Free PMC article.
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Birth weight and diazoxide unresponsiveness strongly predict the likelihood of congenital hyperinsulinism due to a mutation in ABCC8 or KCNJ11.
Hewat TI, Yau D, Jerome JCS, Laver TW, Houghton JAL, Shields BM, Flanagan SE, Patel KA.
Hewat TI, et al.
Eur J Endocrinol. 2021 Oct 30;185(6):813-818. doi: 10.1530/EJE-21-0476.
Eur J Endocrinol. 2021.
PMID: 34633981
Free PMC article.
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Association of birthweight and penetrance of diabetes in individuals with HNF4A-MODY: a cohort study.
Locke JM, Dusatkova P, Colclough K, Hughes AE, Dennis JM, Shields B, Flanagan SE, Shepherd MH, Dempster EL, Hattersley AT, Weedon MN, Pruhova S, Patel KA.
Locke JM, et al.
Diabetologia. 2022 Jan;65(1):246-249. doi: 10.1007/s00125-021-05581-6. Epub 2021 Oct 7.
Diabetologia. 2022.
PMID: 34618178
Free PMC article.
No abstract available.
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Unreliability of genotyping arrays for detecting very rare variants in human genetic studies: Example from a recent study of MC4R.
Weedon MN, Wright CF, Patel KA, Frayling TM.
Weedon MN, et al.
Cell. 2021 Apr 1;184(7):1651. doi: 10.1016/j.cell.2021.03.015.
Cell. 2021.
PMID: 33798434
Free PMC article.
No abstract available.
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Loss of MANF Causes Childhood-Onset Syndromic Diabetes Due to Increased Endoplasmic Reticulum Stress.
Montaser H, Patel KA, Balboa D, Ibrahim H, Lithovius V, Näätänen A, Chandra V, Demir K, Acar S, Ben-Omran T, Colclough K, Locke JM, Wakeling M, Lindahl M, Hattersley AT, Saarimäki-Vire J, Otonkoski T.
Montaser H, et al.
Diabetes. 2021 Apr;70(4):1006-1018. doi: 10.2337/db20-1174. Epub 2021 Jan 26.
Diabetes. 2021.
PMID: 33500254
Free PMC article.
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