Hart LM' - Search Results

1

Pharmacogenomics of GLP-1 receptor agonists: a genome-wide analysis of observational data and large randomised controlled trials.

Dawed AY, Mari A, Brown A, McDonald TJ, Li L, Wang S, Hong MG, Sharma S, Robertson NR, Mahajan A, Wang X, Walker M, Gough S, Hart LM', Zhou K, Forgie I, Ruetten H, Pavo I, Bhatnagar P, Jones AG, Pearson ER; DIRECT consortium. Dawed AY, et al. Lancet Diabetes Endocrinol. 2023 Jan;11(1):33-41. doi: 10.1016/S2213-8587(22)00340-0. Lancet Diabetes Endocrinol. 2023. PMID: 36528349 Free article.

2

Preserved GLP-1 and exaggerated GIP secretion in type 2 diabetes and relationships with triglycerides and ALT.

Alssema M, Rijkelijkhuizen JM, Holst JJ, Teerlink T, Scheffer PG, Eekhoff EM, Gastaldelli A, Mari A, Hart LM, Nijpels G, Dekker JM. Alssema M, et al. Eur J Endocrinol. 2013 Sep 12;169(4):421-30. doi: 10.1530/EJE-13-0487. Print 2013 Oct. Eur J Endocrinol. 2013. PMID: 23864340

3

Multi-omics subgroups associated with glycaemic deterioration in type 2 diabetes: an IMI-RHAPSODY Study.

Li S, Dragan I, Tran VDT, Fung CH, Kuznetsov D, Hansen MK, Beulens JWJ, Hart LM', Slieker RC, Donnelly LA, Gerl MJ, Klose C, Mehl F, Simons K, Elders PJM, Pearson ER, Rutter GA, Ibberson M. Li S, et al. Among authors: hart lm. Front Endocrinol (Lausanne). 2024 Mar 6;15:1350796. doi: 10.3389/fendo.2024.1350796. eCollection 2024. Front Endocrinol (Lausanne). 2024. PMID: 38510703 Free PMC article.

4

Association of the insulin-receptor variant Met-985 with hyperglycemia and non-insulin-dependent diabetes mellitus in the Netherlands: a population-based study.

Hart LM, Stolk RP, Heine RJ, Grobbee DE, van der Does FE, Maassen JA. Hart LM, et al. Am J Hum Genet. 1996 Nov;59(5):1119-25. Am J Hum Genet. 1996. PMID: 8900242 Free PMC article. Clinical Trial.

5

Prevalence of variants in candidate genes for type 2 diabetes mellitus in The Netherlands: the Rotterdam study and the Hoorn study.

Hart LM, Stolk RP, Dekker JM, Nijpels G, Grobbee DE, Heine RJ, Maassen JA. Hart LM, et al. J Clin Endocrinol Metab. 1999 Mar;84(3):1002-6. doi: 10.1210/jcem.84.3.5563. J Clin Endocrinol Metab. 1999. PMID: 10084586

6

Reduced second phase insulin secretion in carriers of a sulphonylurea receptor gene variant associating with Type II diabetes mellitus.

Hart LM, Dekker JM, van Haeften TW, Ruige JB, Stehouwer CD, Erkelens DW, Heine RJ, Maassen JA. Hart LM, et al. Diabetologia. 2000 Apr;43(4):515-9. doi: 10.1007/s001250051337. Diabetologia. 2000. PMID: 10819247

7

Association of a leucine(7)-to-proline(7) polymorphism in the signal peptide of neuropeptide Y with high serum cholesterol and LDL cholesterol levels.

Karvonen MK, Pesonen U, Koulu M, Niskanen L, Laakso M, Rissanen A, Dekker JM, Hart LM, Valve R, Uusitupa MI. Karvonen MK, et al. Nat Med. 1998 Dec;4(12):1434-7. doi: 10.1038/4027. Nat Med. 1998. PMID: 9846584 Clinical Trial.

8

Variants in the sulphonylurea receptor gene: association of the exon 16-3t variant with Type II diabetes mellitus in Dutch Caucasians.

Hart LM, de Knijff P, Dekker JM, Stolk RP, Nijpels G, van der Does FE, Ruige JB, Grobbee DE, Heine RJ, Maassen JA. Hart LM, et al. Diabetologia. 1999 May;42(5):617-20. doi: 10.1007/s001250051203. Diabetologia. 1999. PMID: 10333056

9

The impact of genetic variation in the G6PC2 gene on insulin secretion depends on glycemia.

Heni M, Ketterer C, Hart LM, Ranta F, van Haeften TW, Eekhoff EM, Dekker JM, Boomsma DI, Nijpels G, Kramer MH, Diamant M, Simonis-Bik AM, Heine RJ, de Geus EJ, Schäfer SA, Machicao F, Ullrich S, Thamer C, Stefan N, Staiger H, Häring HU, Fritsche A. Heni M, et al. J Clin Endocrinol Metab. 2010 Dec;95(12):E479-84. doi: 10.1210/jc.2010-0860. Epub 2010 Sep 8. J Clin Endocrinol Metab. 2010. PMID: 20826583

10

Characterization of a novel mitochondrial DNA deletion in a patient with a variant of the Pearson marrow-pancreas syndrome.

van den Ouweland JM, de Klerk JB, van de Corput MP, Dirks RW, Raap AK, Scholte HR, Huijmans JG, Hart LM, Bruining GJ, Maassen JA. van den Ouweland JM, et al. Eur J Hum Genet. 2000 Mar;8(3):195-203. doi: 10.1038/sj.ejhg.5200444. Eur J Hum Genet. 2000. PMID: 10780785

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