Sadler MC - Search Results

1

Exploiting the mediating role of the metabolome to unravel transcript-to-phenotype associations.

Auwerx C, Sadler MC, Woh T, Reymond A, Kutalik Z, Porcu E. Auwerx C, et al. Elife. 2023 Mar 9;12:e81097. doi: 10.7554/eLife.81097. Elife. 2023. PMID: 36891970 Free PMC article.

2

Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome.

Porcu E, Sadler MC, Lepik K, Auwerx C, Wood AR, Weihs A, Sleiman MSB, Ribeiro DM, Bandinelli S, Tanaka T, Nauck M, Völker U, Delaneau O, Metspalu A, Teumer A, Frayling T, Santoni FA, Reymond A, Kutalik Z. Porcu E, et al. Nat Commun. 2021 Sep 24;12(1):5647. doi: 10.1038/s41467-021-25805-y. Nat Commun. 2021. PMID: 34561431 Free PMC article.

3

Mendelian randomization to assess causality between uromodulin, blood pressure and chronic kidney disease.

Ponte B, Sadler MC, Olinger E, Vollenweider P, Bochud M, Padmanabhan S, Hayward C, Kutalik Z, Devuyst O. Ponte B, et al. Kidney Int. 2021 Dec;100(6):1282-1291. doi: 10.1016/j.kint.2021.08.032. Epub 2021 Oct 9. Kidney Int. 2021. PMID: 34634361 Free article.

4

The individual and global impact of copy-number variants on complex human traits.

Auwerx C, Lepamets M, Sadler MC, Patxot M, Stojanov M, Baud D, Mägi R; Estonian Biobank Research Team; Porcu E, Reymond A, Kutalik Z. Auwerx C, et al. Am J Hum Genet. 2022 Apr 7;109(4):647-668. doi: 10.1016/j.ajhg.2022.02.010. Epub 2022 Mar 2. Am J Hum Genet. 2022. PMID: 35240056 Free PMC article.

5

From pharmacogenetics to pharmaco-omics: Milestones and future directions.

Auwerx C, Sadler MC, Reymond A, Kutalik Z. Auwerx C, et al. HGG Adv. 2022 Mar 16;3(2):100100. doi: 10.1016/j.xhgg.2022.100100. eCollection 2022 Apr 14. HGG Adv. 2022. PMID: 35373152 Free PMC article. Review.

6

Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.

Giannuzzi G, Chatron N, Mannik K, Auwerx C, Pradervand S, Willemin G, Hoekzema K, Nuttle X, Chrast J, Sadler MC, Porcu E; 16p11.2 Consortium; Herault Y, Isidor B, Gilbert-Dussardier B, Eichler EE, Kutalik Z, Reymond A. Giannuzzi G, et al. NPJ Genom Med. 2022 Jun 17;7(1):38. doi: 10.1038/s41525-022-00308-x. NPJ Genom Med. 2022. PMID: 35715439 Free PMC article.

7

Sex- and age-dependent genetics of longevity in a heterogeneous mouse population.

Bou Sleiman M, Roy S, Gao AW, Sadler MC, von Alvensleben GVG, Li H, Sen S, Harrison DE, Nelson JF, Strong R, Miller RA, Kutalik Z, Williams RW, Auwerx J. Bou Sleiman M, et al. Science. 2022 Sep 30;377(6614):eabo3191. doi: 10.1126/science.abo3191. Epub 2022 Sep 30. Science. 2022. PMID: 36173858 Free PMC article.

8

Quantifying the role of transcript levels in mediating DNA methylation effects on complex traits and diseases.

Sadler MC, Auwerx C, Lepik K, Porcu E, Kutalik Z. Sadler MC, et al. Nat Commun. 2022 Dec 7;13(1):7559. doi: 10.1038/s41467-022-35196-3. Nat Commun. 2022. PMID: 36477627 Free PMC article.

9

The impact of 22q11.2 copy-number variants on human traits in the general population.

Zamariolli M, Auwerx C, Sadler MC, van der Graaf A, Lepik K, Schoeler T, Moysés-Oliveira M, Dantas AG, Melaragno MI, Kutalik Z. Zamariolli M, et al. Am J Hum Genet. 2023 Feb 2;110(2):300-313. doi: 10.1016/j.ajhg.2023.01.005. Epub 2023 Jan 26. Am J Hum Genet. 2023. PMID: 36706759 Free PMC article.

10

Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.

Giannuzzi G, Chatron N, Mannik K, Auwerx C, Pradervand S, Willemin G, Hoekzema K, Nuttle X, Chrast J, Sadler MC, Porcu E; 16p11.2 Consortium; Herault Y, Isidor B, Gilbert-Dussardier B, Eichler EE, Kutalik Z, Reymond A. Giannuzzi G, et al. NPJ Genom Med. 2023 May 24;8(1):9. doi: 10.1038/s41525-023-00354-z. NPJ Genom Med. 2023. PMID: 37225732 Free PMC article. No abstract available.

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