Smeets HJ - Search Results

1

Simultaneous genotyping of nine polymorphisms in xenobiotic-metabolizing enzymes by multiplex PCR amplification and single base extension.

Knaapen AM, Ketelslegers HB, Gottschalk RW, Janssen RG, Paulussen AD, Smeets HJ, Godschalk RW, Van Schooten FJ, Kleinjans JC, Van Delft JH. Knaapen AM, et al. Among authors: smeets hj. Clin Chem. 2004 Sep;50(9):1664-8. doi: 10.1373/clinchem.2004.034058. Clin Chem. 2004. PMID: 15331501 No abstract available.

2

A functional polymorphism of the mu-opioid receptor gene (OPRM1) influences cue-induced craving for alcohol in male heavy drinkers.

van den Wildenberg E, Wiers RW, Dessers J, Janssen RG, Lambrichs EH, Smeets HJ, van Breukelen GJ. van den Wildenberg E, et al. Among authors: smeets hj. Alcohol Clin Exp Res. 2007 Jan;31(1):1-10. doi: 10.1111/j.1530-0277.2006.00258.x. Alcohol Clin Exp Res. 2007. PMID: 17207095

3

Serotonin transporter polymorphisms and the occurrence of adverse events during treatment with selective serotonin reuptake inhibitors.

Smits K, Smits L, Peeters F, Schouten J, Janssen R, Smeets H, van Os J, Prins M. Smits K, et al. Int Clin Psychopharmacol. 2007 May;22(3):137-43. doi: 10.1097/YIC.0b013e328014822a. Int Clin Psychopharmacol. 2007. PMID: 17414739

4

Polyhydramnios and cerebellar atrophy: a prenatal presentation of mitochondrial encephalomyopathy caused by mutations in the FBXL4 gene.

van Rij MC, Jansen FA, Hellebrekers DM, Onkenhout W, Smeets HJ, Hendrickx AT, Gottschalk RW, Steggerda SJ, Peeters-Scholte CM, Haak MC, Hilhorst-Hofstee Y. van Rij MC, et al. Among authors: smeets hj. Clin Case Rep. 2016 Mar 16;4(4):425-8. doi: 10.1002/ccr3.511. eCollection 2016 Apr. Clin Case Rep. 2016. PMID: 27099744 Free PMC article.

5

A comprehensive strategy for exome-based preconception carrier screening.

Sallevelt SCEH, de Koning B, Szklarczyk R, Paulussen ADC, de Die-Smulders CEM, Smeets HJM. Sallevelt SCEH, et al. Genet Med. 2017 May;19(5):583-592. doi: 10.1038/gim.2016.153. Epub 2016 Oct 27. Genet Med. 2017. PMID: 28492530 Free article.

6

Preimplantation genetic diagnosis for mitochondrial DNA mutations: analysis of one blastomere suffices.

Sallevelt SCEH, Dreesen JCFM, Coonen E, Paulussen ADC, Hellebrekers DMEI, de Die-Smulders CEM, Smeets HJM, Lindsey P. Sallevelt SCEH, et al. J Med Genet. 2017 Oct;54(10):693-697. doi: 10.1136/jmedgenet-2017-104633. Epub 2017 Jul 1. J Med Genet. 2017. PMID: 28668821

7

The influence of 5-HTTLPR and STin2 polymorphisms in the serotonin transporter gene on treatment effect of selective serotonin reuptake inhibitors in depressive patients.

Smits KM, Smits LJ, Peeters FP, Schouten JS, Janssen RG, Smeets HJ, van Os J, Prins MH. Smits KM, et al. Among authors: smeets hj. Psychiatr Genet. 2008 Aug;18(4):184-90. doi: 10.1097/YPG.0b013e3283050aca. Psychiatr Genet. 2008. PMID: 18628680

8

HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency.

Paulussen AD, Raes A, Jongbloed RJ, Gilissen RA, Wilde AA, Snyders DJ, Smeets HJ, Aerssens J. Paulussen AD, et al. Among authors: smeets hj. Cardiovasc Res. 2005 Aug 15;67(3):467-75. doi: 10.1016/j.cardiores.2005.05.017. Cardiovasc Res. 2005. PMID: 15958262

9

Modeling genetic and environmental factors to increase heritability and ease the identification of candidate genes for birth weight: a twin study.

Gielen M, Lindsey PJ, Derom C, Smeets HJ, Souren NY, Paulussen AD, Derom R, Nijhuis JG. Gielen M, et al. Among authors: smeets hj. Behav Genet. 2008 Jan;38(1):44-54. doi: 10.1007/s10519-007-9170-3. Epub 2007 Dec 22. Behav Genet. 2008. PMID: 18157630 Free PMC article.

10

Mitochondrial DNA copy number in colorectal cancer: between tissue comparisons, clinicopathological characteristics and survival.

van Osch FH, Voets AM, Schouten LJ, Gottschalk RW, Simons CC, van Engeland M, Lentjes MH, van den Brandt PA, Smeets HJ, Weijenberg MP. van Osch FH, et al. Among authors: smeets hj. Carcinogenesis. 2015 Dec;36(12):1502-10. doi: 10.1093/carcin/bgv151. Epub 2015 Oct 17. Carcinogenesis. 2015. PMID: 26476438

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