Creemers JW - Search Results

1

Common nonsynonymous variants in PCSK1 confer risk of obesity.

Benzinou M, Creemers JW, Choquet H, Lobbens S, Dina C, Durand E, Guerardel A, Boutin P, Jouret B, Heude B, Balkau B, Tichet J, Marre M, Potoczna N, Horber F, Le Stunff C, Czernichow S, Sandbaek A, Lauritzen T, Borch-Johnsen K, Andersen G, Kiess W, Körner A, Kovacs P, Jacobson P, Carlsson LM, Walley AJ, Jørgensen T, Hansen T, Pedersen O, Meyre D, Froguel P. Benzinou M, et al. Among authors: creemers jw. Nat Genet. 2008 Aug;40(8):943-5. doi: 10.1038/ng.177. Epub 2008 Jul 6. Nat Genet. 2008. PMID: 18604207

2

A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity.

Philippe J, Stijnen P, Meyre D, De Graeve F, Thuillier D, Delplanque J, Gyapay G, Sand O, Creemers JW, Froguel P, Bonnefond A. Philippe J, et al. Among authors: creemers jw. Int J Obes (Lond). 2015 Feb;39(2):295-302. doi: 10.1038/ijo.2014.96. Epub 2014 Jun 3. Int J Obes (Lond). 2015. PMID: 24890885

3

Functional and clinical relevance of novel and known PCSK1 variants for childhood obesity and glucose metabolism.

Löffler D, Behrendt S, Creemers JWM, Klammt J, Aust G, Stanik J, Kiess W, Kovacs P, Körner A. Löffler D, et al. Mol Metab. 2016 Dec 8;6(3):295-305. doi: 10.1016/j.molmet.2016.12.002. eCollection 2017 Mar. Mol Metab. 2016. PMID: 28271036 Free PMC article.

4

Genetic and functional characterization of PCSK1.

Choquet H, Stijnen P, Creemers JW. Choquet H, et al. Among authors: creemers jw. Methods Mol Biol. 2011;768:247-53. doi: 10.1007/978-1-61779-204-5_13. Methods Mol Biol. 2011. PMID: 21805247

5

Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity.

Creemers JW, Choquet H, Stijnen P, Vatin V, Pigeyre M, Beckers S, Meulemans S, Than ME, Yengo L, Tauber M, Balkau B, Elliott P, Jarvelin MR, Van Hul W, Van Gaal L, Horber F, Pattou F, Froguel P, Meyre D. Creemers JW, et al. Diabetes. 2012 Feb;61(2):383-90. doi: 10.2337/db11-0305. Epub 2011 Dec 30. Diabetes. 2012. PMID: 22210313 Free PMC article.

6

Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene.

Jackson RS, Creemers JW, Ohagi S, Raffin-Sanson ML, Sanders L, Montague CT, Hutton JC, O'Rahilly S. Jackson RS, et al. Among authors: creemers jw. Nat Genet. 1997 Jul;16(3):303-6. doi: 10.1038/ng0797-303. Nat Genet. 1997. PMID: 9207799

7

The association of common variants in PCSK1 with obesity: a HuGE review and meta-analysis.

Stijnen P, Tuand K, Varga TV, Franks PW, Aertgeerts B, Creemers JW. Stijnen P, et al. Among authors: creemers jw. Am J Epidemiol. 2014 Dec 1;180(11):1051-65. doi: 10.1093/aje/kwu237. Epub 2014 Oct 29. Am J Epidemiol. 2014. PMID: 25355447 Review.

8

PCSK1 Mutations and Human Endocrinopathies: From Obesity to Gastrointestinal Disorders.

Stijnen P, Ramos-Molina B, O'Rahilly S, Creemers JW. Stijnen P, et al. Among authors: creemers jw. Endocr Rev. 2016 Aug;37(4):347-71. doi: 10.1210/er.2015-1117. Epub 2016 May 17. Endocr Rev. 2016. PMID: 27187081 Review.

9

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism.

Challis BG, Pritchard LE, Creemers JW, Delplanque J, Keogh JM, Luan J, Wareham NJ, Yeo GS, Bhattacharyya S, Froguel P, White A, Farooqi IS, O'Rahilly S. Challis BG, et al. Among authors: creemers jw. Hum Mol Genet. 2002 Aug 15;11(17):1997-2004. doi: 10.1093/hmg/11.17.1997. Hum Mol Genet. 2002. PMID: 12165561

10

Endoplasmic reticulum-associated degradation of the mouse PC1/3-N222D hypomorph and human PCSK1 mutations contributes to obesity.

Stijnen P, Brouwers B, Dirkx E, Ramos-Molina B, Van Lommel L, Schuit F, Thorrez L, Declercq J, Creemers JW. Stijnen P, et al. Among authors: creemers jw. Int J Obes (Lond). 2016 Jun;40(6):973-81. doi: 10.1038/ijo.2016.3. Epub 2016 Jan 20. Int J Obes (Lond). 2016. PMID: 26786350

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