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Items: 1 to 20 of 61

1.

Mutation analysis of WNT10B in obese children, adolescents and adults.

Van Camp JK, Zegers D, Verhulst SL, Van Hoorenbeeck K, Massa G, Verrijken A, Desager KN, Van Gaal LF, Van Hul W, Beckers S.

Endocrine. 2013 Aug;44(1):107-13. doi: 10.1007/s12020-012-9824-7. Epub 2012 Oct 27.

PMID:
23104151
2.

Genetic association between WNT10B polymorphisms and obesity in a Belgian case-control population is restricted to males.

Van Camp JK, Beckers S, Zegers D, Verrijken A, Van Gaal LF, Van Hul W.

Mol Genet Metab. 2012 Mar;105(3):489-93. doi: 10.1016/j.ymgme.2011.11.197. Epub 2011 Dec 2.

PMID:
22189080
3.

WNT10B mutations in human obesity.

Christodoulides C, Scarda A, Granzotto M, Milan G, Dalla Nora E, Keogh J, De Pergola G, Stirling H, Pannacciulli N, Sethi JK, Federspil G, Vidal-Puig A, Farooqi IS, O'Rahilly S, Vettor R.

Diabetologia. 2006 Apr;49(4):678-84. Epub 2006 Feb 14.

4.

Prevalence of rare MC3R variants in obese cases and lean controls.

Zegers D, Beckers S, Hendrickx R, Van Camp JK, Van Hoorenbeeck K, Desager KN, Massa G, Van Gaal LF, Van Hul W.

Endocrine. 2013 Oct;44(2):386-90. doi: 10.1007/s12020-012-9862-1. Epub 2012 Dec 24.

PMID:
23264184
5.

Missense mutations and polymorphisms of the MC4R gene in Polish obese children and adolescents in relation to the relative body mass index.

Nowacka-Woszuk J, Cieslak J, Skowronska B, Majewska KA, Stankiewicz W, Fichna P, Switonski M.

J Appl Genet. 2011 Aug;52(3):319-23. doi: 10.1007/s13353-011-0036-2. Epub 2011 Mar 15.

6.

No important role for genetic variation in the Chibby gene in monogenic and complex obesity.

Van Camp JK, Zegers D, Verhulst SL, Van Hoorenbeeck K, Massa G, Verrijken A, Desager KN, Van Gaal LF, Van Hul W, Beckers S.

Mol Biol Rep. 2013 Jul;40(7):4491-8. doi: 10.1007/s11033-013-2541-3. Epub 2013 May 5.

PMID:
23645032
7.

Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjects.

Siddiq A, Gueorguiev M, Samson C, Hercberg S, Heude B, Levy-Marchal C, Jouret B, Weill J, Meyre D, Walley A, Froguel P.

Diabetologia. 2007 Mar;50(3):574-84. Epub 2007 Jan 18.

PMID:
17235527
8.

Investigation of common and rare genetic variation in the BAMBI genomic region in light of human obesity.

Van Camp JK, De Freitas F, Zegers D, Beckers S, Verhulst SL, Van Hoorenbeeck K, Massa G, Verrijken A, Desager KN, Van Gaal LF, Van Hul W.

Endocrine. 2016 May;52(2):277-86. doi: 10.1007/s12020-015-0778-4. Epub 2015 Oct 26.

PMID:
26499194
9.

Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.

Friedel S, Reichwald K, Scherag A, Brumm H, Wermter AK, Fries HR, Koberwitz K, Wabitsch M, Meitinger T, Platzer M, Biebermann H, Hinney A, Hebebrand J.

BMC Genet. 2007 May 3;8:17.

10.

Genetic and structural variation in the SH2B1 gene in the Belgian population.

Aerts E, Beckers S, Zegers D, Van Camp JK, Van Hoorenbeeck K, Massa G, Verrijken A, Mertens IL, Verhulst SL, Rooman RR, Van Gaal LF, Van Hul W.

Mol Genet Metab. 2015 Aug;115(4):193-8. doi: 10.1016/j.ymgme.2015.05.010. Epub 2015 May 27.

PMID:
26031769
11.

Identification of sequence variants in the UBL5 (ubiquitin-like 5 or BEACON) gene in obese children by PCR-SSCP: no evidence for association with obesity.

Sentinelli F, Romeo S, Cambuli VM, Cossu E, Cavallo MG, Zavarella S, Spoletini M, Buzzetti R, Baroni MG.

J Pediatr Endocrinol Metab. 2008 Dec;21(12):1139-45.

PMID:
19189687
12.

Screening for genetic variants in BDNF that contribute to childhood obesity.

Zegers D, Hendrickx R, Verrijken A, Van Hoorenbeeck K, Van Camp JK, de Craemer V, Rooman RP, Desager KN, Massa G, Van Gaal LF, Van Hul W, Beckers S.

Pediatr Obes. 2014 Feb;9(1):36-42. doi: 10.1111/j.2047-6310.2012.00131.x. Epub 2013 Jan 16.

PMID:
23325614
13.

A functional promoter polymorphism -607G>C of WNT10B is associated with abdominal fat in Korean female subjects.

Kim IC, Cha MH, Kim DM, Lee H, Moon JS, Choi SM, Kim KS, Yoon Y.

J Nutr Biochem. 2011 Mar;22(3):252-8. doi: 10.1016/j.jnutbio.2010.02.002. Epub 2010 Jun 25.

PMID:
20579865
14.

Genetic association study of WNT10B polymorphisms with BMD and adiposity parameters in Danish and Belgian males.

Van Camp JK, Beckers S, Zegers D, Boudin E, Nielsen TL, Andersen M, Roef G, Taes Y, Brixen K, Van Hul W.

Endocrine. 2013 Aug;44(1):247-54. doi: 10.1007/s12020-012-9869-7. Epub 2013 Jan 17.

PMID:
23325361
15.

Identification of three novel genetic variants in the melanocortin-3 receptor of obese children.

Zegers D, Beckers S, de Freitas F, Peeters AV, Mertens IL, Verhulst SL, Rooman RP, Timmermans JP, Desager KN, Massa G, Van Gaal LF, Van Hul W.

Obesity (Silver Spring). 2011 Jan;19(1):152-9. doi: 10.1038/oby.2010.127. Epub 2010 Jun 10.

16.

Mutation analysis of NR0B2 among 1545 Danish men identifies a novel c.278G>A (p.G93D) variant with reduced functional activity.

Echwald SM, Andersen KL, Sørensen TI, Larsen LH, Andersen T, Tonooka N, Tomura H, Takeda J, Pedersen O.

Hum Mutat. 2004 Nov;24(5):381-7.

PMID:
15459958
17.

Nucleotide variation of sFRP5 gene is not associated with obesity in children and adolescents.

Van Camp JK, Beckers S, Zegers D, Verhulst SL, Van Hoorenbeeck K, Massa G, Verrijken A, Desager KN, Van Gaal LF, Van Hul W.

Mol Biol Rep. 2016 Oct;43(10):1041-7. doi: 10.1007/s11033-016-4050-7. Epub 2016 Aug 6.

PMID:
27497818
18.

No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in Germans.

Wang HJ, Wermter AK, Nguyen TT, Scherag A, Reichwald K, Waldenmaier B, Lichtner P, Bettecken T, Hebebrand J, Hinney A.

Horm Metab Res. 2007 Nov;39(11):840-4.

PMID:
17992642
19.

Identification and functional characterization of three novel human melanocortin-4 receptor gene variants in an obese Chinese population.

Rong R, Tao YX, Cheung BM, Xu A, Cheung GC, Lam KS.

Clin Endocrinol (Oxf). 2006 Aug;65(2):198-205.

PMID:
16886960
20.

Expression and the clinical significance of Wnt10a and Wnt10b in endometrial cancer are associated with the Wnt/β-catenin pathway.

Chen H, Wang Y, Xue F.

Oncol Rep. 2013 Feb;29(2):507-14. doi: 10.3892/or.2012.2126. Epub 2012 Nov 7.

PMID:
23135473

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