Ribasés M - Search Results

1

Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.

Winsvold BS, Harder AVE, Ran C, Chalmer MA, Dalmasso MC, Ferkingstad E, Tripathi KP, Bacchelli E, Børte S, Fourier C, Petersen AS, Vijfhuizen LS, Magnusson SH, O'Connor E, Bjornsdottir G, Häppölä P, Wang YF, Callesen I, Kelderman T, Gallardo VJ, de Boer I, Olofsgård FJ, Heinze K, Lund N, Thomas LF, Hsu CL, Pirinen M, Hautakangas H, Ribasés M, Guerzoni S, Sivakumar P, Yip J, Heinze A, Küçükali F, Ostrowski SR, Pedersen OB, Kristoffersen ES, Martinsen AE, Artigas MS, Lagrata S, Cainazzo MM, Adebimpe J, Quinn O, Göbel C, Cirkel A, Volk AE, Heilmann-Heimbach S, Skogholt AH, Gabrielsen ME, Wilbrink LA, Danno D, Mehta D, Guðbjartsson DF; HUNT All-In Headache, The International Headache Genetics Consortium, DBDS Genomic Consortium; Rosendaal FR, Willems van Dijk K, Fronczek R, Wagner M, Scherer M, Göbel H, Sleegers K, Sveinsson OA, Pani L, Zoli M, Ramos-Quiroga JA, Dardiotis E, Steinberg A, Riedel-Heller S, Sjöstrand C, Thorgeirsson TE, Stefansson H, Southgate L, Trembath RC, Vandrovcova J, Noordam R, Paemeleire K, Stefansson K, Fann CS, Waldenlind E, Tronvik E, Jensen RH, Chen SP, Houlden H, Terwindt GM, Kubisch C, Maestrini E, Vikelis M, Pozo-Rosich P, Belin AC, Matharu M, van d… See abstract for full author list ➔ Winsvold BS, et al. Among authors: ribases m. Ann Neurol. 2023 Oct;94(4):713-726. doi: 10.1002/ana.26743. Epub 2023 Aug 7. Ann Neurol. 2023. PMID: 37486023 Free PMC article.

2

The 5-HT(2A) -1438G/A polymorphism in anorexia nervosa: a combined analysis of 316 trios from six European centres.

Gorwood P, Adès J, Bellodi L, Cellini E, Collier DA, Di Bella D, Di Bernardo M, Estivill X, Fernandez-Aranda F, Gratacos M, Hebebrand J, Hinney A, Hu X, Karwautz A, Kipman A, Mouren-Siméoni MC, Nacmias B, Ribasés M, Remschmidt H, Ricca V, Rotella CM, Sorbi S, Treasure J; EC Framework V 'Factors in Healthy Eating' consortium. Gorwood P, et al. Among authors: ribases m. Mol Psychiatry. 2002;7(1):90-4. doi: 10.1038/sj.mp.4000938. Mol Psychiatry. 2002. PMID: 11803452

3

Contribution of the serotoninergic system to anxious and depressive traits that may be partially responsible for the phenotypical variability of bulimia nervosa.

Ribasés M, Fernández-Aranda F, Gratacòs M, Mercader JM, Casasnovas C, Núñez A, Vallejo J, Estivill X. Ribasés M, et al. J Psychiatr Res. 2008 Jan;42(1):50-7. doi: 10.1016/j.jpsychires.2006.09.001. Epub 2006 Oct 20. J Psychiatr Res. 2008. PMID: 17055531

4

Altered brain-derived neurotrophic factor blood levels and gene variability are associated with anorexia and bulimia.

Mercader JM, Ribasés M, Gratacòs M, González JR, Bayés M, de Cid R, Badía A, Fernández-Aranda F, Estivill X. Mercader JM, et al. Among authors: ribases m. Genes Brain Behav. 2007 Nov;6(8):706-16. doi: 10.1111/j.1601-183X.2007.00301.x. Epub 2007 Mar 21. Genes Brain Behav. 2007. PMID: 17376155 Free article.

5

5' UTR-region SNP in the NTRK3 gene is associated with panic disorder.

Armengol L, Gratacòs M, Pujana MA, Ribasés M, Martín-Santos R, Estivill X. Armengol L, et al. Among authors: ribases m. Mol Psychiatry. 2002;7(9):928-30. doi: 10.1038/sj.mp.4001134. Mol Psychiatry. 2002. PMID: 12399943 No abstract available.

6

Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa.

Gabrovsek M, Brecelj-Anderluh M, Bellodi L, Cellini E, Di Bella D, Estivill X, Fernandez-Aranda F, Freeman B, Geller F, Gratacos M, Haigh R, Hebebrand J, Hinney A, Holliday J, Hu X, Karwautz A, Nacmias B, Ribases M, Remschmidt H, Komel R, Sorbi S, Tomori M, Treasure J, Wagner G, Zhao J, Collier DA. Gabrovsek M, et al. Among authors: ribases m. Am J Med Genet B Neuropsychiatr Genet. 2004 Jan 1;124B(1):68-72. doi: 10.1002/ajmg.b.20085. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14681918

7

Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations.

Ribasés M, Gratacòs M, Fernández-Aranda F, Bellodi L, Boni C, Anderluh M, Cavallini MC, Cellini E, Di Bella D, Erzegovesi S, Foulon C, Gabrovsek M, Gorwood P, Hebebrand J, Hinney A, Holliday J, Hu X, Karwautz A, Kipman A, Komel R, Nacmias B, Remschmidt H, Ricca V, Sorbi S, Wagner G, Treasure J, Collier DA, Estivill X. Ribasés M, et al. Hum Mol Genet. 2004 Jun 15;13(12):1205-12. doi: 10.1093/hmg/ddh137. Epub 2004 Apr 28. Hum Mol Genet. 2004. PMID: 15115760

8

Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation.

Pons R, Serrano M, Ormazabal A, Toma C, Garcia-Cazorla A, Area E, Ribasés M, Kanavakis E, Drakaki K, Giannakopoulos A, Orfanou I, Youroukos S, Cormand B, Artuch R. Pons R, et al. Among authors: ribases m. Mov Disord. 2010 Jun 15;25(8):1086-90. doi: 10.1002/mds.23002. Mov Disord. 2010. PMID: 20198643

9

Implication of chromosome 18 in hypertension by sibling pair and association analyses: putative involvement of the RKHD2 gene.

Guzmán B, Cormand B, Ribasés M, González-Núñez D, Botey A, Poch E. Guzmán B, et al. Among authors: ribases m. Hypertension. 2006 Nov;48(5):883-91. doi: 10.1161/01.HYP.0000244085.52918.a0. Epub 2006 Oct 2. Hypertension. 2006. PMID: 17015768

10

Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB.

Ribasés M, Ramos-Quiroga JA, Hervás A, Bosch R, Bielsa A, Gastaminza X, Artigas J, Rodriguez-Ben S, Estivill X, Casas M, Cormand B, Bayés M. Ribasés M, et al. Mol Psychiatry. 2009 Jan;14(1):71-85. doi: 10.1038/sj.mp.4002100. Epub 2007 Oct 16. Mol Psychiatry. 2009. PMID: 17938636

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