Year |
Citation |
Score |
2020 |
Munn-Chernoff MA, Johnson EC, Chou YL, Coleman JRI, Thornton LM, Walters RK, Yilmaz Z, Baker JH, Hübel C, Gordon S, Medland SE, Watson HJ, Gaspar HA, Bryois J, Hinney A, ... ... Docampo E, et al. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addiction Biology. e12880. PMID 32064741 DOI: 10.1111/Adb.12880 |
0.65 |
|
2019 |
Watson HJ, Yilmaz Z, Thornton LM, Hübel C, Coleman JRI, Gaspar HA, Bryois J, Hinney A, Leppä VM, Mattheisen M, Medland SE, Ripke S, Yao S, Giusti-Rodríguez P, ... ... Docampo E, et al. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nature Genetics. PMID 31308545 DOI: 10.1038/s41588-019-0439-2 |
0.657 |
|
2018 |
Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... Docampo E, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/Science.Aap8757 |
0.608 |
|
2016 |
Ombrello MJ, Arthur VL, Remmers EF, Hinks A, Tachmazidou I, Grom AA, Foell D, Martini A, Gattorno M, Özen S, Prahalad S, Zeft AS, Bohnsack JF, Ilowite NT, Mellins ED, ... ... Docampo E, et al. Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications. Annals of the Rheumatic Diseases. PMID 27927641 DOI: 10.1136/Annrheumdis-2016-210324 |
0.425 |
|
2015 |
Ombrello MJ, Remmers EF, Tachmazidou I, Grom A, Foell D, Haas JP, Martini A, Gattorno M, Özen S, Prahalad S, Zeft AS, Bohnsack JF, Mellins ED, Ilowite NT, Russo R, ... ... Docampo E, et al. HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis. Proceedings of the National Academy of Sciences of the United States of America. PMID 26598658 DOI: 10.1073/Pnas.1520779112 |
0.477 |
|
2015 |
Escaramís G, Docampo E, Rabionet R. A decade of structural variants: description, history and methods to detect structural variation. Briefings in Functional Genomics. 14: 305-14. PMID 25877305 DOI: 10.1093/Bfgp/Elv014 |
0.591 |
|
2015 |
Almirall M, Docampo E, Estivill X, Maymó J. Genetic characteristics of rheumatic patients developing inflammatory skin lesions induced by biologic therapy. Reumatologia Clinica. 11: 126-7. PMID 25218411 DOI: 10.1016/J.Reumae.2014.07.009 |
0.361 |
|
2014 |
Docampo E, EscaramÃs G, Gratacòs M, Villatoro S, Puig A, Kogevinas M, Collado A, Carbonell J, Rivera J, Vidal J, Alegre J, Estivill X, Rabionet R. Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system. Pain. 155: 1102-9. PMID 24582949 DOI: 10.1016/J.Pain.2014.02.016 |
0.683 |
|
2014 |
Boraska V, Franklin CS, Floyd JA, Thornton LM, Huckins LM, Southam L, Rayner NW, Tachmazidou I, Klump KL, Treasure J, Lewis CM, Schmidt U, Tozzi F, Kiezebrink K, Hebebrand J, ... ... Docampo E, et al. A genome-wide association study of anorexia nervosa. Molecular Psychiatry. 19: 1085-94. PMID 24514567 DOI: 10.1038/Mp.2013.187 |
0.63 |
|
2013 |
Docampo E, Collado A, EscaramÃs G, Carbonell J, Rivera J, Vidal J, Alegre J, Rabionet R, Estivill X. Cluster analysis of clinical data identifies fibromyalgia subgroups. Plos One. 8: e74873. PMID 24098674 DOI: 10.1371/Journal.Pone.0074873 |
0.606 |
|
2013 |
Rodriguez-Revenga L, Madrigal I, Blanch-Rubió J, Elurbe DM, Docampo E, Collado A, Vidal J, Carbonell J, Estivill X, Mila M. Screening for the presence of FMR1 premutation alleles in women with fibromyalgia. Gene. 512: 305-8. PMID 23111161 DOI: 10.1016/J.Gene.2012.10.016 |
0.416 |
|
2013 |
Docampo E, Escaramis G, Rabionet R, Carbonell J, Rivera J, Alegre J, Vidal J, Estivill X, Collado A. OP0067 Cluster analysis of clinical data identifies fibromyalgia subgroups Annals of the Rheumatic Diseases. 71: 76.1-76. DOI: 10.1136/Annrheumdis-2012-Eular.1750 |
0.624 |
|
2012 |
Docampo E, Ribasés M, Gratacòs M, Bruguera E, Cabezas C, Sánchez-Mora C, Nieva G, Puente D, Argimon-Pallàs JM, Casas M, Rabionet R, Estivill X. Association of neurexin 3 polymorphisms with smoking behavior. Genes, Brain, and Behavior. 11: 704-11. PMID 22716474 DOI: 10.1111/J.1601-183X.2012.00815.X |
0.639 |
|
2011 |
Docampo E, Giardina E, Riveira-Muñoz E, de Cid R, Escaramís G, Perricone C, Fernández-Sueiro JL, Maymó J, González-Gay MA, Blanco FJ, Hüffmeier U, Lisbona MP, Martín J, Carracedo A, Reis A, et al. Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: a study in Spanish and Italian populations and meta-analysis. Arthritis and Rheumatism. 63: 1860-5. PMID 21400479 DOI: 10.1002/Art.30340 |
0.641 |
|
2010 |
Docampo E, Rabionet R, Riveira-Muñoz E, Escaramís G, Julià A, Marsal S, Martín JE, González-Gay MA, Balsa A, Raya E, Martín J, Estivill X. Deletion of the late cornified envelope genes, LCE3C and LCE3B, is associated with rheumatoid arthritis. Arthritis and Rheumatism. 62: 1246-51. PMID 20213803 DOI: 10.1002/Art.27381 |
0.629 |
|
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