Publications and communications of Elisa DOCAMPO MARTINEZ

Grotzinger, A. D., Werme, J., Peyrot, W. J., Frei, O., de Leeuw, C., Bicks, L. K., Guo, Q., Margolis, M. P., Coombes, B. J., Batzler, A., Pazdernik, V., Biernacka, J. M., Andreassen, O. A., Anttila, V., Børglum, A. D., Breen, G., Cai, N., Demontis, D., Edenberg, H. J., ... Docampo Martínez, E. (January 2026). Mapping the genetic landscape across 14 psychiatric disorders. Nature, 649 (8096), 406 - 415. doi:10.1038/s41586-025-09820-3

Lopez Delhoulle, V., De Voeght, A., NECHIFOR - POTORAC, I., Sépulchre, E., Willems, E., Pétrossians, P., Fernandez Carazo, R., KOOPMANSCH, B., Docampo Martínez, E., Bours, V., Bulk, S.* , & Lambert, F.*. (16 October 2025). A Spectrum of Tumorigenesis in an IDH1-Mosaic Patient with Ollier Disease [Poster presentation]. 7th INTERNATIONAL CONFERENCE ACUTE MYELOID LEUKEMIA “MOLECULAR AND TRANSLATIONAL”: ADVANCES IN BIOLOGY AND TREATMENT, Estoril, Portugal.

Lu, Z.-A., Ploner, A., Birgegård, A., Eating Disorders Working Group of the Psychiatric Genomics Consortium, Landén, M., Bulik, C. M., Bergen, S. E., & Docampo Martínez, E. (2025). Leveraging transdiagnostic genetic liability to psychiatric disorders to dissect clinical outcomes of anorexia nervosa. Molecular Psychiatry. doi:10.1038/s41380-025-03264-x

COLLIN, S., revencu, N., Docampo Martínez, E., Bours, V., & Harvengt, J. (18 September 2025). A new NOTCH2 Variant in Hajdu-Cheney Syndrome: Case report and literature update [Poster presentation]. ESPE-OSCAR Science Symposium.

Docampo Martínez, E. (June 2025). Aspects génétiques des pathologies de l’aorte thoracique [Paper presentation]. Journée de l'aorte, Liège, Belgium.

Docampo Martínez, E. (2025). Testing génétique dans les pathologies pulmonaires interstitielles et vasculaires [Paper presentation]. Symposium annuel interhospitalier Sud-Belgique de pathologies interstitielles et vasculaires pulmonaires, Liège, Belgium.

Correia Marques, M., Rubin, D., Shuldiner, E. G., Datta, M., Schmitz, E., Gutierrez Cruz, G., Patt, A., Bennett, E., Grom, A., Foell, D., Gattorno, M., Bohnsack, J., Yeung, R. S. M., Prahalad, S., Mellins, E., Anton, J., Len, C. A., Oliveira, S., Woo, P., ... Docampo Martínez, E. (October 2024). Enrichment of Rare Variants of Hemophagocytic Lymphohistiocytosis Genes in Systemic Juvenile Idiopathic Arthritis. Arthritis and Rheumatology, 76 (10), 1566 - 1572. doi:10.1002/art.42938

Lu, Z.-A., Ploner, A., Birgegård, A., Eating Disorders Working Group of the Psychiatric Genomics Consortium, Bulik, C. M., Bergen, S. E., & Docampo Martínez, E. (27 August 2024). Shared Genetic Architecture Between Schizophrenia and Anorexia Nervosa: A Cross-trait Genome-Wide Analysis. Schizophrenia Bulletin, 50 (5), 1255 - 1265. doi:10.1093/schbul/sbae087

Bertrand, D., Joly, J., Neerinckx, B., Durez, P., Lenaerts, J., Joos, R., Thevissen, K., Zwaenepoel, T., Vanhoof, J., Di Romana, S., Taelman, V., Van Essche, E., Corluy, L., Ribbens, C., Berghe, M. V., Devinck, M., Ajeganova, S., Durnez, A., Boutsen, Y., ... The CareRA2020 Study group (Other coll.). (07 August 2024). Effectiveness of methotrexate and bridging glucocorticoids with or without early introduction of a 6-month course of etanercept in early RA: results of the 2-year, pragmatic, randomised CareRA2020 trial. RMD Open, 10 (3), 004535. doi:10.1136/rmdopen-2024-004535

Chatelain, C., KUKOR, L., BULK, S., Bours, V., & Docampo Martínez, E. (12 April 2024). SKI missense variant c.539C>T p.(Thr180Met), a recurrent variant in Shprintzen-Goldberg syndrome: a case report and review of literature [Poster presentation]. Annual Symposium : Single cells, to care or not to care?, Leuven, Belgium.

Harvengt, J., Docampo Martínez, E., Jacquinet, A., Alkan, S., Martin, M., Debray, F.-G., BULK, S., & Bours, V. (12 April 2024). New paradigms in clinical geneticist practice in the era of emerging therapies: examples of two pediatric syndromes [Poster presentation]. BESHG Annual Symposium 2024.

Fouquet, C., Revencu, N., Docampo Martínez, E., Bours, V., Boeckx, N., Bart, L., & Harvengt, J. (April 2024). Loeys-Dietz syndrome associated with truncating variants in PMEPA1 gene: First description of the phenotypic spectrum in three Belgian families [Poster presentation]. BeSHG Annual Meeting.

CREVECOEUR, J., Docampo, E., Martin, M., & Bours, V. (2024). INTÉRÊT DE L’UTILISATION DES SCORES DE RISQUES POLYGÉNIQUES DANS LE DÉPISTAGE DU CANCER DU SEIN ET LA MÉDECINE DE PRÉVENTION. Revue Médicale de Liège, 79 (6), 372 - 378.

Docampo Martínez, E., Reenaers, C., Van Kemseke, C., Latour, P., Seidel, L., Louis, E., & Ribbens, C. (2024). Joint involvement in inflammatory bowel disease: an observational study [Poster presentation]. 13th International Congress on Spondyloarthritides, Gand, Belgium.

Lehane, F., Malaise, O., Von Frenckell, C., OTTO, B., Docampo Martínez, E., & Ribbens, C. (2024). Hypophosphatasia Presenting as a Chronic Diffuse Pain Syndrome with Extra-Articular Calcifications. Journal of Clinical Medicine, 13 (8), 2263. doi:10.3390/jcm13082263

Fouquet, C., Leroi, N., Coupier, J., Docampo Martínez, E., Bulk, S., & Bours, V. (17 March 2023). Discordancy in interpretation of a BRCA1 variant in the Belgian population [Poster presentation]. BeSHG Annual Meeting 2023.

Lehane, F., Von Frenckell, C., Docampo Martínez, E., Ribbens, C., & Malaise, O. (March 2023). Fibromyalgia … 
But does your liver agree with this diagnosis? [Paper presentation]. Bone Curriculum Symposium 2023.

Mina, M., JACQUERIE, P., Docampo Martínez, E., & Malaise, O. (September 2022). Z-score at +4.4 … Perfect is the enemy of good [Paper presentation]. Belgian Congress of Rheumatology.

KEMPENEERS, C., Bricmont, N., Bonhiver, R., GUISSARD, F., HOUGRAND, O., DELVENNE, P., JACQUINET, A., HARVENGT, J., DOCAMPO MARTINEZ, E., BOURS, V., Benchimol, L., POIRRIER, A.-L., LEFEBVRE, P., CALMES, D., LOUIS, R., & SEGHAYE, M.-C. (17 March 2022). Ciliary videomicroscopy at room temperature lacks sensitivity for PCD diagnosis [Poster presentation]. Congress of the BVK-SBP, Brussels, Belgium.

DOCAMPO MARTINEZ, E., MARTIN, M., GANGOLF, M., HARVENGT, J., BULK, S., SEGERS, K., LEROI, N., LETE, C., PALMARICCIOTTI, V., Freire Chadrina, M., LAMBERT, F., & Bours, V. (2021). Hérédité et cancer. Revue Médicale de Liège, 76 (5-6), 327-336.

DOCAMPO MARTINEZ, E., MARTIN, M., Marnette, J., & Bours, V. (06 March 2020). LTBP3 mutation identified in a patient with a severe valvular disease [Poster presentation]. 20th Annual Meeting of the Belgian Society of Human Genetics.

Bryois, J., Skene, N. G., Hansen, T. F., Kogelman, L. J. A., Watson, H. J., Liu, Z., Brueggeman, L., Breen, G., Bulik, C. M., Arenas, E., Hjerling-Leffler, J., Sullivan, P. F., & DOCAMPO MARTINEZ, E. (Other coll.). (2020). Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. Nature Genetics, 52 (5), 482-493. doi:10.1038/s41588-020-0610-9

Docampo Martínez, E. (2020). Les maladies génétiques du tissus conjonctif [Paper presentation]. Formation continue de l'Association Royale des Médecins de l'Université de Liège (AMLG), Liège, Belgium.

Munn-Chernoff, M. A., Johnson, E. C., Chou, Y.-L., Coleman, J. R. I., Thornton, L. M., Walters, R. K., Yilmaz, Z., Baker, J. H., Hübel, C., Gordon, S., Medland, S. E., Watson, H. J., Gaspar, H. A., Bryois, J., Hinney, A., Leppä, V. M., Mattheisen, M., Ripke, S., Yao, S., ... Agrawal, A. (2020). Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addiction Biology, 12880. doi:10.1111/adb.12880

Docampo Martínez, E. (07 December 2019). La vérité sur l'hyperlaxité [Paper presentation]. 80 réunion du groupement Belge de Pédiatres de Langue Française, Gembloux, Belgium.

DOCAMPO MARTINEZ, E. (Other coll.). (2019). Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell, 179 (7), 1469-1482.e11. doi:10.1016/j.cell.2019.11.020

Watson, H. J., Yilmaz, Z., Thornton, L. M., Hubel, C., Coleman, J. R. I., Gaspar, H. A., Bryois, J., Hinney, A., Leppa, V. M., Mattheisen, M., Medland, S. E., Ripke, S., Yao, S., Giusti-Rodriguez, P., Hanscombe, K. B., Purves, K. L., Adan, R. A. H., Alfredsson, L., Ando, T., ... Bulik, C. M. (2019). Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nature Genetics, 51 (8), 1207-1214. doi:10.1038/s41588-019-0439-2

Yao, S., Kuja-Halkola, R., Martin, J., Lu, Y., Lichtenstein, P., Norring, C., Birgegard, A., Yilmaz, Z., Hubel, C., Watson, H., Baker, J., Almqvist, C., Thornton, L. M., Magnusson, P. K., Bulik, C. M., Larsson, H., & DOCAMPO MARTINEZ, E. (Other coll.). (2019). Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches. Biological Psychiatry, 86 (8), 577-586. doi:10.1016/j.biopsych.2019.04.036

KUKOR, L., BERTOLI, S., Bours, V., BULK, S., & DOCAMPO MARTINEZ, E. (16 February 2018). Ehlers-Danlos syndrome in the University Hospital of Liege [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium.

Anttila, V., Bulik-Sullivan, B., Finucane, H. K., Walters, R. K., Bras, J., Duncan, L., Escott-Price, V., Falcone, G. J., Gormley, P., Malik, R., Patsopoulos, N. A., Ripke, S., Wei, Z., Yu, D., Lee, P. H., Turley, P., Grenier-Boley, B., Chouraki, V., Kamatani, Y., ... Neale, B. M. (2018). Analysis of shared heritability in common disorders of the brain. Science, 360 (6395). doi:10.1126/science.aap8757

Arthur, V. L., Shuldiner, E., Remmers, E. F., Hinks, A., Grom, A. A., Foell, D., Martini, A., Gattorno, M., Ozen, S., Prahalad, S., Zeft, A. S., Bohnsack, J. F., Ilowite, N. T., Mellins, E. D., Russo, R., Len, C., Oliveira, S., Yeung, R. S. M., Rosenberg, A. M., ... DOCAMPO MARTINEZ, E. (Other coll.). (2018). IL1RN Variation Influences Both Disease Susceptibility and Response to Recombinant Human Interleukin-1 Receptor Antagonist Therapy in Systemic Juvenile Idiopathic Arthritis. Arthritis and Rheumatology. doi:10.1002/art.40498

Duncan, L., Yilmaz, Z., Gaspar, H., Walters, R., Goldstein, J., Anttila, V., Bulik-Sullivan, B., Ripke, S., Thornton, L. M., Hinney, A., Daly, M., Sullivan, P. F., Zeggini, E., Breen, G., Bulik, C. M., & DOCAMPO MARTINEZ, E. (Other coll.). (2017). Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa. American Journal of Psychiatry, 201716121402. doi:10.1176/appi.ajp.2017.16121402

Ghisdal, L., Baron, C., Lebranchu, Y., Viklicky, O., Konarikova, A., Naesens, A., Kuypers, D., Dinic, M., Alamartine, E., Touchard, G., Antoine, T., Essig, M., Rerolle, J. P., Merville, P., Taupin, J. L., Le Meur, Y., Grall - Jezequel, A., Glowacki, F., Noel, C., ... Abramowicz M. (2017). Genome-wide Association Study of Acute Renal Graft Rejection. American Journal of Transplantation, 17 (1), 201-2019. doi:10.1111/ajt.13912

Hinney, A., Kesselmeier, M., Jall, S., Volckmar, A.-L., Focker, M., Antel, J., Heid, I. M., Winkler, T. W., Grant, S. F. A., Guo, Y., Bergen, A. W., Kaye, W., Berrettini, W., Hakonarson, H., Herpertz-Dahlmann, B., de Zwaan, M., Herzog, W., Ehrlich, S., Zipfel, S., ... DOCAMPO MARTINEZ, E. (Other coll.). (2017). Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index. Molecular Psychiatry, 22 (2), 192-201. doi:10.1038/mp.2016.71

Huang, H.* , Fang, M.* , Jostins, L.* , Umicevic - Mirkov, M., Boucher, G., Anderson, C. A., Andersen, V., Cleynen, I., Cortes, A., Crins, F., D'Amato, M., Deffontaine, V., Dmitrieva, J. B., DOCAMPO MARTINEZ, E., Elansary, M., Farh, K. K.-H., Franke, A., Gori, A.-S., Goyette, P., ... Barrett, J. C.*. (2017). Fine-mapping inflammatory bowel disease loci to single-variant resolution. Nature, 547 (7662), 173-178. doi:10.1038/nature22969

Huckins, L. M., Hatzikotoulas, K., Southam, L., Thornton, L. M., Steinberg, J., Aguilera-McKay, F., Treasure, J., Schmidt, U., Gunasinghe, C., Romero, A., Curtis, C., Rhodes, D., Moens, J., Kalsi, G., Dempster, D., Leung, R., Keohane, A., Burghardt, R., Ehrlich, S., ... DOCAMPO MARTINEZ, E. (Other coll.). (2017). Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa. Molecular Psychiatry. doi:10.1038/mp.2017.88

Li, D., Chang, X., Connolly, J. J., Tian, L., Liu, Y., Bhoj, E. J., Robinson, N., Abrams, D., Li, Y. R., Bradfield, J. P., Kim, C. E., Li, J., Wang, F., Snyder, J., Lemma, M., Hou, C., Wei, Z., Guo, Y., Qiu, H., ... DOCAMPO MARTINEZ, E. (Other coll.). (2017). Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling. Scientific Reports, 7 (1), 8379. doi:10.1038/s41598-017-06409-3

Li, D., Chang, X., Connolly, J. J., Tian, L., Liu, Y., Bhoj, E. J., Robinson, N., Abrams, D., Li, Y. R., Bradfield, J. P., Kim, C. E., Li, J., Wang, F., Snyder, J., Lemma, M., Hou, C., Wei, Z., Guo, Y., Qiu, H., ... DOCAMPO MARTINEZ, E. (Other coll.). (2017). A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling. Scientific Reports, 7 (1), 3847. doi:10.1038/s41598-017-01674-8

Ombrello, M. J., Arthur, V. L., Remmers, E. F., Hinks, A., Tachmazidou, I., Grom, A. A., Foell, D., Martini, A., Gattorno, M., Ozen, S., Prahalad, S., Zeft, A. S., Bohnsack, J. F., Ilowite, N. T., Mellins, E. D., Russo, R., Len, C., Hilario, M. O. E., Oliveira, S., ... Thomson, W. (2016). Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications. Annals of the Rheumatic Diseases. doi:10.1136/annrheumdis-2016-210324

Docampo Martínez, E., Fang, M., Dmitrieva, J. B., Theatre, E., Elansary, M., Mariman, R., Gori, A.-S., Mni, M., Crins, F., Coppieters, W., Louis, E., & Georges, M. (09 November 2015). Prioritizing likely causative genes in GWAS identified risk loci for immune-mediated inflammatory disorders using cell-type specific eQTL information [Paper presentation]. The American College of Rheumatology Annual Meeting, San Francisco, United States - California.

Docampo Martínez, E., Fang, M., Dmitrieva, J. B., Theatre, E., Elansary, M., Mariman, R., Gori, A.-S., Mini, M., Crins, F., Coppieters, W., LOUIS, E., & Georges, M. (05 May 2015). Prioritizing likely causative genes in GWAS identified risk loci for immune-mediated inflammatory disorders using cell-type specific eQTL information [Poster presentation]. cold spring harbor laboratory THE BIOLOGY OF GENOMES.

Almirall, M., Docampo Martinez, E., Estivill, X., & Maymo, J. (2015). Genetic characteristics of rheumatic patients developing inflammatory skin lesions induced by biologic therapy. Reumatologiá Clinica, 11 (2), 126-7. doi:10.1016/j.reuma.2014.07.007

Docampo Martínez, E., Dmitrieva, J. B., Fang, M., Theatre, E., Elansary, M., Mariman, R., Mni, M., Crins, F., Gori, A.-S., Louis, E., & Georges, M. (2015). Detection of trans-eQTL effects associated with an ulcerative colitis risk locus [Poster presentation]. Gordon research seminar & conference on Quantitative Genetics & Genomics, Luca, Italy.

Escaramis, G., Docampo Martinez, E., & Rabionet, R. (2015). A decade of structural variants: description, history and methods to detect structural variation. Briefings in Functional Genomics, 14 (5), 305-14. doi:10.1093/bfgp/elv014

Ombrello, M. J., Remmers, E. F., Tachmazidou, I., Grom, A., Foell, D., Haas, J.-P., Martini, A., Gattorno, M., Ozen, S., Prahalad, S., Zeft, A. S., Bohnsack, J. F., Mellins, E. D., Ilowite, N. T., Russo, R., Len, C., Hilario, M. O. E., Oliveira, S., Yeung, R. S. M., ... Woo, P. (2015). 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, 112 (52), 15970-5. doi:10.1073/pnas.1520779112

Docampo Martínez, E., Theatre, E., Dmitrieva, J. B., Elansary, M., Mariman, R., Mni, M., Crins, F., Gori, A.-S., Fang, M., LOUIS, E., & Georges, M. (24 April 2014). Identifying Inflammatory Bowel Disease causative genes through trans-eQTLs mapping within GWAS loci [Poster presentation]. BeMGI.

Gori, A.-S., LECUT, C., Theatre, E., Momozawa, Y., Docampo Martínez, E., Mariman, R., Dmitrieva, J. B., Elansary, M., Charloteaux, B., Defontaine, V., Mni, M., Crins, F., LOUIS, E., Georges, M., & Oury, C. (24 April 2014). Combined use of GWAS and eQTL information to identify genes controlling platelet biology [Poster presentation]. BeMGI. doi:10.13140/RG.2.1.4044.9763

Mariman, R., Coppieters, W., Elansary, M., Karim, L., Crins, F., Mni, M., Gori, A.-S., Aoun, N., Docampo Martínez, E., Dmitrieva, J. B., Fang, M., Theatre, E., Eppe, G., & Georges, M. (24 April 2014). Identification of molecular components of the host-microbiota-connectome by using "Omics Approaches" [Poster presentation]. BeMGI.

Boraska, V., Franklin, C. S., Floyd, J. A. B., Thornton, L. M., Huckins, L. M., Southam, L., Rayner, N. W., Tachmazidou, I., Klump, K. L., Treasure, J., Lewis, C. M., Dedoussis, G., Dikeos, D., Gonidakis, F., Tziouvas, K., Tsitsika, A., Papezova, H., Slachtova, L., Martaskova, D., ... Maj, M. (2014). A genome-wide association study of anorexia nervosa. Molecular Psychiatry, 19 (10), 1085-94. doi:10.1038/mp.2013.187

Docampo Martinez, E., Escaramis, G., Gratacos, M., Villatoro, S., Puig, A., Kogevinas, M., Collado, A., Carbonell, J., Rivera, J., Vidal, J., Alegre, J., Estivill, X., & Rabionet, R. (2014). Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system. Pain, 155 (6), 1102-9. doi:10.1016/j.pain.2014.02.016

Huckins, L. M., Boraska, V., Franklin, C. S., Floyd, J. A. B., Southam, L., Sullivan, P. F., Bulik, C. M., Collier, D. A., Tyler-Smith, C., Zeggini, E., Tachmazidou, I., & Docampo Martinez, E. (Other coll.). (2014). Using ancestry-informative markers to identify fine structure across 15 populations of European origin. European Journal of Human Genetics, 22 (10), 1190-200. doi:10.1038/ejhg.2014.1

Rodriguez Ravenga, L., Docampo Martínez, E.* , Collado, A., & Mila, M. (2014). Genetic influence on fibromyalgia. In B. Danneskiold-Samsø, Novel Insights into the Pathophysiology and Treatment of Fibromyalgia. Copenhague, Denmark: Future medecine.

Docampo Martínez, E. (2013). IDENTIFICATION OF GENETIC SUSCEPTIBILITY FACTORS FOR FIBROMYALGIA [Doctoral thesis, University of Barcelona]. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/192741

Blanch, J., Guanabens, N., Lisbona, M. P., Docampo Martínez, E., & Ruiz, D. (2013). Effects of calcium and vitamin D with and without lactulose on bone mineral density in postmenopausal women with osteopenia: a randomized controlled pilot trial. Revista de Osteoporosis y Metabolismo Mineral.

Docampo Martinez, E., Collado, A., Escaramis, G., Carbonell, J., Rivera, J., Vidal, J., Alegre, J., Rabionet, R., & Estivill, X. (2013). Cluster analysis of clinical data identifies fibromyalgia subgroups. PLoS ONE, 8 (9), 74873. doi:10.1371/journal.pone.0074873

Rodriguez-Revenga, L., Madrigal, I., Blanch-Rubio, J., Elurbe, D. M., Docampo Martinez, E., Collado, A., Vidal, J., Carbonell, J., Estivill, X., & Mila, M. (2013). Screening for the presence of FMR1 premutation alleles in women with fibromyalgia. Gene, 512 (2), 305-8. doi:10.1016/j.gene.2012.10.016

Docampo Martínez, E., Escaramis, G., Rabionet, R., Carbonell, J., & Estivill, X. (06 June 2012). Cluster analysis of clinical data identifies fibromyalgia subgroups [Paper presentation]. EULAR annual meeting, Berlin, Germany.

Docampo Martinez, E., Ribases, M., Gratacos, M., Bruguera, E., Cabezas, C., Sanchez-Mora, C., Nieva, G., Puente, D., Argimon-Pallas, J. M., Casas, M., Rabionet, R., & Estivill, X. (2012). Association of neurexin 3 polymorphisms with smoking behavior. Genes, Brain, and Behavior, 11 (6), 704-11. doi:10.1111/j.1601-183X.2012.00815.x

Docampo Martinez, E., Giardina, E., Riveira-Munoz, E., de Cid, R., Escaramis, G., Perricone, C., Fernandez-Sueiro, J. L., Maymo, J., Gonzalez-Gay, M. A., Blanco, F. J., Huffmeier, U., Lisbona, M. P., Martin, J., Carracedo, A., Reis, A., Rabionet, R., Novelli, G., & Estivill, X. (2011). 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 (7), 1860-5. doi:10.1002/art.30340

Estivill, X., Rabionet, R., Ribases, M., Gratacos, M., Montfort, M., & Docampo Martínez, E. (2011). Association of Neurexin 3 variants with nicotine dependence [Poster presentation]. The genomics of Common Diseases 2011, Hinxton, United Kingdom.

Docampo Martínez, E. (2010). Asociacion de dos genes del complejo de diferecenciacion epidermica, LCE3c y LC3B en artritis psoriasica [Paper presentation]. Congreso anual de la sociedad espanola de reumatologia, Tarragona, Spain.

Docampo Martinez, E., Rabionet, R., Riveira-Munoz, E., Escaramis, G., Julia, A., Marsal, S., Martin, J. E., Gonzalez-Gay, M. A., Balsa, A., Raya, E., Martin, J., & Estivill, X. (2010). Deletion of the late cornified envelope genes, LCE3C and LCE3B, is associated with rheumatoid arthritis. Arthritis and Rheumatism, 62 (5), 1246-51. doi:10.1002/art.27381

Docampo Martinez, E., Ciria, M., Serra-Burges, J., Blanch, J., Perez Edo, L., & Carbonell, J. (2009). Factores predictivos de nueva fractura tras vertebroplastia. Medicina Clinica, 133 (1), 17-9. doi:10.1016/j.medcli.2008.07.027

Docampo Martínez, E., Rabionet, R., Riveira, E., Julia, A., Marsal, S., Balsa, A., & Estvill, X. (2009). Deletion of the late cornified envelope genes, LCE3C and LCE3B, is a new susceptibility factor for rheumatoid arthritis [Poster presentation]. American Society of Human Genetics annual meeting, Hawai, United States.

Rabionet, R., Docampo Martínez, E., Riveira, E., Matesanz, F., Marsal, S., Roquer, J., Giardina, E., & Estivill, X. (2009). Copy number variation in the late cornified envelope cluster in autoimmune disorders [Poster presentation]. The biology of genomes, New York, United States.

Docampo Martínez, E. (2008). Genomic structural variation in multiple sclerosis [Master’s dissertation, Universitat de Barcelona]. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/339942

Docampo Martínez, E. (01 June 2008). Genomic structural variation in patients with Multiple Sclerosis [Poster presentation]. European Society of human genetics annual meeting, Barcelone, Spain.

Rossello, L., Palliso, F., Ferrer, J., Docampo Martinez, E., Calvet, J., Benito, P., & Serra, J. (2008). Osteonecrosis vertebral y vertebroplastia percutanea. Reumatologiá Clinica, 4 (4), 162-5. doi:10.1016/S1699-258X(08)71827-8

Taverner, D., Lisbona, M. P., Segales, N., Docampo Martinez, E., Calvet, J., Castro, S., & Benito, P. (2008). Eficacia de la gabapentina en el tratamiento del sindrome del tunel carpiano. Medicina Clinica, 130 (10), 371-3. doi:10.1157/13117468

Taverner, D., Monfort, J., Docampo Martinez, E., & Pou, M. (2008). Artritis septica por Propionibacterium acnes. Medicina Clinica, 131 (18), 718-9. doi:10.1157/13129130

Calvet, J., Lisbona, M. P., Docampo Martínez, E., Maymo, J., & Carbonell, J. (2007). Ultrasound evaluation of inflammatory lesions in hands. Are there any differences between RA and SLE? [Poster presentation]. EULAR Annual European Congress of Rheumotology.

Rovira Cañellas, M., Serra Burgés, J., Muntané Sánchez, A., & Docampo Martínez, E. (2007). Painful vertebrae with negative MRI and bone scintigraphy : is vertebroplasty indicated? [Poster presentation]. XIX Meeting of Ibero Latino American society of Neuroradiology, XXXVI meeting of Spanish society of neuroradiology, Sevilla, Spain.

Docampo Martínez, E. (2006). Inpatients in a rheumatology unit: inmigrants vs autochthonous [Poster presentation]. Congreso anual de la sociedad espanola de reumatologia, Valencia, Spain.

Docampo Martínez, E. (2005). Male osteoporosis: Study of osteoblast function through cellular cultures [Paper presentation]. Network for Male osteoporosis (NEMO) Meeting, Gand, Belgium.

Docampo Martínez, E., Calvet, J., & Pros, A. (2005). Subcutaneous fat biopsy in a tertiary care center [Poster presentation]. Congreso anual de la sociedad espanola de reumatologia, Las Palmas de Gran Canaria, Spain.

Garcia-Miguel, J., Docampo Martinez, E., Blanch, J., & Benito, P. (2005). Calcinosis cutanea fistulizante en la dermatopolimiositis idiopatica del adulto. Medicina Clinica, 125 (19), 758. doi:10.1016/s0025-7753(05)72179-5