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2001 1
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2018 3
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2023 0

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Page 1
Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis.
Rabionet R, Remesal A, Mensa-Vilaró A, Murías S, Alcobendas R, González-Roca E, Ruiz-Ortiz E, Antón J, Iglesias E, Modesto C, Comas D, Puig A, Drechsel O, Ossowski S, Yagüe J, Merino R, Estivill X, Arostegui JI. Rabionet R, et al. Among authors: puig a. Sci Rep. 2019 Mar 14;9(1):4579. doi: 10.1038/s41598-019-40874-2. Sci Rep. 2019. PMID: 30872671 Free PMC article.
Identification of Gene Mutations and Fusion Genes in Patients with Sézary Syndrome.
Prasad A, Rabionet R, Espinet B, Zapata L, Puiggros A, Melero C, Puig A, Sarria-Trujillo Y, Ossowski S, Garcia-Muret MP, Estrach T, Servitje O, Lopez-Lerma I, Gallardo F, Pujol RM, Estivill X. Prasad A, et al. Among authors: puig a. J Invest Dermatol. 2016 Jul;136(7):1490-1499. doi: 10.1016/j.jid.2016.03.024. Epub 2016 Mar 30. J Invest Dermatol. 2016. PMID: 27039262 Free article.
Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders.
Mercader JM, Saus E, Agüera Z, Bayés M, Boni C, Carreras A, Cellini E, de Cid R, Dierssen M, Escaramís G, Fernández-Aranda F, Forcano L, Gallego X, González JR, Gorwood P, Hebebrand J, Hinney A, Nacmias B, Puig A, Ribasés M, Ricca V, Romo L, Sorbi S, Versini A, Gratacòs M, Estivill X. Mercader JM, et al. Among authors: puig a. Hum Mol Genet. 2008 May 1;17(9):1234-44. doi: 10.1093/hmg/ddn013. Epub 2008 Jan 18. Hum Mol Genet. 2008. PMID: 18203754 Clinical Trial.
Regions-based illustrative visualization of multimodal datasets.
Abellán P, Tost D, Grau S, Puig A. Abellán P, et al. Among authors: puig a. Comput Med Imaging Graph. 2013 Jun;37(4):263-71. doi: 10.1016/j.compmedimag.2013.04.002. Epub 2013 May 6. Comput Med Imaging Graph. 2013. PMID: 23660135