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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 3
2007 3
2009 2
2011 3
2012 5
2013 11
2014 12
2015 10
2016 12
2017 10
2018 6
2019 9
2020 6
2021 10
2022 8
2023 3
2024 3

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97 results

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Page 1
Analytical validation of HER2DX genomic test for early-stage HER2-positive breast cancer.
Marín-Aguilera M, Jares P, Sanfeliu E, Villacampa G, Hernández-Lllán E, Martínez-Puchol AI, Shankar S, González-Farré B, Waks AG, Brasó-Maristany F, Pardo F, Manning DK, Abery JA, Curaba J, Moon L, Gordon O, Galván P, Wachirakantapong P, Castillo O, Nee CM, Blasco P, Senevirathne TH, Sirenko V, Martínez-Sáez O, Aguirre A, Krop IE, Li Z, Spellman P, Metzger Filho O, Polyak K, Michaels P, Puig-Butillé JA, Vivancos A, Matito J, Buckingham W, Perou CM, Villagrasa-González P, Prat A, Parker JS, Paré L. Marín-Aguilera M, et al. Among authors: puig butille ja. ESMO Open. 2024 Mar;9(3):102903. doi: 10.1016/j.esmoop.2024.102903. Epub 2024 Mar 6. ESMO Open. 2024. PMID: 38452436 Free PMC article.
Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndrome.
Elias-Mas A, Potrony M, Bague J, Cutler DJ, Alvarez-Mora MI, Torres T, Barcos T, Puig-Butille JA, Rubio M, Madrigal I, Puig S, Allen EG, Rodriguez-Revenga L. Elias-Mas A, et al. Among authors: puig butille ja. Front Aging Neurosci. 2023 Jan 6;14:1073258. doi: 10.3389/fnagi.2022.1073258. eCollection 2022. Front Aging Neurosci. 2023. PMID: 36688175 Free PMC article.
A novel approach for the non-invasive diagnosis of pulmonary nodules using low-depth whole-genome sequencing of cell-free DNA.
Zhang B, Liang H, Liu W, Zhou X, Qiao S, Li F, Tian P, Li C, Ma Y, Zhang H, Zhang Z, Nanjo S, Russo A, Puig-Butillé JA, Wu K, Wang C, Zhao X, Yue D. Zhang B, et al. Among authors: puig butille ja. Transl Lung Cancer Res. 2022 Oct;11(10):2094-2110. doi: 10.21037/tlcr-22-647. Transl Lung Cancer Res. 2022. PMID: 36386459 Free PMC article.
Clinical utility of liquid biopsy for monitoring patients with NRAS-mutant medium-to-giant congenital melanocytic nevi.
Calbet-Llopart N, Tell-Martí G, Mateu J, Feito M, Martínez S, Puig S, Malvehy J, Carrera C, Puig-Butillé JA. Calbet-Llopart N, et al. Among authors: puig butille ja. J Eur Acad Dermatol Venereol. 2023 Feb;37(2):e200-e203. doi: 10.1111/jdv.18584. Epub 2022 Oct 13. J Eur Acad Dermatol Venereol. 2023. PMID: 36151998 No abstract available.
Synchronous primary cutaneous melanomas: a descriptive study of their clinical features, histology, genetic background of the patients and clinical outcomes.
Antúnez-Lay A, Podlipnik S, Carrera C, Potrony M, Tell-Martí G, Badenas C, Puig-Butille JA, Espinosa N, Puig S, Malvehy J. Antúnez-Lay A, et al. Among authors: puig butille ja. J Eur Acad Dermatol Venereol. 2022 Dec;36(12):2364-2372. doi: 10.1111/jdv.18467. Epub 2022 Aug 27. J Eur Acad Dermatol Venereol. 2022. PMID: 35882522
Oncogenic properties via MAPK signaling of the SOX5-RAF1 fusion gene identified in a wild-type NRAS/BRAF giant congenital nevus.
Vinyals A, Ferreres JR, Calbet-Llopart N, Ramos R, Tell-Martí G, Carrera C, Marcoval J, Puig S, Malvehy J, Puig-Butillé JA, Fabra À. Vinyals A, et al. Among authors: puig butille ja. Pigment Cell Melanoma Res. 2022 Jul;35(4):450-460. doi: 10.1111/pcmr.13044. Epub 2022 May 31. Pigment Cell Melanoma Res. 2022. PMID: 35587097
97 results