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

Year Number of Results
1958 1
1972 1
1974 1
1975 2
1977 2
1978 3
1980 1
1986 1
1992 1
1997 2
1999 1
2000 3
2001 1
2002 3
2003 5
2004 4
2005 3
2006 3
2007 3
2008 6
2009 3
2010 5
2011 3
2012 2
2013 3
2014 5
2015 4
2016 6
2017 3
2018 4
2019 1
2020 5
2021 10
2022 6
2023 6
2024 10
2025 1

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111 results

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Page 1
Comprehensive approach to children with cerebral palsy.
Cantero MJP, Medinilla EEM, Martínez AC, Gutiérrez SG. Cantero MJP, et al. Among authors: martinez ac. An Pediatr (Engl Ed). 2021 Oct;95(4):276.e1-276.e11. doi: 10.1016/j.anpede.2021.07.002. Epub 2021 Sep 12. An Pediatr (Engl Ed). 2021. PMID: 34526244 Free article.
OPTN/SRTR 2022 Annual Data Report: Heart.
Colvin MM, Smith JM, Ahn YS, Handarova DK, Martinez AC, Lindblad KA, Israni AK, Snyder JJ. Colvin MM, et al. Among authors: martinez ac. Am J Transplant. 2024 Feb;24(2S1):S305-S393. doi: 10.1016/j.ajt.2024.01.016. Am J Transplant. 2024. PMID: 38431362
Interferon and B-cell Signatures Inform Precision Medicine in Lupus Nephritis.
Parodis I, Lindblom J, Toro-Domínguez D, Beretta L, Borghi MO, Castillo J, Carnero-Montoro E, Enman Y, Mohan C, Alarcón-Riquelme ME, Barturen G, Nikolopoulos D; PRECISESADS Clinical Consortium. Parodis I, et al. Kidney Int Rep. 2024 Mar 13;9(6):1817-1835. doi: 10.1016/j.ekir.2024.03.014. eCollection 2024 Jun. Kidney Int Rep. 2024. PMID: 38899167 Free PMC article.
Endometrial Carcinomas With Subclonal Loss of Mismatch Repair Proteins: A Clinicopathologic and Genomic Study.
Mendoza RP, Wang P, Schulte JJ, Tjota MY, Jani I, Martinez AC, Haridas R, Wanjari P, Steinhardt G, Brown N, Betz BL, Chapel DB, Kertowidjojo E, Yamada SD, Bennett JA. Mendoza RP, et al. Among authors: martinez ac. Am J Surg Pathol. 2023 May 1;47(5):589-598. doi: 10.1097/PAS.0000000000002031. Epub 2023 Mar 3. Am J Surg Pathol. 2023. PMID: 36866757
Molecular characterisation of lupus low disease activity state (LLDAS) and DORIS remission by whole-blood transcriptome-based pathways in a pan-European systemic lupus erythematosus cohort.
Parodis I, Lindblom J, Barturen G, Ortega-Castro R, Cervera R, Pers JO, Genre F, Hiepe F, Gerosa M, Kovács L, De Langhe E, Piantoni S, Stummvoll G, Vasconcelos C, Vigone B, Witte T; PRECISESADS Clinical Consortium; Alarcón-Riquelme ME, Beretta L. Parodis I, et al. Ann Rheum Dis. 2024 Jun 12;83(7):889-900. doi: 10.1136/ard-2023-224795. Ann Rheum Dis. 2024. PMID: 38373843 Free PMC article.
Molecular subtypes explain lupus epigenomic heterogeneity unveiling new regulatory genetic risk variants.
Castellini-Pérez O, Povedano E, Barturen G, Martínez-Bueno M, Iakovliev A, Kerick M, López-Domínguez R, Marañón C, Martín J, Ballestar E; PRECISEADS Clinical Consortium; PRECISEADS Flow Cytometry Study Group; Borghi MO, Qiu W, Zhu C, Shankara S, Spiliopoulou A, de Rinaldis E, Carnero-Montoro E, Alarcón-Riquelme ME. Castellini-Pérez O, et al. NPJ Genom Med. 2024 Jul 16;9(1):38. doi: 10.1038/s41525-024-00420-0. NPJ Genom Med. 2024. PMID: 39013887 Free PMC article.
Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis.
Kerick M, Acosta-Herrera M, Simeón-Aznar CP, Callejas JL, Assassi S; International SSc Group; Proudman SM, Nikpour M; Australian Scleroderma Interest Group (ASIG); PRECISESADS Clinical Consortium; Hunzelmann N, Moroncini G, de Vries-Bouwstra JK, Orozco G, Barton A, Herrick AL, Terao C, Allanore Y, Fonseca C, Alarcón-Riquelme ME, Radstake TRDJ, Beretta L, Denton CP, Mayes MD, Martin J. Kerick M, et al. NPJ Genom Med. 2022 Oct 5;7(1):57. doi: 10.1038/s41525-022-00327-8. NPJ Genom Med. 2022. PMID: 36198672 Free PMC article.
111 results