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

Year Number of Results
2008 1
2009 2
2010 4
2011 2
2012 4
2013 4
2014 2
2016 1
2017 3
2018 2
2019 2
2020 5
2021 3
2022 4
2023 4
2024 2

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36 results

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Page 1
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
Garcia-Pelaez J, Barbosa-Matos R, Lobo S, Dias A, Garrido L, Castedo S, Sousa S, Pinheiro H, Sousa L, Monteiro R, Maqueda JJ, Fernandes S, Carneiro F, Pinto N, Lemos C, Pinto C, Teixeira MR, Aretz S, Bajalica-Lagercrantz S, Balmaña J, Blatnik A, Benusiglio PR, Blanluet M, Bours V, Brems H, Brunet J, Calistri D, Capellá G, Carrera S, Colas C, Dahan K, de Putter R, Desseignés C, Domínguez-Garrido E, Egas C, Evans DG, Feret D, Fewings E, Fitzgerald RC, Coulet F, Garcia-Barcina M, Genuardi M, Golmard L, Hackmann K, Hanson H, Holinski-Feder E, Hüneburg R, Krajc M, Lagerstedt-Robinson K, Lázaro C, Ligtenberg MJL, Martínez-Bouzas C, Merino S, Michils G, Novaković S, Patiño-García A, Ranzani GN, Schröck E, Silva I, Silveira C, Soto JL, Spier I, Steinke-Lange V, Tedaldi G, Tejada MI, Woodward ER, Tischkowitz M, Hoogerbrugge N, Oliveira C. Garcia-Pelaez J, et al. Among authors: pinto n. Lancet Oncol. 2023 Jan;24(1):91-106. doi: 10.1016/S1470-2045(22)00643-X. Epub 2022 Nov 24. Lancet Oncol. 2023. PMID: 36436516 Free PMC article.
Forensic genetics and genomics: Much more than just a human affair.
Arenas M, Pereira F, Oliveira M, Pinto N, Lopes AM, Gomes V, Carracedo A, Amorim A. Arenas M, et al. Among authors: pinto n. PLoS Genet. 2017 Sep 21;13(9):e1006960. doi: 10.1371/journal.pgen.1006960. eCollection 2017 Sep. PLoS Genet. 2017. PMID: 28934201 Free PMC article. Review.
Big data in forensic genetics.
Amorim A, Pinto N. Amorim A, et al. Among authors: pinto n. Forensic Sci Int Genet. 2018 Nov;37:102-105. doi: 10.1016/j.fsigen.2018.08.001. Epub 2018 Aug 2. Forensic Sci Int Genet. 2018. PMID: 30142461
Exact likelihood ratio calculations for pairwise cases.
Egeland T, Pinto N, Amorim A. Egeland T, et al. Among authors: pinto n. Forensic Sci Int Genet. 2017 Jul;29:218-224. doi: 10.1016/j.fsigen.2017.04.018. Epub 2017 Apr 27. Forensic Sci Int Genet. 2017. PMID: 28482259
Paternal and maternal mutations in X-STRs: A GHEP-ISFG collaborative study.
Pinto N, Pereira V, Tomas C, Loiola S, Carvalho EF, Modesti N, Maxzud M, Marcucci V, Cano H, Cicarelli R, Januario B, Bento A, Brito P, Burgos G, Paz-Cruz E, Díez-Juárez L, Vannelli S, Pontes ML, Berardi G, Furfuro S, Fernandez A, Sumita D, Bobillo C, García MG, Gusmão L. Pinto N, et al. Forensic Sci Int Genet. 2020 May;46:102258. doi: 10.1016/j.fsigen.2020.102258. Epub 2020 Feb 5. Forensic Sci Int Genet. 2020. PMID: 32066109
Risk Variants in Three Alzheimer's Disease Genes Show Association with EEG Endophenotypes.
Macedo A, Gómez C, Rebelo MÂ, Poza J, Gomes I, Martins S, Maturana-Candelas A, Pablo VG, Durães L, Sousa P, Figueruelo M, Rodríguez M, Pita C, Arenas M, Álvarez L, Hornero R, Lopes AM, Pinto N. Macedo A, et al. Among authors: pinto n. J Alzheimers Dis. 2021;80(1):209-223. doi: 10.3233/JAD-200963. J Alzheimers Dis. 2021. PMID: 33522999 Free PMC article.
36 results