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

Year Number of Results
2002 1
2003 1
2005 1
2006 3
2007 3
2008 2
2009 4
2010 3
2011 2
2012 8
2013 12
2014 11
2015 12
2016 11
2017 13
2018 20
2019 29
2020 46
2021 46
2022 25
2023 20
2024 10

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251 results

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Page 1
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, Dong S, Wamsley B, Klei L, Wang L, Hao SP, Stevens CR, Cusick C, Babadi M, Banks E, Collins B, Dodge S, Gabriel SB, Gauthier L, Lee SK, Liang L, Ljungdahl A, Mahjani B, Sloofman L, Smirnov AN, Barbosa M, Betancur C, Brusco A, Chung BHY, Cook EH, Cuccaro ML, Domenici E, Ferrero GB, Gargus JJ, Herman GE, Hertz-Picciotto I, Maciel P, Manoach DS, Passos-Bueno MR, Persico AM, Renieri A, Sutcliffe JS, Tassone F, Trabetti E, Campos G, Cardaropoli S, Carli D, Chan MCY, Fallerini C, Giorgio E, Girardi AC, Hansen-Kiss E, Lee SL, Lintas C, Ludena Y, Nguyen R, Pavinato L, Pericak-Vance M, Pessah IN, Schmidt RJ, Smith M, Costa CIS, Trajkova S, Wang JYT, Yu MHC; Autism Sequencing Consortium (ASC); Broad Institute Center for Common Disease Genomics (Broad-CCDG); iPSYCH-BROAD Consortium; Cutler DJ, De Rubeis S, Buxbaum JD, Daly MJ, Devlin B, Roeder K, Sanders SJ, Talkowski ME. Fu JM, et al. Among authors: costa cis. Nat Genet. 2022 Sep;54(9):1320-1331. doi: 10.1038/s41588-022-01104-0. Epub 2022 Aug 18. Nat Genet. 2022. PMID: 35982160 Free PMC article.
Proceedings of the 3rd IPLeiria's International Health Congress : Leiria, Portugal. 6-7 May 2016.
Tomás CC, Oliveira E, Sousa D, Uba-Chupel M, Furtado G, Rocha C, Teixeira A, Ferreira P, Alves C, Gisin S, Catarino E, Carvalho N, Coucelo T, Bonfim L, Silva C, Franco D, González JA, Jardim HG, Silva R, Baixinho CL, Presado MªH, Marques MªF, Cardoso ME, Cunha M, Mendes J, Xavier A, Galhardo A, Couto M, Frade JG, Nunes C, Mesquita JR, Nascimento MS, Gonçalves G, Castro C, Mártires A, Monteiro MªJ, Rainho C, Caballero FP, Monago FM, Guerrero JT, Monago RM, Trigo AP, Gutierrez ML, Milanés GM, Reina MG, Villanueva AG, Piñero AS, Aliseda IR, Ramirez FB, Ribeiro A, Quelhas A, Manso C, Caballero FP, Guerrero JT, Monago FM, Santos RB, Jimenez NR, Nuñez CG, Gomez IR, Fernandez MªJL, Marquez LA, Moreno AL, Huertas MªJT, Ramirez FB, Seabra D, Salvador MªC, Braga L, Parreira P, Salgueiro-Oliveira A, Arreguy-Sena C, Oliveira BF, Henriques MªA, Santos J, Lebre S, Marques A, Festas C, Rodrigues S, Ribeiro A, Lumini J, Figueiredo AG, Hernandez-Martinez FJ, Campi L, Quintana-Montesdeoca MªP, Jimenez-Diaz JF, Rodriguez-De-Vera BC, Parente A, Mata MªA, Pereira AMª, Fernandes A, Brás M, Pinto MªR, Parreira P, Basto ML, Rei AC, Mónico LM, Sousa G, Morna C, Freitas O, Freitas G, Jardim A, Vasconcelos … See abstract for full author list ➔ Tomás CC, et al. Among authors: costa c. BMC Health Serv Res. 2016 Jul 6;16 Suppl 3(Suppl 3):200. doi: 10.1186/s12913-016-1423-5. BMC Health Serv Res. 2016. PMID: 27409075 Free PMC article.
Juvenile amyopathic dermatomyositis.
Napolitano M, Megna M, Squillace L, Costa C, Scalvenzi M. Napolitano M, et al. Among authors: costa c. G Ital Dermatol Venereol. 2019 Apr;154(2):215-216. doi: 10.23736/S0392-0488.17.05696-6. Epub 2017 Jul 11. G Ital Dermatol Venereol. 2019. PMID: 28704993 No abstract available.
Waste exposure and skin diseases.
Megna M, Napolitano M, Costa C, Balato N, Patruno C. Megna M, et al. Among authors: costa c. G Ital Dermatol Venereol. 2017 Aug;152(4):379-382. doi: 10.23736/S0392-0488.17.05505-5. Epub 2017 Feb 16. G Ital Dermatol Venereol. 2017. PMID: 28209048 Review.
A rare evolution of porokeratosis.
Mascolo M, Patri A, Pace M, Costa C, Varricchio S, Travaglino A, Scalvenzi M. Mascolo M, et al. Among authors: costa c. Ital J Dermatol Venerol. 2022 Feb;157(1):102-104. doi: 10.23736/S2784-8671.20.06630-4. Epub 2020 Oct 21. Ital J Dermatol Venerol. 2022. PMID: 33084264 No abstract available.
[Childhood obesity].
da Costa CD, Ferreira MG, Amaral R. da Costa CD, et al. Acta Med Port. 2010 May-Jun;23(3):379-84. Epub 2010 Jun 14. Acta Med Port. 2010. PMID: 20654255 Free article. Portuguese.
Dystrophin genetic variants and autism.
Passos-Bueno MR, Costa CIS, Zatz M. Passos-Bueno MR, et al. Among authors: costa cis. Discov Ment Health. 2022 Mar 24;2(1):4. doi: 10.1007/s44192-022-00008-z. Discov Ment Health. 2022. PMID: 37861890 Free PMC article.
Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes.
Costa CIS, da Silva Montenegro EM, Zarrei M, de Sá Moreira E, Silva IMW, de Oliveira Scliar M, Wang JYT, Zachi EC, Branco EV, da Costa SS, Lourenço NCV, Vianna-Morgante AM, Rosenberg C, Krepischi ACV, Scherer SW, Passos-Bueno MR. Costa CIS, et al. Clin Genet. 2022 Jan;101(1):134-141. doi: 10.1111/cge.14072. Epub 2021 Nov 15. Clin Genet. 2022. PMID: 34664255
Rituximab in Steroid-Dependent Podocytopathies.
Costa C, Antunes A, Oliveira J, Pereira M, Godinho I, Fernandes P, Jorge S, Lopes JA, Gameiro J. Costa C, et al. Glomerular Dis. 2024 Jul 1;4(1):129-136. doi: 10.1159/000539922. eCollection 2024 Jan-Dec. Glomerular Dis. 2024. PMID: 39144474 Free PMC article.
Expert opinion on sonidegib efficacy, safety and tolerability.
Villani A, Fabbrocini G, Costa C, Ocampo-Garza SS, Lallas A, Scalvenzi M. Villani A, et al. Among authors: costa c. Expert Opin Drug Saf. 2021 Aug;20(8):877-882. doi: 10.1080/14740338.2021.1921734. Epub 2021 May 12. Expert Opin Drug Saf. 2021. PMID: 33888008 Review.
251 results