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

Year Number of Results
1963 1
1967 1
1969 2
1970 2
1971 2
1972 4
1973 7
1974 3
1975 1
1976 2
1977 3
1978 6
1979 2
1980 4
1981 3
1982 1
1983 1
1984 2
1985 4
1986 4
1987 3
1988 2
1989 4
1990 4
1991 4
1992 4
1993 3
1994 5
1995 3
1996 6
1997 11
1998 9
1999 2
2000 10
2001 9
2002 2
2003 5
2004 10
2005 6
2006 16
2007 12
2008 12
2009 12
2010 12
2011 18
2012 10
2013 13
2014 13
2015 18
2016 16
2017 14
2018 20
2019 26
2020 26
2021 31
2022 30
2023 27
2024 23

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453 results

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Page 1
Overview of current learning theories for medical educators.
Torre DM, Daley BJ, Sebastian JL, Elnicki DM. Torre DM, et al. Among authors: sebastian jl. Am J Med. 2006 Oct;119(10):903-7. doi: 10.1016/j.amjmed.2006.06.037. Am J Med. 2006. PMID: 17000227 Review. No abstract available.
Efficacy and safety of a soft contact lens to control myopia progression.
Garcia-Del Valle AM, Blázquez V, Gros-Otero J, Infante M, Culebras A, Verdejo A, Sebastián J, García M, Bueno S, Piñero DP. Garcia-Del Valle AM, et al. Among authors: sebastian j. Clin Exp Optom. 2021 Jan;104(1):14-21. doi: 10.1111/cxo.13077. Clin Exp Optom. 2021. PMID: 32342559 Free article. Clinical Trial.
GIGYF1 disruption associates with autism and impaired IGF-1R signaling.
Chen G, Yu B, Tan S, Tan J, Jia X, Zhang Q, Zhang X, Jiang Q, Hua Y, Han Y, Luo S, Hoekzema K, Bernier RA, Earl RK, Kurtz-Nelson EC, Idleburg MJ, Madan-Khetarpal S, Clark R, Sebastian J, Fernandez-Jaen A, Alvarez S, King SD, Ramos LL, Santos MLS, Martin DM, Brooks D, Symonds JD, Cutcutache I, Pan Q, Hu Z, Yuan L, Eichler EE, Xia K, Guo H. Chen G, et al. Among authors: sebastian j. J Clin Invest. 2022 Oct 3;132(19):e159806. doi: 10.1172/JCI159806. J Clin Invest. 2022. PMID: 35917186 Free PMC article.
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, Kvarnung M, Lindstrand A, Nordgren A, Gecz J, Iascone M, Cereda A, Scatigno A, Maitz S, Zanni G, Bertini E, Zweier C, Schuhmann S, Wiesener A, Pepper M, Panjwani H, Torti E, Abid F, Anselm I, Srivastava S, Atwal P, Bacino CA, Bhat G, Cobian K, Bird LM, Friedman J, Wright MS, Callewaert B, Petit F, Mathieu S, Afenjar A, Christensen CK, White KM, Elpeleg O, Berger I, Espineli EJ, Fagerberg C, Brasch-Andersen C, Hansen LK, Feyma T, Hughes S, Thiffault I, Sullivan B, Yan S, Keller K, Keren B, Mignot C, Kooy F, Meuwissen M, Basinger A, Kukolich M, Philips M, Ortega L, Drummond-Borg M, Lauridsen M, Sorensen K, Lehman A; CAUSES Study; Lopez-Rangel E, Levy P, Lessel D, Lotze T, Madan-Khetarpal S, Sebastian J, Vento J, Vats D, Benman LM, Mckee S, Mirzaa GM, Muss C, Pappas J, Peeters H, Romano C, Elia M, Galesi O, Simon MEH, van Gassen KLI, Simpson K, Stratton R, Syed S, Thevenon J, Palafoll IV, Vitobello A, Bournez M, Faivre L, Xia K; SPARK Consortium; Earl RK, Nowakowski T, Bernier RA, Eichler EE. Gillentine MA, et al. Among authors: sebastian j. Genome Med. 2021 Apr 19;13(1):63. doi: 10.1186/s13073-021-00870-6. Genome Med. 2021. PMID: 33874999 Free PMC article.
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.
Radio FC, Pang K, Ciolfi A, Levy MA, Hernández-García A, Pedace L, Pantaleoni F, Liu Z, de Boer E, Jackson A, Bruselles A, McConkey H, Stellacci E, Lo Cicero S, Motta M, Carrozzo R, Dentici ML, McWalter K, Desai M, Monaghan KG, Telegrafi A, Philippe C, Vitobello A, Au M, Grand K, Sanchez-Lara PA, Baez J, Lindstrom K, Kulch P, Sebastian J, Madan-Khetarpal S, Roadhouse C, MacKenzie JJ, Monteleone B, Saunders CJ, Jean Cuevas JK, Cross L, Zhou D, Hartley T, Sawyer SL, Monteiro FP, Secches TV, Kok F, Schultz-Rogers LE, Macke EL, Morava E, Klee EW, Kemppainen J, Iascone M, Selicorni A, Tenconi R, Amor DJ, Pais L, Gallacher L, Turnpenny PD, Stals K, Ellard S, Cabet S, Lesca G, Pascal J, Steindl K, Ravid S, Weiss K, Castle AMR, Carter MT, Kalsner L, de Vries BBA, van Bon BW, Wevers MR, Pfundt R, Stegmann APA, Kerr B, Kingston HM, Chandler KE, Sheehan W, Elias AF, Shinde DN, Towne MC, Robin NH, Goodloe D, Vanderver A, Sherbini O, Bluske K, Hagelstrom RT, Zanus C, Faletra F, Musante L, Kurtz-Nelson EC, Earl RK, Anderlid BM, Morin G, van Slegtenhorst M, Diderich KEM, Brooks AS, Gribnau J, Boers RG, Finestra TR, Carter LB, Rauch A, Gasparini P, Boycott KM, Barakat TS, Graham JM Jr, Fai… See abstract for full author list ➔ Radio FC, et al. Among authors: sebastian j. Am J Hum Genet. 2021 Mar 4;108(3):502-516. doi: 10.1016/j.ajhg.2021.01.015. Epub 2021 Feb 16. Am J Hum Genet. 2021. PMID: 33596411 Free PMC article.
Upholding the reputation of nurses: Academic integrity.
Hurn PD, Karagory PM, Sebastian JG, Hagerty BM, Stamler LL, LaFramboise LM. Hurn PD, et al. Among authors: sebastian jg. Nurs Outlook. 2020 Jul-Aug;68(4):383-384. doi: 10.1016/j.outlook.2020.05.003. Epub 2020 Jun 13. Nurs Outlook. 2020. PMID: 32546325 No abstract available.
Systemic Involvement in Immunoglobulin G4-Related Ophthalmic Disease.
Lai KKH, Aljufairi FMAA, Sebastian JU, Yip CCY, Wei Y, Jia R, Cheuk W, Cheng ACO, Chin JKY, Chu CY, Kwong CH, Yip NKF, Li KKW, Chan WH, Yip WWK, Young AL, Chan E, Ko CKL, Chan CKM, Yuen HKL, Chen LJ, Tham CCY, Pang CP, Chong KKL. Lai KKH, et al. Among authors: sebastian ju. Ocul Immunol Inflamm. 2024 Oct;32(8):1852-1858. doi: 10.1080/09273948.2023.2280709. Epub 2023 Dec 6. Ocul Immunol Inflamm. 2024. PMID: 38055933 Review.
Serotonin syndrome.
Evans CE, Sebastian J. Evans CE, et al. Among authors: sebastian j. Emerg Med J. 2007 Apr;24(4):e20. doi: 10.1136/emj.2006.040550. Emerg Med J. 2007. PMID: 17384366 Free PMC article.
Sex Differences in Susceptibility to Coccidioidomycosis.
McHardy I, Reagan KL, Sebastian JF, Barker B, Bays DJ, Dandekar S, Cohen SH, Jennings KE, Sykes J, Thompson GR 3rd. McHardy I, et al. Among authors: sebastian jf. Open Forum Infect Dis. 2022 Feb 16;9(3):ofab543. doi: 10.1093/ofid/ofab543. eCollection 2022 Mar. Open Forum Infect Dis. 2022. PMID: 35252466 Free PMC article.
453 results