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

Year Number of Results
1978 1
1985 1
1986 1
1987 1
1988 4
1989 2
1990 2
1991 1
1992 3
1993 4
1994 5
1996 6
1997 2
1999 2
2000 4
2001 2
2002 4
2003 7
2004 6
2005 9
2006 9
2007 11
2008 5
2009 9
2010 16
2011 10
2012 16
2013 17
2014 14
2015 11
2016 20
2017 10
2018 7
2019 7
2020 7
2021 11
2022 7
2023 8
2024 3

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228 results

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Page 1
Esketamine Nasal Spray versus Quetiapine for Treatment-Resistant Depression.
Reif A, Bitter I, Buyze J, Cebulla K, Frey R, Fu DJ, Ito T, Kambarov Y, Llorca PM, Oliveira-Maia AJ, Messer T, Mulhern-Haughey S, Rive B, von Holt C, Young AH, Godinov Y; ESCAPE-TRD Investigators. Reif A, et al. N Engl J Med. 2023 Oct 5;389(14):1298-1309. doi: 10.1056/NEJMoa2304145. N Engl J Med. 2023. PMID: 37792613 Clinical Trial.
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.
Kaur M, Blair J, Devkota B, Fortunato S, Clark D, Lawrence A, Kim J, Do W, Semeo B, Katz O, Mehta D, Yamamoto N, Schindler E, Al Rawi Z, Wallace N, Wilde JJ, McCallum J, Liu J, Xu D, Jackson M, Rentas S, Tayoun AA, Zhe Z, Abdul-Rahman O, Allen B, Angula MA, Anyane-Yeboa K, Argente J, Arn PH, Armstrong L, Basel-Salmon L, Baynam G, Bird LM, Bruegger D, Ch'ng GS, Chitayat D, Clark R, Cox GF, Dave U, DeBaere E, Field M, Graham JM Jr, Gripp KW, Greenstein R, Gupta N, Heidenreich R, Hoffman J, Hopkin RJ, Jones KL, Jones MC, Kariminejad A, Kogan J, Lace B, Leroy J, Lynch SA, McDonald M, Meagher K, Mendelsohn N, Micule I, Moeschler J, Nampoothiri S, Ohashi K, Powell CM, Ramanathan S, Raskin S, Roeder E, Rio M, Rope AF, Sangha K, Scheuerle AE, Schneider A, Shalev S, Siu V, Smith R, Stevens C, Tkemaladze T, Toimie J, Toriello H, Turner A, Wheeler PG, White SM, Young T, Loomes KM, Pipan M, Harrington AT, Zackai E, Rajagopalan R, Conlin L, Deardorff MA, McEldrew D, Pie J, Ramos F, Musio A, Kline AD, Izumi K, Raible SE, Krantz ID. Kaur M, et al. Among authors: shalev s. Am J Med Genet A. 2023 Aug;191(8):2113-2131. doi: 10.1002/ajmg.a.63247. Epub 2023 Jun 28. Am J Med Genet A. 2023. PMID: 37377026
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.
Rice GI, Forte GM, Szynkiewicz M, Chase DS, Aeby A, Abdel-Hamid MS, Ackroyd S, Allcock R, Bailey KM, Balottin U, Barnerias C, Bernard G, Bodemer C, Botella MP, Cereda C, Chandler KE, Dabydeen L, Dale RC, De Laet C, De Goede CG, Del Toro M, Effat L, Enamorado NN, Fazzi E, Gener B, Haldre M, Lin JP, Livingston JH, Lourenco CM, Marques W Jr, Oades P, Peterson P, Rasmussen M, Roubertie A, Schmidt JL, Shalev SA, Simon R, Spiegel R, Swoboda KJ, Temtamy SA, Vassallo G, Vilain CN, Vogt J, Wermenbol V, Whitehouse WP, Soler D, Olivieri I, Orcesi S, Aglan MS, Zaki MS, Abdel-Salam GM, Vanderver A, Kisand K, Rozenberg F, Lebon P, Crow YJ. Rice GI, et al. Among authors: shalev sa. Lancet Neurol. 2013 Dec;12(12):1159-69. doi: 10.1016/S1474-4422(13)70258-8. Epub 2013 Oct 30. Lancet Neurol. 2013. PMID: 24183309 Free PMC article.
Medical genetics in Israel's diverse population.
Shalev SA, Zlotogora J, Shalata A, Levy-Lahad E. Shalev SA, et al. Lancet. 2017 Jun 24;389(10088):2453-2455. doi: 10.1016/S0140-6736(17)30875-9. Epub 2017 May 8. Lancet. 2017. PMID: 28495108 No abstract available.
Bacteriological aspects of Darier's disease.
Dodiuk-Gad R, Cohen-Barak E, Ziv M, Shani-Adir A, Shalev S, Chazan B, Raz R, Colodner R, Amichai B, Zlotogorski A, Keness Y, Rozenman D. Dodiuk-Gad R, et al. Among authors: shalev s. J Eur Acad Dermatol Venereol. 2013 Nov;27(11):1405-9. doi: 10.1111/jdv.12025. Epub 2012 Oct 19. J Eur Acad Dermatol Venereol. 2013. PMID: 23078077
Learning disabilities in Darier's disease patients.
Dodiuk-Gad R, Lerner M, Breznitz Z, Cohen-Barak E, Ziv M, Shani-Adir A, Amichai B, Zlotogorski A, Shalev S, Rozenman D. Dodiuk-Gad R, et al. Among authors: shalev s. J Eur Acad Dermatol Venereol. 2014 Mar;28(3):314-9. doi: 10.1111/jdv.12103. Epub 2013 Feb 15. J Eur Acad Dermatol Venereol. 2014. PMID: 23410204
ARCI7 Revisited and Repositioned.
Mohamad J, Malchin N, Shalev S, Sarig O, Sprecher E. Mohamad J, et al. Among authors: shalev s. J Invest Dermatol. 2017 Apr;137(4):970-972. doi: 10.1016/j.jid.2016.12.008. Epub 2016 Dec 21. J Invest Dermatol. 2017. PMID: 28011144 Free article. No abstract available.
Bi-allelic FRA10AC1 variants in a multisystem human syndrome.
Banka S, Shalev S, Park SM, Wood KA, Thomas HB, Wright HL, Alyahya M, Bankier S, Alimi O, Chervinsky E, Zeef LAH, O'Keefe RT. Banka S, et al. Among authors: shalev s. Brain. 2022 Oct 21;145(10):e86-e89. doi: 10.1093/brain/awac262. Brain. 2022. PMID: 35871492 No abstract available.
SAM syndrome is characterized by extensive phenotypic heterogeneity.
Taiber S, Samuelov L, Mohamad J, Barak EC, Sarig O, Shalev SA, Lestringant G, Sprecher E. Taiber S, et al. Among authors: shalev sa. Exp Dermatol. 2018 Jul;27(7):787-790. doi: 10.1111/exd.13551. Exp Dermatol. 2018. PMID: 29604126 Review.
228 results