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Results by year

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

Year Number of Results
1956 1
1963 1
1969 1
1971 1
1972 1
1973 5
1975 3
1976 1
1977 3
1978 1
1980 3
1981 3
1982 4
1983 1
1984 3
1985 3
1986 5
1987 3
1988 4
1989 5
1990 8
1991 5
1992 5
1993 6
1994 4
1995 4
1996 2
1997 7
1998 2
1999 2
2000 3
2001 1
2002 4
2003 1
2004 7
2005 6
2006 6
2007 18
2008 18
2009 12
2010 10
2011 12
2012 24
2013 21
2014 13
2015 10
2016 29
2017 40
2018 33
2019 26
2020 35
2021 31
2022 38
2023 39
2024 16

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Publication date

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508 results

Results by year

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Page 1
Neuroethics.
Kushner T, Giordano J. Kushner T, et al. Among authors: giordano j. Camb Q Healthc Ethics. 2017 Oct;26(4):524-526. doi: 10.1017/S0963180117000056. Camb Q Healthc Ethics. 2017. PMID: 28937336 No abstract available.
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Petrovski S, Aggarwal V, Giordano JL, Stosic M, Wou K, Bier L, Spiegel E, Brennan K, Stong N, Jobanputra V, Ren Z, Zhu X, Mebane C, Nahum O, Wang Q, Kamalakaran S, Malone C, Anyane-Yeboa K, Miller R, Levy B, Goldstein DB, Wapner RJ. Petrovski S, et al. Among authors: giordano jl. Lancet. 2019 Feb 23;393(10173):758-767. doi: 10.1016/S0140-6736(18)32042-7. Epub 2019 Jan 31. Lancet. 2019. PMID: 30712878
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.
Lowther C, Valkanas E, Giordano JL, Wang HZ, Currall BB, O'Keefe K, Pierce-Hoffman E, Kurtas NE, Whelan CW, Hao SP, Weisburd B, Jalili V, Fu J, Wong I, Collins RL, Zhao X, Austin-Tse CA, Evangelista E, Lemire G, Aggarwal VS, Lucente D, Gauthier LD, Tolonen C, Sahakian N, Stevens C, An JY, Dong S, Norton ME, MacKenzie TC, Devlin B, Gilmore K, Powell BC, Brandt A, Vetrini F, DiVito M, Sanders SJ, MacArthur DG, Hodge JC, O'Donnell-Luria A, Rehm HL, Vora NL, Levy B, Brand H, Wapner RJ, Talkowski ME. Lowther C, et al. Among authors: giordano jl. Am J Hum Genet. 2023 Sep 7;110(9):1454-1469. doi: 10.1016/j.ajhg.2023.07.010. Epub 2023 Aug 17. Am J Hum Genet. 2023. PMID: 37595579 Free PMC article.
Genomics of stillbirth.
Giordano JL, Wapner RJ. Giordano JL, et al. Semin Perinatol. 2024 Feb;48(1):151866. doi: 10.1016/j.semperi.2023.151866. Epub 2023 Dec 19. Semin Perinatol. 2024. PMID: 38238216
Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series.
Brar BK, Thompson MG, Vora NL, Gilmore K, Blakemore K, Miller KA, Giordano J, Dufke A, Wong B, Stover S, Lianoglou B, Van den Veyver I, Dempsey E, Rosner M, Chong K, Chitayat D, Sparks TN, Norton ME, Wapner R, Baranano K, Jelin AC; Fetal Sequencing Consortium. Brar BK, et al. Among authors: giordano j. Prenat Diagn. 2022 Dec;42(13):1686-1693. doi: 10.1002/pd.6269. Epub 2022 Nov 28. Prenat Diagn. 2022. PMID: 36403095 Free PMC article. Review.
Vaccination Disagreement Between Parents.
Giordano J. Giordano J. Am Fam Physician. 2022 May 1;105(5):544-546. Am Fam Physician. 2022. PMID: 35559638 No abstract available.
Man with Intermittent Bradycardia.
Cooper BL, Nemri KA, Giordano JA. Cooper BL, et al. Among authors: giordano ja. Ann Emerg Med. 2020 Nov;76(5):586-589. doi: 10.1016/j.annemergmed.2020.02.016. Ann Emerg Med. 2020. PMID: 33097117 Review. No abstract available.
Deep brain stimulation for obsessive-compulsive disorder: a crisis of access.
Visser-Vandewalle V, Andrade P, Mosley PE, Greenberg BD, Schuurman R, McLaughlin NC, Voon V, Krack P, Foote KD, Mayberg HS, Figee M, Kopell BH, Polosan M, Joyce EM, Chabardes S, Matthews K, Baldermann JC, Tyagi H, Holtzheimer PE, Bervoets C, Hamani C, Karachi C, Denys D, Zrinzo L, Blomstedt P, Naesström M, Abosch A, Rasmussen S, Coenen VA, Schlaepfer TE, Dougherty DD, Domenech P, Silburn P, Giordano J, Lozano AM, Sheth SA, Coyne T, Kuhn J, Mallet L, Nuttin B, Hariz M, Okun MS. Visser-Vandewalle V, et al. Among authors: giordano j. Nat Med. 2022 Aug;28(8):1529-1532. doi: 10.1038/s41591-022-01879-z. Nat Med. 2022. PMID: 35840727 No abstract available.
Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts.
Woo XY, Giordano J, Srivastava A, Zhao ZM, Lloyd MW, de Bruijn R, Suh YS, Patidar R, Chen L, Scherer S, Bailey MH, Yang CH, Cortes-Sanchez E, Xi Y, Wang J, Wickramasinghe J, Kossenkov AV, Rebecca VW, Sun H, Mashl RJ, Davies SR, Jeon R, Frech C, Randjelovic J, Rosains J, Galimi F, Bertotti A, Lafferty A, O'Farrell AC, Modave E, Lambrechts D, Ter Brugge P, Serra V, Marangoni E, El Botty R, Kim H, Kim JI, Yang HK, Lee C, Dean DA 2nd, Davis-Dusenbery B, Evrard YA, Doroshow JH, Welm AL, Welm BE, Lewis MT, Fang B, Roth JA, Meric-Bernstam F, Herlyn M, Davies MA, Ding L, Li S, Govindan R, Isella C, Moscow JA, Trusolino L, Byrne AT, Jonkers J, Bult CJ, Medico E, Chuang JH; PDXNET Consortium; EurOPDX Consortium. Woo XY, et al. Among authors: giordano j. Nat Genet. 2021 Jan;53(1):86-99. doi: 10.1038/s41588-020-00750-6. Epub 2021 Jan 7. Nat Genet. 2021. PMID: 33414553 Free PMC article.
508 results