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

Year Number of Results
1982 1
1983 1
1987 1
1988 1
1991 1
1994 1
2003 3
2004 3
2005 6
2006 2
2007 1
2009 2
2010 6
2011 9
2012 5
2013 4
2014 8
2015 16
2016 10
2017 12
2018 13
2019 17
2020 22
2021 21
2022 13
2023 23
2024 5

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183 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: giorgio e. 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.
DLG4-related synaptopathy: a new rare brain disorder.
Rodríguez-Palmero A, Boerrigter MM, Gómez-Andrés D, Aldinger KA, Marcos-Alcalde Í, Popp B, Everman DB, Lovgren AK, Arpin S, Bahrambeigi V, Beunders G, Bisgaard AM, Bjerregaard VA, Bruel AL, Challman TD, Cogné B, Coubes C, de Man SA, Denommé-Pichon AS, Dye TJ, Elmslie F, Feuk L, García-Miñaúr S, Gertler T, Giorgio E, Gruchy N, Haack TB, Haldeman-Englert CR, Haukanes BI, Hoyer J, Hurst ACE, Isidor B, Soller MJ, Kushary S, Kvarnung M, Landau YE, Leppig KA, Lindstrand A, Kleinendorst L, MacKenzie A, Mandrile G, Mendelsohn BA, Moghadasi S, Morton JE, Moutton S, Müller AJ, O'Leary M, Pacio-Míguez M, Palomares-Bralo M, Parikh S, Pfundt R, Pode-Shakked B, Rauch A, Repnikova E, Revah-Politi A, Ross MJ, Ruivenkamp CAL, Sarrazin E, Savatt JM, Schlüter A, Schönewolf-Greulich B, Shad Z, Shaw-Smith C, Shieh JT, Shohat M, Spranger S, Thiese H, Mau-Them FT, van Bon B, van de Burgt I, van de Laar IMBH, van Drie E, van Haelst MM, van Ravenswaaij-Arts CM, Verdura E, Vitobello A, Waldmüller S, Whiting S, Zweier C, Prada CE, de Vries BBA, Dobyns WB, Reiter SF, Gómez-Puertas P, Pujol A, Tümer Z. Rodríguez-Palmero A, et al. Among authors: giorgio e. Genet Med. 2021 May;23(5):888-899. doi: 10.1038/s41436-020-01075-9. Epub 2021 Feb 17. Genet Med. 2021. PMID: 33597769 Free article.
The Histone Code of Senescence.
Paluvai H, Di Giorgio E, Brancolini C. Paluvai H, et al. Among authors: di giorgio e. Cells. 2020 Feb 18;9(2):466. doi: 10.3390/cells9020466. Cells. 2020. PMID: 32085582 Free PMC article. Review.
RNA therapeutics for neurological diseases.
Brentari I, Zadorozhna M, Denti MA, Giorgio E. Brentari I, et al. Among authors: giorgio e. Br Med Bull. 2023 Sep 12;147(1):50-61. doi: 10.1093/bmb/ldad010. Br Med Bull. 2023. PMID: 37210633 Review.
MEF2 and the tumorigenic process, hic sunt leones.
Di Giorgio E, Hancock WW, Brancolini C. Di Giorgio E, et al. Biochim Biophys Acta Rev Cancer. 2018 Dec;1870(2):261-273. doi: 10.1016/j.bbcan.2018.05.007. Epub 2018 Jun 5. Biochim Biophys Acta Rev Cancer. 2018. PMID: 29879430 Free article. Review.
Lamin B1 as a key modulator of the developing and aging brain.
Koufi FD, Neri I, Ramazzotti G, Rusciano I, Mongiorgi S, Marvi MV, Fazio A, Shin M, Kosodo Y, Cani I, Giorgio E, Cortelli P, Manzoli L, Ratti S. Koufi FD, et al. Among authors: giorgio e. Front Cell Neurosci. 2023 Aug 31;17:1263310. doi: 10.3389/fncel.2023.1263310. eCollection 2023. Front Cell Neurosci. 2023. PMID: 37720548 Free PMC article. Review.
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
Mingardo E, Beaman G, Grote P, Nordenskjöld A, Newman W, Woolf AS, Eckstein M, Hilger AC, Dworschak GC, Rösch W, Ebert AK, Stein R, Brusco A, Di Grazia M, Tamer A, Torres FM, Hernandez JL, Erben P, Maj C, Olmos JM, Riancho JA, Valero C, Hostettler IC, Houlden H, Werring DJ, Schumacher J, Gehlen J, Giel AS, Buerfent BC, Arkani S, Åkesson E, Rotstein E, Ludwig M, Holmdahl G, Giorgio E, Berettini A, Keene D, Cervellione RM, Younsi N, Ortlieb M, Oswald J, Haid B, Promm M, Neissner C, Hirsch K, Stehr M, Schäfer FM, Schmiedeke E, Boemers TM, van Rooij IALM, Feitz WFJ, Marcelis CLM, Lacher M, Nelson J, Ure B, Fortmann C, Gale DP, Chan MMY, Ludwig KU, Nöthen MM, Heilmann S, Zwink N, Jenetzky E, Odermatt B, Knapp M, Reutter H. Mingardo E, et al. Among authors: giorgio e. Commun Biol. 2022 Nov 9;5(1):1203. doi: 10.1038/s42003-022-04092-3. Commun Biol. 2022. PMID: 36352089 Free PMC article.
Editorial: Molecular and cellular mechanisms for cancer therapy resistance.
Battaglia AM, Giorgio E, Petriaggi L, Biamonte F, Momeny M. Battaglia AM, et al. Among authors: giorgio e. Front Oncol. 2023 Nov 29;13:1340318. doi: 10.3389/fonc.2023.1340318. eCollection 2023. Front Oncol. 2023. PMID: 38094612 Free PMC article. No abstract available.
Selective class IIa HDAC inhibitors: myth or reality.
Di Giorgio E, Gagliostro E, Brancolini C. Di Giorgio E, et al. Cell Mol Life Sci. 2015 Jan;72(1):73-86. doi: 10.1007/s00018-014-1727-8. Epub 2014 Sep 5. Cell Mol Life Sci. 2015. PMID: 25189628 Review.
183 results