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

Year Number of Results
2002 5
2003 9
2004 12
2005 10
2006 8
2007 12
2008 15
2009 17
2010 12
2011 9
2012 25
2013 12
2014 10
2015 14
2016 12
2017 12
2018 9
2019 9
2020 17
2021 18
2022 13
2023 5
2024 22
2025 2

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260 results

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Page 1
Simpson-Golabi-Behmel syndrome.
Vaisfeld A, Neri G. Vaisfeld A, et al. Among authors: neri g. Am J Med Genet C Semin Med Genet. 2024 Dec;196(4):e32088. doi: 10.1002/ajmg.c.32088. Epub 2024 May 20. Am J Med Genet C Semin Med Genet. 2024. PMID: 38766979 Review.
Elements of morphology: standard terminology for the head and face.
Allanson JE, Cunniff C, Hoyme HE, McGaughran J, Muenke M, Neri G. Allanson JE, et al. Among authors: neri g. Am J Med Genet A. 2009 Jan;149A(1):6-28. doi: 10.1002/ajmg.a.32612. Am J Med Genet A. 2009. PMID: 19125436 Free PMC article.
Dermatological manifestations, management, and care in RASopathies.
Kavamura MI, Leoni C, Neri G. Kavamura MI, et al. Among authors: neri g. Am J Med Genet C Semin Med Genet. 2022 Dec;190(4):452-458. doi: 10.1002/ajmg.c.32027. Epub 2022 Dec 21. Am J Med Genet C Semin Med Genet. 2022. PMID: 36541891 Review.
Fragile X syndrome.
Terracciano A, Chiurazzi P, Neri G. Terracciano A, et al. Among authors: neri g. Am J Med Genet C Semin Med Genet. 2005 Aug 15;137C(1):32-7. doi: 10.1002/ajmg.c.30062. Am J Med Genet C Semin Med Genet. 2005. PMID: 16010677 Review.
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations.
Lepri F, De Luca A, Stella L, Rossi C, Baldassarre G, Pantaleoni F, Cordeddu V, Williams BJ, Dentici ML, Caputo V, Venanzi S, Bonaguro M, Kavamura I, Faienza MF, Pilotta A, Stanzial F, Faravelli F, Gabrielli O, Marino B, Neri G, Silengo MC, Ferrero GB, Torrrente I, Selicorni A, Mazzanti L, Digilio MC, Zampino G, Dallapiccola B, Gelb BD, Tartaglia M. Lepri F, et al. Among authors: neri g. Hum Mutat. 2011 Jul;32(7):760-72. doi: 10.1002/humu.21492. Epub 2011 Apr 28. Hum Mutat. 2011. PMID: 21387466 Free PMC article.
Autologous anti-GD2 CAR T cells efficiently target primary human glioblastoma.
Chiavelli C, Prapa M, Rovesti G, Silingardi M, Neri G, Pugliese G, Trudu L, Dall'Ora M, Golinelli G, Grisendi G, Vinet J, Bestagno M, Spano C, Papapietro RV, Depenni R, Di Emidio K, Pasetto A, Nascimento Silva D, Feletti A, Berlucchi S, Iaccarino C, Pavesi G, Dominici M. Chiavelli C, et al. Among authors: neri g. NPJ Precis Oncol. 2024 Feb 1;8(1):26. doi: 10.1038/s41698-024-00506-z. NPJ Precis Oncol. 2024. PMID: 38302615 Free PMC article.
Choriocapillaris in Age-Related Macular Degeneration.
Neri G, Olivieri C, Serafino S, Viggiano P, Marolo P, Reibaldi M, Borrelli E. Neri G, et al. Turk J Ophthalmol. 2024 Aug 28;54(4):228-234. doi: 10.4274/tjo.galenos.2024.04608. Turk J Ophthalmol. 2024. PMID: 39205438 Free PMC article. Review.
X-linked intellectual disability update 2017.
Neri G, Schwartz CE, Lubs HA, Stevenson RE. Neri G, et al. Am J Med Genet A. 2018 Jun;176(6):1375-1388. doi: 10.1002/ajmg.a.38710. Epub 2018 Apr 25. Am J Med Genet A. 2018. PMID: 29696803 Free PMC article. Review.
Deep Learning in Neovascular Age-Related Macular Degeneration.
Borrelli E, Serafino S, Ricardi F, Coletto A, Neri G, Olivieri C, Ulla L, Foti C, Marolo P, Toro MD, Bandello F, Reibaldi M. Borrelli E, et al. Among authors: neri g. Medicina (Kaunas). 2024 Jun 17;60(6):990. doi: 10.3390/medicina60060990. Medicina (Kaunas). 2024. PMID: 38929607 Free PMC article. Review.
Personal journeys to and in human genetics and dysmorphology.
Schwartz CE, Aylsworth AS, Allanson J, Battaglia A, Carey JC, Curry CJ, Davies KE, Eichler EE, Graham JM Jr, Hall B, Hall JG, Holmes LB, Hoyme HE, Hunter A, Innis J, Johnson J, Keppler-Noreuil KM, Leroy JG, Moore C, Nelson DL, Neri G, Opitz JM, Picketts D, Raymond FL, Shalev SA, Stevenson RE, Stumpel CTRM, Sutherland G, Viskochil DH, Weaver DD, Zackai EH. Schwartz CE, et al. Among authors: neri g. Am J Med Genet A. 2024 Jun;194(6):e63514. doi: 10.1002/ajmg.a.63514. Epub 2024 Feb 8. Am J Med Genet A. 2024. PMID: 38329159
260 results