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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 18
2026 2

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273 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.
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.
CFC syndrome.
Neri G, Kavamura MI, Zollino M, Opitz JM. Neri G, et al. Am J Med Genet A. 2003 Feb 1;116A(4):410. doi: 10.1002/ajmg.a.10012. Am J Med Genet A. 2003. PMID: 12522802 No abstract available.
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.
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.
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.
The Helena syndromes.
Neri G. Neri G. Am J Med Genet A. 2006 Oct 1;140(19):2007-12. doi: 10.1002/ajmg.a.31415. Am J Med Genet A. 2006. PMID: 16906537 Review.
Distinct neurological disorders with ATP1A3 mutations.
Heinzen EL, Arzimanoglou A, Brashear A, Clapcote SJ, Gurrieri F, Goldstein DB, Jóhannesson SH, Mikati MA, Neville B, Nicole S, Ozelius LJ, Poulsen H, Schyns T, Sweadner KJ, van den Maagdenberg A, Vilsen B; ATP1A3 Working Group. Heinzen EL, et al. Lancet Neurol. 2014 May;13(5):503-14. doi: 10.1016/S1474-4422(14)70011-0. Lancet Neurol. 2014. PMID: 24739246 Free PMC article. Review.
273 results