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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 6
2024 7

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244 results

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Page 1
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.
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.
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.
DNA Methylation in the Diagnosis of Monogenic Diseases.
Cerrato F, Sparago A, Ariani F, Brugnoletti F, Calzari L, Coppedè F, De Luca A, Gervasini C, Giardina E, Gurrieri F, Lo Nigro C, Merla G, Miozzo M, Russo S, Sangiorgi E, Sirchia SM, Squeo GM, Tabano S, Tabolacci E, Torrente I, Genuardi M, Neri G, Riccio A. Cerrato F, et al. Among authors: neri g. Genes (Basel). 2020 Mar 26;11(4):355. doi: 10.3390/genes11040355. Genes (Basel). 2020. PMID: 32224912 Free PMC article. Review.
The ring 14 syndrome.
Zollino M, Ponzi E, Gobbi G, Neri G. Zollino M, et al. Among authors: neri g. Eur J Med Genet. 2012 May;55(5):374-80. doi: 10.1016/j.ejmg.2012.03.009. Epub 2012 Apr 14. Eur J Med Genet. 2012. PMID: 22564756 Review.
Overgrowth in myth and art.
Boccuto L, Neri G. Boccuto L, et al. Among authors: neri g. Am J Med Genet C Semin Med Genet. 2021 Jun;187(2):176-181. doi: 10.1002/ajmg.c.31910. Epub 2021 May 13. Am J Med Genet C Semin Med Genet. 2021. PMID: 33982857
XLMR genes: update 2007.
Chiurazzi P, Schwartz CE, Gecz J, Neri G. Chiurazzi P, et al. Among authors: neri g. Eur J Hum Genet. 2008 Apr;16(4):422-34. doi: 10.1038/sj.ejhg.5201994. Epub 2008 Jan 16. Eur J Hum Genet. 2008. PMID: 18197188 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.
Overgrowth syndromes: a classification.
Neri G, Moscarda M. Neri G, et al. Endocr Dev. 2009;14:53-60. doi: 10.1159/000207476. Endocr Dev. 2009. PMID: 19293574 Review.
244 results