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

Year Number of Results
1959 2
1962 1
1963 4
1964 3
1965 7
1966 4
1967 4
1968 2
1969 4
1970 4
1971 5
1973 4
1974 5
1975 2
1976 4
1977 4
1978 11
1979 6
1980 8
1981 6
1982 10
1983 9
1984 9
1985 9
1986 3
1987 10
1988 14
1989 13
1990 19
1991 17
1992 14
1993 11
1994 21
1995 20
1996 37
1997 18
1998 15
1999 28
2000 20
2001 19
2002 21
2003 25
2004 26
2005 22
2006 17
2007 22
2008 30
2009 26
2010 20
2011 18
2012 36
2013 25
2014 15
2015 25
2016 23
2017 25
2018 26
2019 19
2020 34
2021 36
2022 32
2023 21
2024 38
2025 2

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933 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.
Oral-facial-skeletal syndromes.
Neri G, Gurrieri F, Genuardi M. Neri G, et al. Am J Med Genet. 1995 Nov 20;59(3):365-8. doi: 10.1002/ajmg.1320590317. Am J Med Genet. 1995. PMID: 8599363 Review. No abstract available.
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.
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.
X-linked mental retardation.
Neri G, Chiurazzi P. Neri G, et al. Adv Genet. 1999;41:55-94. doi: 10.1016/s0065-2660(08)60151-0. Adv Genet. 1999. PMID: 10494617 Review. No abstract available.
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.
The cardiofaciocutaneous syndrome.
Roberts A, Allanson J, Jadico SK, Kavamura MI, Noonan J, Opitz JM, Young T, Neri G. Roberts A, et al. Among authors: neri g. J Med Genet. 2006 Nov;43(11):833-42. doi: 10.1136/jmg.2006.042796. Epub 2006 Jul 6. J Med Genet. 2006. PMID: 16825433 Free PMC article. Review.
Vitamins and mast cells.
Anogeianaki A, Castellani ML, Tripodi D, Toniato E, De Lutiis MA, Conti F, Felaco P, Fulcheri M, Theoharides TC, Galzio R, Caraffa A, Antinolfi P, Cuccurullo C, Ciampoli C, Felaco M, Cerulli G, Pandolfi F, Sabatino G, Neri G, Shaik-Dasthagirisaheb YB. Anogeianaki A, et al. Among authors: neri g. Int J Immunopathol Pharmacol. 2010 Oct-Dec;23(4):991-6. doi: 10.1177/039463201002300403. Int J Immunopathol Pharmacol. 2010. PMID: 21244748 Free article. Review.
More on the Noonan-CFC controversy.
Neri G, Zollino M. Neri G, et al. Am J Med Genet. 1996 Oct 16;65(2):100. doi: 10.1002/(SICI)1096-8628(19961016)65:2<100::AID-AJMG2>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8911597 No abstract available.
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.
933 results