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Results by year

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

Year Number of Results
1970 1
1971 4
1972 3
1973 4
1974 1
1975 3
1976 3
1977 5
1978 1
1979 1
1980 6
1981 2
1982 5
1983 5
1984 2
1985 1
1986 2
1987 2
1988 2
1989 4
1990 3
1991 5
1992 2
1993 7
1994 6
1995 6
1996 6
1997 4
1998 11
1999 4
2000 9
2001 3
2002 3
2003 6
2004 5
2005 8
2006 13
2007 27
2008 27
2009 22
2010 18
2011 20
2012 20
2013 19
2014 28
2015 16
2016 7
2017 14
2018 9
2019 6
2020 13
2021 14
2022 6
Text availability
Article attribute
Article type
Publication date

Search Results

371 results
Results by year
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Page 1
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain.
Liu S, Aldinger KA, Cheng CV, Kiyama T, Dave M, McNamara HK, Zhao W, Stafford JM, Descostes N, Lee P, Caraffi SG, Ivanovski I, Errichiello E, Zweier C, Zuffardi O, Schneider M, Papavasiliou AS, Perry MS, Humberson J, Cho MT, Weber A, Swale A, Badea TC, Mao CA, Garavelli L, Dobyns WB, Reinberg D. Liu S, et al. Among authors: zuffardi o. Mol Cell. 2021 Nov 18;81(22):4663-4676.e8. doi: 10.1016/j.molcel.2021.09.020. Epub 2021 Oct 11. Mol Cell. 2021. PMID: 34637754 Free PMC article.
Array technology in prenatal diagnosis.
Zuffardi O, Vetro A, Brady P, Vermeesch J. Zuffardi O, et al. Semin Fetal Neonatal Med. 2011 Apr;16(2):94-8. doi: 10.1016/j.siny.2010.12.001. Epub 2011 Jan 5. Semin Fetal Neonatal Med. 2011. PMID: 21208835 Review.
The genetics of small-vessel disease.
Bersano A, Debette S, Zanier ER, Lanfranconi S, De Simoni MG, Zuffardi O, Micieli G. Bersano A, et al. Among authors: zuffardi o. Curr Med Chem. 2012;19(24):4124-41. doi: 10.2174/092986712802430081. Curr Med Chem. 2012. PMID: 22680632 Review.
Reply to Sajantila and Budowle.
Barton DE, Claustres M, Kozich V, Dequeker E, Fowler B, Hehir-Kwa JY, Miller K, Oosterwijk C, Peterlin B, van Ravenswaaij-Arts C, Zimmermann U, Zuffardi O, Hastings RJ. Barton DE, et al. Among authors: zuffardi o. Eur J Hum Genet. 2016 Mar;24(3):330. doi: 10.1038/ejhg.2014.290. Epub 2015 Jan 14. Eur J Hum Genet. 2016. PMID: 25585701 Free PMC article. No abstract available.
Xp duplications and sex reversal.
Zanaria E, Bardoni B, Dabovic B, Calvari V, Fraccaro M, Zuffardi O, Camerino G. Zanaria E, et al. Among authors: zuffardi o. Philos Trans R Soc Lond B Biol Sci. 1995 Nov 29;350(1333):291-6. doi: 10.1098/rstb.1995.0164. Philos Trans R Soc Lond B Biol Sci. 1995. PMID: 8570694 Review.
PRKACB and Carney complex.
Forlino A, Vetro A, Garavelli L, Ciccone R, London E, Stratakis CA, Zuffardi O. Forlino A, et al. Among authors: zuffardi o. N Engl J Med. 2014 Mar 13;370(11):1065-7. doi: 10.1056/NEJMc1309730. Epub 2014 Feb 26. N Engl J Med. 2014. PMID: 24571725 No abstract available.
Ring syndrome: still true?
Rossi E, Messa J, Zuffardi O. Rossi E, et al. Among authors: zuffardi o. J Med Genet. 2008 Nov;45(11):766-8. doi: 10.1136/jmg.2008.060442. J Med Genet. 2008. PMID: 18978335 No abstract available.
Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European study.
Raviglione F, Douzgou S, Scala M, Mingarelli A, D'Arrigo S, Freri E, Darra F, Giglio S, Bonaglia MC, Pantaleoni C, Mastrangelo M, Epifanio R, Elia M, Saletti V, Morlino S, Vari MS, De Liso P, Pavaine J, Spaccini L, Cattaneo E, Gardella E, Møller RS, Marchese F, Colonna C, Gandioli C, Gobbi G, Ram D, Palumbo O, Carella M, Germano M, Tonduti D, De Angelis D, Caputo D, Bergonzini P, Novara F, Zuffardi O, Verrotti A, Orsini A, Bonuccelli A, De Muto MC, Trivisano M, Vigevano F, Granata T, Bernardina BD, Tranchina A, Striano P. Raviglione F, et al. Among authors: zuffardi o. Seizure. 2021 May;88:60-72. doi: 10.1016/j.seizure.2021.03.025. Epub 2021 Mar 30. Seizure. 2021. PMID: 33831796 Free article.
Guidelines for molecular karyotyping in constitutional genetic diagnosis.
Vermeesch JR, Fiegler H, de Leeuw N, Szuhai K, Schoumans J, Ciccone R, Speleman F, Rauch A, Clayton-Smith J, Van Ravenswaaij C, Sanlaville D, Patsalis PC, Firth H, Devriendt K, Zuffardi O. Vermeesch JR, et al. Among authors: zuffardi o. Eur J Hum Genet. 2007 Nov;15(11):1105-14. doi: 10.1038/sj.ejhg.5201896. Epub 2007 Jul 18. Eur J Hum Genet. 2007. PMID: 17637806 Review.
371 results