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

Year Number of Results
1999 1
2000 1
2001 1
2003 1
2004 3
2005 1
2006 1
2007 3
2008 3
2009 2
2010 1
2011 1
2012 1
2013 1
2015 1
2016 1
2017 1
2018 5
2019 2
2020 2
2021 1
2022 2
2024 0

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33 results

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Page 1
The 22q11.2 deletion syndrome.
Emanuel BS, McDonald-McGinn D, Saitta SC, Zackai EH. Emanuel BS, et al. Among authors: saitta sc. Adv Pediatr. 2001;48:39-73. Adv Pediatr. 2001. PMID: 11480765 Review.
MAP'ing CNS development and cognition: an ERKsome process.
Samuels IS, Saitta SC, Landreth GE. Samuels IS, et al. Among authors: saitta sc. Neuron. 2009 Jan 29;61(2):160-7. doi: 10.1016/j.neuron.2009.01.001. Neuron. 2009. PMID: 19186160 Free PMC article. Review.
Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care.
Pirozzi F, Berkseth M, Shear R, Gonzalez L, Timms AE, Sulc J, Pao E, Oyama N, Forzano F, Conti V, Guerrini R, Doherty ES, Saitta SC, Lockwood CM, Pritchard CC, Dobyns WB, Novotny E, Wright JNN, Saneto RP, Friedman S, Hauptman J, Ojemann J, Kapur RP, Mirzaa GM. Pirozzi F, et al. Among authors: saitta sc. Brain. 2022 Apr 29;145(3):925-938. doi: 10.1093/brain/awab376. Brain. 2022. PMID: 35355055 Free PMC article.
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients.
Levin MD, Saitta SC, Gripp KW, Wenger TL, Ganesh J, Kalish JM, Epstein MR, Smith R, Czosek RJ, Ware SM, Goldenberg P, Myers A, Chatfield KC, Gillespie MJ, Zackai EH, Lin AE. Levin MD, et al. Among authors: saitta sc. Am J Med Genet A. 2018 Aug;176(8):1711-1722. doi: 10.1002/ajmg.a.38854. Epub 2018 Jul 28. Am J Med Genet A. 2018. PMID: 30055033 Free PMC article.
Further delineation of an entity caused by CREBBP and EP300 mutations but not resembling Rubinstein-Taybi syndrome.
Menke LA; DDD study; Gardeitchik T, Hammond P, Heimdal KR, Houge G, Hufnagel SB, Ji J, Johansson S, Kant SG, Kinning E, Leon EL, Newbury-Ecob R, Paolacci S, Pfundt R, Ragge NK, Rinne T, Ruivenkamp C, Saitta SC, Sun Y, Tartaglia M, Terhal PA, van Essen AJ, Vigeland MD, Xiao B, Hennekam RC. Menke LA, et al. Among authors: saitta sc. Am J Med Genet A. 2018 Apr;176(4):862-876. doi: 10.1002/ajmg.a.38626. Epub 2018 Feb 20. Am J Med Genet A. 2018. PMID: 29460469
33 results