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

Year Number of Results
2002 3
2003 3
2004 8
2005 6
2006 3
2007 1
2008 7
2009 6
2010 9
2011 9
2012 12
2013 9
2014 5
2015 6
2016 6
2017 14
2018 8
2019 17
2020 8
2021 11
2022 10
2023 2
2024 4

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140 results

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Page 1
Spina bifida.
Mitchell LE, Adzick NS, Melchionne J, Pasquariello PS, Sutton LN, Whitehead AS. Mitchell LE, et al. Lancet. 2004 Nov 20-26;364(9448):1885-95. doi: 10.1016/S0140-6736(04)17445-X. Lancet. 2004. PMID: 15555669 Review.
Genetic epidemiology of neural tube defects.
Lupo PJ, Agopian AJ, Castillo H, Castillo J, Clayton GH, Dosa NP, Hopson B, Joseph DB, Rocque BG, Walker WO, Wiener JS, Mitchell LE. Lupo PJ, et al. Among authors: mitchell le. J Pediatr Rehabil Med. 2017 Dec 11;10(3-4):189-194. doi: 10.3233/PRM-170456. J Pediatr Rehabil Med. 2017. PMID: 29125517 Free PMC article. Review.
Review of evidence for environmental causes of uveal coloboma.
Selzer EB, Blain D, Hufnagel RB, Lupo PJ, Mitchell LE, Brooks BP. Selzer EB, et al. Among authors: mitchell le. Surv Ophthalmol. 2022 Jul-Aug;67(4):1031-1047. doi: 10.1016/j.survophthal.2021.12.008. Epub 2021 Dec 31. Surv Ophthalmol. 2022. PMID: 34979194 Free PMC article. Review.
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
Zhao Y, Diacou A, Johnston HR, Musfee FI, McDonald-McGinn DM, McGinn D, Crowley TB, Repetto GM, Swillen A, Breckpot J, Vermeesch JR, Kates WR, Digilio MC, Unolt M, Marino B, Pontillo M, Armando M, Di Fabio F, Vicari S, van den Bree M, Moss H, Owen MJ, Murphy KC, Murphy CM, Murphy D, Schoch K, Shashi V, Tassone F, Simon TJ, Shprintzen RJ, Campbell L, Philip N, Heine-Suñer D, García-Miñaúr S, Fernández L; International 22q11.2 Brain and Behavior Consortium; Bearden CE, Vingerhoets C, van Amelsvoort T, Eliez S, Schneider M, Vorstman JAS, Gothelf D, Zackai E, Agopian AJ, Gur RE, Bassett AS, Emanuel BS, Goldmuntz E, Mitchell LE, Wang T, Morrow BE. Zhao Y, et al. Among authors: mitchell le. Am J Hum Genet. 2020 Jan 2;106(1):26-40. doi: 10.1016/j.ajhg.2019.11.010. Epub 2019 Dec 20. Am J Hum Genet. 2020. PMID: 31870554 Free PMC article.
Epidemiology of neural tube defects.
Mitchell LE. Mitchell LE. Am J Med Genet C Semin Med Genet. 2005 May 15;135C(1):88-94. doi: 10.1002/ajmg.c.30057. Am J Med Genet C Semin Med Genet. 2005. PMID: 15800877 Review.
X-chromosome association studies of congenital heart defects.
Agopian AJ, Hoang TT, Goldmuntz E, Hakonarson H, Musfee FI, Mitchell LE; Pediatric Cardiac Genomics Consortium. Agopian AJ, et al. Among authors: mitchell le. Am J Med Genet A. 2020 Jan;182(1):250-254. doi: 10.1002/ajmg.a.61411. Epub 2019 Nov 15. Am J Med Genet A. 2020. PMID: 31729158 Free PMC article. No abstract available.
140 results