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

Year Number of Results
1994 1
1995 2
1998 4
2000 3
2001 2
2002 2
2003 3
2004 8
2005 5
2006 11
2007 5
2008 7
2009 4
2010 4
2011 3
2012 4
2013 4
2014 3
2015 2
2016 2
2017 6
2018 11
2019 7
2020 8
2021 10
2022 13
2023 12
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2025 7

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147 results

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Page 1
Spina Bifida.
Iskandar BJ, Finnell RH. Iskandar BJ, et al. N Engl J Med. 2022 Aug 4;387(5):444-450. doi: 10.1056/NEJMra2116032. N Engl J Med. 2022. PMID: 35921452 Review. No abstract available.
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus.
Jin SC, Dong W, Kundishora AJ, Panchagnula S, Moreno-De-Luca A, Furey CG, Allocco AA, Walker RL, Nelson-Williams C, Smith H, Dunbar A, Conine S, Lu Q, Zeng X, Sierant MC, Knight JR, Sullivan W, Duy PQ, DeSpenza T, Reeves BC, Karimy JK, Marlier A, Castaldi C, Tikhonova IR, Li B, Peña HP, Broach JR, Kabachelor EM, Ssenyonga P, Hehnly C, Ge L, Keren B, Timberlake AT, Goto J, Mangano FT, Johnston JM, Butler WE, Warf BC, Smith ER, Schiff SJ, Limbrick DD Jr, Heuer G, Jackson EM, Iskandar BJ, Mane S, Haider S, Guclu B, Bayri Y, Sahin Y, Duncan CC, Apuzzo MLJ, DiLuna ML, Hoffman EJ, Sestan N, Ment LR, Alper SL, Bilguvar K, Geschwind DH, Günel M, Lifton RP, Kahle KT. Jin SC, et al. Among authors: iskandar bj. Nat Med. 2020 Nov;26(11):1754-1765. doi: 10.1038/s41591-020-1090-2. Epub 2020 Oct 19. Nat Med. 2020. PMID: 33077954 Free PMC article.
Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations.
Zhao S, Mekbib KY, van der Ent MA, Allington G, Prendergast A, Chau JE, Smith H, Shohfi J, Ocken J, Duran D, Furey CG, Hao LT, Duy PQ, Reeves BC, Zhang J, Nelson-Williams C, Chen D, Li B, Nottoli T, Bai S, Rolle M, Zeng X, Dong W, Fu PY, Wang YC, Mane S, Piwowarczyk P, Fehnel KP, See AP, Iskandar BJ, Aagaard-Kienitz B, Moyer QJ, Dennis E, Kiziltug E, Kundishora AJ, DeSpenza T Jr, Greenberg ABW, Kidanemariam SM, Hale AT, Johnston JM, Jackson EM, Storm PB, Lang SS, Butler WE, Carter BS, Chapman P, Stapleton CJ, Patel AB, Rodesch G, Smajda S, Berenstein A, Barak T, Erson-Omay EZ, Zhao H, Moreno-De-Luca A, Proctor MR, Smith ER, Orbach DB, Alper SL, Nicoli S, Boggon TJ, Lifton RP, Gunel M, King PD, Jin SC, Kahle KT. Zhao S, et al. Among authors: iskandar bj. Nat Commun. 2023 Nov 17;14(1):7452. doi: 10.1038/s41467-023-43062-z. Nat Commun. 2023. PMID: 37978175 Free PMC article.
Spina Bifida. Reply.
Iskandar BJ, Finnell RH. Iskandar BJ, et al. N Engl J Med. 2022 Oct 27;387(17):1628. doi: 10.1056/NEJMc2211513. N Engl J Med. 2022. PMID: 36300989 No abstract available.
The Nomenclature of Chiari Malformations.
Cools MJ, Wellons JC 3rd, Iskandar BJ. Cools MJ, et al. Among authors: iskandar bj. Neurosurg Clin N Am. 2023 Jan;34(1):1-7. doi: 10.1016/j.nec.2022.08.003. Epub 2022 Nov 2. Neurosurg Clin N Am. 2023. PMID: 36424049 Review.
Syringomyelia in hereditary multiple exostosis.
Legare JM, Modaff P, Iskandar BJ, Pauli RM. Legare JM, et al. Among authors: iskandar bj. Am J Med Genet A. 2016 Nov;170(11):2956-2959. doi: 10.1002/ajmg.a.37854. Epub 2016 Aug 2. Am J Med Genet A. 2016. PMID: 27480811
147 results