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

Year Number of Results
1992 1
1993 1
1995 1
1996 1
1997 2
1998 1
2000 1
2002 2
2003 2
2004 1
2005 3
2007 2
2008 5
2009 1
2011 6
2012 2
2013 2
2015 1
2016 1
2017 3
2018 3
2019 2
2020 4
2021 3
2022 1
2023 1
2024 0

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49 results

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Page 1
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.
Holtz AM, VanCoillie R, Vansickle EA, Carere DA, Withrow K, Torti E, Juusola J, Millan F, Person R, Guillen Sacoto MJ, Si Y, Wentzensen IM, Pugh J, Vasileiou G, Rieger M, Reis A, Argilli E, Sherr EH, Aldinger KA, Dobyns WB, Brunet T, Hoefele J, Wagner M, Haber B, Kotzaeridou U, Keren B, Heron D, Mignot C, Heide S, Courtin T, Buratti J, Murugasen S, Donald KA, O'Heir E, Moody S, Kim KH, Burton BK, Yoon G, Campo MD, Masser-Frye D, Kozenko M, Parkinson C, Sell SL, Gordon PL, Prokop JW, Karaa A, Bupp C, Raby BA. Holtz AM, et al. Among authors: sell sl. Genet Med. 2022 Oct;24(10):2065-2078. doi: 10.1016/j.gim.2022.07.005. Epub 2022 Aug 18. Genet Med. 2022. PMID: 35980381 Free PMC article.
POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies.
Smallwood K, Watt KEN, Ide S, Baltrunaite K, Brunswick C, Inskeep K, Capannari C, Adam MP, Begtrup A, Bertola DR, Demmer L, Demo E, Devinsky O, Gallagher ER, Guillen Sacoto MJ, Jech R, Keren B, Kussmann J, Ladda R, Lansdon LA, Lunke S, Mardy A, McWalters K, Person R, Raiti L, Saitoh N, Saunders CJ, Schnur R, Skorvanek M, Sell SL, Slavotinek A, Sullivan BR, Stark Z, Symonds JD, Wenger T, Weber S, Whalen S, White SM, Winkelmann J, Zech M, Zeidler S, Maeshima K, Stottmann RW, Trainor PA, Weaver KN. Smallwood K, et al. Among authors: sell sl. Am J Hum Genet. 2023 May 4;110(5):809-825. doi: 10.1016/j.ajhg.2023.03.014. Epub 2023 Apr 18. Am J Hum Genet. 2023. PMID: 37075751 Free PMC article.
Changing your practice.
Van Sell SL. Van Sell SL. RN. 2008 Mar;71(3):9. RN. 2008. PMID: 18399049 No abstract available.
Help stop self-injury.
Van Sell SL, O'Quin L, Oliphant E, Shull P, Johnston E, Nguyen C. Van Sell SL, et al. RN. 2005 Nov;68(11):54-8; quiz 59. RN. 2005. PMID: 16334382 No abstract available.
Stress incontinence: it's no laughing matter.
Bray B, Van Sell SL, Miller-Anderson M. Bray B, et al. Among authors: van sell sl. RN. 2007 Apr;70(4):25-9; quiz 30. RN. 2007. PMID: 17479692 Review. No abstract available.
Family presence during resuscitation.
Strasen J, Van Sell SL, Sheriff S. Strasen J, et al. Among authors: van sell sl. Nurs Manage. 2015 Oct;46(10):46-50. doi: 10.1097/01.NUMA.0000471581.01067.32. Nurs Manage. 2015. PMID: 26397875 No abstract available.
MicroRNA profiling identifies a novel compound with antidepressant properties.
Sell SL, Boone DR, Weisz HA, Cardenas C, Willey HE, Bolding IJ, Micci MA, Falduto MT, Torres KEO, DeWitt DS, Prough DS, Hellmich HL. Sell SL, et al. PLoS One. 2019 Aug 23;14(8):e0221163. doi: 10.1371/journal.pone.0221163. eCollection 2019. PLoS One. 2019. PMID: 31442236 Free PMC article.
HNRNPR Variants that Impair Homeobox Gene Expression Drive Developmental Disorders in Humans.
Duijkers FA, McDonald A, Janssens GE, Lezzerini M, Jongejan A, van Koningsbruggen S, Leeuwenburgh-Pronk WG, Wlodarski MW, Moutton S, Tran-Mau-Them F, Thauvin-Robinet C, Faivre L, Monaghan KG, Smol T, Boute-Benejean O, Ladda RL, Sell SL, Bruel AL, Houtkooper RH, MacInnes AW. Duijkers FA, et al. Among authors: sell sl. Am J Hum Genet. 2019 Jun 6;104(6):1040-1059. doi: 10.1016/j.ajhg.2019.03.024. Epub 2019 May 9. Am J Hum Genet. 2019. PMID: 31079900 Free PMC article.
49 results