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

Year Number of Results
1986 3
1987 2
1988 4
1989 2
1990 4
1991 1
1993 1
1994 2
1995 3
1996 4
1997 1
1998 2
1999 1
2001 2
2002 3
2003 1
2004 2
2005 3
2006 4
2007 4
2008 2
2010 4
2011 1
2012 1
2013 2
2016 3
2017 1
2018 3
2019 5
2021 1
2022 0
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69 results
Results by year
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Page 1
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord J, McMullan DJ, Eberhardt RY, Rinck G, Hamilton SJ, Quinlan-Jones E, Prigmore E, Keelagher R, Best SK, Carey GK, Mellis R, Robart S, Berry IR, Chandler KE, Cilliers D, Cresswell L, Edwards SL, Gardiner C, Henderson A, Holden ST, Homfray T, Lester T, Lewis RA, Newbury-Ecob R, Prescott K, Quarrell OW, Ramsden SC, Roberts E, Tapon D, Tooley MJ, Vasudevan PC, Weber AP, Wellesley DG, Westwood P, White H, Parker M, Williams D, Jenkins L, Scott RH, Kilby MD, Chitty LS, Hurles ME, Maher ER; Prenatal Assessment of Genomes and Exomes Consortium. Lord J, et al. Among authors: quarrell ow. Lancet. 2019 Feb 23;393(10173):747-757. doi: 10.1016/S0140-6736(18)31940-8. Epub 2019 Jan 31. Lancet. 2019. PMID: 30712880 Free PMC article.
Syndromes with lissencephaly.
Pilz DT, Quarrell OW. Pilz DT, et al. Among authors: quarrell ow. J Med Genet. 1996 Apr;33(4):319-23. doi: 10.1136/jmg.33.4.319. J Med Genet. 1996. PMID: 8730288 Free PMC article. Review. No abstract available.
Huntington's disease: prediction and prevention.
Harper PS, Quarrell OW, Youngman S. Harper PS, et al. Among authors: quarrell ow. Philos Trans R Soc Lond B Biol Sci. 1988 Jun 15;319(1194):285-98. doi: 10.1098/rstb.1988.0050. Philos Trans R Soc Lond B Biol Sci. 1988. PMID: 2900522 Review.
Managing juvenile Huntington's disease.
Quarrell OW, Nance MA, Nopoulos P, Paulsen JS, Smith JA, Squitieri F. Quarrell OW, et al. Neurodegener Dis Manag. 2013 Jun 1;3(3):10.2217/nmt.13.18. doi: 10.2217/nmt.13.18. Neurodegener Dis Manag. 2013. PMID: 24416077 Free PMC article.
Familial visceral neuropathy: a defined entity?
Roper EC, Gibson A, McAlindon ME, Williams LH, Cook JA, Kandler RH, Quarrell OW. Roper EC, et al. Among authors: quarrell ow. Am J Med Genet A. 2005 Sep 1;137A(3):249-54. doi: 10.1002/ajmg.a.30880. Am J Med Genet A. 2005. PMID: 16088914 Review.
Large-scale open-source three-dimensional growth curves for clinical facial assessment and objective description of facial dysmorphism.
Matthews HS, Palmer RL, Baynam GS, Quarrell OW, Klein OD, Spritz RA, Hennekam RC, Walsh S, Shriver M, Weinberg SM, Hallgrimsson B, Hammond P, Penington AJ, Peeters H, Claes PD. Matthews HS, et al. Among authors: quarrell ow. Sci Rep. 2021 Jun 9;11(1):12175. doi: 10.1038/s41598-021-91465-z. Sci Rep. 2021. PMID: 34108542 Free PMC article.
A hypomorphic allele of SLC35D1 results in Schneckenbecken-like dysplasia.
Rautengarten C, Quarrell OW, Stals K, Caswell RC, De Franco E, Baple E, Burgess N, Jokhi R, Heazlewood JL, Offiah AC, Ebert B, Ellard S. Rautengarten C, et al. Among authors: quarrell ow. Hum Mol Genet. 2019 Nov 1;28(21):3543-3551. doi: 10.1093/hmg/ddz200. Hum Mol Genet. 2019. PMID: 31423530 Free PMC article.
Defining pediatric huntington disease: Time to abandon the term Juvenile Huntington Disease?
Quarrell OWJ, Nance MA, Nopoulos P, Reilmann R, Oosterloo M, Tabrizi SJ, Furby H, Saft C, Roos RAC, Squitieri F, Landwehrmeyer GB, Burgunder JM; Juvenile Huntington Disease Working Group of the European Huntington Disease Network. Quarrell OWJ, et al. Mov Disord. 2019 Apr;34(4):584-585. doi: 10.1002/mds.27640. Epub 2019 Feb 20. Mov Disord. 2019. PMID: 30788860 No abstract available.
27 years of prenatal diagnosis for Huntington disease in the United Kingdom.
Piña-Aguilar RE, Simpson SA, Alshatti A, Clarke A, Craufurd D, Dorkins H, Doye K, Lahiri N, Lashwood A, Lynch C, Miller C, Morton S, O'Driscoll M, Quarrell OW, Rae D, Strong M, Tomlinson C, Turnpenny P, Miedzybrodzka Z; UK HD Predictive Testing Consortium. Piña-Aguilar RE, et al. Among authors: quarrell ow. Genet Med. 2019 Jul;21(7):1639-1643. doi: 10.1038/s41436-018-0367-z. Epub 2018 Dec 14. Genet Med. 2019. PMID: 30546084 Free article.
69 results