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Results by year

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 1
2023 3
2024 0

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Search Results

72 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.
Prevalence and Incidence of Huntington's Disease.
Strong M, Quarrell OW. Strong M, et al. Among authors: quarrell ow. Mov Disord. 2023 Aug;38(8):1570-1572. doi: 10.1002/mds.29532. Mov Disord. 2023. PMID: 37565397 No abstract available.
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.
Biallelic variants in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype-phenotype correlation study.
Loong L, Tardivo A, Knaus A, Hashim M, Pagnamenta AT, Alt K, Böhrer-Rabel H, Caro-Llopis A, Cole T, Distelmaier F, Edery P, Ferreira CR, Jezela-Stanek A, Kerr B, Kluger G, Krawitz PM, Kuhn M, Lemke JR, Lesca G, Lynch SA, Martinez F, Maxton C, Mierzewska H, Monfort S, Nicolai J, Orellana C, Pal DK, Płoski R, Quarrell OW, Rosello M, Rydzanicz M, Sabir A, Śmigiel R, Stegmann APA, Stewart H, Stumpel C, Szczepanik E, Tzschach A, Wolfe L, Taylor JC, Murakami Y, Kinoshita T, Bayat A, Kini U. Loong L, et al. Among authors: quarrell ow. Genet Med. 2023 Jan;25(1):37-48. doi: 10.1016/j.gim.2022.09.007. Epub 2022 Nov 2. Genet Med. 2023. PMID: 36322149 Free article.
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.
Dystonia in Pediatric Huntington's Disease; Prominent and Possibly Painful.
Ketels MMA, Quarrell OW, Oosterloo M. Ketels MMA, et al. Among authors: quarrell ow. Mov Disord Clin Pract. 2023 Aug 18;10(10):1552-1553. doi: 10.1002/mdc3.13850. eCollection 2023 Oct. Mov Disord Clin Pract. 2023. PMID: 37868924 Free PMC article. No abstract available.
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.
Maxillonasal dysplasia (Binder's syndrome).
Quarrell OW, Koch M, Hughes HE. Quarrell OW, et al. J Med Genet. 1990 Jun;27(6):384-7. doi: 10.1136/jmg.27.6.384. J Med Genet. 1990. PMID: 2359101 Free PMC article. No abstract available.
72 results