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Results by year

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

Year Number of Results
1985 1
1986 3
1987 2
1988 4
1989 3
1990 5
1991 1
1993 2
1994 2
1995 3
1996 4
1997 2
1998 5
1999 2
2001 3
2002 6
2003 1
2004 2
2005 4
2006 5
2007 5
2008 3
2010 4
2011 4
2012 6
2013 7
2014 4
2015 2
2016 5
2017 2
2018 3
2019 7
2021 2
2022 2
2023 1
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Article attribute
Article type
Publication date

Search Results

109 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.
Diagnostic genetic testing for Huntington's disease.
Craufurd D, MacLeod R, Frontali M, Quarrell O, Bijlsma EK, Davis M, Hjermind LE, Lahiri N, Mandich P, Martinez A, Tibben A, Roos RA; Working Group on Genetic Counselling and Testing of the European Huntington's Disease Network (EHDN). Craufurd D, et al. Among authors: quarrell o. Pract Neurol. 2015 Feb;15(1):80-4. doi: 10.1136/practneurol-2013-000790. Epub 2014 Aug 28. Pract Neurol. 2015. PMID: 25169240 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.
Predictive genetic testing for Motor neuron disease: time for a guideline?
McNeill A, Amador MD, Bekker H, Clarke A, Crook A, Cummings C, McEwen A, McDermott C, Quarrell O, Renieri A, Roggenbuck J, Salmon K, Volk A, Weishaupt J; International Alliance of ALS/MND Associations. McNeill A, et al. Among authors: quarrell o. Eur J Hum Genet. 2022 Jun;30(6):635-636. doi: 10.1038/s41431-022-01093-y. Epub 2022 Apr 5. Eur J Hum Genet. 2022. PMID: 35379930 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.
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.
A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practice.
Wadrup F, Holden S, MacLeod R, Miedzybrodzka Z, Németh AH, Owens S, Pasalodos S, Quarrell O, Clarke AJ; UK Huntington’s Disease Predictive Testing Consortium. Wadrup F, et al. Among authors: quarrell o. Eur J Hum Genet. 2019 Aug;27(8):1215-1224. doi: 10.1038/s41431-019-0375-8. Epub 2019 Mar 19. Eur J Hum Genet. 2019. PMID: 30890781 Free PMC article. Review.
109 results