Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
2002 9
2003 9
2004 9
2005 2
2006 4
2007 9
2008 9
2009 12
2010 10
2011 9
2012 9
2013 7
2014 9
2015 10
2016 10
2017 11
2018 14
2019 16
2020 12
Text availability
Article attribute
Article type
Publication date

Search Results

154 results
Results by year
Filters applied: . Clear all
Page 1
Utility of ctDNA to support patient selection for early phase clinical trials: the TARGET study.
Rothwell DG, Ayub M, Cook N, Thistlethwaite F, Carter L, Dean E, Smith N, Villa S, Dransfield J, Clipson A, White D, Nessa K, Ferdous S, Howell M, Gupta A, Kilerci B, Mohan S, Frese K, Gulati S, Miller C, Jordan A, Eaton H, Hickson N, O'Brien C, Graham D, Kelly C, Aruketty S, Metcalf R, Chiramel J, Tinsley N, Vickers AJ, Kurup R, Frost H, Stevenson J, Southam S, Landers D, Wallace A, Marais R, Hughes AM, Brady G, Dive C, Krebs MG. Rothwell DG, et al. Among authors: Wallace A. Nat Med. 2019 May;25(5):738-743. doi: 10.1038/s41591-019-0380-z. Epub 2019 Apr 22. Nat Med. 2019. PMID: 31011204
A standardized framework for the validation and verification of clinical molecular genetic tests.
Mattocks CJ, Morris MA, Matthijs G, Swinnen E, Corveleyn A, Dequeker E, Müller CR, Pratt V, Wallace A; EuroGentest Validation Group. Mattocks CJ, et al. Among authors: Wallace A. Eur J Hum Genet. 2010 Dec;18(12):1276-88. doi: 10.1038/ejhg.2010.101. Epub 2010 Jul 28. Eur J Hum Genet. 2010. PMID: 20664632 Free PMC article.
Schwannomatosis: a genetic and epidemiological study.
Evans DG, Bowers NL, Tobi S, Hartley C, Wallace AJ, King AT, Lloyd SKW, Rutherford SA, Hammerbeck-Ward C, Pathmanaban ON, Freeman SR, Ealing J, Kellett M, Laitt R, Thomas O, Halliday D, Ferner R, Taylor A, Duff C, Harkness EF, Smith MJ. Evans DG, et al. Among authors: Wallace AJ. J Neurol Neurosurg Psychiatry. 2018 Nov;89(11):1215-1219. doi: 10.1136/jnnp-2018-318538. Epub 2018 Jun 16. J Neurol Neurosurg Psychiatry. 2018. PMID: 29909380
A Dominantly Inherited 5' UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer.
Evans DGR, van Veen EM, Byers HJ, Wallace AJ, Ellingford JM, Beaman G, Santoyo-Lopez J, Aitman TJ, Eccles DM, Lalloo FI, Smith MJ, Newman WG. Evans DGR, et al. Among authors: Wallace AJ. Am J Hum Genet. 2018 Aug 2;103(2):213-220. doi: 10.1016/j.ajhg.2018.07.002. Am J Hum Genet. 2018. PMID: 30075112 Free PMC article.
HNRNPA1 promotes recognition of splice site decoys by U2AF2 in vivo.
Howard JM, Lin H, Wallace AJ, Kim G, Draper JM, Haeussler M, Katzman S, Toloue M, Liu Y, Sanford JR. Howard JM, et al. Among authors: Wallace AJ. Genome Res. 2018 May;28(5):689-698. doi: 10.1101/gr.229062.117. Epub 2018 Apr 12. Genome Res. 2018. PMID: 29650551 Free PMC article.
The Manchester International Consensus Group recommendations for the management of gynecological cancers in Lynch syndrome.
Crosbie EJ, Ryan NAJ, Arends MJ, Bosse T, Burn J, Cornes JM, Crawford R, Eccles D, Frayling IM, Ghaem-Maghami S, Hampel H, Kauff ND, Kitchener HC, Kitson SJ, Manchanda R, McMahon RFT, Monahan KJ, Menon U, Møller P, Möslein G, Rosenthal A, Sasieni P, Seif MW, Singh N, Skarrott P, Snowsill TM, Steele R, Tischkowitz M; Manchester International Consensus Group, Evans DG. Crosbie EJ, et al. Genet Med. 2019 Oct;21(10):2390-2400. doi: 10.1038/s41436-019-0489-y. Epub 2019 Mar 28. Genet Med. 2019. PMID: 30918358 Free PMC article.
Performance testing protocol for closed-system transfer devices used during pharmacy compounding and administration of hazardous drugs.
Wilkinson AS, Allwood MC, Morris CP, Wallace A, Finnis R, Kaminska E, Stonkute D, Szramowska M, Miller J, Pengelly I, Hemingway M. Wilkinson AS, et al. Among authors: Wallace A. PLoS One. 2018 Oct 31;13(10):e0205263. doi: 10.1371/journal.pone.0205263. eCollection 2018. PLoS One. 2018. PMID: 30379831 Free PMC article.
Pathology update to the Manchester Scoring System based on testing in over 4000 families.
Evans DG, Harkness EF, Plaskocinska I, Wallace AJ, Clancy T, Woodward ER, Howell TA, Tischkowitz M, Lalloo F. Evans DG, et al. Among authors: Wallace AJ. J Med Genet. 2017 Oct;54(10):674-681. doi: 10.1136/jmedgenet-2017-104584. Epub 2017 May 10. J Med Genet. 2017. PMID: 28490612
Revisiting neurofibromatosis type 2 diagnostic criteria to exclude LZTR1-related schwannomatosis.
Smith MJ, Bowers NL, Bulman M, Gokhale C, Wallace AJ, King AT, Lloyd SK, Rutherford SA, Hammerbeck-Ward CL, Freeman SR, Evans DG. Smith MJ, et al. Among authors: Wallace AJ. Neurology. 2017 Jan 3;88(1):87-92. doi: 10.1212/WNL.0000000000003418. Epub 2016 Nov 16. Neurology. 2017. PMID: 27856782 Free PMC article.
154 results
Jump to page
Feedback