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

Year Number of Results
1945 1
1946 1
1947 1
1974 2
1988 1
1993 1
1995 1
1996 3
1997 2
2001 1
2004 1
2005 4
2007 2
2008 1
2009 4
2010 3
2011 3
2012 6
2013 4
2014 2
2015 5
2016 3
2017 2
2018 6
2019 6
2020 7
2021 11
2022 8
2023 6
2024 6

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91 results

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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: prescott k. 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.
Learning from pragmatic local research.
Prescott K, Winzor G, Jumaa P. Prescott K, et al. Infect Prev Pract. 2021 Sep;3(3):100171. doi: 10.1016/j.infpip.2021.100171. Epub 2021 Aug 21. Infect Prev Pract. 2021. PMID: 34568806 Free PMC article. No abstract available.
Hand hygiene: a COVID beneficiary?
Prescott K, Mahida N, Wilkinson M, Gray J. Prescott K, et al. J Hosp Infect. 2021 May;111:4-5. doi: 10.1016/j.jhin.2021.03.017. Epub 2021 Mar 22. J Hosp Infect. 2021. PMID: 33766546 Free PMC article. No abstract available.
The SHDRA syndrome-associated gene TMEM260 encodes a protein-specific O-mannosyltransferase.
Larsen ISB, Povolo L, Zhou L, Tian W, Mygind KJ, Hintze J, Jiang C, Hartill V, Prescott K, Johnson CA, Mullegama SV, McConkie-Rosell A, McDonald M, Hansen L, Vakhrushev SY, Schjoldager KT, Clausen H, Worzfeld T, Joshi HJ, Halim A. Larsen ISB, et al. Among authors: prescott k. Proc Natl Acad Sci U S A. 2023 May 23;120(21):e2302584120. doi: 10.1073/pnas.2302584120. Epub 2023 May 15. Proc Natl Acad Sci U S A. 2023. PMID: 37186866 Free PMC article.
Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrum.
Priestley JRC, Deshwar AR, Murthy H, D'Agostino MD, Dupuis L, Gangaram B, Gray C, Jobling R, Pannia E, Platzer K, Prescott K, Redman M, Rippert AL, Rosenfeld JA, Scott DA, Wang YW, Schmederer Z, Dalal A, Sarma AS, Skraban C, Dowling JJ, Mendoza-Londono R, Slavotinek A, Bhoj EJ. Priestley JRC, et al. Among authors: prescott k. Genet Med. 2023 Aug;25(8):100863. doi: 10.1016/j.gim.2023.100863. Epub 2023 Apr 28. Genet Med. 2023. PMID: 37125634
Outcome assessments in rheumatoid arthritis.
Gilek-Seibert K, Prescott K, Kazi S. Gilek-Seibert K, et al. Among authors: prescott k. Curr Rheumatol Rep. 2013 Nov;15(11):370. doi: 10.1007/s11926-013-0370-y. Curr Rheumatol Rep. 2013. PMID: 24072601 Review.
Contribution of retrotransposition to developmental disorders.
Gardner EJ, Prigmore E, Gallone G, Danecek P, Samocha KE, Handsaker J, Gerety SS, Ironfield H, Short PJ, Sifrim A, Singh T, Chandler KE, Clement E, Lachlan KL, Prescott K, Rosser E, FitzPatrick DR, Firth HV, Hurles ME. Gardner EJ, et al. Among authors: prescott k. Nat Commun. 2019 Oct 11;10(1):4630. doi: 10.1038/s41467-019-12520-y. Nat Commun. 2019. PMID: 31604926 Free PMC article.
De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement.
Lu S, Ma M, Mao X, Bacino CA, Jankovic J, Sutton VR, Bartley JA, Wang X, Rosenfeld JA, Beleza-Meireles A, Chauhan J, Pan X, Li M, Liu P, Prescott K, Amin S, Davies G, Wangler MF, Dai Y, Bellen HJ. Lu S, et al. Among authors: prescott k. Am J Hum Genet. 2022 Oct 6;109(10):1932-1943. doi: 10.1016/j.ajhg.2022.09.005. Am J Hum Genet. 2022. PMID: 36206744 Free PMC article.
Predictive language processing in young autistic children.
Prescott KE, Mathée-Scott J, Reuter T, Edwards J, Saffran J, Ellis Weismer S. Prescott KE, et al. Autism Res. 2022 May;15(5):892-903. doi: 10.1002/aur.2684. Epub 2022 Feb 9. Autism Res. 2022. PMID: 35142078 Free PMC article.
91 results