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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2012 | 1 |
2013 | 2 |
2015 | 1 |
2016 | 2 |
2018 | 1 |
2024 | 0 |
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7 results
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Page 1
Cellular correlates of selfish spermatogonial selection.
Andrology. 2016 May;4(3):550-3. doi: 10.1111/andr.12185. Epub 2016 Apr 26.
Andrology. 2016.
PMID: 27115825
Free PMC article.
No abstract available.
Visualizing the origins of selfish de novo mutations in individual seminiferous tubules of human testes.
Maher GJ, McGowan SJ, Giannoulatou E, Verrill C, Goriely A, Wilkie AO.
Maher GJ, et al.
Proc Natl Acad Sci U S A. 2016 Mar 1;113(9):2454-9. doi: 10.1073/pnas.1521325113. Epub 2016 Feb 8.
Proc Natl Acad Sci U S A. 2016.
PMID: 26858415
Free PMC article.
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"Selfish spermatogonial selection": a novel mechanism for the association between advanced paternal age and neurodevelopmental disorders.
Goriely A, McGrath JJ, Hultman CM, Wilkie AO, Malaspina D.
Goriely A, et al.
Am J Psychiatry. 2013 Jun;170(6):599-608. doi: 10.1176/appi.ajp.2013.12101352.
Am J Psychiatry. 2013.
PMID: 23639989
Free PMC article.
Review.
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Selfish mutations dysregulating RAS-MAPK signaling are pervasive in aged human testes.
Maher GJ, Ralph HK, Ding Z, Koelling N, Mlcochova H, Giannoulatou E, Dhami P, Paul DS, Stricker SH, Beck S, McVean G, Wilkie AOM, Goriely A.
Maher GJ, et al.
Genome Res. 2018 Dec;28(12):1779-1790. doi: 10.1101/gr.239186.118. Epub 2018 Oct 24.
Genome Res. 2018.
PMID: 30355600
Free PMC article.
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Selfish spermatogonial selection: evidence from an immunohistochemical screen in testes of elderly men.
Lim J, Maher GJ, Turner GD, Dudka-Ruszkowska W, Taylor S, Rajpert-De Meyts E, Goriely A, Wilkie AO.
Lim J, et al.
PLoS One. 2012;7(8):e42382. doi: 10.1371/journal.pone.0042382. Epub 2012 Aug 6.
PLoS One. 2012.
PMID: 22879958
Free PMC article.
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GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: identification of a population at risk of leukemia.
Roberts I, Alford K, Hall G, Juban G, Richmond H, Norton A, Vallance G, Perkins K, Marchi E, McGowan S, Roy A, Cowan G, Anthony M, Gupta A, Ho J, Uthaya S, Curley A, Rasiah SV, Watts T, Nicholl R, Bedford-Russell A, Blumberg R, Thomas A, Gibson B, Halsey C, Lee PW, Godambe S, Sweeney C, Bhatnagar N, Goriely A, Campbell P, Vyas P; Oxford-Imperial Down Syndrome Cohort Study Group.
Roberts I, et al.
Blood. 2013 Dec 5;122(24):3908-17. doi: 10.1182/blood-2013-07-515148. Epub 2013 Sep 10.
Blood. 2013.
PMID: 24021668
Free PMC article.
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Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.
Taylor JC, Martin HC, Lise S, Broxholme J, Cazier JB, Rimmer A, Kanapin A, Lunter G, Fiddy S, Allan C, Aricescu AR, Attar M, Babbs C, Becq J, Beeson D, Bento C, Bignell P, Blair E, Buckle VJ, Bull K, Cais O, Cario H, Chapel H, Copley RR, Cornall R, Craft J, Dahan K, Davenport EE, Dendrou C, Devuyst O, Fenwick AL, Flint J, Fugger L, Gilbert RD, Goriely A, Green A, Greger IH, Grocock R, Gruszczyk AV, Hastings R, Hatton E, Higgs D, Hill A, Holmes C, Howard M, Hughes L, Humburg P, Johnson D, Karpe F, Kingsbury Z, Kini U, Knight JC, Krohn J, Lamble S, Langman C, Lonie L, Luck J, McCarthy D, McGowan SJ, McMullin MF, Miller KA, Murray L, Németh AH, Nesbit MA, Nutt D, Ormondroyd E, Oturai AB, Pagnamenta A, Patel SY, Percy M, Petousi N, Piazza P, Piret SE, Polanco-Echeverry G, Popitsch N, Powrie F, Pugh C, Quek L, Robbins PA, Robson K, Russo A, Sahgal N, van Schouwenburg PA, Schuh A, Silverman E, Simmons A, Sørensen PS, Sweeney E, Taylor J, Thakker RV, Tomlinson I, Trebes A, Twigg SR, Uhlig HH, Vyas P, Vyse T, Wall SA, Watkins H, Whyte MP, Witty L, Wright B, Yau C, Buck D, Humphray S, Ratcliffe PJ, Bell JI, Wilkie AO, Bentley D, Donnelly P, McVean G.
Taylor JC, et al.
Nat Genet. 2015 Jul;47(7):717-726. doi: 10.1038/ng.3304. Epub 2015 May 18.
Nat Genet. 2015.
PMID: 25985138
Free PMC article.
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