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

Year Number of Results
1998 1
1999 1
2000 1
2001 1
2003 2
2004 5
2005 2
2006 2
2007 5
2008 4
2009 10
2010 12
2011 8
2012 6
2013 7
2014 7
2015 12
2016 6
2017 5
2018 6
2019 4
2020 11
2021 2
2022 4
2024 0

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108 results

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Page 1
Mouse genomic and cellular annotations.
Long H, Reeves R, Simon MM. Long H, et al. Mamm Genome. 2022 Mar;33(1):19-30. doi: 10.1007/s00335-021-09936-7. Epub 2022 Feb 5. Mamm Genome. 2022. PMID: 35124726 Free PMC article. Review.
Making sense of the linear genome, gene function and TADs.
Long HS, Greenaway S, Powell G, Mallon AM, Lindgren CM, Simon MM. Long HS, et al. Epigenetics Chromatin. 2022 Jan 29;15(1):4. doi: 10.1186/s13072-022-00436-9. Epigenetics Chromatin. 2022. PMID: 35090532 Free PMC article.
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes.
Lana-Elola E, Cater H, Watson-Scales S, Greenaway S, Müller-Winkler J, Gibbins D, Nemes M, Slender A, Hough T, Keskivali-Bond P, Scudamore CL, Herbert E, Banks GT, Mobbs H, Canonica T, Tosh J, Noy S, Llorian M, Nolan PM, Griffin JL, Good M, Simon M, Mallon AM, Wells S, Fisher EMC, Tybulewicz VLJ. Lana-Elola E, et al. Dis Model Mech. 2021 Oct 1;14(10):dmm049157. doi: 10.1242/dmm.049157. Epub 2021 Oct 15. Dis Model Mech. 2021. PMID: 34477842 Free PMC article.
LAMA: automated image analysis for the developmental phenotyping of mouse embryos.
Horner NR, Venkataraman S, Armit C, Casero R, Brown JM, Wong MD, van Eede MC, Henkelman RM, Johnson S, Teboul L, Wells S, Brown SD, Westerberg H, Mallon AM. Horner NR, et al. Development. 2021 Mar 24;148(18):dev192955. doi: 10.1242/dev.192955. Development. 2021. PMID: 33574040 Free PMC article.
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.
Swan AL, Schütt C, Rozman J, Del Mar Muñiz Moreno M, Brandmaier S, Simon M, Leuchtenberger S, Griffiths M, Brommage R, Keskivali-Bond P, Grallert H, Werner T, Teperino R, Becker L, Miller G, Moshiri A, Seavitt JR, Cissell DD, Meehan TF, Acar EF, Lelliott CJ, Flenniken AM, Champy MF, Sorg T, Ayadi A, Braun RE, Cater H, Dickinson ME, Flicek P, Gallegos J, Ghirardello EJ, Heaney JD, Jacquot S, Lally C, Logan JG, Teboul L, Mason J, Spielmann N, McKerlie C, Murray SA, Nutter LMJ, Odfalk KF, Parkinson H, Prochazka J, Reynolds CL, Selloum M, Spoutil F, Svenson KL, Vales TS, Wells SE, White JK, Sedlacek R, Wurst W, Lloyd KCK, Croucher PI, Fuchs H, Williams GR, Bassett JHD, Gailus-Durner V, Herault Y, Mallon AM, Brown SDM, Mayer-Kuckuk P, Hrabe de Angelis M; IMPC Consortium. Swan AL, et al. PLoS Genet. 2020 Dec 28;16(12):e1009190. doi: 10.1371/journal.pgen.1009190. eCollection 2020 Dec. PLoS Genet. 2020. PMID: 33370286 Free PMC article.
108 results