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Title Authors Journal Year of Publication DOI Pubmed ID
Reproducibility and replicability of rodent phenotyping in preclinical studies N. Kafkafi; J. Agassi; E.J. Chesler; J.C. Crabbe; W.E. Crusio; D. Eilam; R. Gerlai; I. Golani; A. Gomez-Marin; R. Heller; F. Iraqi; I. Jaljuli; N.A. Karp; H. Morgan; G. Nicholson; D.W. Pfaff; S.H. Richter; P.B. Stark; O. Stiedl; V. Stodden; L.M. Tarantino; V. Tucci; W. Valdar; R.W. Williams; H. Wurbel; Y. Benjamini Neurosci Biobehav Rev 2018 10.1016/j.neubiorev.2018.01.003
Identification of genetic elements in metabolism by high-throughput mouse phenotyping J. Rozman; B. Rathkolb; M.A. Oestereicher; C. Schutt; A.C. Ravindranath; S. Leuchtenberger; S. Sharma; M. Kistler; M. Willershauser; R. Brommage; T.F. Meehan; J. Mason; H. Haselimashhadi; T. Hough; A.M. Mallon; S. Wells; L. Santos; C.J. Lelliott; J.K. White; T. Sorg; M.F. Champy; L.R. Bower; C.L. Reynolds; A.M. Flenniken; S.A. Murray; L.M.J. Nutter; K.L. Svenson; D. West; G.P. Tocchini-Valentini; A.L. Beaudet; F. Bosch; R.B. Braun; M.S. Dobbie; X. Gao; Y. Herault; A. Moshiri; B.A. Moore; K.C.Kent Lloyd; C. McKerlie; H. Masuya; N. Tanaka; P. Flicek; H.E. Parkinson; R. Sedlacek; J.K. Seong; C.L. Wang; M. Moore; S.D. Brown; M.H. Tschop; W. Wurst; M. Klingenspor; E. Wolf; J. Beckers; F. Machicao; A. Peter; H. Staiger; H.U. Haring; H. Grallert; M. Campillos; H. Maier; H. Fuchs; V. Gailus-Durner; T. Werner; H. de Angelis Nat Commun 2018 10.1038/s41467-017-01995-2

PMC5773596

High-throughput mouse phenomics for characterizing mammalian gene function S.D.M. Brown; C.C. Holmes; A.M. Mallon; T.F. Meehan; D. Smedley; S. Wells Nat Rev Genet 2018 10.1038/s41576-018-0005-2
Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition K.S. Small; M. Todorcevic; M. Civelek; J.S.ElSaye Moustafa; X. Wang; M.M. Simon; J. Fernandez-Tajes; A. Mahajan; M. Horikoshi; A. Hugill; C.A. Glastonbury; L. Quaye; M.J. Neville; S. Sethi; M. Yon; C. Pan; N. Che; A. Vinuela; P.C. Tsai; A. Nag; A. Buil; G. Thorleifsson; A. Raghavan; Q. Ding; A.P. Morris; J.T. Bell; U. Thorsteinsdottir; K. Stefansson; M. Laakso; I. Dahlman; P. Arner; A.L. Gloyn; K. Musunuru; A.J. Lusis; R.D. Cox; F. Karpe; M.I. McCarthy Nat Genet 2018 10.1038/s41588-018-0088-x
An N-ethyl-N-nitrosourea (ENU)-induced Tyr265Stop mutation of the DNA polymerase accessory subunit gamma 2 (Polg2) is associated with renal calcification in mice C.M. Gorvin; B.N. Ahmad; M.J. Stechman; N.Y. Loh; T.A. Hough; P. Leo; M. Marshall; S. Sethi; L. Bentley; S.E. Piret; A. Reed; J. Jeyabalan; P.T. Christie; S. Wells; M.M. Simon; A.M. Mallon; H. Schulz; N. Huebner; M.A. Brown; R.D. Cox; S.D. Brown; R.V. Thakker J Bone Miner Res 2018 10.1002/jbmr.3624
The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation V. Munoz-Fuentes; P. Cacheiro; T.F. Meehan; J.A. Aguilar-Pimentel; S.D.M. Brown; A.M. Flenniken; P. Flicek; A. Galli; H.H. Mashhadi; H. de Angelis; J.K. Kim; K.C.K. Lloyd; C. McKerlie; H. Morgan; S.A. Murray; L.M.J. Nutter; P.T. Reilly; J.R. Seavitt; J.K. Seong; M. Simon; H. Wardle-Jones; A.M. Mallon; D. Smedley; H.E. Parkinson Conserv Genet 2018 10.1007/s10592-018-1072-9

PMC6061128

Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition K.S. Small; M. Todorcevic; M. Civelek; J.S.ElSaye Moustafa; X. Wang; M.M. Simon; J. Fernandez-Tajes; A. Mahajan; M. Horikoshi; A. Hugill; C.A. Glastonbury; L. Quaye; M.J. Neville; S. Sethi; M. Yon; C. Pan; N. Che; A. Vinuela; P.C. Tsai; A. Nag; A. Buil; G. Thorleifsson; A. Raghavan; Q. Ding; A.P. Morris; J.T. Bell; U. Thorsteinsdottir; K. Stefansson; M. Laakso; I. Dahlman; P. Arner; A.L. Gloyn; K. Musunuru; A.J. Lusis; R.D. Cox; F. Karpe; M.I. McCarthy Nat Genet 2018 10.1038/s41588-018-0088-x
A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies G. Banks; G. Lassi; A. Hoerder-Suabedissen; F. Tinarelli; M.M. Simon; A. Wilcox; P. Lau; T.N. Lawson; S. Johnson; A. Rutman; M. Sweeting; J.E. Chesham; A.R. Barnard; N. Horner; H. Westerberg; L.B. Smith; Z. Molnar; M.H. Hastings; R.A. Hirst; V. Tucci; P.M. Nolan Mol Psychiatry 2017 10.1038/mp.2017.54
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction M.R. Bowl; M.M. Simon; N.J. Ingham; S. Greenaway; L. Santos; H. Cater; S. Taylor; J. Mason; N. Kurbatova; S. Pearson; L.R. Bower; D.A. Clary; H. Meziane; P. Reilly; O. Minowa; L. Kelsey; G.P. Tocchini-Valentini; X. Gao; A. Bradley; W.C. Skarnes; M. Moore; A.L. Beaudet; M.J. Justice; J. Seavitt; M.E. Dickinson; W. Wurst; M.H. de Angelis; Y. Herault; S. Wakana; L.M.J. Nutter; A.M. Flenniken; C. McKerlie; S.A. Murray; K.L. Svenson; R.E. Braun; D.B. West; K.C.K. Lloyd; D.J. Adams; J. White; N. Karp; P. Flicek; D. Smedley; T.F. Meehan; H.E. Parkinson; L.M. Teboul; S. Wells; K.P. Steel; A.M. Mallon; S.D.M. Brown Nat Commun 2017 10.1038/s41467-017-00595-4

PMC5638796

A mutation in Nischarin causes otitis media via LIMK1 and NF-kappaB pathways M. Crompton; T. Purnell; H.E. Tyrer; A. Parker; G. Ball; R.E. Hardisty-Hughes; R. Gale; D. Williams; C.H. Dean; M.M. Simon; A.M. Mallon; S. Wells; M.F. Bhutta; M.J. Burton; H. Tateossian; S.D.M. Brown PLoS Genet 2017 10.1371/journal.pgen.1006969

PMC5570507

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