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Ann-Marie Mallon
Ann-Marie Mallon
MRC Harwell
Verified email at har.mrc.ac.uk
Title
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Cited by
Year
High-throughput discovery of novel developmental phenotypes
ME Dickinson, AM Flenniken, X Ji, L Teboul, MD Wong, JK White, ...
Nature 537 (7621), 508-514, 2016
7152016
Promoting coherent minimum reporting guidelines for biological and biomedical investigations: the MIBBI project
CF Taylor, D Field, SA Sansone, J Aerts, R Apweiler, M Ashburner, ...
Nature biotechnology 26 (8), 889-896, 2008
5772008
Promoting coherent minimum reporting guidelines for biological and biomedical investigations: the MIBBI project
CF Taylor, D Field, SA Sansone, J Aerts, R Apweiler, M Ashburner, ...
Nature biotechnology 26 (8), 889-896, 2008
5772008
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains
MM Simon, S Greenaway, JK White, H Fuchs, V Gailus-Durner, S Wells, ...
Genome biology 14 (7), 1-22, 2013
3892013
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31
P Mburu, M Mustapha, A Varela, D Weil, A El-Amraoui, RH Holme, ...
Nature genetics 34 (4), 421-428, 2003
3422003
Using ontologies to describe mouse phenotypes
GV Gkoutos, ECJ Green, AM Mallon, JM Hancock, D Davidson
Genome biology 6 (1), 1-10, 2005
2612005
The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data
G Koscielny, G Yaikhom, V Iyer, TF Meehan, H Morgan, J Atienza-Herrero, ...
Nucleic acids research 42 (D1), D802-D809, 2014
2392014
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium
TF Meehan, N Conte, DB West, JO Jacobsen, J Mason, J Warren, ...
Nature genetics 49 (8), 1231-1238, 2017
1772017
The gene mutated in bare patches and striated mice encodes a novel 3β-hydroxysteroid dehydrogenase
XY Liu, AW Dangel, RI Kelley, W Zhao, P Denny, M Botcherby, ...
Nature genetics 22 (2), 182-187, 1999
1731999
Prevalence of sexual dimorphism in mammalian phenotypic traits
NA Karp, J Mason, AL Beaudet, Y Benjamini, L Bower, RE Braun, ...
Nature communications 8 (1), 1-12, 2017
1672017
Mouse large-scale phenotyping initiatives: Overview of the European mouse disease clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project
A Ayadi, MC Birling, J Bottomley, J Bussell, H Fuchs, M Fray, ...
Mammalian Genome 23 (9), 600-610, 2012
1382012
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics
MH De Angelis, G Nicholson, M Selloum, JK White, H Morgan, ...
Nature genetics 47 (9), 969-978, 2015
1252015
Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair
J Mianné, L Chessum, S Kumar, C Aguilar, G Codner, M Hutchison, ...
Genome medicine 8 (1), 1-12, 2016
1022016
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
MR Bowl, MM Simon, NJ Ingham, S Greenaway, L Santos, H Cater, ...
Nature communications 8 (1), 1-11, 2017
982017
EuroPhenome: a repository for high-throughput mouse phenotyping data
H Morgan, T Beck, A Blake, H Gates, N Adams, G Debouzy, S Leblanc, ...
Nucleic acids research 38 (suppl_1), D577-D585, 2010
902010
EuroPhenome and EMPReSS: online mouse phenotyping resource
AM Mallon, A Blake, JM Hancock
Nucleic acids research 36 (suppl_1), D715-D718, 2007
832007
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease
PK Potter, MR Bowl, P Jeyarajan, L Wisby, A Blease, ME Goldsworthy, ...
Nature communications 7 (1), 1-13, 2016
792016
Applying the ARRIVE guidelines to an in vivo database
NA Karp, TF Meehan, H Morgan, JC Mason, A Blake, N Kurbatova, ...
PLoS biology 13 (5), e1002151, 2015
672015
Building mouse phenotype ontologies
GV Gkoutos, ECJ Green, AM Mallon, JM Hancock, D Davidson
Biocomputing 2004, 178-189, 2003
672003
Comparative genome sequence analysis of the Bpa/Str region in mouse and man
AM Mallon, M Platzer, R Bate, G Gloeckner, MRM Botcherby, G Nordsiek, ...
Genome Research 10 (6), 758-775, 2000
642000
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