Search details
1.
The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven Axis.
Cell
; 162(3): 607-21, 2015 Jul 30.
Article
in English
| MEDLINE | ID: mdl-26232227
2.
Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background.
Am J Hum Genet
; 110(10): 1817-1824, 2023 10 05.
Article
in English
| MEDLINE | ID: mdl-37659414
3.
Multivariate phenotype analysis enables genome-wide inference of mammalian gene function.
PLoS Biol
; 20(8): e3001723, 2022 08.
Article
in English
| MEDLINE | ID: mdl-35944064
4.
The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease.
Nucleic Acids Res
; 51(D1): D1038-D1045, 2023 01 06.
Article
in English
| MEDLINE | ID: mdl-36305825
5.
LAMA: automated image analysis for the developmental phenotyping of mouse embryos.
Development
; 148(18)2021 03 24.
Article
in English
| MEDLINE | ID: mdl-33574040
6.
High-throughput mouse phenomics for characterizing mammalian gene function.
Nat Rev Genet
; 19(6): 357-370, 2018 06.
Article
in English
| MEDLINE | ID: mdl-29626206
7.
A framework for longitudinal latent factor modelling of treatment response in clinical trials with applications to Psoriatic Arthritis and Rheumatoid Arthritis.
J Biomed Inform
; : 104641, 2024 Apr 18.
Article
in English
| MEDLINE | ID: mdl-38642627
8.
Genic constraint against nonsynonymous variation across the mouse genome.
BMC Genomics
; 24(1): 562, 2023 Sep 22.
Article
in English
| MEDLINE | ID: mdl-37736706
9.
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.
Mamm Genome
; 34(2): 180-199, 2023 06.
Article
in English
| MEDLINE | ID: mdl-37294348
10.
High-throughput discovery of genetic determinants of circadian misalignment.
PLoS Genet
; 16(1): e1008577, 2020 01.
Article
in English
| MEDLINE | ID: mdl-31929527
11.
Interoperability of statistical models in pandemic preparedness: principles and reality.
Stat Sci
; 37(2): 183-206, 2022 May.
Article
in English
| MEDLINE | ID: mdl-35664221
12.
Modelling the genetic aetiology of complex disease: human-mouse conservation of noncoding features and disease-associated loci.
Biol Lett
; 18(3): 20210630, 2022 03.
Article
in English
| MEDLINE | ID: mdl-35317627
13.
Advancing data science in drug development through an innovative computational framework for data sharing and statistical analysis.
BMC Med Res Methodol
; 21(1): 250, 2021 11 14.
Article
in English
| MEDLINE | ID: mdl-34773974
14.
A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease.
BMC Genomics
; 21(1): 754, 2020 Nov 02.
Article
in English
| MEDLINE | ID: mdl-33138777
15.
A bioimage informatics platform for high-throughput embryo phenotyping.
Brief Bioinform
; 19(1): 41-51, 2018 01 01.
Article
in English
| MEDLINE | ID: mdl-27742664
16.
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.
PLoS Genet
; 13(8): e1006969, 2017 Aug.
Article
in English
| MEDLINE | ID: mdl-28806779
17.
The digital revolution in phenotyping.
Brief Bioinform
; 17(5): 819-30, 2016 09.
Article
in English
| MEDLINE | ID: mdl-26420780
18.
Applying the ARRIVE Guidelines to an In Vivo Database.
PLoS Biol
; 13(5): e1002151, 2015 May.
Article
in English
| MEDLINE | ID: mdl-25992600
19.
The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation.
Conserv Genet
; 19(4): 995-1005, 2018.
Article
in English
| MEDLINE | ID: mdl-30100824
20.
Introduction to Mammalian Genome Special Issue: Mammalian Genetic Resources.
Mamm Genome
; 33(1): 1-3, 2022 03.
Article
in English
| MEDLINE | ID: mdl-35044497