| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.
|
Cell
|
2009
|
3.63
|
|
2
|
Rapamycin extends murine lifespan but has limited effects on aging.
|
J Clin Invest
|
2013
|
2.23
|
|
3
|
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.
|
Genome Biol
|
2013
|
2.04
|
|
4
|
Active delivery of trefoil factors by genetically modified Lactococcus lactis prevents and heals acute colitis in mice.
|
Gastroenterology
|
2004
|
1.99
|
|
5
|
Targeted estrogen delivery reverses the metabolic syndrome.
|
Nat Med
|
2012
|
1.51
|
|
6
|
Mouse phenotyping.
|
Methods
|
2010
|
1.43
|
|
7
|
ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta.
|
PLoS Genet
|
2008
|
1.37
|
|
8
|
Mitochondrial dysfunction and decrease in body weight of a transgenic knock-in mouse model for TDP-43.
|
J Biol Chem
|
2014
|
1.37
|
|
9
|
Systemic first-line phenotyping.
|
Methods Mol Biol
|
2009
|
1.26
|
|
10
|
Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia.
|
J Cell Sci
|
2011
|
1.24
|
|
11
|
Prdm5 regulates collagen gene transcription by association with RNA polymerase II in developing bone.
|
PLoS Genet
|
2012
|
1.09
|
|
12
|
Innovations in phenotyping of mouse models in the German Mouse Clinic.
|
Mamm Genome
|
2012
|
1.09
|
|
13
|
Requirement of the RNA-editing enzyme ADAR2 for normal physiology in mice.
|
J Biol Chem
|
2011
|
1.05
|
|
14
|
A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine model.
|
Arthritis Rheum
|
2011
|
1.04
|
|
15
|
Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolism.
|
Am J Physiol Renal Physiol
|
2009
|
1.02
|
|
16
|
Mutation of the Na(+)-K(+)-2Cl(-) cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.
|
Am J Physiol Renal Physiol
|
2010
|
0.93
|
|
17
|
Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in mice.
|
Hum Mol Genet
|
2013
|
0.93
|
|
18
|
A broad phenotypic screen identifies novel phenotypes driven by a single mutant allele in Huntington's disease CAG knock-in mice.
|
PLoS One
|
2013
|
0.89
|
|
19
|
Microphthalmia, parkinsonism, and enhanced nociception in Pitx3 ( 416insG ) mice.
|
Mamm Genome
|
2009
|
0.89
|
|
20
|
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.
|
Mamm Genome
|
2012
|
0.88
|
|
21
|
Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathology.
|
FASEB J
|
2012
|
0.87
|
|
22
|
Pleiotropic effects in Eya3 knockout mice.
|
BMC Dev Biol
|
2008
|
0.86
|
|
23
|
SMC6 is an essential gene in mice, but a hypomorphic mutant in the ATPase domain has a mild phenotype with a range of subtle abnormalities.
|
DNA Repair (Amst)
|
2013
|
0.86
|
|
24
|
Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processes.
|
PLoS One
|
2009
|
0.85
|
|
25
|
Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms.
|
Hum Mol Genet
|
2012
|
0.85
|
|
26
|
New ENU-induced semidominant mutation, Ali18, causes inflammatory arthritis, dermatitis, and osteoporosis in the mouse.
|
Mamm Genome
|
2006
|
0.84
|
|
27
|
Neurobeachin, a regulator of synaptic protein targeting, is associated with body fat mass and feeding behavior in mice and body-mass index in humans.
|
PLoS Genet
|
2012
|
0.83
|
|
28
|
Mouse nuclear myosin I knock-out shows interchangeability and redundancy of myosin isoforms in the cell nucleus.
|
PLoS One
|
2013
|
0.82
|
|
29
|
Standardized, systemic phenotypic analysis of Umod(C93F) and Umod(A227T) mutant mice.
|
PLoS One
|
2013
|
0.80
|
|
30
|
An ENU mutagenesis-derived mouse model with a dominant Jak1 mutation resembling phenotypes of systemic autoimmune disease.
|
Am J Pathol
|
2013
|
0.78
|
|
31
|
Modeling hepatic osteodystrophy in Abcb4 deficient mice.
|
Bone
|
2013
|
0.77
|
|
32
|
Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.
|
J Biomed Sci
|
2014
|
0.77
|
|
33
|
Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines.
|
Eur J Oral Sci
|
2012
|
0.76
|
|
34
|
Long-term experiment to study the development, interaction, and influencing factors of DEXA parameters.
|
Mamm Genome
|
2013
|
0.76
|
|
35
|
Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels.
|
Biometals
|
2015
|
0.75
|