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Author Details
Full Name
Stephen Lyon
Affiliation
ORCID
Career Start Year
2007
Papers
12
H Index
8
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36228616
Obesity caused by an OVOL2 mutation reveals dual roles of OVOL2 in promoting thermogenesis and limiting white adipogenesis.
2022
34782469
De novo germline mutation in the dual specificity phosphatase 10 gene accelerates autoimmune diabetes.
Proc Natl Acad Sci U S A
2021
33905568
Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice.
Journal of Bone and Mineral Research
2021
34260399
Thousands of induced germline mutations affecting immune cells identified by automated meiotic mapping coupled with machine learning.
Proceedings of the National Academy of Sciences of the United States of America
2021
32457148
Forward genetic analysis using OCT screening identifies <i>Sfxn3</i> mutations leading to progressive outer retinal degeneration in mice.
Proc Natl Acad Sci U S A
2020
29382827
Probability of phenotypically detectable protein damage by ENU-induced mutations in the Mutagenetix database.
Nat Commun
2018
26642356
NLRP3 activation and mitosis are mutually exclusive events coordinated by NEK7, a new inflammasome component.
Nature Immunology
2016
26269570
Comparison of predicted and actual consequences of missense mutations.
Proceedings of the National Academy of Sciences of the United States of America
2015
25605905
Real-time resolution of point mutations that cause phenovariance in mice.
Proc Natl Acad Sci U S A
2015
23095377
ENU-induced phenovariance in mice: inferences from 587 mutations.
BMC Research Notes
2012
17965093
The Molecule Pages database.
Nucleic Acids Res
2008
17192258
The alliance for cellular signaling plasmid collection: a flexible resource for protein localization studies and signaling pathway analysis.
Mol Cell Proteomics
2007
1 - 12 of 12
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