scispace - formally typeset
P

Ping-Zi Wen

Researcher at University of California, Los Angeles

Publications -  10
Citations -  409

Ping-Zi Wen is an academic researcher from University of California, Los Angeles. The author has contributed to research in topics: Locus (genetics) & Quantitative trait locus. The author has an hindex of 9, co-authored 10 publications receiving 385 citations.

Papers
More filters
Journal ArticleDOI

Unraveling inflammatory responses using systems genetics and gene-environment interactions in macrophages

TL;DR: A systems genetics strategy is used to examine the role of common genetic variation in macrophage responses to inflammatory stimuli and identified the gene 2310061C15Rik as a regulator of inflammatory responses in Macrophages.
Journal ArticleDOI

High-Resolution Mapping of Gene Expression Using Association in an Outbred Mouse Stock

TL;DR: This article applied whole-genome association analysis to hepatic gene expression traits in an outbred mouse population, the MF1 stock, and replicated expression QTL (eQTL) identified in previous studies of F2 intercross mice.
Journal ArticleDOI

Genetic control of HDL levels and composition in an interspecific mouse cross (CAST/Ei × C57BL/6J)

TL;DR: Low HDL lipid levels exhibited complex inheritance, as 12 quantitative trait loci with significant or suggestive likelihood of observed data scores were identified and novel genes are likely to be important in the control of HDL metabolism.
Journal ArticleDOI

Systems genetics of susceptibility to obesity-induced diabetes in mice.

TL;DR: The results show that the genetics of diabetes susceptibility are enormously complex and a number of quantitative trait loci contributing to diabetes-related traits were identified, notably on chromosomes 4, 6, 7, 9, 10, 11, 12, and 19.
Journal ArticleDOI

Dissection of multigenic obesity traits in congenic mouse strains

TL;DR: Characterization of the MOB congenics localized the effects of genes that underlie obesity-related traits to an introgressed interval unique to the middle MOB congenic, whereas significant differences between the lipid and insulin profiles of the middle and distal Mob congenics implicated the presence of at least two genes thatUnderlie these traits.