Peter S Chines
Overview
Explore the profile of Peter S Chines including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
66
Citations
20618
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Tenney A, Di Gioia S, Webb B, Chan W, de Boer E, Garnai S, et al.
Nat Genet
. 2023 Jun;
55(7):1149-1163.
PMID: 37386251
Hereditary congenital facial paresis type 1 (HCFP1) is an autosomal dominant disorder of absent or limited facial movement that maps to chromosome 3q21-q22 and is hypothesized to result from facial...
2.
Taylor D, Jackson A, Narisu N, Hemani G, Erdos M, Chines P, et al.
Proc Natl Acad Sci U S A
. 2019 May;
116(22):10883-10888.
PMID: 31076557
We integrate comeasured gene expression and DNA methylation (DNAme) in 265 human skeletal muscle biopsies from the FUSION study with >7 million genetic variants and eight physiological traits: height, waist,...
3.
Cohen J, Manoli I, Dowdell K, Krogmann T, Tamura D, Radecki P, et al.
Blood
. 2019 May;
133(26):2753-2764.
PMID: 31064750
Patients with classic hydroa vacciniforme-like lymphoproliferative disorder (HVLPD) typically have high levels of Epstein-Barr virus (EBV) DNA in T cells and/or natural killer (NK) cells in blood and skin lesions...
4.
Lawlor N, Marquez E, Orchard P, Narisu N, Shamim M, Thibodeau A, et al.
Cell Rep
. 2019 Jan;
26(3):788-801.e6.
PMID: 30650367
EndoC-βH1 is emerging as a critical human β cell model to study the genetic and environmental etiologies of β cell (dys)function and diabetes. Comprehensive knowledge of its molecular landscape is...
5.
Zou L, Erdos M, Taylor D, Chines P, Varshney A, Parker S, et al.
BMC Genomics
. 2018 May;
19(1):390.
PMID: 29792182
Background: Bisulfite sequencing is widely employed to study the role of DNA methylation in disease; however, the data suffer from biases due to coverage depth variability. Imputation of methylation values...
6.
Taylor D, Knowles D, Scott L, Ramirez A, Casale F, Wolford B, et al.
PLoS One
. 2018 Apr;
13(4):e0195788.
PMID: 29659628
From whole organisms to individual cells, responses to environmental conditions are influenced by genetic makeup, where the effect of genetic variation on a trait depends on the environmental context. RNA-sequencing...
7.
Teslovich T, Kim D, Yin X, Stancakova A, Jackson A, Wielscher M, et al.
Hum Mol Genet
. 2018 Feb;
27(9):1664-1674.
PMID: 29481666
Comprehensive metabolite profiling captures many highly heritable traits, including amino acid levels, which are potentially sensitive biomarkers for disease pathogenesis. To better understand the contribution of genetic variation to amino...
8.
Flannick J, Fuchsberger C, Mahajan A, Teslovich T, Agarwala V, Gaulton K, et al.
Sci Data
. 2018 Jan;
5:180002.
PMID: 29360107
This corrects the article DOI: 10.1038/sdata.2017.179.
9.
Jun G, Manning A, Almeida M, Zawistowski M, Wood A, Teslovich T, et al.
Proc Natl Acad Sci U S A
. 2017 Dec;
115(2):379-384.
PMID: 29279374
A major challenge in evaluating the contribution of rare variants to complex disease is identifying enough copies of the rare alleles to permit informative statistical analysis. To investigate the contribution...
10.
Flannick J, Fuchsberger C, Mahajan A, Teslovich T, Agarwala V, Gaulton K, et al.
Sci Data
. 2017 Dec;
4:170179.
PMID: 29257133
To investigate the genetic basis of type 2 diabetes (T2D) to high resolution, the GoT2D and T2D-GENES consortia catalogued variation from whole-genome sequencing of 2,657 European individuals and exome sequencing...