Results 21 to 30 of about 49,899 (262)

Genome-wide pathway analysis in glioma

open access: yesNeoplasma, 2015
The aim of this study was to identify candidate single-nucleotide polymorphisms (SNPs) that may play a role in the susceptibility to glioma, to elucidate their potential mechanisms, and to generate SNP-to-gene-to-pathway hypotheses.A genome-wide association study (GWAS) dataset of glioma including 509,345 SNPs from 1,856 glioma patients and 4,955 ...
Y H, Lee, G G, Song
openaire   +3 more sources

Genome wide analysis reveals heparan sulfate epimerase modulates TDP-43 proteinopathy.

open access: yesPLoS Genetics, 2019
Pathological phosphorylated TDP-43 protein (pTDP) deposition drives neurodegeneration in amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD-TDP).
Nicole F Liachko   +6 more
doaj   +1 more source

Genome wide molecular analysis of minimally differentiated acute myeloid leukemia

open access: yesHaematologica, 2009
Background Minimally differentiated acute myeloid leukemia is heterogeneous in karyotype and is defined by immature morphological and molecular characteristics.
Fernando P.G. Silva   +12 more
doaj   +1 more source

Genome wide identification of recessive cancer genes by combinatorial mutation analysis. [PDF]

open access: yesPLoS ONE, 2008
We devised a novel procedure to identify human cancer genes acting in a recessive manner. Our strategy was to combine the contributions of the different types of genetic alterations to loss of function: amino-acid substitutions, frame-shifts, gene ...
Stefano Volinia   +8 more
doaj   +1 more source

Meta-Analysis in Genome-Wide Association Studies [PDF]

open access: yesPharmacogenomics, 2009
The advent of genome-wide association studies has allowed considerable progress in the identification and robust replication of common gene variants that confer susceptibility to common diseases and other phenotypes of interest. These genetic effect sizes are almost invariably moderate to small in magnitude and single studies, even if large, are ...
Zeggini, E., Ioannidis, J. P.
openaire   +3 more sources

Genome-Wide Gene-Based Multi-Trait Analysis

open access: yesFrontiers in Genetics, 2020
Genome-wide association studies focusing on a single phenotype have been broadly conducted to identify genetic variants associated with a complex disease.
Yamin Deng   +5 more
doaj   +1 more source

Genome‐wide analysis of the AP2/ERF gene family inSalix arbutifolia

open access: yesFEBS Open Bio, 2015
AP2/ERF genes encode transcriptional regulators with a variety of functions in plant growth and development and in response to biotic and abiotic stresses.
Guodong Rao   +4 more
doaj   +1 more source

Genome-wide pathway analysis in neuroblastoma

open access: yesTumor Biology, 2013
The aim of this study was to identify candidate single-nucleotide polymorphisms (SNPs) that might play a role in susceptibility to neuroblastoma, elucidate their potential mechanisms, and generate SNP-to-gene-to-pathway hypotheses. A genome-wide association study (GWAS) dataset of neuroblastoma that included 442,976 SNPs from 1,627 neuroblastoma ...
Young Ho, Lee   +2 more
openaire   +2 more sources

Approximate conditional phenotype analysis based on genome wide association summary statistics

open access: yesScientific Reports, 2021
Because single genetic variants may have pleiotropic effects, one trait can be a confounder in a genome-wide association study (GWAS) that aims to identify loci associated with another trait.
Peitao Wu   +5 more
doaj   +1 more source

Comprehensive Analysis of SiNPs on the Genome-Wide Transcriptional Changes in Caenorhabditis elegans

open access: yesInternational Journal of Nanomedicine, 2020
Shuang Liang,1,2,* Junchao Duan,1,2,* Hejing Hu,1,2 Jingyi Zhang,1,2 Shan Gao,2,3 Haiming Jing,2,3 Guojun Li,2,3 Zhiwei Sun1,2 1Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing 100069, People ...
Liang S   +7 more
doaj  

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