User profiles for M. Gloudemans
Michael J GloudemansPhD Student in Biomedical Informatics, Stanford University Verified email at stanford.edu Cited by 4665 |
Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer's and Parkinson's diseases
Genome-wide association studies of neurological diseases have identified thousands of
variants associated with disease phenotypes. However, most of these variants do not alter …
variants associated with disease phenotypes. However, most of these variants do not alter …
RNA editing underlies genetic risk of common inflammatory diseases
A major challenge in human genetics is to identify the molecular mechanisms of trait-associated
and disease-associated variants. To achieve this, quantitative trait locus (QTL) mapping …
and disease-associated variants. To achieve this, quantitative trait locus (QTL) mapping …
[PDF][PDF] Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease
Long non-coding RNA (lncRNA) genes have well-established and important impacts on
molecular and cellular functions. However, among the thousands of lncRNA genes, it is still a …
molecular and cellular functions. However, among the thousands of lncRNA genes, it is still a …
Multiple causal variants underlie genetic associations in humans
… work and members of the M. Bassik laboratory for experimental advice. We also thank R. …
Montgomery laboratory for general guidance and feedback on this work and members of the M. …
Montgomery laboratory for general guidance and feedback on this work and members of the M. …
Abundant associations with gene expression complicate GWAS follow-up
To the Editor—Genome-wide association studies (GWAS) are rapidly expanding the catalog
of trait-and disease-associated variants. With increasing cohort size and phenotyping, …
of trait-and disease-associated variants. With increasing cohort size and phenotyping, …
Co-expression networks reveal the tissue-specific regulation of transcription and splicing
…, D Garrido-Martín, G Gliner, MJ Gloudemans… - Genome …, 2017 - genome.cshlp.org
Gene co-expression networks capture biologically important patterns in gene expression
data, enabling functional analyses of genes, discovery of biomarkers, and interpretation of …
data, enabling functional analyses of genes, discovery of biomarkers, and interpretation of …
[PDF][PDF] Genetic regulatory mechanisms of smooth muscle cells map to coronary artery disease risk loci
…, M Pjanic, T Wang, T Nguyen, M Gloudemans… - The American Journal of …, 2018 - cell.com
Coronary artery disease (CAD) is the leading cause of death globally. Genome-wide association
studies (GWASs) have identified more than 95 independent loci that influence CAD risk…
studies (GWASs) have identified more than 95 independent loci that influence CAD risk…
[HTML][HTML] Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx
Background Population structure among study subjects may confound genetic association
studies, and lack of proper correction can lead to spurious findings. The Genotype-Tissue …
studies, and lack of proper correction can lead to spurious findings. The Genotype-Tissue …
Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics
Induced pluripotent stem cells (iPSCs) are an established cellular system to study the impact
of genetic variants in derived cell types and developmental contexts. However, in their …
of genetic variants in derived cell types and developmental contexts. However, in their …
Identifying cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis
…, ADH Gewirtz, G Gliner, MJ Gloudemans… - Genome …, 2017 - genome.cshlp.org
The impact of inherited genetic variation on gene expression in humans is well-established.
The majority of known expression quantitative trait loci (eQTLs) impact expression of local …
The majority of known expression quantitative trait loci (eQTLs) impact expression of local …