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Author Details
Full Name
Swneke D Bailey
Affiliation
Research Institute of the McGill University Health Centre
ORCID
Career Start Year
2006
Papers
40
H Index
23
Expertise
CM4AI Collaborator
Antoine Forget (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36059037
Soluble factors in malignant ascites promote the metastatic adhesion of gastric adenocarcinoma cells.
Gastric Cancer
2023
37563798
Tumour extracellular vesicles induce neutrophil extracellular traps to promote lymph node metastasis.
J Extracell Vesicles
2023
34767138
Inhibition of LPS-mediated TLR4 activation abrogates gastric adenocarcinoma-associated peritoneal metastasis.
Clin Exp Metastasis
2022
36446943
Author Correction: Failure of human rhombic lip differentiation underlies medulloblastoma formation.
Nature
2022
36212399
To bind or not to bind: Cistromic reprogramming in prostate cancer.
Front Oncol
2022
36131014
Failure of human rhombic lip differentiation underlies medulloblastoma formation.
Nature
2022
34880227
A predominant enhancer co-amplified with the SOX2 oncogene is necessary and sufficient for its expression in squamous cancer.
Nat Commun
2021
33741928
The transcriptional landscape of Shh medulloblastoma.
Nat Commun
2021
33115806
Chromatin Looping Shapes KLF5-Dependent Transcriptional Programs in Human Epithelial Cancers.
Cancer Res
2020
32094913
Author Correction: Human somatic cell mutagenesis creates genetically tractable sarcomas.
Nat Genet
2020
30816925
C3D: a tool to predict 3D genomic interactions between cis-regulatory elements.
Bioinformatics
2019
31664194
Recurrent noncoding U1Â snRNA mutations drive cryptic splicing in SHH medulloblastoma.
Nature
2019
29633758
Publisher Correction: ZNF143 provides sequence specificity to secure chromatin interactions at gene promoters.
Nat Commun
2018
29921600
Mammary molecular portraits reveal lineage-specific features and progenitor cell vulnerabilities.
J Cell Biol
2018
26727462
Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study.
Sci Rep
2016
27498878
The Transcriptional Repressor Polycomb Group Factor 6, PCGF6, Negatively Regulates Dendritic Cell Activation and Promotes Quiescence.
Cell Rep
2016
27526323
Modulation of long noncoding RNAs by risk SNPs underlying genetic predispositions to prostate cancer.
Nat Genet
2016
27571262
Noncoding somatic and inherited single-nucleotide variants converge to promote ESR1 expression in breast cancer.
Nat Genet
2016
26908456
Pre-neoplastic epigenetic disruption of transcriptional enhancers in chronic inflammation.
Oncotarget
2016
25452129
BioID identifies novel c-MYC interacting partners in cultured cells and xenograft tumors.
J Proteomics
2015
25995231
ABC: a tool to identify SNVs causing allele-specific transcription factor binding from ChIP-Seq experiments.
Bioinformatics
2015
25645053
ZNF143 provides sequence specificity to secure chromatin interactions at gene promoters.
Nat Commun
2015
24362726
Variation at the DPP4 locus influences apolipoprotein B levels in South Asians and exhibits heterogeneity in Europeans related to BMI.
Diabetologia
2014
25473436
Enhancer alterations in cancer: a source for a cell identity crisis.
Genome Med
2014
24981860
Human-chromatin-related protein interactions identify a demethylase complex required for chromosome segregation.
Cell Rep
2014
24553142
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy.
Nature
2014
24661571
Laying a solid foundation for Manhattan--'setting the functional basis for the post-GWAS era'.
Trends Genet
2014
23603917
Genetic information and the prediction of incident type 2 diabetes in a high-risk multiethnic population: the EpiDREAM genetic study.
Diabetes Care
2013
21840418
The HDL proteome in acute coronary syndromes shifts to an inflammatory profile.
Biochim Biophys Acta
2012
23001124
Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression.
Nat Genet
2012
22665440
Integrative functional genomics identifies an enhancer looping to the SOX9 gene disrupted by the 17q24.3 prostate cancer risk locus.
Genome Res
2012
22022235
The effect of chromosome 9p21 variants on cardiovascular disease may be modified by dietary intake: evidence from a case/control and a prospective study.
PLoS Med
2011
19844255
Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects.
Eur J Hum Genet
2010
20858904
Fine mapping of the insulin-induced gene 2 identifies a variant associated with LDL cholesterol and total apolipoprotein B levels.
Circ Cardiovasc Genet
2010
20628086
Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes Care
2010
17805225
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
Eur J Hum Genet
2008
18974833
Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies.
PLoS One
2008
18316358
Genetic variants of FTO influence adiposity, insulin sensitivity, leptin levels, and resting metabolic rate in the Quebec Family Study.
Diabetes
2008
17608621
Familial combined hyperlipidaemia: how can genetic disorders be common, complex and comprehensible?
Clin Sci (Lond)
2007
17003359
Common polymorphisms in the promoter of the visfatin gene (PBEF1) influence plasma insulin levels in a French-Canadian population.
Diabetes
2006
1 - 40 of 40
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