Publication & Citation Trends
Publications
0 total
Common Oncogene Mutations and Novel SND1-BRAF Transcript Fusion in Lung Adenocarcinoma from Never Smokers OA
Cited by 46
Semantic Scholar
MG-129 The development of a genetic newborn screening assay for permanent hearing loss using blood spots – a collaboration between newborn screening ontario (NSO) and the infant hearing program (IHP)
Cited by 2
Semantic Scholar
The development of a genetic newborn screening assay for permanent hearing loss using blood spots — A collaboration between Newborn Screening Ontario (NSO) and the Infant Hearing Program (IHP)
Cited by 0
Semantic Scholar
PCDH10 promoter hypermethylation is frequent in most histologic subtypes of mature lymphoid malignancies and occurs early in lymphomagenesis OA
Cited by 23
Semantic Scholar
Promoter methylation‐mediated inactivation of PCDH10 in acute lymphoblastic leukemia contributes to chemotherapy resistance
Cited by 34
Semantic Scholar
Discovery of DNA Hypermethylation Using a DHPLC Screening Strategy OA
Cited by 9
Semantic Scholar
Research Topics
Epigenetics and DNA Methylation
(3)
Hearing, Cochlea, Tinnitus, Genetics
(2)
Lung Cancer Treatments and Mutations
(2)
Cancer Genomics and Diagnostics
(2)
RNA modifications and cancer
(2)
Affiliations
Transgenomic (United States)
Sequenom (United States)