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Samantha L. Wilson
Researcher at University of British Columbia
Publications - 24
Citations - 494
Samantha L. Wilson is an academic researcher from University of British Columbia. The author has contributed to research in topics: dNaM & DNA methylation. The author has an hindex of 12, co-authored 24 publications receiving 358 citations. Previous affiliations of Samantha L. Wilson include Boston Children's Hospital & Family Research Institute.
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Journal ArticleDOI
Placental epigenetic clocks: estimating gestational age using placental DNA methylation levels
Yunsung Lee,Sanaa Choufani,Rosanna Weksberg,Samantha L. Wilson,Samantha L. Wilson,Victor Yuan,Victor Yuan,Amber Burt,Carmen J. Marsit,Ake T. Lu,Beate Ritz,Jon Bohlin,Håkon K. Gjessing,Håkon K. Gjessing,Jennifer R. Harris,Per Magnus,Alexandra M. Binder,Wendy P. Robinson,Wendy P. Robinson,Astanand Jugessur,Astanand Jugessur,Steve Horvath +21 more
TL;DR: It is shown that epigenetic clocks derived from cord blood or other tissues do not accurately estimate gestational age in placental samples, and placental clocks closely track fetal age during development and may have interesting applications.
Journal ArticleDOI
Epigenetic regulation of placental gene expression in transcriptional subtypes of preeclampsia.
Katherine Leavey,Samantha L. Wilson,Shannon Bainbridge,Shannon Bainbridge,Wendy P. Robinson,Brian J. Cox +5 more
TL;DR: DNA methylation alterations underlying a portion of the transcriptional development of “canonical” PE in cluster 2 and “immunological”PE in cluster 3 are established, however, a significant number of the observed methylation changes were not associated with corresponding changes in gene expression, indicating that alternate methods of gene regulation will need to be explored.
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Mining DNA methylation alterations towards a classification of placental pathologies.
TL;DR: Despite large changes observed in EOPE, there were challenges in reproducing genome-wide DNAm hits that are discussed, and DNAm profiling may provide an independent tool to refine clinical/pathological diagnoses into subgroups with more uniform pathology.
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Number of Children and Telomere Length in Women: A Prospective, Longitudinal Evaluation
Cindy K. Barha,Courtney W. Hanna,Courtney W. Hanna,Katrina G. Salvante,Samantha L. Wilson,Samantha L. Wilson,Wendy P. Robinson,Wendy P. Robinson,Rachel MacKay Altman,Pablo A. Nepomnaschy +9 more
TL;DR: Investigation of the relationship between the number of surviving children born to a woman and telomere length over 13 years in a group of 75 Kaqchikel Mayan women found women who had fewer children exhibited shorter TLs than those who had more children, contrary to LHT's prediction.
Journal ArticleDOI
Detecting somatic mosaicism: considerations and clinical implications.
A.S.A. Cohen,A.S.A. Cohen,Samantha L. Wilson,Samantha L. Wilson,Joanne Trinh,X.C. Ye,X.C. Ye +6 more
TL;DR: Somatic mosaicism is defined with a brief overview of its main mechanisms in concrete clinical examples, the impact of next‐generation sequencing technologies in its detection is discussed, and the clinical implications associated with a discovery in the clinic are expanded.