Author details

Full Name

Angela Brooks-Wilson

Affiliation

ORCID

Career Start Year

1988

Papers

217

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37546854	Systematic assessment of long-read RNA-seq methods for transcript identification and quantification.	bioRxiv	2023
36368129	Profiling the immune landscape in mucinous ovarian carcinoma.	Gynecol Oncol	2023
37666943	Correction: Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes.	Leukemia	2023
37688655	Physiological phenotypes have optimal values relevant to healthy aging: sweet spots deduced from the Canadian Longitudinal Study on Aging.		2023
37398362	Detecting haplotype-specific transcript variation in long reads with FLAIR2.		2023
36572991	CCNE1 and survival of patients with tubo-ovarian high-grade serous carcinoma: An Ovarian Tumor Tissue Analysis consortium study.	Cancer	2023
36948887	p53 and ovarian carcinoma survival: an Ovarian Tumor Tissue Analysis consortium study.	J Pathol Clin Res	2023
36697831	Author Correction: Genomic basis for RNA alterations in cancer.	Nature	2023
37379307	Gene and pathway based burden analyses in familial lymphoid cancer cases: Rare variants in immune pathway genes.		2023
36688720	Lifetime ovulatory years and risk of epithelial ovarian cancer: a multinational pooled analysis.	J Natl Cancer Inst	2023
37487637	Full-length transcript alterations in human bronchial epithelial cells with S34F mutations.		2023
35202586	SRSF1 governs progenitor-specific alternative splicing to maintain adult epithelial tissue homeostasis and renewal.	Dev Cell	2022
35767963	Penalized Logistic Regression Analysis for Genetic Association Studies of Binary Phenotypes.	Human Heredity	2022
36092819	An expression-based variant impact phenotyping protocol to predict the impact of gene variants in cell lines.	STAR Protocols	2022
35418701	Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women.	Sci Rep	2022
35858545	Mutant KRAS regulates transposable element RNA and innate immunity via KRAB zinc-finger genes.	Cell Rep	2022
35353015	Cell Painting predicts impact of lung cancer variants.	Mol Biol Cell	2022
34351578	Interactions between exposure to polycyclic aromatic hydrocarbons and xenobiotic metabolism genes, and risk of breast cancer.		2022
35233977	Functional MRI evaluation of cognitive effects of carotid stenosis revascularization.	Brain and Behavior	2022
35244686	B-Cell NHL Subtype Risk Associated with Autoimmune Conditions and PRS.	Cancer Epidemiol Biomarkers Prev	2022
34612777	Anticipation in multiple-case lymphoid cancer families after controlling for ascertainment biases.	Leukemia and Lymphoma	2021
33574182	Reintroduction of the archaic variant of <i>NOVA1</i> in cortical organoids alters neurodevelopment.	Science	2021
34047695	Inflammation drives alternative first exon usage to regulate immune genes including a novel iron-regulated isoform of <i>Aim2</i>.	Elife	2021
34622145	Genome-wide homozygosity and risk of four non-Hodgkin lymphoma subtypes.	J Transl Genet Genom	2021
31504207	Allele-Specific Transcript Abundance: A Pilot Study in Healthy Centenarians.		2020
31600786	Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathways.	Hum Mol Genet	2020
32188845	Full-length transcript characterization of SF3B1 mutation in chronic lymphocytic leukemia reveals downregulation of retained introns.	Nature Communications	2020
32064237	Genetically Determined Height and Risk of Non-hodgkin Lymphoma.	Front Oncol	2020
32178631	Dietary patterns in the healthy oldest old in the healthy aging study and the Canadian longitudinal study of aging: a cohort study.	BMC Geriatrics	2020
32169998	Birth Order, Sibship Size, Childhood Environment and Immune-Related Disorders, and Risk of Lymphoma in Lymphoid Cancer Families.	Cancer Epidemiology Biomarkers and Prevention	2020
32108027	Lipid Trait Variants and the Risk of Non-Hodgkin Lymphoma Subtypes: A Mendelian Randomization Study.	Cancer Epidemiol Biomarkers Prev	2020
31819268	Author Correction: Nanopore native RNA sequencing of a human poly(A) transcriptome.	Nat Methods	2020
31764964	SimRVSequences: an R package to simulate genetic sequence data for pedigrees.		2020
32444850	Visualizing and interpreting cancer genomics data via the Xena platform.	Nat Biotechnol	2020
32699076	Tattoos and Hematologic Malignancies in British Columbia, Canada.	Cancer Epidemiology Biomarkers and Prevention	2020
32555365	Clinical and pathological associations of PTEN expression in ovarian cancer: a multicentre study from the Ovarian Tumour Tissue Analysis Consortium.	Br J Cancer	2020
30712845	A Murine Model of Chronic Lymphocytic Leukemia Based on B Cell-Restricted Expression of Sf3b1 Mutation and Atm Deletion.	Cancer Cell	2019
30169793	Cohort Profile: The British Columbia Generations Project (BCGP).	International Journal of Epidemiology	2019
30601841	Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk.	PLoS ONE	2019
30499236	A comprehensive gene-environment interaction analysis in Ovarian Cancer using genome-wide significant common variants.	Int J Cancer	2019
29901523	Ovarian Carcinoma Histotype: Strengths and Limitations of Integrating Morphology With Immunohistochemical Predictions.	Int J Gynecol Pathol	2019
30819100	10-year follow-up of the Super-Seniors Study: compression of morbidity and genetic factors.	BMC Geriatrics	2019
31491388	A Pan-cancer Transcriptome Analysis Reveals Pervasive Regulation through Alternative Promoters.	Cell	2019
31407831	Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.	Genet Epidemiol	2019
31001917	Evaluation of vitamin D biosynthesis and pathway target genes reveals UGT2A1/2 and EGFR polymorphisms associated with epithelial ovarian cancer in African American Women.	Cancer Med	2019
29795606	The Super-Seniors Study: Phenotypic characterization of a healthy 85+ population.	PLoS ONE	2018
29979793	Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility.	PLoS One	2018
30356812	Simulating pedigrees ascertained for multiple disease-affected relatives.	Source Code for Biology and Medicine	2018
30059005	An alternative splicing switch in FLNB promotes the mesenchymal cell state in human breast cancer.	Elife	2018
30282833	Splicing modulation sensitizes chronic lymphocytic leukemia cells to venetoclax by remodeling mitochondrial apoptotic dependencies.	JCI Insight	2018