Author details

Full Name

Celia M T Greenwood

Affiliation

ORCID

Career Start Year

1988

Papers

235

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37534032	Development of risk prediction models for depression combining genetic and early life risk factors.		2023
36280454	Circulating Proteins Influencing Psychiatric Disease: A Mendelian Randomization Study.	Biol Psychiatry	2023
37761864	A Review of the Epigenetic Clock: Emerging Biomarkers for Asthma and Allergic Disease.	Genes (Basel)	2023
37830501	Identifying Rare Genetic Determinants for Improved Polygenic Risk Prediction of Bone Mineral Density and Fracture Risk.	J Bone Miner Res	2023
36969007	Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases.	Front Oncol	2023
36833203	Molecular Genetic Characteristics of <i>FANCI</i>, a Proposed New Ovarian Cancer Predisposing Gene.	Genes (Basel)	2023
37270501	Novel insights into systemic sclerosis using a sensitive computational method to analyze whole-genome bisulfite sequencing data.		2023
36948466	Genetic predisposition to depression and inflammation impacts symptom burden and survival in patients with head and neck cancer: A longitudinal study.	J Affect Disord	2023
36635386	Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases.	Nat Genet	2023
37069249	Circulating proteins to predict COVID-19 severity.	Sci Rep	2023
37124505	GD2 and GD3 gangliosides as diagnostic biomarkers for all stages and subtypes of epithelial ovarian cancer.		2023
37368847	Dose-dependent Association of Alcohol Consumption With Obesity and Type 2 Diabetes: Mendelian Randomization Analyses.	J Clin Endocrinol Metab	2023
35147782	An effector index to predict target genes at GWAS loci.	Hum Genet	2022
36376796	Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals.	Clin Proteomics	2022
36250789	Genetic determinants of polygenic prediction accuracy within a population.	Genetics	2022
35460399	Polygenic risk score as a possible tool for identifying familial monogenic causes of complex diseases.	Genet Med	2022
35710731	Capturing additional genetic risk from family history for improved polygenic risk prediction.	Commun Biol	2022
35947648	Single base-pair resolution analysis of DNA binding motif with MoMotif reveals an oncogenic function of CTCF zinc-finger 1 mutation.	Nucleic Acids Research	2022
35753057	A Bayesian hierarchical model for improving measurement of 5mC and 5hmC levels: Toward revealing associations between phenotypes and methylation states.	Genet Epidemiol	2022
35689460	Identifying Causes of Fracture Beyond Bone Mineral Density: Evidence From Human Genetics.	J Bone Miner Res	2022
35565380	The Genetic and Molecular Analyses of <i>RAD51C</i> and <i>RAD51D</i> Identifies Rare Variants Implicated in Hereditary Ovarian Cancer from a Genetically Unique Population.	Cancers (Basel)	2022
35869146	The rise to power of the microbiome: power and sample size calculation for microbiome studies.	Mucosal Immunology	2022
36418427	Dementia with Lewy bodies post-mortem brains reveal differentially methylated CpG sites with biomarker potential.	Communications Biology	2022
36819922	Considering strategies for SNP selection in genetic and polygenic risk scores.		2022
34389974	Combined polygenic risk scores of different psychiatric traits predict general and specific psychopathology in childhood.	Journal of Child Psychology and Psychiatry and Allied Disciplines	2022
34861889	A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene.	Genome Med	2021
32278003	Maternal Prenatal Mood, Pregnancy-Specific Worries, and Early Child Psychopathology: Findings From the DREAM BIG Consortium.	J Am Acad Child Adolesc Psychiatry	2021
32438470	A novel statistical method for modeling covariate effects in bisulfite sequencing derived measures of DNA methylation.	Biometrics	2021
34181531	Resistance to different anthracycline chemotherapeutics elicits distinct and actionable primary metabolic dependencies in breast cancer.	eLife	2021
34020575	A 10-color flow cytometry panel for diagnosis and minimal residual disease in chronic lymphocytic leukemia.	Leukemia and Lymphoma	2021
34174944	Detecting cord blood cell type-specific epigenetic associations with gestational diabetes mellitus and early childhood growth.	Clinical Epigenetics	2021
33803939	Candidate Markers of Olaparib Response from Genomic Data Analyses of Human Cancer Cell Lines.	Cancers (Basel)	2021
33633408	A Neanderthal OAS1 isoform protects individuals of European ancestry against COVID-19 susceptibility and severity.	Nat Med	2021
33481004	Understanding the impact of preprocessing pipelines on neuroimaging cortical surface analyses.	Gigascience	2021
33536041	Improved prediction of fracture risk leveraging a genome-wide polygenic risk score.	Genome Med	2021
34053674	Early or Late Gestational Exposure to Maternal Immune Activation Alters Neurodevelopmental Trajectories in Mice: An Integrated Neuroimaging, Behavioral, and Transcriptional Study.	Biol Psychiatry	2021
33788949	A Polygenic Risk Score to Predict Future Adult Short Stature Among Children.	J Clin Endocrinol Metab	2021
33931971	Copy number and transcriptome alterations associated with metastatic lesion response to treatment in colorectal cancer.	Clinical and Translational Medicine	2021
32911998	Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome.	Am J Psychiatry	2021
33110269	Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening.	Genet Med	2021
33414497	Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability.	Molecular Psychiatry	2021
33390174	Neuropsychiatric symptoms are early indicators of an upcoming metabolic decline in Alzheimer's disease.	Translational Neurodegeneration	2021
33386395	High Systolic Blood Pressure at Hospital Admission Is an Important Risk Factor in Models Predicting Outcome of COVID-19 Patients.	American Journal of Hypertension	2021
34468045	Block coordinate descent algorithm improves variable selection and estimation in error-in-variables regression.	Genet Epidemiol	2021
34573331	Thousands of CpGs Show DNA Methylation Differences in ACPA-Positive Individuals.	Genes	2021
30626458	Distinguishing differential susceptibility, diathesis-stress, and vantage sensitivity: Beyond the single gene and environment model.	Development and Psychopathology	2020
31697315	MDiNE: a model to estimate differential co-occurrence networks in microbiome studies.		2020
31642105	Suicidal ideation is common in autosomal dominant Alzheimer's disease at-risk persons.	International Journal of Geriatric Psychiatry	2020
32365090	Simultaneous SNP selection and adjustment for population structure in high dimensional prediction models.	PLoS Genetics	2020
32000781	Polygenic risk for coronary heart disease acts through atherosclerosis in type 2 diabetes.	Cardiovasc Diabetol	2020