P. Awadalla

The evolution of SARS-CoV-2 seroprevalence in Canada: a time-series study, 2020–2023
202343 citationsauthor #5
Lung adenocarcinoma promotion by air pollutants
2023538 citationsauthor #61
Author Correction: Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
20231 citationsauthor #124
Author Correction: Pan-cancer analysis of whole genomes
20238 citationsauthor #44
Depression, anxiety, and the risk of cancer: An individual participant data meta‐analysis
202338 citationsauthor #13
Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts
202373 citationsauthor #12
Author Correction: Comprehensive molecular characterization of mitochondrial genomes in human cancers
20231 citationsauthor #62
Author Correction: Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
20237 citationsauthor #156
Author Correction: The evolutionary history of 2,658 cancers
20234 citationsauthor #119
Pre-diagnosis plasma cell-free DNA methylome profiling up to seven years prior to clinical detection reveals early signatures of breast cancer
20232 citationsauthor #11
Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
20234 citationsauthor #122
Author Correction: Patterns of somatic structural variation in human cancer genomes
20234 citationsauthor #124
Author Correction: Genomic basis for RNA alterations in cancer
20230 citationsauthor #38
Provincial variation in colorectal cancer screening adherence in Canada; evidence from the Canadian Partnership for Tomorrow’s Health
20238 citationsauthor #3
Author Correction: Pathway and network analysis of more than 2500 whole cancer genomes
20222 citationsauthor #175
Normal sex and age-specific parameters in a multi-ethnic population: a cardiovascular magnetic resonance study of the Canadian Alliance for Healthy Hearts and Minds cohort
202234 citationsauthor #7
Abstract 6090: Disentangling subclonal dynamics in growing tumors using stochastic simulations and Bayesian neural networks
20220 citationsauthor #2
Pan-cancer classification of single cells in the tumour microenvironment
202257 citationsauthor #3
Abstract 1221: Comprehensive cell-type classification of tumor and normal cells from single cell RNA sequencing in pan cancer settings
20220 citationsauthor #2
Cohort Profile: The Ontario Health Study (OHS).
202211 citationsauthor #12
Recombination affects allele-specific expression of deleterious variants in human populations
20228 citationsauthor #9
Lifestyle factors and lung cancer risk among never smokers in the Canadian Partnership for Tomorrow’s Health (CanPath)
202216 citationsauthor #14
Lung Adenocarcinoma Promotion by 1 Air Pollutants 2
20220 citationsauthor #62
Abstract 2228: A multi-omic perspective of how selection shapes blood cancer risk phenotypes in aging populations
20220 citationsauthor #6
Author Correction: Inferring structural variant cancer cell fraction
20220 citationsauthor #121
Meta-analysis fine-mapping is often miscalibrated at single-variant resolution
202281 citationsauthor #126
Understanding the evolution of tumours using hybrid deep generative models
20220 citationsauthor #2
3229 – MODELING CLONAL HEMATOPOIESIS AND THE PRE-LEUKEMIC STATE WITH CHR13Q DELETION IN HUMAN HEMATOPOIETIC STEM CELLS
20220 citationsauthor #5
Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin
202224 citationsauthor #33
Correction to: Lifestyle factors and lung cancer risk among never smokers in the Canadian Partnership for Tomorrow’s Health (CanPath)
20223 citationsauthor #14
The cell-free DNA methylome captures distinctions between localized and metastatic prostate tumors
202242 citationsauthor #19
Building knowledge, optimising physical and mental health and setting up healthier life trajectories in South African women (Bukhali): a preconception randomised control trial part of the Healthy Life Trajectories Initiative (HeLTI)
202243 citationsauthor #7
Abstract 3385: Pre-diagnosis plasma cell-free DNA methylation profiling reveals signatures of cancers up to7 years prior to clinical detection
20220 citationsauthor #7
Inferring ongoing cancer evolution from single tumour biopsies using synthetic supervised learning
20215 citationsauthor #2
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour
2021119 citationsauthor #12
Using image-based haplotype alignments to map global adaptation of SARS-CoV-2
20211 citationsauthor #3
The relationship between reproductive lifespan and coronary artery disease
20210 citationsauthor #5
Score tests for scale effects, with application to genomic analysis
20210 citationsauthor #3
Correction to: Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control
20210 citationsauthor #30
Effect of Cognitive Reserve on the Association of Vascular Brain Injury With Cognition
202127 citationsauthor #4
P-13 The Utility of Occupational Health Data in the Canadian Partnership for Tomorrow’s Health (CanPath)
20210 citationsauthor #2
Psychosocial factors and cancer incidence (PSY‐CA): Protocol for individual participant data meta‐analyses
202114 citationsauthor #11
Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control
202138 citationsauthor #30
Abstract 2602: Leveraging cell-free methylome markers for early cancer detection
20210 citationsauthor #10
Psychosocial factors and cancer incidence (PSY-CA): Protocol for individual participant datameta-analyses
20210 citationsauthor #11
Publisher Correction: Identification of 371 genetic variants for age at first sex and birth linked to externalising behavior
20210 citationsauthor #12
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
20211,605 citationsauthor #96
Clonal hematopoiesis is associated with risk of severe Covid-19
2020112 citationsauthor #37
Diabetes, Brain Infarcts, Cognition and Small Vessels in the Canadian Alliance for Healthy Hearts and Minds Study.
202018 citationsauthor #5
Sex differences in oncogenic mutational processes
202091 citationsauthor #97
High-coverage whole-genome analysis of 1220 cancers reveals hundreds of genes deregulated by rearrangement-mediated cis-regulatory alterations
202059 citationsauthor #11
Long-term exposure to a mixture of industrial SO2, NO2, and PM2.5 and anti-citrullinated protein antibody positivity
202027 citationsauthor #7
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples
202045 citationsauthor #171
Interacting evolutionary pressures drive mutation dynamics and health outcomes in aging blood
202017 citationsauthor #12
Genomic basis for RNA alterations in cancer
2020347 citationsauthor #38
High-depth African genomes inform human migration and health
202011 citationsauthor #72
Integration of intra-sample contextual error modeling for improved detection of somatic mutations from deep sequencing
202010 citationsauthor #8
The Canadian Alliance for Healthy Hearts and Minds: How Well Does It Reflect the Canadian Population?
20204 citationsauthor #11
Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies.
202017 citationsauthor #11
Reduced Cognitive Assessment Scores Among Individuals With Magnetic Resonance Imaging–Detected Vascular Brain Injury
20208 citationsauthor #5
High-depth African genomes inform human migration and health
2020279 citationsauthor #72
Patterns of somatic structural variation in human cancer genomes
2020686 citationsauthor #124
Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples
20201 citationsauthor #171
133 - The Canadian Partnership for Tomorrow Project: Canada’s Longitudinal Population Laboratory
20190 citationsauthor #1
Polygenic risk scores predict diabetic complications and their response to therapy
20193 citationsauthor #29
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
2019640 citationsauthor #64
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
2019280 citationsauthor #10
Rheumatoid arthritis-relevant DNA methylation changes identified in ACPA-positive asymptomatic individuals using methylome capture sequencing
201919 citationsauthor #6
Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances
2019228 citationsauthor #13
Gene-by-environment interactions in urban populations modulate risk phenotypes
20180 citationsauthor #13
Uromodulin in a Pathway Between Decreased Renal Urate Excretion and Albuminuria
20183 citationsauthor #8
Aberrant PRDM9 expression impacts the pan-cancer genomic landscape
201829 citationsauthor #10
Gene-by-environment interactions in urban populations modulate risk phenotypes
2018106 citationsauthor #13
The Canadian Urban Environmental Health Research Consortium – a protocol for building a national environmental exposure data platform for integrated analyses of urban form and health
201883 citationsauthor #7
The Canadian Partnership for Tomorrow Project: a pan-Canadian platform for research on chronic disease prevention
201886 citationsauthor #2
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis
2018506 citationsauthor #89
Genomic basis for RNA alterations revealed by whole-genome analyses of 27 cancer types
201727 citationsauthor #37
Relaxed Selection During a Recent Human Expansion
201753 citationsauthor #17
Motif Disruption Domains Lead To Cancer Gene Expression Rewiring
20172 citationsauthor #6
The impact of recombination on human mutation load and disease
201734 citationsauthor #4
Relaxed Selection During a Recent Human Expansion
201753 citationsauthor #16
Pan-cancer study of heterogeneous RNA aberrations
201715 citationsauthor #59
Abstract SY10-02: Pan-cancer study of recurrent and heterogeneous RNA aberrations and association with whole-genome variants
20171 citationsauthor #2
Genomic and Environmental Contributions to Chronic Diseases in Urban Populations
20171 citationsauthor #12
Clinical, Genetic, and Urinary Factors Associated with Uromodulin Excretion.
201642 citationsauthor #6
Rationale, design, and methods for Canadian alliance for healthy hearts and minds cohort study (CAHHM) – a Pan Canadian cohort study
201641 citationsauthor #3
Gain-of-function missense variant in SLC12A2, encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophrenia.
201642 citationsauthor #6
A haplotype-based normalization technique for the analysis and detection of allele specific expression
201611 citationsauthor #4
Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.
201625 citationsauthor #9
Comparative Analysis of Iron Homeostasis in Sub-Saharan African Children with Sickle Cell Disease and Their Unaffected Siblings
20167 citationsauthor #4
Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease
201663 citationsauthor #10
ARMC5 mutations in a large French-Canadian family with cortisol-secreting β-adrenergic/vasopressin responsive bilateral macronodular adrenal hyperplasia.
201657 citationsauthor #7
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis.
201668 citationsauthor #13
Recombination affects accumulation of damaging and disease-associated mutations in human populations
201583 citationsauthor #8
Association of age-dependent height and bone mineral density decline with increased arterial stiffness and rate of fractures in hypertensive individuals
201534 citationsauthor #7
Allele-specific expression reveals interactions between genetic variation and environment
2015129 citationsauthor #11
Impact of the X Chromosome and sex on regulatory variation
201599 citationsauthor #16
Recombination impacts damaging and disease mutation accumulation in human populations
20140 citationsauthor #8
High-Resolution Genomic Analysis of Human Mitochondrial RNA Sequence Variation
2014100 citationsauthor #9
Genomic architecture of sickle cell disease in West African children
201421 citationsauthor #11

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