Author details

Full Name

Paul L Auer

Affiliation

ORCID

Career Start Year

2010

Papers

142

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
37745480	Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium.	bioRxiv	2023
37905118	Determinants of mosaic chromosomal alteration fitness.	medRxiv	2023
37732240	A General Approach to Adjusting Genetic Studies for Assortative Mating.		2023
37904051	Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.	Nat Genet	2023
37558590	Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19.	Blood Cells Mol Dis	2023
37777527	Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality.	Nat Commun	2023
37609271	The Relationship of Duffy Gene Polymorphism, High Sensitivity C-Reactive Protein, and Long-term Outcomes.	medRxiv	2023
37345498	On asymptotic distributions of several test statistics for familial relatedness in linear mixed models.		2023
36778386	Structural variation across 138,134 samples in the TOPMed consortium.	Res Sq	2023
37277705	Comparison of multiple imputation and other methods for the analysis of imputed genotypes.	BMC Genomics	2023
36899395	Prognostic landscape of mitochondrial genome in myelodysplastic syndrome after stem-cell transplantation.	J Hematol Oncol	2023
37398003	Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.	medRxiv	2023
36747810	Structural variation across 138,134 samples in the TOPMed consortium.	bioRxiv	2023
37041565	Whole-genome sequencing identifies novel predictors for hematopoietic cell transplant outcomes for patients with myelodysplastic syndrome: a CIBMTR study.		2023
37533140	Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait.	Clin J Am Soc Nephrol	2023
35262092	Genetic Examination of Hematological Parameters in SARS-CoV-2 Infection and COVID-19.	medRxiv	2022
35837690	Prenatal Socioeconomic Disadvantage and Epigenetic Alterations at Birth Among Children Born to White British and Pakistani Mothers in the Born in Bradford Study.	Epigenetics	2022
35580243	Latent Class Models of Early-life Trauma and Incident Breast Cancer.	Epidemiology	2022
35504290	TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data.	Am J Hum Genet	2022
36208382	Contemporary evaluation of estrogen receptor and progesterone receptor expression in breast cancer-associated stroma.	Breast Cancer Research and Treatment	2022
35939862	Early life trauma and adult leucocyte telomere length.	Psychoneuroendocrinology	2022
35552711	Whole-exome sequencing of 14â¿¿389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.	Hum Mol Genet	2022
35418701	Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women.	Sci Rep	2022
36481753	Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program.	Nat Commun	2022
36474046	Finding causal genes underlying risk for coronary artery disease.	Nature Genetics	2022
32766691	Individualized multi-omic pathway deviation scores using multiple factor analysis.	Biostatistics	2022
34727735	Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project.	Stroke	2022
34553764	Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.	Hum Mol Genet	2022
34582791	Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.	Am J Hum Genet	2021
32359158	Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk.	J Natl Cancer Inst	2021
34292776	Risk of Late-Onset Breast Cancer in Genetically Predisposed Women.	J Clin Oncol	2021
33910371	Soluble CD14 Levels in the Jackson Heart Study: Associations With Cardiovascular Disease Risk and Genetic Variants.	Arteriosclerosis, Thrombosis, and Vascular Biology	2021
33471974	A Population-Based Study of Genes Previously Implicated in Breast Cancer.	N Engl J Med	2021
34107879	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	BMC Genomics	2021
33887194	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.	Am J Hum Genet	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
34101481	Risk of Breast Cancer Among Carriers of Pathogenic Variants in Breast Cancer Predisposition Genes Varies by Polygenic Risk Score.	J Clin Oncol	2021
33992829	Impact of Epigenomic Hypermethylation at TP53 on Allogeneic Hematopoietic Cell Transplantation Outcomes for Myelodysplastic Syndromes.	Transplantation and Cellular Therapy	2021
34087167	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.	Am J Hum Genet	2021
32918779	Mendelian randomization analysis with survival outcomes.	Genetic Epidemiology	2021
33175443	A unified linear mixed model for familial relatedness and population structure in genetic association studies.	Genetic Epidemiology	2021
32851660	Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer.	Int J Cancer	2021
33268503	Effect of Sickle Cell Trait and <i>APOL1</i> Genotype on the Association of Soluble uPAR with Kidney Function Measures in Black Americans.	Clin J Am Soc Nephrol	2021
35047852	From GWAS variant to function: A study of â¿¼148,000 variants for blood cell traits.	HGG Adv	2021
34407845	Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.	Breast Cancer Res	2021
34517814	Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study.	BMC Genomics	2021
34706549	Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Black Adults.	Circ Genom Precis Med	2021
32888493	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Cell	2020
31902252	Comparative and Functional Genomic Resource for Mechanistic Studies of Human Blood Pressure-Associated Single Nucleotide Polymorphisms.	Hypertension	2020