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Genomic, phenomic, and geographic associations of leukocyte telomere length in the United States
Genomic, phenomic, and geographic associations of leukocyte telomere length in the United States
medRxiv - The Preprint Server for Health Sciences
Polygenic risk scores for precision psychiatry: a study on the effect heterogeneity of antidepressants
Polygenic risk scores for precision psychiatry: a study on the effect heterogeneity of antidepressants
medRxiv - The Preprint Server for Health Sciences
Transcriptome-wide association study of Alzheimer disease reveals many differentially expressed genes and multiple biological pathways in brain tissue from African American donors
Transcriptome-wide association study of Alzheimer disease reveals many differentially expressed genes and multiple biological pathways in brain tissue from African American donors
medRxiv - The Preprint Server for Health Sciences
Spatially resolved mapping of cells associated with human complex traits
Spatially resolved mapping of cells associated with human complex traits
medRxiv - The Preprint Server for Health Sciences
Clinical syndromes linked to biallelic germline variants in MCM8 and MCM9
Clinical syndromes linked to biallelic germline variants in MCM8 and MCM9
medRxiv - The Preprint Server for Health Sciences
Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications
Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications
medRxiv - The Preprint Server for Health Sciences
Improved heritability partitioning and enrichment analyses using summary statistics with graphREML
Improved heritability partitioning and enrichment analyses using summary statistics with graphREML
medRxiv - The Preprint Server for Health Sciences
An accurate genetic colocalization method for the HLA locus
An accurate genetic colocalization method for the HLA locus
medRxiv - The Preprint Server for Health Sciences
Identification of actionable genetic variants in 4,198 Scottish volunteers from the Viking Genes research cohort and implementation of return of results
Identification of actionable genetic variants in 4,198 Scottish volunteers from the Viking Genes research cohort and implementation of return of results
medRxiv - The Preprint Server for Health Sciences
Genomic characterization uncovers transmission dynamics of Marburg Virus in Rwanda following a single zoonotic spillover event
Genomic characterization uncovers transmission dynamics of Marburg Virus in Rwanda following a single zoonotic spillover event
medRxiv - The Preprint Server for Health Sciences
ANALYSIS OF GLOMERULAR TRANSCRIPTOMES FROM NEPHROTIC PATIENTS SUGGEST APOL1 RISK VARIANTS IMPACT PARIETAL EPITHELIAL CELLS
ANALYSIS OF GLOMERULAR TRANSCRIPTOMES FROM NEPHROTIC PATIENTS SUGGEST APOL1 RISK VARIANTS IMPACT PARIETAL EPITHELIAL CELLS
medRxiv - The Preprint Server for Health Sciences
Genetic regulation of TERT splicing contributes to reduced or elevated cancer risk by altering cellular longevity and replicative potential
Genetic regulation of TERT splicing contributes to reduced or elevated cancer risk by altering cellular longevity and replicative potential
medRxiv - The Preprint Server for Health Sciences
MPSE provides fast, flexible, and efficient means to identify newborns who will benefit from whole genome sequencing within the first 48 hours of NICU admission
MPSE provides fast, flexible, and efficient means to identify newborns who will benefit from whole genome sequencing within the first 48 hours of NICU admission
medRxiv - The Preprint Server for Health Sciences
Successful classification of clinical pediatric leukemia genetic subtypes via structural variant detection using HiFi long-read sequencing
Successful classification of clinical pediatric leukemia genetic subtypes via structural variant detection using HiFi long-read sequencing
medRxiv - The Preprint Server for Health Sciences
Single-nucleus transcriptome-wide association study of human brain disorders
Single-nucleus transcriptome-wide association study of human brain disorders
medRxiv - The Preprint Server for Health Sciences
Comparative Performance of Polygenic Risk Scores for Atherosclerotic Cardiovascular Disease Subtypes in the All of Us Research Program
Comparative Performance of Polygenic Risk Scores for Atherosclerotic Cardiovascular Disease Subtypes in the All of Us Research Program
medRxiv - The Preprint Server for Health Sciences
Potential causal links between genetic variants in SAMM50, SUGP1, MAU2, and GATAD2A and liver fat in individuals with normal weight
Potential causal links between genetic variants in SAMM50, SUGP1, MAU2, and GATAD2A and liver fat in individuals with normal weight
medRxiv - The Preprint Server for Health Sciences
Unsupervised cardiac MRI phenotyping with 3D diffusion autoencoders reveals novel genetic insights
Unsupervised cardiac MRI phenotyping with 3D diffusion autoencoders reveals novel genetic insights
medRxiv - The Preprint Server for Health Sciences
Evaluation of DNA-poli: study protocol of a randomised controlled trial to assess a digital platform for family cascade genetic testing and predictive genetic counselling
Evaluation of DNA-poli: study protocol of a randomised controlled trial to assess a digital platform for family cascade genetic testing and predictive genetic counselling
medRxiv - The Preprint Server for Health Sciences
A 5-transcript signature for discriminating viral and bacterial etiology in pediatric pneumonia
A 5-transcript signature for discriminating viral and bacterial etiology in pediatric pneumonia
medRxiv - The Preprint Server for Health Sciences
Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy
Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy
medRxiv - The Preprint Server for Health Sciences
Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling
Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling
medRxiv - The Preprint Server for Health Sciences
The Great Genotyper: A Graph-Based Method for Population Genotyping of Small and Structural Variants
The Great Genotyper: A Graph-Based Method for Population Genotyping of Small and Structural Variants
medRxiv - The Preprint Server for Health Sciences
Inherited infertility- mapping loci associated with impaired female reproduction
Inherited infertility- mapping loci associated with impaired female reproduction
medRxiv - The Preprint Server for Health Sciences
Identification of a Novel SLC2A9 Gene Association with LDL-C levels and Evaluation of Polygenic Scores in a Multi-Ancestry Genome Wide Association Study
Identification of a Novel SLC2A9 Gene Association with LDL-C levels and Evaluation of Polygenic Scores in a Multi-Ancestry Genome Wide Association Study
medRxiv - The Preprint Server for Health Sciences
Global Perspectives on Returning Genetic Research Results in Parkinson's Disease
Global Perspectives on Returning Genetic Research Results in Parkinson's Disease
medRxiv - The Preprint Server for Health Sciences
Non-linear genetic regulation of the blood plasma proteome
Non-linear genetic regulation of the blood plasma proteome
medRxiv - The Preprint Server for Health Sciences
Overlap between COPD genetic association results and transcriptional quantitative trait loci
Overlap between COPD genetic association results and transcriptional quantitative trait loci
medRxiv - The Preprint Server for Health Sciences
The Association between Endometriosis and Immunological diseases
The Association between Endometriosis and Immunological diseases
medRxiv - The Preprint Server for Health Sciences
High incidence and geographic distribution of cleft palate cases in Finland are associated with a regulatory variant in IRF6
High incidence and geographic distribution of cleft palate cases in Finland are associated with a regulatory variant in IRF6
medRxiv - The Preprint Server for Health Sciences
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