|
| 37961088 | Comparing ancestry calibration approaches for a trans-ancestry colorectal cancer polygenic risk score. | medRxiv | 2024 |
| 37961088 | Comparing ancestry calibration approaches for a trans-ancestry colorectal cancer polygenic risk score. | medRxiv | 2024 |
| 36824881 | Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia. | medRxiv | 2023 |
| 37662324 | Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count genetics. | medRxiv | 2023 |
| 37808736 | Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition. | bioRxiv | 2023 |
| 37898691 | Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. | Sci Rep | 2023 |
| 37883979 | Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing. | Am J Hum Genet | 2023 |
| 37790445 | Genetic Sex Validation for Sample Tracking in Clinical Testing. | Res Sq | 2023 |
| 37560121 | Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2A. | Neurol Genet | 2023 |
| 37968452 | Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. | Sci Rep | 2023 |
| 37783704 | Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations. | Nat Commun | 2023 |
| 37559024 | Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approach. | BMC Pulm Med | 2023 |
| 38065071 | Genomic medicine year in review: 2023. | Am J Hum Genet | 2023 |
| 37470892 | Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system. | Breast Cancer Res Treat | 2023 |
| 36824881 | Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia. | medRxiv | 2023 |
| 37461624 | Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies <i>LRRC4C, LHX5-AS1</i> and nominates ancestry-specific loci <i>PTPRK</i> , <i>GRB14</i> , and <i>KIAA0825</i> as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. | medRxiv | 2023 |
| 37071725 | Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results. | Circ Genom Precis Med | 2023 |
| 37194416 | Dominant-negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome. | Ann Clin Transl Neurol | 2023 |
| 36798371 | Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2A. | bioRxiv | 2023 |
| 36621880 | Returning integrated genomic risk and clinical recommendations: The eMERGE study. | Genet Med | 2023 |
| 36540998 | Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index. | Pac Symp Biocomput | 2023 |
| 36789420 | Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity. | medRxiv | 2023 |
| 37526719 | Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry. | JAMA | 2023 |
| 36846987 | Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions. | J Am Heart Assoc | 2023 |
| 37808736 | Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition. | bioRxiv | 2023 |
| 37560121 | Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2A. | Neurol Genet | 2023 |
| 37526719 | Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry. | JAMA | 2023 |
| 37559024 | Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approach. | BMC Pulm Med | 2023 |
| 37662324 | Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count genetics. | medRxiv | 2023 |
| 38065071 | Genomic medicine year in review: 2023. | Am J Hum Genet | 2023 |
| 37898691 | Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. | Sci Rep | 2023 |
| 37790445 | Genetic Sex Validation for Sample Tracking in Clinical Testing. | Res Sq | 2023 |
| 37883979 | Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing. | Am J Hum Genet | 2023 |
| 37783704 | Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations. | Nat Commun | 2023 |
| 37968452 | Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. | Sci Rep | 2023 |
| 37470892 | Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system. | Breast Cancer Res Treat | 2023 |
| 37071725 | Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results. | Circ Genom Precis Med | 2023 |
| 37194416 | Dominant-negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome. | Ann Clin Transl Neurol | 2023 |
| 37461624 | Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies <i>LRRC4C, LHX5-AS1</i> and nominates ancestry-specific loci <i>PTPRK</i> , <i>GRB14</i> , and <i>KIAA0825</i> as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. | medRxiv | 2023 |
| 36789420 | Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity. | medRxiv | 2023 |
| 36621880 | Returning integrated genomic risk and clinical recommendations: The eMERGE study. | Genet Med | 2023 |
| 36846987 | Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions. | J Am Heart Assoc | 2023 |
| 36540998 | Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index. | Pac Symp Biocomput | 2023 |
| 36798371 | Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2A. | bioRxiv | 2023 |
| 34302314 | Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment. | J Genet Couns | 2022 |
| 36372681 | Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics. | Obesity (Silver Spring) | 2022 |
| 35595084 | Multiancestral polygenic risk score for pediatric asthma. | J Allergy Clin Immunol | 2022 |
| 35594287 | Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities. | PLoS One | 2022 |
| 35710995 | Genome-wide polygenic score to predict chronic kidney disease across ancestries. | Nat Med | 2022 |
| 35522237 | ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial. | Genet Med | 2022 |