Search Results - "DAVIS, Lea K"
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Weldon, Bateson, and the origins of genetics: Reflections on the unraveling and rebuilding of a scientific community
Published in PLoS genetics (27-10-2022)“…“Science, like most forms of human activity, is occasionally liable to lose sight of its ultimate ends under a flood of controversy, the strugglings of…”
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2
Sex modifies the effect of genetic risk scores for polycystic ovary syndrome on metabolic phenotypes
Published in PLoS genetics (31-05-2023)“…Females with polycystic ovary syndrome (PCOS), the most common endocrine disorder in women, have an increased risk of developing cardiometabolic disorders such…”
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3
Integrative genomic analyses identify susceptibility genes underlying COVID-19 hospitalization
Published in Nature communications (27-07-2021)“…Despite rapid progress in characterizing the role of host genetics in SARS-Cov-2 infection, there is limited understanding of genes and pathways that…”
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4
Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation
Published in Neuropsychopharmacology (New York, N.Y.) (01-03-2017)“…Loneliness is a complex biological trait that has been associated with numerous negative health outcomes. The measurement and environmental determinants of…”
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5
A genome-wide association study of polycystic ovary syndrome identified from electronic health records
Published in American journal of obstetrics and gynecology (01-10-2020)“…Polycystic ovary syndrome is the most common endocrine disorder affecting women of reproductive age. A number of criteria have been developed for clinical…”
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6
Examination of the shared genetic basis of anorexia nervosa and obsessive–compulsive disorder
Published in Molecular psychiatry (01-09-2020)“…Anorexia nervosa (AN) and obsessive–compulsive disorder (OCD) are often comorbid and likely to share genetic risk factors. Hence, we examine their shared…”
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Genetic investigation of the contribution of body composition to anorexia nervosa in an electronic health record setting
Published in Translational psychiatry (19-11-2022)“…Anorexia nervosa (AN) is a psychiatric disorder defined by anthropometric symptoms, such as low body weight, and cognitive-behavioral symptoms, such as…”
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8
Contextualizing genetic risk score for disease screening and rare variant discovery
Published in Nature communications (20-07-2021)“…Studies of the genetic basis of complex traits have demonstrated a substantial role for common, small-effect variant polygenic burden (PB) as well as…”
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The physical and psychiatric health conditions related to autism genetic scores, across genetic ancestries, sexes and age-groups in electronic health records
Published in Journal of neurodevelopmental disorders (16-06-2023)“…Although polygenic scores (PGS) for autism have been related to various psychiatric and medical conditions, most studies to date have been conducted in…”
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10
Medical and genetic correlates of long-term buprenorphine treatment in the electronic health records
Published in Translational psychiatry (10-01-2024)“…Despite the benefits associated with longer buprenorphine treatment duration (i.e., >180 days) (BTD) for opioid use disorder (OUD), retention remains poor…”
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11
Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction
Published in Nature communications (13-11-2024)“…Myasthenia gravis (MG) is a rare autoantibody-mediated disease affecting the neuromuscular junction. We performed a genome-wide association study of 5708 MG…”
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12
Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease
Published in Genome medicine (13-01-2021)“…Clinical laboratory (lab) tests are used in clinical practice to diagnose, treat, and monitor disease conditions. Test results are stored in electronic health…”
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13
Developing a phenotype risk score for tic disorders in a large, clinical biobank
Published in Translational psychiatry (28-07-2024)“…Tics are a common feature of early-onset neurodevelopmental disorders, characterized by involuntary and repetitive movements or sounds. Despite affecting up to…”
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14
Dense phenotyping from electronic health records enables machine learning-based prediction of preterm birth
Published in BMC medicine (28-09-2022)“…Identifying pregnancies at risk for preterm birth, one of the leading causes of worldwide infant mortality, has the potential to improve prenatal care…”
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15
Structural Architecture of SNP Effects on Complex Traits
Published in American journal of human genetics (06-11-2014)“…Despite the discovery of copy-number variation (CNV) across the genome nearly 10 years ago, current SNP-based analysis methodologies continue to collapse the…”
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Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry
Published in BMC genomics (26-02-2024)“…Polycystic ovary syndrome (PCOS) is a complex multifactorial disorder with a substantial genetic component. However, the clinical manifestations of PCOS are…”
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17
A dimensional perspective on the genetics of obsessive-compulsive disorder
Published in Translational psychiatry (21-07-2021)“…This review covers recent findings in the genomics of obsessive-compulsive disorder (OCD), obsessive-compulsive symptoms, and related traits from a dimensional…”
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Development and multi-site external validation of a generalizable risk prediction model for bipolar disorder
Published in Translational psychiatry (25-01-2024)“…Bipolar disorder is a leading contributor to disability, premature mortality, and suicide. Early identification of risk for bipolar disorder using…”
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The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene
Published in Scientific reports (02-08-2021)“…Inflammation increases the risk of cardiometabolic disease. Delineating specific inflammatory pathways and biomarkers of their activity could identify the…”
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Pancreatic islet beta cell-specific deletion of G6pc2 reduces fasting blood glucose
Published in Journal of molecular endocrinology (01-05-2020)“…The G6PC1, G6PC2 and G6PC3 genes encode distinct glucose-6-phosphatase catalytic subunit (G6PC) isoforms. In mice, germline deletion of G6pc2 lowers fasting…”
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