Works by Davis, Lea K.
Results: 53
Developing a phenotype risk score for tic disorders in a large, clinical biobank.
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- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-03011-w
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- Article
Medical and genetic correlates of long-term buprenorphine treatment in the electronic health records.
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- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-023-02713-x
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- Article
Genome-wide analysis of copy number variants in age-related macular degeneration.
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- Human Genetics, 2011, v. 129, n. 1, p. 91, doi. 10.1007/s00439-010-0904-6
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- Article
Sexual Trauma, Polygenic Scores, and Mental Health Diagnoses and Outcomes.
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- JAMA Psychiatry, 2025, v. 82, n. 1, p. 75, doi. 10.1001/jamapsychiatry.2024.3426
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- Article
Genetic Liability to Posttraumatic Stress Disorder Symptoms and Its Association With Cardiometabolic and Respiratory Outcomes.
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- JAMA Psychiatry, 2024, v. 81, n. 1, p. 34, doi. 10.1001/jamapsychiatry.2023.4127
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- Article
Calcium-Sensing Receptor Polymorphisms at rs1801725 Are Associated with Increased Risk of Secondary Malignancies.
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- Journal of Personalized Medicine, 2021, v. 11, n. 7, p. 642, doi. 10.3390/jpm11070642
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- Article
Genome-wide association study of alcohol use disorder identification test (AUDIT) scores in 20 328 research participants of European ancestry.
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- 2019
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- journal article
Automated Phenotyping Tool for Identifying Developmental Language Disorder Cases in Health Systems Data (APT-DLD): A New Research Algorithm for Deployment in Large-Scale Electronic Health Record Systems.
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- Journal of Speech, Language & Hearing Research, 2020, v. 63, n. 9, p. 3019, doi. 10.1044/2020_JSLHR-19-00397
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- Article
In Search of Genomic Stability: Characterizing Copy Number Stable Regions.
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- Human Mutation, 2011, v. 32, n. 8, p. v, doi. 10.1002/humu.21572
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- Article
STAMS: STRING-assisted module search for genome wide association studies and application to autism.
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- Bioinformatics, 2016, v. 32, n. 24, p. 3815, doi. 10.1093/bioinformatics/btw530
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- Article
Sex-Adjusted Model for End-stage Liver Disease Scores for Liver Transplant Allocation—Reply.
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- JAMA Surgery, 2022, v. 157, n. 12, p. 1167, doi. 10.1001/jamasurg.2022.4150
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- Article
Proposing a Sex-Adjusted Sodium-Adjusted MELD Score for Liver Transplant Allocation.
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- 2022
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- journal article
Copy number variations on chromosome 12q14 in patients with normal tension glaucoma.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2482, doi. 10.1093/hmg/ddr123
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- Article
The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area.
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- Cerebral Cortex, 2021, v. 31, n. 4, p. 1873, doi. 10.1093/cercor/bhaa327
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- Article
Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
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- Molecular Autism, 2017, v. 8, p. 1, doi. 10.1186/s13229-017-0130-3
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- Article
Frequency of benign neutropenia among Black versus White individuals undergoing a bone marrow assessment.
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- Journal of Cellular & Molecular Medicine, 2022, v. 26, n. 13, p. 3628, doi. 10.1111/jcmm.17346
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- Article
Weldon, Bateson, and the origins of genetics: Reflections on the unraveling and rebuilding of a scientific community.
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- PLoS Genetics, 2022, v. 18, n. 10, p. 1, doi. 10.1371/journal.pgen.1010379
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- Article
Improving the computation efficiency of polygenic risk score modeling: faster in Julia.
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- Life Science Alliance, 2022, v. 5, n. 12, p. 1, doi. 10.26508/lsa.202201382
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- Article
Use of the PsycheMERGE Network to Investigate the Association Between Depression Polygenic Scores and White Blood Cell Count.
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- 2021
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- journal article
Genetic association signal near NTN4 in Tourette syndrome.
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- 2014
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- journal article
Genetic association signal near NTN 4 in Tourette syndrome.
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- Annals of Neurology, 2014, v. 76, n. 2, p. 310, doi. 10.1002/ana.24215
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- Article
Confronting ethical and social issues related to the genetics of musicality.
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- Annals of the New York Academy of Sciences, 2023, v. 1522, n. 1, p. 5, doi. 10.1111/nyas.14972
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- Article
Medical phenome of musicians: an investigation of health records collected on 9803 musically active individuals.
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- Annals of the New York Academy of Sciences, 2021, v. 1505, n. 1, p. 156, doi. 10.1111/nyas.14671
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- Article
Epidemiology of Functional Seizures Among Adults Treated at a University Hospital.
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- JAMA Network Open, 2020, v. 3, n. 12, p. e2027920, doi. 10.1001/jamanetworkopen.2020.27920
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- Article
The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-95154-9
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- Article
Strength of Genetic Associations with Thyrotropin Values Differs Between Populations with Similarity to African and European Reference Populations.
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- Thyroid, 2025, v. 35, n. 2, p. 131, doi. 10.1089/thy.2024.0525
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- Article
A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05624-4
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- Article
A practical approach to identifying autistic adults within the electronic health record.
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- Autism Research: Official Journal of the International Society for Autism Research, 2023, v. 16, n. 1, p. 52, doi. 10.1002/aur.2849
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- Article
Polygenic burden in focal and generalized epilepsies.
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- 2019
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- journal article
Dense phenotyping from electronic health records enables machine learning-based prediction of preterm birth.
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- BMC Medicine, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12916-022-02522-x
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- Article
Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture.
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- PLoS Genetics, 2013, v. 9, n. 10, p. 1, doi. 10.1371/journal.pgen.1003864
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Genetic investigation of the contribution of body composition to anorexia nervosa in an electronic health record setting.
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- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02251-y
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- Article
Phenomewide Association Study of Health Outcomes Associated With the Genetic Correlates of 25 Hydroxyvitamin D Concentration and Vitamin D Binding Protein Concentration.
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- Twin Research & Human Genetics, 2024, v. 27, n. 2, p. 69, doi. 10.1017/thg.2024.19
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- Article
Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease.
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- Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-020-00820-8
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- Article
Estimating Uterine Fibroid SNP-Based Heritability in European American Women with Imaging-Confirmed Fibroids.
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- Human Heredity, 2019, v. 84, n. 2, p. 73, doi. 10.1159/000501335
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- Article
LGBTQ+ Perspectives on Conducting Genomic Research on Sexual Orientation and Gender Identity.
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- Behavior Genetics, 2022, v. 52, n. 4/5, p. 246, doi. 10.1007/s10519-022-10105-y
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- Article
The Biological Contributions to Gender Identity and Gender Diversity: Bringing Data to the Table.
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- Behavior Genetics, 2018, v. 48, n. 2, p. 95, doi. 10.1007/s10519-018-9889-z
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- Article
Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes.
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- Bioinformatics, 2015, v. 31, n. 2, p. 187, doi. 10.1093/bioinformatics/btu591
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- Article
Fate or coincidence: do COPD and major depression share genetic risk factors?
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- Human Molecular Genetics, 2021, v. 30, n. 7, p. 619, doi. 10.1093/hmg/ddab068
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- Article
The physical and psychiatric health conditions related to autism genetic scores, across genetic ancestries, sexes and age-groups in electronic health records.
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- Journal of Neurodevelopmental Disorders, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s11689-023-09485-x
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- Article
Genetic Thyrotropin Regulation of Atrial Fibrillation Risk Is Mediated Through an Effect on Height.
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- 2021
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- journal article
Characterizing the Clinical and Genetic Spectrum of Polycystic Ovary Syndrome in Electronic Health Records.
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- 2021
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- journal article
Sex modifies the effect of genetic risk scores for polycystic ovary syndrome on metabolic phenotypes.
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- PLoS Genetics, 2023, v. 19, n. 5, p. 1, doi. 10.1371/journal.pgen.1010764
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- Article
Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitativet trait loci.
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- Molecular Autism, 2012, v. 3, n. 1, p. 3, doi. 10.1186/2040-2392-3-3
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- Article
Life is pain: Fibromyalgia as a nexus of multiple liability distributions.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2023, v. 192, n. 7/8, p. 171, doi. 10.1002/ajmg.b.32949
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- Article
A phenome‐wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2022, v. 189, n. 6, p. 185, doi. 10.1002/ajmg.b.32911
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- Article
International Society of Psychiatric Genetics Ethics Committee: Issues facing us.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 8, p. 543, doi. 10.1002/ajmg.b.32736
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- Article
Sex differences in the genetic architecture of obsessive–compulsive disorder.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 6, p. 351, doi. 10.1002/ajmg.b.32687
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The new science of sex differences in neuropsychiatric traits.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 6, p. 333, doi. 10.1002/ajmg.b.32747
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Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry.
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- BMC Genomics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s12864-024-09990-w
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- Article