المؤلفون: Jacqueline A. Piekos, Jacklyn N. Hellwege, Yanfei Zhang, Eric S. Torstenson, Gail P. Jarvik, Ozan Dikilitas, Iftikhar J. Kullo, Daniel J. Schaid, David R. Crosslin, Sarah A. Pendergrass, Ming Ta Michael Lee, Dan Roden, Josh C. Denny, Todd L. Edwards, Digna R. Velez Edwards

المصدر: Human Genetics. 141:1739-1748

مصطلحات موضوعية: Genetics, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::210ae589328184702a161524b5814ab0Test
https://doi.org/10.1007/s00439-022-02442-zTest

المؤلفون: Ian B. Stanaway, David Fasel, Sarah A. Pendergrass, Yatong K. Li, Melody R. Palmer, Hakon Hakonarson, Chunhua Weng, Sunghwan Sohn, David Cronkite, Eric B. Larson, Gail P. Jarvik, David R. Crosslin, Rongling Li, Iftikhar J. Kullo, Adam S. Gordon, David Carrell, Daniel Seung Kim, Xiaomeng Du, QiPing Feng, Samuel K. Handelman, Patrick M. A. Sleiman, Marc S. Williams, Elisabeth A. Rosenthal, Elizabeth K. Speliotes

المصدر: Genetic Epidemiology

مصطلحات موضوعية: medicine.medical_specialty, Epidemiology, Carotid arteries, Bilateral carotid artery stenosis, Locus (genetics), Genome-wide association study, Polymorphism, Single Nucleotide, Gastroenterology, 03 medical and health sciences, Internal medicine, carotid artery atherosclerosis, medicine, Humans, Carotid Stenosis, Genetic Predisposition to Disease, Research Articles, Genetics (clinical), genome‐wide association study, 030304 developmental biology, 0303 health sciences, Models, Genetic, business.industry, 030305 genetics & heredity, Atherosclerotic disease, Genomics, Odds ratio, medicine.disease, Confidence interval, Stenosis, electronic health records, business, Genome-Wide Association Study, Lipoprotein(a), Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68ec6ab9cbd68d69ae19ae8d44180244Test
https://doi.org/10.1002/gepi.22360Test

المؤلفون: Bertram Müller-Myhsok, John B. Harley, Patrick M. A. Sleiman, Anastasia Lucas, Murray H. Brilliant, Beibei Jiang, Jiayan Zhou, Molly A. Hall, John M. Wallace, Jason H. Moore, John McGuigan, Shefali S. Verma, Yuki Bradford, Hakon Hakonarson, Kristel Van Steen, Yanfei Zhang, Krzysztof Kiryluk, Sarah A. Pendergrass, Kristin Passero, Marylyn D. Ritchie, Peggy L. Peissig

المصدر: PLoS Genetics, Vol 17, Iss 6, p e1009534 (2021)
PLoS Genetics

مصطلحات موضوعية: Cancer Research, Heredity, Eye Diseases, Single Nucleotide Polymorphisms, Datasets as Topic, Genome-wide association study, SUSCEPTIBILITY, QH426-470, DISEASE, Homozygosity, Macular Degeneration, 0302 clinical medicine, Medical Conditions, Gene Frequency, Medicine and Health Sciences, Genetics (clinical), Genetics & Heredity, 0303 health sciences, Heterozygosity, Genomics, BREAST-CANCER RISK, Genetic Mapping, ISCHEMIC-STROKE, Phenotype, Hypertension, symbols, Life Sciences & Biomedicine, Research Article, Single-nucleotide polymorphism, Variant Genotypes, Computational biology, Biology, Polymorphism, Single Nucleotide, Cataract, 03 medical and health sciences, symbols.namesake, Genetic model, LOCUS, Genome-Wide Association Studies, Genetics, Humans, Allele, GENOME-WIDE ASSOCIATION, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Alleles, 030304 developmental biology, TOOLS, Science & Technology, EMERGE NETWORK, Models, Genetic, Cataracts, ELECTRONIC MEDICAL-RECORDS, Biology and Life Sciences, Computational Biology, Human Genetics, Glaucoma, Genome Analysis, POLYMORPHISM, Minor allele frequency, Ophthalmology, Bonferroni correction, Diabetes Mellitus, Type 2, Genetic Loci, Lens Disorders, Multiple comparisons problem, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: Electronic-eCollection

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2417c0b12ab33679e6e18047153250dcTest
https://doaj.org/article/b37fdfc15813491fa1c98bc3372f6d22Test

المؤلفون: David J. Carey, Yanfei Zhang, Lisa Bang, Marta Byrska-Bishop, Ming Ta Michael Lee, Anurag Verma, Yu Zhang, Sarah A. Pendergrass, Marylyn D. Ritchie, Dokyoon Kim, Jason E. Miller

المصدر: American Journal of Human Genetics

مصطلحات موضوعية: 0301 basic medicine, Epigenomics, Single-nucleotide polymorphism, Computational biology, Disease, Biology, Polymorphism, Single Nucleotide, Article, Autoimmune Diseases, 03 medical and health sciences, 0302 clinical medicine, Pleiotropy, Genetic variation, Genetics, Electronic Health Records, Humans, DiscovEHR study, Genetics (clinical), Genetic Association Studies, Genetic association, PheWAS, electronic health record, Biobank, Genetic architecture, 030104 developmental biology, Phenotype, Cardiovascular Diseases, 030220 oncology & carcinogenesis, human disease network, Diagnosis code, EHR-based population study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24380b6f02bf466199da0c8e95637057Test
http://europepmc.org/articles/PMC6323551Test

المؤلفون: Diego R. Mazzotti, Allan I. Pack, Sarah A. Pendergrass, Navya Shilpa Josyula, Brendan T. Keenan, Christopher R. Bauer, Beth A. Malow, Janet D. Robishaw, Olivia J. Veatch, Kanika Bagai

المصدر: BMC Medical Genomics
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-14 (2020)

مصطلحات موضوعية: Male, 0301 basic medicine, lcsh:Internal medicine, Candidate gene, lcsh:QH426-470, Genotype, Single-nucleotide polymorphism, Disease, Health records, Bioinformatics, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Diabetes mellitus, Ethnicity, Genetics, medicine, Humans, Electronic health records, SNP, Genetic Predisposition to Disease, lcsh:RC31-1245, Genetics (clinical), Genetic association, Pleiotropy, Sleep Apnea, Obstructive, Genetic heterogeneity, business.industry, Sleep disorders, Middle Aged, medicine.disease, Obstructive sleep apnea, Human genetics, nervous system diseases, 3. Good health, respiratory tract diseases, lcsh:Genetics, Phenotype, 030104 developmental biology, Systematic review, 030228 respiratory system, Case-Control Studies, Female, business, 030217 neurology & neurosurgery, Genome-Wide Association Study, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dd9599d928809239d82a2ecc223e101Test

المؤلفون: Joseph B. Leader, Marylyn D. Ritchie, Sarah A. Pendergrass, Yu Zhang, Anastasia Lucas, Anqa Khan, Dustin N. Hartzel, Shefali S. Verma, Daniel R. Lavage, Anurag Verma, Navya Shilpa Josyula

المصدر: The American Journal of Human Genetics. 102:592-608

مصطلحات موضوعية: 0301 basic medicine, Context (language use), Genome-wide association study, Single-nucleotide polymorphism, Disease, Biology, Article, Open Reading Frames, 03 medical and health sciences, International Classification of Diseases, Genetics, Electronic Health Records, Humans, Medical diagnosis, Genetics (clinical), Genetic association, Clinical Laboratory Techniques, Genome, Human, Sequence Analysis, RNA, Reproducibility of Results, Molecular Sequence Annotation, Chromatin, Minor allele frequency, Phenotype, 030104 developmental biology, Gene Expression Regulation, Haplotypes, Genetic epidemiology, DNA, Intergenic, Genome-Wide Association Study, Demography

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02c785761e829bca4b1242823e513500Test
https://doi.org/10.1016/j.ajhg.2018.02.017Test

المؤلفون: Yunin Ludena-Rodriguez, Molly A. Hall, Santhosh Girirajan, Marylyn D. Ritchie, Dokyoon Kim, Kyoungmi Kim, Heather E. Volk, Irva Hertz-Picciotto, Debashis Ghosh, Scott B. Selleck, Rebecca J. Schmidt, Robin L Hansen, Shefali S. Verma, Sarah A. Pendergrass

المصدر: Autism Research. 10:1470-1480

مصطلحات موضوعية: 0301 basic medicine, Genetics, General Neuroscience, Environmental exposure, Biology, Heritability, medicine.disease, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Missing heritability problem, Genetic variation, medicine, Genetic predisposition, Autism, Neurology (clinical), Copy-number variation, Gene–environment interaction, 030217 neurology & neurosurgery, Genetics (clinical), Demography

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::496fee267fe6b6c057591668dbb83b1bTest
https://doi.org/10.1002/aur.1799Test

المؤلفون: Anurag Verma, Gene D. Morse, Eric S. Daar, Charles S. Venuto, Shefali S. Verma, Yuki Bradford, David W. Haas, Marylyn D. Ritchie, Sarah A. Pendergrass

المصدر: Pharmacogenetics and Genomics

مصطلحات موضوعية: CD4-Positive T-Lymphocytes, Male, 0301 basic medicine, Oncology, PharmGKB, Pharmacogenomic Variants, Pilot Projects, Genome-wide association study, law.invention, chemistry.chemical_compound, 0302 clinical medicine, Randomized controlled trial, law, Prospective Studies, 030212 general & internal medicine, General Pharmacology, Toxicology and Pharmaceutics, Prospective cohort study, Genetics (clinical), Middle Aged, 3. Good health, Phenotype, Anti-Retroviral Agents, ComputingMethodologies_DOCUMENTANDTEXTPROCESSING, Molecular Medicine, Female, medicine.drug, Adult, medicine.medical_specialty, Efavirenz, antiretroviral therapy, phenome-wide association studies, Context (language use), Polymorphism, Single Nucleotide, 03 medical and health sciences, Apolipoproteins E, Internal medicine, Genetics, medicine, Humans, Lymphocyte Count, Molecular Biology, pharmacogenomics, Acquired Immunodeficiency Syndrome, clinical trials, business.industry, Original Articles, Atazanavir, Clinical trial, Cytochrome P-450 CYP2B6, 030104 developmental biology, chemistry, Apolipoprotein A-V, HIV-1, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe41f7dc237817633f3dbd02cda76e7aTest
https://doi.org/10.1097/fpc.0000000000000263Test

المؤلفون: Todd L. Edwards, Ayush Giri, Jacklyn N. Hellwege, Katherine E. Hartmann, Elizabeth A. Stewart, Janina M. Jeff, Michael J. Bray, Sarah A. Pendergrass, Eric S. Torstenson, Jacob M. Keaton, Sarah H. Jones, Radhika P. Gogoi, Helena Kuivaniemi, Kathryn L. Jackson, Abel N. Kho, Iftikhar J. Kullo, Catherine A. McCarty, Hae Kyung Im, Jennifer A. Pacheco, Jyotishman Pathak, Marc S. Williams, Gerard Tromp, Eimear E. Kenny, Peggy L. Peissig, Joshua C. Denny, Dan M. Roden, Digna R. Velez Edwards

المصدر: Frontiers in Genetics
Frontiers in Genetics, Vol 10 (2019)

مصطلحات موضوعية: 0301 basic medicine, lcsh:QH426-470, Uterine fibroids, Single-nucleotide polymorphism, Locus (genetics), Genome-wide association study, Biology, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, SNP, uterine fibroids, Allele, 1000 Genomes Project, Genetics (clinical), Original Research, genetically predicted gene expression (GPGE), genome-wide association study (GWAS), trans-ethnic, medicine.disease, genetic architecture, 3. Good health, lcsh:Genetics, 030104 developmental biology, meta-analysis electronic health record (EHR), Genetic marker, 030220 oncology & carcinogenesis, Molecular Medicine

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::886d2027e6af7537cf7d80e6ffca1c29Test
https://doi.org/10.3389/fgene.2019.00511Test

المؤلفون: Sarah A. Pendergrass, Dana C. Crawford

المصدر: Current Protocols in Human Genetics. 100

مصطلحات موضوعية: 0301 basic medicine, Computer science, Vital signs, Disease, Health records, Precision medicine, medicine.disease, Response to treatment, Article, Data warehouse, 03 medical and health sciences, Laboratory test, Phenotype, 030104 developmental biology, 0302 clinical medicine, Genetics, medicine, Data Mining, Electronic Health Records, Humans, 030212 general & internal medicine, Clinical imaging, Medical emergency, Algorithms, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aa93d0413ae6bbf19bf8e294e3b274fTest
https://doi.org/10.1002/cphg.80Test