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1دورية أكاديميةMeasurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing
المؤلفون: Kingsmore, Stephen F, Henderson, Audrey, Owen, Mallory J, Clark, Michelle M, Hansen, Christian, Dimmock, David, Chambers, Christina D, Jeliffe-Pawlowski, Laura L, Hobbs, Charlotte
المصدر: npj Genomic Medicine. 5(1)
مصطلحات موضوعية: Human Genome, Infant Mortality, Pediatric, Clinical Research, Genetics, Good Health and Well Being, Molecular medicine
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/44t8t8x2Test
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2دورية أكاديمية
المؤلفون: Dimmock, David P, Clark, Michelle M, Gaughran, Mary, Cakici, Julie A, Caylor, Sara A, Clarke, Christina, Feddock, Michele, Chowdhury, Shimul, Salz, Lisa, Cheung, Cynthia, Bird, Lynne M, Hobbs, Charlotte, Wigby, Kristen, Farnaes, Lauge, Bloss, Cinnamon S, Kingsmore, Stephen F, Investigators, the RCIGM, Bainbridge, Matthew N, Barea, Jaime, Batalov, Sergey, Bezares, Zaira, Braun, Joshua JA, Del Campo, Miguel, Carroll, Jeanne, Cohenmeyer, Casey, Coufal, Nicole G, Diaz, Carlos, Ding, Yan, Ellsworth, Katarzyna, Evans, Marva, Feigenbaum, Annette, Friedman, Jennifer, Gleeson, Joe, Hansen, Christian, Honold, Jose, James, Kiely, Jones, Marilyn C, Kimball, Amy, Knight, Gail, Van Der Kraan, Lucitia, Lane, Brian, Le, Jennie, Leibel, Sandra, Lenberg, Jerica, Mashburn, Dana, Moyer, Laurel, Mulrooney, Patrick, Nahas, Shareef, Oh, Daeheon, Orendain, Daniken, Oriol, Albert, Ortiz-Arechiga, Maria, Prince, Lance, Rego, Seema, Reyes, Iris, Sanford, Erica, Sauer, Charles, Schwanemann, Leila, Speziale, Mark, Suttner, Denise, Sweeney, Nathaly, Song, Richard, Tokita, Mari, Veeraraghavan, Narayanan, Watkins, Kelly, Wong, Terence, Wright, Meredith S, Yamada, Catherine
المصدر: American Journal of Human Genetics. 107(5)
مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Health Sciences, Genetics, Clinical Trials and Supportive Activities, Clinical Research, Biotechnology, Infectious Diseases, Pediatric, Human Genome, Good Health and Well Being, Chromosome Mapping, Clinical Decision-Making, Critical Illness, Disease Management, Female, Genetic Diseases, Inborn, Genetic Testing, Genome, Human, Humans, Infant, Infant, Newborn, Intensive Care Units, Neonatal, Logistic Models, Male, Prospective Studies, Time Factors, Whole Genome Sequencing, RCIGM Investigators, NSIGHT2, clinical utility, diagnostic testing outcomes, healthcare cost-benefit analysis, neonatal intensive care unit, pediatric intensive care unit, rapid whole-exome sequencing, rapid whole-genome sequencing, ultra-rapid whole-genome sequencing, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences
وصف الملف: application/pdf
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3دورية أكاديمية
المؤلفون: Sanford, Erica F, Clark, Michelle M, Farnaes, Lauge, Williams, Matthew R, Perry, James C, Ingulli, Elizabeth G, Sweeney, Nathaly M, Doshi, Ami, Gold, Jeffrey J, Briggs, Benjamin, Bainbridge, Matthew N, Feddock, Michele, Watkins, Kelly, Chowdhury, Shimul, Nahas, Shareef A, Dimmock, David P, Kingsmore, Stephen F, Coufal, Nicole G
المصدر: Pediatric Critical Care Medicine. 20(11)
مصطلحات موضوعية: Human Genome, Pediatric Research Initiative, Genetics, Clinical Research, Patient Safety, Pediatric, Detection, screening and diagnosis, 4.1 Discovery and preclinical testing of markers and technologies, Generic health relevance, Good Health and Well Being, Adolescent, Child, Child, Preschool, Critical Illness, Female, Genetic Diseases, Inborn, Humans, Infant, Intensive Care Units, Pediatric, Male, Precision Medicine, Retrospective Studies, Whole Genome Sequencing, clinical utility, diagnostic utility, genomics, pediatric critical care, precision medicine, whole genome sequencing, RCIGM Investigators, Nursing, Paediatrics and Reproductive Medicine, Pediatrics
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/7165w94qTest
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4دورية أكاديمية
المؤلفون: Kingsmore, Stephen F, Cakici, Julie A, Clark, Michelle M, Gaughran, Mary, Feddock, Michele, Batalov, Sergey, Bainbridge, Matthew N, Carroll, Jeanne, Caylor, Sara A, Clarke, Christina, Ding, Yan, Ellsworth, Katarzyna, Farnaes, Lauge, Hildreth, Amber, Hobbs, Charlotte, James, Kiely, Kint, Cyrielle I, Lenberg, Jerica, Nahas, Shareef, Prince, Lance, Reyes, Iris, Salz, Lisa, Sanford, Erica, Schols, Peter, Sweeney, Nathaly, Tokita, Mari, Veeraraghavan, Narayanan, Watkins, Kelly, Wigby, Kristen, Wong, Terence, Chowdhury, Shimul, Wright, Meredith S, Dimmock, David, Investigators, the RCIGM, Bezares, Zaira, Bloss, Cinnamon, Braun, Joshua JA, Diaz, Carlos, Mashburn, Dana, Tamang, Dorjee, Orendain, Daniken, Friedman, Jenni, Gleeson, Joe, Barea, Jaime, Chiang, George, Cohenmeyer, Casey, Coufal, Nicole G, Evans, Marva, Honold, Jose, Hovey, Raymond L, Kimball, Amy, Lane, Brian, Le, Crystal, Le, Jennie, Leibel, Sandra, Moyer, Laurel, Mulrooney, Patrick, Oh, Daeheon, Ordonez, Paulina, Oriol, Albert, Ortiz-Arechiga, Maria, Puckett, Laura, Speziale, Mark, Suttner, Denise, Van Der Kraan, Lucitia, Knight, Gail, Sauer, Charles, Song, Richard, White, Sarah, Wise, Audra, Yamada, Catherine
المصدر: American Journal of Human Genetics. 105(4)
مصطلحات موضوعية: Human Genome, Pediatric, Clinical Research, Genetics, Clinical Trials and Supportive Activities, Good Health and Well Being, Genetic Testing, Humans, Infant, Infant, Newborn, Exome Sequencing, Whole Genome Sequencing, RCIGM Investigators, diagnosis, genetic disease, genomic medicine, infant, intensive care unit, precision medicine, ultra-rapid whole-genome sequencing, whole-exome sequencing, whole-genome sequencing, Biological Sciences, Medical and Health Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/9h05k7vhTest
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5دورية أكاديمية
المؤلفون: Cakici, Julie A., Dimmock, David, Caylor, Sara, Gaughran, Mary, Clarke, Christina, Triplett, Cynthia, Clark, Michelle M., Kingsmore, Stephen F., Bloss, Cinnamon S.
المصدر: Clinical Therapeutics ; volume 45, issue 8, page 736-744 ; ISSN 0149-2918
مصطلحات موضوعية: Pharmacology (medical), Pharmacology
الإتاحة: https://doi.org/10.1016/j.clinthera.2023.06.014Test
https://api.elsevier.com/content/article/PII:S0149291823002205?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0149291823002205?httpAccept=text/plainTest -
6دورية أكاديمية
المؤلفون: Janowitz Koch, Ilana, Clark, Michelle M, Thompson, Michael J, Deere-Machemer, Kerry A, Wang, Jun, Duarte, Lionel, Gnanadesikan, Gitanjali E, McCoy, Eskender L, Rubbi, Liudmilla, Stahler, Daniel R, Pellegrini, Matteo, Ostrander, Elaine A, Wayne, Robert K, Sinsheimer, Janet S, vonHoldt, Bridgett M
المصدر: Molecular Ecology. 25(8)
مصطلحات موضوعية: Biological Sciences, Genetics, Human Genome, Biotechnology, Animals, DNA Methylation, DNA Transposable Elements, Dogs, Domestication, Evolution, Molecular, Inheritance Patterns, Pedigree, Polymorphism, Genetic, Sequence Analysis, DNA, Species Specificity, Wolves, canid, domestication, genome regulation, methylation, Evolutionary Biology, Biological sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/06p8k9fhTest
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7دورية أكاديمية
المؤلفون: Clark, Michelle M, Chazara, Olympe, Sobel, Eric M, Gjessing, Håkon K, Magnus, Per, Moffett, Ashley, Sinsheimer, Janet S
المصدر: Human Heredity. 81(4)
مصطلحات موضوعية: Genetics, Pediatric, Clinical Research, Perinatal Period - Conditions Originating in Perinatal Period, 2.1 Biological and endogenous factors, Aetiology, Reproductive health and childbirth, Birth Weight, Cohort Studies, Female, Fetal Development, Genome-Wide Association Study, Genotype, HLA-C Antigens, Humans, Pregnancy, Receptors, KIR, Maternal-fetal genotype interaction, KIR, HLA, Gene-gene interaction, Family-based association, Quantitative traits, Variance components, Intergenerational effects, The Norwegian Mother and Child Cohort (MoBa) Study, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/26t3q4shTest
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8دورية أكاديمية
المصدر: Annals of human genetics. 80(1)
مصطلحات موضوعية: Humans, Genetic Predisposition to Disease, Likelihood Functions, Linear Models, Pedigree, Pregnancy, Gene Frequency, Genotype, Quantitative Trait, Heritable, Polymorphism, Single Nucleotide, Models, Genetic, Computer Simulation, Female, Genome-Wide Association Study, Maternal-fetal genotype incompatibility, family-based association, gene-gene interaction, intergenerational effects, measured genotype analysis, pedigree GWAS, quantitative traits, score test, variance components, Genetics, Pediatric, Human Genome, 2.1 Biological and endogenous factors, Reproductive health and childbirth, Maternal-fetal genotype incompatibility, family-based association, gene-gene interaction, intergenerational effects, measured genotype analysis, pedigree GWAS, quantitative traits, score test, variance components, Genetics & Heredity, Clinical Sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/5hf703dkTest
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9دورية أكاديمية
المؤلفون: James, Kiely N., Clark, Michelle M., Camp, Brandon, Kint, Cyrielle, Schols, Peter, Batalov, Sergey, Briggs, Benjamin, Veeraraghavan, Narayanan, Chowdhury, Shimul, Kingsmore, Stephen F.
المساهمون: U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute
المصدر: npj Genomic Medicine ; volume 5, issue 1 ; ISSN 2056-7944
مصطلحات موضوعية: Genetics (clinical), Genetics, Molecular Biology
الإتاحة: https://doi.org/10.1038/s41525-020-00140-1Test
https://www.nature.com/articles/s41525-020-00140-1.pdfTest
https://www.nature.com/articles/s41525-020-00140-1Test -
10دورية أكاديمية
المؤلفون: Cakici, Julie A., Dimmock, David P., Caylor, Sara A., Gaughran, Mary, Clarke, Christina, Triplett, Cynthia, Clark, Michelle M., Kingsmore, Stephen F., Bloss, Cinnamon S.
المساهمون: National Institutes of Health
المصدر: The American Journal of Human Genetics ; volume 107, issue 5, page 953-962 ; ISSN 0002-9297
مصطلحات موضوعية: Genetics (clinical), Genetics
الإتاحة: https://doi.org/10.1016/j.ajhg.2020.10.004Test
https://api.elsevier.com/content/article/PII:S0002929720303621?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0002929720303621?httpAccept=text/plainTest