المؤلفون: Variants, Commission on Novel Technologies for Neurodevelopmental Copy Number, Buttermore, Elizabeth, Chamberlain, Stormy, Cody, Jannine, Costain, Gregory, Dang, Louis, DeWoody, Andrew, DeWoody, Yssa, Dies, Kira, Eichler, Evan, Girirajan, Santhosh, Gramm, Marie, Halladay, Alycia, Lal, Dennis, Lalli, Matthew, Levy, Tess, Logsdon, Glennis, Lowenstein, Daniel, Mefford, Heather, Mulle, Jennifer, Muotri, Alysson, Murphy, Melissa, Palma, Eduardo Perez, Pinter, Stefan, Pollak, Rebecca, Purcell, Ryan, Samaco, Rodney, Shah, Bina, Singh, Karun, So, Joyce, Sundberg, Maria, Veeraragavan, Surabi, Vogel-Farley, Vanessa, Wynshaw-Boris, Anthony

المصدر: American Journal of Human Genetics. 109(8)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Human Genome, Intellectual and Developmental Disabilities (IDD), Neurosciences, Brain Disorders, DNA Copy Number Variations, Genome, Humans, Neurodevelopmental Disorders, Patient Advocacy, Phenotype, Commission on Novel Technologies for Neurodevelopmental Copy Number Variants, CNVs, biobank, community engagement, copy-number variants, genomic disorders, iPSCs, inclusion, infrastructure, long-read sequencing, neurodevelopment, neurological, patient centered, patient led, structural variants, systematic phenotyping, team science, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3tc3h13fTest

المؤلفون: Sen, Kuntal, Ananth, Amitha, Gottlieb-Smith, Rachel, Calalme, Daniel, Strelzik, Jeffrey, Baranano, Kristin, Emrick, Lisa, Ziobro, Julie, Habela, Christa, Ream, Margie, Mithal, Divakar, Gropman, Andrea, Dang, Louis

المصدر: Genetics in Medicine Open ; volume 2, page 101466 ; ISSN 2949-7744

الإتاحة: https://doi.org/10.1016/j.gimo.2024.101466Test
https://api.elsevier.com/content/article/PII:S2949774424006125?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S2949774424006125?httpAccept=text/plainTest

المؤلفون: Dang, Louis T.

المصدر: Epilepsy Currents ; volume 23, issue 2, page 130-132 ; ISSN 1535-7597 1535-7511

مصطلحات موضوعية: Neurology (clinical)

الإتاحة: https://doi.org/10.1177/15357597221149265Test

المؤلفون: Gottlieb-Smith, Rachel, Sen, Kuntal, Dang, Louis T., Strelzik, Jeffrey A.

المصدر: Pediatric Neurology ; volume 152, page 62 ; ISSN 0887-8994

مصطلحات موضوعية: Neurology (clinical), Developmental Neuroscience, Neurology, Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1016/j.pediatrneurol.2023.12.017Test
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المؤلفون: Xin, Ziyin, Cai, Yujun, Dang, Louis T., Burke, Hannah M. S., Revote, Jerico, Charitakis, Natalie, Bienroth, Denis, Nim, Hieu T., Li, Yuan-Fang, Ramialison, Mirana

المساهمون: Australian Research Council, National Health and Medical Research Council

المصدر: BMC Bioinformatics ; volume 23, issue 1 ; ISSN 1471-2105

مصطلحات موضوعية: Applied Mathematics, Computer Science Applications, Molecular Biology, Biochemistry, Structural Biology

الإتاحة: https://doi.org/10.1186/s12859-022-04594-1Test

المؤلفون: Dang, Louis

المساهمون: National Institutes of Health

المصدر: Epilepsy Currents ; volume 22, issue 4, page 255-257 ; ISSN 1535-7597 1535-7511

مصطلحات موضوعية: Neurology (clinical)

الإتاحة: https://doi.org/10.1177/15357597221101278Test

المؤلفون: Dang, Louis T.

المصدر: Epilepsy Currents ; volume 22, issue 5, page 315-317 ; ISSN 1535-7597 1535-7511

مصطلحات موضوعية: Neurology (clinical)

الإتاحة: https://doi.org/10.1177/15357597221113704Test

المؤلفون: Buttermore, Elizabeth, Chamberlain, Stormy, Cody, Jannine, Costain, Gregory, Dang, Louis, DeWoody, Andrew, DeWoody, Yssa, Dies, Kira, Eichler, Evan, Girirajan, Santhosh, Gramm, Marie, Halladay, Alycia, Lal, Dennis, Lalli, Matthew, Levy, Tess, Logsdon, Glennis, Lowenstein, Daniel, Mefford, Heather, Mulle, Jennifer, Muotri, Alysson, Murphy, Melissa, Perez Palma, Eduardo, Pinter, Stefan, Pollak, Rebecca, Purcell, Ryan, Samaco, Rodney, Shah, Bina, Singh, Karun, So, Joyce, Sundberg, Maria, Veeraragavan, Surabi, Vogel-Farley, Vanessa, Wynshaw-Boris, Anthony

المصدر: The American Journal of Human Genetics ; volume 109, issue 8, page 1353-1365 ; ISSN 0002-9297

الإتاحة: https://doi.org/10.1016/j.ajhg.2022.07.003Test
https://api.elsevier.com/content/article/PII:S000292972200307X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S000292972200307X?httpAccept=text/plainTest

المؤلفون: Sloan-Heggen, Christina, Pritchard, Amanda Barone, Barks, John, Dang, Louis, Desch, Karl, Quasney, Michael, Russell, Mark, Innis, Jeffrey

المصدر: Genetics in Medicine ; volume 24, issue 3, page S158 ; ISSN 1098-3600

مصطلحات موضوعية: Genetics (clinical)

الإتاحة: https://doi.org/10.1016/j.gim.2022.01.284Test
https://api.elsevier.com/content/article/PII:S109836002200301X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S109836002200301X?httpAccept=text/plainTest

المؤلفون: Gupta, Gita, O’ Brien, Louise, Dang, Louis, Shellhaas, Renée

المصدر: Sleep ; volume 44, issue Supplement_2, page A278-A278 ; ISSN 0161-8105 1550-9109

مصطلحات موضوعية: Physiology (medical), Neurology (clinical)

الإتاحة: https://doi.org/10.1093/sleep/zsab072.711Test
http://academic.oup.com/sleep/article-pdf/44/Supplement_2/A278/37657963/zsab072.711.pdfTest