-
1دورية أكاديمية
المؤلفون: Tychele N. Turner
المصدر: BMC Bioinformatics, Vol 24, Iss 1, Pp 1-6 (2023)
مصطلحات موضوعية: De novo variants, De novo variation, Genomics, Genetics, Computer applications to medicine. Medical informatics, R858-859.7, Biology (General), QH301-705.5
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1471-2105
-
2دورية أكاديمية
المؤلفون: Naeimeh Tayebi, Brian Leon‐Ricardo, Kevin McCall, Elvisa Mehinovic, Kristin Engelstad, Vincent Huynh, Tychele N. Turner, Judy Weisenberg, Liu L. Thio, Paul Hruz, Robin S. B. Williams, Darryl C. De Vivo, Vincent Petit, Gabe Haller, Christina A. Gurnett
المصدر: Annals of Clinical and Translational Neurology, Vol 10, Iss 5, Pp 787-801 (2023)
مصطلحات موضوعية: Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2328-9503
-
3دورية أكاديمية
المؤلفون: Natasha Marrus, Tychele N. Turner, Elizabeth Forsen, Drew Bolster, Alison Marvin, Andrew Whitehouse, Laura Klinger, Christina A. Gurnett, J. N. Constantino
المصدر: Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-13 (2021)
مصطلحات موضوعية: Personalized medicine, Genetic counseling, Family studies, Reproductive health planning, Early detection, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
-
4دورية أكاديمية
المؤلفون: Kesavan Meganathan, Ramachandran Prakasam, Dustin Baldridge, Paul Gontarz, Bo Zhang, Fumihiko Urano, Azad Bonni, Susan E. Maloney, Tychele N. Turner, James E. Huettner, John N. Constantino, Kristen L. Kroll
المصدر: BMC Biology, Vol 19, Iss 1, Pp 1-26 (2021)
مصطلحات موضوعية: Induced pluripotent stem cells, Cortical neurons, Psychiatric disease, Neurodevelopmental disorders, Copy number variants, Chromosome 15q13.3 duplication, Biology (General), QH301-705.5
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1741-7007
-
5دورية أكاديمية
المؤلفون: Evin M. Padhi, Tristan J. Hayeck, Zhang Cheng, Sumantra Chatterjee, Brandon J. Mannion, Marta Byrska-Bishop, Marjolaine Willems, Lucile Pinson, Sylvia Redon, Caroline Benech, Kevin Uguen, Séverine Audebert-Bellanger, Cédric Le Marechal, Claude Férec, Stephanie Efthymiou, Fatima Rahman, Shazia Maqbool, Reza Maroofian, Henry Houlden, Rajeeva Musunuri, Giuseppe Narzisi, Avinash Abhyankar, Riana D. Hunter, Jennifer Akiyama, Lauren E. Fries, Jeffrey K. Ng, Elvisa Mehinovic, Nick Stong, Andrew S. Allen, Diane E. Dickel, Raphael A. Bernier, David U. Gorkin, Len A. Pennacchio, Michael C. Zody, Tychele N. Turner
المصدر: Human Genomics, Vol 15, Iss 1, Pp 1-15 (2021)
مصطلحات موضوعية: Autism, Neurodevelopmental disorder, Enhancer, Gene regulatory network, EBF3, hs737, Medicine, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1479-7364
-
6دورية أكاديمية
المؤلفون: Ashley N. Hall, Tychele N. Turner, Christine Queitsch
المصدر: Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2045-2322
-
7دورية أكاديمية
المؤلفون: Eleanor I. Sams, Jeffrey K. Ng, Victoria Tate, Ying-Chen Claire Hou, Yang Cao, Lucinda Antonacci-Fulton, Khadija Belhassan, Julie Neidich, Robi D. Mitra, F. Sessions Cole, Patricia Dickson, Jeffrey Milbrandt, Tychele N. Turner
المصدر: HGG Advances, Vol 3, Iss 1, Pp 100081- (2022)
مصطلحات موضوعية: syndrome, 9p, CNV, deletion, duplication, developmental, Genetics, QH426-470
وصف الملف: electronic resource
-
8دورية أكاديمية
المصدر: Genome Medicine, Vol 9, Iss 1, Pp 1-16 (2017)
مصطلحات موضوعية: Autism spectrum disorder, De novo mutations, Developmental disorders, Epilepsy, Intellectual disability, Neurodevelopmental disorders, Medicine, Genetics, QH426-470
وصف الملف: electronic resource
-
9دورية أكاديمية
المؤلفون: Rachel K. Earl, Tychele N. Turner, Heather C. Mefford, Caitlin M. Hudac, Jennifer Gerdts, Evan E. Eichler, Raphael A. Bernier
المصدر: Molecular Autism, Vol 8, Iss 1, Pp 1-15 (2017)
مصطلحات موضوعية: Autism, DYRK1A, Genetic syndrome, Genetically defined subtype, Disruptive mutation, Clinical phenotype, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
-
10