المؤلفون: Drury, Vanessa, Drake, Sam, Sun, Nawei, Alkhairo, Hasan, Arbelaez, Juan, Duhn, Clif, Bal, Vanessa, Langley, Kate, Martin, Joanna, Hoekstra, Pieter, Dietrich, Andrea, Xing, Jinchuan, Heiman, Gary, Tischfield, Jay, Fernandez, Thomas, Owen, Michael, ODonovan, Michael, Thapar, Anita, State, Matthew, Wang, Sheng, Willsey, Arthur, Wang, Belinda

المصدر: Nature Communications. 14(1)

مصطلحات موضوعية: Humans, Male, Female, Attention Deficit Disorder with Hyperactivity, Tourette Syndrome, Autistic Disorder, Autism Spectrum Disorder, Neurodevelopmental Disorders

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/4nh8c7mh
https://escholarship.org/content/qt4nh8c7mh/qt4nh8c7mh.pdf

المؤلفون: Young, David M, Duhn, Clif, Gilson, Michael, Nojima, Mai, Yuruk, Deniz, Kumar, Aparna, Yu, Weimiao, Sanders, Stephan J

المصدر: Current Protocols in Neuroscience. 94(1)

مصطلحات موضوعية: Information and Computing Sciences, Applied Computing, Biomedical Imaging, Neurosciences, Bioengineering, Networking and Information Technology R&D (NITRD), Mental Health, Animals, Atlases as Topic, Brain, Humans, Image Processing, Computer-Assisted, Imaging, Three-Dimensional, Software, 3D atlas, graphical interface, image processing, microscopy images, tissue clearing

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/4cz0k1dt

المؤلفون: An, Joon-Yong, Lin, Kevin, Zhu, Lingxue, Werling, Donna M, Dong, Shan, Brand, Harrison, Wang, Harold Z, Zhao, Xuefang, Schwartz, Grace B, Collins, Ryan L, Currall, Benjamin B, Dastmalchi, Claudia, Dea, Jeanselle, Duhn, Clif, Gilson, Michael C, Klei, Lambertus, Liang, Lindsay, Markenscoff-Papadimitriou, Eirene, Pochareddy, Sirisha, Ahituv, Nadav, Buxbaum, Joseph D, Coon, Hilary, Daly, Mark J, Kim, Young Shin, Marth, Gabor T, Neale, Benjamin M, Quinlan, Aaron R, Rubenstein, John L, Sestan, Nenad, State, Matthew W, Willsey, A Jeremy, Talkowski, Michael E, Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J

المصدر: Science. 362(6420)

مصطلحات موضوعية: Human Genome, Genetics, Biotechnology, Intellectual and Developmental Disabilities (IDD), Mental Health, Brain Disorders, Autism, Pediatric, 2.1 Biological and endogenous factors, Aetiology, Mental health, Autism Spectrum Disorder, Binding Sites, Conserved Sequence, DNA Mutational Analysis, Genetic Loci, Genetic Variation, Humans, Mutation, Pedigree, Promoter Regions, Genetic, Risk, Transcription Factors, General Science & Technology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3476g3p5

المؤلفون: Wang, Sheng, Mandell, Jeffrey D, Kumar, Yogesh, Sun, Nawei, Morris, Montana T, Arbelaez, Juan, Nasello, Cara, Dong, Shan, Duhn, Clif, Zhao, Xin, Yang, Zhiyu, Padmanabhuni, Shanmukha S, Yu, Dongmei, King, Robert A, Dietrich, Andrea, Khalifa, Najah, Dahl, Niklas, Huang, Alden Y, Neale, Benjamin M, Coppola, Giovanni, Mathews, Carol A, Scharf, Jeremiah M, Tourette International Collaborative Genetics Study (TIC Genetics), Tourette Syndrome Genetics Southern and Eastern Europe Initiative (TSGENESEE), Tourette Association of America International Consortium for Genetics (TAAICG), Fernandez, Thomas V, Buxbaum, Joseph D, De Rubeis, Silvia, Grice, Dorothy E, Xing, Jinchuan, Heiman, Gary A, Tischfield, Jay A, Paschou, Peristera, Willsey, A Jeremy, State, Matthew W

المصدر: Cell reports. 24(13)

مصطلحات موضوعية: Tourette International Collaborative Genetics Study, Tourette Syndrome Genetics Southern and Eastern Europe Initiative, Tourette Association of America International Consortium for Genetics, Humans, Tourette Syndrome, Cadherins, Receptors, Cell Surface, Pedigree, Cell Polarity, Adult, Child, Female, Male, DNA Copy Number Variations, TIC Genetics, Tourette disorder, cell polarity, copy number variants, de novo variants, gene discovery, microarray genotyping, multiplex, simplex, whole exome sequencing, Clinical Research, Pediatric, Biotechnology, Genetics, Brain Disorders, Human Genome, Intellectual and Developmental Disabilities (IDD), Neurodegenerative, 2.1 Biological and endogenous factors, Aetiology, Biochemistry and Cell Biology, Medical Physiology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/31c79634

المؤلفون: Werling, Donna M, Brand, Harrison, An, Joon-Yong, Stone, Matthew R, Zhu, Lingxue, Glessner, Joseph T, Collins, Ryan L, Dong, Shan, Layer, Ryan M, Markenscoff-Papadimitriou, Eirene, Farrell, Andrew, Schwartz, Grace B, Wang, Harold Z, Currall, Benjamin B, Zhao, Xuefang, Dea, Jeanselle, Duhn, Clif, Erdman, Carolyn A, Gilson, Michael C, Yadav, Rachita, Handsaker, Robert E, Kashin, Seva, Klei, Lambertus, Mandell, Jeffrey D, Nowakowski, Tomasz J, Liu, Yuwen, Pochareddy, Sirisha, Smith, Louw, Walker, Michael F, Waterman, Matthew J, He, Xin, Kriegstein, Arnold R, Rubenstein, John L, Sestan, Nenad, McCarroll, Steven A, Neale, Benjamin M, Coon, Hilary, Willsey, A Jeremy, Buxbaum, Joseph D, Daly, Mark J, State, Matthew W, Quinlan, Aaron R, Marth, Gabor T, Roeder, Kathryn, Devlin, Bernie, Talkowski, Michael E, Sanders, Stephan J

المصدر: Nature Genetics. 50(5)

مصطلحات موضوعية: Biological Sciences, Genetics, Human Genome, Biotechnology, Brain Disorders, Intellectual and Developmental Disabilities (IDD), Mental Health, Autism, 2.1 Biological and endogenous factors, Autism Spectrum Disorder, Female, Genetic Predisposition to Disease, Genome, Genome-Wide Association Study, Humans, INDEL Mutation, Male, Polymorphism, Single Nucleotide, Protein Isoforms, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/29v6r8tv
https://escholarship.org/content/qt29v6r8tv/qt29v6r8tv.pdf

المؤلفون: Wang, Sheng, Wang, Belinda, Drury, Vanessa, Drake, Sam, Sun, Nawei, Alkhairo, Hasan, Arbelaez, Juan, Duhn, Clif, Bromberg, Yana, Brown, Lawrence W., Cao, Xiaolong, Cheon, Keun-Ah, Cheong, Kyungun, Choi, Hannyung, Coffey, Barbara J., Deng, Li, Fremer, Carolin, Garcia-Delgar, Blanca, Gilbert, Donald L., Glover, Danea, Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heyman, Isobel, Hong, Hyun Ju, Huyser, Chaim, Kim, Heejoo, Kim, Young Key, Kim, Eunjoo, Kim, Young-Shin, King, Robert A., Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Lee, Junghan, Leventhal, Bennett L., Madruga-Garrido, Marcos, Mingbunjerdsuk, Dararat, Mir, Pablo, Morer, Astrid, Murphy, Tara L., Müller-Vahl, Kirsten, Münchau, Alexander, Nasello, Cara, Oh, Dong Hun, Plessen, Kerstin J., Roessner, Veit, Shin, Eun-Young, Song, Dong-Ho, Song, Jungeun, Thackray, Joshua K., Visscher, Frank, Zinner, Samuel H., Bal, Vanessa H., Langley, Kate, Martin, Joanna, Hoekstra, Pieter J., Dietrich, Andrea, Xing, Jinchuan, Heiman, Gary A., Tischfield, Jay A., Fernandez, Thomas V., Owen, Michael J., O’Donovan, Michael C., Thapar, Anita, State, Matthew W., Willsey, A. Jeremy

المصدر: Wang , S , Wang , B , Drury , V , Drake , S , Sun , N , Alkhairo , H , Arbelaez , J , Duhn , C , Bromberg , Y , Brown , L W , Cao , X , Cheon , K-A , Cheong , K , Choi , H , Coffey , B J , Deng , L , Fremer , C , Garcia-Delgar , B , Gilbert , D L , Glover , D , Grice , D E , Hagstrøm , J , Hedderly , T , Heyman , I ....

الاتاحة: https://research.vumc.nl/en/publications/8865cb1b-bc85-4b85-95ee-a13a1116b107
https://doi.org/10.1038/s41467-023-43776-0
http://www.scopus.com/inward/record.url?scp=85178887598&partnerID=8YFLogxK

المؤلفون: National Institute of Mental Health (US), Tourette Association of America, Human Genetics Institute of New Jersey, Tourette Syndrome Association of New Jersey, Wang, Sheng, Wang, Belinda, Drury, Vanessa, Drake, Sam, Sun, Nawei, Alkhairo, Hasan, Arbelaez, Juan, Duhn, Clif, Tourette International Collaborative Genetics (TIC Genetics), Madruga, Marcos, Mir, Pablo, Bal, Vanessa H., Langley, Kate, Martin, Joanna, Hoekstra, Pieter J., Dietrich, Andrea, Xing, Jinchuan, Heiman, Gary A., Tischfield, Jay A., Fernández, Thomas V., Owen, Michael J., O’Donovan, Michael C., Thapar, Anita, State, Matthew W., Willsey, A. Jeremy

مصطلحات الفهرس: Autism spectrum disorders, Neurodevelopmental disorders, artículo

URL: http://hdl.handle.net/10261/352762
https://doi.org/10.1038/s41467-023-43776-0
Publisher's version
Summary data, including Chr X variant calls and phenotype information, is de-identified and included in the Bitbucket repository located at (https://shengw@bitbucket.org/willseylab/chrx_analysis.git). Data from SSC and SPARK data accessible upon application and approval through Simons Foundation for Autism Research Initiative SFARIbase (https://base.sfari.org). Researchers must submit a project with an IRB approval or exemption notice. TS data are accessible through four sources, including Tourette International Collaborative Genetics (TIC Genetics) Study (https://tic-genetics.org/, dbGaP: https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001423); Tourette Association of America International Consortium for Genetics (https://tourette.org/), BioProject: PRJNA384389; Tourette Syndrome Genetics Southern and Eastern Europe Initiative (http://tsgenesee.mbg.duth.gr/index.html); Upsala Tourette Cohort (see https://pubmed.ncbi.nlm.nih.gov/30257206/). Newly generated TS data are deposited in the existing TIC Genetics Study dbGaP study. Researchers must get approved by the relevant Data Access Committee(s) (DAC(s)) upon providing a written Research Use Statement following dbGaP instruction. EE data are accessible by submitting an application to the Steering Committee for the Epi4K Consortium (https://www.epi4k.org/collab/). Variants for the DD project are available at https://github.com/hilarymartin/DDD_chrX.git. Variants for 1000 Genomes Project samples are publicly available at http://ftp.1000genomes.ebi.ac.uk/vol1/ftp/. ADHD data are deposited into BioProject: PRJNA1003909.
The underlying dataset has been published as supplementary material of the article in the publisher platform at https://doi.org/10.1038/s41467-023-43776-0
https://doi.org/10.1038/s41467-023-43776-0
Sí

المؤلفون: Werling, Donna, Werling, Donna, Brand, Harrison, An, Joon-Yong, Stone, Matthew, Zhu, Lingxue, Glessner, Joseph, Collins, Ryan, Dong, Shan, Layer, Ryan, Markenscoff-Papadimitriou, Eirene, Farrell, Andrew, Schwartz, Grace, Wang, Harold, Currall, Benjamin, Zhao, Xuefang, Dea, Jeanselle, Duhn, Clif, Erdman, Carolyn, Gilson, Michael, Yadav, Rachita, Handsaker, Robert, Kashin, Seva, Klei, Lambertus, Mandell, Jeffrey, Nowakowski, Tomasz, Liu, Yuwen, Pochareddy, Sirisha, Smith, Louw, Waterman, Matthew, He, Xin, Sestan, Nenad, McCarroll, Steven, Neale, Benjamin, Coon, Hilary, Buxbaum, Joseph, Daly, Mark, State, Matthew, Quinlan, Aaron, Marth, Gabor, Roeder, Kathryn, Devlin, Bernie, Talkowski, Michael, Kriegstein, Arnold, Rubenstein, John, Sanders, Stephan, Willsey, Arthur, Walker, Michael

المصدر: Nature Genetics; vol 50, iss 5

مصطلحات الفهرس: Autism Spectrum Disorder, Female, Genetic Predisposition to Disease, Genome, Genome-Wide Association Study, Humans, INDEL Mutation, Male, Polymorphism, Single Nucleotide, Protein Isoforms, article

URL: https://escholarship.org/uc/item/29v6r8tv
https://escholarship.org/

المؤلفون: Karlinsey, Robert L, Yi, Keewook, Duhn, Clif W

المصدر: Bioinspiration & Biomimetics ; volume 1, issue 1, page 12-19 ; ISSN 1748-3182 1748-3190

الاتاحة: http://dx.doi.org/10.1088/1748-3182/1/1/002

المؤلفون: Karlinsey, Robert L, Hara, Anderson T, Yi, Keewook, Duhn, Clif W

المصدر: Biomedical Materials ; volume 1, issue 1, page 16-23 ; ISSN 1748-6041 1748-605X

الاتاحة: http://dx.doi.org/10.1088/1748-6041/1/1/003

المؤلفون: Karlinsey, Robert L, Hara, Anderson T, Yi, Keewook, Duhn, Clif W

المصدر: Biomedical Materials (17486041); Mar2006, Vol. 1 Issue 1, p16-23, 8p

المؤلفون: Karlinsey, Robert L., Hara, Anderson T., Duhn, Clif W.

المصدر: Advances in Science and Technology; October 2006, Vol. 45 Issue: 1 p17-21, 5p

المؤلفون: Wang, Sheng, Mandell, Jeffrey D., Kumar, Yogesh, Sun, Nawei, Morris, Montana T., Arbelaez, Juan, Nasello, Cara, Dong, Shan, Duhn, Clif, Zhao, Xin, Yang, Zhiyu, Padmanabhuni, Shanmukha S., Yu, Dongmei, King, Robert A., Dietrich, Andrea, Khalifa, Najah, Dahl, Niklas, Huang, Alden Y., Neale, Benjamin M., Coppola, Giovanni, Mathews, Carol A., Scharf, Jeremiah M., Abdulkadir, Mohamed, Arbelaez, Juan, Bodmer, Benjamin, Bromberg, Yana, Brown, Lawrence W., Cheon, Keun-Ah, Coffey, Barbara J., Deng, Li, Dietrich, Andrea, Dong, Shan, Duhn, Clif, Elzerman, Lonneke, Fernandez, Thomas V., Fremer, Carolin, Garcia-Delgar, Blanca, Gilbert, Donald L., Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heiman, Gary A., Heyman, Isobel, Hoekstra, Pieter J., Hong, Hyun Ju, Huyser, Chaim, Kim, Eun-Joo, Kim, Young Key, Kim, Young-Shin, King, Robert A., Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Leventhal, Bennett L, Ludolph, Andrea G., Madruga-Garrido, Marcos, Mandell, Jeffrey D., Maras, Athanasios, Mir, Pablo, Morer, Astrid, Morris, Montana T, Müller-Vahl, Kirsten, Münchau, Alexander, Murphy, Tara L., Nasello, Cara, Plessen, Kerstin J., Poisner, Hannah, Roessner, Veit, Sanders, Stephan J., Shin, Eun-Young, Song, Dong-Ho, Song, Jungeun, State, Matthew W., Sun, Nawei, Thackray, Joshua K., Tischfield, Jay A., Tübing, Jennifer, Visscher, Frank, Wanderer, Sina, Wang, Sheng, Willsey, A Jeremy, Woods, Martin, Xing, Jinchuan, Zhang, Yeting, Zhao, Xin, Zinner, Samuel H., Androutsos, Christos, Barta, Csaba, Farkas, Luca, Fichna, Jakub, Georgitsi, Marianthi, Janik, Piotr, Karagiannidis, Iordanis, Koumoula, Anastasia, Nagy, Peter, Paschou, Peristera, Puchala, Joanna, Rizzo, Renata, Szejko, Natalia, Szymanska, Urszula, Tarnok, Zsanett, Tsironi, Vaia, Wolanczyk, Tomasz, Zekanowski, Cezary, Barr, Cathy L., Batterson, James R., Berlin, Cheston, Bruun, Ruth D., Budman, Cathy L., Cath, Danielle C., Chouinard, Sylvain, Coppola, Giovanni, Cox, Nancy J., Darrow, Sabrina, Davis, Lea K., Dion, Yves, Freimer, Nelson B., Grados, Marco A., Hirschtritt, Matthew E., Huang, Alden Y., Illmann, Cornelia, King, Robert A., Kurlan, Roger, Leckman, James F., Lyon, Gholson J., Malaty, Irene A., Mathews, Carol A., MacMahon, William M., Neale, Benjamin M., Okun, Michael S., Osiecki, Lisa, Pauls, David L., Posthuma, Danielle, Ramensky, Vasily, Robertson, Mary M., Rouleau, Guy A., Sandor, Paul, Scharf, Jeremiah M., Singer, Harvey S., Smit, Jan, Sul, Jae-Hoon, Yu, Dongmei, Fernandez, Thomas V., Buxbaum, Joseph D., De Rubeis, Silvia, Grice, Dorothy E., Xing, Jinchuan, Heiman, Gary A., Tischfield, Jay A., Paschou, Peristera, Willsey, A. Jeremy, State, Matthew W.

المصدر: Cell Reports; September 2018, Vol. 24 Issue: 13 p3441-3454.e12