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Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

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dc.contributor.authorWang, Sheng-
dc.contributor.authorWang, Belinda-
dc.contributor.authorDrury, Vanessa-
dc.contributor.authorDrake, Sam-
dc.contributor.authorSun, Nawei-
dc.contributor.authorAlkhairo, Hasan-
dc.contributor.authorArbelaez, Juan-
dc.contributor.authorDuhn, Clif-
dc.contributor.authorBromberg, Yana-
dc.contributor.authorBrown, Lawrence W.-
dc.contributor.authorCao, Xiaolong-
dc.contributor.authorCheon, Keun-Ah-
dc.contributor.authorCheong, Kyungun-
dc.contributor.authorChoi, Hannyung-
dc.contributor.authorCoffey, Barbara J.-
dc.contributor.authorDeng, Li-
dc.contributor.authorFremer, Carolin-
dc.contributor.authorGarcia-Delgar, Blanca-
dc.contributor.authorGilbert, Donald L.-
dc.contributor.authorGlover, Danea-
dc.contributor.authorGrice, Dorothy E.-
dc.contributor.authorHagstrøm, Julie-
dc.contributor.authorHedderly, Tammy-
dc.contributor.authorHeyman, Isobel-
dc.contributor.authorHong, Hyun Ju-
dc.contributor.authorHuyser, Chaim-
dc.contributor.authorKim, Heejoo-
dc.contributor.authorKim, Young Key-
dc.contributor.authorKim, Eunjoo-
dc.contributor.authorKim, Young-Shin-
dc.contributor.authorKing, Robert A.-
dc.contributor.authorKoh, Yun-Joo-
dc.contributor.authorKook, Sodahm-
dc.contributor.authorKuperman, Samuel-
dc.contributor.authorLee, Junghan-
dc.contributor.authorLeventhal, Bennett L.-
dc.contributor.authorMadruga-Garrido, Marcos-
dc.contributor.authorMingbunjerdsuk, Dararat-
dc.contributor.authorMir, Pablo-
dc.contributor.authorMorer, Astrid-
dc.contributor.authorMurphy, Tara L.-
dc.contributor.authorMüller-Vahl, Kirsten-
dc.contributor.authorMünchau, Alexander-
dc.contributor.authorNasello, Cara-
dc.contributor.authorOh, Dong Hun-
dc.contributor.authorPlessen, Kerstin J.-
dc.contributor.authorRoessner, Veit-
dc.contributor.authorShin, Eun-Young-
dc.contributor.authorSong, Dong-Ho-
dc.contributor.authorSong, Jungeun-
dc.contributor.authorThackray, Joshua K.-
dc.contributor.authorVisscher, Frank-
dc.contributor.authorZinner, Samuel H.-
dc.contributor.authorBal, Vanessa H.-
dc.contributor.authorLangley, Kate-
dc.contributor.authorMartin, Joanna-
dc.contributor.authorHoekstra, Pieter J.-
dc.contributor.authorDietrich, Andrea-
dc.contributor.authorXing, Jinchuan-
dc.contributor.authorHeiman, Gary A.-
dc.contributor.authorTischfield, Jay A.-
dc.contributor.authorFernandez, Thomas V.-
dc.contributor.authorOwen, Michael J.-
dc.contributor.authorO’Donovan, Michael C.-
dc.contributor.authorThapar, Anita-
dc.contributor.authorState, Matthew W.-
dc.contributor.authorWillsey, A. Jeremy-
dc.contributor.author김은주-
dc.date.accessioned2026-05-22T07:28:27Z-
dc.date.available2026-05-22T07:28:27Z-
dc.date.created2026-05-18-
dc.date.issued2023-12-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/212372-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherNature Pub. Group-
dc.relation.isPartOfNature Communications-
dc.relation.isPartOfNATURE COMMUNICATIONS-
dc.titleRare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD-
dc.typeArticle-
dc.contributor.googleauthorWang, Sheng-
dc.contributor.googleauthorWang, Belinda-
dc.contributor.googleauthorDrury, Vanessa-
dc.contributor.googleauthorDrake, Sam-
dc.contributor.googleauthorSun, Nawei-
dc.contributor.googleauthorAlkhairo, Hasan-
dc.contributor.googleauthorArbelaez, Juan-
dc.contributor.googleauthorDuhn, Clif-
dc.contributor.googleauthorBromberg, Yana-
dc.contributor.googleauthorBrown, Lawrence W.-
dc.contributor.googleauthorCao, Xiaolong-
dc.contributor.googleauthorCheon, Keun-Ah-
dc.contributor.googleauthorCheong, Kyungun-
dc.contributor.googleauthorChoi, Hannyung-
dc.contributor.googleauthorCoffey, Barbara J.-
dc.contributor.googleauthorDeng, Li-
dc.contributor.googleauthorFremer, Carolin-
dc.contributor.googleauthorGarcia-Delgar, Blanca-
dc.contributor.googleauthorGilbert, Donald L.-
dc.contributor.googleauthorGlover, Danea-
dc.contributor.googleauthorGrice, Dorothy E.-
dc.contributor.googleauthorHagstrøm, Julie-
dc.contributor.googleauthorHedderly, Tammy-
dc.contributor.googleauthorHeyman, Isobel-
dc.contributor.googleauthorHong, Hyun Ju-
dc.contributor.googleauthorHuyser, Chaim-
dc.contributor.googleauthorKim, Heejoo-
dc.contributor.googleauthorKim, Young Key-
dc.contributor.googleauthorKim, Eunjoo-
dc.contributor.googleauthorKim, Young-Shin-
dc.contributor.googleauthorKing, Robert A.-
dc.contributor.googleauthorKoh, Yun-Joo-
dc.contributor.googleauthorKook, Sodahm-
dc.contributor.googleauthorKuperman, Samuel-
dc.contributor.googleauthorLee, Junghan-
dc.contributor.googleauthorLeventhal, Bennett L.-
dc.contributor.googleauthorMadruga-Garrido, Marcos-
dc.contributor.googleauthorMingbunjerdsuk, Dararat-
dc.contributor.googleauthorMir, Pablo-
dc.contributor.googleauthorMorer, Astrid-
dc.contributor.googleauthorMurphy, Tara L.-
dc.contributor.googleauthorMüller-Vahl, Kirsten-
dc.contributor.googleauthorMünchau, Alexander-
dc.contributor.googleauthorNasello, Cara-
dc.contributor.googleauthorOh, Dong Hun-
dc.contributor.googleauthorPlessen, Kerstin J.-
dc.contributor.googleauthorRoessner, Veit-
dc.contributor.googleauthorShin, Eun-Young-
dc.contributor.googleauthorSong, Dong-Ho-
dc.contributor.googleauthorSong, Jungeun-
dc.contributor.googleauthorThackray, Joshua K.-
dc.contributor.googleauthorVisscher, Frank-
dc.contributor.googleauthorZinner, Samuel H.-
dc.contributor.googleauthorBal, Vanessa H.-
dc.contributor.googleauthorLangley, Kate-
dc.contributor.googleauthorMartin, Joanna-
dc.contributor.googleauthorHoekstra, Pieter J.-
dc.contributor.googleauthorDietrich, Andrea-
dc.contributor.googleauthorXing, Jinchuan-
dc.contributor.googleauthorHeiman, Gary A.-
dc.contributor.googleauthorTischfield, Jay A.-
dc.contributor.googleauthorFernandez, Thomas V.-
dc.contributor.googleauthorOwen, Michael J.-
dc.contributor.googleauthorO’Donovan, Michael C.-
dc.contributor.googleauthorThapar, Anita-
dc.contributor.googleauthorState, Matthew W.-
dc.contributor.googleauthorWillsey, A. Jeremy-
dc.identifier.doi10.1038/s41467-023-43776-0-
dc.relation.journalcodeJ02293-
dc.identifier.eissn2041-1723-
dc.identifier.pmid38057346-
dc.contributor.affiliatedAuthorCheon, Keun-Ah-
dc.contributor.affiliatedAuthorCheong, Kyungun-
dc.contributor.affiliatedAuthorChoi, Hannyung-
dc.contributor.affiliatedAuthorKim, Eunjoo-
dc.contributor.affiliatedAuthorLee, Junghan-
dc.contributor.affiliatedAuthorOh, Dong Hun-
dc.contributor.affiliatedAuthorSong, Dong-Ho-
dc.identifier.scopusid2-s2.0-85178887598-
dc.identifier.wosid001135959900006-
dc.citation.volume14-
dc.citation.number1-
dc.identifier.bibliographicCitationNature Communications, Vol.14(1), 2023-12-
dc.identifier.rimsid92898-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordPlusDE-NOVO MUTATIONS-
dc.subject.keywordPlusTRANSMISSION DISEQUILIBRIUM TEST-
dc.subject.keywordPlusDEFICIT HYPERACTIVITY DISORDER-
dc.subject.keywordPlusSPECTRUM DISORDER-
dc.subject.keywordPlusFRAGILE-X-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusPOPULATION-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCHILDREN-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.identifier.articleno8077-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Psychiatry (정신과학교실) > 1. Journal Papers

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