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AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

IF1.5
论文数28
被引数
期刊论文 28
发表时间
A Global Prospective Harmonization Framework for Suicidality, Anhedonia, and Obsessive-Compulsive Symptoms in Psychiatric Genetic Studies: A Cross-Continental Study Within the Ancestral Population Network全球展望下的协调框架:用于精神遗传学研究中自杀倾向、快感缺乏和强迫症状的跨大陆祖先人群网络研究
delete2026-09-01
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deleteDiaz-Zuluaga, Ana M.; Anderberg, Jacey L.; Ramirez-Diaz, Ana M.; Marques, Andrea Horvath; Rast, Catherine E.; Bustamante, Daniel; Jonker, Deborah; Valencia-Echeverry, Johanna; Kyebuzibwa, Joseph; Munoz, Josselyn S.; van der Walt, Kristien; Ramirez, Mauricio Castano; Wootton, Olivia; Frederick, Renee M.; Stroud, Rocky E.; Gur, Ruben; Rhee, Sang Jin; Jha, Shaili C.; Gichuru, Stella; Service, Susan; Reus, Victor I.; Dickens, Akena; Lopez-Jaramillo, Carlos; Bearden, Carrie E.; Stein, Dan J.; Susser, Ezra S.; Crowley, James J.; Flint, Jonathan; Kendler, Kenneth S.; Atwoli, Lukoye; Pato, Michele T.; Freimer, Nelson B.; Ophoff, Roel A.; Ahn, Yong Min; Olde Loohuis, Loes; Storch, Eric A.; Gelaye, Bizu
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Genome-Wide Association Study of Symptom Change Following Cognitive Behavioral Therapy for Common Mental Disorders认知行为疗法对常见精神障碍症状变化的基因组关联研究
delete2026-03-01
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PREAI
deleteBackman, Julia; Kravchenko, Olly; Halvorsen, Matthew; de Schipper, Elles; Ivanova, Ekaterina; Kaldo, Viktor; Isacsson, Nils Hentati; Eide, Thorstein Olsen; Hoffler, Kira D.; Mattheisen, Manuel; Hansen, Bjarne; Kvale, Gerd; Hagen, Kristen; Haavik, Jan; Mataix-cols, David; Crowley, James J.; Wallert, John; Ruck, Christian
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Longitudinal Behavior Phenotype Hallmarks in RNU4-2 Syndrome: Implications for Clinical ManagementRNU4-2综合征中的纵向行为表型特征:对临床管理的启示
delete2026-02-01
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deleteAjmone, Paola Francesca; Rigamonti, Claudia; Brasca, Francesca; Milani, Donatella; Ortigosa, Chiara Ranci; Iascone, Maria; Goisis, Lucrezia; Torella, Annalaura; Costantino, Maria Antonella
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Novel Variants Identified in Families With SNX27-Related Neurodevelopmental Disorder, Aiding in Characterizing Its Genotypic and Phenotypic Spectrum在SNX27相关神经发育障碍家族中鉴定出的新型变异,有助于表征其基因型和表型谱
delete2026-01-01
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PREAI
deleteShan, Tayyaba; Hussain, Abrar; Acharya, Anushree; Hussain, Mulazim; Li, Yumei; Hussain, Hafiz Muhammad Jafar; Afshan, Kiran; Leal, Suzanne M.; Chen, Rui; Mir, Asif; Schrauwen, Isabelle; Firasat, Sabika
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Black EquaLity in OCD NeuroGenomics (BELONG): Study Protocol强迫症神经基因组学中的黑人平等(BELONG):研究方案
delete2026-01-01
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PREAI
deleteWilliams, Iasha J.; Marquez, Dalia Y.; Lopez-lengowski, Kara E.; Bommiasamy, Malini; Onyeka, Ogechi (cynthia); Underwood, Slayton J.; Avery, Juliana E.; Gluckman, Jacob; Pichardo, Thariana; Chandler, Rhea; Brown, Yulu; Mangen, Katie; Choplin, Emma Grace; Richardson, Sonyia C.; Buxbaum, Joseph D.; Storch, Eric A.; Crowley, James J.; Hankerson, Sidney H.; Grice, Dorothy E.
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