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- [31] Loss of the Intellectual Disability and Autism Gene Cc2d1a and Its Homolog Cc2d1b Differentially Affect Spatial Memory, Anxiety, and HyperactivityFRONTIERS IN GENETICS, 2018, 9Zamarbide, Marta论文数: 0 引用数: 0 h-index: 0机构: George Washington Univ, Sch Med & Hlth Sci, GW Inst Neurosci, Dept Pharmacol & Physiol, Washington, DC 20052 USA George Washington Univ, Sch Med & Hlth Sci, GW Inst Neurosci, Dept Pharmacol & Physiol, Washington, DC 20052 USAOaks, Adam W.论文数: 0 引用数: 0 h-index: 0机构: George Washington Univ, Sch Med & Hlth Sci, GW Inst Neurosci, Dept Pharmacol & Physiol, Washington, DC 20052 USA George Washington Univ, Sch Med & Hlth Sci, GW Inst Neurosci, Dept Pharmacol & Physiol, Washington, DC 20052 USAPond, Heather L.论文数: 0 引用数: 0 h-index: 0机构: George Washington Univ, Sch Med & Hlth Sci, GW Inst Neurosci, Dept Pharmacol & Physiol, Washington, DC 20052 USA George Washington Univ, Sch Med & Hlth Sci, GW Inst Neurosci, Dept Pharmacol & Physiol, Washington, DC 20052 USAAdelman, Julia S.论文数: 0 引用数: 0 h-index: 0机构: George Washington Univ, Sch Med & Hlth Sci, GW Inst Neurosci, Dept Pharmacol & Physiol, Washington, DC 20052 USA George Washington Univ, Sch Med & Hlth Sci, GW Inst Neurosci, Dept Pharmacol & Physiol, Washington, DC 20052 USAManzini, M. Chiara论文数: 0 引用数: 0 h-index: 0机构: George Washington Univ, Sch Med & Hlth Sci, GW Inst Neurosci, Dept Pharmacol & Physiol, Washington, DC 20052 USA George Washington Univ, Autism & Neurodev Disorders Inst, Washington, DC 20052 USA George Washington Univ, Sch Med & Hlth Sci, GW Inst Neurosci, Dept Pharmacol & Physiol, Washington, DC 20052 USA
- [32] Identification of CC2D1A homozygous mutation as a cause of Joubert Syndrome with obsessive compulsive disorderFEBS OPEN BIO, 2018, 8 : 291 - 292Ergoren, M. C.论文数: 0 引用数: 0 h-index: 0机构: Near East Univ, Fac Med, Dept Med Biol, Nicosia, Cyprus Near East Univ, Expt Hlth Res Ctr Hlth Sci, Nicosia, Cyprus Near East Univ, Fac Med, Dept Med Biol, Nicosia, CyprusEngindereli, Y.论文数: 0 引用数: 0 h-index: 0机构: Near East Univ, Dept Child & Adolescent Psychiat, Fac Med, Nicosia, Cyprus Near East Univ, Fac Med, Dept Med Biol, Nicosia, CyprusCulhaoglu, B. Kaymakamzade论文数: 0 引用数: 0 h-index: 0机构: Near East Univ, Dept Neurol, Fac Med, Nicosia, Cyprus Near East Univ, Fac Med, Dept Med Biol, Nicosia, Cyprus
- [33] The Mammalian Orthologs of Drosophila Lgd, CC2D1A and CC2D1B, Function in the Endocytic Pathway, but Their Individual Loss of Function Does Not Affect Notch SignallingPLOS GENETICS, 2015, 11 (12):Drusenheimer, Nadja论文数: 0 引用数: 0 h-index: 0机构: Univ Dusseldorf, Inst Genet, Dusseldorf, Germany Univ Dusseldorf, Inst Genet, Dusseldorf, GermanyMigdal, Bernhard论文数: 0 引用数: 0 h-index: 0机构: Univ Dusseldorf, Inst Genet, Dusseldorf, Germany Univ Dusseldorf, Inst Genet, Dusseldorf, GermanyJaeckel, Sandra论文数: 0 引用数: 0 h-index: 0机构: German Ctr Neurodegenerat Dis DZNE, Tubingen, Germany Univ Dusseldorf, Inst Genet, Dusseldorf, Germany论文数: 引用数: h-index:机构:Scheider, Kristina论文数: 0 引用数: 0 h-index: 0机构: Univ Dusseldorf, Inst Genet, Dusseldorf, Germany Univ Dusseldorf, Inst Genet, Dusseldorf, GermanySchulz, Katharina论文数: 0 引用数: 0 h-index: 0机构: Univ Dusseldorf, Inst Genet, Dusseldorf, Germany Univ Dusseldorf, Inst Genet, Dusseldorf, GermanyGroeper, Jieny论文数: 0 引用数: 0 h-index: 0机构: Univ Dusseldorf, Inst Genet, Dusseldorf, Germany Univ Dusseldorf, Inst Genet, Dusseldorf, GermanyKoehrer, Karl论文数: 0 引用数: 0 h-index: 0机构: Univ Dusseldorf, Biol & Med Res Ctr BMFZ, Genom & Transcript Lab GTL, Dusseldorf, Germany Univ Dusseldorf, Inst Genet, Dusseldorf, GermanyKlein, Thomas论文数: 0 引用数: 0 h-index: 0机构: Univ Dusseldorf, Inst Genet, Dusseldorf, Germany Univ Dusseldorf, Inst Genet, Dusseldorf, Germany
- [34] Oxytocin treatment rescues irritability-like behavior in Cc2d1a conditional knockout miceNEUROPSYCHOPHARMACOLOGY, 2024, 49 (11) : 1792 - 1802Cheng, Kuan-Hsiang论文数: 0 引用数: 0 h-index: 0机构: Natl Cheng Kung Univ, Inst Basic Med Sci, Coll Med, Tainan, Taiwan Natl Cheng Kung Univ, Inst Basic Med Sci, Coll Med, Tainan, TaiwanHung, Yu-Chieh论文数: 0 引用数: 0 h-index: 0机构: Natl Cheng Kung Univ, Inst Basic Med Sci, Coll Med, Tainan, Taiwan Natl Cheng Kung Univ, Inst Basic Med Sci, Coll Med, Tainan, TaiwanLing, Pin论文数: 0 引用数: 0 h-index: 0机构: Natl Cheng Kung Univ, Inst Basic Med Sci, Coll Med, Tainan, Taiwan Natl Cheng Kung Univ, Coll Med, Dept Microbiol & Immunol, Tainan, Taiwan Natl Cheng Kung Univ, Inst Basic Med Sci, Coll Med, Tainan, Taiwan论文数: 引用数: h-index:机构:
- [35] Novel alterations of CC2D1A as a candidate gene in a Turkish sample of patients with autism spectrum disorderINTERNATIONAL JOURNAL OF NEUROSCIENCE, 2022, 132 (11) : 1072 - 1079论文数: 引用数: h-index:机构:Onal, Muge Gulcihan论文数: 0 引用数: 0 h-index: 0机构: Erciyes Univ, Genome & Stem Cell Ctr GENKOK, Kayseri, Turkey Erciyes Univ, Halil Bayraktar Vocat Sch Hlth Coll, Kayseri, Turkey Erciyes Univ, Dept Med Biol, Med Fac, TR-38039 Kayseri, Turkey论文数: 引用数: h-index:机构:Nalbantoglu, Ufuk论文数: 0 引用数: 0 h-index: 0机构: Erciyes Univ, Genome & Stem Cell Ctr GENKOK, Kayseri, Turkey Erciyes Univ, Dept Comp Engn, Fac Engn, Kayseri, Turkey Erciyes Univ, Dept Med Biol, Med Fac, TR-38039 Kayseri, TurkeyOzkul, Yusuf论文数: 0 引用数: 0 h-index: 0机构: Erciyes Univ, Genome & Stem Cell Ctr GENKOK, Kayseri, Turkey Erciyes Univ, Dept Med Genet, Med Fac, Kayseri, Turkey Erciyes Univ, Dept Med Biol, Med Fac, TR-38039 Kayseri, TurkeyCanatan, Halit论文数: 0 引用数: 0 h-index: 0机构: Erciyes Univ, Dept Med Biol, Med Fac, TR-38039 Kayseri, Turkey Erciyes Univ, Dept Med Biol, Med Fac, TR-38039 Kayseri, TurkeyOztop, Didem Behice论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Dept Child Psychiat, Fac Med, Ankara, Turkey Erciyes Univ, Dept Med Biol, Med Fac, TR-38039 Kayseri, Turkey
- [36] A nonsense CC2D1A variant is associated with congenital anomalies, motor delay, hypotonia, and slight deformitiesHELIYON, 2024, 10 (06)Yi, Sheng论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Clin Res Ctr Pediat Dis, Guangxi Key Lab Reprod Hlth & Birth Defects Preven, Guangxi Key Lab Precis Med Genet Dis,Guangxi Key L, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R ChinaTang, Xianglian论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Clin Res Ctr Pediat Dis, Guangxi Key Lab Reprod Hlth & Birth Defects Preven, Guangxi Key Lab Precis Med Genet Dis,Guangxi Key L, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R ChinaZhang, Qiang论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Clin Res Ctr Pediat Dis, Guangxi Key Lab Reprod Hlth & Birth Defects Preven, Guangxi Key Lab Precis Med Genet Dis,Guangxi Key L, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R ChinaLiang, Yu论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Dept Pathol, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R ChinaHuang, Jing论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Dept Obstet, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R ChinaZhang, Shujie论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Clin Res Ctr Pediat Dis, Guangxi Key Lab Reprod Hlth & Birth Defects Preven, Guangxi Key Lab Precis Med Genet Dis,Guangxi Key L, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R ChinaHuang, Limei论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Clin Res Ctr Pediat Dis, Guangxi Key Lab Reprod Hlth & Birth Defects Preven, Guangxi Key Lab Precis Med Genet Dis,Guangxi Key L, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R ChinaYi, Shang论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Clin Res Ctr Pediat Dis, Guangxi Key Lab Reprod Hlth & Birth Defects Preven, Guangxi Key Lab Precis Med Genet Dis,Guangxi Key L, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R ChinaHuang, Minpan论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Clin Res Ctr Pediat Dis, Guangxi Key Lab Reprod Hlth & Birth Defects Preven, Guangxi Key Lab Precis Med Genet Dis,Guangxi Key L, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R ChinaQin, Zailong论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Clin Res Ctr Pediat Dis, Guangxi Key Lab Reprod Hlth & Birth Defects Preven, Guangxi Key Lab Precis Med Genet Dis,Guangxi Key L, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Lab Genet & Metab, Nanning 530003, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R ChinaLuo, Jingsi论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Clin Res Ctr Pediat Dis, Guangxi Key Lab Reprod Hlth & Birth Defects Preven, Guangxi Key Lab Precis Med Genet Dis,Guangxi Key L, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Lab Genet & Metab, Nanning 530003, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonomo, Guangxi Birth Defects Res & Prevent Inst, Genet & Metab Cent Lab, Nanning, Peoples R China
- [37] Conditional Deletion of CC2D1A Reduces Hippocampal Synaptic Plasticity and Impairs Cognitive Function through Rac1 HyperactivationJOURNAL OF NEUROSCIENCE, 2019, 39 (25): : 4959 - 4975Yang, Cheng-Yi论文数: 0 引用数: 0 h-index: 0机构: Natl Cheng Kung Univ, Coll Med, Inst Basic Med Sci, Tainan 70101, Taiwan Natl Cheng Kung Univ, Coll Med, Inst Basic Med Sci, Tainan 70101, TaiwanYu, Ting-Hsuan论文数: 0 引用数: 0 h-index: 0机构: Natl Cheng Kung Univ, Coll Med, Inst Basic Med Sci, Tainan 70101, Taiwan Natl Cheng Kung Univ, Coll Med, Inst Basic Med Sci, Tainan 70101, TaiwanWen, Wan-Ling论文数: 0 引用数: 0 h-index: 0机构: Natl Cheng Kung Univ, Coll Med, Dept Pharmacol, Tainan 70101, Taiwan Natl Cheng Kung Univ, Coll Med, Inst Basic Med Sci, Tainan 70101, TaiwanLing, Pin论文数: 0 引用数: 0 h-index: 0机构: Natl Cheng Kung Univ, Coll Med, Dept Microbiol & Immunol, Tainan 70101, Taiwan Natl Cheng Kung Univ, Coll Med, Inst Basic Med Sci, Tainan 70101, Taiwan论文数: 引用数: h-index:机构:
- [38] CC2D1A Regulates Human Intellectual and Social Function as well as NF-κB Signaling HomeostasisCELL REPORTS, 2014, 8 (03): : 647 - 655Manzini, M. Chiara论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Howard Hughes Med Inst, Chevy Chase, MD 20815 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USAXiong, Lan论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal, Montreal Mental Hlth Univ Inst, Res Ctr, Dept Psychiat, Montreal, PQ H1N 3V2, Canada Univ Montreal Hosp, Res Ctr, Montreal, PQ H2L 2W5, Canada Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USAShaheen, Ranad论文数: 0 引用数: 0 h-index: 0机构: King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USATambunan, Dimira E.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Howard Hughes Med Inst, Chevy Chase, MD 20815 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USADi Costanzo, Stefania论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Howard Hughes Med Inst, Chevy Chase, MD 20815 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USAMitisalis, Vanessa论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Howard Hughes Med Inst, Chevy Chase, MD 20815 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USATischfield, David J.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Howard Hughes Med Inst, Chevy Chase, MD 20815 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USACinquino, Antonella论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Howard Hughes Med Inst, Chevy Chase, MD 20815 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USAGhaziuddin, Mohammed论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan Hlth Syst, Dept Child & Adolescent Psychiat, Ann Arbor, MI 48109 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USAChristian, Mehtab论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal Hosp, Res Ctr, Montreal, PQ H2L 2W5, Canada Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USAJiang, Qin论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal, Montreal Mental Hlth Univ Inst, Res Ctr, Dept Psychiat, Montreal, PQ H1N 3V2, Canada Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USALaurent, Sandra论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal Hosp, Res Ctr, Montreal, PQ H2L 2W5, Canada Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USANanjiani, Zohair A.论文数: 0 引用数: 0 h-index: 0机构: Univ Karachi, Ma Ayesha Mem Ctr, Karachi 75350, Pakistan Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USARasheed, Saima论文数: 0 引用数: 0 h-index: 0机构: Autism Inst, Karachi 74000, Pakistan Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USAHill, R. Sean论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Howard Hughes Med Inst, Chevy Chase, MD 20815 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USALizarraga, Sofia B.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Howard Hughes Med Inst, Chevy Chase, MD 20815 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USAGleason, Danielle论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Howard Hughes Med Inst, Chevy Chase, MD 20815 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USASabbagh, Diya论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Howard Hughes Med Inst, Chevy Chase, MD 20815 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USASalih, Mustafa A.论文数: 0 引用数: 0 h-index: 0机构: King Saud Univ, Coll Med, Dept Pediat, Div Pediat Neurol, Riyadh 11461, Saudi Arabia Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USAAlkuraya, Fowzan S.论文数: 0 引用数: 0 h-index: 0机构: King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USAWalsh, Christopher A.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Howard Hughes Med Inst, Chevy Chase, MD 20815 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA
- [39] A novel framework for functional annotation of variants of uncertain significance in ID/ASD risk gene CC2D1AHUMAN MOLECULAR GENETICS, 2024, 33 (14) : 1229 - 1240Bhattacharya, Aniket论文数: 0 引用数: 0 h-index: 0机构: Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, 89 French St, New Brunswick, NJ 08901 USA Rutgers Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, 89 French St, New Brunswick, NJ 08901 USA Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, 89 French St, New Brunswick, NJ 08901 USAParlanti, Paola论文数: 0 引用数: 0 h-index: 0机构: Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, 89 French St, New Brunswick, NJ 08901 USA Rutgers Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, 89 French St, New Brunswick, NJ 08901 USA Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, 89 French St, New Brunswick, NJ 08901 USACavallo, Luca论文数: 0 引用数: 0 h-index: 0机构: Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, 89 French St, New Brunswick, NJ 08901 USA Rutgers Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, 89 French St, New Brunswick, NJ 08901 USA Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, 89 French St, New Brunswick, NJ 08901 USAFarrow, Edward论文数: 0 引用数: 0 h-index: 0机构: George Washington Univ, Dept Pharmacol & Physiol, Sch Med & Hlth Sci, 2121 1St NW, Washington, DC 20052 USA Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, 89 French St, New Brunswick, NJ 08901 USASpivey, Tyler论文数: 0 引用数: 0 h-index: 0机构: George Washington Univ, Dept Pharmacol & Physiol, Sch Med & Hlth Sci, 2121 1St NW, Washington, DC 20052 USA Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, 89 French St, New Brunswick, NJ 08901 USA论文数: 引用数: h-index:机构:Mari, Francesca论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, Viale Bracci 2, I-53100 Siena, Italy Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, 89 French St, New Brunswick, NJ 08901 USAManzini, M. Chiara论文数: 0 引用数: 0 h-index: 0机构: Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, 89 French St, New Brunswick, NJ 08901 USA Rutgers Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, 89 French St, New Brunswick, NJ 08901 USA Child Hlth Inst New Jersey, 89 French St Room 3274, New Brunswick, NJ 08901 USA Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, 89 French St, New Brunswick, NJ 08901 USA
- [40] Regulation of CHMP4/ESCRT-III Function in Human Immunodeficiency Virus Type 1 Budding by CC2D1AJOURNAL OF VIROLOGY, 2012, 86 (07) : 3746 - 3756Usami, Yoshiko论文数: 0 引用数: 0 h-index: 0机构: Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01655 USA Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01655 USAPopov, Sergei论文数: 0 引用数: 0 h-index: 0机构: Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01655 USA Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01655 USAWeiss, Eric R.论文数: 0 引用数: 0 h-index: 0机构: Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01655 USA Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01655 USAVriesema-Magnuson, Christie论文数: 0 引用数: 0 h-index: 0机构: Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01655 USA Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01655 USACalistri, Arianna论文数: 0 引用数: 0 h-index: 0机构: Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01655 USAGoettlinger, Heinrich G.论文数: 0 引用数: 0 h-index: 0机构: Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01655 USA Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01655 USA