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- [1] Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations[J]. NATURE GENETICS, 2011, 43 (06) : 585 - U125O'Roak, Brian J.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA论文数: 引用数: h-index:机构:Lee, Choli论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USAVives, Laura论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USASchwartz, Jerrod J.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USAGirirajan, Santhosh论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USAKarakoc, Emre论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USAMacKenzie, Alexandra P.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USANg, Sarah B.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USABaker, Carl论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USARieder, Mark J.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USANickerson, Deborah A.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA论文数: 引用数: h-index:机构:Fisher, Simon E.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England Max Planck Inst Psycholinguist, Language & Genet Dept, Nijmegen, Netherlands Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USAShendure, Jay论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USAEichler, Evan E.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA Howard Hughes Med Inst, Washington, DC USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA
- [2] Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations[J]. Nature Genetics, 2011, 43 : 585 - 589Brian J O'Roak论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesPelagia Deriziotis论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesCholi Lee论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesLaura Vives论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesJerrod J Schwartz论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesSanthosh Girirajan论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesEmre Karakoc论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesAlexandra P MacKenzie论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesSarah B Ng论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesCarl Baker论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesMark J Rieder论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesDeborah A Nickerson论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesRaphael Bernier论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesSimon E Fisher论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesJay Shendure论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome SciencesEvan E Eichler论文数: 0 引用数: 0 h-index: 0机构: University of Washington School of Medicine,Department of Genome Sciences
- [3] WHOLE GENOME SEQUENCING TO IDENTIFY DE NOVO MUTATIONS IN BIPOLAR DISORDER[J]. EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2017, 27 : S384 - S384Goes, Fernando论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Baltimore, MD 21218 USA Johns Hopkins Univ, Baltimore, MD 21218 USAPirooznia, Mehdi论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Baltimore, MD 21218 USA Johns Hopkins Univ, Baltimore, MD 21218 USATehan, Martin论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Baltimore, MD 21218 USA Johns Hopkins Univ, Baltimore, MD 21218 USAWolyniec, Paula论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Baltimore, MD 21218 USA Johns Hopkins Univ, Baltimore, MD 21218 USAMcGrath, John论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Baltimore, MD 21218 USA Johns Hopkins Univ, Baltimore, MD 21218 USANested, Gerald论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Baltimore, MD 21218 USA Johns Hopkins Univ, Baltimore, MD 21218 USAApulver, Ann论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Baltimore, MD 21218 USA Johns Hopkins Univ, Baltimore, MD 21218 USA
- [4] Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations[J]. Molecular Psychiatry, 2016, 21 : 885 - 893M Kataoka论文数: 0 引用数: 0 h-index: 0机构: Laboratory for Molecular Dynamics of Mental Disorders,Department of Child NeuropsychiatryN Matoba论文数: 0 引用数: 0 h-index: 0机构: Laboratory for Molecular Dynamics of Mental Disorders,Department of Child NeuropsychiatryT Sawada论文数: 0 引用数: 0 h-index: 0机构: Laboratory for Molecular Dynamics of Mental Disorders,Department of Child NeuropsychiatryA-A Kazuno论文数: 0 引用数: 0 h-index: 0机构: Laboratory for Molecular Dynamics of Mental Disorders,Department of Child NeuropsychiatryM Ishiwata论文数: 0 引用数: 0 h-index: 0机构: Laboratory for Molecular Dynamics of Mental Disorders,Department of Child NeuropsychiatryK Fujii论文数: 0 引用数: 0 h-index: 0机构: Laboratory for Molecular Dynamics of Mental Disorders,Department of Child NeuropsychiatryK Matsuo论文数: 0 引用数: 0 h-index: 0机构: Laboratory for Molecular Dynamics of Mental Disorders,Department of Child NeuropsychiatryA Takata论文数: 0 引用数: 0 h-index: 0机构: Laboratory for Molecular Dynamics of Mental Disorders,Department of Child NeuropsychiatryT Kato论文数: 0 引用数: 0 h-index: 0机构: Laboratory for Molecular Dynamics of Mental Disorders,Department of Child Neuropsychiatry
- [5] Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations[J]. MOLECULAR PSYCHIATRY, 2016, 21 (07) : 885 - 893Kataoka, M.论文数: 0 引用数: 0 h-index: 0机构: RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, Japan Univ Tokyo, Grad Sch Med, Dept Child Neuropsychiat, Tokyo, Japan RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, JapanMatoba, N.论文数: 0 引用数: 0 h-index: 0机构: RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, Japan Univ Tokyo, Grad Sch Frontier Sci, Dept Computat Biol & Med Sci, Chiba, Japan RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, JapanSawada, T.论文数: 0 引用数: 0 h-index: 0机构: RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, Japan RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, JapanKazuno, A-A论文数: 0 引用数: 0 h-index: 0机构: RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, Japan RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, JapanIshiwata, M.论文数: 0 引用数: 0 h-index: 0机构: RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, Japan RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, JapanFujii, K.论文数: 0 引用数: 0 h-index: 0机构: RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, Japan Dokkyo Med Univ, Sch Med, Dept Psychiat, Mibu, Tochigi, Japan RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, JapanMatsuo, K.论文数: 0 引用数: 0 h-index: 0机构: Yamaguchi Univ, Dept Neurosci, Grad Sch Med, Div Neuropsychiat, Yamaguchi, Japan RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, JapanTakata, A.论文数: 0 引用数: 0 h-index: 0机构: RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, Japan RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, JapanKato, T.论文数: 0 引用数: 0 h-index: 0机构: RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, Japan RIKEN Brain Sci Inst, Lab Mol Dynam Mental Disorders, 2-1 Hirosawa Wako, Saitama 3510198, Japan
- [6] Erratum: Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations[J]. Nature Genetics, 2012, 44 : 471 - 471Brian J O'Roak论文数: 0 引用数: 0 h-index: 0Pelagia Deriziotis论文数: 0 引用数: 0 h-index: 0Choli Lee论文数: 0 引用数: 0 h-index: 0Laura Vives论文数: 0 引用数: 0 h-index: 0Jerrod J Schwartz论文数: 0 引用数: 0 h-index: 0Santhosh Girirajan论文数: 0 引用数: 0 h-index: 0Emre Karakoc论文数: 0 引用数: 0 h-index: 0Alexandra P MacKenzie论文数: 0 引用数: 0 h-index: 0Sarah B Ng论文数: 0 引用数: 0 h-index: 0Carl Baker论文数: 0 引用数: 0 h-index: 0Mark J Rieder论文数: 0 引用数: 0 h-index: 0Deborah A Nickerson论文数: 0 引用数: 0 h-index: 0Raphael Bernier论文数: 0 引用数: 0 h-index: 0Simon E Fisher论文数: 0 引用数: 0 h-index: 0Jay Shendure论文数: 0 引用数: 0 h-index: 0Evan E Eichler论文数: 0 引用数: 0 h-index: 0
- [7] Search for de novo mutations in bipolar disorder[J]. BIPOLAR DISORDERS, 2019, 21 : 40 - 40Nishioka, M.论文数: 0 引用数: 0 h-index: 0机构: RIKEN Ctr Brain Sci, Lab Mol Dynam Mental Disorders, Saitama, Japan RIKEN Ctr Brain Sci, Lab Mol Dynam Mental Disorders, Saitama, Japan
- [8] Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia[J]. JOURNAL OF MEDICAL GENETICS, 2014, 51 (03) : 197 - 202Yu, Lan论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USABennett, James T.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Div Med Genet, Dept Pediat, Seattle, WA 98115 USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAWynn, Julia论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USACarvill, Gemma L.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Div Med Genet, Dept Pediat, Seattle, WA 98115 USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USACheung, Yee Him论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAShen, Yufeng论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Dept Biomed Informat, New York, NY 10032 USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAMychaliska, George B.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan Hlth Syst, Dept Surg, Ann Arbor, MI USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAAzarow, Kenneth S.论文数: 0 引用数: 0 h-index: 0机构: Univ Nebraska, Coll Med, Dept Surg, Omaha, NE 68198 USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USACrombleholme, Timothy M.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Colorado, Div Pediat Gen Thorac & Fetal Surg, Colorado Fetal Care Ctr, Aurora, CO USA Univ Colorado, Sch Med, Aurora, CO USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAChung, Dai H.论文数: 0 引用数: 0 h-index: 0机构: Vanderbilt Univ, Med Ctr, Dept Pediat Surg, Nashville, TN USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAPotoka, Douglas论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Sch Med, Dept Pediat Surg, Pittsburgh, PA USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAWarner, Brad W.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Dept Pediat Surg, St Louis, MO USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USABucher, Brian论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Dept Pediat Surg, St Louis, MO USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USALim, Foong-Yen论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Div Pediat Gen Thorac & Fetal Surg, Ctr Mol Fetal Therapy, Cincinnati, OH 45229 USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAPietsch, John论文数: 0 引用数: 0 h-index: 0机构: Vanderbilt Univ, Med Ctr, Dept Pediat Surg, Nashville, TN USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAStolar, Charles论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Div Pediat Surg, Dept Surg, New York, NY 10032 USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAAspelund, Gudrun论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Div Pediat Surg, Dept Surg, New York, NY 10032 USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAArkovitz, Marc S.论文数: 0 引用数: 0 h-index: 0机构: Tel Hashomer Med Ctr, Div Pediat Surg, Tel Hashomer, Israel Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAMefford, Heather论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Div Med Genet, Dept Pediat, Seattle, WA 98115 USA Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USAChung, Wendy K.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USA Columbia Univ, Med Ctr, Div Mol Genet, Dept Pediat, New York, NY 10032 USA
- [9] LACK OF A UNIFYING DIAGNOSIS: WHOLE EXOME SEQUENCING IDENTIFIES 2 DE NOVO MUTATIONS IN A PATIENT WITH A COMPLEX PHENOTYPE[J]. JOURNAL OF INVESTIGATIVE MEDICINE, 2017, 65 (01) : 242 - 242Martin, M. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Davis, Sacramento, CA USA Univ Calif Davis, Sacramento, CA USA
- [10] Exome sequencing to identify de novo mutations in sporadic ALS trios[J]. NATURE NEUROSCIENCE, 2013, 16 (07) : 851 - U98Chesi, Alessandra论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAStaahl, Brett T.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Howard Hughes Med Inst, Sch Med, Stanford, CA 94305 USA Stanford Univ, Dept Dev Biol, Sch Med, Stanford, CA 94305 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAJovicic, Ana论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USACouthouis, Julien论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAFasolino, Maria论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Neurosci Grad Grp, Perelman Sch Med, Philadelphia, PA 19104 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USARaphael, Alya R.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAYamazaki, Tomohiro论文数: 0 引用数: 0 h-index: 0机构: Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAElias, Laura论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Howard Hughes Med Inst, Sch Med, Stanford, CA 94305 USA Stanford Univ, Dept Dev Biol, Sch Med, Stanford, CA 94305 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA论文数: 引用数: h-index:机构:Kelly, Crystal论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Neurol, Atlanta, GA 30322 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAWilliams, Kelly L.论文数: 0 引用数: 0 h-index: 0机构: Australian & New Zealand Army Corps Res Inst, Northcott Neurosci Lab, Sydney, NSW, Australia Univ Sydney, Sydney Med Sch, Sydney, NSW 2006, Australia Macquarie Univ, Australian Sch Adv Med, Sydney, NSW 2109, Australia Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAFifita, Jennifer A.论文数: 0 引用数: 0 h-index: 0机构: Australian & New Zealand Army Corps Res Inst, Northcott Neurosci Lab, Sydney, NSW, Australia Macquarie Univ, Australian Sch Adv Med, Sydney, NSW 2109, Australia Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAMaragakis, Nicholas J.论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USANicholson, Garth A.论文数: 0 引用数: 0 h-index: 0机构: Australian & New Zealand Army Corps Res Inst, Northcott Neurosci Lab, Sydney, NSW, Australia Univ Sydney, Sydney Med Sch, Sydney, NSW 2006, Australia Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAKing, Oliver D.论文数: 0 引用数: 0 h-index: 0机构: Univ Massachusetts, Sch Med, Dept Cell & Dev Biol, Worcester, MA USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAReed, Robin论文数: 0 引用数: 0 h-index: 0机构: Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USACrabtree, Gerald R.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Howard Hughes Med Inst, Sch Med, Stanford, CA 94305 USA Stanford Univ, Dept Dev Biol, Sch Med, Stanford, CA 94305 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USABlair, Ian P.论文数: 0 引用数: 0 h-index: 0机构: Australian & New Zealand Army Corps Res Inst, Northcott Neurosci Lab, Sydney, NSW, Australia Univ Sydney, Sydney Med Sch, Sydney, NSW 2006, Australia Macquarie Univ, Australian Sch Adv Med, Sydney, NSW 2109, Australia Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAGlass, Jonathan D.论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Neurol, Atlanta, GA 30322 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USAGitler, Aaron D.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA