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- [1] Inflammatory Proteomic Analysis of 22q11.2 Deletion SyndromeJournal of Clinical Immunology, 2024, 44Valentina Frusone论文数: 0 引用数: 0 h-index: 0机构: Drexel University,Division of Allergy Immunology, ARC 1216Kelly Maurer论文数: 0 引用数: 0 h-index: 0机构: Drexel University,Division of Allergy Immunology, ARC 1216Beverly S. Emanuel论文数: 0 引用数: 0 h-index: 0机构: Drexel University,Division of Allergy Immunology, ARC 1216Donna McDonald-McGinn论文数: 0 引用数: 0 h-index: 0机构: Drexel University,Division of Allergy Immunology, ARC 1216Kathleen E. Sullivan论文数: 0 引用数: 0 h-index: 0机构: Drexel University,Division of Allergy Immunology, ARC 1216
- [2] 22q11.2 deletion syndromeNATURE REVIEWS DISEASE PRIMERS, 2015, 1McDonald-McGinn, Donna M.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USA Univ Penn, Clin Genet Ctr, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA 19104 USA Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USASullivan, Kathleen E.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA 19104 USA Univ Penn, Div Allergy & Immunol, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USAMarino, Bruno论文数: 0 引用数: 0 h-index: 0机构: Univ Roma La Sapienza, Dept Pediat, Rome, Italy Lorillard Spencer Cenci Fdn, Rome, Italy Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USAPhilip, Nicole论文数: 0 引用数: 0 h-index: 0机构: Assistance Publ Hop Marseille, Dept Med Genet, Marseille, France Aix Marseille Univ, INSERM, GMGF UMR S 910, Marseille, France Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USASwillen, Ann论文数: 0 引用数: 0 h-index: 0机构: Univ Leuven, Fac Rehabil Sci, Leuven, Belgium Univ Hosp Gasthuisberg, Ctr Human Genet, Leuven, Belgium Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USAVorstman, Jacob A. S.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Brain Ctr Rudolf Magnus, Dept Psychiat, Utrecht, Netherlands Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USAZackai, Elaine H.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USA Univ Penn, Clin Genet Ctr, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA 19104 USA Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USAEmanuel, Beverly S.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA 19104 USA Univ Penn, Div Human Genet, 22q & You Ctr, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USAVermeesch, Joris R.论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USAMorrow, Bernice E.论文数: 0 引用数: 0 h-index: 0机构: Albert Einstein Coll Med, Dept Genet, New York, NY USA Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USAScambler, Peter J.论文数: 0 引用数: 0 h-index: 0机构: UCL, Dev Biol Birth Defects Sect, Inst Child Hlth, London, England Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USABassett, Anne S.论文数: 0 引用数: 0 h-index: 0机构: Univ Toronto, Dalglish Family Hearts & Minds Clin Delet Syndrom, Toronto Gen Hosp, Univ Hlth Network, Toronto, ON, Canada Univ Toronto, Clin Genet Res Program, Ctr Addict & Mental Hlth, Toronto, ON, Canada Univ Penn, Div Human Genet, 22q & You Ctr, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USA
- [4] 22q11.2 deletion syndromeNature Reviews Disease Primers, 1Donna M. McDonald-McGinn论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of PennsylvaniaKathleen E. Sullivan论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of PennsylvaniaBruno Marino论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of PennsylvaniaNicole Philip论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of PennsylvaniaAnn Swillen论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of PennsylvaniaJacob A. S. Vorstman论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of PennsylvaniaElaine H. Zackai论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of PennsylvaniaBeverly S. Emanuel论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of PennsylvaniaJoris R. Vermeesch论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of PennsylvaniaBernice E. Morrow论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of PennsylvaniaPeter J. Scambler论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of PennsylvaniaAnne S. Bassett论文数: 0 引用数: 0 h-index: 0机构: 22q and You Center,Division of Human Genetics, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of Pennsylvania
- [5] Genetic analysis of the 22q11.2 deletion syndromePEDIATRIC RESEARCH, 2000, 47 (04) : 238A - 238ABaldini, A论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USAVitelli, F论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USASu, DR论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USAWang, Y论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USALindsay, EA论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Houston, TX 77030 USA Baylor Coll Med, Houston, TX 77030 USA
- [6] 22q11.2 deletion syndrome and schizophreniaACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2020, 52 (11) : 1181 - 1190Qin, Xianzheng论文数: 0 引用数: 0 h-index: 0机构: Nanchang Univ, Gueen Mary Sch, Nanchang 330031, Jiangxi, Peoples R China Nanchang Univ, Gueen Mary Sch, Nanchang 330031, Jiangxi, Peoples R ChinaChen, Jiang论文数: 0 引用数: 0 h-index: 0机构: Nanchang Univ, Inst Life Sci, Lab Synapt Dev & Plast, Nanchang 330031, Jiangxi, Peoples R China Nanchang Univ, Gueen Mary Sch, Nanchang 330031, Jiangxi, Peoples R ChinaZhou, Tian论文数: 0 引用数: 0 h-index: 0机构: Nanchang Univ, Sch Basic Med Sci, Nanchang 330031, Jiangxi, Peoples R China Nanchang Univ, Gueen Mary Sch, Nanchang 330031, Jiangxi, Peoples R China
- [7] Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion SyndromeGENES, 2022, 13 (11)Heung, Tracy论文数: 0 引用数: 0 h-index: 0机构: Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, Canada Univ Hlth Network, Dalglish Family 22q Clin, Toronto, ON M5G 2C4, Canada Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, CanadaConroy, Brigid论文数: 0 引用数: 0 h-index: 0机构: Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, Canada Univ Toronto, Fac Med, Undergrad Med Educ, Toronto, ON M5S 1A4, Canada Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, CanadaMalecki, Sarah论文数: 0 引用数: 0 h-index: 0机构: Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, Canada Univ Toronto, Dept Med, Toronto, ON M5S 1A4, Canada Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, CanadaHa, Joanne论文数: 0 引用数: 0 h-index: 0机构: Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, Canada Univ Hlth Network, Dalglish Family 22q Clin, Toronto, ON M5G 2C4, Canada Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, CanadaBoot, Erik论文数: 0 引用数: 0 h-index: 0机构: Univ Hlth Network, Dalglish Family 22q Clin, Toronto, ON M5G 2C4, Canada S Heeren Loo, Advisium, NL-3818 LA Amersfoort, Netherlands Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, CanadaCorral, Maria论文数: 0 引用数: 0 h-index: 0机构: Univ Hlth Network, Dalglish Family 22q Clin, Toronto, ON M5G 2C4, Canada Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, CanadaBassett, Anne S.论文数: 0 引用数: 0 h-index: 0机构: Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, Canada Univ Hlth Network, Dalglish Family 22q Clin, Toronto, ON M5G 2C4, Canada Univ Toronto, Dept Psychiat, Toronto, ON M5S 1A4, Canada Toronto Gen Hosp Res Inst, Toronto, ON M5G 2C4, Canada Campbell Family Mental Hlth Res Inst, Toronto, ON M5G 2C1, Canada Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON M5S 2S1, Canada
- [8] Camptodactyly and the 22q11.2 deletion syndromeAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (02) : 515 - 518Couser, Natario L.论文数: 0 引用数: 0 h-index: 0机构: Univ North Carolina Chapel Hill, Dept Pediat, Div Genet & Metab, Sch Med, Chapel Hill, NC USA Univ North Carolina Chapel Hill, Dept Ophthalmol, Chapel Hill, NC USA Univ North Carolina Chapel Hill, Dept Pediat, Div Genet & Metab, Sch Med, Chapel Hill, NC USAPande, Chetna K.论文数: 0 引用数: 0 h-index: 0机构: Texas Tech Hlth Sci Ctr, Paul L Foster Sch Med, El Paso, TX USA Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA Univ North Carolina Chapel Hill, Dept Pediat, Div Genet & Metab, Sch Med, Chapel Hill, NC USAWalsh, Jonathan M.论文数: 0 引用数: 0 h-index: 0机构: Univ North Carolina Chapel Hill, Dept Otolaryngol Head & Neck Surg, Chapel Hill, NC USA Johns Hopkins Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Baltimore, MD 21205 USA Univ North Carolina Chapel Hill, Dept Pediat, Div Genet & Metab, Sch Med, Chapel Hill, NC USATepperberg, James论文数: 0 引用数: 0 h-index: 0机构: LabCorp, Res Triangle Pk, NC USA Univ North Carolina Chapel Hill, Dept Pediat, Div Genet & Metab, Sch Med, Chapel Hill, NC USAAylsworth, Arthur S.论文数: 0 引用数: 0 h-index: 0机构: Univ North Carolina Chapel Hill, Dept Pediat, Div Genet & Metab, Sch Med, Chapel Hill, NC USA Univ North Carolina Chapel Hill, Dept Genet, Chapel Hill, NC USA Univ North Carolina Chapel Hill, Dept Pediat, Div Genet & Metab, Sch Med, Chapel Hill, NC USA
- [9] 22Q11.2 DELETION SYNDROME IS ASSOCIATED WITH AN INFLAMMATORY PLASMA SIGNATURENEUROPSYCHOPHARMACOLOGY, 2024, 49 : 403 - 403Michalski, Christina论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USAIslam, Mojahidul论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USAParker, David论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USAImes, Sidney论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USARuban, Gabrielle论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USACuthbert, Bruce论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USAHenshey, Brett论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USALee, Grace论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USAMassa, Nicholas论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USAOusley, Opal论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USAWalker, Elaine论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USAGoldsmith, David论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USAPearce, Bradley论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USACubells, Joseph论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USADuncan, Erica论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USASharma, Ashish论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USAWen, Zhexing论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA USA Emory Univ, Sch Med, Atlanta, GA USA
- [10] Schizophrenia and 22q11.2 deletion syndromeCurrent Psychiatry Reports, 2008, 10 (2) : 148 - 157Bassett A.S.论文数: 0 引用数: 0 h-index: 0机构: Centre for Addiction and Mental Health, Toronto, ON M6J 1H4 Centre for Addiction and Mental Health, Toronto, ON M6J 1H4Chow E.W.C.论文数: 0 引用数: 0 h-index: 0机构: Centre for Addiction and Mental Health, Toronto, ON M6J 1H4 Centre for Addiction and Mental Health, Toronto, ON M6J 1H4