共 50 条
- [1] Heterozygous HMGB1 loss-of-function variants are associated with developmental delay and microcephalyCLINICAL GENETICS, 2021, 100 (04) : 386 - 395Uguen, Kevin论文数: 0 引用数: 0 h-index: 0机构: CHRU Brest, Serv Genet Med, Brest, France Univ Brest, INSERM, EFS, Brest, France CHRU Brest, Serv Genet Med, Brest, FranceKrysiak, Kilannin论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA CHRU Brest, Serv Genet Med, Brest, FranceAudebert-Bellanger, Severine论文数: 0 引用数: 0 h-index: 0机构: CHRU Brest, Serv Genet Med, Brest, France CHRU Brest, Serv Genet Med, Brest, FranceRedon, Sylvia论文数: 0 引用数: 0 h-index: 0机构: CHRU Brest, Serv Genet Med, Brest, France Univ Brest, INSERM, EFS, Brest, France CHRU Brest, Serv Genet Med, Brest, FranceBenech, Caroline论文数: 0 引用数: 0 h-index: 0机构: Univ Brest, INSERM, EFS, Brest, France CHRU Brest, Serv Genet Med, Brest, FranceViora-Dupont, Eleonore论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants, FHU TRANSLAD, Ctr Reference Anomalies Dev & Syndromes Malformat, Dijon, France CHRU Brest, Serv Genet Med, Brest, FranceTran Mau-Them, Frederic论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Pole Biol, Unite Fonct Innovat Diagnost Genom Malad Rares 62, Dijon, France Univ Bourgogne, INSERM, UMR1231, GAD,FHU TRANSLAD, Dijon, France CHRU Brest, Serv Genet Med, Brest, FranceRondeau, Sophie论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, AP HP, Federat Genet Med, Paris, France CHRU Brest, Serv Genet Med, Brest, FranceElsharkawi, Ibrahim论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA CHRU Brest, Serv Genet Med, Brest, FranceGranadillo, Jorge L.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA CHRU Brest, Serv Genet Med, Brest, France论文数: 引用数: h-index:机构:Soares, Celia Azevedo论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Porto, Ctr Genet Med Jacinto Magalhaes, Serv Genet Med, Porto, Portugal Univ Porto, Inst Ciencias Biomed Abel Salazar, Unit Multidisciplinary Res Biomed, Porto, Portugal CHRU Brest, Serv Genet Med, Brest, FranceTkachenko, Nataliya论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Porto, Ctr Genet Med Jacinto Magalhaes, Serv Genet Med, Porto, Portugal CHRU Brest, Serv Genet Med, Brest, FranceM. Amudhavalli, Shivarajan论文数: 0 引用数: 0 h-index: 0机构: Childrens Mercy Hosp, Dept Clin Genet, Kansas City, MO 64108 USA CHRU Brest, Serv Genet Med, Brest, FranceEngleman, Kendra论文数: 0 引用数: 0 h-index: 0机构: Childrens Mercy Hosp, Dept Clin Genet, Kansas City, MO 64108 USA CHRU Brest, Serv Genet Med, Brest, France论文数: 引用数: h-index:机构:Deleuze, Jean-Francois论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Saclay, CEA, Ctr Natl Rech Genom Humaine, Evry, France CHRU Brest, Serv Genet Med, Brest, FranceBezieau, Stephane论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, 9 Quai Moncousu, F-44093 Nantes, France Univ Nantes, CNRS, INSERM, Nantes, France CHRU Brest, Serv Genet Med, Brest, FranceOdent, Sylvie论文数: 0 引用数: 0 h-index: 0机构: CHU Rennes, Ctr Labellise Anomalies Dev CLAD Ouest, Ctr Reference Anomalies Dev, Serv Genet Clin,Ctr Reference Deficiences Intelle, F-35203 Rennes, France Univ Rennes, Inst Genet & Dev Rennes, UMR 6290, Rennes, France CHRU Brest, Serv Genet Med, Brest, FranceToutain, Annick论文数: 0 引用数: 0 h-index: 0机构: Univ Tours, CHU Tours, Serv Genet, Tours, France CHRU Brest, Serv Genet Med, Brest, FranceBonneau, Dominique论文数: 0 引用数: 0 h-index: 0机构: CHU Angers, CNRS, UMR 6015, Dept Biochim & Genet Mitochondrial & Cardiovasc P, Angers, France CHRU Brest, Serv Genet Med, Brest, France论文数: 引用数: h-index:机构:Faivre, Laurence论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants, FHU TRANSLAD, Ctr Reference Anomalies Dev & Syndromes Malformat, Dijon, France Univ Bourgogne, INSERM, UMR1231, GAD,FHU TRANSLAD, Dijon, France CHRU Brest, Serv Genet Med, Brest, FranceRio, Marlene论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, AP HP, Federat Genet Med, Paris, France CHRU Brest, Serv Genet Med, Brest, FranceLe Marechal, Cedric论文数: 0 引用数: 0 h-index: 0机构: CHRU Brest, Serv Genet Med, Brest, France Univ Brest, INSERM, EFS, Brest, France CHRU Brest, Serv Genet Med, Brest, FranceFerec, Claude论文数: 0 引用数: 0 h-index: 0机构: CHRU Brest, Serv Genet Med, Brest, France Univ Brest, INSERM, EFS, Brest, France CHRU Brest, Serv Genet Med, Brest, FranceRepnikova, Elena论文数: 0 引用数: 0 h-index: 0机构: Univ Missouri, Childrens Mercy Hosp, Med Sch, Dept Pathol, Kansas City, MO 65211 USA CHRU Brest, Serv Genet Med, Brest, FranceCao, Yang论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA CHRU Brest, Serv Genet Med, Brest, France
- [2] Two new cases with HMGB1 loss-of-function variantsEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 184 - 184Rio, Marlene论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, France Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, FranceCourtin, Thomas论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, France Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, FranceRondeau, Sophie论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, France Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, FranceLesieursebellin, Marion论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, France Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, FranceAttie-Bitach, Tania论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, France Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, FranceCormier-Daire, Valerie论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, France Univ Paris Cite, Necker Hosp, APHP Ctr, Genom Med Rare Disorders, Paris, France
- [3] Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephalyHUMAN GENETICS, 2024, 143 (03) : 455 - 469Herbst, Charlotte论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, Germany Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyBothe, Viktoria论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, Germany Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyWegler, Meret论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, Germany Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyAxer-Schaefer, Susanne论文数: 0 引用数: 0 h-index: 0机构: Bielefeld Univ, Krankenhaus Mara Bethel Epilepsy Ctr, Dept Epileptol, Med Sch OWL, Campus Bethel, Bielefeld, Germany Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyAudebert-Bellanger, Severine论文数: 0 引用数: 0 h-index: 0机构: Dept Genet, CHU Brest, F-29000 Brest, France Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyGecz, Jozef论文数: 0 引用数: 0 h-index: 0机构: Univ Adelaide, Robinson Res Inst, Adelaide, SA, Australia Univ Adelaide, Robinson Res Inst, Adelaide, SA, Australia Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyCogne, Benjamin论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, F-44000 Nantes, France Nantes Univ, Inst Thorax, CHU Nantes, CNRS,INSERM, F-44000 Nantes, France Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyFeldman, Hagit Baris论文数: 0 引用数: 0 h-index: 0机构: Tel Aviv Sourasky Med Ctr, Genet Inst, Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genom Ctr, Tel Aviv, Israel Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyHorn, Anselm H. C.论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg, Inst Biochem, Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg, Erlangen Natl High Performance Comp Ctr, Erlangen, Germany Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyHurst, Anna C. E.论文数: 0 引用数: 0 h-index: 0机构: Univ Alabama Birmingham, Dept Genet, Birmingham, AL USA Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyKelly, Melissa A.论文数: 0 引用数: 0 h-index: 0机构: HudsonAlpha Inst Biotechnol, HudsonAlpha Clin Serv Lab, Huntsville, AL USA Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyKruer, Michael C.论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Phoenix Childrens Hosp, Barrow Neurol Inst, Coll Med, Phoenix, AZ USA Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyKurolap, Alina论文数: 0 引用数: 0 h-index: 0机构: Tel Aviv Sourasky Med Ctr, Genet Inst, Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genom Ctr, Tel Aviv, Israel Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyLaquerriere, Annie论文数: 0 引用数: 0 h-index: 0机构: Univ Rouen Normandie, Dept Anat, Inserm U1245, F-76000 Rouen, France Univ Rouen Normandie, CHU Rouen, F-76000 Rouen, France Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyLi, Megan论文数: 0 引用数: 0 h-index: 0机构: Invitae Corp, San Francisco, CA USA Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyMark, Paul R.论文数: 0 引用数: 0 h-index: 0机构: Helen DeVos Childrens Hosp, Div Med Genet, Corewell Hlth, Grand Rapids, MI USA Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyMorawski, Markus论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Paul Flechsig Inst, Med Fac, Ctr Neuropathol & Brain Res, Leipzig, Germany Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, Germany论文数: 引用数: h-index:机构:Pastinen, Tomi论文数: 0 引用数: 0 h-index: 0机构: Childrens Mercy Hosp, Genom Med Ctr, Kansas City, MO USA Univ Missouri Kansas City, Sch Med, Kansas City, MO USA Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyPolster, Tilman论文数: 0 引用数: 0 h-index: 0机构: Bielefeld Univ, Krankenhaus Mara Bethel Epilepsy Ctr, Dept Epileptol, Med Sch OWL, Campus Bethel, Bielefeld, Germany Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, Germany论文数: 引用数: h-index:机构:SeSong, Jang论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Genom Med Inst, Seoul, South Korea Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanySticht, Heinrich论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg, Inst Biochem, Erlangen, Germany Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyStieler, Jens T.论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Paul Flechsig Inst, Med Fac, Ctr Neuropathol & Brain Res, Leipzig, Germany Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyThifffault, Isabelle论文数: 0 引用数: 0 h-index: 0机构: Childrens Mercy Hosp, Genom Med Ctr, Kansas City, MO USA Univ Missouri Kansas City, Sch Med, Kansas City, MO USA Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, Germanyvan Eyk, Clare L.论文数: 0 引用数: 0 h-index: 0机构: Univ Adelaide, Robinson Res Inst, Adelaide, SA, Australia Univ Adelaide, Robinson Res Inst, Adelaide, SA, Australia Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyMarcorelles, Pascale论文数: 0 引用数: 0 h-index: 0机构: Dept Anat, CHU Brest, F-29000 Brest, France Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyVezain-Mouchard, Myriam论文数: 0 引用数: 0 h-index: 0机构: Univ Rouen Normandie, CHU Rouen, F-76000 Rouen, France Univ Rouen Normandie, Dept Genet, F-76000 Rouen, France Univ Rouen Normandie, Reference Ctr Dev Disorders, Inserm U1245, F-76000 Rouen, France Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyAbou Jamra, Rami论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, Germany Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, GermanyOppermann, Henry论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, Germany Univ Leipzig, Med Ctr, Inst Human Genet, D-04103 Leipzig, Germany
- [4] Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephalyHuman Genetics, 2024, 143 : 455 - 469Charlotte Herbst论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsViktoria Bothe论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsMeret Wegler论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsSusanne Axer-Schaefer论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsSéverine Audebert-Bellanger论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsJozef Gecz论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsBenjamin Cogne论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsHagit Baris Feldman论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsAnselm H. C. Horn论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsAnna C. E. Hurst论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsMelissa A. Kelly论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsMichael C. Kruer论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsAlina Kurolap论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsAnnie Laquerriere论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsMegan Li论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsPaul R. Mark论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsMarkus Morawski论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsMathilde Nizon论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsTomi Pastinen论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsTilman Polster论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsPascale Saugier-Veber论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsJang SeSong论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsHeinrich Sticht论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsJens T. Stieler论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsIsabelle Thifffault论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsClare L. van Eyk论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsPascale Marcorelles论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsMyriam Vezain-Mouchard论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsRami Abou Jamra论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human GeneticsHenry Oppermann论文数: 0 引用数: 0 h-index: 0机构: University of Leipzig Medical Center,Institute of Human Genetics
- [5] Loss-of-Function CARS1 Variants in a Patient With Microcephaly, Developmental Delay, and a Brittle Hair PhenotypeMOLECULAR GENETICS & GENOMIC MEDICINE, 2025, 13 (02):论文数: 引用数: h-index:机构:Kuo, Molly E.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Michigan, Med Sch, Cellular & Mol Biol Program, Ann Arbor, MI 48109 USA Univ Michigan, Med Sch, Med Scientist Training Program, Ann Arbor, MI USA Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USASmith, Desiree E. C.论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Amsterdam UMC, Lab Genet Metab Dis, Amsterdam, Netherlands Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USAMendes, Marisa I.论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Amsterdam UMC, Lab Genet Metab Dis, Amsterdam, Netherlands Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USASalamons, Gajja S.论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Amsterdam UMC, Lab Genet Metab Dis, Amsterdam, Netherlands Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USANemcovic, Marek论文数: 0 引用数: 0 h-index: 0机构: Slovak Acad Sci, Inst Chem, Dept Glycobiol, Bratislava, Slovakia Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USAKodrikova, Rebeka论文数: 0 引用数: 0 h-index: 0机构: Slovak Acad Sci, Inst Chem, Dept Glycobiol, Bratislava, Slovakia Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USASestak, Sergej论文数: 0 引用数: 0 h-index: 0机构: Slovak Acad Sci, Inst Chem, Dept Glycobiol, Bratislava, Slovakia Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USAStancheva, Malina论文数: 0 引用数: 0 h-index: 0机构: Med Dent Ctr Mediva, Sofia, Bulgaria Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USAAntonellis, Anthony论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Michigan, Med Sch, Cellular & Mol Biol Program, Ann Arbor, MI 48109 USA Univ Michigan, Med Sch, Dept Neurol, Ann Arbor, MI 48109 USA Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USA
- [6] De novo loss-of-function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomaliesAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (05) : 1319 - 1327Mullegama, Sureni V.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Clin Genom Ctr, 695 Charles E Young Dr South, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAKlein, Steven D.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAMulatinho, Milene V.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USASenaratne, Tharanga Niroshini论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USASingh, Kathryn论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Irvine, Div Genet & Genom Med, Irvine, CA USA Miller Childrens & Womens Hosp Long Beach, Long Beach, CA USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USANguyen, Dzung C.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAGallant, Natalie M.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Irvine, Div Genet & Genom Med, Irvine, CA USA Miller Childrens & Womens Hosp Long Beach, Long Beach, CA USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAStrom, Samuel P.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Clin Genom Ctr, 695 Charles E Young Dr South, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAGhahremani, Shahnaz论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Radiol, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USARao, Nagesh P.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAMartinez-Agosto, Julian A.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, UCLA Clin Genom Ctr, 695 Charles E Young Dr South, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
- [7] Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizuresAMERICAN JOURNAL OF HUMAN GENETICS, 2022, 109 (04) : 571 - 586Lu, Shenzhao论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Duncan Neurol Res Inst, Houston, TX 77030 USA Baylor Coll Med, Howard Hughes Med Inst, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAHernan, Rebecca论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pediat, New York, NY 10032 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAMarcogliese, Paul C.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Duncan Neurol Res Inst, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAHuang, Yan论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Duncan Neurol Res Inst, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAGertler, Tracy S.论文数: 0 引用数: 0 h-index: 0机构: Ann & Robert H Lurie Childrens Hosp Chicago, Dept Pediat, Div Neurol, Chicago, IL 60611 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAAkcaboy, Meltem论文数: 0 引用数: 0 h-index: 0机构: Dr Sami Ulus Matern & Childrens Hlth & Dis Traini, Dept Pediat, Ankara, Turkey Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USALiu, Shiyong论文数: 0 引用数: 0 h-index: 0机构: Army Med Univ, Xinqiao Hosp, Dept Neurosurg, Chongqing 400037, Peoples R China Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAChung, Hyung-lok论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Duncan Neurol Res Inst, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAPan, Xueyang论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Duncan Neurol Res Inst, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USASun, Xiaoqin论文数: 0 引用数: 0 h-index: 0机构: Army Med Univ, Xinqiao Hosp, Dept Neurosurg, Chongqing 400037, Peoples R China Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAOguz, Melahat Melek论文数: 0 引用数: 0 h-index: 0机构: Dr Sami Ulus Matern & Childrens Hlth & Dis Traini, Dept Pediat, Ankara, Turkey Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAOztoprak, Ulkuhan论文数: 0 引用数: 0 h-index: 0机构: Dr Sami Ulus Matern & Childrens Hlth & Dis Traini, Dept Pediat Neurol, Ankara, Turkey Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAde Baaij, Jeroen H. F.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Radboud Inst Mol Life Sci, Dept Physiol, Med Ctr, NL-6500 HB Nijmegen, Netherlands Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAIvanisevic, Jelena论文数: 0 引用数: 0 h-index: 0机构: Ann & Robert H Lurie Childrens Hosp Chicago, Dept Pediat, Div Neurol, Chicago, IL 60611 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAMcGinnis, Erin论文数: 0 引用数: 0 h-index: 0机构: Ann & Robert H Lurie Childrens Hosp Chicago, Dept Pediat, Div Neurol, Chicago, IL 60611 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USASacoto, Maria J. Guillen论文数: 0 引用数: 0 h-index: 0机构: GeneDx Inc, Gaithersburg, MD 20877 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAChung, Wendy K.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pediat, New York, NY 10032 USA Columbia Univ, Dept Med, Med Ctr, New York, NY 10032 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USABellen, Hugo J.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Duncan Neurol Res Inst, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
- [8] Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental featuresHUMAN GENETICS AND GENOMICS ADVANCES, 2024, 5 (02):Ansari, Morad论文数: 0 引用数: 0 h-index: 0机构: Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, Scotland Univ Edinburgh, Inst Genet & Canc, MRC, Human Genet Unit, Edinburgh, Midlothian, Scotland Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandFaour, Kamli N. W.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA Boston Childrens Hosp, Cornelia Lange Syndrome & Related Disorders Clin, Boston, MA 02115 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandShimamura, Akiko论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Hematol & Oncol, Boston, MA USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandGrimes, Graeme论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, Inst Genet & Canc, MRC, Human Genet Unit, Edinburgh, Midlothian, Scotland Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandKao, Emeline M.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Inst Centers Clin & Translat Res, Boston, MA USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandDenhoff, Erica R.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Inst Centers Clin & Translat Res, Boston, MA USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandBlatnik, Ana论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, Inst Genet & Canc, MRC, Human Genet Unit, Edinburgh, Midlothian, Scotland Inst Oncol Ljubljana, Dept Clin Canc Genet, Ljubljana, Slovenia Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandBen-Isvy, Daniel论文数: 0 引用数: 0 h-index: 0机构: Massachusetts Gen Hosp, Ctr Genom Med, Boston, MA 02114 USA Broad Inst MIT & Harvard, Med & Populat Genet, Cambridge, MA 02142 USA Harvard Med Sch, Div Med Sci, Boston, MA 02115 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandWang, Lily论文数: 0 引用数: 0 h-index: 0机构: Massachusetts Gen Hosp, Ctr Genom Med, Boston, MA 02114 USA Broad Inst MIT & Harvard, Med & Populat Genet, Cambridge, MA 02142 USA Harvard Med Sch, Div Med Sci, Boston, MA 02115 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandHelm, Benjamin M.论文数: 0 引用数: 0 h-index: 0机构: Indiana Univ Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46202 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, Scotland论文数: 引用数: h-index:机构:Breman, Amy M.论文数: 0 引用数: 0 h-index: 0机构: Indiana Univ Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46202 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandBijlsma, Emilia K.论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Dept Clin Genet, Med Ctr, Leiden, Netherlands Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, Scotland论文数: 引用数: h-index:机构:de Ravel, Thomy J. L.论文数: 0 引用数: 0 h-index: 0机构: UZ Leuven, Leuven Univ Hosp, Ctr Human Genet, Leuven, Belgium Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandFusaro, Vincent论文数: 0 引用数: 0 h-index: 0机构: Invitae, San Francisco, CA USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandFryer, Alan论文数: 0 引用数: 0 h-index: 0机构: Alder Hey Childrens Hosp Liverpool, Dept Clin Genet, Liverpool, Merseyside, England Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandNykamp, Keith论文数: 0 引用数: 0 h-index: 0机构: Invitae, San Francisco, CA USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandStuhn, Lara G.论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandHaack, Tobias B.论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandKorenke, G. Christoph论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp Oldenburg, Dept Neuropaediat & Metab Dis, Oldenburg, Germany Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandConstantinou, Panayioti论文数: 0 引用数: 0 h-index: 0机构: Queen Elizabeth Univ Hosp, West Scotland Ctr Genom Med, Glasgow, Lanark, Scotland Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandBujakowksa, Kinga M.论文数: 0 引用数: 0 h-index: 0机构: Massachusetts Eye & Ear Infirm, Boston, MA 02114 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandLow, Karen J.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Bristol & Weston NHS Fdn Trust, Bristol, Avon, England Univ Bristol, Bristol, Avon, England Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandPlace, Emily论文数: 0 引用数: 0 h-index: 0机构: Massachusetts Eye & Ear Infirm, Boston, MA 02114 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandHumberson, Jennifer论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia Hlth Syst, Charlottesville, VA USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandNapier, Melanie P.论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandHoffman, Jessica论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandJuusola, Jane论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandDeardorff, Matthew A.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Los Angeles, Dept Pathol, Los Angeles, CA 90027 USA Childrens Hosp Los Angeles, Dept Pediat, Los Angeles, CA 90027 USA Univ Southern Calif, Los Angeles, CA 90007 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandShao, Wanqing论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Res Comp, Informat Technol, Boston, MA USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandRockowitz, Shira论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA Boston Childrens Hosp, Res Comp, Informat Technol, Boston, MA USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Boston, MA USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandKrantz, Ian论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandKaur, Maninder论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandRaible, Sarah论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandDortenzio, Victoria论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandKliesch, Sabine论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Munster, Ctr Reprod Med & Androl, Dept Clin & Surg Androl, Munster, Germany Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandSinger-Berk, Moriel论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Med & Populat Genet, Cambridge, MA 02142 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandGroopman, Emily论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA Broad Inst MIT & Harvard, Med & Populat Genet, Cambridge, MA 02142 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandDiTroia, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Med & Populat Genet, Cambridge, MA 02142 USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandBallal, Sonia论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Cornelia Lange Syndrome & Related Disorders Clin, Boston, MA 02115 USA Boston Childrens Hosp, Div Gastroenterol, Boston, MA USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandSrivastava, Siddharth论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Cornelia Lange Syndrome & Related Disorders Clin, Boston, MA 02115 USA Boston Childrens Hosp, Div Neurol, Boston, MA USA Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandRothfelder, Kathrin论文数: 0 引用数: 0 h-index: 0机构: Zentrum Humangenet, Tubingen, Germany Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandBiskup, Saskia论文数: 0 引用数: 0 h-index: 0机构: Zentrum Humangenet, Tubingen, Germany Ctr Genom & Transcript CeGaT, Tubingen, Germany Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandRzasa, Jessica论文数: 0 引用数: 0 h-index: 0机构: London Hlth Sci Ctr, Mol Diagnost Program, London, ON, Canada London Hlth Sci Ctr, Verspeeten Clin Genome Ctr, London, ON, Canada Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandKerkhof, Jennifer论文数: 0 引用数: 0 h-index: 0机构: London Hlth Sci Ctr, Mol Diagnost Program, London, ON, Canada London Hlth Sci Ctr, Verspeeten Clin Genome Ctr, London, ON, Canada Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandMcConkey, Haley论文数: 0 引用数: 0 h-index: 0机构: London Hlth Sci Ctr, Mol Diagnost Program, London, ON, Canada London Hlth Sci Ctr, Verspeeten Clin Genome Ctr, London, ON, Canada Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandSadikovic, Bekim论文数: 0 引用数: 0 h-index: 0机构: London Hlth Sci Ctr, Mol Diagnost Program, London, ON, Canada London Hlth Sci Ctr, Verspeeten Clin Genome Ctr, London, ON, Canada Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandHilton, Sarah论文数: 0 引用数: 0 h-index: 0机构: Manchester Univ NHS Fdn Trust, Manchester Ctr Genom Med, Hlth Innovat Manchester, Manchester, Lancs, England Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, ScotlandBanka, Siddharth论文数: 0 引用数: 0 h-index: 0机构: Manchester Univ NHS Fdn Trust, Manchester Ctr Genom Med, Hlth Innovat Manchester, Manchester, Lancs, England Univ Manchester, Fac Biol Med & Hlth, Sch Biol Sci, Div Evolut Infect & Genom, Manchester, Lancs, England Western Gen Hosp, South East Scotland Genet Serv, Edinburgh, Midlothian, Scotland
- [9] Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disordersNature Neuroscience, 2016, 19 : 571 - 577Tarjinder Singh论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryMitja I Kurki论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryDavid Curtis论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryShaun M Purcell论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryLucy Crooks论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryJeremy McRae论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryJaana Suvisaari论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryHimanshu Chheda论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryDouglas Blackwood论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryGerome Breen论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryOlli Pietiläinen论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatrySebastian S Gerety论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryMuhammad Ayub论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryMoira Blyth论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryTrevor Cole论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryDavid Collier论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryEve L Coomber论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryNick Craddock论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryMark J Daly论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryJohn Danesh论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryMarta DiForti论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryAlison Foster论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryNelson B Freimer论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryDaniel Geschwind论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryMandy Johnstone论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryShelagh Joss论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryGeorg Kirov论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryJarmo Körkkö论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryOuti Kuismin论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryPeter Holmans论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryChristina M Hultman论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryConrad Iyegbe论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryJouko Lönnqvist论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryMinna Männikkö论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatrySteve A McCarroll论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryPeter McGuffin论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryAndrew M McIntosh论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryAndrew McQuillin论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryJukka S Moilanen论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryCarmel Moore论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryRobin M Murray论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryRuth Newbury-Ecob论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryWillem Ouwehand论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryTiina Paunio论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryElena Prigmore论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryElliott Rees论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryDavid Roberts论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryJennifer Sambrook论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryPamela Sklar论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of PsychiatryDavid St Clair论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Institute,Division of Psychiatric Genomics, Department of Psychiatry
- [10] Further Delineation of the Microcephaly-Micromelia Syndrome Associated with Loss-of-Function Variants in DONSONMOLECULAR SYNDROMOLOGY, 2019, 10 (03) : 171 - 176Abdelrahman, Hanadi A.论文数: 0 引用数: 0 h-index: 0机构: United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Pathol, Al Ain, U Arab Emirates United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Pathol, Al Ain, U Arab EmiratesJohn, Anne论文数: 0 引用数: 0 h-index: 0机构: United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Pathol, Al Ain, U Arab Emirates United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Pathol, Al Ain, U Arab EmiratesAli, Bassam R.论文数: 0 引用数: 0 h-index: 0机构: United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Pathol, Al Ain, U Arab Emirates United Arab Emirates Univ, Coll Med & Hlth Sci, Zayed Ctr Hlth Sci, Al Ain, U Arab Emirates United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Pathol, Al Ain, U Arab EmiratesAl-Gazali, Lihadh论文数: 0 引用数: 0 h-index: 0机构: United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Pediat, PO 17666, Al Ain, U Arab Emirates United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Pathol, Al Ain, U Arab Emirates