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المؤلفون: Sund KL; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Liu J; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.; Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio, USA., Lee J; Bionano Genomics, San Diego, California, USA., Garbe J; University of Minnesota Genomics Center, University of Minnesota, Minneapolis, Minnesota, USA., Abdelhamed Z; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Maag C; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Hallinan B; Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio, USA.; Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Wu SW; Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio, USA.; Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Sperry E; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Deshpande A; University of Minnesota Genomics Center, University of Minnesota, Minneapolis, Minnesota, USA., Stottmann R; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.; Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio, USA., Smolarek TA; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.; Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio, USA., Dyer LM; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.; Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio, USA., Hestand MS; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.; Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio, USA.

المصدر: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Jul 23, pp. e63818. Date of Electronic Publication: 2024 Jul 23.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

المؤلفون: Virolainen SJ; Division of Human Genetics and.; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.; Immunology Graduate Program and.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA., Satish L; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.; Division of Asthma Research, Cincinnati Children's Hospital, Cincinnati, Ohio, USA., Biagini JM; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.; Division of Asthma Research, Cincinnati Children's Hospital, Cincinnati, Ohio, USA., Chaib H; Division of Human Genetics and.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA., Chang WC; Division of Asthma Research, Cincinnati Children's Hospital, Cincinnati, Ohio, USA., Dexheimer PJ; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA., Dixon MR; Division of Human Genetics and., Dunn K; Division of Human Genetics and.; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA., Fletcher D; Division of Human Genetics and., Forney C; Division of Human Genetics and.; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA., Granitto M; Division of Human Genetics and.; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA., Hestand MS; Pacific Biosciences, Menlo Park, California, USA., Hurd M; Division of Asthma Research, Cincinnati Children's Hospital, Cincinnati, Ohio, USA., Kauffman K; Division of Human Genetics and.; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA., Lawson L; Division of Human Genetics and.; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA., Martin LJ; Division of Human Genetics and.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA., Peña LD; Division of Human Genetics and.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA., Phelan KJ; Division of Asthma Research, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.; Medical Scientist Training Program, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA., Shook M; Division of Human Genetics and.; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA., Weirauch MT; Division of Human Genetics and.; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.; Immunology Graduate Program and.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.; Divisions of Developmental Biology and Bioinformatics and Allergy and Immunology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA., Khurana Hershey GK; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.; Division of Asthma Research, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.; Medical Scientist Training Program, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA., Kottyan LC; Division of Human Genetics and.; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.; Immunology Graduate Program and.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.; Divisions of Developmental Biology and Bioinformatics and Allergy and Immunology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.

المصدر: JCI insight [JCI Insight] 2024 Apr 02; Vol. 9 (9). Date of Electronic Publication: 2024 Apr 02.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 101676073 Publication Model: Electronic Cited Medium: Internet ISSN: 2379-3708 (Electronic) Linking ISSN: 23793708 NLM ISO Abbreviation: JCI Insight Subsets: MEDLINE

مواضيع طبية MeSH: Filaggrin Proteins* , Dermatitis, Atopic*/genetics , Dermatitis, Atopic*/pathology , Loss of Function Mutation* , Phenotype* , Intermediate Filament Proteins*/genetics, Humans ; Male ; Female ; Child, Preschool ; Prospective Studies ; Infant ; Genetic Predisposition to Disease ; Child ; Food Hypersensitivity/genetics

المؤلفون: Cleynen I; Department of Human Genetics, KU Leuven, Leuven, Belgium., Engchuan W; The Centre for Applied Genomics (TCAG), The Hospital for Sick Children, Toronto, ON, Canada., Hestand MS; Department of Human Genetics, KU Leuven, Leuven, Belgium.; Department of Pediatrics, University of Cincinnati, Cincinnati, OH, USA.; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA., Heung T; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON, Canada.; Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, ON, Canada., Holleman AM; Department of Epidemiology, Emory University, Atlanta, GA, USA., Johnston HR; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA., Monfeuga T; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK., McDonald-McGinn DM; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA, USA.; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., Gur RE; Department of Psychiatry and Lifespan Brain Institute, Penn Medicine-CHOP, University of Pennsylvania, Philadelphia, PA, USA., Morrow BE; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA., Swillen A; Department of Human Genetics, KU Leuven, Leuven, Belgium.; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium., Vorstman JAS; Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Psychiatry, University Medical Center Utrecht, Utrecht, The Netherlands.; Department of Psychiatry, University of Toronto, Toronto, ON, Canada., Bearden CE; Departments of Psychiatry and Biobehavioral Sciences and Psychology, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA, USA., Chow EWC; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON, Canada.; Department of Psychiatry, University of Toronto, Toronto, ON, Canada., van den Bree M; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK., Emanuel BS; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., Vermeesch JR; Department of Human Genetics, KU Leuven, Leuven, Belgium., Warren ST; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA., Owen MJ; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK., Chopra P; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA., Cutler DJ; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA., Duncan R; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA., Kotlar AV; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA., Mulle JG; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA., Voss AJ; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA., Zwick ME; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA., Diacou A; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA., Golden A; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA., Guo T; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA., Lin JR; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA., Wang T; Department of Epidemiology & Population Health, Albert Einstein College of Medicine, Bronx, NY, USA., Zhang Z; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA., Zhao Y; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA., Marshall C; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.; Division of Genome Diagnostics, Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, ON, Canada., Merico D; The Centre for Applied Genomics (TCAG), The Hospital for Sick Children, Toronto, ON, Canada.; Deep Genomics Inc., Toronto, ON, Canada., Jin A; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., Lilley B; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., Salmons HI; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., Tran O; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., Holmans P; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK., Pardinas A; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK., Walters JTR; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK., Demaerel W; Department of Human Genetics, KU Leuven, Leuven, Belgium., Boot E; Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, ON, Canada., Butcher NJ; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON, Canada., Costain GA; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON, Canada.; Hospital for Sick Children, Toronto, ON, Canada., Lowther C; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON, Canada., Evers R; School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands., van Amelsvoort TAMJ; School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands., van Duin E; School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands., Vingerhoets C; School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands., Breckpot J; Department of Human Genetics, KU Leuven, Leuven, Belgium.; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium., Devriendt K; Department of Human Genetics, KU Leuven, Leuven, Belgium.; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium., Vergaelen E; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium., Vogels A; Department of Human Genetics, KU Leuven, Leuven, Belgium.; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium., Crowley TB; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., McGinn DE; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., Moss EM; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., Sharkus RJ; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., Unolt M; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., Zackai EH; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA, USA.; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA, USA., Calkins ME; Department of Psychiatry and Lifespan Brain Institute, Penn Medicine-CHOP, University of Pennsylvania, Philadelphia, PA, USA., Gallagher RS; Department of Psychiatry and Lifespan Brain Institute, Penn Medicine-CHOP, University of Pennsylvania, Philadelphia, PA, USA., Gur RC; Department of Psychiatry and Lifespan Brain Institute, Penn Medicine-CHOP, University of Pennsylvania, Philadelphia, PA, USA., Tang SX; Department of Psychiatry and Lifespan Brain Institute, Penn Medicine-CHOP, University of Pennsylvania, Philadelphia, PA, USA., Fritsch R; Universidad de Chile, Santiago, Chile., Ornstein C; Universidad de Chile, Santiago, Chile., Repetto GM; Clinica Alemana Universidad del Desarrollo, Santiago, Chile., Breetvelt E; Department of Psychiatry, University of Toronto, Toronto, ON, Canada.; Department of Psychiatry, Hospital for Sick Children, Toronto, ON, Canada., Duijff SN; Department of Pediatrics, University Medical Center Utrecht, Utrecht, Netherlands., Fiksinski A; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON, Canada.; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands., Moss H; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK., Niarchou M; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK., Murphy KC; Royal College of Surgeons in Ireland, Dublin, Ireland., Prasad SE; Royal College of Surgeons in Ireland, Dublin, Ireland., Daly EM; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London, London, UK., Gudbrandsen M; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London, London, UK., Murphy CM; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London, London, UK., Murphy DG; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London, London, UK., Buzzanca A; Department of Human Neurosciences, University Sapienza of Rome, Rome, Italy., Fabio FD; Department of Human Neurosciences, University Sapienza of Rome, Rome, Italy., Digilio MC; Ospedale Bambino Gesu Pediatric Hospital, Rome, Italy., Pontillo M; Child and Adolescence Neuropsychiatry Unit, Department of Neuroscience, IRCSS Bambino Gesù Children's Hospital of Rome, Rome, Italy., Marino B; Sapienza University, Rome, Italy., Vicari S; Child and Adolescence Neuropsychiatry Unit, Department of Neuroscience, IRCSS Bambino Gesù Children's Hospital of Rome, Rome, Italy., Coleman K; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA., Cubells JF; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.; Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA., Ousley OY; Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA., Carmel M; Felsenstein Medical Research Center, Petach Tikva, Israel.; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel., Gothelf D; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.; The Child Psychiatry Division, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel., Mekori-Domachevsky E; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.; The Child Psychiatry Division, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel., Michaelovsky E; Felsenstein Medical Research Center, Petach Tikva, Israel.; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel., Weinberger R; The Child Psychiatry Division, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel., Weizman A; Felsenstein Medical Research Center, Petach Tikva, Israel.; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.; Geha Mental Health Center, Petach Tikva, Israel., Kushan L; Departments of Psychiatry and Biobehavioral Sciences and Psychology, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA, USA., Jalbrzikowski M; Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA., Armando M; Developmental Imaging and Psychopathology, Department of Psychiatry, University of Geneva, Geneva, Switzerland., Eliez S; Developmental Imaging and Psychopathology, Department of Psychiatry, University of Geneva, Geneva, Switzerland., Sandini C; Developmental Imaging and Psychopathology, Department of Psychiatry, University of Geneva, Geneva, Switzerland., Schneider M; Developmental Imaging and Psychopathology, Department of Psychiatry, University of Geneva, Geneva, Switzerland., Béna FS; Department of Medical Genetics, Geneva University Hospitals, Geneva, Switzerland., Antshel KM; Department of Psychology, Syracuse University, Syracuse, NY, USA., Fremont W; Department of Psychiatry and Behavioral Sciences, SUNY Upstate Medical University, Syracuse, NY, USA., Kates WR; Department of Psychiatry and Behavioral Sciences, SUNY Upstate Medical University, Syracuse, NY, USA., Belzeaux R; Pôle de psychiatrie, Hopital Sainte Marguerite, Batiment Solaris, APHM, Marseille, France., Busa T; Departement de Genetique Medicale Hôpital d'Enfants de la Timone, APHM, Marseille, France., Philip N; Departement de Genetique Medicale Aix Marseille Univ, INSERM, GMGF, APHM, Marseille, France., Campbell LE; University of Newcastle, Callaghan, Australia., McCabe KL; University of Newcastle, Callaghan, Australia.; University of California Davis, Davis, CA, USA., Hooper SR; Department of Allied Health Sciences, School of Medicine, University of North Carolina-Chapel Hill, Chapel Hill, NC, USA., Schoch K; Department of Pediatrics, Division of Medical Genetics, Duke University School of Medicine, Durham, NC, USA., Shashi V; Department of Pediatrics, Division of Medical Genetics, Duke University School of Medicine, Durham, NC, USA., Simon TJ; MIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis, Davis, CA, USA., Tassone F; Department of Microbiology and Molecular Medicine, University of California Davis, Davis, CA, USA., Arango C; Department of Child and Adolescent Psychiatry, Hospital General Universitario Gregorio Marañón, IiSGM, CIBERSAM, School of Medicine, Universidad Complutense, Madrid, Spain., Fraguas D; Department of Child and Adolescent Psychiatry, Hospital General Universitario Gregorio Marañón, IiSGM, CIBERSAM, School of Medicine, Universidad Complutense, Madrid, Spain., García-Miñaúr S; Institute of Medical and Molecular Genetics (INGEMM), La Paz University Hospital, Madrid, Spain., Morey-Canyelles J; Hospital Universitari Son Espases, Palma, Spain., Rosell J; Hospital Universitari Son Espases, Palma, Spain., Suñer DH; Laboratorio Unidad de Diagnóstico Molecular y Genética Clínica, Hospital Universitari Son Espases, Palma de Mallorca, Spain., Raventos-Simic J; Hospital Universitari Son Espases, Palma, Spain., Epstein MP; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA. mpepste@emory.edu., Williams NM; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK. williamsnm@cardiff.ac.uk., Bassett AS; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON, Canada. anne.bassett@utoronto.ca.; Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, ON, Canada. anne.bassett@utoronto.ca.; Department of Psychiatry, University of Toronto, Toronto, ON, Canada. anne.bassett@utoronto.ca.

مؤلفون مشاركون: International 22q11.2DS Brain and Behavior Consortium

المصدر: Molecular psychiatry [Mol Psychiatry] 2021 Aug; Vol. 26 (8), pp. 4496-4510. Date of Electronic Publication: 2020 Feb 03.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5578 (Electronic) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: DiGeorge Syndrome*/genetics , Psychotic Disorders* , Schizophrenia*/genetics, Adult ; Case-Control Studies ; Cohort Studies ; Humans

المؤلفون: Linthorst J; Department of Clinical Genetics, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.; Delft Bioinformatics Lab, Delft University of Technology, Delft, The Netherlands., Meert W; Department of Human Genetics, KU Leuven, Leuven, Belgium., Hestand MS; Department of Human Genetics, KU Leuven, Leuven, Belgium., Korlach J; Pacific Biosciences, Menlo Park, CA, USA., Vermeesch JR; Department of Human Genetics, KU Leuven, Leuven, Belgium., Reinders MJT; Delft Bioinformatics Lab, Delft University of Technology, Delft, The Netherlands., Holstege H; Department of Clinical Genetics, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands. h.holstege@amsterdamumc.nl.; Delft Bioinformatics Lab, Delft University of Technology, Delft, The Netherlands. h.holstege@amsterdamumc.nl.; Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands. h.holstege@amsterdamumc.nl.

المصدر: Translational psychiatry [Transl Psychiatry] 2020 Nov 02; Vol. 10 (1), pp. 369. Date of Electronic Publication: 2020 Nov 02.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Nature Pub. Group Country of Publication: United States NLM ID: 101562664 Publication Model: Electronic Cited Medium: Internet ISSN: 2158-3188 (Electronic) Linking ISSN: 21583188 NLM ISO Abbreviation: Transl Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Genome, Human* , Minisatellite Repeats*/genetics, Aged, 80 and over ; Brain ; Female ; Haplotypes ; Humans ; Sequence Analysis, DNA

المؤلفون: Unolt M; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA. unolt.marta@gmail.com.; Department of Pediatrics, Sapienza University of Rome, Rome, Italy. unolt.marta@gmail.com., Kammoun M; Center for Human Genetics, KU Leuven, Leuven, Belgium., Nowakowska B; Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland., Graham GE; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada., Crowley TB; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA., Hestand MS; Center for Human Genetics, KU Leuven, Leuven, Belgium., Demaerel W; Center for Human Genetics, KU Leuven, Leuven, Belgium., Geremek M; Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland., Emanuel BS; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA., Zackai EH; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA., Vermeesch JR; Center for Human Genetics, KU Leuven, Leuven, Belgium., McDonald-McGinn D; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2020 Feb; Vol. 22 (2), pp. 326-335. Date of Electronic Publication: 2019 Sep 02.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

مواضيع طبية MeSH: Cell Cycle Proteins/*genetics , DiGeorge Syndrome/*genetics, Alleles ; Cell Cycle Proteins/metabolism ; Child ; Child, Preschool ; Chromosome Deletion ; Chromosomes/genetics ; Chromosomes, Human, Pair 22/genetics ; Craniosynostoses/genetics ; DiGeorge Syndrome/metabolism ; Female ; Heart Defects, Congenital/genetics ; Humans ; Male ; Phenotype ; Retrospective Studies

المؤلفون: Vervoort L; Department of Human Genetics, KU Leuven, Leuven, Belgium., Demaerel W; Department of Human Genetics, KU Leuven, Leuven, Belgium., Rengifo LY; Department of Human Genetics, KU Leuven, Leuven, Belgium., Odrzywolski A; Department of Human Genetics, KU Leuven, Leuven, Belgium.; Department of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland., Vergaelen E; Department of Human Genetics, KU Leuven, Leuven, Belgium., Hestand MS; Department of Human Genetics, KU Leuven, Leuven, Belgium.; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.; Department of Pediatrics, University of Cincinnati, Cincinnati, OH, USA., Breckpot J; Department of Human Genetics, KU Leuven, Leuven, Belgium., Devriendt K; Department of Human Genetics, KU Leuven, Leuven, Belgium., Swillen A; Department of Human Genetics, KU Leuven, Leuven, Belgium., McDonald-McGinn DM; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA., Fiksinski AM; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.; The Dalglish Family 22q Clinic and Centre for Addiction and Mental Health, Toronto, ON, Canada., Zinkstok JR; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands., Morrow BE; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA., Heung T; The Dalglish Family 22q Clinic and Centre for Addiction and Mental Health, Toronto, ON, Canada.; Department of Psychiatry, University of Toronto, Toronto, ON, Canada., Vorstman JAS; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.; The Dalglish Family 22q Clinic and Centre for Addiction and Mental Health, Toronto, ON, Canada., Bassett AS; The Dalglish Family 22q Clinic and Centre for Addiction and Mental Health, Toronto, ON, Canada.; Department of Psychiatry, University of Toronto, Toronto, ON, Canada., Chow EWC; Department of Psychiatry, University of Toronto, Toronto, ON, Canada.; Clinical Genetics Service, Centre for Addiction and Mental Health, Toronto, ON, Canada., Shashi V; Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA., Vermeesch JR; Department of Human Genetics, KU Leuven, Leuven, Belgium.

مؤلفون مشاركون: International 22q11.2 Brain, Behavior Consortium

المصدر: Human molecular genetics [Hum Mol Genet] 2019 Nov 15; Vol. 28 (22), pp. 3724-3733.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: DiGeorge Syndrome/*genetics , DiGeorge Syndrome/*metabolism , Homologous Recombination/*genetics, Adult ; Alleles ; Chromosome Breakpoints ; Chromosome Deletion ; Chromosome Inversion/genetics ; Chromosome Mapping/methods ; Chromosomes/genetics ; Chromosomes, Human, Pair 22/genetics ; Female ; Humans ; In Situ Hybridization, Fluorescence/methods ; Male ; Segmental Duplications, Genomic/genetics ; Whole Genome Sequencing/methods

المؤلفون: Kalbfleisch TS; 1Department of Biochemistry and Molecular Genetics, School of Medicine, University of Louisville, Louisville, KY 40292 USA., Rice ES; 2Department of Biomolecular Engineering, UC Santa Cruz, Santa Cruz, CA 95064 USA., DePriest MS Jr; 1Department of Biochemistry and Molecular Genetics, School of Medicine, University of Louisville, Louisville, KY 40292 USA., Walenz BP; 3Genome Informatics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892 USA., Hestand MS; 4Center for Human Genetics, Katholieke University Leuven (KU Leuven), 3000 Leuven, Belgium., Vermeesch JR; 4Center for Human Genetics, Katholieke University Leuven (KU Leuven), 3000 Leuven, Belgium., O'Connell BL; 2Department of Biomolecular Engineering, UC Santa Cruz, Santa Cruz, CA 95064 USA.; 16Present Address: Medical and Molecular Genetics, Oregon Health and Science University, Portland, OR 97239 USA., Fiddes IT; 2Department of Biomolecular Engineering, UC Santa Cruz, Santa Cruz, CA 95064 USA.; 510x Genomics, Inc., Pleasanton, CA 94566 USA., Vershinina AO; 6Department of Ecology and Evolutionary Biology, UC Santa Cruz, Santa Cruz, CA 95064 USA., Saremi NF; 2Department of Biomolecular Engineering, UC Santa Cruz, Santa Cruz, CA 95064 USA., Petersen JL; 7Department of Animal Science, University of Nebraska - Lincoln, Lincoln, NE 68583-0908 USA., Finno CJ; 8Department of Population Health and Reproduction, University of California, Davis, CA 95616 USA., Bellone RR; 8Department of Population Health and Reproduction, University of California, Davis, CA 95616 USA.; 9Veterinary Genetics Laboratory, University of California, Davis, CA 95616 USA., McCue ME; 10Department of Veterinary Population Medicine, University of Minnesota, St. Paul, MN 55108 USA., Brooks SA; 11UF Genetics Institute, Department of Animal Sciences, University of Florida, Gainesville, FL 32611 USA., Bailey E; 12Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington, KY 40546 USA., Orlando L; 13Centre for GeoGenetics, Natural History Museum of Denmark, 1350K Copenhagen, Denmark.; Laboratoire d'Anthropobiologie Moléculaire et d'Imagerie de Synthèse UMR 5288, Université de Toulouse, CNRS, Université Paul Sabatier, Toulouse, France., Green RE; 2Department of Biomolecular Engineering, UC Santa Cruz, Santa Cruz, CA 95064 USA., Miller DC; 15Baker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853 USA., Antczak DF; 15Baker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853 USA., MacLeod JN; 12Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington, KY 40546 USA.

المصدر: Communications biology [Commun Biol] 2019 Sep 11; Vol. 2, pp. 342. Date of Electronic Publication: 2019 Sep 11 (Print Publication: 2019).

نوع المنشور: Published Erratum

بيانات الدورية: Publisher: Nature Publishing Group UK Country of Publication: England NLM ID: 101719179 Publication Model: eCollection Cited Medium: Internet ISSN: 2399-3642 (Electronic) Linking ISSN: 23993642 NLM ISO Abbreviation: Commun Biol Subsets: PubMed not MEDLINE

المؤلفون: Demaerel W; Departement of Human Genetics, KU Leuven, Leuven, 3000 Belgium., Mostovoy Y; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, California 94158, USA., Yilmaz F; Department of Integrative Biology, University of Colorado Denver, Denver, Colorado 80204, USA.; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado Denver, Aurora, Colorado 80045, USA., Vervoort L; Departement of Human Genetics, KU Leuven, Leuven, 3000 Belgium., Pastor S; Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA., Hestand MS; Departement of Human Genetics, KU Leuven, Leuven, 3000 Belgium.; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.; Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio 45221, USA., Swillen A; Departement of Human Genetics, KU Leuven, Leuven, 3000 Belgium., Vergaelen E; Departement of Human Genetics, KU Leuven, Leuven, 3000 Belgium., Geiger EA; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado Denver, Aurora, Colorado 80045, USA., Coughlin CR; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado Denver, Aurora, Colorado 80045, USA., Chow SK; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, California 94158, USA., McDonald-McGinn D; Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA., Morrow B; Department of Genetics, Albert Einstein College of Medicine, Bronx, New York 10461, USA., Kwok PY; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, California 94158, USA., Xiao M; School of Biomedical Engineering, Drexel University, Philadelphia, Pennsylvania 19104, USA., Emanuel BS; Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA., Shaikh TH; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado Denver, Aurora, Colorado 80045, USA., Vermeesch JR; Departement of Human Genetics, KU Leuven, Leuven, 3000 Belgium.

المصدر: Genome research [Genome Res] 2019 Sep; Vol. 29 (9), pp. 1389-1401.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Cold Spring Harbor Laboratory Press Country of Publication: United States NLM ID: 9518021 Publication Model: Print Cited Medium: Internet ISSN: 1549-5469 (Electronic) Linking ISSN: 10889051 NLM ISO Abbreviation: Genome Res Subsets: MEDLINE

مواضيع طبية MeSH: Repetitive Sequences, Nucleic Acid*, 22q11 Deletion Syndrome/*genetics , Chromosome Mapping/*methods , Chromosomes, Human, Pair 22/*genetics, Animals ; Cell Line ; Chromosomal Instability ; Evolution, Molecular ; Humans ; In Situ Hybridization, Fluorescence ; Primates/genetics

المؤلفون: Hestand MS; Department of Clinical Genetics, VU University Medical Center Amsterdam, Amsterdam, The Netherlands.; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA., Bessem M; Department of Clinical Genetics, VU University Medical Center Amsterdam, Amsterdam, The Netherlands., van Rijn P; Department of Clinical Genetics, VU University Medical Center Amsterdam, Amsterdam, The Netherlands., de Menezes RX; Department of Epidemiology and Biostatistics, VU University Medical Center Amsterdam, Amsterdam, The Netherlands., Sie D; Department of Clinical Genetics, VU University Medical Center Amsterdam, Amsterdam, The Netherlands., Bakker I; Department of Clinical Genetics, VU University Medical Center Amsterdam, Amsterdam, The Netherlands., Boon EMJ; Department of Clinical Genetics, VU University Medical Center Amsterdam, Amsterdam, The Netherlands., Sistermans EA; Department of Clinical Genetics, VU University Medical Center Amsterdam, Amsterdam, The Netherlands., Weiss MM; Department of Clinical Genetics, VU University Medical Center Amsterdam, Amsterdam, The Netherlands. j.weiss@vumc.nl.

المصدر: European journal of human genetics : EJHG [Eur J Hum Genet] 2019 Feb; Vol. 27 (2), pp. 198-202. Date of Electronic Publication: 2018 Sep 25.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Chromosome Disorders/*diagnosis , Genetic Testing/*methods , Prenatal Diagnosis/*methods, Body Mass Index ; Chromosome Disorders/epidemiology ; Chromosome Disorders/genetics ; Chromosomes, Human, Y/genetics ; False Negative Reactions ; Female ; Genetic Testing/standards ; Gestational Age ; Humans ; Male ; Maternal Age ; Pregnancy ; Prenatal Diagnosis/standards