Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders.
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| Title: | Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. |
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| Authors: | Brunet T; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany., Berutti R; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany., Dill V; Department of Medicine III, Technical University of Munich, Klinikum rechts der Isar, 81675 Munich, Germany., Hecker JS; Department of Medicine III, Technical University of Munich, Klinikum rechts der Isar, 81675 Munich, Germany., Choukair D; Division of Paediatric Endocrinology and Diabetology, University Children's Hospital, 69120 Heidelberg, Germany., Andres S; Center of Human Genetics and Laboratory Diagnostics, 82152 Martinsried, Germany., Deschauer M; Department of Neurology, Technical University of Munich, School of Medicine, 81675 Munich, Germany., Diehl-Schmid J; Technical University of Munich, School of Medicine, Department of Psychiatry and Psychotherapy, 81675 Munich, Germany.; Munich Cluster for Systems Neurology (SyNergy), 81377 Munich, Germany., Krenn M; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Department of Neurology, Medical University of Vienna, 1090 Vienna, Austria., Eckstein G; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany.; Core Facility Genomics, Helmholtz Center Munich, Neuherberg 85764, Germany., Graf E; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany., Gasser T; Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, 72076 Tübingen, Germany.; German Center for Neurodegenerative Diseases (DZNE), 72076 Tübingen, Germany., Strom TM; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany., Hoefele J; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany., Götze KS; Department of Medicine III, Technical University of Munich, Klinikum rechts der Isar, 81675 Munich, Germany., Meitinger T; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany., Wagner M; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany. |
| Source: | Human molecular genetics [Hum Mol Genet] 2022 Jul 21; Vol. 31 (14), pp. 2386-2395. |
| Publication Type: | Journal Article |
| Journal Info: | 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 |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 35179199 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Brunet+T%22">Brunet T</searchLink>; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany.<br /><searchLink fieldCode="AU" term="%22Berutti+R%22">Berutti R</searchLink>; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany.<br /><searchLink fieldCode="AU" term="%22Dill+V%22">Dill V</searchLink>; Department of Medicine III, Technical University of Munich, Klinikum rechts der Isar, 81675 Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Hecker+JS%22">Hecker JS</searchLink>; Department of Medicine III, Technical University of Munich, Klinikum rechts der Isar, 81675 Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Choukair+D%22">Choukair D</searchLink>; Division of Paediatric Endocrinology and Diabetology, University Children's Hospital, 69120 Heidelberg, Germany.<br /><searchLink fieldCode="AU" term="%22Andres+S%22">Andres S</searchLink>; Center of Human Genetics and Laboratory Diagnostics, 82152 Martinsried, Germany.<br /><searchLink fieldCode="AU" term="%22Deschauer+M%22">Deschauer M</searchLink>; Department of Neurology, Technical University of Munich, School of Medicine, 81675 Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Diehl-Schmid+J%22">Diehl-Schmid J</searchLink>; Technical University of Munich, School of Medicine, Department of Psychiatry and Psychotherapy, 81675 Munich, Germany.; Munich Cluster for Systems Neurology (SyNergy), 81377 Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Krenn+M%22">Krenn M</searchLink>; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Department of Neurology, Medical University of Vienna, 1090 Vienna, Austria.<br /><searchLink fieldCode="AU" term="%22Eckstein+G%22">Eckstein G</searchLink>; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany.; Core Facility Genomics, Helmholtz Center Munich, Neuherberg 85764, Germany.<br /><searchLink fieldCode="AU" term="%22Graf+E%22">Graf E</searchLink>; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Gasser+T%22">Gasser T</searchLink>; Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, 72076 Tübingen, Germany.; German Center for Neurodegenerative Diseases (DZNE), 72076 Tübingen, Germany.<br /><searchLink fieldCode="AU" term="%22Strom+TM%22">Strom TM</searchLink>; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Hoefele+J%22">Hoefele J</searchLink>; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Götze+KS%22">Götze KS</searchLink>; Department of Medicine III, Technical University of Munich, Klinikum rechts der Isar, 81675 Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Meitinger+T%22">Meitinger T</searchLink>; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Wagner+M%22">Wagner M</searchLink>; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, 81675 Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2022 Jul 21; Vol. 31 (14), pp. 2386-2395. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=35179199 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/hmg/ddac034 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 2386 Titles: – TitleFull: Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Brunet T – PersonEntity: Name: NameFull: Berutti R – PersonEntity: Name: NameFull: Dill V – PersonEntity: Name: NameFull: Hecker JS – PersonEntity: Name: NameFull: Choukair D – PersonEntity: Name: NameFull: Andres S – PersonEntity: Name: NameFull: Deschauer M – PersonEntity: Name: NameFull: Diehl-Schmid J – PersonEntity: Name: NameFull: Krenn M – PersonEntity: Name: NameFull: Eckstein G – PersonEntity: Name: NameFull: Graf E – PersonEntity: Name: NameFull: Gasser T – PersonEntity: Name: NameFull: Strom TM – PersonEntity: Name: NameFull: Hoefele J – PersonEntity: Name: NameFull: Götze KS – PersonEntity: Name: NameFull: Meitinger T – PersonEntity: Name: NameFull: Wagner M IsPartOfRelationships: – BibEntity: Dates: – D: 21 M: 07 Text: 2022 Jul 21 Type: published Y: 2022 Identifiers: – Type: issn-electronic Value: 1460-2083 Numbering: – Type: volume Value: 31 – Type: issue Value: 14 Titles: – TitleFull: Human molecular genetics Type: main |
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