Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders.

Saved in:
Bibliographic Details
Title: Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders.
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
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 35179199
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
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
ResultId 1