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    • Research Interests
    Intellectual Disabil...Intellectual DisabilityDna MethylationPrenatal DiagnosisEpilepsyMutation2010202020072025
    20082024

    Papers共 104 篇Author StatisticsCo-AuthorSimilar Experts

    By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选
    时间
    引用量
    主题
    期刊级别
    合作者
    合作机构
    All20252024202320222021202020192018201720162015201420132012201120102009200820072006
    Williams-Beuren Syndrome and Epilepsy: A Retrospective Analysis of 589 Patients
    Johanna Pohl, Harry Nuss,Almuth Caliebe,Angela Gosch, Elke Reutershahn,Rainer Pankau,Hiltrud Muhle
    JOURNAL OF CHILD NEUROLOGY (2025)
    Cited0Views1WOSBibtex
    0
    1
    Role of CACNG2 Variants in Human Pathology
    EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 496-496
    Cited0Views2Bibtex
    0
    2
    Expansion of the Symptoms Associated with Bi-Allelic Variants in TRAPPC12
    Inga Nagel, Michelle Meyenborg,Christel Eckmann-Scholz,Malte Spielmann,Almuth Caliebe
    EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 241-242
    Cited0Views0Bibtex
    0
    0
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    Author Statistics
    00.20.40.60.81#Papers#CitationH-IndexG-IndexSociabilityDiversityActivity

    #Papers: 104

    #Citation: 3487

    H-Index: 31

    G-Index: 57

    Sociability: 7

    Diversity: 3

    Activity: 53

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    • 合作者
    • 学生
    • 导师
    Reiner Siebert合作论文数
    Institut Für Humangenetik, Universitätsklinikum Ulm31
    Hiltrud Muhle合作论文数
    19
    Gabriele Gillessen-Kaesbach合作论文数
    16
    Bens Susanne合作论文数
    13
    Inga Nagel合作论文数
    Institut für Humangenetik, Christian-Albrechts-Universität zu Kiel13
    Ingo Helbig合作论文数
    University Medical Center Schleswig-Holstein Department of Neuropediatrics Kiel Campus12
    Malte Spielmann合作论文数
    Brigham and Women’s Hospital, Harvard Medical School12
    Ole Ammerpohl合作论文数
    12
    Paul-Martin Holterhus合作论文数
    10
    Inga Vater合作论文数
    9
    Ulrich Stephani合作论文数
    9
    Norbert Arnold合作论文数
    Univ Hosp Schleswig Holstein, Dept Gynecol & Obstet, Kiel, Germany8
    Christel Eckmann-Scholz合作论文数
    8
    Nadine Hornig合作论文数
    8
    Helbig Katherine L合作论文数
    8
    Dagmar Wieczorek合作论文数
    8
    Simone Heidemann合作论文数
    7
    McWalter Kirsty合作论文数
    7
    C Von Kaisenberg合作论文数
    7
    José Ignacio Martín-Subero合作论文数
    August Pi Sunyer Biomedical Research Institute, Hospital Clínic de Barcelona7
    Yorck Hellenbroich合作论文数
    7
    Amy Lacroix合作论文数
    6
    Dianne Laboy Cintron合作论文数
    6
    Rachel Westman合作论文数
    6
    Jennifer N. Dines合作论文数
    6
    Katie Golden-Grant合作论文数
    6
    Leah Fleming合作论文数
    6
    Jenny Thies合作论文数
    6
    Alice Basinger合作论文数
    6
    Dmitriy M. Niyazov合作论文数
    6
    Alison M Muir合作论文数
    Univ Washington, Dept Pediat, Div Med Genet, Seattle, WA 98195 USA6
    Amber Begtrup合作论文数
    Genedx, Inc.6
    Ganka Douglas合作论文数
    6
    Kolja Becker合作论文数
    6
    Megan T Cho合作论文数
    National Human Genome Research Institute, National Institutes of Health6
    Angela Sun合作论文数
    6
    Dalton Joline C合作论文数
    6
    Pendziwiat Manuela合作论文数
    6
    Kolarova Julia合作论文数
    6
    Millan Francisca合作论文数
    6
    Kautza Monika合作论文数
    6
    Holger Tonnies合作论文数
    6
    Heather C. Mefford合作论文数
    Department of pediatrics, Division of Genetic Medicine, University of Washington;Cell & Molecular Biology Department, Center for Pediatric Neurological Disease Research, St. Jude Children's Research Hospital;Medical Genetics Clinic, Seattle Children’s Hospital;Center for Integrative Brain Research, Seattle Children’s Hospital6
    Peter I. Karachunski合作论文数
    College of Biological Sciences, University of Minnesota6
    Can Ficicioglu合作论文数
    6
    René Santer合作论文数
    6
    Karin Buiting合作论文数
    Institut fur Humangenetik, Universitatsklinikum Essen, Essen, Germany;6
    J. Lawrence Merritt合作论文数
    6
    Kristin G. Monaghan合作论文数
    6
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