Gunnar Schmidt - Institut für Humangenetik, Medizinische Hochschule Hannover

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论文共 51 篇作者统计合作学者相似作者

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Limitations in Next-Generation Sequencing-Based Genotyping of Breast Cancer Polygenic Risk Score Loci

Alexandra Baumann,Christian Ruckert, Christoph Meier, Tim Hutschenreiter,Robert Remy, Benedikt Schnur, Marvin Doebel, Rudel Christian Nkouamedjo Fankep,Dariush Skowronek, Oliver Kutz,Norbert Arnold, Anna-Lena Katzke,Michael Forster, Anna-Lena Kobiela, Katharina Thiedig,Andreas Zimmer,Julia Ritter,Bernhard H. F. Weber,Ellen Honisch,Karl Hackmann,Gunnar Schmidt,Marc Sturm,Corinna Ernst, Marvin Dobel,Stephan Drukewitz,Christoph Engel,Peter Frommolt,Eva Gross,Johannes Helmuth, Zarah Kowalzyk,Maximilian Radtke,Juliane Ramser, Steffen Uebe,Shan Wang-Gohrke

EUROPEAN JOURNAL OF HUMAN GENETICSno. 8 (2024): 987-997

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Germline Variants in Patients Developing Second Malignant Neoplasms after Therapy for Pediatric Acute Lymphoblastic Leukemia—a Case-Control Study

Stefanie V. Junk,Alisa Förster,Gunnar Schmidt,Martin Zimmermann,Birthe Fedders, Bernd Haermeyer,Anke K. Bergmann,Anja Möricke,Gunnar Cario,Bernd Auber,Martin Schrappe,Christian P. Kratz,Martin Stanulla

LEUKEMIAno. 4 (2024): 887-892

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Corrigendum: Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1

Manfred Anim,Georgios Sogkas,Gunnar Schmidt,Natalia Dubrowinskaja,Torsten Witte,Reinhold Ernst Schmidt,Faranaz Atschekzei

Frontiers in immunology (2023): 1212029-1212029

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Comparison of Methylation Estimates Obtained Via MinION Nanopore Sequencing and Sanger Bisulfite Sequencing in the TRPA1 Promoter Region

Sara Gombert,Kirsten Jahn,Hansi Pathak,Alexandra Burkert,Gunnar Schmidt,Lutz Wiehlmann,Colin Davenport,Björn Brändl,Franz-Josef Müller,Andreas Leffler,Maximilian Deest,Helge Frieling

BMC Medical Genomicsno. 1 (2023)

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Mobile element insertions as potential cancer predisposition in high-risk HBOC patients

Janin Klein,Annette Otto, Gina Kastens,Gunnar Schmidt,Thilo Doerk,Brigitte Schlegelberger,Doris Steinemann,Winfried Hofmann

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 571-571

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Diagnostic Genomic Sequencing in Critically Ill Children

Bernd Auber,Gunnar Schmidt,Chen Du,Sandra von Hardenberg

MEDIZINISCHE GENETIKno. 2 (2023): 105-113

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Parallel Deletion and Duplication at 7q11.23 in a Silent Carrier for Two Reciprocal Syndromic Disorders

Jonathan Lukas Luehmann,Gunnar Schmidt,Bernd Auber,Anke Katharina Bergmann,Oliver Brandau, Anja Louis, Sabine Hentze, Katrin Eisfeld,Brigitte Schlegelberger,Ruediger Klaes,Doris Steinemann

American Journal of Medical Genetics Part A（2023）

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A holistic approach to maximise diagnostic output in trio exome sequencing

Sandra von Hardenberg,Hannah Wallaschek,Chen Du,Gunnar Schmidt,Bernd Auber

Frontiers in pediatrics (2023): 1183891-1183891

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A Novel Alu Element Insertion in ATM Induces Exon Skipping in Suspected HBOC Patients

Janin Klein,Aldrige B. B. Allister,Gunnar Schmidt,Annette Otto, Kai Heinecke, Jordis Bax-Knoche,Carmela Beger, Sarah Becker,Stephan Bartels,Tim Ripperger,Jens Bohne,Thilo Doerk,Brigitte Schlegelberger,Winfried Hofmann,Doris Steinemann

Human Mutation（2023）

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