Depth of Sequencing Plays a Determining Role in the Characterization of Phage Display Peptide Libraries by NGS by Ane Beth Sloth, Babak Bakhshinejad, Camilla Stavnsbjerg, Maria Rossing, Andreas Kjaer

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Highly impaired platelet ultrastructure in two families with novel IKZF5 variants by Eva Leinoe, Mimi Kjaersgaard, Eva Zetterberg, Sisse Ostrowski, Andreas Greinacher, Maria Rossing

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Germline RET Leu56Met Variant Is Likely Not Causative of Multiple Endocrine Neoplasia Type 2 by Anna Reimer Hansen, Line Borgwardt, Åse Krogh Rasmussen, Christian Godballe, Christian Godballe, Morten Møller Poulsen, Filipe G. Vieira, Jes Sloth Mathiesen, Jes Sloth Mathiesen, Maria Rossing, Maria Rossing

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uPAR (PLAUR) Marks Two Intra-Tumoral Subtypes of Glioblastoma: Insights from Single-Cell RNA Sequencing by Yue He, Kristina B. V. Døssing, Maria Rossing, Frederik Otzen Bagger, Andreas Kjaer

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Amplicon-Based NGS Panels for Actionable Cancer Target Identification in Follicular Cell-Derived Thyroid Neoplasia by Majbritt Busk Madsen, Katalin Kiss, Finn Cilius Nielsen, Finn Noe Bennedbæk, Maria Rossing

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Detection of circulating tumor-derived material in peripheral blood of pediatric sarcoma patients: A systematic review by Eva Kristine Ruud Kjær, Christian Bach Vase, Maria Rossing, Lise Barlebo Ahlborn, Lisa Lyngsie Hjalgrim

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A novel homozygous GFI1B variant in 2 sisters with thrombocytopenia and severe bleeding tendency by Nanna Brøns, Carlo Zaninetti, Sisse Rye Ostrowski, Jesper Petersen, Andreas Greinacher, Maria Rossing, Eva Leinøe

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Quantitative Evaluation of Stem-like Markers of Human Glioblastoma Using Single-Cell RNA Sequencing Datasets by Yue He, Kristina B. V. Døssing, Ane Beth Sloth, Xuening He, Maria Rossing, Andreas Kjaer

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Genotype–phenotype associations in PPGLs in 59 patients with variants in SDHX genes by Ailsa Maria Main, Maria Rossing, Line Borgwardt, Birgitte Grønkær Toft, Åse Krogh Rasmussen, Ulla Feldt-Rasmussen

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Analysis of Compositional Bias in a Commercial Phage Display Peptide Library by Next-Generation Sequencing by Ane Beth Sloth, Babak Bakhshinejad, Malte Jensen, Camilla Stavnsbjerg, Mikkel Baldtzer Liisberg, Maria Rossing, Andreas Kjaer

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Germline heterozygous variants in genes associated with familial hemophagocytic lymphohistiocytosis as a cause of increased bleeding by Marcus Fager Ferrari, Eva Leinoe, Maria Rossing, Eva Norström, Karin Strandberg, Tobias Steen Sejersen, Klaus Qvortrup, Eva Zetterberg

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Severe Congenital Thrombocytopenia Characterized by Decreased Platelet Sialylation and Moderate Complement Activation Caused by Novel Compound Heterozygous Variants in GNE by Karolina I. Smolag, Marcus Fager Ferrari, Eva Zetterberg, Eva Leinoe, Torben Ek, Anna M. Blom, Maria Rossing, Myriam Martin

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Prevalence of Pathogenic Germline DICER1 Variants in Young Individuals Thyroidectomised Due to Goitre – A National Danish Cohort by Mays Altaraihi, Thomas van Overeem Hansen, Eric Santoni-Rugiu, Maria Rossing, Åse Krogh Rasmussen, Anne-Marie Gerdes, Karin Wadt

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Building flexible and robust analysis frameworks for molecular subtyping of cancers by Christina Bligaard Pedersen, Benito Campos, Lasse Rene, Helene Scheel Wegener, Neeraja M. Krishnan, Binay Panda, Kristoffer Vitting‐Seerup, Maria Rossing, Frederik Otzen Bagger, Lars Rønn Olsen

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Importance of Comprehensive Molecular Profiling for Clinical Outcome in Children With Recurrent Cancer by Olga Østrup, Karsten Nysom, David Scheie, Ane Y. Schmidt, Rene Mathiasen, Lisa L. Hjalgrim, Tina E. Olsen, Jane Skjøth-Rasmussen, Birthe M. Henriksen, Finn C. Nielsen, Peder S. Wehner, Henrik Schrøder, Astrid M. Sehested, Catherine Rechnitzer, Maria Rossing

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Adrenal suppression in patients with chronic obstructive pulmonary disease treated with glucocorticoids: Role of specific glucocorticoid receptor polymorphisms. by Pradeesh Sivapalan, Stina Willemoes Borresen, Josefin Eklöf, Marianne Klose, Freja S Holm, Ulla Feldt-Rasmussen, Maria Rossing, Niklas R Jørgensen, Rasmus L Marvig, Mohamad Isam Saeed, Torgny Wilcke, Niels Seersholm, Alexander G Mathioudakis, Jørgen Vestbo, Jens-Ulrik Stæhr Jensen

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Case Report: Giant Paraganglioma of the Skull Base With Two Somatic Mutations in SDHB and PTEN Genes by Ailsa Maria Main, Ailsa Maria Main, Götz Benndorf, Götz Benndorf, Ulla Feldt-Rasmussen, Ulla Feldt-Rasmussen, Kåre Fugleholm, Thomas Kistorp, Anand C. Loya, Anand C. Loya, Lars Poulsgaard, Åse Krogh Rasmussen, Maria Rossing, Christine Sølling, Marianne Christina Klose

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Replication of newly proposed TNM staging system for medullary thyroid carcinoma: a nationwide study by Jes Sloth Mathiesen, Jens Peter Kroustrup, Peter Vestergaard, Per Løgstrup Poulsen, Åse Krogh Rasmussen, Ulla Feldt-Rasmussen, Sten Schytte, Stefano Christian Londero, Henrik Baymler Pedersen, Christoffer Holst Hahn, Jens Bentzen, Sören Möller, Mette Gaustadnes, Maria Rossing, Finn Cilius Nielsen, Kim Brixen, Christian Godballe

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A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data by Migle Gabrielaite, Mathias Husted Torp, Malthe Sebro Rasmussen, Sergio Andreu-Sánchez, Filipe Garrett Vieira, Christina Bligaard Pedersen, Savvas Kinalis, Majbritt Busk Madsen, Miyako Kodama, Gül Sude Demircan, Arman Simonyan, Christina Westmose Yde, Lars Rønn Olsen, Rasmus L. Marvig, Olga Østrup, Maria Rossing, Finn Cilius Nielsen, Ole Winther, Frederik Otzen Bagger

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Incidence and prevalence of sporadic and hereditary MTC in Denmark 1960–2014: a nationwide study by Jes Sloth Mathiesen, Jens Peter Kroustrup, Peter Vestergaard, Kirstine Stochholm, Per Løgstrup Poulsen, Åse Krogh Rasmussen, Ulla Feldt-Rasmussen, Sten Schytte, Stefano Christian Londero, Henrik Baymler Pedersen, Christoffer Holst Hahn, Bjarki Ditlev Djurhuus, Jens Bentzen, Sören Möller, Mette Gaustadnes, Maria Rossing, Finn Cilius Nielsen, Kim Brixen, Anja Lisbeth Frederiksen, Christian Godballe

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