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Massive parallel sequencing of head and neck conventional squamous cell carcinomas: A comprehensive review

2024 . Nadal, Alfons | Cardesa, Antonio | Agaimy, Abbas | Almangush, Alhadi | Franchi, Alessandro | Hellquist, Henrik | Leivo, Ilmo | Zidar, Nina | Ferlito, Alfio

Implementation of circulating tumour DNA multi-target mutation testing in plasma: a perspective from an external quality assessment providers’ survey

2023 . Fairley, Jennifer A. | Badrick, Tony | Denis, Marc G. | Dimitrova, Lora | Goodall, Rebecca | Maas, Joerg | Normanno, Nicola | Patton, Simon J. | Rouleau, Etienne | Russo, Antonio | Stockley, Tracy L. | Deans, Zandra

Mutational status may supersede tumor size in predicting the presence of aggressive pathologic features in well differentiated thyroid cancer

2022 . Semsar-Kazerooni, Koorosh | Morand, Grégoire B. | Payne, Alexandra E. | da Silva, Sabrina D. | Forest, Véronique-Isabelle | Hier, Michael P. | Pusztaszeri, Marc P. | Tamilia, Michael | Payne, Richard J.

SWI/SNF-deficient undifferentiated/rhabdoid carcinoma of the gallbladder carrying a POLE mutation in a 30-year-old woman: a case report

2021 . Gerber, Tiemo S. | Agaimy, Abbas | Hartmann, Arndt | Habekost, Michael | Roth, Wilfried | Stenzinger, Albrecht | Schirmacher, Peter | Straub, Beate K.

Spatial distance between sites of sampling associated with genetic variation among Neospora caninum in aborted bovine foetuses from northern Italy

2021 . Villa, Luca | Maksimov, Pavlo | Luttermann, Christine | Tuschy, Mareen | Gazzonis, Alessia Libera | Zanzani, Sergio | MORTARINO, MICHELE | Conraths, Franz | Manfredi, Maria Teresa | Schares, Gereon R. M.

Classification of NF1 microdeletions and its importance for establishing genotype/phenotype correlations in patients with NF1 microdeletions

2021 . Kehrer-Sawatzki, Hildegard | Cooper, David N.

A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects

2021 . Markus, Fenja | Kannengießer, Annika | Näder, Patricia | Atigbire, Paul | Scholten, Alexander | Vössing, Christine | Bültmann, Eva | Korenke, G. Christoph | Owczarek-Lipska, Marta | Neidhardt, John

Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxia

2021 . Nolte, Dagmar | Kang, Jun-Suk | Hofmann, Amrei | Schwaab, Eva | Krämer, Heidrun H. | Müller, Ulrich

Factor IX p.A37V mutation causes severe bleeding in a patient with phenprocoumon therapy

2021 . Mülling, Nils | Rosery, Vivian | Reinhardt, H. Christian | Hanoun, Maher

A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutations

2021 . Hartung, Benno | Tank, Anne | Dittmann, Sven | Ritz-Timme, Stefanie | Schulze-Bahr, Eric

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