Professur für Diagnostische Molekularpathologie


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

Distinct genetic alterations and luminal molecular subtype in nested variant of urothelial carcinoma (2019) Weyerer V, Weisser R, Moskalev E, Haller F, Stoehr R, Eckstein M, Zinnall U, et al. Journal article Tumour mutational burden analysis: implementation in routine diagnostics (2019) Kroeze L, Kamping E, Von Rhein D, Jansen E, De Voer R, Barberis M, Botling J, et al. Conference contribution Frequency of GNAS mutation in intramuscular myxoma (2019) Erber R, Stöhr R, Haller F, Hartmann A, Agaimy A Conference contribution Digit ratio (2D:4D) and academic success as measured by achievement in the academic degree "Habilitation" (2019) Tektas OY, Kapsner L, Lemmer M, Bouna-Pyrrou P, Lewczuk P, Lenz B, Kornhuber J Journal article Successful targeting of BRAF V600E mutation with vemurafenib in a treatment-resistant extragonadal non-seminomatous germ cell tumor (2019) Meintker L, Haller F, Tögel L, Schmidt D, Waibel H, Mackensen A, Meidenbauer N Conference contribution Report of the working group on molecular pathology Bericht der Arbeitsgemeinschaft Molekularpathologie (2019) Haller F, Lassmann S, Siebolts U Journal article Coding and Non-coding: Molecular Portrait of GIST and its Clinical Implication (2018) Bure I, Haller F, Zaletaev DV Journal article Transcriptome and protein interaction profiling in cancer cells with mutations in histone H3.3 (2018) Lim J, Park JH, Baude A, Fellenberg J, Zustin J, Haller F, Kruecken I, et al. Journal article Recurrent Mutations within the Amino-Terminal Region of ?-Catenin Are Probable Key Molecular Driver Events in Sinonasal Hemangiopericytoma (2015) Haller F, Bieg M, Moskalev E, Barthelmeß S, Geddert H, Boltze C, Diessl N, et al. Journal article Solitary fibrous tumors/hemangiopericytomas with different variants of the NAB2-STAT6 gene fusion are characterized by specific histomorphology and distinct clinicopathological features (2014) Barthelmeß S, Geddert H, Boltze C, Moskalev E, Bieg M, Sirbu H, Brors B, et al. Journal article