Concepedia

Author

Andreas Schlattl

Boehringer Ingelheim (Austria)ORCID

Also Known As

Andreas Schlattl, Schlattl, Andreas

51

Publications

6K

Citations

13

H-Index

29

Concepts

All Affiliations

Boehringer Ingelheim (Austria)European Bioinformatics InstituteEuropean Molecular Biology LaboratoryMedical University of ViennaResearch Institute of Molecular Pathology
AS

About

Andreas Schlattl is an author at Boehringer Ingelheim (Austria) specializing in cell biology, medicine, and tumor biology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

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325

2

Cell Biology

4

4

325

3

Pathology

2

2

224

4

Health Sciences

1

1

135

5

Molecular Genetics

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57

Andreas Schlattl

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13

Publications

6K

Citations

13

H-Index

YearCitations

DELLY: structural variant discovery by integrated paired-end and split-read analysis

Tobias Rausch, Thomas Zichner, Andreas Schlattl,

Bioinformatics

2012

2.6K

An integrated map of structural variation in 2,504 human genomes

Peter H. Sudmant, Tobias Rausch, Eugene J. Gardner,

Nature

2015

2.6K

Werner syndrome helicase is a selective vulnerability of microsatellite instability-high tumor cells

Simone Lieb, Silvia Blaha-Ostermann, Elisabeth Kamper,

eLife

2019

135

Synthetic lethality between the cohesin subunits STAG1 and STAG2 in diverse cancer contexts

Petra van der Lelij, Simone Lieb, Julian Jude,

eLife

2017

127

Relating CNVs to transcriptome data at fine resolution: Assessment of the effect of variant size, type, and overlap with functional regions

Andreas Schlattl, Simon Anders, Sebastian M. Waszak,

Genome Research

2011

117

The Baker's Yeast Diploid Genome Is Remarkably Stable in Vegetative Growth and Meiosis

Koodali T Nishant, Wu Wei, Eugenio Mancera,

PLoS Genetics

2010

104

A Novel RAF Kinase Inhibitor with DFG-Out–Binding Mode: High Efficacy in BRAF-Mutant Tumor Xenograft Models in the Absence of Normal Tissue Hyperproliferation

Irene C. Waizenegger, Anke Baum, Steffen Steurer,

Molecular Cancer Therapeutics

2016

89

Systematic Inference of Copy-Number Genotypes from Personal Genome Sequencing Data Reveals Extensive Olfactory Receptor Gene Content Diversity

Sebastian M. Waszak, Yehudit Hasin-Brumshtein, Thomas Zichner,

PLoS Computational Biology

2010

63

Interrogation of cancer gene dependencies reveals paralog interactions of autosome and sex chromosome-encoded genes

Anna Köferle, Andreas Schlattl, Alexandra Hörmann,

Cell Reports

2022

57

SMARCA2-deficiency confers sensitivity to targeted inhibition of SMARCA4 in esophageal squamous cell carcinoma cell lines

Katharina Ehrenhöfer-Wölfer, Teresa Puchner, Cornelia Schwarz,

Scientific Reports

2019

49

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