Author

Anne Buttgereit

Bayer (Germany)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Assay:DNA methylation· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:clustering· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Concepción MarañóniD· 2 shared Elena Carnero‐MontoroiD· 2 shared Francesc Català‐MolliD· 2 shared Guillermo BartureniD· 2 shared Manuel Martínez‐BuenoiD· 2 shared María TerueliD· 2 shared Martin KerickiD· 2 shared Zuzanna Makowska· 2 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Concepción MarañónORCID

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2 papers

Recent·Most cited

Integrative Analysis Reveals a Molecular Stratification of Systemic Autoimmune Diseases

Guillermo Barturen, Sepideh Babaei, Francesc Català‐Moll, Manuel Martínez‐Bueno, Zuzanna Makowska, Jordi Martorell‐Marugán, Pedro Carmona‐Sáez, Daniel Toro Dominguez, Elena Carnero‐Montoro, María Teruel, Martin Kerick, Marialbert Acosta‐Herrera, Lucas Le Lann, Christophe Jamin, Javier Rodríguez‐Ubreva, , Montserrat Alvarez

The paper identifies four molecular clusters in systemic autoimmune diseases using transcriptome and methylome data, showing three stable aberrant patterns and one non-specific cluster.

Arthritis & Rheumatology · Dec 8, 2020Peer-reviewedGenetic & Genomic Medicine

An integrative multi-omics approach in Sjogrens Syndrome identifies novel genetic drivers with regulatory function and disease-specificity

María Teruel, Guillermo Barturen, Manuel Martínez‐Bueno, Miguel Barroso, Olivia Castelli, Elena Povedano, Martin Kerick, Francesc Català‐Moll, Zuzanna Makowska, Anne Buttgereit, PRECISESADS Flow Cytometry Study Group, Jacques‐Olivier Pers, Concepción Marañón, Esteban Ballestar, Javier J. Martin, , Marta Eugenia Alarcón-Riquelme

This study identifies novel genetic drivers in Sjogrens Syndrome through an integrative multi-omics approach, revealing epigenetic signatures and regulatory variants associated with the disease.

medRxiv · Sep 14, 2020 · PreprintGenetic & Genomic Medicine