Author

Laura T. Jiménez-Barrón

Max Planck Institute of PsychiatryORCID 0000-0002-6790-7366Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Laura T. Jiménez-Barrón1 paper

Biology Disciplines

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Developmental Biology· 1 Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Research Focus:variant effect prediction· 2 Assay:bulk RNA-seq· 1 Research Focus:fine-mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Lucia TrastullaiD· 2 shared Michael J. ZilleriD· 2 shared Vanessa MurekiD· 2 shared Alexander HerholtiD· 1 shared Anders Dupont BørglumiD· 1 shared Andrea Byrnes· 1 shared Andrew McQuilliniD· 1 shared Anna Hausruckinger· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Lucia TrastullaORCID

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3 papers

Recent·Most cited

Distinct genetic liability profiles define clinically relevant patient strata across common diseases

Lucia Trastulla, Georgii V. Dolgalev, Sylvain Moser, Laura T. Jiménez-Barrón, Till F. M. Andlauer, Moritz von Scheidt, Douglas M. Ruderfer, Stephan Ripke, Andrew McQuillin, Eli A. Stahl, Enrico Domenici, Rolf Adolfsson, Ingrid Agartz, Esben Agerbo, Margot Albus, , Thomas Folkmann Hansen

The paper identifies genetically distinct patient subgroups across diseases by analyzing polygenic risk and pathway convergence.

Nature Communications · Jul 1, 2024Peer-reviewedGenetic & Genomic Medicine

Cell type and condition specific functional annotation of schizophrenia associated non-coding genetic variants

Christine K. Rummel, Miriam Gagliardi, Alexander Herholt, Ruhel Ahmad, Vanessa Murek, Liesa Weigert, Anna Hausruckinger, Susanne Maidl, Laura T. Jiménez-Barrón, Lucia Trastulla, Mathias Eder, Moritz J. Rossner, Michael J. Ziller

The paper functionally annotates schizophrenia-associated non-coding variants by identifying cell type and condition specific molecular functions and target genes.

bioRxiv · Jun 27, 2023 · PreprintGenomics

Human-specific enrichment of schizophrenia risk-genes in callosal neurons of the developing neocortex

Emanuela Zuccaro, Vanessa Murek, Kwanho Kim, Hsu-Hsin Chen, Sara Mancinelli, Paul Oyler-Castrillo, Laura T. Jiménez-Barrón, Chiara Gerhardinger, Juliana R. Brown, Andrea Byrnes, Benjamin M. Neale, Joshua Z. Levin, Michael J. Ziller, Simona Lodato, Paola Arlotta

The paper identifies human-specific enrichment of schizophrenia risk genes in callosal neurons of the developing neocortex using comparative transcriptomic analysis across species and developmental stages.

bioRxiv · Sep 10, 2021 · PreprintDevelopmental Biology