Author

Nazan Puluca

Deutsches Herzzentrum MünchenORCID 0000-0003-2605-1247Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Cell Biology· 1 Developmental Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Assay:scRNA-seq· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Claudia Abou‐Ajram· 2 shared Elisa Mastantuono· 2 shared Harald LahmiD· 2 shared Irina Neb· 2 shared Julie CleuziouiD· 2 shared Lutz HeiniD· 2 shared Markus KraneiD· 2 shared Martina DreßeniD· 2 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersDevelopmental Biology

Claudia Abou‐Ajram

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Cell BiologySciencePeer-reviewedMay 12, 2022

The Tabula Sapiens: a multiple organ single cell transcriptomic atlas of humans

Robert C. Jones, Jim Karkanias, Mark A. Krasnow…·Andrea R. Yung

Nearly 500,000 cells from 24 human tissues, many from one donor, characterize over 400 cell types and enable within-donor study of T-cell clones, B-cell mutation rates and splicing.

1,058 citationstop 1%

humanscRNA-seq

𝕏 PostBluesky

Developmental BiologyCirculationPeer-reviewedOct 25, 2021

Sequential defects in cardiac lineage commitment and maturation cause hypoplastic left heart syndrome

Markus Krane, Martina Dreßen, Gianluca Santamaria…·Alessandra Moretti

This study identifies sequential defects in cardiac lineage commitment and maturation in hypoplastic left heart syndrome using multi-omics approaches and iPSC modeling.

62 citations

humanwhole-exome sequencing

𝕏 PostBluesky

GenomicsJournal of Clinical InvestigationPeer-reviewedNov 17, 2020

Genome-wide association study in European patients with congenital heart disease identifies risk loci for transposition of the great arteries and anomalies of the thoracic arteries and veins and expression of discovered candidate genes in the developing heart

Harald Lahm, Meiwen Jia, Martina Dreßen…·Markus Krane

This study identifies genetic risk loci for congenital heart disease subtypes and shows candidate genes play essential roles in heart development.

112 citationstop 4%

humanGWAS summary statistics

𝕏 PostBluesky