Author

Marion B. Kiechle

TUM KlinikumORCID 0000-0003-4237-2657Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Bioengineering· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Research Focus:cell type annotation· 1 Assay:imaging· 1 Approach:microscopy & imaging analysis· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alison M. DunningiD· 1 shared Anders KvistiD· 1 shared Andrea S. VendrameiD· 1 shared Andreas HadjisavvasiD· 1 shared Anna González‐NeiraiD· 1 shared Anna PukalukiD· 1 shared Arnaud DroitiD· 1 shared Audrey Y. JungiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 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

1 shared paperGenetic & Genomic Medicine

Alison M. DunningORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

A General High-throughput Mucus Microrheology Platform for Quantitative and Scalable Mucus Phenotyping

Feng Ling, Ayşe Tuğçe Şahin, Bernardo Miller Naranjo, Stefano Aime, Doris Roth, Anna Pukaluk, Niels Tepho, Romina Augustin, Benedetta Zampa, Andrea S. Vendrame, Mark-Christian Klassen, Ellen Emken, Marion B. Kiechle, Mircea Gabriel Stoleriu, Pontus Mertsch, , Janna C. Nawroth

This paper introduces a high-throughput mucus microrheology platform using Differential Dynamic Microscopy to quantify mucus properties across various conditions and applications.

Advanced Science · Sep 28, 2026Peer-reviewedBioengineering

Exome sequencing identifies novel susceptibility genes and defines the contribution of coding variants to breast cancer risk.

Naomi Wilcox, Martine Dumont, Anna González‐Neira, Sara Carvalho, Charles Joly Beauparlant, Marco Crotti, Craig Luccarini, Penny Soucy, Stéphane Dubois, Rocío Núñez‐Torres, Guillermo Pita, M. Rosario Alonso, Núria Álvarez, Caroline Baynes, Heiko Becher, , Jacques Simard

The paper uses whole-exome sequencing data to identify novel breast cancer susceptibility genes and assess the contribution of coding variants to breast cancer risk.

medRxiv · Jun 17, 2022 · PreprintGenetic & Genomic Medicine