Author

Mark Tullett

St Richard's Hospital

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

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:phylogenetics / evolution· 1

Frequent Co-Authors

David J. AdamsiD· 2 shared Ingrid FerreiraiD· 2 shared Alejandro Jiménez-SáncheziD· 1 shared Alethia Álvarez‐CanoiD· 1 shared Alfredo Hidalgo‐MirandaiD· 1 shared Amanda JiangiD· 1 shared Carla Daniela Robles‐EspinozaiD· 1 shared Christian Molina‐AguilariD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 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 papersGenetic & Genomic Medicine

David J. AdamsORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Ancestry and somatic profile predict acral melanoma origin and prognosis

Patricia Basurto‐Lozada, Martha Estefania Vázquez‐Cruz, Christian Molina‐Aguilar, Amanda Jiang, Dekker C. Deacon, Dennis Cerrato-Izaguirre, Irving Simonin Wilmer, Fernanda Guadalupe Arriaga-González, Kenya L. Contreras-Ramírez, Emiliano Ferro-Rodríguez, Jamie Billington, Eric T. Dawson, J. Rene C. Wong-Ramirez, Johana Itzel Ramos-Galguera, Alethia Álvarez‐Cano, , Carla Daniela Robles‐Espinoza

This study analyzes acral melanoma genomes and transcriptomes from Mexican patients, finding ancestry-related mutation patterns and survival differences.

medRxiv · Sep 21, 2024 · PreprintGenetic & Genomic Medicine

Multi-site clonality analyses uncovers pervasive subclonal heterogeneity and branching evolution across melanoma metastases

Roy Rabbie, Naser Ansari‐Pour, Oliver M. Cast, Doreen Lau, Francis Scott, Sarah Joanne Welsh, Christine Parkinson, Leila Khoja, Luiza Moore, Mark Tullett, Kim Wong, Ingrid Ferreira, Julia M. Martínez Gómez, Mitchell Paul Levesque, Ferdia Aidan Gallagher, , David J. Adams

The paper analyzes whole-genome sequencing data from melanoma metastases to show that branched evolution is common and that subclonal heterogeneity is prevalent in metastatic melanoma.

Nature Communications · Aug 27, 2020Peer-reviewedGenomics