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Jamie Trotman

10PUBLICATIONS
27CO-AUTHORS
Molecular targetsNeurosciences not elsewhere classifiedGenetic immunologyGenomicsNeurogenetics
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Journal

Publications (10)

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|Apr 24, 2026
Somatic PLCG1 Mutation in a Vascular Tumor of an Infant.

|Apr 25, 2025
Mediastinal NUT Carcinoma With Raised Serum Alpha-Fetoprotein Mimicking a Malignant Germ Cell Tumor: Suspicion Raised Due to Negative Serum miR-371a-3p Levels.

Sheng-Yuan Kan, Cinzia G Scarpini, Dawn Ward

|Apr 19, 2025
Congenital Langerhans Cell Histiocytosis With Novel KLC1::RAF1 Gene Fusion Identified Through Routine Whole-Genome Sequencing.

Fiona E Wright, Gemma Barnard, Shivani Bailey

|Apr 14, 2025
Lingual hamartoma-like lipoblastoma: the diagnostic value of routine whole-genome sequencing.

Sheng-Yuan Kan, Ashley Ferro, James A Watkins

|Oct 09, 2024
A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumor.

Shathar Mahmood, Sarah M Leiter, Poe Phyu

|Jul 12, 2024
Introduction and impact of routine whole genome sequencing in the diagnosis and management of sarcoma.

James A Watkins, Jamie Trotman, John A Tadross

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Frequent Collaborators

6 joint publications

Matthew J Murray

4 joint publications

John A Tadross

3 joint publications

Sam Behjati

3 joint publications

Patrick Tarpey

3 joint publications

Sarah M Leiter

3 joint publications

Catherine E Hook

3 joint publications

James Watkins

2 joint publications

G A Amos Burke

2 joint publications

Sheng-Yuan Kan

1 joint publications

Rebecca Green

Frequent Collaborators

6 joint publications

Matthew J Murray

4 joint publications

John A Tadross

3 joint publications

Sam Behjati

3 joint publications

Patrick Tarpey

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