Morghan C Lucas

16PUBLICATIONS
136CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cancer geneticsGene expression (incl. microarray and other genome-wide approaches)Cell and nuclear divisionPredictive and prognostic markers
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Publications (16)

|Aug 21, 2026
Toward the clinical application of long-read sequencing in repeat-expansion disorders.

|Mar 11, 2026
Validation structures for sequence variants of uncertain significance in hereditary cancer.

Morghan C Lucas, Thomas Keßler, Anna Benet-Pagès

|Dec 05, 2025
Improving genetic diagnosis of hereditary tumor syndromes: From expanded gene panels to functional genomics.

Mayra Sauer, Morghan C Lucas, Vitus Prokosch

|Sep 03, 2025
Repeat-associated ataxias in a German patient cohort analysed by targeted parallel long-read sequencing.

Hannes Erdmann, Annalisa Schaub, Morghan C Lucas

|May 03, 2025
A series of reviews in familial cancer: genetic cancer risk in context variants of uncertain significance in MMR genes: which procedures should be followed?

Morghan C Lucas, Thomas Keßler, Florentine Scharf

|Dec 20, 2024
Updated Structure of CNBP Repeat Expansions in Patients With Myotonic Dystrophy Type 2 and Its Implication for Standard Diagnostics.

Martin Wendlandt, Hannes Erdmann, Simone Rost

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Frequent Collaborators

5 joint publications

Thomas R Cox

5 joint publications

Eva Maria Novoa

4 joint publications

David Herrmann

4 joint publications

Paul Timpson