Marta Futema

9PUBLICATIONS
90CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cardiology (incl. cardiovascular diseases)Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsGene mapping
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Publications (9)

|Oct 10, 2026
The genetic landscape of myotonic dystrophy type 1: insights from nearly one million genomes.

|Aug 13, 2026
COPI Coatomer Regulates Several Steps of HDL Metabolism.

|Feb 10, 2026
Frequency of familial hypercholesterolaemia-causing genetic variants in the 100 000 Genomes Project cohort: whole genome sequencing analyses of 77 260 participants.

Marta Futema, Martin Bird, Ash Haeger

|Nov 14, 2025
Brugada Syndrome: an exemplar for the genomic basis of sudden death.

Rebecca L M Griffiths, Roddy Walsh, Marta Futema

|Jul 24, 2025
Novel start codon variant in the 5'UTR of LDLR associated with familial hypercholesterolaemia.

Martin Bird, Chris Jyun-Peng Tung, Alan M Pittman

|Feb 26, 2025
Rare disease gene association discovery in the 100,000 Genomes Project.

Valentina Cipriani, Letizia Vestito, Emma F Magavern

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Frequent Collaborators

3 joint publications

Elijah R Behr

2 joint publications

Steve E Humphries

2 joint publications

Grigorios Panteloglou

2 joint publications

Alaa Othman