Marta Futema

7PUBLICATIONS
68CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsCardiology (incl. cardiovascular diseases)Gene mappingEpigenetics (incl. genome methylation and epigenomics)
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Publications (7)

|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

|Nov 12, 2024
Variants in LPA are associated with familial hypercholesterolaemia: whole genome sequencing analysis in the 100 000 Genomes Project.

Martin Bird, Antoine Rimbert, Alan Michael Pittman

|Jul 06, 2023
Prevalence of FH-Causing Variants and Impact on LDL-C Concentration in European, South Asian, and African Ancestry Groups of the UK Biobank-Brief Report.

Jasmine Gratton, Steve E Humphries, Marta Futema

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Frequent Collaborators

3 joint publications

Elijah R Behr

2 joint publications

Alan M Pittman

2 joint publications

Martin Bird

1 joint publications

Roddy Walsh