Marta Futema
8PUBLICATIONS
89CO-AUTHORS

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Publications (8)
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|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
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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
2 joint publications
Roger Meier
2 joint publications
Arnold von Eckardstein
2 joint publications
Simon F Norrelykke
2 joint publications
Alan M Pittman
2 joint publications
Jan Albert Kuivenhoven
2 joint publications
Bart van de Sluis