Prevalence of familial hypercholesterolaemia (FH)-causing variants and impact on LDL-C concentration in European, South Asian, and African ancestry groups of the UK Biobank av J. Gratton, S.E. Humphries, M. Futema

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How many individuals with Familial Hypercholesterolaemia (FH) need to be identified to achieve the NHS 2019 Long Term Plan ambition? av S.E. Humphries, J.Gratton, K. Haralambos, M. Futema

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Genomic Research to Identify Novel Pathways in the Development of Abdominal Aortic Aneurysm av Seamus C. Harrison, Anastasia Z. Kalea, Michael V. Holmes, Obi Agu, Steve E. Humphries

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Genome-Wide DNA Methylation in Mixed Ancestry Individuals with Diabetes and Prediabetes from South Africa av Tandi E. Matsha, Carmen Pheiffer, Stephen E. Humphries, Junaid Gamieldien, Rajiv T. Erasmus, Andre P. Kengne

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Oceanic adults, coastal juveniles: tracking the habitat use of whale sharks off the Pacific coast of Mexico av Dení Ramírez-Macías, Nuno Queiroz, Simon J. Pierce, Nicolas E. Humphries, David W. Sims, Juerg M. Brunnschweiler

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Comparing the performance of the novel FAMCAT algorithms and established case-finding criteria for familial hypercholesterolaemia in primary care av Joe Kai, Nadeem Qureshi, Stephen Weng, Ralph K Akyea, Jo Leonardi-Bee, Steve E Humphries, Brittany Dutton

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Modelling a two-stage adult population screen for autosomal dominant familial hypercholesterolaemia: cross-sectional analysis within the UK Biobank av Joan K Morris, Reecha Sofat, Steve E Humphries, Marta Futema, Amand Floriaan Schmidt, Chris Finan, Jasmine Gratton

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Immunological Aspects of Chytridiomycosis av Laura F. Grogan, Josephine E. Humphries, Jacques Robert, Chantal M. Lanctôt, Catherine J. Nock, David A. Newell, Hamish I. McCallum

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Higher Responsiveness to Rosuvastatin in Polygenic versus Monogenic Hypercholesterolemia: A Propensity Score Analysis av Agnieszka Mickiewicz, Marta Futema, Agnieszka Ćwiklinska, Agnieszka Kuchta, Maciej Jankowski, Mariusz Kaszubowski, Magdalena Chmara, Bartosz Wasąg, Marcin Fijałkowski, Miłosz Jaguszewski, Steve E. Humphries, Marcin Gruchała

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How many FH genetic tests were performed by the UK Genetic Laboratory Hubs in 2022? av S.E. Humphries, R. Challis, K. Downes, E. Howard, T. Legerton, C. Macanulty, S. Morgan, A. O’Rouke, D. O’Sullivan, A. Taylor-Beadling, E. Thompson, E. Watson, G. Norbury

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Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays. av Andrew J P Smith, Philip Howard, Sonia Shah, Per Eriksson, Stefan Stender, Claudia Giambartolomei, Lasse Folkersen, Anne Tybjærg-Hansen, Meena Kumari, Jutta Palmen, Aroon D Hingorani, Philippa J Talmud, Steve E Humphries

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Measuring deoxygenation effects on marine predators: A new animal‐attached archival tag recording in situ dissolved oxygen, temperature, fine‐scale movements and behaviour av Ivo daCosta, David W. Sims, Bruno Loureiro, Matt J. Waller, Freya C. Womersley, Alexandra Loveridge, Nicolas E. Humphries, Emily J. Southall, Marisa Vedor, Gonzalo Mucientes, Sophie Prendergast, Jorge Fontes, Pedro Afonso, Bruno C. L. Macena, Yuuki Y. Watanabe, Nuno Queiroz

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Alternative cascade-testing protocols for identifying and managing patients with familial hypercholesterolaemia: systematic reviews, qualitative study and cost-effectiveness analys... av Nadeem Qureshi, Bethan Woods, Rita Neves de Faria, Pedro Saramago Goncalves, Edward Cox, Jo Leonardi-Bee, Laura Condon, Stephen Weng, Ralph K Akyea, Barbara Iyen, Paul Roderick, Steve E Humphries, William Rowlands, Melanie Watson, Kate Haralambos, Ryan Kenny, Dev Datta, Zosia Miedzybrodzka, Christopher Byrne, Joe Kai

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