Research
Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank
BMJ 2019; 364 doi: https://doi.org/10.1136/bmj.k5222 (Published 16 January 2019) Cite this as: BMJ 2019;364:k5222Linked opinion
Haemochromatosis is linked to more disease than previously thought
Data supplement
Web extra
- Data Supplement - Supplementary information: additional methods, results, and figures, including a link to additional tables
Related articles
- News Published: 24 January 2019; BMJ 364 doi:10.1136/bmj.l320
- Correction Published: 23 October 2019; BMJ 367 doi:10.1136/bmj.l6157
- Practice Published: 26 July 2023; BMJ 382 doi:10.1136/bmj-2023-076750
See more
- Introductory AddressProv Med Surg J October 03, 1840, s1-1 (1) 1-4; DOI: https://doi.org/10.1136/bmj.s1-1.1.1
- Report of the Meeting of the Eastern Branch of the Provincial Association at Bury St. Edmond'sProv Med Surg J October 03, 1840, s1-1 (1) 10-13; DOI: https://doi.org/10.1136/bmj.s1-1.1.10
- Mr. Warburton's Bill for the Regulation of the Medical ProfessionProv Med Surg J October 03, 1840, s1-1 (1) 13-15; DOI: https://doi.org/10.1136/bmj.s1-1.1.13
- An Atlas of Plates, illustrative of the Principles and Practice of Obstetric Medicine and Surgery, with descriptive LetterpressProv Med Surg J October 03, 1840, s1-1 (1) 4; DOI: https://doi.org/10.1136/bmj.s1-1.1.4
- A Practical Treatise on the Diseases peculiar to Women, illustrated by Cases, &cProv Med Surg J October 03, 1840, s1-1 (1) 4-5; DOI: https://doi.org/10.1136/bmj.s1-1.1.4-a
Cited by...
- Prospective cohort for early detection of liver cancer (Pearl): a study protocol
- HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank
- Targeting PKC alleviates iron overload in diabetes and hemochromatosis
- HFE genotypes, haemochromatosis diagnosis status and clinical penetrance to age 80 in the UK Biobank community cohort
- Managing raised ferritin in primary care
- Haemochromatosis genetic variants and musculoskeletal outcomes: 11.5 year follow-up in the UK Biobank cohort study
- Haemochromatosis genetic variants and musculoskeletal outcomes: 11.5 year follow-up in the UK Biobank cohort study
- Haemochromatosis genetic variants and musculoskeletal outcomes: 11.5 year follow-up in the UK Biobank cohort study
- Selection bias as an explanation for the observed protective association of childhood adiposity with breast cancer
- Causal associations between iron status and sepsis: a Mendelian randomisation analysis
- Penetrance of HFE haemochromatosis variants to clinical disease: polygenic risk score associations in UK Biobank
- Hereditary haemochromatosis beyond liver cancer: increased risk of prostate cancer during an 11-year follow-up
- Relating Global and Local Connectome Changes to Dementia and Targeted Gene Expression in Alzheimers Disease
- Hemochromatosis mutations, dementia and brain iron deposition: a prospective cohort study
- The undiagnosed disease burden associated with alpha-1 antitrypsin deficiency genotypes
- Seven days in medicine: 16-22 January 2019