Items where authors include "Hoffmann, P"
Article
Fritz, N, Berens, S, Dong, Y et al. (52 more authors) (2022) The serotonin receptor 3E variant is a risk factor for female IBS-D. Journal of Molecular Medicine, 100 (11). pp. 1617-1627. ISSN 0946-2716
Ferrada, MA, Savic, S orcid.org/0000-0001-7910-0554, Ospina Cardona, D et al. (29 more authors) (2022) Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis. Blood, 140 (13). pp. 1496-1506. ISSN 0006-4971
Niemi, MEK, Karjalainen, J, Liao, RG et al. (3763 more authors) (2021) Mapping the human genetic architecture of COVID-19. Nature, 600 (7889). pp. 472-477. ISSN 0028-0836
Ferrada, MA, Sikora, KA, Luo, Y et al. (32 more authors) (2021) Somatic Mutations in UBA1 Define a Distinct Subset of Relapsing Polychondritis Patients With VEXAS. Arthritis and Rheumatology, 73 (10). pp. 1886-1895. ISSN 2326-5191
Beck, DB, Ferrada, MA, Sikora, KA et al. (59 more authors) (2020) Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease. New England Journal of Medicine. NEJMoa2026834. ISSN 0028-4793
Went, M, Sud, A, Speedy, H et al. (52 more authors) (2018) Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology. Blood Cancer Journal, 9. ARTN 1. ISSN 2044-5385
Vijayakrishnan, J, Studd, J, Broderick, P et al. (37 more authors) (2018) Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. Nature Communications, 9 (1). 1340. ISSN 2041-1723
Vijayakrishnan, J, Kumar, R, Henrion, MYR et al. (26 more authors) (2017) A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1. Leukemia, 31 (3). pp. 573-579. ISSN 0887-6924
Webb, TR, Erdmann, J, Stirrups, KE et al. (131 more authors) (2017) Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. Journal of the American College of Cardiology, 69 (7). pp. 823-836. ISSN 0735-1097
Vijayakrishnan, J, Kumar, R, Henrion, M Y R et al. (26 more authors) (2017) A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1. Leukemia. pp. 573-579. ISSN 0887-6924
Mitchell, JS, Li, N, Weinhold, N et al. (55 more authors) (2016) Genome-wide association study identifies multiple susceptibility loci for multiple myeloma. Nature Communications, 7. 12050.
Johnson, DC, Weinhold, N, Mitchell, J et al. (18 more authors) (2016) Genetic factors influencing the risk of multiple myeloma bone disease. Leukemia, 30 (4). pp. 883-888. ISSN 0887-6924
Johnson, DC, Weinhold, N, Mitchell, JS et al. (19 more authors) (2016) Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma. Nature Communications, 7. 10290.
Vijayakrishnan, J, Henrion, M, Moorman, AV et al. (24 more authors) (2015) The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A. Scientific Reports, 5. 15065. ISSN 2045-2322
Conference or Workshop Item
Ferrada, M, Savic, S, Alessi, H et al. (18 more authors) (2021) Genotype and Transfusion Dependence Predicts Mortality in VEXAS Syndrome, a Newly Described Disease with Overlap Inflammatory and Hematologic Features. In: ACR Convergence 2021, 05-09 Nov 2021, Virtual.
Proceedings Paper
Niesler, B, Hattensperger, N, Martinez, C et al. (43 more authors) (2018) The Serotonin receptor 3E subunit variant HTR3E c.*76G> A is confirmed as a risk factor for IBS- D in females. In: Neurogastroenterology and Motility. FNM 2018 – 3rd Meeting of the Federation of Neurogastroenterology and Motility, 29 Aug - 01 Sep 2018, Amsterdam, The Netherlands. Wiley .