Items where authors include "Brennan, P."

Article

Stafford-Smith, B., Gurasashvili, J., Peter, M. et al. (19 more authors) (2024) “I’m quite proud of how we’ve handled it”: health professionals’ experiences of returning additional findings from the 100,000 genomes project. European Journal of Human Genetics. ISSN 1018-4813

Pagnamenta, A.T. orcid.org/0000-0001-7334-0602, Yu, J., Walker, S. et al. (65 more authors) (2024) The impact of inversions across 33,924 families with rare disease from a national genome sequencing project. The American Journal of Human Genetics, 111 (6). pp. 1140-1164. ISSN 0002-9297

Homer, J.J., Winter, S.C. orcid.org/0000-0002-8152-816X, Abbey, E.C. et al. (172 more authors) (2024) Head and Neck Cancer: United Kingdom National Multidisciplinary Guidelines, Sixth Edition. The Journal of Laryngology & Otology, 138 (Supplement S1). S1-S224. ISSN 0022-2151

Zhao, X., Yang, M., Fan, J. et al. (45 more authors) (2024) Identification of genetically predicted DNA methylation markers associated with non–small cell lung cancer risk among 34,964 cases and 448,579 controls. Cancer, 130 (6). pp. 913-926. ISSN 0008-543X

Wang, X., Zhang, Z., Ding, Y. et al. (34 more authors) (2024) Impact of individual level uncertainty of lung cancer polygenic risk score (PRS) on risk stratification. Genome Medicine, 16. 22. ISSN 1756-994X

Tavabie, O.D., Abbott, J., Abeysekera, K.W.M. et al. (97 more authors) (2024) Regional variations in inpatient decompensated cirrhosis mortality may be associated with access to specialist care: results from a multicentre retrospective study. Frontline Gastroenterology, 15 (1). pp. 3-13. ISSN 2041-4137

Tavabie, O.D., Abbott, J., Abeysekera, K.W. et al. (97 more authors) (2023) Defining characteristics and outcomes for patients with non-alcoholic fatty liver disease admitted to hospital with decompensated cirrhosis. Journal of Hepatology, 79 (4). e165-e167. ISSN 0168-8278

Fares, A.F., Li, Y., Jiang, M. et al. (52 more authors) (2023) Association between duration of smoking abstinence before non-small-cell lung cancer diagnosis and survival: a retrospective, pooled analysis of cohort studies. The Lancet Public Health, 8 (9). e691-e700. ISSN 2468-2667

Shi, J. orcid.org/0000-0001-8606-4707, Shiraishi, K. orcid.org/0000-0002-5821-7400, Choi, J. orcid.org/0000-0002-0955-2384 et al. (219 more authors) (2023) Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population. Nature Communications, 14 (1). 3043. ISSN 2041-1723

Williams, S.T., Chatzikyriakou, P., Carroll, P.V. et al. (34 more authors) (2022) SDHC phaeochromocytoma and paraganglioma: A UK‐wide case series. Clinical Endocrinology, 96 (4). pp. 499-512. ISSN 0300-0664

Rosenberger, A., Muttray, N., Hung, R.J. et al. (37 more authors) (2022) Gene–gene interaction of AhRwith and within the Wntcascade affects susceptibility to lung cancer. European Journal of Medical Research, 27. 14. ISSN 2047-783X

Rosenberger, A., Tozzi, V., Bickeböller, H. et al. (38 more authors) (2022) Iam hiQ—a novel pair of accuracy indices for imputed genotypes. BMC Bioinformatics, 23 (1). 50.

Qin, N., Li, Y., Wang, C. et al. (41 more authors) (2021) Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma. Frontiers of Medicine, 15 (2). pp. 275-291. ISSN 2095-0217

Zhou, W., Liu, G., Hung, R.J. et al. (29 more authors) (2021) Causal relationships between body mass index, smoking, and lung cancer: univariable and multivariable mendelian randomization. International Journal of Cancer, 148 (5). pp. 1077-1086. ISSN 0020-7136

Bossé, Y., Li, Z., Xia, J. et al. (45 more authors) (2020) Transcriptome‐wide association study reveals candidate causal genes for lung cancer. International Journal of Cancer, 146 (7). pp. 1862-1878. ISSN 0020-7136

Dai, J., Huang, M., Amos, C.I. et al. (36 more authors) (2020) Genome‐wide association study of INDELs identified four novel susceptibility loci associated with lung cancer risk. International Journal of Cancer, 146 (10). pp. 2855-2864. ISSN 0020-7136

Kachuri, L., Saarela, O., Bojesen, S.E. et al. (67 more authors) (2019) Mendelian randomization and mediation analysis of leukocyte telomere length and risk of lung and head and neck cancers. International Journal of Epidemiology , 48 (3). pp. 751-766. ISSN 0300-5771

Li, Y., Xiao, X., Bossé, Y. et al. (77 more authors) (2019) Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development. Oncotarget, 10 (19). pp. 1760-1774. ISSN 1949-2553

Kolias, A.G., Edlmann, E., Thelin, E.P. et al. (26 more authors) (2018) Dexamethasone for adult patients with a symptomatic chronic subdural haematoma (Dex-CSDH) trial: study protocol for a randomised controlled trial. Trials, 19. 670. ISSN 1745-6215

Rosenberger, A. orcid.org/0000-0001-7848-1332, Hung, R.J., Christiani, D.C. et al. (36 more authors) (2018) Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners. International Archives of Occupational and Environmental Health, 91. pp. 937-950. ISSN 0340-0131

Ferreiro-Iglesias, A., Lesseur, C., McKay, J. et al. (70 more authors) (2018) Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity. Nature Communications, 9 (1). 3927. ISSN 2041-1723

Li, Y., Xiao, X., Han, Y. et al. (73 more authors) (2018) Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population. Carcinogenesis, 39 (3). pp. 336-346. ISSN 0143-3334

McKay, J.D., Hung, R.J., Han, Y. et al. (138 more authors) (2017) Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Nature Genetics, 49 (7). pp. 1126-1132. ISSN 1061-4036

Carreras-Torres, R., Johansson, M., Haycock, P.C. et al. (61 more authors) (2017) Obesity, metabolic factors and risk of different histological types of lung cancer: A Mendelian randomization study. PLoS One, 12 (6). e0177875.

Shimelis, H., Mesman, R.L.S., Von Nicolai, C. et al. (130 more authors) (2017) BRCA2 hypomorphic missense variants confer moderate risks of breast cancer. Cancer Research, 77 (11). pp. 2789-2799. ISSN 0008-5472

Ghoussaini, M, French, J.D., Michailidou, K. et al. (122 more authors) (2016) Evidence that the 5p12 variant rs10941679 confers susceptibility to estrogen receptor positive breast cancer through FGF10 and MRPS30 regulation. American Journal of Human Genetics, 99 (4). pp. 903-911. ISSN 0002-9297

Horne, H.N., Chung, C.E., Zhang, H. et al. (112 more authors) (2016) Fine-mapping of the 1p11.2 breast cancer susceptibility locus. PLoS One, 11 (8). e0160316. ISSN 1932-6203

Zeng, C., Guo, X., Long, J. et al. (234 more authors) (2016) Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus. Breast Cancer Research, 18 (1). 64. ISSN 1465-542X

Berndt, S.I., Camp, N.J., Skibola, C.F. et al. (123 more authors) (2016) Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia. Nature Communications, 7. 10933. ISSN 2041-1723

Dunning, A.M., Michailidou, K., Kuchenbaecker, K.B. et al. (245 more authors) (2016) Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170. Nature Genetics. ISSN 1061-4036

Orr, N., Dudbridge, F., Dryden, N. et al. (213 more authors) (2015) Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2. Human Molecular Genetics, 24 (10). 2966 - 2984. ISSN 0964-6906

Michailidou, K., Beesley, J., Lindstrom, S. et al. (245 more authors) (2015) Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. Nature Genetics, 47. pp. 373-380. ISSN 1061-4036

Cozen, W., Timofeeva, M. N., Diepstra, A. et al. (63 more authors) (2014) A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus. Nature Communications. 3856. ISSN 2041-1723

Johnson, N., Dudbridge, F., Orr, N. et al. (182 more authors) (2014) Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study. Breast Cancer Research , 16 (3). R51. ISSN 1465-5411

Berndt, S.I., Skibola, C.F., Joseph, V. et al. (127 more authors) (2013) Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. Nature Genetics, 45 (8). pp. 868-876. ISSN 1061-4036

Cote, M.L., Liu, M., Bonassi, S. et al. (56 more authors) (2012) Increased risk of lung cancer in individuals with a family history of the disease: A pooled analysis from the International Lung Cancer Consortium. European Journal of Cancer, 48 (13). pp. 1957-1968. ISSN 0959-8049

Hein, R., Maranian, M., Hopper, J.L. et al. (168 more authors) (2012) Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC). PLoS ONE, 7 (8). e42380. ISSN 1932-6203

Johansson, M., Roberts, A., Chen, D. et al. (48 more authors) (2012) Using Prior Information from the Medical Literature in GWAS of Oral Cancer Identifies Novel Susceptibility Variant on Chromosome 4 - the AdAPT Method. PLoS ONE, 7 (5). e36888. ISSN 1932-6203

Stevens, K.N., Garcia-Closas, M., Fredericksen, Z. et al. (101 more authors) (2011) Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk. British Journal of Cancer, 105. pp. 1934-1939. ISSN 0007-0920

Garcia-Closas, M., Hall, P., Nevanlinna, H. et al. (110 more authors) (2008) Heterogeneity of Breast Cancer Associations with Five Susceptibility Loci by Clinical and Pathological Characteristics. PLoS Genetics, 4 (4). e1000054. ISSN 1553-7404