Items where authors include "Law, MH"
Article
Haycock, PC, Borges, MC, Burrows, K et al. (32 more authors) (2023) The association between genetically elevated polyunsaturated fatty acids and risk of cancer. eBioMedicine, 91. 104510. ISSN 2352-3964
Sugier, P-E, Lucotte, EA, Domenighetti, C et al. (91 more authors) (2023) Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers. Movement Disorders, 38 (4). pp. 604-615. ISSN 0885-3185
Long, E, Yin, J, Funderburk, KM et al. (20 more authors) (2022) Massively parallel reporter assays and variant scoring identified functional variants and target genes for melanoma loci and highlighted cell-type specificity. American Journal of Human Genetics, 109 (12). pp. 2210-2229. ISSN 0002-9297
Liyanage, U, MacGregor, S, Bishop, DT orcid.org/0000-0002-8752-8785 et al. (24 more authors) (2022) Multi-trait genetic analysis identifies auto-immune loci associated with cutaneous melanoma. The Journal of investigative dermatology, 142 (8). pp. 1607-1616. ISSN 0022-202X
Steinberg, J, Iles, MM orcid.org/0000-0002-2603-6509, Lee, JY et al. (11 more authors) (2022) Independent evaluation of melanoma polygenic risk scores in UK and Australian prospective cohorts. British Journal of Dermatology, 186 (5). pp. 823-834. ISSN 0007-0963
Ong, J-S, Dixon-Suen, SC, Han, X et al. (21 more authors) (2021) A comprehensive re-assessment of the association between vitamin D and cancer susceptibility using Mendelian randomization. Nature Communications, 12 (1). 246. ISSN 2041-1723
Cardinale, A, Cantalupo, S, Lasorsa, VA et al. (20 more authors) (2021) Functional annotation and investigation of the 10q24.33 melanoma risk locus identifies a common variant that influences transcriptional regulation of OBFC1. Human Molecular Genetics. ISSN 0964-6906
Zhang, T, Choi, J, Dilshat, R et al. (14 more authors) (2021) Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanisms. American Journal of Human Genetics (AJHG), 108 (9). pp. 1631-1646. ISSN 0002-9297
Xu, M, Mehl, L, Zhang, T et al. (25 more authors) (2021) A UVB-responsive common variant at chromosome band 7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor, AHR. American journal of human genetics, 108 (9). pp. 1611-1630. ISSN 0002-9297
Yang, F, Mortlock, S, MacGregor, S et al. (5 more authors) (2021) Genetic Relationship Between Endometriosis and Melanoma. Frontiers in Reproductive Health, 3. 711123. ISSN 2673-3153
Chen, H, Majumdar, A, Wang, L et al. (75 more authors) (2021) Large-scale cross-cancer fine-mapping of the 5p15.33 region reveals multiple independent signals. HGG advances, 2 (3). 100041. ISSN 2666-2477
Laskar, R, Ferreiro‐Iglesias, A, Bishop, DT et al. (11 more authors) (2020) Risk factors for melanoma by anatomical site: an evaluation of aetiological heterogeneity. British Journal of Dermatology. ISSN 0007-0963
Choi, J, Zhang, T, Vu, A et al. (24 more authors) (2020) Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma. Nature Communications, 11 (1). 2718. ISSN 2041-1723
Mangantig, E, MacGregor, S, Iles, MM orcid.org/0000-0002-2603-6509 et al. (17 more authors) (2020) Germline variants are associated with increased primary melanoma tumor thickness at diagnosis. Human Molecular Genetics, 29 (21). pp. 3578-3587. ISSN 0964-6906
Olsen, CM, Pandeya, N, Law, MH et al. (7 more authors) (2020) Does polygenic risk influence associations between sun exposure and melanoma?: a prospective cohort analysis. British Journal of Dermatology, 183 (2). pp. 303-310. ISSN 0007-0963
Dusingize, JC, Olsen, CM, An, J et al. (10 more authors) (2020) Body mass index and height and risk of cutaneous melanoma: Mendelian randomization analyses. International Journal of Epidemiology, 49 (4). pp. 1236-1245. ISSN 0300-5771
Law, MH, Aoude, LG, Duffy, DL et al. (19 more authors) (2020) Multiplex melanoma families are enriched for polygenic risk. Human Molecular Genetics. ISSN 0964-6906
Zhang, YD, Hurson, AN, Zhang, H et al. (102 more authors) (2020) Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers. Nature Communications, 11. 3353.
Landi, MT, Bishop, DT orcid.org/0000-0002-8752-8785, MacGregor, S et al. (158 more authors) (2020) Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nature Genetics, 52 (5). pp. 494-504. ISSN 1061-4036
Dube, U, Ibanez, L, Budde, JP et al. (9 more authors) (2020) Correction to: Overlapping genetic architecture between Parkinson disease and melanoma. Acta Neuropathologica, 139 (5). p. 963. ISSN 0001-6322
Avitabile, M, Succoio, M, Testori, A et al. (25 more authors) (2020) Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 gene. Carcinogenesis, 41 (3). pp. 284-295. ISSN 0143-3334
Dube, U, Ibanez, L, Budde, JP et al. (9 more authors) (2020) Overlapping genetic architecture between Parkinson disease and melanoma. Acta Neuropathologica, 139 (2). pp. 347-364. ISSN 0001-6322
Liyanage, UE, Law, MH, Melanoma Meta-analysis Consortium et al. (3 more authors) (2020) Is there a causal relationship between vitamin D and melanoma risk? : A Mendelian randomization study. British Journal of Dermatology, 182 (1). pp. 97-103. ISSN 0007-0963
Ntritsos, G, Dimou, N, Kypreou, K et al. (10 more authors) (2019) Assessment of melanoma candidate genes in a meta‐analysis of 16 534 melanoma cases. Journal of the European Academy of Dermatology and Venereology, 33 (10). e369-e370. ISSN 0926-9959
Duffy, DL, Zhu, G, Li, X et al. (42 more authors) (2019) Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 10. 299. ISSN 2041-1723
Gu, F, Chen, T-H, Pfeiffer, RM et al. (27 more authors) (2018) Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma. Human Molecular Genetics, 27 (23). pp. 4145-4156. ISSN 0964-6906
Cust, AE, Drummond, M, Kanetsky, PA et al. (18 more authors) (2018) Assessing the incremental contribution of common genomic variants to melanoma risk prediction in two population-based studies. Journal of Investigative Dermatology, 138 (12). pp. 2617-2624. ISSN 0022-202X
Duffy, DL, Zhu, G, Li, X et al. (42 more authors) (2018) Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 9. 4774. ISSN 2041-1723
Zhang, T, Choi, J, Kovacs, MA et al. (15 more authors) (2018) Cell-type–specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes. Genome Research, 28 (11). pp. 1621-1635. ISSN 1088-9051
Liyanage, UE, Law, MH, Ong, JS et al. (7 more authors) (2018) Polyunsaturated fatty acids and risk of melanoma: A Mendelian randomisation analysis. International Journal of Cancer, 143 (3). pp. 508-514. ISSN 0020-7136
Choi, J, Xu, M, Makowski, MM et al. (16 more authors) (2017) A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth via regulation of MITF. Nature Genetics, 49 (9). pp. 1287-1413. ISSN 1061-4036
Telomeres Mendelian Randomization Collaboration, Haycock, PC, Burgess, S et al. (196 more authors) (2017) Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study. JAMA Oncology, 3 (5). pp. 636-651. ISSN 2374-2437
Lubbe, SJ, Escott-Price, V, Brice, A et al. (16 more authors) (2016) Rare variants analysis of cutaneous malignant melanoma genes in Parkinson’s disease. Neurobiology of Aging, 48. 222.e1-222.e7. ISSN 0197-4580
Freitag, DF, Butterworth, AS, Willeit, P et al. (150 more authors) (2015) Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis. Lancet Diabetes and Endocrinology, 3 (4). pp. 243-253. ISSN 2213-8587
Monograph
Choi, J, Zhang, T, Vu, A et al. (21 more authors) (2019) Massively parallel reporter assays combined with cell-type specific eQTL informed multiple melanoma loci and identified a pleiotropic function of HIV-1 restriction gene, MX2, in melanoma promotion. Working Paper. Cold Spring Harbor Laboratory (Submitted)
Conference or Workshop Item
Lindstrom, S, Kar, S, Wang, L et al. (25 more authors) (2020) Cross-cancer GWAS meta-analysis of more than 370,000 cases and 530,000 controls identifies multiple novel cancer risk regions. In: AACR Annual Meeting 2020, 27 Apr - 24 Jun 2020, Philadelphia, PA, USA.
Liyanage, UE, Law, MH, Han, X et al. (8 more authors) (2019) Abstract 1592: Genome-wide meta-analysis of keratinocytic cancers identifies 26 novel risk loci. In: AACR Annual Meeting 2019, 29 Mar - 03 Apr 2019, Atlanta, GA, USA.
Preprint
Olsen, CM, Pandeya, N, Law, MH et al. (6 more authors) (2019) Ultraviolet radiation exposure and melanoma: evidence for gene-environment interaction in a large prospective cohort. [Preprint]