Items where authors include "Brown, KM"

Article

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

Castaneda-Garcia, C, Iyer, V, Nsengimana, J et al. (11 more authors) (2022) Defining novel causal SNPs and linked phenotypes at melanoma-associated loci. Human Molecular Genetics, 31 (17). pp. 2845-2856. ISSN 0964-6906

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

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

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

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

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

Laskar, RS, Muller, DC, Li, P et al. (105 more authors) (2019) Sex specific associations in genome wide association analysis of renal cell carcinoma. European Journal of Human Genetics, 27. pp. 1589-1598. ISSN 1018-4813

Johansson, M, Carreras-Torres, R, Scelo, G et al. (110 more authors) (2019) The influence of obesity-related factors in the etiology of renal cell carcinoma—A mendelian randomization study. PLoS Medicine, 16 (1). e1002724. ISSN 1549-1277

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

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

Fang, J, Jia, J, Makowski, M et al. (38 more authors) (2018) Publisher correction: Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148. Nature Communications, 9. p. 16159.

Machiela, MJ, Hofmann, JN, Carreras-Torres, R et al. (109 more authors) (2017) Genetic variants related to longer telomere length are associated with increased risk of renal cell carcinoma. European Urology, 72 (5). pp. 747-754. ISSN 0302-2838

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

Scelo, G, Purdue, MP, Brown, KM et al. (120 more authors) (2017) Genome-wide association study identifies multiple risk loci for renal cell carcinoma. Nature Communications, 8. 15724. ISSN 2041-1723

Fang, J, Jia, J, Makowski, M et al. (41 more authors) (2017) Functional characterisation of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148. Nature Communications, 8. 15034. ISSN 2041-1723

Harland, M, Petljak, M, Robles-Espinoza, CD et al. (13 more authors) (2016) Germline TERT promoter mutations are rare in familial melanoma. Familial Cancer, 15 (1). pp. 139-144. ISSN 1389-9600

Law, M, Bishop, DT orcid.org/0000-0002-8752-8785, Lee, JE et al. (78 more authors) (2015) Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics, 47 (9). pp. 987-995. ISSN 1061-4036

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)