关注
Myriam Brossard
Myriam Brossard
Postdoctoral Researcher
在 lunenfeld.ca 的电子邮件经过验证
标题
引用次数
引用次数
年份
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
F Demenais, P Margaritte-Jeannin, KC Barnes, WOC Cookson, ...
Nature genetics 50 (1), 42-53, 2018
5172018
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
MH Law, DT Bishop, JE Lee, M Brossard, NG Martin, EK Moses, F Song, ...
Nature genetics 47 (9), 987-995, 2015
2562015
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
MT Landi, DT Bishop, S MacGregor, MJ Machiela, AJ Stratigos, P Ghiorzo, ...
Nature genetics 52 (5), 494-504, 2020
1882020
The effect on melanoma risk of genes previously associated with telomere length
MM Iles, DT Bishop, JC Taylor, NK Hayward, M Brossard, AE Cust, ...
Journal of the National Cancer Institute 106 (10), dju267, 2014
1362014
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
DL Duffy, G Zhu, X Li, M Sanna, MM Iles, LC Jacobs, DM Evans, S Yazar, ...
Nature communications 9 (1), 4774, 2018
1152018
Cell-type–specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes
T Zhang, J Choi, MA Kovacs, J Shi, M Xu, AM Goldstein, AJ Trower, ...
Genome research 28 (11), 1621-1635, 2018
822018
Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma
J Choi, T Zhang, A Vu, J Ablain, MM Makowski, LM Colli, M Xu, ...
Nature communications 11 (1), 2718, 2020
802020
Assessing the incremental contribution of common genomic variants to melanoma risk prediction in two population-based studies
AE Cust, M Drummond, PA Kanetsky, GJ Mann, H Schmid, JL Hopper, ...
Journal of Investigative Dermatology 138 (12), 2617-2624, 2018
542018
gpart: human genome partitioning and visualization of high-density SNP data by identifying haplotype blocks
SA Kim, M Brossard, D Roshandel, AD Paterson, SB Bull, YJ Yoo
Bioinformatics 35 (21), 4419-4421, 2019
452019
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions
JH Barrett, JC Taylor, C Bright, M Harland, AM Dunning, LA Akslen, ...
International journal of cancer 136 (6), 1351-1360, 2015
452015
SigMod: an exact and efficient method to identify a strongly interconnected disease-associated module in a gene network
Y Liu, M Brossard, D Roqueiro, P Margaritte-Jeannin, C Sarnowski, ...
Bioinformatics 33 (10), 1536-1544, 2017
302017
The nuclear factor I/A (NFIA) gene is associated with the asthma plus rhinitis phenotype
MH Dizier, P Margaritte-Jeannin, AM Madore, M Moffatt, M Brossard, ...
Journal of allergy and clinical immunology 134 (3), 576-582. e1, 2014
232014
Network-assisted analysis of GWAS data identifies a functionally-relevant gene module for childhood-onset asthma
Y Liu, M Brossard, C Sarnowski, A Vaysse, M Moffatt, ...
Scientific reports 7 (1), 938, 2017
202017
Interaction between the DNAH9 gene and early smoke exposure in bronchial hyperresponsiveness
MH Dizier, R Nadif, P Margaritte-Jeannin, SJ Barton, C Sarnowski, ...
European Respiratory Journal 47 (4), 1072-1081, 2016
192016
Integrated pathway and epistasis analysis reveals interactive effect of genetic variants at TERF1 and AFAP1L2 loci on melanoma risk
M Brossard, S Fang, A Vaysse, Q Wei, WV Chen, H Mohamdi, E Maubec, ...
International journal of cancer 137 (8), 1901-1909, 2015
182015
Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families
X Liang, RM Pfeiffer, WQ Li, M Brossard, LS Burke, W Wheeler, D Calista, ...
Journal of Investigative Dermatology 134 (2), 481-487, 2014
172014
A comprehensive genome‐wide analysis of melanoma Breslow thickness identifies interaction between CDC42 and SCIN genetic variants
A Vaysse, S Fang, M Brossard, Q Wei, WV Chen, H Mohamdi, ...
International journal of cancer 139 (9), 2012-2020, 2016
142016
A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults
E Bouzigon, R Nadif, EE Thompson, MP Concas, S Kuldanek, G Du, ...
Clinical & Experimental Allergy 45 (4), 797-806, 2015
142015
Large-scale cross-cancer fine-mapping of the 5p15. 33 region reveals multiple independent signals
H Chen, A Majumdar, L Wang, S Kar, KM Brown, H Feng, C Turman, ...
Human Genetics and Genomics Advances 2 (3), 2021
132021
New susceptibility loci for cutaneous melanoma risk and progression revealed using a porcine model
E Bourneuf, J Estellé, A Blin, F Créchet, M del Pilar Schneider, H Gilbert, ...
Oncotarget 9 (45), 27682, 2018
122018
系统目前无法执行此操作,请稍后再试。
文章 1–20