Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: IL31RA[original query] |
---|
Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci. PLoS genetics 2011 Mar 7 (3): e1002026. Nguyen Le B, Diskin Sharon J, Capasso Mario, Wang Kai, Diamond Maura A, Glessner Joseph, Kim Cecilia, Attiyeh Edward F, Mosse Yael P, Cole Kristina, Iolascon Achille, Devoto Marcella, Hakonarson Hakon, Li Hongzhe K, Maris John |
ANKRD55 and DHCR7 are novel multiple sclerosis risk loci. Genes and immunity 2012 Apr 13 (3): 253-7. Alloza I, Otaegui D, de Lapuente A Lopez, Antigüedad A, Varadé J, Núñez C, Arroyo R, Urcelay E, Fernandez O, Leyva L, Fedetz M, Izquierdo G, Lucas M, Oliver-Martos B, Alcina A, Saiz A, Blanco Y, Comabella M, Montalban X, Olascoaga J, Matesanz F, Vandenbroeck |
Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility. Carcinogenesis 2013 Mar 34 (3): 605-11. Capasso Mario, Diskin Sharon J, Totaro Francesca, Longo Luca, De Mariano Marilena, Russo Roberta, Cimmino Flora, Hakonarson Hakon, Tonini Gian Paolo, Devoto Marcella, Maris John M, Iolascon Achil |
HSD17B12 gene rs11037575 C>T polymorphism confers neuroblastoma susceptibility in a Southern Chinese population. OncoTargets and therapy 2017 10 1969-1975. Zhang Zhuorong, Zou Yan, Zhu Jinhong, Zhang Ruizhong, Yang Tianyou, Wang Fenghua, Xia Huimin, He Jing, Feng Zhich |
The Clinical Spectrum of Multiple Endocrine Neoplasia Type 2A with Cutaneous Lichen Amyloidosis in Ethnic Han Chinese. Cancer investigation 2018 2 36 (2): 141-151. Qi Xiao-Ping, Zhao Jian-Qiang, Cao Zhi-Lie, Fu Er, Li Feng, Zhao Yi-Hua, Wang Guang-Ping, Li Peng-Fei, Ma Wo-Long, Guo Jian, Jia Ho |
Clinical and genetic features of Chinese patients with lichen and macular primary localized cutaneous amyloidosis. Clinical and experimental dermatology 2019 2 44 (4): e110-e117. Lu P, Wu F-F, Rong Z-L, Fang C, Deng C-C, Bin L-H, Yang |
A genome-wide association study on frequent exacerbation of asthma depending on smoking status. Respiratory medicine 2022 5 199 106877. Son Ji-Hye, Park Jong-Sook, Lee Jong-Uk, Kim Min Kyung, Min Sun-Ah, Park Choon-Sik, Chang Hun S |
Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55-IL6ST Gene Region in Immature Dendritic Cells. Frontiers in immunology 2022 2 12 816930. Mena Jorge, Alloza Iraide, Tulloch Navarro Raquel, Aldekoa Ane, Díez García Javier, Villanueva Etxebarria Ane, Lindskog Cecilia, Antigüedad Alfredo, Boyero Sabas, Mendibe-Bilbao María Del Mar, Álvarez de Arcaya Amaya, Sánchez Menoyo José Luis, Midaglia Luciana, Villarrubia Noelia, Malhotra Sunny, Montalban Xavier, Villar Luisa María, Comabella Manuel, Vandenbroeck Ko |
Genetic association of IL2RA, IL17RA, IL23R, and IL31RA single nucleotide polymorphisms with alopecia areata. Saudi journal of biological sciences 2022 Nov 29 (11): 103460. Alghamdi Mansour A, Al-Eitan Laith N, Aljamal Hanan A, Shati Ayed A, Alshehri Mohammed |
Identification of rare coding variants associated with Kawasaki disease by whole exome sequencing. Genomics & informatics 2022 1 19 (4): e38. Kim Jae-Jung, Hong Young Mi, Yun Sin Weon, Lee Kyung-Yil, Yoon Kyung Lim, Han Myung-Ki, Kim Gi Beom, Kil Hong-Ryang, Song Min Seob, Lee Hyoung Doo, Ha Kee Soo, Jun Hyun Ok, Choi Byung-Ok, Oh Yeon-Mok, Yu Jeong Jin, Jang Gi Young, Lee Jong-Keuk, |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: