Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: NAV2[original query] |
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Follow-up association study of linkage regions reveals multiple candidate genes for carotid plaque in Dominicans. Atherosclerosis 2012 Jul 223 (1): 177-83. Dong Chuanhui, Beecham Ashley, Wang Liyong, Blanton Susan H, Rundek Tatjana, Sacco Ralph |
Family-based association analysis of NAV2 gene with the risk and age at onset of Alzheimer's disease. Journal of neuroimmunology 2017 Sep 310 60-65. Wang Ke-Sheng, Liu Ying, Xu Chun, Liu Xuefeng, Luo Xinggua |
Exonic mutations in SCN9A (NaV1.7) are found in a minority of patients with erythromelalgia. Scandinavian journal of pain 2018 6 5 (4): 217-225. Zhang Zhiping, Schmelz Martin, Segerdahl Märta, Quiding Hans, Centerholt Carina, Juréus Anna, Carr Thomas Hedley, Whiteley Jessica, Salter Hugh, Kvernebo Mari Skylstad, Ørstavik Kristin, Helås Tormod, Kleggetveit Inge-Petter, Lunden Lars Kristian, Jørum Ell |
Genetic associations with age of menopause in familial longevity. Menopause (New York, N.Y.) 2019 Jun . Bae Harold, Lunetta Kathryn L, Murabito Joanne M, Andersen Stacy L, Schupf Nicole, Perls Thomas, Sebastiani Paola, |
Use of Deep-Learning Genomics to Discriminate Healthy Individuals from Those with Alzheimer's Disease or Mild Cognitive Impairment.
Behavioural neurology 2021 8 2021 3359103. Li Lanlan, Yang Yeying, Zhang Qi, Wang Jiao, Jiang Jiehui, Neuroimaging Initiative Alzheimer's Disea |
Neoantigen-reactive T cells exhibit effective anti-tumor activity against colorectal cancer. Human vaccines & immunotherapeutics 2021 Mar 1-11. Yu Yaojun, Zhang Jing, Ni Leyi, Zhu Yuesheng, Yu Hejie, Teng Yangyang, Lin Limiao, Xue Zhanxiong, Xue Xiangyang, Shen Xian, Song Haiping, Su Xiaoping, Sun Weihong, Cai Zhenzh |
Risk Variants in Three Alzheimer's Disease Genes Show Association with EEG Endophenotypes. Journal of Alzheimer's disease : JAD 2021 Jan . Macedo Ana, Gómez Carlos, Rebelo Miguel Ângelo, Poza Jesús, Gomes Iva, Martins Sandra, Maturana-Candelas Aarón, Pablo Víctor Gutiérrez-de, Durães Luis, Sousa Patrícia, Figueruelo Manuel, Rodríguez María, Pita Carmen, Arenas Miguel, Álvarez Luis, Hornero Roberto, Lopes Alexandra M, Pinto Nád |
Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus. NPJ genomic medicine 2022 11 7 (1): 70. Gallego-Martinez Alvaro, Escalera-Balsera Alba, Trpchevska Natalia, Robles-Bolivar Paula, Roman-Naranjo Pablo, Frejo Lidia, Perez-Carpena Patricia, Bulla Jan, Gallus Silvano, Canlon Barbara, Cederroth Christopher R, Lopez-Escamez Jose |
Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis. Human genomics 2023 10 17 (1): 88. Susanna Nousiainen, Outi Kuismin, Siiri Reinikka, Roosa Manninen, Sara Khamaiseh, Mari Kuivalainen, Anna Terho, Sari Koivurova, Maarit Niinimäki, Kari Salokas, Markku Varjosalo, Anne Ahtikoski, Ralf Bützow, Outi Lindgren, Outi Uimari, Pia Vahteris |
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- Page last updated:Apr 22, 2024
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