日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Genome-wide association testing beyond SNPs

超越SNP的全基因组关联检测

Harris, Laura; McDonagh, Ellen M; Zhang, Xiaolei; Fawcett, Katherine; Foreman, Amy; Daneck, Petr; Sergouniotis, Panagiotis I; Parkinson, Helen; Mazzarotto, Francesco; Inouye, Michael; Hollox, Edward J; Birney, Ewan; Fitzgerald, Tomas

Genomics of chronic dry cough unravels neurological pathways

慢性干咳的基因组学研究揭示了神经通路

Coley, Kayesha; John, Catherine; Ghouse, Jonas; Shepherd, David J; Shrine, Nick; Izquierdo, Abril G; Kanoni, Stavroula; Magavern, Emma F; Packer, Richard; McGarvey, Lorcan; Smith, Jaclyn A; Bundgaard, Henning; Ostrowski, Sisse R; Erikstrup, Christian; Pedersen, Ole B V; van Heel, David A; Hennah, William; Marttila, Mikko; Free, Robert C; Hollox, Edward J; Wain, Louise V; Tobin, Martin D; Batini, Chiara

Constitutive inflammation and epithelial-mesenchymal transition dictate sensitivity to nivolumab in CONFIRM: a placebo-controlled, randomised phase III trial

CONFIRM:一项安慰剂对照、随机 III 期试验表明,构成性炎症和上皮-间质转化决定了对纳武利尤单抗的敏感性。

Fennell, Dean A; Hill, Kayleigh; Zhang, Min; Poile, Charlotte; Ewings, Sean; Baitei, Essa Y; Dzialo, Joanna; Nusrat, Nada; Rogel, Jan; Faulkner, Daniel; Ottensmeier, Christian; Califano, Raffaele; Hanna, Gerard G; Danson, Sarah; Steele, Nicola; Nye, Mavis; Johnson, Lucy; Mallard, Kim; Lord, Joanne; Middleton, Calley; Szlosarek, Peter; Chan, Sam; Darlison, Liz; Wells-Jordan, Peter; Richards, Cathy; Harber, James; Bzura, Aleksandra; Spicer, Jake; Pritchard, Catrin; Kamata, Tamihiro; Hahne, Jens C; Jama, Maymun; Hollox, Edward J; Lester, Jason F; Luo, Jin-Li; Zhou, Zisen; Yang, Hongji; Zhou, Huiyu; Klampatsa, Astero; Griffiths, Gareth O

Impact of β-defensin 103 (DEFB103) copy number variation on bull sperm parameters and post-insemination uterine gene expression

β-防御素103 (DEFB103) 拷贝数变异对公牛精子参数和授精后子宫基因表达的影响

Sidekli, Ozge; Hollox, Edward J; Fair, Sean; Meade, Kieran G

A gut microbiota rheostat forecasts responsiveness to PD-L1 and VEGF blockade in mesothelioma

肠道菌群调节器可预测间皮瘤对PD-L1和VEGF阻断疗法的反应性

Zhang, Min; Bzura, Aleksandra; Baitei, Essa Y; Zhou, Zisen; Spicer, Jake B; Poile, Charlotte; Rogel, Jan; Branson, Amy; King, Amy; Barber, Shaun; Kamata, Tamihiro; Dzialo, Joanna; Harber, James; Greystoke, Alastair; Nusrat, Nada; Faulkner, Daniel; Sun, Qianqian; Nolan, Luke; Hahne, Jens C; Scotland, Molly; Walter, Harriet; Darlison, Liz; Morgan, Bruno; Bajaj, Amrita; Brookes, Cassandra; Hollox, Edward J; Lubawska, Dominika; Jama, Maymun; Griffiths, Gareth; Nakas, Apostolos; Kutywayo, Kudzayi; Luo, Jin-Li; Klampatsa, Astero; Cooper, Andrea; Halder, Koirobi; Wells-Jordan, Peter; Zhou, Huiyu; Dudbridge, Frank; Thomas, Anne; Richards, Catherine Jane; Pritchard, Catrin; Yang, Hongji; Barer, Michael; Fennell, Dean A

Fc gamma receptors: Their evolution, genomic architecture, genetic variation, and impact on human disease

Fcγ受体:它们的进化、基因组结构、遗传变异及其对人类疾病的影响

Frampton, Sarah; Smith, Rosanna; Ferson, Lili; Gibson, Jane; Hollox, Edward J; Cragg, Mark S; Strefford, Jonathan C

Association study of human leukocyte antigen variants and idiopathic pulmonary fibrosis

人类白细胞抗原变异与特发性肺纤维化的关联研究

Guillen-Guio, Beatriz; Paynton, Megan L; Allen, Richard J; Chin, Daniel P W; Donoghue, Lauren J; Stockwell, Amy; Leavy, Olivia C; Hernandez-Beeftink, Tamara; Reynolds, Carl; Cullinan, Paul; Martinez, Fernando; Booth, Helen L; Fahy, William A; Hall, Ian P; Hart, Simon P; Hill, Mike R; Hirani, Nik; Hubbard, Richard B; McAnulty, Robin J; Millar, Ann B; Navaratnam, Vidya; Oballa, Eunice; Parfrey, Helen; Saini, Gauri; Sayers, Ian; Tobin, Martin D; Whyte, Moira K B; Adegunsoye, Ayodeji; Kaminski, Naftali; Ma, Shwu-Fan; Strek, Mary E; Zhang, Yingze; Fingerlin, Tasha E; Molina-Molina, Maria; Neighbors, Margaret; Sheng, X Rebecca; Oldham, Justin M; Maher, Toby M; Molyneaux, Philip L; Flores, Carlos; Noth, Imre; Schwartz, David A; Yaspan, Brian L; Jenkins, R Gisli; Wain, Louise V; Hollox, Edward J

β-Defensin gene copy number variation in cattle

牛β-防御素基因拷贝数变异

Sidekli, Ozge; Oketch, John; Fair, Sean; Meade, Kieran G; Hollox, Edward J

A comparison of software for analysis of rare and common short tandem repeat (STR) variation using human genome sequences from clinical and population-based samples

比较用于分析罕见和常见短串联重复序列(STR)变异的软件,这些软件使用来自临床和人群样本的人类基因组序列。

Oketch, John W; Wain, Louise V; Hollox, Edward J

Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease

全基因组关联研究揭示了促甲状腺激素与甲状腺疾病之间的新基因、通路和关联。

Williams, Alexander T; Chen, Jing; Coley, Kayesha; Batini, Chiara; Izquierdo, Abril; Packer, Richard; Abner, Erik; Kanoni, Stavroula; Shepherd, David J; Free, Robert C; Hollox, Edward J; Brunskill, Nigel J; Ntalla, Ioanna; Reeve, Nicola; Brightling, Christopher E; Venn, Laura; Adams, Emma; Bee, Catherine; Wallace, Susan E; Pareek, Manish; Hansell, Anna L; Esko, Tõnu; Stow, Daniel; Jacobs, Benjamin M; van Heel, David A; Hennah, William; Rao, Balasubramanya S; Dudbridge, Frank; Wain, Louise V; Shrine, Nick; Tobin, Martin D; John, Catherine