Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: NMI[original query] |
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The effects of common genetic variants in oncogenes on ovarian cancer survival. Clinical cancer research : an official journal of the American Association for Cancer Research 2008 Sep 14 (18): 5833-9. Quaye Lydia, Gayther Simon A, Ramus Susan J, Di Cioccio Richard A, McGuire Valerie, Hogdall Estrid, Hogdall Claus, Blaakr Jan, Easton Douglas F, Ponder Bruce A J, Jacobs Ian, Kjaer Susanne Kruger, Whittemore Alice S, Pearce Celeste Leigh, Pharoah Paul D P, Song Hongl |
Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer. British journal of cancer 2009 Mar 100 (6): 993-1001. Quaye L, Song H, Ramus S J, Gentry-Maharaj A, Høgdall E, DiCioccio R A, McGuire V, Wu A H, Van Den Berg D J, Pike M C, Wozniak E, Doherty J A, Rossing M A, Ness R B, Moysich K B, Høgdall C, Blaakaer J, , Easton D F, Ponder B A J, Jacobs I J, Menon U, Whittemore A S, Krüger-Kjaer S, Pearce C L, Pharoah P D P, Gayther S |
The development of multiple bladder tumour recurrences in relation to the FGFR3 mutation status of the primary tumour. The Journal of pathology 2009 May 218 (1): 104-12. Kompier Lucie C, van der Aa Madelon N M, Lurkin Irene, Vermeij Marcel, Kirkels Wim J, Bangma Chris H, van der Kwast Theodorus H, Zwarthoff Ellen |
Fibroblast growth factor receptor 3 mutation analysis on voided urine for surveillance of patients with low-grade non-muscle-invasive bladder cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 2010 Jun 16 (11): 3011-8. Zuiverloon Tahlita C M, van der Aa Madelon N M, van der Kwast Theo H, Steyerberg Ewout W, Lingsma Hester F, Bangma Chris H, Zwarthoff Ellen |
FGFR3, HRAS, KRAS, NRAS and PIK3CA mutations in bladder cancer and their potential as biomarkers for surveillance and therapy. PloS one 2010 5 (11): e13821. Kompier Lucie C, Lurkin Irene, van der Aa Madelon N M, van Rhijn Bas W G, van der Kwast Theo H, Zwarthoff Ellen |
Subependymal nodules and giant cell tumours in tuberous sclerosis complex patients: prevalence on MRI in relation to gene mutation. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2012 Aug . Michelozzi C, Di Leo G, Galli F, Silva Barbosa F, Labriola F, Sardanelli F, Cornalba G |
Genetic variants in N-myc (and STAT) interactor and susceptibility to glioma in a Chinese Han population. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Mar 36 (3): 1579-88. Meng Delong, Li Xiaoying, Zhang Shuo, Zhao Yingjie, Song Xiao, Chen Yuanyuan, Wang Shiming, Mao Ying, Chen Hongyan, Lu Da |
Mosaic and Intronic Mutations in TSC1/TSC2 Explain the Majority of TSC Patients with No Mutation Identified by Conventional Testing. PLoS genetics 2015 Nov 11 (11): e1005637. Tyburczy Magdalena E, Dies Kira A, Glass Jennifer, Camposano Susana, Chekaluk Yvonne, Thorner Aaron R, Lin Ling, Krueger Darcy, Franz David N, Thiele Elizabeth A, Sahin Mustafa, Kwiatkowski David |
TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study. Orphanet journal of rare diseases 2018 9 13 (1): 157. de Vries Petrus J, Belousova Elena, Benedik Mirjana P, Carter Tom, Cottin Vincent, Curatolo Paolo, Dahlin Maria, D'Amato Lisa, d'Augères Guillaume B, Ferreira José C, Feucht Martha, Fladrowski Carla, Hertzberg Christoph, Jozwiak Sergiusz, Kingswood J Chris, Lawson John A, Macaya Alfons, Marques Ruben, Nabbout Rima, O'Callaghan Finbar, Qin Jiong, Sander Valentin, Sauter Matthias, Shah Seema, Takahashi Yukitoshi, Touraine Renaud, Youroukos Sotiris, Zonnenberg Bernard, Jansen Anna C, |
Pattern of TSC1 and TSC2 germline mutations in Russian patients with tuberous sclerosis. Journal of human genetics 2018 Feb . Suspitsin Evgeny N, Yanus Grigoriy A, Dorofeeva Marina Yu, Ledashcheva Tatiana A, Nikitina Nataliya V, Buyanova Galina V, Saifullina Elena V, Sokolenko Anna P, Imyanitov Evgeny |
Mutation landscape of TSC1/TSC2 in Chinese patients with tuberous sclerosis complex. Journal of human genetics 2020 9 66 (3): 227-236. Meng Yuhuan, Yu Changshun, Chen Meijun, Yu Xiaokang, Sun Mingming, Yan Hui, Zhao Weiwei, Yu Shih |
Genotype and Phenotype Analysis of Chinese Children With Tuberous Sclerosis Complex: A Pediatric Cohort Study. Frontiers in genetics 2020 3 11 204. Ding Yifeng, Wang Ji, Zhou Shuizhen, Zhou Yuanfeng, Zhang Linmei, Yu Lifei, Wang |
Lymphangioleiomyomatosis Association with Underlying Genotype in Patients with Tuberous Sclerosis Complex. Annals of the American Thoracic Society 2020 Nov . Tian Xinlun, Glass Jennifer E, Kwiatkowski David J, Towbin Alexander J, Li Yinan, Sund Kristen L, Krueger Darcy A, Franz David N, McCormack Francis X, Gupta Nisha |
Fibroblast Growth Factor Receptor 3 Mutation as a Prognostic Indicator in Patients with Urothelial Carcinoma: A Systematic Review and Meta-analysis. European urology open science 2020 Oct 21 61-68. Khalid Sidra, Basulaiman Bassam Mohammed, Emack Jeffrey, Booth Christopher M, Duran Ignacio, Robinson Andrew G, Berman David, Smoragiewicz Martin, Amir Eitan, Vera-Badillo Francisco |
A multistep approach to the genotype-phenotype analysis of Polish patients with tuberous sclerosis complex. European journal of medical genetics 2021 8 64 (10): 104309. B?bol-Pokora Katarzyna, Bielska Marta, Bobeff Katarzyna, Jatczak-Pawlik Izabela, Borkowska Julita, Kotulska Katarzyna, Jó?wiak Sergiusz, M?ynarski Wojciech, Treli?ska Joan |
Correlation between epilepsy and genotype: A large retrospective tuberous sclerosis complex cohort. Seizure 2021 7 91 273-277. Ding Yifeng, Zhou Yuanfeng, Yu Lifei, Zhang Linmei, Zhou Shuizhen, Wang Yi, Wang |
The Phenotypic Spectrum of Tuberous Sclerosis Complex: A Canadian Cohort. Child neurology open 2021 5 8 2329048X211012817. Alsowat Daad, Whitney Robyn, Hewson Stacy, Jain Puneet, Chan Valerie, Kabir Nadia, Amburgey Kimberly, Noone Damien, Lemaire Mathieu, McCoy Blathnaid, Zak Mar |
Prognostic significance of LRIG2 and LRIG3 proteins in urothelial bladder carcinoma. Journal of immunoassay & immunochemistry 2021 11 43 (3): 308-332. M Serag El-Dien Marwa, Fathy Mahmoud Shereen, Alhanafy Alshimaa Mahmoud, Mohamed Zanaty Fouad, Shawky Holah Nan |
Analysis of renal lesions in Chinese tuberous sclerosis complex patients with different types of TSC gene mutations. Genetics and molecular biology 2022 5 45 (2): e20200387. Wang Wenda, Zhao Yang, Wang Xu, Wang Zhan, Cai Yi, Li Hanzhong, Zhang Yus |
A novel inflammatory signature for evaluating immune microenvironment status in soft tissue sarcoma. Frontiers in oncology 2022 10 12 990670. Li Zhehong, Zheng Honghong, Liu Lirui, Fen Zhen, Cao Haiying, Yang Jilong, Wei Junqia |
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- Page last updated:Apr 29, 2024
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