HuGE Literature Finder
Records 1-30
|
A comprehensive analysis of somatic alterations in Chinese ovarian cancer patients.
Scientific reports 2021 Jan 11 (1): 387. Zhang Yingli, Shi Xiaoliang, Zhang Jiejie, Chen Xi, Zhang Peng, Liu Angen, Zhu T |
|
Differences in Genomic Alterations Between Brain Metastases and Primary Tumors.
Neurosurgery 2020 Dec . Dono Antonio, Takayasu Takeshi, Yan Yuanqing, Bundrant Bethany E, Arevalo Octavio, Lopez-Garcia Carlos A, Esquenazi Yoshua, Ballester Leomar |
|
Genetic and nongenetic factors associated with CADASIL: A retrospective cohort study.
Journal of the neurological sciences 2020 Oct 419 117178. Ospina Carolina, Arboleda-Velasquez Joseph F, Aguirre-Acevedo Daniel Camilo, Zuluaga-Castaño Yesica, Velilla Lina, Garcia Gloria P, Quiroz Yakeel T, Lopera Francis |
|
Genomic profiles and clinical outcomes of de novo blastoid/pleomorphic MCL are distinct from those of transformed MCL.
Blood advances 2020 Mar 4 (6): 1038-1050. Jain Preetesh, Zhang Shaojun, Kanagal-Shamanna Rashmi, Ok Chi Young, Nomie Krystle, Gonzalez Graciela Nogueras, Gonzalez-Pagan Omarya, Hill Holly A, Lee Hun Ju, Fayad Luis, Westin Jason, Nastoupil Loretta, Hagemeister Frederick, Chen Wendy, Oriabure Onyeka, Badillo Maria, Jiang Changying, Yixin Yao, Li Shaoying, Tang Guilin, Yin C Cameron, Patel Keyur P, Medeiros Leonard Jeffrey, Nair Ranjit, Ahmed Sairah, Iyer Swaminathan P, Thirumurthi Selvi, Champlin Richard, Xu Guofan, Tinsu Pan, Santos David, Wang Ruiping, Han Guangchun, Zhang Jianhua, Song Xingzhi, Neelapu Sattva, Romaguera Jorge, Futreal Andy, Flowers Christopher, Fowler Nathan, Wang Linghua, Wang Michael |
|
Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies.
Acta neuropathologica communications 2020 Jan 8 (1): 5. Orme Tatiana, Hernandez Dena, Ross Owen A, Kun-Rodrigues Celia, Darwent Lee, Shepherd Claire E, Parkkinen Laura, Ansorge Olaf, Clark Lorraine, Honig Lawrence S, Marder Karen, Lemstra Afina, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Morgan Kevin, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Holton Janice, Compta Yaroslau, Van Deerlin Vivianna, Trojanowski John Q, Serrano Geidy E, Beach Thomas G, Lesage Suzanne, Galasko Douglas, Masliah Eliezer, Santana Isabel, Pastor Pau, Tienari Pentti J, Myllykangas Liisa, Oinas Minna, Revesz Tamas, Lees Andrew, Boeve Brad F, Petersen Ronald C, Ferman Tanis J, Escott-Price Valentina, Graff-Radford Neill, Cairns Nigel J, Morris John C, Pickering-Brown Stuart, Mann David, Halliday Glenda, Stone David J, Dickson Dennis W, Hardy John, Singleton Andrew, Guerreiro Rita, Bras Jo |
|
GGC repeat expansion of NOTCH2NLC in adult patients with leukoencephalopathy.
Annals of neurology 2019 Aug . Okubo Masaki, Doi Hiroshi, Fukai Ryoko, Fujita Atsushi, Mitsuhashi Satomi, Hashiguchi Shunta, Kishida Hitaru, Ueda Naohisa, Morihara Keisuke, Ogasawara Akihiro, Kawamoto Yuko, Takahashi Tatsuya, Takahashi Keita, Nakamura Haruko, Kunii Misako, Tada Mikiko, Katsumoto Atsuko, Fukuda Hiromi, Mizuguchi Takeshi, Miyatake Satoko, Miyake Noriko, Suzuki Junichiro, Ito Yasuhiro, Sone Jun, Sobue Gen, Takeuchi Hideyuki, Matsumoto Naomichi, Tanaka Fumia |
|
Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates.
Respiratory research 2019 Aug 20 (1): 174. Liu Xu, Mei Mei, Chen Xiang, Lu Yulan, Dong Xinran, Hu Liyuan, Hu Xiaojing, Cheng Guoqiang, Cao Yun, Yang Lin, Zhou Wenh |
|
Effect of gene-gene and gene-environment interaction on the risk of first-ever stroke and poststroke death.
Molecular genetics & genomic medicine 2019 Jul e846. Feng Congrui, Yang Yunyun, Yang Shujun, Tu Xin, Wang Yibo, Song Yiqing, Hui Rutai, Zhang Wei |
|
Genetic polymorphisms and transcription profiles associated with intracranial aneurysm: a key role for NOTCH3.
Aging 2019 Jul 11 . Li Mengqi, Dong Xinlong, Chen Shi, Wang Weihan, Yang Chao, Li Bochuan, Liang Degang, Yang Weidong, Liu Xiaozhi, Yang Xin |
|
Novel and Recurring NOTCH3 Mutations in Two Chinese Patients with CADASIL.
Neuro-degenerative diseases 2019 Jun 1-8. Chen Xiangyu, Deng Sheng, Xu Hongbo, Hou Deren, Hu Pengzhi, Yang Yan, Wen Jie, Deng Hao, Yuan Lam |
|
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.
JAMA network open 2019 Mar 2 (3): e191350. Patel Devanshi, Mez Jesse, Vardarajan Badri N, Staley Lyndsay, Chung Jaeyoon, Zhang Xiaoling, Farrell John J, Rynkiewicz Michael J, Cannon-Albright Lisa A, Teerlink Craig C, Stevens Jeffery, Corcoran Christopher, Gonzalez Murcia Josue D, Lopez Oscar L, Mayeux Richard, Haines Jonathan L, Pericak-Vance Margaret A, Schellenberg Gerard, Kauwe John S K, Lunetta Kathryn L, Farrer Lindsay A, |
|
Common Variants rs3815188 and rs1043994 on Notch3 Gene Confer Susceptibility to Lung Cancer: A Hospital-Based Case-Control Study.
Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer 2019 38 (1): 61-68. Yagci Emine, Degirmenci Irfan, Ozbayer Cansu, Ak Guntulu, Saydam Faruk, Metintas Muzaff |
|
Next Generation Sequencing Analysis in Early Onset Dementia Patients.
Journal of Alzheimer's disease : JAD 2019 67 (1): 243-256. Bonvicini Cristian, Scassellati Catia, Benussi Luisa, Di Maria Emilio, Maj Carlo, Ciani Miriam, Fostinelli Silvia, Mega Anna, Bocchetta Martina, Lanzi Gaetana, Giacopuzzi Edoardo, Ferraboli Sergio, Pievani Michela, Fedi Virginia, Defanti Carlo Alberto, Giliani Silvia, , Frisoni Giovanni Battista, Ghidoni Roberta, Gennarelli Massi |
|
The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1-6 pathogenic variant are associated with a more severe phenotype and lower survival compared with EGFr 7-34 pathogenic variant.
Genetics in medicine : official journal of the American College of Medical Genetics 2018 Jul . Rutten Julie W, Van Eijsden Bastian J, Duering Marco, Jouvent Eric, Opherk Christian, Pantoni Leonardo, Federico Antonio, Dichgans Martin, Markus Hugh S, Chabriat Hugues, Lesnik Oberstein Saskia A |
|
Genomic landscape and prognostic analysis of mantle cell lymphoma.
Cancer gene therapy 2018 May . Yang Ping, Zhang Weilong, Wang Jing, Liu Yuanyuan, An Ran, Jing Hongm |
|
Genetic analysis of adult leukoencephalopathy patients using a custom-designed gene panel.
Clinical genetics 2018 Apr . Kunii M, Doi H, Ishii Y, Ohba C, Tanaka K, Tada M, Fukai R, Hashiguchi S, Kishida H, Ueda N, Kudo Y, Kugimoto C, Nakano T, Udaka N, Miyatake S, Miyake N, Saitsu H, Ito Y, Takahashi K, Nakamura H, Tomita-Katsumoto A, Takeuchi H, Koyano S, Matsumoto N, Tanaka |
|
[Association between polymorphism in notch signaling pathway and lung cancer risk].
Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] 2018 Mar 52 (3): 243-252. Xu Q P, Xiao R D, Xiong W M, He F, Cai |
|
RNF213-related susceptibility of Japanese CADASIL patients to intracranial arterial stenosis.
Journal of human genetics 2018 Mar . Yeung Wing Tung Esther, Mizuta Ikuko, Watanabe-Hosomi Akiko, Yokote Akiyoshi, Koizumi Takashi, Mukai Mao, Kinoshita Masako, Ohara Tomoyuki, Mizuno Toshi |
|
Whole genome sequencing identifies novel NOTCH3 mutations for leukoaraiosis.
Biochemical and biophysical research communications 2018 Feb . Shi Wen-Lei, Zhang Yong-Biao, Wei Wei, Gao Hong-Yan, Huang Yong-H |
|
Study of NOTCH1 and FBXW7 Mutations and Its Prognostic Significance in South Indian T-Cell Acute Lymphoblastic Leukemia.
Journal of pediatric hematology/oncology 2018 01 40 (1): e1-e8. Valliyammai Natarajan, Nancy Nirmala K, Sagar Tenali G, Rajkumar Thangaraj |
|
COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls.
Neurology 2017 Sep . Rannikmäe Kristiina, Sivakumaran Vhinoth, Millar Henry, Malik Rainer, Anderson Christopher D, Chong Mike, Dave Tushar, Falcone Guido J, Fernandez-Cadenas Israel, Jimenez-Conde Jordi, Lindgren Arne, Montaner Joan, O'Donnell Martin, Paré Guillaume, Radmanesh Farid, Rost Natalia S, Slowik Agnieszka, Söderholm Martin, Traylor Matthew, Pulit Sara L, Seshadri Sudha, Worrall Brad B, Woo Daniel, Markus Hugh S, Mitchell Braxton D, Dichgans Martin, Rosand Jonathan, Sudlow Cathie L M, |
|
Identification of Novel Breast Cancer Risk Loci.
Cancer research 2017 Aug . Chan Claire Hian Tzer, Munusamy Prabhakaran, Loke Sau Yeen, Koh Geok Ling, Wong Edward Sern Yuen, Law Hai Yang, Yoon Chui Sheun, Tan Min-Han, Yap Yoon Sim, Ang Peter, Lee Ann Siew G |
|
Polymorphisms in Genes Related to Epithelial-Mesenchymal Transition and Risk of Non-Small Cell Lung Cancer.
Carcinogenesis 2017 Aug . Xie Kunlin, Ye Yuanqing, Zeng Yong, Gu Jian, Yang Hushan, Wu Xife |
|
Prognostic value of Notch receptors in postsurgical patients with hepatitis B virus-related hepatocellular carcinoma.
Cancer medicine 2017 May . Yu Tingdong, Han Chuangye, Zhu Guangzhi, Liao Xiwen, Qin Wei, Yang Chengkun, Liu Zhen, Su Hao, Liu Xiaoguang, Yu Long, Liu Zhengtao, Lu Sicong, Chen Zhiwei, Liang Yu, Huang Jianlu, Qin Xue, Gui Ying, Li Jiaquan, Peng T |
|
Mutational Profile of Metastatic Breast Cancers: A Retrospective Analysis.
PLoS medicine 2016 Dec 13 (12): e1002201. Lefebvre Celine, Bachelot Thomas, Filleron Thomas, Pedrero Marion, Campone Mario, Soria Jean-Charles, Massard Christophe, Lévy Christelle, Arnedos Monica, Lacroix-Triki Magali, Garrabey Julie, Boursin Yannick, Deloger Marc, Fu Yu, Commo Frédéric, Scott Véronique, Lacroix Ludovic, Dieci Maria Vittoria, Kamal Maud, Diéras Véronique, Gonçalves Anthony, Ferrerro Jean-Marc, Romieu Gilles, Vanlemmens Laurence, Mouret Reynier Marie-Ange, Théry Jean-Christophe, Le Du Fanny, Guiu Séverine, Dalenc Florence, Clapisson Gilles, Bonnefoi Hervé, Jimenez Marta, Le Tourneau Christophe, André Fabri |
|
Archetypal NOTCH3 mutations frequent in public exome: implications for CADASIL.
Annals of clinical and translational neurology 2016 Nov 3 (11): 844-853. Rutten Julie W, Dauwerse Hans G, Gravesteijn Gido, van Belzen Martine J, van der Grond Jeroen, Polke James M, Bernal-Quiros Manuel, Lesnik Oberstein Saskia A |
|
The Association Between the Genetic Variants of the NOTCH3 Gene and Ischemic Stroke Risk.
Medical science monitor : international medical journal of experimental and clinical research 2016 Oct 22 3910-3914. Yuan Xiaoling, Dong Zife |
|
Combined effects of age and polymorphisms in Notch3 in the pathogenesis of cerebral infarction disease.
Metabolic brain disease 2016 Jul . Zhu Chun-Yu, Wang Yue, Zeng Qing-Xuan, Qian Yu, Li Huan, Yang Zi-Xia, Yang Ya-Mei, Zhang Qiong, Li Fei-Feng, Liu Shu-L |
|
Ischemic Stroke and Six Genetic Variants in CRP, EPHX2, FGA, and NOTCH3 Genes: A Meta-Analysis.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2016 Jun . González-Giraldo Yeimy, Barreto George E, Fava Cristiano, Forero Diego |
|
Exome sequencing of oral squamous cell carcinoma in users of Arabian snuff reveals novel candidates for driver genes.
International journal of cancer 2016 Mar . Al-Hebshi Nezar Noor, Li Shiyong, Nasher Akram Thabet, El-Setouhy Maged, Alsanosi Rashad, Blancato Jan, Loffredo Christoph |
- Page last reviewed:Oct 1, 2020
- Page last updated:Apr 22, 2021
- Content source: