Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 36 Records) |
| Query Trace: Disease and Notch2[original query] |
|---|
| The genetic landscape of dural marginal zone lymphomas. Oncotarget 2016 Jul 7 (28): 43052-43061. Ganapathi Karthik A, Jobanputra Vaidehi, Iwamoto Fabio, Jain Preti, Chen Jinli, Cascione Luciano, Nahum Odelia, Levy Brynn, Xie Yi, Khattar Pallavi, Hoehn Daniela, Bertoni Francesco, Murty Vundavalli V, Pittaluga Stefania, Jaffe Elaine S, Alobeid Bachir, Mansukhani Mahesh M, Bhagat Govi |
| Clinicopathological analysis of ATRX, DAXX and NOTCH receptor expression in angiosarcomas. Histopathology 2017 Aug . Panse Gauri, Chrisinger John Sa, Leung Cheuk H, Ingram Davis R, Khan Samia, Wani Khalida, Lin Heather, Lazar Alexander J, Wang Wei-Li |
THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome.
Cellular and molecular gastroenterology and hepatology 2016 Sep 2 (5): 663-675.e2. Tsai Ellen A, Gilbert Melissa A, Grochowski Christopher M, Underkoffler Lara A, Meng He, Zhang Xiaojie, Wang Michael M, Shitaye Hailu, Hankenson Kurt D, Piccoli David, Lin Henry, Kamath Binita M, Devoto Marcella, Spinner Nancy B, Loomes Kathleen |
| Alagille Syndrome. Clinics in liver disease 2018 9 22 (4): 625-641. Mitchell Ellen, Gilbert Melissa, Loomes Kathleen |
| Epistatic Association of CD14 and NOTCH2 Genetic Polymorphisms with Biliary Atresia in a Southern Chinese Population. Molecular therapy. Nucleic acids 2018 Oct 13 590-595. Lin Zefeng, Xie Xiaoli, Lin Huiting, Fu Ming, Su Liang, Tong Yanlu, Chen Hongjiao, Wang Hezhen, Zhao Jinglu, Xia Huimin, Zhang Yan, Zhang Ruizho |
| Functional evidence implicating NOTCH2 missense mutations in primary ovarian insufficiency etiology. Human mutation 2018 10 40 (1): 25-30. Patiño Liliana C, Beau Isabelle, Morel Adrien, Delemer Brigitte, Young Jacques, Binart Nadine, Laissue Pa |
| Unraveling transformation of follicular lymphoma to diffuse large B-cell lymphoma. PloS one 2019 2 14 (2): e0212813. González-Rincón Julia, Méndez Miriam, Gómez Sagrario, García Juan F, Martín Paloma, Bellas Carmen, Pedrosa Lucía, Rodríguez-Pinilla Socorro M, Camacho Francisca I, Quero Cristina, Pérez-Callejo David, Rueda Antonio, Llanos Marta, Gómez-Codina José, Piris Miguel A, Montes-Moreno Santiago, Bárcena Carmen, Rodríguez-Abreu Delvys, Menárguez Javier, de la Cruz-Merino Luis, Monsalvo Silvia, Parejo Consuelo, Royuela Ana, Kwee Ivo, Cascione Luciano, Arribas Alberto, Bertoni Francesco, Mollejo Manuela, Provencio Mariano, Sánchez-Beato Margari |
| Association between tumor mutation profile and clinical outcomes among Hispanic Latina women with triple-negative breast cancer. PloS one 2020 9 15 (9): e0238262. Philipovskiy Alexander, Dwivedi Alok K, Gamez Roberto, McCallum Richard, Mukherjee Debabrata, Nahleh Zeina, Aguilera Renato J, Gaur Sum |
| Genomic Alterations and MYD88 Variant Mapping in Patients with Diffuse Large B-Cell Lymphoma and Response to Ibrutinib. Targeted oncology 2020 4 15 (2): 221-230. Jiang Shiyu, Qin Yan, Gui Lin, Liu Peng, Jiang Hongxin, Liu Biao, Yang Jianliang, Yang Sheng, He Xiaohui, Zhou Shengyu, Du Xinhua, Yi Yuting, Lin Jing, Shi Yuank |
| Genetic lesions in MYC and STAT3 drive oncogenic transcription factor overexpression in plasmablastic lymphoma. Haematologica 2020 4 106 (4): 1120-1128. Garcia-Reyero Julia, Martinez Magunacelaya Nerea, Gonzalez de Villambrosia Sonia, Loghavi Sanam, Gomez Mediavilla Angela, Tonda Raul, Beltran Sergi, Gut Marta, Pereña Gonzalez Ainara, d'Ámore Emanuele, Visco Carlo, Khoury Joseph D, Montes-Moreno Santia |
| Exon Coverage Variations Between Cancer Tissues and Adjacent Non-Cancerous Tissues are Prognostic Factors in Gastric Cancer. OncoTargets and therapy 2020 13 61-70. Pan Xuan, Wang Yajing, Li Chenchen, Zhou Zhaofei, Zhong Yuejiao, Feng Jifeng, Lu Jianw |
| Rare Variants of Putative Candidate Genes Associated With Sporadic Meniere's Disease in East Asian Population. Frontiers in neurology 2019 10 1424. Oh Eun Hye, Shin Jin-Hong, Kim Hyang-Sook, Cho Jae Wook, Choi Seo Young, Choi Kwang-Dong, Rhee Je-Keun, Lee Seowhang, Lee Changwook, Choi Jae-Hw |
| Genetic Variation in CCL5 Signaling Genes and Triple Negative Breast Cancer: Susceptibility and Prognosis Implications. Frontiers in oncology 2019 9 1328. Shan Jingxuan, Chouchane Aziz, Mokrab Younes, Saad Mohamad, Boujassoum Salha, Sayaman Rosalyn W, Ziv Elad, Bouaouina Noureddine, Remadi Yasmine, Gabbouj Sallouha, Roelands Jessica, Ma Xiaojing, Bedognetti Davide, Chouchane Lot |
| Radiation Response Prediction Model Based on Integrated Clinical and Genomic Data Analysis. Cancer research and treatment 2021 Aug . Jang Bum-Sup, Chang Ji-Hyun, Jeon Seung Hyuck, Song Myung Geun, Lee Kyung-Hun, Im Seock-Ah, Kim Jong-Il, Kim Tae-You, Chie Eui K |
| Sex and Menopause Modify the Effect of Single Nucleotide Polymorphism Genotypes on Fibrosis in NAFLD. Hepatology communications 2021 4 5 (4): 598-607. Wegermann Kara, Garrett Melanie E, Zheng Jiayin, Coviello Andrea, Moylan Cynthia A, Abdelmalek Manal F, Chow Shein-Chung, Guy Cynthia D, Diehl Anna Mae, Ashley-Koch Allison, Suzuki Aya |
| Genomic characteristics in neoadjuvant chemoradiotherapy for locally advanced esophageal squamous cell carcinoma. Journal of gastrointestinal oncology 2021 1 11 (6): 1105-1112. He Wenwu, Leng Xuefeng, Wang Kangning, Mao Tiaoqin, Peng Lin, Fang Qiang, Xiao Wenguang, Han Yongt |
| Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance. Frontiers in endocrinology 2021 1 11 582516. Li Lele, Gao Fenqi, Fan Lijun, Su Chang, Liang Xuejun, Gong ChunX |
| Mutation analysis of circulating tumor DNA and paired ascites and tumor tissues in ovarian cancer. Experimental and therapeutic medicine 2022 8 24 (3): 542. Jie Xiaoxiang, Du Ming, Zhang Meng, Jin Xiayu, Cai Qingqing, Xu Congjian, Zhang Xiaoy |
| Pediatric-Type Indolent B-Cell Lymphomas With Overlapping Clinical, Pathologic, and Genetic Features. The American journal of surgical pathology 2022 7 46 (10): 1397-1406. Lim Sojung, Lim Ka Young, Koh Jiwon, Bae Jeong Mo, Yun Hongseok, Lee Cheol, Kim Young A, Paik Jin Ho, Jeon Yoon Kyu |
| Identification of Germline Mutations in Genes Involved in Classic FAP in Patients from Northern Brazil. Cancer diagnosis & prognosis 2022 5 2 (3): 405-410. DI Felipe Ávila Alcantara Diego, Lima Júnior Sergio Figueiredo, DE Assumpção Paulo Pimentel, Lamarão Leticia Martins, DE Castro Sant'anna Carla, Moreira-Nunes Caroline Aquino, Burbano Rommel Rodrigu |
| On the association between Chiari malformation type 1, bone mineral density and bone related genes. Bone reports 2022 3 16 101181. Martínez-Gil Núria, Mellibovsky Leonardo, Manzano-López González Demián, Patiño Juan David, Cozar Monica, Rabionet Raquel, Grinberg Daniel, Balcells Susan |
| Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders. The Journal of clinical endocrinology and metabolism 2022 3 107 (7): e3048-e3057. Oheim Ralf, Tsourdi Elena, Seefried Lothar, Beller Gisela, Schubach Max, Vettorazzi Eik, Stürznickel Julian, Rolvien Tim, Ehmke Nadja, Delsmann Alena, Genest Franca, Krüger Ulrike, Zemojtel Tomasz, Barvencik Florian, Schinke Thorsten, Jakob Franz, Hofbauer Lorenz C, Mundlos Stefan, Kornak U |
| Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hip. Molecular genetics and genomics : MGG 2022 12 298 (2): 329-342. Dembic Maja, van Brakel Andersen Lars, Larsen Martin Jakob, Mechlenburg Inger, Søballe Kjeld, Hertz Jens Micha |
| Prevailing Antagonistic Risks in Pleiotropic Associations with Alzheimer's Disease and Diabetes. Journal of Alzheimer's disease : JAD 2023 6 . Alexander M Kulminski, Fan Feng, Elena Loiko, Alireza Nazarian, Yury Loika, Irina Culminska |
| Molecular associations of response to the new generation BTK inhibitor zanubrutinib in marginal zone lymphoma. Blood advances 2023 3 . Tatarczuch Maciej, Waltham Mark, Shortt Jake, Polekhina Galina, Hawkes Eliza A, Ho Shir-Jing, Trotman Judith, Brasacchio Daniella, Co Melannie, Li Jessica, Ramakrishnan Vanitha, Dunne Karin, Opat Stephen S, Gregory Gareth |
| Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants. American journal of medical genetics. Part A 2023 3 . Sok Pagna, Sabo Aniko, Almli Lynn M, Jenkins Mary M, Nembhard Wendy N, Agopian A J, Bamshad Michael J, Blue Elizabeth E, Brody Lawrence C, Brown Austin L, Browne Marilyn L, Canfield Mark A, Carmichael Suzan L, Chong Jessica X, Dugan-Perez Shannon, Feldkamp Marcia L, Finnell Richard H, Gibbs Richard A, Kay Denise M, Lei Yunping, Meng Qingchang, Moore Cynthia A, Mullikin James C, Muzny Donna, Olshan Andrew F, Pangilinan Faith, Reefhuis Jennita, Romitti Paul A, Schraw Jeremy M, Shaw Gary M, Werler Martha M, Harpavat Sanjiv, Lupo Philip J, |
| Decoding type 2 diabetes mellitus genetic risk variants in Pakistani Pashtun ethnic population using the nascent whole exome sequencing and MassARRAY genotyping: A case-control association study. PloS one 2023 2 18 (1): e0281070. Jan Asif, Zakiullah , Ali Sajid, Muhammad Basir, Arshad Amina, Shah Yasar, Bahadur Haji, Khan Hamayun, Khuda Fazli, Akbar Rani, Ijaz Kir |
| NOTCH pathway mutation contributes to inferior prognosis in HBV-infected chronic lymphocytic leukemia. Annals of hematology 2023 11 . Chun-Yu Shang, Li-Ye Bei, Jia-Zhu Wu, Hao-Rui Sheng, Hua Yin, Jin-Hua Liang, Li Wang, Jian-Yong Li, Yue Li, Wei |
| Identification of biomarker associated with Trop2 in breast cancer: implication for targeted therapy. Discover oncology 2024 9 15 (1): 413. Jianguo Lai, Shuxuan Deng, Jiyuan Cao, Yongqi Ren, Zanmei Xu, Xiaofang Qi, Mian Xu, Ning Li |
| Genetic and prognostic analysis of blastoid and pleomorphic mantle cell lymphoma: a multicenter analysis in China. Annals of hematology 2024 1 . Ping Yang, Shuo-Zi Liu, Chun-Yuan Li, Wei-Long Zhang, Jing Wang, Ying-Tong Chen, Sen Li, Cui-Ling Liu, Hui Liu, Qing-Qing Cai, Wei Zhang, Hong-Mei Ji |
- Page last reviewed:Feb 1, 2024
- Content source: