Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 61 Records) |
Query Trace: Genome editing[original query] |
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Clinical phenotypes combined with saturation genome editing identifying the pathogenicity of BRCA1 variants of uncertain significance in breast cancer. Familial cancer 2020 Aug . Wan Qiting, Hu Li, Ouyang Tao, Li Jinfeng, Wang Tianfeng, Fan Zhaoqing, Fan Tie, Lin Benyao, Xu Ye, Xie Yunt |
T-box transcription factor 3 governs a transcriptional program for the function of the mouse atrioventricular conduction system. Proceedings of the National Academy of Sciences of the United States of America 2020 Jul . Mohan Rajiv A, Bosada Fernanda M, van Weerd Jan H, van Duijvenboden Karel, Wang Jianan, Mommersteeg Mathilda T M, Hooijkaas Ingeborg B, Wakker Vincent, de Gier-de Vries Corrie, Coronel Ruben, Boink Gerard J J, Bakkers Jeroen, Barnett Phil, Boukens Bas J, Christoffels Vincent |
A Key GWAS-Identified Genetic Variant Contributes to Hyperlipidemia by Upregulating miR-320a. iScience 2020 12 23 (12): 101788. Yin Zhongwei, Zhao Yanru, Du Hengzhi, Nie Xiang, Li Huaping, Fan Jiahui, He Mengying, Dai Beibei, Zhang Xudong, Yuan Shuai, Wen Zheng, Chen Chen, Wang Dao W |
Functional validation of CHMP7 as an ADHD risk gene. Translational psychiatry 2020 11 10 (1): 385. Dark Callum, Williams Caitlin, Bellgrove Mark A, Hawi Ziarih, Bryson-Richardson Robert |
Regulatory variants at 2q33.1 confer schizophrenia risk by modulating distal gene TYW5 expression. Brain : a journal of neurology 2021 9 145 (2): 770-786. Li Shiwu, Li Jiao, Liu Jiewei, Wang Junyang, Li Xiaoyan, Huo Yongxia, Li Yifan, Liu Yixing, Li Ming, Xiao Xiao, Luo Xiong-Ji |
Frequent loss of heterozygosity in CRISPR-Cas9-edited early human embryos. Proceedings of the National Academy of Sciences of the United States of America 2021 5 118 (22): . Alanis-Lobato Gregorio, Zohren Jasmin, McCarthy Afshan, Fogarty Norah M E, Kubikova Nada, Hardman Emily, Greco Maria, Wells Dagan, Turner James M A, Niakan Kathy |
Lupus Susceptibility Region Containing CDKN1B rs34330 Mechanistically Influences Expression and Function of Multiple Target Genes, Also Linked to Proliferation and Apoptosis. Arthritis & rheumatology (Hoboken, N.J.) 2021 May . Singh Bhupinder, Maiti Guru P, Zhou Xujie, Fazel-Najafabadi Mehdi, Bae Sang-Cheol, Sun Celi, Terao Chikashi, Okada Yukinori, Heng Chua Kek, Kochi Yuta, Guthridge Joel M, Zhang Hong, Weirauch Matthew, James Judith A, Harley John B, Varshney Gaurav K, Looger Loren L, Nath Swapan |
CRISPR-based genome editing in primary human pancreatic islet cells. Nature communications 2021 4 12 (1): 2397. Bevacqua Romina J, Dai Xiaoqing, Lam Jonathan Y, Gu Xueying, Friedlander Mollie S H, Tellez Krissie, Miguel-Escalada Irene, Bonàs-Guarch Silvia, Atla Goutham, Zhao Weichen, Kim Seung Hyun, Dominguez Antonia A, Qi Lei S, Ferrer Jorge, MacDonald Patrick E, Kim Seung |
Altered Visual Function in a Larval Zebrafish Knockout of Neurodevelopmental Risk Gene pdzk1. Investigative ophthalmology & visual science 2021 3 62 (3): 29. Xie Jiaheng, Jusuf Patricia R, Bui Bang V, Dudczig Stefanie, Sztal Tamar E, Goodbourn Patrick |
Derivation of stem cell line UMi028-A-2 containing a CRISPR/Cas9 induced Alzheimer's disease risk variant p.S1038C in the TTC3 gene. Stem cell research 2021 2 52 102258. Laverde-Paz Mayra Juliana, Nuytemans Karen, Wang Liyong, Vance Jeffery M, Pericak-Vance Margaret A, Dykxhoorn Derek M, Cukier Holly |
Thrombin-deficient mutant of medaka, a model fish, displays serious retardation in blood coagulation. Bioscience, biotechnology, and biochemistry 2021 2 85 (4): 824-833. Watanabe Yuko, Oguri Rina, Suzuki Risa, Meng Qi, Ishikawa Yuta, Tatsukawa Hideki, Hashimoto Hisashi, Hitomi Kiyota |
Mouse Embryonic Fibroblasts Isolated From Nthl1 D227Y Knockin Mice Exhibit Defective DNA Repair and Increased Genome Instability. DNA repair 2021 11 109 103247. Marsden Carolyn G, Das Lipsa, Nottoli Timothy P, Kathe Scott D, Doublié Sylvie, Wallace Susan S, Sweasy Joann |
Plasma Concentration of 12-Hydroxyeicosatetraenoic Acid, Single Nucleotide Polymorphisms of 12-Lipooxygenase Gene and Vaso-Occlusion in Sickle Cell Disease. Frontiers in genome editing 2021 10 3 722190. Duru Augustine Nwakuche, Ocheni Sunday, Ibegbulam Obike, Okpala Ihean |
SNPs associated with colorectal cancer at 15q13.3 affect risk enhancers that modulate GREM1 gene expression. Human mutation 2021 Jan . Fortini Barbara K, Tring Stephanie, Devall Matthew A, Ali Mourad Wagdy, Plummer Sarah J, Casey Grah |
Prevalence and reclassification of BRCA1 and BRCA2 variants in a large, unselected Chinese Han breast cancer cohort. Journal of hematology & oncology 2021 Jan 14 (1): 18. Liu Yun, Wang Honglian, Wang Xin, Liu Jiaqi, Li Junjian, Wang Xiang, Zhang Yun, Bai Zhigang, Zhou Qinghua, Wu Ying, Shen Yi, Weng Xiaoling, Liu Fatao, Guo Jiancheng, Di Lijun, Gires Olivier, Zhang Zhongtao, Chen Yiding, Wang Hongx |
Comparative evolutionary genetics of deleterious load in sorghum and maize. Nature plants 2021 1 7 (1): 17-24. Lozano Roberto, Gazave Elodie, Dos Santos Jhonathan P R, Stetter Markus G, Valluru Ravi, Bandillo Nonoy, Fernandes Samuel B, Brown Patrick J, Shakoor Nadia, Mockler Todd C, Cooper Elizabeth A, Taylor Perkins M, Buckler Edward S, Ross-Ibarra Jeffrey, Gore Michael |
Genetic regulatory and biological implications of the 10q24.32 schizophrenia risk locus. Brain : a journal of neurology 2022 9 . Wang Junyang, Liu Jiewei, Li Shiwu, Li Xiaoyan, Yang Jinfeng, Dang Xinglun, Mu Changgai, Li Yifan, Li Kaiqin, Li Jiao, Chen Rui, Liu Yixing, Huang Di, Zhang Zhijun, Luo Xiong Ji |
A common SNP in Chrna5 enhances morphine reward in female mice. Neuropharmacology 2022 8 218 109218. Brynildsen Julia K, Yang Kechun, Lemchi Crystal, Dani John A, De Biasi Mariella, Blendy Julie |
Functional genomic analysis delineates regulatory mechanisms of GWAS-identified bipolar disorder risk variants. Genome medicine 2022 5 14 (1): 53. Chen Rui, Yang Zhihui, Liu Jiewei, Cai Xin, Huo Yongxia, Zhang Zhijun, Li Ming, Chang Hong, Luo Xiong-Ji |
Functional genomics elucidates regulatory mechanisms of Parkinson's disease-associated variants. BMC medicine 2022 2 20 (1): 68. Chen Rui, Liu Jiewei, Li Shiwu, Li Xiaoyan, Huo Yongxia, Yao Yong-Gang, Xiao Xiao, Li Ming, Luo Xiong-Ji |
On- and Off-Target Analyses of CRISPR-Cas12b Genome Editing Systems in Rice. The CRISPR journal 2022 11 6 (1): 62-74. Gurel Filiz, Wu Yuechao, Pan Changtian, Cheng Yanhao, Li Gen, Zhang Tao, Qi Yipi |
CRISPR/Cas9 genome editing demonstrates functionality of the autoimmunity-associated SNP rs12946510. Biochimica et biophysica acta. Molecular basis of disease 2022 11 1869 (2): 166599. Ustiugova Alina S, Ekaterina Dvorianinova M, Nataliya Melnikova V, Alexey Dmitriev A, Dmitry Kuprash V, Marina Afanasyeva |
Absence of copy number gain of EGFR: A possible predictive marker of long-term response to afatinib. Cancer science 2022 11 . Nakamura Tomomi, Sato Akemi, Nakashima Chiho, Abe Tomonori, Iwanaga Kentaro, Umeguchi Hitomi, Kawaguchi Atsushi, Sueoka-Aragane Nao |
Loss of the Atrial Fibrillation-Related Gene, Zfhx3, Results in Atrial Dilation and Arrhythmias. Circulation research 2023 7 . Heather S Jameson, Alan Hanley, Matthew C Hill, Ling Xiao, Jiangchuan Ye, Aneesh Bapat, Elsa Ronzier, Amelia Weber Hall, William J Hucker, Sebastian Clauss, Miranda Barazza, Elizabeth Silber, Julie Mina, Nathan R Tucker, Robert W Mills, Jin-Tang Dong, David J Milan, Patrick T Ellin |
A comparison of three different delivery methods for achieving CRISPR/Cas9 mediated genome editing in Cichorium intybus L. Frontiers in plant science 2023 5 14 1111110. Umberto Salvagnin, Katharina Unkel, Thorben Sprink, Paul Bundock, Robert Sevenier, Milica Bogdanovi?, Sla?ana Todorovi?, Katarina Cankar, Johanna Christina Hakkert, Elio Schijlen, Ronald Nieuwenhuis, Maria Hingsamer, Veronika Kulmer, Michael Kernitzkyi, Dirk Bosch, Stefan Martens, Mickael Maln |
An IL1RL1 genetic variant lowers soluble ST2 levels and the risk effects of APOE-?4 in female patients with Alzheimer's disease. Nature aging 2023 4 2 (7): 616-634. Yuanbing Jiang, Xiaopu Zhou, Hiu Yi Wong, Li Ouyang, Fanny C F Ip, Vicky M N Chau, Shun-Fat Lau, Wei Wu, Daniel Y K Wong, Heukjin Seo, Wing-Yu Fu, Nicole C H Lai, Yuewen Chen, Yu Chen, Estella P S Tong, , Vincent C T Mok, Timothy C Y Kwok, Kin Y Mok, Maryam Shoai, Benoit Lehallier, Patricia Morán Losada, Eleanor O'Brien, Tenielle Porter, Simon M Laws, John Hardy, Tony Wyss-Coray, Colin L Masters, Amy K Y Fu, Nancy Y |
A regulatory variant at 19p13.3 is associated with primary biliary cholangitis risk and ARID3A expression. Nature communications 2023 3 14 (1): 1732. Li You, Li Zhiqiang, Chen Ruiling, Lian Min, Wang Hanxiao, Wei Yiran, You Zhengrui, Zhang Jun, Li Bo, Li Yikang, Huang Bingyuan, Chen Yong, Liu Qiaoyan, Lyu Zhuwan, Liang Xueying, Miao Qi, Xiao Xiao, Wang Qixia, Fang Jingyuan, Shi YongYong, Liu Xiangdong, Seldin Michael F, Gershwin M Eric, Tang Ruqi, Ma Xio |
Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variation. Nature communications 2023 12 14 (1): 7702. Elizabeth J Radford, Hong-Kee Tan, Malin H L Andersson, James D Stephenson, Eugene J Gardner, Holly Ironfield, Andrew J Waters, Daniel Gitterman, Sarah Lindsay, Federico Abascal, Iñigo Martincorena, Anna Kolesnik-Taylor, Elise Ng-Cordell, Helen V Firth, Kate Baker, John R B Perry, David J Adams, Sebastian S Gerety, Matthew E Hurl |
Three linked variants have opposing regulatory effects on isovaleryl-CoA dehydrogenase gene expression. Human molecular genetics 2023 11 . Elizabeth A Brown, Susan Kales, Michael James Boyle, Joseph Vitti, Dylan Kotliar, Steve Schaffner, Ryan Tewhey, Pardis C Sabe |
Genetic inhibition of angiopoietin-like protein-3, lipids, and cardiometabolic risk. European heart journal 2024 1 . Émilie Gobeil, Jérôme Bourgault, Patricia L Mitchell, Ursula Houessou, Eloi Gagnon, Arnaud Girard, Audrey Paulin, Hasanga D Manikpurage, Valérie Côté, Christian Couture, Simon Marceau, Yohan Bossé, Sébastien Thériault, Patrick Mathieu, Marie-Claude Vohl, André Tchernof, Benoit J Arsenau |
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- Page last updated:Apr 22, 2024
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