Mapping cis- and trans-regulatory effects across multiple tissues in twins

The Multiple Tissue Human Expression Resource (MuTHER) Consortium, Grundberg, Elin, Small, Kerrin S, Hedman, Åsa K, Nica, Alexandra C, Buil, Alfonso, Keildson, Sarah, Bell, Jordana T +44 more·2012·Nature Genetics

DOI 10.1038/ng.2394

Cited by (748)

Items 401–500 of 748

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Ana Viñuela, Andrew Anand Brown, Alfonso Buil, Pei-Chien Tsai, Matthew N Davies, Jordana T. Bell, Emmanouil T. Dermitzakis, Tim D. Spector, Kerrin S. Small · 2016 · bioRxiv (Cold Spring Harbor Laboratory)
Differential contribution of cis and trans gene transcription regulatory mechanisms in amygdala and prefrontal cortex and modulation by social stress
Reuveni, Eli, Getselter, Dmitry, Oron, Oded, Elliott, Evan · 2018 · Scientific Reports
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Kenneth R. Day, Lindsay L. Waite, Arnald Alonso, Marguerite R. Irvin, Degui Zhi, Krista S. Thibeault, Stella W. Aslibekyan, Bertha Hidalgo, Ingrid B. Borecki, José María Ordovás et al. · 2016 · PLoS ONE
Lupus Susceptibility Region Containing CDKN1B rs34330 Mechanistically Influences Expression and Function of Multiple Target Genes, Also Linked to Proliferation and Apoptosis
Bhupinder Singh, Guru Prasad Maiti, Xujie Zhou, Mehdi Fazel‐Najafabadi, Sang‐Cheol Bae, Celi Sun, Chikashi C. Terao, Yukinori Okada, Kek Heng Chua, Yuta Kochi et al. · 2021 · Arthritis & Rheumatology
Multiple epistatic DNA variants in a single gene affect gene expression in trans
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Integrated multiomics approach identifies calcium and integrin-binding protein-2 as a novel gene for pulse wave velocity
Massimo Mangino, Marina Cecelja, Cristina Menni, Pei-Chien Tsai, Wei Yuan, Kerrin S. Small, Jordana T. Bell, Gary F. Mitchell, Phil Chowienczyk, Tim D. Spector · 2015 · Journal of Hypertension
Genetic and epigenetic variants contributing to clofarabine cytotoxicity
Michael T. Eadon, Heather E. Wheeler, Amy L. Stark, Xu Zhang, Erika L. Moen, Shannon M. Delaney, Hae Kyung Im, Patrick N. Cunningham, Wei Zhang, M. Eileen Dolan · 2013 · Human Molecular Genetics
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Cristina Menni, Sarah Metrustry, Georg Ehret, Anna F. Dominiczak, Phil Chowienczyk, Tim D. Spector, Sandosh Padmanabhan, Ana Maria Valdes · 2017 · PLoS ONE
Polymorphisms in genes related to epithelial–mesenchymal transition and risk of non-small cell lung cancer
Kunlin Xie, Yuanqing Ye, Yong Zeng, Jian Hong Gu, Hushan Yang, Xifeng Wu · 2017 · Carcinogenesis
A Penalized Regression Framework for Building Polygenic Risk Models Based on Summary Statistics From Genome-Wide Association Studies and Incorporating External Information
Ting-Huei Chen, Nilanjan Chatterjee, Maria Teresa Landi, Jianxin Shi · 2020 · Journal of the American Statistical Association
Leveraging functional annotation to identify genes associated with complex diseases
Wei Liu, Mo Li, Wenfeng Zhang, Geyu Zhou, Xing Wu, Jiawei Wang, Qiongshi Lu, Hongyu Zhao · 2020 · PLoS Computational Biology
Epigenetic Regulation of Estrogen Receptor Genes’ Expressions in Adipose Tissue in the Course of Obesity
Krzysztof Koźniewski, Michał Wąsowski, Marta Izabela Jonas, Wojciech Lisik, Maurycy Jonas, Artur Binda, Paweł Jaworski, Wiesław Tarnowski, Bartlomiej Henryk Noszczyk, Monika Puzianowska‐Kuźnicka et al. · 2022 · International Journal of Molecular Sciences
Gene Silencing and Haploinsufficiency of Csk Increase Blood Pressure
Hyeon-Ju Lee, Ji‐One Kang, Sung-Moon Kim, Sumin Ji, So‐Yon Park, Marina E. Kim, Baigalmaa Jigden, Ji Eun Lim, Sue‐Yun Hwang, Young‐Ho Lee et al. · 2016 · PLoS ONE
Gene expression and adaptive noncoding changes during human evolution
Courtney C. Babbitt, Ralph Haygood, William Nielsen, Gregory A. Wray · 2017 · BMC Genomics
Genetic risk variants for autoimmune diseases that influence gene expression in thymus
Ingvild Gabrielsen, Silja Svanstrøm Amundsen, Hanna Helgeland, Siri T. Flåm, Nimo Hatinoor, Kristian Holm, Marte Kathrine Viken, Benedicte Alexandra Lie · 2016 · Human Molecular Genetics
Illuminating links between cis-regulators and trans-acting variants in the human prefrontal cortex
Shuang Liu, Hyejung Won, Declan Clarke, Nana Matoba, Saniya Khullar, Yudi Mu, Daifeng Wang, Mark Gerstein · 2022 · Genome Medicine
Association of Early Childhood Caries with Bitter Taste Receptors: A Meta-Analysis of Genome-Wide Association Studies and Transcriptome-Wide Association Study
Ekaterina Orlova, Tom Dudding, Jonathan M. Chernus, Rasha N. Alotaibi, Simon J. Haworth, Richard J. Crout, Myoung Keun Lee, Nandita Mukhopadhyay, Eleanor Feingold, Steven Marc Levy et al. · 2022 · Genes
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Shahid Ullah Khan, Sumbul Saeed, Amnah Mohammed Alsuhaibani, Sumaya Fatima, Khalil ur Rehman, Umber Zaman, Muneeb Ullah, Moamen Salah El-Deen Refat, Kun Lu · 2023 · Current Problems in Cardiology
High-Resolution Genetic Maps Identify Multiple Type 2 Diabetes Loci at Regulatory Hotspots in African Americans and Europeans
Winston Lau, Toby Andrew, Nikolas Maniatis · 2017 · The American Journal of Human Genetics
Identifying Multi-Omics Causers and Causal Pathways for Complex Traits
Huaizhen Qin, Tianhua Niu, Jinying Zhao · 2019 · Frontiers in Genetics
Systems-based approaches for investigation of inter-tissue communication
Marcus Michael Seldin, Aldons Jake Lusis · 2019 · Journal of Lipid Research
Transcriptome profiling in adult attention-deficit hyperactivity disorder.
Niall Mortimer, C. Sánchez-Mora, P. Rovira, L. Vilar-Ribó, V. Richarte, M. Corrales, C. Fadeuilhe, O. Rivero, K. Lesch, M. Casas et al. · 2020 · European Neuropsychopharmacology
Systematic review of gastric cancer-associated genetic variants, gene-based meta-analysis, and gene-level functional analysis to identify candidate genes for drug development
Sangjun Lee, Han‐Kwang Yang, Hyuk-Joon Lee, Do Joong Park, Seong‐Ho Kong, Sue K. Park · 2022 · Frontiers in Genetics
Interpretation of the role of germline and somatic non-coding mutations in cancer: expression and chromatin conformation informed analysis
Michael Pudjihartono, Jo Kate Perry, Cristin Gregor Print, Justin Martin O'Sullivan, William S. Schierding · 2022 · Clinical Epigenetics
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Lei Yang, Zelin Yang, Chunjian Zuo, Xiaolong Lv, Tianyu Liu, Chenhao Jia, Huanwen Chen · 2022 · Frontiers in Oncology
An independent component analysis confounding factor correction framework for identifying broad impact expression quantitative trait loci
Jin Hyun Ju, Sushila A. Shenoy, Ronald G. Crystal, Jason G. Mezey · 2017 · PLoS Computational Biology
A genome-wide survey of copy number variations reveals an asymmetric evolution of duplicated genes in rice
Fengli Zhao, Yuexing Wang, Jianshu Zheng, Yanling Wen, Minghao Qu, Shujing Kang, Shigang Wu, Xiaojuan Deng, Kai Hong, Sanfeng Li et al. · 2020 · BMC Biology
Partitioning gene-mediated disease heritability without eQTLs
Daniel J. Weiner, Steven Gazal, Elise Robinson, Luke Jen O’Connor · 2022 · The American Journal of Human Genetics
eQTL mapping identifies insertion- and deletion-specific eQTLs in multiple tissues
Jinyan Huang, Jun Chen, Jorge Esparza, Jun Ding, James T. Elder, Gonçalo R. Abecasis, Young-Ae Lee, Mark G. Lathrop, Miriam F. Moffatt, William Cookson et al. · 2015 · Nature Communications
Variants in thePSCAgene associated with risk of cancer and nonneoplastic diseases: systematic research synopsis, meta-analysis and epidemiological evidence
Huijie Cui, Mingshuang Tang, Min Zhang, Shanshan Liu, Siyu Chen, Ziqian Zeng, Zhuozhi Shen, Bin Song, Jiachun Lü, Hong Jia et al. · 2018 · Carcinogenesis
The lncRNA LOC102549805 (U1) modulates neurotoxicity of HIV-1 Tat protein
Bahareh Torkzaban, Kalimuthusamy Natarajaseenivasan, Taha Mohseni Ahooyi, Masoud Shekarabi, Shohreh Amini, Dianne Langford, Kamel Khalili · 2020 · Cell Death and Disease
Adipose methylome integrative-omic analyses reveal genetic and dietary metabolic health drivers and insulin resistance classifiers
Colette Christiansen, Max Tomlinson, Melissa Eliot, Emma Nilsson, Ricardo Costeira, Yujing Xia, Sergio Villicaña, Olatz Mompeó, Philippa M. Wells, Juan Castillo Fernandez et al. · 2022 · Genome Medicine
Integrating eQTL and GWAS data characterises established and identifies novel migraine risk loci
Ammarah Ghaffar, Dale R. Nyholt · 2023 · Human Genetics
Transcriptomic risk scores for attention deficit/hyperactivity disorder
Judit Cabana‐Domínguez, Natalia Llonga, Lorena Arribas, Silvia Alemany, Laura Vilar‐Ribó, Ditte Demontis, Christian Fadeuilhe, Montse Corrales F, Vanesa Richarte B, Anders Dupont Børglum et al. · 2023 · Molecular Psychiatry
Mapping and annotating genomic loci to prioritize genes and implicate distinct polygenic adaptations for skin color
Beomsu Kim, Dan Say Kim, Joong‐Gon Shin, Sangseob Leem, Minyoung Cho, Hanji Kim, Ki‐Nam Gu, Jung Yeon Seo, Seung Won You, Alicia R. Martin et al. · 2024 · Nature Communications
The heritability and patterns of DNA methylation in normal human colorectum
Amy Rowlatt, Gustavo A. Hernandez-Suarez, María Carolina Sanabria‐Salas, Martha Lucía Serrano, Konrad Rawlik, Eva Hernández‐Illán, Cristina Alenda, Adela Castillejo, José Luís Soto, Chris Haley et al. · 2016 · Human Molecular Genetics
A comprehensive genome‐wide analysis of melanoma Breslow thickness identifies interaction between CDC42 and SCIN genetic variants
Amaury Vaysse, Shenying Fang, Myriam Brossard, Qingyi Wei, Wei V. Chen, Hamida Mohamdi, Lynda Vincent-Fétita, Patricia Margaritte‐Jeannin, Nolwenn Lavielle, E. Maubec et al. · 2016 · International Journal of Cancer
Characterizing the Relation Between Expression QTLs and Complex Traits: Exploring the Role of Tissue Specificity
Hill Fung Ip, Rick Jansen, Abdel Abdellaoui, Meike Bartels, Dorret Irene Boomsma, Michel Guillaume Nivard · 2018 · Behavior Genetics
Trans-Ethnic Mapping of BANK1 Identifies Two Independent SLE-Risk Linkage Groups Enriched for Co-Transcriptional Splicing Marks
Manuel Martínez‐Bueno, N. Yu. Oparina, Mikhail G. Dozmorov, Miranda C. Marion, Mary E. Comeau, Gary S. Gilkeson, Diane L. Kamen, Michael H. Weisman, Jane E. Salmon, Joseph W. McCune et al. · 2018 · International Journal of Molecular Sciences
Transcript specific regulation of expression influences susceptibility to multiple sclerosis
Maria Ban, Wenjia Liao, Amie Baker, Alastair Compston, John W. Thorpe, Paul David Molyneux, M Fraser, Jyoti Khadake, Joanne Jones, Alasdair J. Coles et al. · 2020 · European Journal of Human Genetics
Capturing functional epigenomes for insight into metabolic diseases
Fiona Allum, Elin Grundberg · 2020 · Molecular Metabolism
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TTSH RA Study Group, Liuh Ling Goh, Mei Yun Yong, Wei Qiang See, Edward Yu Wing Chee, Pei Qi Lim, Ee Tzun Koh, Khai Pang Leong · 2017 · Rheumatology International
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Karim Labrèche, Maïlys Daniau, Amit Sud, Philip Law, Louis Royer-Perron, Amy Holroyd, Peter Broderick, Molly Went, Marion Benazra, Guido Ahle et al. · 2019 · Neuro-Oncology
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Letitia M.F. Sng, Peter Campbell Thomson, Daniah Trabzuni · 2019 · Scientific Reports
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Corbin Quick, Li Guan, Zilin Li, Xihao Li, Rounak Dey, Yaowu Liu, Laura J. Scott, Xihong Lin · 2020 · bioRxiv (Cold Spring Harbor Laboratory)
Interaction of an S100A9 gene variant with saturated fat and carbohydrates to modulate insulin resistance in 3 populations of different ancestries1–3
Blanco-Rojo, Ruth, Delgado-Lista, Javier, Lee, Yu-Chi, Lai, Chao-Qiang, Perez-Martinez, Pablo, Rangel-Zuñiga, Oriol, Smith, Caren E, Hidalgo, Bertha, Alcala-Diaz, Juan F, Gomez-Delgado, Francisco et al. · 2016 · The American Journal of Clinical Nutrition
Cumulative Evidence for Relationships Between Multiple Variants in the TERT and CLPTM1L Region and Risk of Cancer and Non-Cancer Disease
Jie Tian, Yan Wang, Yingxian Dong, Junke Chang, Yongming Wu, Shuai Chang, Guowei Che · 2022 · Frontiers in Oncology
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Priya Sudarsanam, Barak A. Cohen · 2014 · PLoS Genetics
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Olga McLeod, Angela Maria Vidigal Silveira, Elsa Valdés‐Márquez, Harry Björkbacka, Peter Almgren, Karl Gertow, Jesper R. Gådin, Alexandra Bäcklund, Bengt Sennblad, Damiano Baldassarre et al. · 2016 · Cytokine
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Matthias Heinig · 2018 · Frontiers in Cardiovascular Medicine
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Suchi Smita, Falko Lange, Olaf Wolkenhauer A, Rüdiger Köhling · 2016 · Biochimica et Biophysica Acta (BBA) - General Subjects
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L Canet, Rafael Cáliz, Carmen B. Lupiañez, Helena M Canhão, Manuel Martinez, Alejandro Escudero‐Contreras, I. Filipescu, Juana Segura-Catena, María José Soto-Pino, Miguel A. Ferrer et al. · 2015 · Pharmacogenetics and Genomics
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Kenan Direk, Winston Lau, Kerrin S. Small, Nikolas Maniatis, Toby Andrew · 2014 · Annals of Human Genetics
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Manuela Sironi, Mara Biasin, Federica Gnudi, Rachele Cagliani, Irma Saulle, Diego Forni, Veronica Rainone, Daria Trabattoni, Micaela Garziano, Francesco Mazzotta et al. · 2014 · PLoS ONE
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Cristina Venturini, Abhishek Nag, Pirro G. Hysi, Jie Jin Wang, Tien Yin Wong, Paul R. Healey, Paul Mitchell, Christopher J. Hammond, Ananth C. Viswanathan · 2014 · British Journal of Ophthalmology
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Michael David Morgan, Étienne Patin, Bernd Jagla, Milena Hasan, Lluís Quintana‐Murci, John C. Marioni · 2020 · PLoS Genetics
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Xiaohua Chen, Hua Du, Binjian Liu, Li Zou, Wei Chen, Yang Yang, Ying Zhu, Yajie Gong, Jianbo Tian, Feng Li et al. · 2015 · PLoS ONE
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Sarah H. Lockwood, Anna S. Guan, Abigail S. Yu, Chi Zhang, Artem Zykovich, Ian F. Korf, Bruce H. Rannala, David Jay Segal · 2014 · G3 Genes Genomes Genetics
Crossing Phenotype Heritability and Candidate Gene Expression in Grafted Black-Lipped Pearl Oyster Pinctada margaritifera, an Animal Chimera
Carole Blay, Serge Planes, Chin‐Long Ky · 2018 · Journal of Heredity
Pathway-Based Factor Analysis of Gene Expression Data Produces Highly Heritable Phenotypes That Associate with Age
Andrew Anand Brown, Zhihao Ding, Ana Viñuela, Dan Glass, Leopold Parts, Tim D. Spector, John Michael Winn, Richard Michael Durbin · 2015 · G3 Genes Genomes Genetics
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Aida Moreno‐Moral, Francesco Pesce, Jacques V. Behmoaras, Enrico G. Petretto · 2016 · Methods in molecular biology
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Jianhua Chen, Ping Yang, Qian Zhang, Ruirui Chen, Peng Wang, Benxiu Liu, Wensheng Sun, Xuemin Jian, Siying Xiang, Juan Zhou et al. · 2021 · Translational Psychiatry
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Diana Avalos, Guillaume Rey, Diogo M. Ribeiro, Anna Ramisch, Emmanouil T. Dermitzakis, Olivier Delaneau · 2023 · Communications Biology
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Rong Li, Jian Hong Gu, John Victor Heymach, Xiang Shu, Lina Zhao, Baohui Han, Yuanqing Ye, Jack A. Roth, Xifeng Wu · 2017 · Carcinogenesis
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Clare C Landefeld, Colin A. Hodgkinson, Primavera A. Spagnolo, Cheryl A. Marietta, Pei‐Hong Shen, Hui Sun, Zhifeng Zhou, Barbara K. Lipska, David A Goldman · 2018 · Translational Psychiatry
Estimation of cis-eQTL Effect Sizes Using a Log of Linear Model
John Palowitch, A. Shabalin, Yi-Hui Zhou, A. Nobel, F. Wright · 2017 · Biometrics
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Junghyun Jung, Go Woon Kim, Byungjo Lee, Jong Wha J. Joo, Wonhee Jang · 2019 · BMC Medical Genomics
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Brian Jo, Yuan Ming He, Benjamin J. Strober, Princy Parsana, François Aguet, Andrew Anand Brown, Stephane E. Castel, Eric R. Gamazon, Ariel DH Gewirtz, Genna Gliner et al. · 2016 · bioRxiv (Cold Spring Harbor Laboratory)
Testing hypotheses on a tree: new error rates and controlling strategies
Marina Bogomolov, Christine B. Peterson, Yoav Benjamini, Chiara Sabatti · 2017 · arXiv (Cornell University)
Transcriptome-wide association study identifies novel candidate susceptibility genes for migraine
Travis J. Meyers, Jie Yin, Victor A. Herrera, Alice Rogot Pressman, Thomas J. Hoffmann, Catherine A. Schaefer, Andrew L. Avins, Hélène Choquet · 2023 · Human Genetics and Genomics Advances
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Henry Wittich, Kristin Ardlie, Kent D. Taylor, Peter Durda, Yongmei Liu, Anna V. Mikhaylova, Christopher R. Gignoux, Michael H. Cho, Stephen S. Rich, Jerome I. Rotter et al. · 2024 · The American Journal of Human Genetics
RNA Biogenesis Instructs Functional Inter-Chromosomal Genome Architecture
Alessandro Bertero · 2021 · Frontiers in Genetics
Molecular Characterization of the Lipid Genome-Wide Association Study Signal on Chromosome 18q11.2 Implicates HNF4A-Mediated Regulation of the TMEM241 Gene
Alejandra Rodríguez, Luis A. Gonzalez, Arthur Ko, Marcus Alvarez, Zong Miao, Yash V. Bhagat, Elina Nikkola, Ivette Cruz‐Bautista, Olimpia Arellano‐Campos, Linda Liliana Muñóz-Hernández et al. · 2016 · Arteriosclerosis Thrombosis and Vascular Biology
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Huanhuan Zhu, Lulu Shang, Xiang Zhou · 2021 · Frontiers in Genetics
Genetic determinants of adiponectin regulation revealed by pregnancy
Marie‐France Hivert, Denise M. Scholtens, Catherine Allard, Michael Nodzenski, Luigi Bouchard, Diane Brisson, Lynn P. Lowe, Ian C. McDowell, Tim Reddy, Zari Dastani et al. · 2017 · Obesity
Many long intergenic non-coding RNAs distally regulate mRNA gene expression levels
Ian C. McDowell, Athma A. Pai, Cong Guo, Christopher M. Vockley, Christopher D. Brown, Timothy E. Reddy, Barbara Elizabeth Engelhardt · 2016 · bioRxiv (Cold Spring Harbor Laboratory)
HLA-A 31:01 is not associated with the development of methotrexate pneumonitis in the UK population: results from a genome-wide association study
James Bluett, Sally-Anne Owen, Jonathan Massey, Ana Alfirevic, Munir Pirmohamed, Darren Plant, Suzanne M. M. Verstappen, Anne C Barton · 2017 · Annals of the Rheumatic Diseases
Ultra-rare variants drive substantial cis -heritability of human gene expression
Ryan D. Hernandez, Lawrence H. Uricchio, Kevin Hartman, Chun Ye, Andrew Dahl, Noah Zaitlen · 2017 · bioRxiv (Cold Spring Harbor Laboratory)
Multiscale causal network models of Alzheimer’s disease identify VGF as a key regulator of disease
Noam D. Beckmann, Wei‐Jye Lin, Minghui Wang, Ariella T. Cohain, Pei Wang, Weiping Ma, Ying‐Chih Wang, Cheng Shi Jiang, Mickaël Audrain, Phillip Comella et al. · 2018 · bioRxiv (Cold Spring Harbor Laboratory)
Conserved properties of genetic architecture of renal and fat transcriptomes in rat models of insulin resistance
Georg Otto, Pamela J. Kaisaki, François Brial, Aurélie Le Lay, Jean‐Baptiste Cazier, Richard Mott, Dominique Gauguier · 2019 · Disease Models & Mechanisms
Potential drug targets for myocardial infarction identified through Mendelian randomization analysis and Genetic colocalization
Jiayu Wu, Qiaoming Fan, Qi He, Qian Zhong, Xianqiong Zhu, Huilian Cai, Xiaolin He, Ying Xu, Yuxuan Huang, Xingwei Di · 2023 · Medicine
Association of Cross-Sectional and Longitudinal Change in Arterial Stiffness With Gene Expression in the Twins UK Cohort
Marina Cecelja, Benyu Jiang, Massimo Mangino, Tim D. Spector, Phil Chowienczyk · 2015 · Hypertension
A systematic comparison of normalization methods for eQTL analysis
Jiajun Yang, Dongyang Wang, Yanbo Yang, Wenqian Yang, Weiwei Jin, Xiaohui Niu, Jing Gong · 2021 · Briefings in Bioinformatics
Transcriptome-based polygenic score links depression-related corticolimbic gene expression changes to sex-specific brain morphology and depression risk
Amy E. Miles, Fernanda C. Dos Santos, Enda M. Byrne, Miguel E. Rentería, Andrew Mark McIntosh, Mark J. Adams, Giorgio Pistis, Enrique Castelao, Martin Preisig, Bernhard Theodor Baune et al. · 2021 · Neuropsychopharmacology
Dynamics of Brain Structure and its Genetic Architecture over the Lifespan
Rachel M. Brouwer, Marieke Klein, Katrina L. Grasby, Hugo Gerard Schnack, Neda Jahanshad, Jalmar Teeuw, Sophia I. Thomopoulos, Emma Sprooten, Carol E. Franz, Nitin Gogtay et al. · 2020 · Zenodo (CERN European Organization for Nuclear Research)
DUSP1Gene Polymorphisms Are Associated with Obesity-Related Metabolic Complications among Severely Obese Patients and Impact on Gene Methylation and Expression
Frédéric Guénard, Luigi Bouchard, André Tchernof, Yves Deshaies, Frédéric Simon Hould, Stéfane Lebel, Picard Marceau, Louis Përusse, Marie‐Claude Vohl · 2013 · International Journal of Genomics
Genetic factors influencing the risk of multiple myeloma bone disease
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RIPK2 polymorphisms and susceptibility to tuberculosis in a Western Chinese Han population
Jiajia Song, Tangyuheng Liu, Lin Jiao, Zhenzhen Zhao, Xuejiao Lina Hu, Qian Wu, Hao Bai, Mengyuan Lv, Zirui Meng, Tao Wu et al. · 2019 · Infection Genetics and Evolution