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Author Correction: The Rho GTPase Rnd1 suppresses mammary tumorigenesis and EMT by restraining Ras-MAPK signalling

Nature cell biology 2019年第4期21卷 534页

作者： Tomoyo Okada Surajit Sinha Ilaria Esposito Gaia Schiavon Miguel A López-Lago Wenjing Su Christine A Pratilas Cristina Abele Jonathan M Hernandez Masahiro Ohara Morihito Okada Agnes Viale Adriana Heguy Nicholas D Socci Anna Sapino Venkatraman E Seshan Stephen Long Giorgio Inghirami Neal Rosen Filippo G Giancotti Cell Biology Program Sloan-Kettering Institute for Cancer Research Memorial Sloan-Kettering Cancer Center New York New York 10065 USA. Department of Surgery Memorial Sloan-Kettering Cancer Center New York 10065 USA. Breast Unit Royal Marsden Hospital London SW3 6JJ UK. Department of Surgery and Center for Cell Engineering Memorial Sloan-Kettering Cancer Center New York 10065 USA. Molecular Pharmacology and Chemistry Program Sloan-Kettering Institute for Cancer Research Memorial Sloan-Kettering Cancer Center New York New York 10065 USA. Department of Pediatrics Memorial Hospital Memorial Sloan-Kettering Cancer Center New York New York 10065 USA. The Sidney Kimmel Comprehensive Cancer Center Johns Hopkins University School of Medicine Baltimore Maryland 21287 USA. Department of Biomedical Sciences and Human Oncology Center of Experimental Medicine and Research University of Torino Torino 10126 Italy. Department of Surgery Memorial Hospital Memorial Sloan-Kettering Cancer Center New York New York 10065 USA. Department of Surgical Oncology Research Institute for Radiation Biology and Medicine Graduate School of Biomedical Sciences Hiroshima University Hiroshima 734-8551 Japan. Genomics Core Facility Memorial Sloan-Kettering Cancer Center New York New York 10065 USA. Geoffrey Beene Translational Oncology Core Facility Memorial Sloan-Kettering Cancer Center New York New York 10065 USA. Department of Pathology Office for Collaborative Science New York University New York 10016 USA. Bioinformatics Core Facility Memorial Sloan-Kettering Cancer Center New York New York 10065 USA. Department of Medical Sciences Center of Experimental Medicine and Research University of Torino Torino 10126 Italy. Department of Epidemiology and Biostatistics Memorial Hospital Memorial Sloan-Kettering Cancer Center New York New York 10065 USA. Structural Biology Program Sloan-Kettering Institute for Cancer Research Memorial Sloan-Kettering Cancer Center New Y

In the version of this Article originally published the same blot was inadvertently presented as both p-Rb and Cyclin A in Fig. 2a. This blot corresponds to the p-Rb panel, as can be seen in the unprocessed version of these blots in Supplementary Fig. 9. The corrected version of the panel is shown below, together with a completely uncropped image of both blots. In addition, in the 'Viral transduction' section of the Methods, the pLKO.1 plasmids encoding short hairpin RNAs targeting human Rnd1 were incorrectly listed as clones TRCN0000018338 and TRCN0000039977. The correct clone numbers are TRCN0000047434 and TRCN0000047435.

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Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (vol 51, pg 659, 2019)

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NATURE GENETICS 2019年第6期51卷 1068-1068页

作者： Huckins, Laura M. Dobbyn, Amanda Ruderfer, Douglas M. Hoffman, Gabriel Wang, Weiqing Pardinas, Antonio F. Rajagopal, Veera M. Als, Thomas D. Nguyen, Hoang T. Girdhar, Kiran Boocock, James Roussos, Panos Fromer, Menachem Kramer, Robin Domenici, Enrico Gamazon, Eric R. Purcell, Shaun Demontis, Ditte Borglum, Anders D. Walters, James T. R. O'Donovan, Michael C. Sullivan, Patrick Owen, Michael J. Devlin, Bernie Sieberts, Solveig K. Cox, Nancy J. Im, Hae Kyung Sklar, Pamela Stahl, Eli A. Pamela Sklar Division of Psychiatric Genomics Icahn School of Medicine at Mount Sinai New York NY USA Department of Genetics and Genomics Icahn School of Medicine at Mount Sinai New York NY USA Department of Psychiatry Icahn School of Medicine at Mount Sinai New York NY USA Icahn Institute for Genomics and Multiscale Biology Icahn School of Medicine at Mount Sinai New York NY USA Vanderbilt University Medical Center Nashville TN USA MRC Centre for Neuropsychiatric Genetics and Genomics Cardiff University Cardiff UK Department of Biomedicine Aarhus University Aarhus Denmark The Lundbeck Foundation Initiative for Integrative Psychiatric Research iPSYCH Denmark Center for Integrative Sequencing Aarhus University Aarhus Denmark Department of Human Genetics David Geffen School of Medicine University of California Los Angeles Los Angeles CA USA Human Brain Collection Core National Institute of Mental Health Bethesda MD USA Laboratory of Neurogenomic Biomarkers Centre for Integrative Biology (CIBIO) University of Trento Trento Italy Clare Hall University of Cambridge Cambridge UK University of North Carolina at Chapel Hill Chapel Hill NC USA Karolinska Institutet Stockholm Sweden Department of Psychiatry University of Pittsburgh Pittsburgh PA USA Systems Biology Sage Bionetworks Seattle WA USA Section of Genetic Medicine Department of Medicine University of Chicago Chicago IL USA Integrated Technology Research Laboratories Pharmaceutical Research Division Takeda Pharmaceutical Company Limited Fujisawa Japan Neuropsychiatry Section Department of Psychiatry Perelman School of Medicine University of Pennsylvania Philadelphia PA USA Neuropsychiatric Signaling Program Department of Psychiatry Perelman School of Medicine University of Pennsylvania Philadelphia PA USA Psychiatry JJ Peters Virginia Medical Center Bronx NY USA Department of Neuroscience Icahn School of Medicine at Mount Sinai New York New York NY USA Friedman Brain Institute

Transcriptomic imputation approaches combine eQTL reference panels with large-scale genotype data in order to test associations between disease and gene expression. These genic associations could elucidate signals in complex genome-wide association study (GWAS) loci and may disentangle the role of different tissues in disease development. We used the largest eQTL reference panel for the dorso-lateral prefrontal cortex (DLPFC) to create a set of gene expression predictors and demonstrate their utility. We applied DLPFC and 12 GTEx-brain predictors to 40,299 schizophrenia cases and 65,264 matched controls for a large transcriptomic imputation study of schizophrenia. We identified 413 genic associations across 13 brain regions. Stepwise conditioning identified 67 non-MHC genes, of which 14 did not fall within previous GWAS loci. We identified 36 significantly enriched pathways, including hexosaminidase-A deficiency, and multiple porphyric disorder pathways. We investigated developmental expression patterns among the 67 non-MHC genes and identified specific groups of pre- and postnatal expression.

关键词： Gene expression Genome-wide association studies Schizophrenia Transcriptomics

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Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk

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Nature genetics 2020年第3期52卷 354页

作者： Iris E Jansen Jeanne E Savage Kyoko Watanabe Julien Bryois Dylan M Williams Stacy Steinberg Julia Sealock Ida K Karlsson Sara Hägg Lavinia Athanasiu Nicola Voyle Petroula Proitsi Aree Witoelar Sven Stringer Dag Aarsland Ina S Almdahl Fred Andersen Sverre Bergh Francesco Bettella Sigurbjorn Bjornsson Anne Brækhus Geir Bråthen Christiaan de Leeuw Rahul S Desikan Srdjan Djurovic Logan Dumitrescu Tormod Fladby Timothy J Hohman Palmi V Jonsson Steven J Kiddle Arvid Rongve Ingvild Saltvedt Sigrid B Sando Geir Selbæk Maryam Shoai Nathan G Skene Jon Snaedal Eystein Stordal Ingun D Ulstein Yunpeng Wang Linda R White John Hardy Jens Hjerling-Leffler Patrick F Sullivan Wiesje M van der Flier Richard Dobson Lea K Davis Hreinn Stefansson Kari Stefansson Nancy L Pedersen Stephan Ripke Ole A Andreassen Danielle Posthuma Department of Complex Trait Genetics Center for Neurogenomics and Cognitive Research Amsterdam Neuroscience VU University Amsterdam the Netherlands. Alzheimer Center Amsterdam Department of Neurology Amsterdam Neuroscience Vrije Universiteit Amsterdam Amsterdam UMC Amsterdam the Netherlands. Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden. deCODE Genetics/ Amgen Reykjavik Iceland. Interdisciplinary Graduate Program Vanderbilt University Nashville TN USA. Institute of Gerontology and Aging Research Network-Jönköping (ARN-J) School of Health and Welfare Jönköping University Jönköping Sweden. NORMENT K.G. Jebsen Centre for Psychosis Research Institute of Clinical Medicine University of Oslo Oslo Norway. Division of Mental Health and Addiction Oslo University Hospital Oslo Norway. Institute of Psychiatry Psychology and Neuroscience King's College London London UK. Institute of Clinical Medicine University of Oslo Oslo Norway. Center for Age-Related Diseases Stavanger University Hospital Stavanger Norway. Department of Neurology Akershus University Hospital Lørenskog Norway. AHUS Campus University of Oslo Oslo Norway. Department of Psychiatry of Old Age Oslo University Hospital Oslo Norway. Department of Community Medicine University of Tromsø Tromsø Norway. Norwegian National Advisory Unit on Ageing and Health Vestfold Hospital Trust Tønsberg Norway. Centre for Old Age Psychiatry Research Innlandet Hospital Trust Ottestad Norway. Department of Geriatric Medicine Landspitali University Hospital Reykjavik Iceland. Geriatric Department Oslo University Hospital Oslo Norway. Department of Neuromedicine and Movement Science Norwegian University of Science and Technology Trondheim Norway. Department of Neurology St Olav's Hospital Trondheim University Hospital Trondheim Norway. Neuroradiology Section Department of Radiology and Biomedical Imaging University of California San Francisco CA USA. Department

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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Corrigendum to “Weight-bearing asymmetry and vertical activity differences in a rat model of post-traumatic knee osteoarthritis” [Osteoarthritis Cartilage 23 (7) (2015) 1178–85]

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Osteoarthritis and Cartilage 2016年第2期24卷 382-382页

作者： Hamilton, C.B. Pest, M.A. Pitelka, V. Ratneswaran, A. Beier, F. Chesworth, B.M. Graduate Program in Health and Rehabilitation Sciences Faculty of Health Sciences University of Western Ontario London ON Canada Collaborative Graduate Program in Musculoskeletal Health Research University of Western Ontario London ON Canada Department of Physiology and Pharmacology Schulich School of Medicine and Dentistry University of Western Ontario London ON Canada School of Physical Therapy Faculty of Health Science Department of Epidemiology and Biostatistics Schulich School of Medicine and Dentistry University of Western Ontario London ON Canada

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Correction to: 2021 Taxonomic update of phylum Negarnaviricota (Riboviria: Orthornavirae), including the large orders Bunyavirales and Mononegavirales

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Archives of virology 2021年第12期166卷 3567-3579页

作者： Jens H Kuhn Scott Adkins Bernard R Agwanda Rim Al Kubrusli Sergey V Alkhovsky Gaya K Amarasinghe Tatjana Avšič-Županc María A Ayllón Justin Bahl Anne Balkema-Buschmann Matthew J Ballinger Christopher F Basler Sina Bavari Martin Beer Nicolas Bejerman Andrew J Bennett Dennis A Bente Éric Bergeron Brian H Bird Carol D Blair Kim R Blasdell Dag-Ragnar Blystad Jamie Bojko Wayne B Borth Steven Bradfute Rachel Breyta Thomas Briese Paul A Brown Judith K Brown Ursula J Buchholz Michael J Buchmeier Alexander Bukreyev Felicity Burt Carmen Büttner Charles H Calisher Mengji Cao Inmaculada Casas Kartik Chandran Rémi N Charrel Qi Cheng Yuya Chiaki Marco Chiapello Il-Ryong Choi Marina Ciuffo J Christopher S Clegg Ian Crozier Elena Dal Bó Juan Carlos de la Torre Xavier de Lamballerie Rik L de Swart Humberto Debat Nolwenn M Dheilly Emiliano Di Cicco Nicholas Di Paola Francesco Di Serio Ralf G Dietzgen Michele Digiaro Olga Dolnik Michael A Drebot J Felix Drexler William G Dundon W Paul Duprex Ralf Dürrwald John M Dye Andrew J Easton Hideki Ebihara Toufic Elbeaino Koray Ergünay Hugh W Ferguson Anthony R Fooks Marco Forgia Pierre B H Formenty Jana Fránová Juliana Freitas-Astúa Jingjing Fu Stephanie Fürl Selma Gago-Zachert George Fú Gāo María Laura García Adolfo García-Sastre Aura R Garrison Thomas Gaskin Jean-Paul J Gonzalez Anthony Griffiths Tony L Goldberg Martin H Groschup Stephan Günther Roy A Hall John Hammond Tong Han Jussi Hepojoki Roger Hewson Jiang Hong Ni Hong Seiji Hongo Masayuki Horie John S Hu Tao Hu Holly R Hughes Florian Hüttner Timothy H Hyndman M Ilyas Risto Jalkanen Dàohóng Jiāng Gilda B Jonson Sandra Junglen Fujio Kadono Karia H Kaukinen Michael Kawate Boris Klempa Jonas Klingström Gary Kobinger Igor Koloniuk Hideki Kondō Eugene V Koonin Mart Krupovic Kenji Kubota Gael Kurath Lies Laenen Amy J Lambert Stanley L Langevin Benhur Lee Elliot J Lefkowitz Eric M Leroy Shaorong Li Longhui Li Jiànróng Lǐ Huazhen Liu Igor S Lukashevich Piet Maes William Marciel de Souza Marco Marklewitz Sergio H Marshall Shin-Yi L Marzano Se Integrated Research Facility at Fort Detrick National Institute of Allergy and Infectious Diseases National Institutes of Health Frederick MD USA. kuhnjens@mail.nih.gov. United States Department of Agriculture Agricultural Research Service US Horticultural Research Laboratory Fort Pierce FL USA. Zoology Department National Museums of Kenya Nairobi Kenya. Jomo Kenyatta University of Agriculture & Technology Nairobi Kenya. Division Phytomedicine Faculty of Life Sciences Humboldt-Universität zu Berlin Berlin Germany. D.I. Ivanovsky Institute of Virology of N.F. Gamaleya National Center on Epidemiology and Microbiology of Ministry of Health of Russian Federation Moscow Russia. Department of Pathology and Immunology Washington University School of Medicine St. Louis MO USA. Faculty of Medicine University of Ljubljana Ljubljana Slovenia. Centro de Biotecnología y Genómica de Plantas Universidad Politécnica de Madrid-Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria Campus de Montegancedo Pozuelo de Alarcón Madrid Spain. Departamento de Biotecnología-Biología Vegetal Escuela Técnica Superior de Ingeniería Agronómica Alimentaria y de Biosistemas Universidad Politécnica de Madrid Madrid Spain. Center for Ecology of Infectious Diseases Department of Infectious Diseases Department of Epidemiology and Biostatistics Insitute of Bioinformatics University of Georgia Athens GA USA. Institute of Novel and Emerging Infectious Diseases Friedrich-Loeffler-Institut Federal Research Institute for Animal Health Greifswald-Insel Riems Germany. Department of Biological Sciences Mississippi State University Mississippi State MS USA. Center for Microbial Pathogenesis Institute for Biomedical Sciences Georgia State University Atlanta GA USA. Edge BioInnovation Consulting and Mgt Frederick MD USA. Institute of Diagnostic Virology Friedrich-Loeffler-Institut Greifswald-Insel Riems Germany. UFyMA INTA-CONICET Cordoba Argentina. Genomics and Bioinformatics D

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Author Correction: Discovery of stimulation-responsive immune enhancers with CRISPR activation

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Nature 2018年第7715期559卷 E13页

作者： Dimitre R Simeonov Benjamin G Gowen Mandy Boontanrart Theodore L Roth John D Gagnon Maxwell R Mumbach Ansuman T Satpathy Youjin Lee Nicolas L Bray Alice Y Chan Dmytro S Lituiev Michelle L Nguyen Rachel E Gate Meena Subramaniam Zhongmei Li Jonathan M Woo Therese Mitros Graham J Ray Gemma L Curie Nicki Naddaf Julia S Chu Hong Ma Eric Boyer Frederic Van Gool Hailiang Huang Ruize Liu Victoria R Tobin Kathrin Schumann Mark J Daly Kyle K Farh K Mark Ansel Chun J Ye William J Greenleaf Mark S Anderson Jeffrey A Bluestone Howard Y Chang Jacob E Corn Alexander Marson Biomedical Sciences Graduate Program University of California San Francisco California 94143 USA. Department of Microbiology and Immunology University of California San Francisco California 94143 USA. Diabetes Center University of California San Francisco California 94143 USA. Innovative Genomics Institute University of California Berkeley California 94720 USA. Department of Molecular and Cell Biology University of California Berkeley Berkeley California 94720 USA. Sandler Asthma Basic Research Center University of California San Francisco California 94143 USA. Center for Personal Dynamic Regulomes Stanford University School of Medicine Stanford California 94305 USA. Program in Epithelial Biology Stanford University School of Medicine Stanford California 94305 USA. Department of Genetics Stanford University School of Medicine Stanford California 94305 USA. Department of Pediatrics University of California San Francisco California 94143 USA. Department of Epidemiology and Biostatistics Department of Bioengineering and Therapeutic Sciences Institute for Human Genetics (IHG) University of California San Francisco California 94143 USA. Biological and Medical Informatics Graduate Program University of California San Francisco California 94158 USA. Broad Institute of MIT and Harvard Cambridge Massachusetts 02142 USA. Analytic and Translational Genetics Unit Massachusetts General Hospital Harvard Medical School Boston Massachusetts 02114 USA. Illumina Inc. 5200 Illumina Way San Diego California 92122 USA. Department of Applied Physics Stanford University Stanford California 94025 USA. Chan Zuckerberg Biohub San Francisco California 94158 USA. Department of Medicine University of California San Francisco California 94143 USA. Innovative Genomics Institute University of California Berkeley California 94720 USA. jcorn@berkeley.edu. Department of Molecular and Cell Biology University of California Berkeley Berkeley Californi

In this Letter, analysis of steady-state regulatory T (Treg) cell percentages from Il2ra enhancer deletion (EDEL) and wild-type (WT) mice revealed no differences between them (Extended Data Fig. 9d). This analysis included two mice whose genotypes were incorrectly assigned. Even after correction of the genotypes, no significant differences in Treg cell percentages were seen when data across experimental cohorts were averaged (as was done in Extended Data Fig. 9d). However, if we normalize the corrected data to account for variation among experimental cohorts, a subtle decrease in EDEL Treg cell percentages is revealed and, using the corrected and normalized data, we have redrawn Extended Data Fig. 9d in Supplementary Fig. 1. The Supplementary Information to this Amendment contains the corrected and reanalysed Extended Data Fig. 9d. The sentence "This enhancer deletion (EDEL) strain also had no obvious T cell phenotypes at steady state (Extended Data Fig. 9)." should read: "This enhancer deletion (EDEL) strain had a small decrease in the percentage of Treg cells (Extended Data Fig. 9).". This error does not affect any of the main figures in the Letter or the data from mice with the human autoimmune-associated single nucleotide polymorphism (SNP) knocked in or with a 12-base-pair deletion at the site (12DEL). In addition, we stated in the Methods that we observed consistent immunophenotypes of EDEL mice across three founders, but in fact, we observed consistent phenotypes in mice from two founders. This does not change any of our conclusions and the original Letter has not been corrected.

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A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women

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Bone Reports 2016年 5卷 233-242页

作者： Taylor, Kira C. Evans, Daniel S. Edwards, Digna R. Velez Edwards, Todd L. Sofer, Tamar Li, Guo Liu, Yongmei Franceschini, Nora Jackson, Rebecca D. Giri, Ayush Donneyong, Macarius Psaty, Bruce Rotter, Jerome I. LaCroix, Andrea Z. Jordan, Joanne M. Robbins, John A. Lewis, Beth Stefanick, Marcia L. Garcia, Melissa Harris, Tamara Cauley, Jane A. North, Kari E. School of Public Health and Information Sciences University of Louisville 485 E Gray St. Louisville 40202 KY United States Gillings School of Global Public Health University of North Carolina at Chapel Hill 137 E. Franklin St. Chapel Hill 27514 NC United States University of North Carolina at Chapel Hill 137 E. Franklin St. Chapel Hill 27514 NC United States California Pacific Medical Center Research Institute 550 16th Street Box 0560 San Francisco 94158-2549 CA United States Vanderbilt Epidemiology Center Department of Obstetrics and Gynecology Vanderbilt Genetics Institute Vanderbilt University 2525 West End Avenue Nashville 37203 TN United States Vanderbilt Genetics Institute Division of Epidemiology Department of Medicine Vanderbilt University 2525 West End Avenue Nashville 37203 TN United States Department of Biostatistics University of Washington UW Tower 15th floor 4333 Brooklyn Ave NE Seattle 98105 United States Cardiovascular Health Research Unit Department of Medicine University of Washington Metropolitan Park East Tower 1730 Minor Ave Suite 1360 Seattle 98101 WA United States Thurston Arthritis Research Center University of North Carolina at Chapel Hill 3300 Thurston Bldg. CB# 7280 Chapel Hill 27599-7280 NC United States The Ohio State University 376 W 10th Avenue Suite 260 Columbus 43210 OH United States Division of Pharmacoepidemiology and Pharmacoeconomics Department of Medicine Brigham and Women's Hospital 1620 Tremont St St 3030 Boston 02120 MA United States Cardiovascular Health Research Unit Departments of Medicine Epidemiology and Health Services University of Washington Institute of Translational Genomics and Population Sciences Los Angeles Biomedical Research Institute and Department of Pediatrics Harbor-UCLA Medical Center 1124 W. Carson Street Bldg. E-5 Torrance 90502 CA United States Fred Hutchinson Cancer Research Center 1100 Fairview Ave N Seattle 98109 WA United States Department of Medicine Uni

Background Osteoporosis is a major public health problem associated with excess disability and mortality. It is estimated that 50–70% of the variation in osteoporotic fracture risk is attributable to genetic factors. The purpose of this hypothesis-generating study was to identify possible genetic determinants of fracture among African American (AA) women in a GWAS meta-analysis. Methods Data on clinical fractures (all fractures except fingers, toes, face, skull or sternum) were analyzed among AA female participants in the Women's Health Initiative (WHI) (N = 8155), Cardiovascular Health Study (CHS) (N = 504), BioVU (N = 704), Health ABC (N = 651), and the Johnston County Osteoarthritis Project (JoCoOA) (N = 291). Affymetrix (WHI) and Illumina (Health ABC, JoCoOA, BioVU, CHS) GWAS panels were used for genotyping, and a 1:1 ratio of YRI:CEU HapMap haplotypes was used as an imputation reference panel. We used Cox proportional hazard models or logistic regression to evaluate the association of ~ 2.5 million SNPs with fracture risk, adjusting for ancestry, age, and geographic region where applicable. We conducted a fixed-effects, inverse variance-weighted meta-analysis. Genome-wide significance was set at P < 5 × 10^− 8. Results One SNP, rs12775980 in an intron of SVIL on chromosome 10p11.2, reached genome-wide significance (P = 4.0 × 10^− 8). Although this SNP has a low minor allele frequency (0.03), there was no evidence for heterogeneity of effects across the studies (I² = 0). This locus was not reported in any previous osteoporosis-related GWA studies. We also interrogated previously reported GWA-significant loci associated with fracture or bone mineral density in our data. One locus (SMOC1) generalized, but overall there was not substantial evidence of generalization. Possible reasons for the lack of generalization are discussed. Conclusion This GWAS meta-analysis of fractures in African American women identified a potentially novel lo

关键词： African American Fracture Genetic association study Genome-wide association study (GWAS) Meta-analysis Osteoporosis

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Metadata Correction: Importance-Performance Analysis of Personal Health Records in Taiwan: A Web-Based Survey

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Journal of medical Internet research 2017年第6期19卷 e209页

作者： Hsiao-Hsien Rau Yi-Syuan Wu Chi-Ming Chu Fu-Chung Wang Min-Huei Hsu Chi-Wen Chang Kang-Hua Chen Yen-Liang Lee Senyeong Kao Yu-Lung Chiu Hsyien-Chia Wen Anis Fuad Chien-Yeh Hsu Hung-Wen Chiu Graduate Institute of Biomedical Informatics Taipei Medical University Taipei Taiwan. Administration Department Healthconn Corp Taipei Taiwan. Institute of Medical Informatics Department of Computer Science of Information Engineering National Cheng Kung University Tainan Taiwan. School Of Public Health National Defense Medical Center Taiepi Taiwan. National Health Insurance Administration Ministry of Health and Welfare Taiepi Taiwan. School of Nursing College of Medicine Chang Gung University Linkou Taiwan. Division of Endocrinology Department of Pediatrics Linkou Chang Gung Memorial Hospital Linkou Taiwan. Internet of Things Laboratory Chunghwa Telecom Laboratories TaoYuen Taiwan. School of Health Care Administration Taipei Medical University Taipei Taiwan. Department of Biostatistics Epidemiology and Population Health Faculty of Medicine Universitas Gadjah Mada Yogyakarta Indonesia. Department of Information Management National Taipei University of Nursing and Health Sciences Taipei Taiwan. Master Program in Global Health and Development Taipei Medical University Taipei Taiwan.

[This corrects the article DOI: .].

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Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations

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Human molecular genetics 2017年第2期26卷 454-465页

作者： Wei Jie Seow Keitaro Matsuo Chao Agnes Hsiung Kouya Shiraishi Minsun Song Hee Nam Kim Maria Pik Wong Yun-Chul Hong H Dean Hosgood Zhaoming Wang I-Shou Chang Jiu-Cun Wang Nilanjan Chatterjee Margaret Tucker Hu Wei Tetsuya Mitsudomi Wei Zheng Jin Hee Kim Baosen Zhou Neil E Caporaso Demetrius Albanes Min-Ho Shin Lap Ping Chung She-Juan An Ping Wang Hong Zheng Yasushi Yatabe Xu-Chao Zhang Young Tae Kim Xiao-Ou Shu Young-Chul Kim Bryan A Bassig Jiang Chang James Chung Man Ho Bu-Tian Ji Michiaki Kubo Yataro Daigo Hidemi Ito Yukihide Momozawa Kyota Ashikawa Yoichiro Kamatani Takayuki Honda Hiromi Sakamoto Hideo Kunitoh Koji Tsuta Shun-Ichi Watanabe Hiroshi Nokihara Yohei Miyagi Haruhiko Nakayama Shingo Matsumoto Masahiro Tsuboi Koichi Goto Zhihua Yin Jianxin Shi Atsushi Takahashi Akiteru Goto Yoshihiro Minamiya Kimihiro Shimizu Kazumi Tanaka Tangchun Wu Fusheng Wei Jason Y Y Wong Fumihiko Matsuda Jian Su Yeul Hong Kim In-Jae Oh Fengju Song Victor Ho Fun Lee Wu-Chou Su Yuh-Min Chen Gee-Chen Chang Kuan-Yu Chen Ming-Shyan Huang Pan-Chyr Yang Hsien-Chih Lin Yong-Bing Xiang Adeline Seow Jae Yong Park Sun-Seog Kweon Chien-Jen Chen Haixin Li Yu-Tang Gao Chen Wu Biyun Qian Daru Lu Jianjun Liu Hyo-Sung Jeon Chin-Fu Hsiao Jae Sook Sung Ying-Huang Tsai Yoo Jin Jung Huan Guo Zhibin Hu Wen-Chang Wang Charles C Chung Charles Lawrence Laurie Burdett Meredith Yeager Kevin B Jacobs Amy Hutchinson Sonja I Berndt Xingzhou He Wei Wu Junwen Wang Yuqing Li Jin Eun Choi Kyong Hwa Park Sook Whan Sung Li Liu Chang Hyun Kang Lingmin Hu Chung-Hsing Chen Tsung-Ying Yang Jun Xu Peng Guan Wen Tan Chih-Liang Wang Alan Dart Loon Sihoe Ying Chen Yi Young Choi Jen-Yu Hung Jun Suk Kim Ho-Il Yoon Qiuyin Cai Chien-Chung Lin In Kyu Park Ping Xu Jing Dong Christopher Kim Qincheng He Reury-Perng Perng Chih-Yi Chen Roel Vermeulen Junjie Wu Wei-Yen Lim Kun-Chieh Chen John K C Chan Minjie Chu Yao-Jen Li Jihua Li Hongyan Chen Chong-Jen Yu Li Jin Yen-Li Lo Ying-Hsiang Chen Joseph F Fraumeni Jie Liu Taiki Yamaji Yang Yang Belynda Hicks Kathleen Wyatt Shengchao A Li Division of Cancer Epidemiology and Genetics National Cancer Institute Bethesda MD USA. Saw Swee Hock School of Public Health National University of Singapore and National University Health System Singapore. Division of Molecular Medicine Aichi Cancer Center Research Institute Nagoya Japan. Institute of Population Health Sciences National Health Research Institutes Zhunan Taiwan. Division of Genome Biology National Cancer Center Research Institute Tokyo Japan. Department of Statistics Sookmyung Women's University Seoul Republic of Korea. Department of Preventive Medicine Chonnam National University Medical School Gwangju Republic of Korea. Department of Pathology The University of Hong Kong Queen Mary Hospital Hong Kong. Department of Preventive Medicine Seoul National University College of Medicine Seoul Republic of Korea. Department of Epidemiology and Population Health Albert Einstein College of Medicine Bronx NY USA. Department of Computational Biology St. Jude Children's Research Hospital Memphis TN 38105 USA. National Institute of Cancer Research National Health Research Institutes Zhunan Taiwan. Ministry of Education Key Laboratory of Contemporary Anthropology School of Life Sciences Fudan University Shanghai People's Republic of China. State Key Laboratory of Genetic Engineering School of Life Sciences Fudan University Shanghai People's Republic of China. Division of Thoracic Surgery Kinki University School of Medicine Sayama Japan. Division of Epidemiology Department of Medicine Vanderbilt University Medical Center and Vanderbilt-Ingram Cancer Center Nashville TN USA. Department of Integrative Bioscience & Biotechnology Sejong University Seoul Republic of Korea. Department of Epidemiology School of Public Health China Medical University Shenyang People's Republic of China. Guangdong Lung Cancer Institute Medical Research Center and Cancer Center of Guangdong General Hospital Guangdong Academy of Medical Sciences Guangzhou People's Republic

To evaluate associations by EGFR mutation status for lung adenocarcinoma risk among never-smoking Asian women, we conducted a meta-analysis of 11 loci previously identified in genome-wide association studies (GWAS). Genotyping in an additional 10,780 never-smoking cases and 10,938 never-smoking controls from Asia confirmed associations with eight known single nucleotide polymorphisms (SNPs). Two new signals were observed at genome-wide significance (P < 5 × 10-8), namely, rs7216064 (17q24.3, BPTF), for overall lung adenocarcinoma risk, and rs3817963 (6p21.3, BTNL2) which is specific to cases with EGFR mutations. In further sub-analyses by EGFR status, rs9387478 (ROS1/DCBLD1) and rs2179920 (HLA-DPB1) showed stronger estimated associations in EGFR-positive compared to EGFR-negative cases. Comparison of the overall associations with published results in Western populations revealed that the majority of these findings were distinct, underscoring the importance of distinct contributing factors for smoking and non-smoking lung cancer. Our results extend the catalogue of regions associated with lung adenocarcinoma in non-smoking Asian women and highlight the importance of how the germline could inform risk for specific tumour mutation patterns, which could have important translational implications.

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Corrigendum to: Report: NIA Workshop on Measures of Physiologic Resiliencies in Human Aging

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The journals of gerontology. Series A, Biological sciences and medical sciences 2018年第7期73卷 995页

作者： Evan C Hadley George A Kuchel Anne B Newman Heather G Allore Jenna M Bartley Cindy S Bergeman Michael L Blinov Cathleen S Colon-Emeric Firdaus S Dabhar Laura L Dugan Chhanda Dutta Basil A Eldadah Luigi Ferrucci James L Kirkland Stephen B Kritchevsky Lewis A Lipsitz Neelesh K Nadkarni May J Reed Kenneth E Schmader Felipe Sierra Stephanie A Studenski Ravi Varadhan Jeremy D Walston Heather E Whitson Raymond Yung Division of Geriatrics and Clinical Gerontology National Institutes of Health National Institute on Aging Bethesda Maryland. Department of Medicine Center on Aging University of Connecticut Health Center Farmington. Department of Epidemiology University of Pittsburgh Graduate School of Public Health. Department of Medicine Division of Geriatric Medicine University of Pittsburgh School of Medicine Pennsylvania. Department of Internal Medicine Section of Geriatrics Yale University School of Medicine New Haven Connecticut. Department of Immunology Center on Aging University of Connecticut Health Center University of Connecticut Farmington. Department of Psychology University of Notre Dame Indiana. R. D. Berlin Center for Cell Analysis and Modeling University of Connecticut School of Medicine University of Connecticut Farmington. Duke University School of Medicine Duke University Medical Center. Durham VA Geriatric Research Education and Clinical Center North Carolina. Department of Psychiatry and Behavioral Sciences Stanford University School of Medicine Stanford University California. Department of Medicine Division of Geriatric Medicine Vanderbilt University School of Medicine Vanderbilt University Nashville Tennessee. Office of the Scientific Director National Institute on Aging National Institutes of Health Bethesda Maryland. Robert and Arlene Kogod Center on Aging Mayo Clinic College of Medicine Mayo Clinic Rochester Minnesota. Department of Gerontology and Geriatrics Sticht Center on Aging Wake Forest University School of Medicine Winston-Salem North Carolina. Beth Israel Deaconess Medical Center Harvard Medical School Boston. Institute for Aging Research Hebrew Senior Life Boston Massachusetts. Division of Geriatric Medicine Department of Internal Medicine School of Medicine University of Washington Seattle. Division of Geriatric Medicine Department of Medicine School of Medicine Duke University. Department of Veterans Affairs Medical Center Durham No

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