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Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information (vol 91, pg 626, 2022)

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BIOLOGICAL PSYCHIATRY 2022年第7期91卷 690-690页

作者： Maihofer, Adam X. Vinkers, Christiaan H. Department of Psychiatry University of California San Diego La Jolla California Department of Family Medicine and Public Health University of California San Diego La Jolla California Center of Excellence for Stress and Mental Health Veterans Affairs Healthcare System San Diego California. Electronic address: amaihofer@health.ucsd.edu. Department of Epidemiology Harvard T.H. Chan School of Public Health Boston Massachusetts Department of Psychiatry Massachusetts General Hospital Boston Massachusetts. Social Genetic and Developmental Psychiatry Centre Institute of Psychiatry Psychology and Neuroscience King's College London London United Kingdom National Institute of Health Research Maudsley Biomedical Research Centre King's College London London United Kingdom. Department of Psychiatry Harvard Medical School Boston Massachusetts Stanley Center for Psychiatric Research Broad Institute of MIT and Harvard Cambridge Massachusetts Center of Excellence in Depression and Anxiety Disorders Belmont Massachusetts. Department of Epidemiology Harvard T.H. Chan School of Public Health Boston Massachusetts Stanley Center for Psychiatric Research Broad Institute of MIT and Harvard Cambridge Massachusetts. Department of Psychiatry University of California San Diego La Jolla California Center of Excellence for Stress and Mental Health Veterans Affairs Healthcare System San Diego California Research Service Veterans Affairs Healthcare System San Diego California. Duke Molecular Physiology Institute Duke University School of Medicine Durham North Carolina. Department of Psychiatry Veterans Affairs Connecticut Healthcare System West Haven Connecticut Department of Psychiatry Yale University School of Medicine New Haven Connecticut. Department of Epidemiology Harvard T.H. Chan School of Public Health Boston Massachusetts Department of Epidemiology Columbia University Mailman School of Public Health New York. Division of Mental Health Atlanta Veterans Affairs Medical Center

BACKGROUND: Posttraumatic stress disorder (PTSD) is heritable and a potential consequence of exposure to traumatic stress. Evidence suggests that a quantitative approach to PTSD phenotype measurement and incorporation... 详细信息

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Author Correction: Transcription phenotypes of pancreatic cancer are driven by genomic events during tumor evolution

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Nature genetics 2020年第4期52卷 463页

作者： Michelle Chan-Seng-Yue Jaeseung C Kim Gavin W Wilson Karen Ng Eugenia Flores Figueroa Grainne M O'Kane Ashton A Connor Robert E Denroche Robert C Grant Jessica McLeod Julie M Wilson Gun Ho Jang Amy Zhang Sheng-Ben Liang Ayelet Borgida Dianne Chadwick Sangeetha Kalimuthu Ilinca Lungu John M S Bartlett Paul M Krzyzanowski Vandana Sandhu Hervé Tiriac Fieke E M Froeling Joanna M Karasinska James T Topham Daniel J Renouf David F Schaeffer Steven J M Jones Marco A Marra Janessa Laskin Runjan Chetty Lincoln D Stein George Zogopoulos Benjamin Haibe-Kains Peter J Campbell David A Tuveson Jennifer J Knox Sandra E Fischer Steven Gallinger Faiyaz Notta Princess Margaret Cancer Centre Toronto Ontario Canada. PanCuRx Translational Research Initiative Ontario Institute for Cancer Research Toronto Ontario Canada. Genomics Technology Program Ontario Institute for Cancer Research Toronto Ontario Canada. Wallace McCain Centre for Pancreatic Cancer Department of Medical Oncology Princess Margaret Centre University Health Network University of Toronto Toronto Ontario Canada. Hepatobiliary/Pancreatic Surgical Oncology Program University Health Network Toronto Ontario Canada. UHN Program in BioSpecimen Sciences University Health Network Toronto Ontario Canada. Lunenfeld-Tanenbaum Research Institute Mount Sinai Hospital Toronto Ontario Canada. Department of Pathology University Health Network and University of Toronto Toronto Ontario Canada. Diagnostic Development Ontario Institute for Cancer Research Toronto Ontario Canada. Cold Spring Harbor Laboratory Cold Spring Harbor NY USA. Lustgarten Foundation Pancreatic Cancer Research Laboratory Cold Spring Harbor NY USA. Department of Surgery University of California San Diego NCI-designated Comprehensive Cancer Center La Jolla CA USA. Department of Surgery and Cancer Imperial College London London UK. Pancreas Centre BC Vancouver British Columbia Canada. Department of Medical Oncology BC Cancer Vancouver British Columbia Canada. Department of Pathology and Laboratory Medicine Vancouver General Hospital Vancouver British Columbia Canada. Canada's Michael Smith Genome Sciences Centre Vancouver British Columbia Canada. Department of Medical Genetics University of British Columbia Vancouver British Columbia Canada. Bioinformatics Ontario Institute for Cancer Research Toronto Ontario Canada. Department of Molecular Genetics University of Toronto Toronto Ontario Canada. Research Institute of the McGill University Health Centre Montreal Quebec Canada. The Goodman Cancer Research Centre of McGill University Montreal Quebec Canada. Department of Medical

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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Author Correction: High p16 expression and heterozygous RB1 loss are biomarkers for CDK4/6 inhibitor resistance in ER+ breast cancer

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Nature Communications 2022年第1期13卷 1页

作者： Marta Palafox Laia Monserrat Andreu Òdena Mònica Sánchez-Guixé Olga Rodríguez Marta Guzmán Judit Grueso Violeta Serra Meritxell Bellet Mafalda Oliveira Marta Capelán Analía Azaro Cristina Saura Guillermo Villacampa Cristina Viaplana Rodrigo Dienstmann Abel Gonzalez-Perez Nuria Lopez-Bigas Fara Brasó-Maristany Aleix Prat Nusaibah Ibrahimi Stefan Michiels Srinivasaraghavan Kannan Chandra S. Verma Leonardo Mina Alicia García-Sanz Maria Teresa Herrera-Abreu Nicholas C. Turner Alejandra Bruna Javier Hernández Faye Su Kui Lin Robert B. Clarke Carlos Caldas Joaquín Arribas Paolo Nuciforo Maurizio Scaltriti Monica Arnedos Experimental Therapeutics Group Vall d’Hebron Institute of Oncology Barcelona Spain CIBERONC Vall d’Hebron Institute of Oncology Barcelona Spain Breast Cancer and Melanoma Group Vall d’Hebron Institute of Oncology Barcelona Spain Department of Medical Oncology Hospital Vall d’Hebron Barcelona Spain Oncology Data Science Group Vall d’Hebron Institute of Oncology Barcelona Spain Institute for Research in Biomedicine (IRB Barcelona) Barcelona Spain Research Program on Biomedical Informatics Universitat Pompeu Fabra Barcelona Spain Institució Catalana de Recerca i Estudis Avançats (ICREA) Barcelona Spain Translational Genomics and Targeted Therapies in Solid Tumors August Pi i Sunyer Biomedical Research Institute (IDIBAPS) Barcelona Spain University of Barcelona Barcelona Spain Department of Medical Oncology Hospital Clinic Barcelona Spain SOLTI Breast Cancer Research Group Barcelona Spain Department of Oncology IOB Institute of Oncology Barcelona Spain Service de Biostatistique et d’Epidémiologie Gustave Roussy Villejuif France Oncostat U1018 Inserm University Paris-Saclay Villejuif France Bioinformatics Institute (A*STAR) Singapore Singapore School of Biological Sciences Nanyang Technological University Singapore Singapore Department of Biological Sciences National University of Singapore Singapore Singapore Medica Scientia Innovation Research (MedSIR) Barcelona Spain The Breast Cancer Now Research Centre London UK Preclinical Modelling of Pediatric Cancer Evolution Group The Institute of Cancer Research London UK Translational Molecular Pathology Vall d’Hebron Institute of Research (VHIR) Barcelona Spain Novartis Pharmaceuticals East Hanover NJ USA Genentech Inc. South San Francisco California USA Breast Biology Group Manchester Breast Centre Manchester UK Cancer Research UK Cambridge UK Growth Factors Laboratory Vall d’Hebron Institute of Oncology Barcelona Spain Department of Biochemistry and Molecular Biology Universitat Autònoma de Bar

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Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

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Genetics in medicine : official journal of the American College of Medical Genetics 2021年第12期23卷 2467页

作者： Sacha Ferdinandusse Kirsty McWalter Heleen Te Brinke Lodewijk IJlst Petra M Mooijer Jos P N Ruiter Alida E M van Lint Mia Pras-Raves Eric Wever Francisca Millan Maria J Guillen Sacoto Amber Begtrup Mark Tarnopolsky Lauren Brady Roger L Ladda Susan L Sell Catherine B Nowak Jessica Douglas Cuixia Tian Elizabeth Ulm Seth Perlman Arlene V Drack Karen Chong Nicole Martin Jennifer Brault Elly Brokamp Camilo Toro William A Gahl Ellen F Macnamara Lynne Wolfe Quinten Waisfisz Petra J G Zwijnenburg Alban Ziegler Magalie Barth Rosemarie Smith Sara Ellingwood Deborah Gaebler-Spira Somayeh Bakhtiari Michael C Kruer Antoine H C van Kampen Ronald J A Wanders Hans R Waterham David Cassiman Frédéric M Vaz Laboratory Genetic Metabolic Diseases Amsterdam UMC University of Amsterdam Department of Clinical Chemistry Amsterdam Gastroenterology Endocrinology Metabolism Amsterdam The Netherlands. s.ferdinandusse@amsterdamumc.nl. GeneDx Gaithersburg MD USA. Laboratory Genetic Metabolic Diseases Amsterdam UMC University of Amsterdam Department of Clinical Chemistry Amsterdam Gastroenterology Endocrinology Metabolism Amsterdam The Netherlands. Core Facility Metabolomics Amsterdam UMC Amsterdam The Netherlands. Bioinformatics Laboratory Department of Epidemiology and Data Science Amsterdam Public Health Research Institute Amsterdam UMC University of Amsterdam Amsterdam The Netherlands. Department of Pediatrics McMaster University Children's Hospital Hamilton ON Canada. Department of Pediatrics Penn State Children's Hospital Hershey PA USA. The Feingold Center for Children Division of Genetics and Genomics Boston Children's Hospital Boston MA USA. Division of Neurology Cincinnati Children's Hospital Medical Center Department of Pediatrics University of Cincinnati College of Medicine Cincinnati OH USA. Division of Human Genetics Cincinnati Children's Hospital Medical Center Cincinnati OH USA. Department of Neurology University of Iowa Hospitals and Clinics Iowa City IA USA. Department of Ophthalmology and Visual Sciences University of Iowa Iowa City IA USA. Mount Sinai Hospital Department of Obstetrics and Gynecology Prenatal Diagnosis and Medical Genetics Program Toronto ON Canada. Vanderbilt University Medical Center Department of Pediatrics Nashville TN USA. NIH Undiagnosed Diseases Program Office of the Clinical Director National Human Genome Research Institute NIH Bethesda MD USA. Department of Clinical Genetics Amsterdam UMC Vrije Universiteit Amsterdam Amsterdam The Netherlands. Genetic department University Hospital Angers Angers France. Division of Genetics Department of Pediatrics Maine Medical Center Portland ME USA. Feinberg Northwest

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Erratum to: The whole genome sequence of the Mediterranean fruit fly, Ceratitis capitata (Wiedemann), reveals insights into the biology and adaptive evolution of a highly invasive pest species

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Genome biology 2017年第1期18卷 11页

作者： Alexie Papanicolaou Marc F Schetelig Peter Arensburger Peter W Atkinson Joshua B Benoit Kostas Bourtzis Pedro Castañera John P Cavanaugh Hsu Chao Christopher Childers Ingrid Curril Huyen Dinh HarshaVardhan Doddapaneni Amanda Dolan Shannon Dugan Markus Friedrich Giuliano Gasperi Scott Geib Georgios Georgakilas Richard A Gibbs Sarah D Giers Ludvik M Gomulski Miguel González-Guzmán Ana Guillem-Amat Yi Han Artemis G Hatzigeorgiou Pedro Hernández-Crespo Daniel S T Hughes Jeffery W Jones Dimitra Karagkouni Panagiota Koskinioti Sandra L Lee Anna R Malacrida Mosè Manni Kostas Mathiopoulos Angela Meccariello Monica Munoz-Torres Shwetha C Murali Terence D Murphy Donna M Muzny Georg Oberhofer Félix Ortego Maria D Paraskevopoulou Monica Poelchau Jiaxin Qu Martin Reczko Hugh M Robertson Andrew J Rosendale Andrew E Rosselot Giuseppe Saccone Marco Salvemini Grazia Savini Patrick Schreiner Francesca Scolari Paolo Siciliano Sheina B Sim George Tsiamis Enric Ureña Ioannis S Vlachos John H Werren Ernst A Wimmer Kim C Worley Antigone Zacharopoulou Stephen Richards Alfred M Handler Hawkesbury Institute for the Environment Western Sydney University Sydney Australia. Justus-Liebig-University Giessen Institute for Insect Biotechnology 35394 Giessen Germany. Department of Biological Sciences Cal Poly Pomona Pomona CA 91768 USA. Department of Entomology and Center for Disease Vector Research University of California Riverside Riverside CA 92521 USA. Interdepartmental Graduate Program in Genetics Genomics & Bioinformatics University of California Riverside Riverside CA 92521 USA. Department of Biological Sciences University of Cincinnati Cincinnati OH 45221 USA. Insect Pest Control Laboratory Joint FAO/IAEA Programme of Nuclear Techniques in Food and Agriculture Seibersdorf Vienna Austria. Department of Environmental and Natural Resources Management University of Patras Agrinio Greece. Department of Environmental Biology Centro de Investigaciones Biológicas CSIC 28040 Madrid Spain. Human Genome Sequencing Center Department of Human and Molecular Genetics Baylor College of Medicine 77030 Houston TX USA. National Agricultural Library USDA 20705 Beltsville MD USA. Georg-August-Universität Göttingen Johann-Friedrich-Blumenbach-Institut für Zoologie und Anthropologie 37077 Göttingen Germany. Department of Biology University of Rochester 14627 Rochester NY USA. Department of Biological Sciences Wayne State University 48202 Detroit MI USA. Department of Biology and Biotechnology University of Pavia 27100 Pavia Italy. USDA-ARS Pacific Basin Agricultural Research Center 96720 Hilo HI USA. DIANA-Lab Department of Electrical & Computer Engineering University of Thessaly 382 21 Volos Greece and Hellenic Pasteur Institute 11521 Athens Greece. Department of Entomology University of Illinois at Urbana-Champaign 61801 Urbana IL USA. Department of Biological Sciences Oakland University 48309 Rochester MI USA. Department of Biochemistry and Biotechnology University of Thessaly Larissa Greece. Department of Biology Univer

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Human genome meeting 2016 : Houston, TX, USA. 28 February - 2 March 2016

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Human genomics 2016年第1期10 Suppl 1卷 12页

作者： A. K. Srivastava Y. Wang R. Huang C. Skinner T. Thompson L. Pollard T. Wood F. Luo R. Stevenson R. Polimanti J. Gelernter X. Lin I. Y. Lim Y. Wu A. L. Teh L. Chen I. M. Aris S. E. Soh M. T. Tint J. L. MacIsaac F. Yap K. Kwek S. M. Saw M. S. Kobor M. J. Meaney K. M. Godfrey Y. S. Chong J. D. Holbrook Y. S. Lee P. D. Gluckman N. Karnani A. Kapoor D. Lee A. Chakravarti C. Maercker F. Graf M. Boutros G. Stamoulis F. Santoni P. Makrythanasis A. Letourneau M. Guipponi N. Panousis M. Garieri P. Ribaux E. Falconnet C. Borel S. E. Antonarakis S. Kumar J. Curran J. Blangero S. Chatterjee J. Akiyama D. Auer C. Berrios L. Pennacchio T. R. Donti G. Cappuccio M. Miller P. Atwal A. Kennedy A. Cardon C. Bacino L. Emrick J. Hertecant F. Baumer B. Porter M. Bainbridge P. Bonnen B. Graham R. Sutton Q. Sun S. Elsea Z. Hu P. Wang Y. Zhu J. Zhao M. Xiong David A. Bennett A. Hidalgo-Miranda S. Romero-Cordoba S. Rodriguez-Cuevas R. Rebollar-Vega E. Tagliabue M. Iorio E. D’Ippolito S. Baroni B. Kaczkowski Y. Tanaka H. Kawaji A. Sandelin R. Andersson M. Itoh T. Lassmann Y. Hayashizaki P. Carninci A. R. R. Forrest C. A. Semple E. A. Rosenthal B. Shirts L. Amendola C. Gallego M. Horike-Pyne A. Burt P. Robertson P. Beyers C. Nefcy D. Veenstra F. Hisama R. Bennett M. Dorschner D. Nickerson J. Smith K. Patterson D. Crosslin R. Nassir N. Zubair T. Harrison U. Peters G. Jarvik F. Menghi K. Inaki X. Woo P. Kumar K. Grzeda A. Malhotra H. Kim D. Ucar P. Shreckengast K. Karuturi J. Keck J. Chuang E. T. Liu B. Ji A. Tyler G. Ananda G. Carter H. Nikbakht M. Montagne M. Zeinieh A. Harutyunyan M. Mcconechy N. Jabado P. Lavigne J. Majewski J. B. Goldstein M. Overman G. Varadhachary R. Shroff R. Wolff M. Javle A. Futreal D. Fogelman L. Bravo W. Fajardo H. Gomez C. Castaneda C. Rolfo J. A. Pinto K. C. Akdemir L. Chin S. Patterson C. Statz S. Mockus S. N. Nikolaev X. I. Bonilla L. Parmentier B. King F. Bezrukov G. Kaya V. Zoete V. Seplyarskiy H. Sharpe T. McKee K. Popadin N. Basset-Seguin R. Ben Chaabene M. Andrianova C. Verdan K. Grosdemange O. Sumara M. E JCSRI Greenwood Genetic Center Greenwood USA School of Computing Clemson University Clemson USA Biochemical Genetics Laboratory Greenwood Genetic Center Greenwood USA Department Psychiatry Yale Sch Med and VA CT Healthcare Center West Haven USA Department Genetics Yale Sch Med and VA CT Healthcare Center West Haven USA Department Neurobiology Yale Sch Med and VA CT Healthcare Center West Haven USA Singapore Institute for Clinical Sciences Singapore Singapore National University of Singapore Singapore Singapore University of British Columbia Vancouver Canada KK Women’s and Children’s Hospital Singapore Singapore University of Southampton and University Hospital Southampton NHS Foundation Trust Southampton UK University of Auckland Auckland New Zealand McKusick-Nathans Institute of Genetic Medicine Johns Hopkins University School of Medicine Baltimore USA Esslingen University of Applied Sciences Esslingen Germany German Cancer Research Center Heidelberg Germany Department of Genetic Medicine and Development University of Geneva Medical School Geneva Switzerland Geneva University Hospitals-HUG Service of Genetic Medicine Geneva Switzerland GE3 Institute of Genetics and Genomics of Geneva University of Geneva Medical School Geneva Switzerland South Texas Diabetes and Obesity Institute School of Medicine University of Texas Rio-Grande Valley Edinburg USA South Texas Diabetes and Obesity Institute School of Medicine University of Texas Rio-Grande Valley Brownsville USA Institute of Genetic Medicine Johns Hopkins University Baltimore USA Genomics Division Lawrence Berkeley National Laboratory Berkeley USA Molecular and Human Genetics Baylor College of Medicine Houston USA Department of Translational Medical Sciences Federico II University Naples Italy Metabolon Inc Durham USA Section of Pediatric Neurology and Neuroscience Baylor College of Medicine Houston USA Tawam Hospital Abu Dhabi United Arab Emirates Stanford Medical School Stanford USA Sch

O1 The metabolomics approach to autism: identification of biomarkers for early detection of autism spectrum disorder A. K. Srivastava, Y. Wang, R. Huang, C. Skinner, T. Thompson, L. Pollard, T. Wood, F. Luo, R. Steven... 详细信息

O1 The metabolomics approach to autism: identification of biomarkers for early detection of autism spectrum disorder A. K. Srivastava, Y. Wang, R. Huang, C. Skinner, T. Thompson, L. Pollard, T. Wood, F. Luo, R. Stevenson O2 Phenome-wide association study for smoking- and drinking-associated genes in 26,394 American women with African, Asian, European, and Hispanic descents R. Polimanti, J. Gelernter O3 Effects of prenatal environment, genotype and DNA methylation on birth weight and subsequent postnatal outcomes: findings from GUSTO, an Asian birth cohort X. Lin, I. Y. Lim, Y. Wu, A. L. Teh, L. Chen, I. M. Aris, S. E. Soh, M. T. Tint, J. L. MacIsaac, F. Yap, K. Kwek, S. M. Saw, M. S. Kobor, M. J. Meaney, K. M. Godfrey, Y. S. Chong, J. D. Holbrook, Y. S. Lee, P. D. Gluckman, N. Karnani, GUSTO study group O4 High-throughput identification of specific qt interval modulating enhancers at the SCN5A locus A. Kapoor, D. Lee, A. Chakravarti O5 Identification of extracellular matrix components inducing cancer cell migration in the supernatant of cultivated mesenchymal stem cells C. Maercker, F. Graf, M. Boutros O6 Single cell allele specific expression (ASE) IN T21 and common trisomies: a novel approach to understand DOWN syndrome and other aneuploidies G. Stamoulis, F. Santoni, P. Makrythanasis, A. Letourneau, M. Guipponi, N. Panousis, M. Garieri, P. Ribaux, E. Falconnet, C. Borel, S. E. Antonarakis O7 Role of microRNA in LCL to IPSC reprogramming S. Kumar, J. Curran, J. Blangero O8 Multiple enhancer variants disrupt gene regulatory network in Hirschsprung disease S. Chatterjee, A. Kapoor, J. Akiyama, D. Auer, C. Berrios, L. Pennacchio, A. Chakravarti O9 Metabolomic profiling for the diagnosis of neurometabolic disorders T. R. Donti, G. Cappuccio, M. Miller, P. Atwal, A. Kennedy, A. Cardon, C. Bacino, L. Emrick, J. Hertecant, F. Baumer, B. Porter, M. Bainbridge, P. Bonnen, B. Graham, R. Sutton, Q. Sun, S. Elsea O10 A novel causal methylation network approach to Alzheimer’s

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Author Correction: Wiskott-Aldrich syndrome protein forms nuclear condensates and regulates alternative splicing

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Nature communications 2022年第1期13卷 5291页

作者： Baolei Yuan Xuan Zhou Keiichiro Suzuki Gerardo Ramos-Mandujano Mengge Wang Muhammad Tehseen Lorena V Cortés-Medina James J Moresco Sarah Dunn Reyna Hernandez-Benitez Tomoaki Hishida Na Young Kim Manal M Andijani Chongwei Bi Manching Ku Yuta Takahashi Jinna Xu Jinsong Qiu Ling Huang Christopher Benner Emi Aizawa Jing Qu Guang-Hui Liu Zhongwei Li Fei Yi Yanal Ghosheh Changwei Shao Maxim Shokhirev Patrizia Comoli Francesco Frassoni John R Yates Xiang-Dong Fu Concepcion Rodriguez Esteban Samir Hamdan Juan Carlos Izpisua Belmonte Mo Li Bioscience Program Biological and Environmental Science and Engineering Division King Abdullah University of Science and Technology (KAUST) Thuwal 23955-6900 Kingdom of Saudi Arabia. Gene Expression Laboratory Salk Institute for Biological Studies 10010 North Torrey Pines Road La Jolla CA 92037 USA. Institute for Advanced Co-Creation Studies Graduate School of Engineering Science Osaka University Osaka Japan. Department of Cell Biology Scripps Research Institute La Jolla CA 92037 USA. The Waitt Advanced Biophotonics Core Facility Salk Institute for Biological Studies 10010 North Torrey Pines Road La Jolla CA 92037 USA. Altos Labs Inc. 5510 Morehouse Drive Suite 300 San Diego CA 92121 USA. Laboratory of Biological Chemistry School of Pharmaceutical Sciences Wakayama Medical University 25-1 Shitibancho Wakayama Wakayama 640-8156 Japan. Next-generation sequencing core Salk Institute for Biological Studies 10010 North Torrey Pines Road La Jolla CA 92037 USA. Life Science Center Tsukuba Advanced Research Alliance University of Tsukuba 1-1-1 Tennoudai Tsukuba Ibaraki 305-8577 Japan. Department of Cellular & Molecular Medicine University of California at San Diego La Jolla CA 92093 USA. Integrative Genomics and Bioinformatics Core Salk Institute for Biological Studies 10010 North Torrey Pines Road La Jolla CA 92037 USA. State Key Laboratory of Membrane Biology Institute of Zoology Chinese Academy of Sciences Beijing 100101 China. University of Southern California 1333 San Pablo Street MMR 618 Los Angeles CA 90033 USA. Ambys Medicines 131 Oyster Point Blvd. Suite 200 South San Francisco CA 94080 USA. Pediatric Hematology/Oncology and Cell Factory Fondazione IRCCS Policlinico San Matteo Pavia Italy. Department of Research Laboratories and Director of Center for Stem Cell and Cell Therapy Instituto G. Gaslini Children Hospital Scientific Institute 16147 Genova Italy. Bioscience Program Biological and Environmental Science and Engineering

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Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

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Nature communications 2021年第1期12卷 1166页

作者： Ditte Demontis Raymond K Walters Veera M Rajagopal Irwin D Waldman Jakob Grove Thomas D Als Søren Dalsgaard Marta Ribasés Jonas Bybjerg-Grauholm Maria Bækvad-Hansen Thomas Werge Merete Nordentoft Ole Mors Preben Bo Mortensen Bru Cormand David M Hougaard Benjamin M Neale Barbara Franke Stephen V Faraone Anders D Børglum The Lundbeck Foundation Initiative for Integrative Psychiatric Research iPSYCH Aarhus Denmark. ditte@biomed.au.dk. Center for Genomics and Personalized Medicine Aarhus Denmark. ditte@biomed.au.dk. Department of Biomedicine - Human Genetics Aarhus University Aarhus Denmark. ditte@biomed.au.dk. Analytic and Translational Genetics Unit Department of Medicine Massachusetts General Hospital and Harvard Medical School Boston MA USA. Stanley Center for Psychiatric Research Broad Institute of MIT and Harvard Cambridge MA USA. The Lundbeck Foundation Initiative for Integrative Psychiatric Research iPSYCH Aarhus Denmark. Center for Genomics and Personalized Medicine Aarhus Denmark. Department of Biomedicine - Human Genetics Aarhus University Aarhus Denmark. Department of Psychology Emory University Atlanta GA USA. Bioinformatics Research Centre Aarhus University Aarhus Denmark. National Centre for Register-Based Research Aarhus University Aarhus Denmark. Psychiatric Genetics Unit Group of Psychiatry Mental Health and Addiction Vall d'Hebron Research Institute (VHIR) Universitat Autònoma de Barcelona Barcelona Catalonia Spain. Department of Psychiatry Hospital Universitari Vall d'Hebron Barcelona Catalonia Spain. Biomedical Network Research Center on Mental Health (CIBERSAM) Instituto de Salud Carlos III Madrid Spain. Departament de Genètica Microbiologia i Estadística Facultat de Biologia Universitat de Barcelona Barcelona Catalonia Spain. Center for Neonatal Screening Department for Congenital Disorders Statens Serum Institut Copenhagen Denmark. GLOBE Institute Center for GeoGenetics University of Copenhagen Copenhagen Denmark. Institute of Biological Psychiatry MHC Sct. Hans Mental Health Services Copenhagen Roskilde Denmark. Department of Clinical Medicine University of Copenhagen Copenhagen Denmark. Copenhagen University Hospital Mental Health Centre Copenhagen Mental Health Services in the Capital Region of Denmark Hellerup Denmark. Department of

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Stroke genetics informs drug discovery and risk prediction across ancestries (vol 611, pg 115, 2022)

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NATURE 2022年第7938期612卷 E7-E7页

作者： Mishra, Aniket Malik, Rainer Hachiya, Tsuyoshi Jurgenson, Tuuli Namba, Shinichi Posner, Daniel C. Kamanu, Frederick K. Koido, Masaru Le Grand, Quentin Shi, Mingyang He, Yunye Georgakis, Marios K. Caro, Ilana Krebs, Kristi Liaw, Yi-Ching Vaura, Felix C. Lin, Kuang Winsvold, Bendik Slagsvold Srinivasasainagendra, Vinodh Parodi, Livia Bae, Hee-Joon Chauhan, Ganesh Chong, Michael R. Tomppo, Liisa Akinyemi, Rufus Roshchupkin, Gennady V. Habib, Naomi Jee, Yon Ho Thomassen, Jesper Qvist Abedi, Vida Carcel-Marquez, Jara Nygaard, Marianne Leonard, Hampton L. Yang, Chaojie Yonova-Doing, Ekaterina Knol, Maria J. Lewis, Adam J. Judy, Renae L. Ago, Tetsuro Amouyel, Philippe Armstrong, Nicole D. Bakker, Mark K. Bartz, Traci M. Bennett, David A. Bis, Joshua C. Bordes, Constance Borte, Sigrid Cain, Anael Ridker, Paul M. Cho, Kelly Chen, Zhengming Cruchaga, Carlos Cole, John W. de Jager, Phil L. de Cid, Rafael Endres, Matthias Ferreira, Leslie E. Geerlings, Mirjam I. Gasca, Natalie C. Gudnason, Vilmundur Hata, Jun He, Jing Heath, Alicia K. Ho, Yuk-Lam Havulinna, Aki S. Hopewell, Jemma C. Hyacinth, I. Hyacinth Inouye, Michael Jacob, Mina A. Jeon, Christina E. Jern, Christina Kamouchi, Masahiro Keene, Keith L. Kitazono, Takanari Kittner, Steven J. Konuma, Takahiro Kumar, Amit Lacaze, Paul Launer, Lenore J. Lee, Keon-Joo Lepik, Kaido Li, Jiang Li, Liming Manichaikul, Ani Markus, Hugh S. Marston, Nicholas A. Meitinger, Thomas Mitchell, Braxton D. Montellano, Felipe A. Morisaki, Takayuki Mosley, Thomas H. Nalls, Mike A. Nordestgaard, Borge G. O'Donnell, Martin J. Okada, Yukinori Onland-Moret, N. Charlotte Ovbiagele, Bruce Peters, Annette Psaty, Bruce M. Rich, Stephen S. Rosand, Jonathan Sabatine, Marc S. Sacco, Ralph L. Saleheen, Danish Sandset, Else Charlotte Salomaa, Veikko Sargurupremraj, Muralidharan Sasaki, Makoto Satizabal, Claudia L. Schmidt, Carsten O. Shimizu, Atsushi Smith, Nicholas L. Sloane, Kelly L. Sutoh, Yoichi Sun, Yan V. Tanno, Kozo Tiedt, Steffen Tatlisumak, Turgut Torres-Aguila, Nuria P. Tiwari, Hemant K. Tregouet, Bordeaux Population Health Research Center University of Bordeaux Inserm UMR 1219 Bordeaux France Department of Public Health Bordeaux University Hospital Bordeaux France Department of Neurology Memory Clinic Bordeaux University Hospital Bordeaux France Department of Neurology Institute for Neurodegenerative Diseases CHU de Bordeaux Bordeaux France Institute for Stroke and Dementia Research (ISD) University Hospital LMU Munich Munich Germany Center for Genomic Medicine Massachusetts General Hospital Boston MA USA Program in Medical and Population Genetics Broad Institute of Harvard and the Massachusetts Institute of Technology Cambridge MA USA Munich Cluster for Systems Neurology Munich Germany German Center for Neurodegenerative Diseases (DZNE) Munich Germany Iwate Tohoku Medical Megabank Organization Iwate Medical University Iwate Japan Estonian Genome Centre Institute of Genomics University of Tartu Tartu Estonia Institute of Mathematics and Statistics University of Tartu Tartu Estonia Department of Computational Biology University of Lausanne Lausanne Switzerland Swiss Institute of Bioinformatics Lausanne Switzerland University Center for Primary Care and Public Health Lausanne Switzerland Department of Statistical Genetics Osaka University Graduate School of Medicine Suita Japan Department of Genome Informatics Graduate School of Medicine The University of Tokyo Tokyo Japan Laboratory for Systems Genetics RIKEN Center for Integrative Medical Sciences Yokohama Japan Laboratory of Statistical Immunology Immunology Frontier Research Center (WPI-IFReC) Osaka University Suita Japan Integrated Frontier Research for Medical Science Division Institute for Open and Transdisciplinary Research Initiatives Osaka University Suita Japan Center for Infectious Disease Education and Research (CiDER) Osaka University Suita Japan Massachusetts Veterans Epidemiology Research and Information Center (MAVERIC) VA Boston Healthcare System Boston MA USA TIMI S

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Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

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Nature genetics 2023年第10期55卷 1778-1779页

作者： Nick Shrine Abril G Izquierdo Jing Chen Richard Packer Robert J Hall Anna L Guyatt Chiara Batini Rebecca J Thompson Chandan Pavuluri Vidhi Malik Brian D Hobbs Matthew Moll Wonji Kim Ruth Tal-Singer Per Bakke Katherine A Fawcett Catherine John Kayesha Coley Noemi Nicole Piga Alfred Pozarickij Kuang Lin Iona Y Millwood Zhengming Chen Liming Li Sara R A Wijnant Lies Lahousse Guy Brusselle Andre G Uitterlinden Ani Manichaikul Elizabeth C Oelsner Stephen S Rich R Graham Barr Shona M Kerr Veronique Vitart Michael R Brown Matthias Wielscher Medea Imboden Ayoung Jeong Traci M Bartz Sina A Gharib Claudia Flexeder Stefan Karrasch Christian Gieger Annette Peters Beate Stubbe Xiaowei Hu Victor E Ortega Deborah A Meyers Eugene R Bleecker Stacey B Gabriel Namrata Gupta Albert Vernon Smith Jian'an Luan Jing-Hua Zhao Ailin F Hansen Arnulf Langhammer Cristen Willer Laxmi Bhatta David Porteous Blair H Smith Archie Campbell Tamar Sofer Jiwon Lee Martha L Daviglus Bing Yu Elise Lim Hanfei Xu George T O'Connor Gaurav Thareja Omar M E Albagha Karsten Suhre Raquel Granell Tariq O Faquih Pieter S Hiemstra Annelies M Slats Benjamin H Mullin Jennie Hui Alan James John Beilby Karina Patasova Pirro Hysi Jukka T Koskela Annah B Wyss Jianping Jin Sinjini Sikdar Mikyeong Lee Sebastian May-Wilson Nicola Pirastu Katherine A Kentistou Peter K Joshi Paul R H J Timmers Alexander T Williams Robert C Free Xueyang Wang John L Morrison Frank D Gilliland Zhanghua Chen Carol A Wang Rachel E Foong Sarah E Harris Adele Taylor Paul Redmond James P Cook Anubha Mahajan Lars Lind Teemu Palviainen Terho Lehtimäki Olli T Raitakari Jaakko Kaprio Taina Rantanen Kirsi H Pietiläinen Simon R Cox Craig E Pennell Graham L Hall W James Gauderman Chris Brightling James F Wilson Tuula Vasankari Tarja Laitinen Veikko Salomaa Dennis O Mook-Kanamori Nicholas J Timpson Eleftheria Zeggini Josée Dupuis Caroline Hayward Ben Brumpton Claudia Langenberg Stefan Weiss Georg Homuth Carsten Oliver Schmidt Nicole Probst-Hensch Marjo-Riitta Jarvelin Alanna C Morrison Ozren Polasek Igor Department of Population Health Sciences University of Leicester Leicester UK. nick.shrine@leicester.ac.uk. Department of Population Health Sciences University of Leicester Leicester UK. Division of Respiratory Medicine and NIHR Nottingham Biomedical Research Centre University of Nottingham Nottingham UK. Leicester National Institute for Health and Care Research Biomedical Research Centre Glenfield Hospital Leicester UK. Channing Division of Network Medicine Division of Pulmonary and Critical Care Medicine Department of Medicine Brigham and Women's Hospital Boston MA USA. Harvard Medical School Boston MA USA. COPD Foundation Washington DC USA. Department of Clinical Science Unversity of Bergen Bergen Norway. Nuffield Department of Population Health University of Oxford Oxford UK. MRC Population Health Research Unit University of Oxford Oxford UK. Department of Epidemiology and Biostatistics School of Public Health Peking University Health Science Center Beijing China. Department of Respiratory Diseases Ghent Universital Hospital Ghent Belgium. Department of Bioanalysis Faculty of Pharmaceutical Sciences Ghent University Ghent Belgium. Department of Epidemiology Eramus Medical Center Rotterdam The Netherlands. Department of Internal Medicine Eramus Medical Center Rotterdam The Netherlands. Center for Public Health Genomics University of Virginia Charlottesville VA USA. Department of Medicine Columbia University Medical Center New York NY USA. Medical Research Council Human Genetics Unit Institute of Genetics and Cancer University of Edinburgh Edinburgh UK. Human Genetics Center Department of Epidemiology Human Genetics and Environmental Sciences School of Public Health The University of Texas Health Science Center at Houston Houston TX USA. MRC Centre for Environment and Health Department of Epidemiology and Biostatistics School of Public Health Imperial College London London UK. Department of Epidemiology and Public Health Swiss Tropical

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