Trans-ethnic genome-wide association study of severe COVID-19

[1]  Mattia G. Bergomi,et al.  Mapping the human genetic architecture of COVID-19 , 2021, Nature.

[2]  Ruth I. Tennen,et al.  Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity , 2021, Nature Genetics.

[3]  L. Bradley,et al.  Lessons in antiviral immunity , 2021, Science.

[4]  Huanming Yang,et al.  Initial whole-genome sequencing and analysis of the host genetic contribution to COVID-19 severity and susceptibility , 2020, Cell discovery.

[5]  S. Pääbo,et al.  The major genetic risk factor for severe COVID-19 is inherited from Neanderthals , 2020, Nature.

[6]  Barbara B. Shih,et al.  Genetic mechanisms of critical illness in COVID-19 , 2020, Nature.

[7]  Jacques Fellay,et al.  Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 , 2020, Science.

[8]  S. Solomon,et al.  Clinical Outcomes in Young US Adults Hospitalized With COVID-19. , 2020, JAMA internal medicine.

[9]  A. Gylfason,et al.  Humoral Immune Response to SARS-CoV-2 in Iceland , 2020, The New England journal of medicine.

[10]  R. Rohs,et al.  Landscape of DNA binding signatures of myocyte enhancer factor-2B reveals a unique interplay of base and shape readout , 2020, Nucleic acids research.

[11]  U. Reimer,et al.  SARS-CoV-2-reactive T cells in healthy donors and patients with COVID-19 , 2020, Nature.

[12]  J. Schuurs-Hoeijmakers,et al.  Presence of Genetic Variants Among Young Men With Severe COVID-19. , 2020, JAMA.

[13]  Tangchun Wu,et al.  Reconstruction of the full transmission dynamics of COVID-19 in Wuhan , 2020, Nature.

[14]  Martin Linster,et al.  SARS-CoV-2-specific T cell immunity in cases of COVID-19 and SARS, and uninfected controls , 2020, Nature.

[15]  M. Hernán,et al.  Prevalence of SARS-CoV-2 in Spain (ENE-COVID): a nationwide, population-based seroepidemiological study , 2020, The Lancet.

[16]  Michael J. Purcaro,et al.  Expanded encyclopaedias of DNA elements in the human and mouse genomes , 2020, Nature.

[17]  C. Reed,et al.  Seroprevalence of Antibodies to SARS-CoV-2 in Six Sites in the United States, March 23-May 3, 2020 , 2020, medRxiv.

[18]  J. Erdmann,et al.  Genomewide Association Study of Severe Covid-19 with Respiratory Failure , 2020, The New England journal of medicine.

[19]  The COVID-19 Host Genetics Initiative The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic , 2020, European Journal of Human Genetics.

[20]  M. He,et al.  Lead exposure and its interactions with oxidative stress polymorphisms on lung function impairment: Results from a longitudinal population-based study. , 2020, Environmental research.

[21]  Jian Chen,et al.  Association between ABO blood groups and risk of SARS‐CoV‐2 pneumonia , 2020, British journal of haematology.

[22]  Eun Ji Kim,et al.  Presenting Characteristics, Comorbidities, and Outcomes Among 5700 Patients Hospitalized With COVID-19 in the New York City Area. , 2020, JAMA.

[23]  Jing Shi,et al.  Risk factors for severity and mortality in adult COVID-19 inpatients in Wuhan , 2020, Journal of Allergy and Clinical Immunology.

[24]  Xihong Lin,et al.  Association of Public Health Interventions With the Epidemiology of the COVID-19 Outbreak in Wuhan, China. , 2020, JAMA.

[25]  S. Merler,et al.  Baseline Characteristics and Outcomes of 1591 Patients Infected With SARS-CoV-2 Admitted to ICUs of the Lombardy Region, Italy. , 2020, JAMA.

[26]  Lei Liu,et al.  Relationship between the ABO Blood Group and the COVID-19 Susceptibility , 2020, medRxiv.

[27]  J. Xiang,et al.  Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study , 2020, The Lancet.

[28]  E. Dong,et al.  An interactive web-based dashboard to track COVID-19 in real time , 2020, The Lancet Infectious Diseases.

[29]  Hongbing Shen,et al.  Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations. , 2019, The Lancet. Respiratory medicine.

[30]  Alicia R. Martin,et al.  Clinical use of current polygenic risk scores may exacerbate health disparities , 2019, Nature Genetics.

[31]  J. Casanova,et al.  Lessons learned from the study of human inborn errors of innate immunity , 2019, The Journal of allergy and clinical immunology.

[32]  D. Hinds,et al.  Eleven loci with new reproducible genetic associations with allergic disease risk , 2019, The Journal of allergy and clinical immunology.

[33]  Juan Burgueño,et al.  Pilot genome-wide association study identifying novel risk loci for type 2 diabetes in a Maya population. , 2018, Gene.

[34]  K. Basso,et al.  MEF2B Instructs Germinal Center Development and Acts as an Oncogene in B Cell Lymphomagenesis. , 2018, Cancer cell.

[35]  Dennis Andersson,et al.  A retrospective cohort study , 2018 .

[36]  H. Teare,et al.  Perceptions of legislation relating to the sharing of genomic biobank results with donors—a survey of BBMRI-ERIC biobanks , 2018, European Journal of Human Genetics.

[37]  Doron Lancet,et al.  GeneHancer: genome-wide integration of enhancers and target genes in GeneCards , 2017, Database J. Biol. Databases Curation.

[38]  T. Wieland,et al.  Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability , 2017, Human Genetics.

[39]  Jacob M. Luber,et al.  HiGlass: web-based visual exploration and analysis of genome interaction maps , 2017, Genome Biology.

[40]  Jessica A. Weber,et al.  The Sentieon Genomics Tools – A fast and accurate solution to variant calling from next-generation sequence data , 2017, bioRxiv.

[41]  J. Stoler,et al.  Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU , 2017, Human Genetics.

[42]  Alan M. Kwong,et al.  Next-generation genotype imputation service and methods , 2016, Nature Genetics.

[43]  Shane A. McCarthy,et al.  Reference-based phasing using the Haplotype Reference Consortium panel , 2016, Nature Genetics.

[44]  Anne W. Ndungu,et al.  Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children , 2016, American journal of human genetics.

[45]  H. Jäck,et al.  Essential control of early B-cell development by Mef2 transcription factors. , 2016, Blood.

[46]  Joseph K. Pickrell,et al.  Detection and interpretation of shared genetic influences on 42 human traits , 2015, Nature Genetics.

[47]  T. Jacques,et al.  Human IFNAR2 deficiency: Lessons for antiviral immunity , 2015, Science Translational Medicine.

[48]  Gabor T. Marth,et al.  A global reference for human genetic variation , 2015, Nature.

[49]  Jun S. Liu,et al.  The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans , 2015, Science.

[50]  Carson C Chow,et al.  Second-generation PLINK: rising to the challenge of larger and richer datasets , 2014, GigaScience.

[51]  Chaolong Wang,et al.  Ancestry estimation and control of population stratification for sequence-based association studies , 2014, Nature Genetics.

[52]  Hongbing Shen,et al.  New loci associated with chronic hepatitis B virus infection in Han Chinese , 2013, Nature Genetics.

[53]  F. Geissmann,et al.  MEF2 Is an In Vivo Immune-Metabolic Switch , 2013, Cell.

[54]  David C. Wilson,et al.  Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease , 2012, Nature.

[55]  Andre Franke,et al.  Genome-wide association study indicates two novel resistance loci for severe malaria , 2012, Nature.

[56]  Shanru Li,et al.  Foxp4 Is Dispensable for T Cell Development, but Required for Robust Recall Responses , 2012, PloS one.

[57]  M. Lu,et al.  Foxp1/4 control epithelial cell fate during lung development and regeneration through regulation of anterior gradient 2 , 2012, Development.

[58]  P. Bugert,et al.  Blood Group ABO Genotyping in Paternity Testing , 2012, Transfusion Medicine and Hemotherapy.

[59]  Eleazar Eskin,et al.  Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies. , 2011, American journal of human genetics.

[60]  Josyf Mychaleckyj,et al.  Robust relationship inference in genome-wide association studies , 2010, Bioinform..

[61]  Michael Boehnke,et al.  LocusZoom: regional visualization of genome-wide association scan results , 2010, Bioinform..

[62]  Zhaoxia Yu,et al.  Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies. , 2009, American journal of human genetics.

[63]  Richard Durbin,et al.  Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .

[64]  E. Olson,et al.  MEF2: a central regulator of diverse developmental programs , 2007, Development.

[65]  Sonja W. Scholz,et al.  Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data , 2007, The Lancet Neurology.

[66]  Sonja W. Scholz,et al.  Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data , 2006, The Lancet Neurology.

[67]  B. Hansen,et al.  Optimal Full Matching and Related Designs via Network Flows , 2006 .

[68]  S. Goff,et al.  Inhibition of HIV-1 gene expression by a fragment of hnRNP U. , 2006, Molecular cell.

[69]  H. Whittle,et al.  Class II cytokine receptor gene cluster is a major locus for hepatitis B persistence. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[70]  J. Sung,et al.  ABO blood group and susceptibility to severe acute respiratory syndrome. , 2005, JAMA.

[71]  Jun O. Liu,et al.  Myocyte Enhancer Factor 2 Mediates Calcium-dependent Transcription of the Interleukin-2 Gene in T Lymphocytes , 2004, Journal of Biological Chemistry.

[72]  Jun O. Liu,et al.  Deletion of Calcineurin and Myocyte Enhancer Factor 2 (MEF2) Binding Domain of Cabin1 Results in Enhanced Cytokine Gene Expression in T Cells , 2001, The Journal of experimental medicine.

[73]  Marc Parmentier,et al.  Resistance to HIV-1 infection in Caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene , 1996, Nature.

[74]  David D. McDonald,et al.  Programs , 1984, CL.