Amanda Y. Chong

ORCID: 0000-0003-4919-2632
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About
Contact & Profiles
Research Areas
  • vaccines and immunoinformatics approaches
  • T-cell and B-cell Immunology
  • IL-33, ST2, and ILC Pathways
  • Chromosomal and Genetic Variations
  • Genomics and Phylogenetic Studies
  • SARS-CoV-2 and COVID-19 Research
  • Polyomavirus and related diseases
  • Genetic Associations and Epidemiology
  • Immune Cell Function and Interaction
  • Immunotherapy and Immune Responses
  • Cytokine Signaling Pathways and Interactions
  • COVID-19 Clinical Research Studies
  • RNA regulation and disease
  • Paleontology and Evolutionary Biology
  • Respiratory viral infections research
  • Parvovirus B19 Infection Studies
  • Evolution and Paleontology Studies
  • Microbial infections and disease research
  • Inflammasome and immune disorders
  • Genetic and phenotypic traits in livestock
  • Tumors and Oncological Cases
  • Immune responses and vaccinations
  • NF-κB Signaling Pathways
  • Genetic diversity and population structure
  • Full-Duplex Wireless Communications

University of Oxford
2019-2025

Centre for Human Genetics
2019-2025

Ludwig Cancer Research
2024-2025

Oxford BioMedica (United Kingdom)
2022

The University of Sydney
2011-2017

Earlham Institute
2017

Fracture Analysis Consultants (United States)
2014

To provide context for the diversification of archosaurs--the group that includes crocodilians, dinosaurs, and birds--we generated draft genomes three crocodilians: Alligator mississippiensis (the American alligator), Crocodylus porosus saltwater crocodile), Gavialis gangeticus Indian gharial). We observed an exceptionally slow rate genome evolution within crocodilians at all levels, including nucleotide substitutions, indels, transposable element content movement, gene family evolution,...

10.1126/science.1254449 article EN Science 2014-12-11
David Ahern Zhichao Ai Mark Ainsworth Chris Allan Alice Allcock and 95 more Brian Angus M. Azim Ansari Carolina V. Arancibia-Cárcamo Dominik Aschenbrenner Moustafa Attar J. Kenneth Baillie Eleanor Barnes Rachael Bashford-Rogers Archana Bashyal Sally Beer G. Berridge Amy Beveridge Sagida Bibi Tihana Bicanic Luke Blackwell Paul Bowness Andrew Brent Andrew Brown John Broxholme David Buck Katie L. Burnham Helen M. Byrne Susana Camara Ivan Candido-Ferreira Philip D. Charles Wentao Chen Yi‐Ling Chen Amanda Y. Chong Elizabeth Clutterbuck Mark Coles Christopher P. Conlon Richard J. Cornall Adam P. Cribbs Fabiola Curion Emma E. Davenport Neil Davidson Simon Davis Calliope A. Dendrou Julie Dequaire Lea Dib James Docker Christina Dold Tao Dong Damien J. Downes Hal Drakesmith Susanna Dunachie David A. Duncan Chris Eijsbouts Robert Esnouf Alexis Espinosa Rachel Etherington Benjamin P. Fairfax Rory Fairhead Hai Fang Shayan Fassih Sally Felle Maria Fernandez Mendoza Ricardo Melo Ferreira Román Fischer Thomas Foord Aden Forrow John Frater Anastasia Fries Verónica Sánchez Lucy C. Garner Clementine Geeves Dominique Georgiou Leila Godfrey Tanya Golubchik Maria Gomez Vazquez Angie Green Hong Harper Heather A. Harrington Raphael Heilig Svenja Hester Jennifer Hill Charles Hinds Clare Hird Ling‐Pei Ho Renee S. Hoekzema Benjamin Hollis Jim R. Hughes Paula Hutton Matthew A. Jackson-Wood Ashwin Jainarayanan Anna James-Bott Kathrin Jansen Katie Jeffery Elizabeth Jones Luke Jostins Georgina Kerr David Kim Paul Klenerman Julian C. Knight Vinod Kumar

Treatment of severe COVID-19 is currently limited by clinical heterogeneity and incomplete description specific immune biomarkers. We present here a comprehensive multi-omic blood atlas for patients with varying severity in an integrated comparison influenza sepsis versus healthy volunteers. identify signatures correlates host response. Hallmarks disease involved cells, their inflammatory mediators networks, including progenitor cells myeloid lymphocyte subsets, features the repertoire,...

10.1016/j.cell.2022.01.012 article EN cc-by Cell 2022-01-21

Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine immunogenicity varies between individuals, and immune responses correlate with efficacy. Using data from 1,076 participants enrolled in ChAdOx1 nCov-19 efficacy trials the United Kingdom, we found that inter-individual variation normalized antibody against SARS-CoV-2 spike its receptor-binding domain (RBD) at 28 days after first vaccination shows genome-wide significant association major histocompatibility complex...

10.1038/s41591-022-02078-6 article EN cc-by Nature Medicine 2022-10-13

Certain infectious agents are recognised causes of cancer and other chronic diseases. To understand the pathological mechanisms underlying such relationships, here we design a Multiplex Serology platform to measure quantitative antibody responses against 45 antigens from 20 including human herpes, hepatitis, polyoma, papilloma, retroviruses, as well Chlamydia trachomatis, Helicobacter pylori Toxoplasma gondii, then assayed random subset 9695 UK Biobank participants. We find seroprevalence...

10.1038/s41467-022-29307-3 article EN cc-by Nature Communications 2022-04-05

Latin America continues to be severely underrepresented in genomics research, and fine-scale genetic histories complex trait architectures remain hidden owing insufficient data1. To fill this gap, the Mexican Biobank project genotyped 6,057 individuals from 898 rural urban localities across all 32 states Mexico at a resolution of 1.8 million genome-wide markers with linked disease information creating valuable nationwide genotype-phenotype database. Here, using ancestry deconvolution...

10.1038/s41586-023-06560-0 article EN cc-by Nature 2023-10-11
Christos P Kotanidis Cheng Xie Donna Maria Alexander Jonathan Rodrigues Katie L. Burnham and 95 more Alexander J. Mentzer Daniel O’Connor Julian C. Knight Muhammad Siddique Helen Lockstone Sheena Thomas Rafail A. Kotronias Evangelos K. Oikonomou Ileana Badi Maria Lyasheva Cheerag Shirodaria Sheila Lumley Bede Constantinides Nicholas Sanderson Gillian Rodger Kevin Chau Archie Lodge Maria Tsakok Fergus Gleeson David Adlam Praveen P. N. Rao Das Indrajeet Aparna Deshpande Amrita Bajaj Benjamin Hudson Vivek Srivastava Shakil Farid George Krasopoulos Rana Sayeed Ling‐Pei Ho Stefan Neubauer David E. Newby Keith M. Channon John Deanfield Charalambos Antoniades David Ahern Zhichao Ai Mark Ainsworth Chris Allan Alice Allcock Brian Angus M. Azim Ansari Carolina V. Arancibia-Cárcamo Dominik Aschenbrenner Moustafa Attar J. Kenneth Baillie Eleanor Barnes Rachael Bashford-Rogers Archana Bashyal Sally Beer G. Berridge Amy Beveridge Sagida Bibi Tihana Bicanic Luke Blackwell Paul Bowness Andrew Brent Andrew Brown John Broxholme David Buck Katie L. Burnham Helen M. Byrne Susana Camara Ivan Candido-Ferreira Philip D. Charles Wentao Chen Yi‐Ling Chen Amanda Y. Chong Elizabeth Clutterbuck Mark Coles Christopher P. Conlon Richard J. Cornall Adam P. Cribbs Fabiola Curion Emma E. Davenport Neil C. Davidson Simon Davis Calliope A. Dendrou Julie Dequaire Lea Dib James Docker Christina Dold Tao Dong Damien J. Downes Hal Drakesmith Susanna Dunachie David A. Duncan Chris Eijsbouts Robert Esnouf Alexis Espinosa Rachel Etherington Benjamin P. Fairfax Rory Fairhead Hai Fang Shayan Fassih

10.1016/s2589-7500(22)00132-7 article EN cc-by The Lancet Digital Health 2022-08-26

The major histocompatibility complex (MHC) is a dynamic genome region with an essential role in the adaptive immunity of vertebrates, especially antigen presentation. MHC generally divided into subregions (classes I, II and III) containing genes similar function across species, but different gene number organisation. Crocodylia (crocodilians) are widely distributed represent evolutionary distinct group among higher genomic organisation within this lineage has been largely unexplored. Here,...

10.1371/journal.pone.0114631 article EN cc-by PLoS ONE 2014-12-11

Crocodilians are thought to be hosts a diverse and divergent complement of endogenous retroviruses (ERVs) but comprehensive investigation is yet performed. The recent sequencing three crocodilian genomes provides an opportunity for more detailed accurate representation the ERV diversity that present in these species. Here we investigate diversity, distribution evolution ERVs from key species, outline processes driving proliferation evolution.ERVs related sequences make up less than 2%...

10.1186/s12977-014-0071-2 article EN cc-by Retrovirology 2014-10-29

How human genetic variation contributes to vaccine effectiveness in infants is unclear, and data are limited on these relationships populations with African ancestries. We undertook analyses of antibody responses from Uganda (n = 1391), Burkina Faso 353) South Africa 755), identifying associations between leukocyte antigen (HLA) response for five eight tested antigens spanning pertussis, diphtheria hepatitis B vaccines. In addition, through HLA typing 1,702 individuals 11 ancestry derived...

10.1038/s41591-024-02944-5 article EN cc-by Nature Medicine 2024-05-01

Abstract Iron is an essential trace element for both humans and pathogens, but its genetic determinants are understudied in Africa where iron deficiency infectious diseases highly prevalent. We conducted genome-wide association studies six iron-related biomarkers 3928 children from five sites across with replication 2868 African American adults. identify a previously unreported loci transferrin GTF3C5, gene regulating cellular iron-uptake, soluble receptor FREM3 , the Dantu locus, hepcidin...

10.1101/2025.03.02.25323069 preprint EN medRxiv (Cold Spring Harbor Laboratory) 2025-03-05

Abstract Cytomegalovirus (CMV) is a globally endemic latent herpes virus that profoundly impacts T cell immunity. We investigated the oncological consequences of CMV infection across 341 prospectively recruited patients receiving immune checkpoint blockade (ICB) for melanoma. + with metastatic melanoma (MM) have higher lymphocyte counts, reduced neutrophil to ratio and divergent CD8 gene expression. Combination anti-CTLA-4/anti-PD-1 ICB, but not single-agent anti-PD-1 induces cytotoxicity...

10.1038/s41591-025-03647-1 article EN cc-by Nature Medicine 2025-04-23

<title>Abstract</title> Sepsis is a heterogeneous clinical syndrome with high mortality rate and personalised stratification strategies are proposed as essential to successful targeted therapeutics. Here, we characterise genetic variation that modulates <italic>MTOR</italic>, critical regulator of metabolism immune responses in sepsis. The effects highly context specific, involving regulatory element affects <italic>MTOR</italic> expression activated T cells opposite direction effect...

10.21203/rs.3.rs-6457289/v1 preprint EN Research Square (Research Square) 2025-05-26

Abstract The platypus O rnithorhynchus anatinus is an endemic monotreme species with a wide latitudinal distribution in eastern A ustralia, including T asmania. Understanding of the phylogeography within this very limited at present and represents gap documentation ustralia's unique biodiversity. We analysed mitochondrial DNA sequences (partial control region complete cytochrome b , portions flanking tRNAs ) 74 individuals from across species. Phylogenetic analysis concatenated corroborated...

10.1111/j.1469-7998.2011.00854.x article EN Journal of Zoology 2011-10-07

Abstract Background Certain infectious agents are recognised causes of cancer and potentially other chronic diseases. Identifying associations understanding pathological mechanisms involving subsequent disease risk will be possible through measuring exposure to multiple in large-scale prospective cohorts such as UK Biobank. Methods Following expert consensus we designed a Multiplex Serology platform capable simultaneously quantitative antibody responses against 45 antigens from 20 implicated...

10.1101/19004960 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2019-08-29

Current Genome-Wide Association Studies (GWAS) rely on genotype imputation to increase statistical power, improve fine-mapping of association signals, and facilitate meta-analyses. Due the complex demographic history Latin America lack balanced representation Native American genomes in current panels, discovery locally relevant disease variants is likely be missed, limiting scope impact biomedical research these populations. Therefore, necessity better diversity genomic databases a...

10.3389/fgene.2021.719791 article EN cc-by Frontiers in Genetics 2022-01-03

Abstract Human polyomaviruses are widespread in humans and can cause severe disease immunocompromised individuals. To identify human genetic determinants of the humoral immune response against polyomaviruses, we performed genome-wide association studies meta-analyses qualitative quantitative immunoglobulin G responses BK polyomavirus (BKPyV), JC (JCPyV), Merkel cellpolyomavirus (MCPyV), WU (WUPyV), 6 (HPyV6) 15,660 individuals European ancestry from three independent studies. We observed...

10.1093/ve/veab058 article EN cc-by Virus Evolution 2021-06-09

The number of gluten-free diet followers without celiac disease (CD) is increasing. However, little known about the characteristics these individuals.

10.1093/ajcn/nqaa291 article EN cc-by American Journal of Clinical Nutrition 2020-10-01
David Ahern Zhichao Ai Mark Ainsworth Chris Allan Alice Allcock and 95 more M. Azim Ansari Carolina V. Arancibia-Cárcamo Dominik Aschenbrenner Moustafa Attar J. Kenneth Baillie Eleanor Barnes Rachael Bashford-Rogers Archana Bashyal Sally Beer G. Berridge Amy Beveridge Sagida Bibi Tihana Bicanic Luke Blackwell Paul Bowness Andrew Brent Andrew Brown John Broxholme David Buck Katie L. Burnham Helen M. Byrne Susana Camara Ivan Candido-Ferreira Philip D. Charles Wentao Chen Yi‐Ling Chen Amanda Y. Chong Elizabeth Clutterbuck Mark Coles Christopher P. Conlon Richard J. Cornall Adam P. Cribbs Fabiola Curion Emma E. Davenport Neil Davidson Simon Davis Calliope A. Dendrou Julie Dequaire Lea Dib James Docker Christina Dold Tao Dong Damien J. Downes Hal Drakesmith Susanna Dunachie David A. Duncan Chris Eijsbouts Robert Esnouf Alexis Espinosa Rachel Etherington Benjamin P. Fairfax Rory Fairhead Hai Fang Shayan Fassih Sally Felle Maria Fernandez Mendoza Ricardo C. Ferreira Román Fischer Thomas Foord Aden Forrow John Frater Anastasia Fries Verónica Sánchez Lucy C. Garner Clementine Geeves Dominique Georgiou Leila Godfrey Tanya Golubchik Maria Gomez Vazquez Angie Green Hong Harper Heather A. Harrington Raphael Heilig Svenja Hester Jennifer Hill Charles Hinds Clare Hird Ling‐Pei Ho Renee S. Hoekzema Benjamin Hollis Jim R. Hughes Paula Hutton Matthew Jackson Ashwin Jainarayanan Anna James-Bott Kathrin Jansen Katie Jeffery Elizabeth Jones Luke Jostins Georgina Kerr David Kim Paul Klenerman Julian C. Knight Vinod Kumar Piyush Kumar Sharma

Summary Treatment of severe COVID-19 is currently limited by clinical heterogeneity and incomplete understanding potentially druggable immune mediators disease. To advance this, we present a comprehensive multi-omic blood atlas in patients with varying severity compare influenza, sepsis healthy volunteers. We identify signatures correlates host response. Hallmarks disease revealed cells, their inflammatory networks as potential therapeutic targets, including progenitor cells specific myeloid...

10.1101/2021.05.11.21256877 preprint EN cc-by medRxiv (Cold Spring Harbor Laboratory) 2021-05-11

Abstract Genetic colocalization analyses are frequently conducted to determine if causal signals at a genetic locus shared between two phenotypes. However, is rarely undertaken the HLA locus, due its complex linkage disequilibrium (LD) and high polymorphism density. This lack of inference method limits our ability translate associations into therapeutic targets. Here we present that uses alleles, instead nucleotide variants, perform traits genes. The method, which call HLA-colocalization,...

10.1101/2024.11.05.24316783 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2024-11-05
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