7 research outputs found
The impact of viral mutations on recognition by SARS-CoV-2 specific T cells.
- Author
- Aanensen DM
- Abudahab K
- Adams A
- Adams H
- Adeniji K
- Afifi S
- Aggarwal D
- Agranoff D
- Agwuh K
- Ahmad SSY
- Ahmed KA
- Aigrain L
- Ail D
- Alcolea-Medina A
- Aldera EL
- Alegria A
- Alex B
- Alikhan N-F
- Allara E
- Allen S
- Amato R
- Andrikopoulos P
- Angus B
- Angyal A
- Annett T
- Aplin S
- Ariani CV
- Armstrong JA
- Asad H
- Ash A
- Ashfield P
- Ashford F
- Ashish A
- Ashworth M
- Asiimwe IG
- Atkinson D
- Atkinson L
- Attwood SW
- Auckland C
- Aydin A
- Bach B
- Baillie JK
- Baker DJ
- Baker P
- Bakshi S
- Balcazar CE
- Ball J
- Barclay WS
- Bari S
- Barlow G
- Barlow SL
- Barnass S
- Barrett JC
- Barrett N
- Barrow M
- Barton E
- Bashton M
- Bassett AR
- Bassford C
- Basude S
- Batra R
- Baxter C
- Baxter D
- Bayzid N
- Beadsworth M
- Beaver C
- Beckett AH
- Beckwith SM
- Bedford L
- Beer R
- Beggs A
- Bellis KL
- Bernatoniene J
- Berridge J
- Berry C
- Berry L
- Bertolusso B
- Best A
- Best N
- Betteridge E
- Bibby D
- Bicknell K
- Binns D
- Birchley A
- Bird PW
- Bishop C
- Blacow R
- Blakey V
- Blane B
- Bogaert D
- Bolt F
- Bonfield J
- Bonner S
- Bonsall D
- Booth L
- Boswell T
- Bosworth A
- Bothma P
- Bourgeois Y
- Boyd O
- Bradley DT
- Breen C
- Brennan B
- Bresner C
- Breuer J
- Bridgett S
- Brittain-Long R
- Bronner IF
- Brooks E
- Broos A
- Brown JR
- Brown R
- Bucca G
- Buchan SL
- Buck D
- Bull M
- Bullock K
- Bulteel N
- Burden T
- Burns PJ
- Burtenshaw A
- Burton-Fanning S
- Byaruhanga T
- Byott M
- Campbell S
- Carabelli AM
- Cargill JS
- Carlile M
- Carlucci N
- Carracedo AD
- Carson G
- Caruth V
- Carvalho SF
- Casey A
- Cass E
- Castigador A
- Catalan J
- Catterall BWA
- Chadwick D
- Chadwick D
- Chalker V
- Chaloner NJ
- Chambler D
- Chand M
- Chand M
- Chappell JG
- Charalampous T
- Chatterton W
- Chaudhry Y
- Chechi K
- Chee N
- Child J
- Chukkambotla S
- Churcher CM
- Clark G
- Clark JJ
- Clark T
- Clarke EA
- Clarke P
- Clohisey S
- Cogger BJ
- Cole K
- Cole S
- Cole S
- Collini P
- Collins J
- Colquhoun R
- Connor M
- Connor TR
- Cook KF
- Cooke GS
- Coombes J
- Cooper L
- Corden S
- Cormie C
- Correia GDS
- Cortes N
- Cosgrove C
- Cotic M
- Cotton S
- Cottrell S
- Coupland L
- Cox A
- Cox H
- Cox M
- Craine N
- Crawford L
- Cross A
- Crown MR
- Crudgington D
- Cumley N
- Cupitt J
- Curran MD
- Curran T
- Cutino-Moguel M-T
- da Silva Filipe A
- da Silva Filipe A
- Dabrera G
- Dalton J
- Darby AC
- Dark P
- Davidson RK
- Davies A
- Davies RM
- Davis C
- Davis T
- Dawson C
- de Angelis D
- De Lacy E
- de Oliveira Martins L
- de Silva TI
- Debebe J
- Denton-Smith R
- Dervisevic S
- Dervisevic S
- Dewar R
- Dey J
- Dias J
- Dincarslan O
- Dobie D
- Docherty AB
- Donegan C
- Dong D
- Dong T
- Donnison P
- Donohue C
- Dorman MJ
- Douthwaite S
- Downing F
- Driscoll M
- Drummond A
- du Plessis L
- Duckworth N
- Dumas M-E
- Dunachie S
- Dunn C
- Dunning J
- DuRand I
- Durham J
- Dushianthan A
- Dyer P
- Dyer T
- Eastick K
- Easton LJ
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- Edgeworth J
- Edwards S
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- Eldirdiri S
- Ellaby N
- Elliott A
- Elliott S
- Eltringham G
- Ensell L
- Erkiert MJ
- Essex S
- Evans A
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- Evans JM
- Everson W
- Eziefula C
- Fairley DJ
- Fallon K
- Fanaie A
- Farr BW
- Fearn C
- Fegan C
- Feltwell T
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- Finn A
- Fisher LWS
- Flaherty L
- Flaviani F
- Fleming VM
- Fletcher T
- Forrest S
- Foster T
- Foster-Nyarko E
- Foulkes BH
- Foulser L
- Fragakis M
- Frampton D
- Francois S
- Fraser C
- Freeman TM
- Fryer H
- Fuchs M
- Fuller W
- Fullerton D
- Gajee K
- Galai K
- Gallagher A
- Gallagher E
- Gallagher MD
- Gallis M
- Gamble C
- Garcia-Dorival I
- Garg A
- Garg S
- Garg S
- Gaskin A
- Gatica-Wilcox B
- Geidelberg L
- Gemmell M
- Georgana I
- George RP
- Gifford L
- Gilbert L
- Girgis ST
- Girvan M
- Gkrania-Klotsas E
- Glaysher S
- Godden J
- Goldsmith A
- Goldstein EJ
- Golubchik T
- Gomes AN
- Gonçalves S
- Goodfellow IG
- Goodwin S
- Goudarzi S
- Gourtovaia M
- Graham C
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- Green LR
- Greenaway J
- Greenhalf W
- Gregory R
- Griffin JL
- Griffiths F
- Guest M
- Gunning P
- Gunson RN
- Gupta RK
- Gupta RK
- Gutierrez B
- Haldenby ST
- Halpin S
- Hamilton WL
- Hansford SE
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- Hardwick H
- Hardy E
- Harris KA
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- Hart J
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- Hartshorn S
- Harvey D
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- Hassan-Ibrahim MO
- Havalda P
- Hawcutt DB
- Heaney J
- Helmer T
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- Hiscox JA
- Hobrok M
- Hodgson L
- Holden MTG
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- Holmes CW
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- Houlihan C
- Howson-Wells HC
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- Hughes J
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- Hutchings S
- Idle G
- Ijaz S
- Illingworth CJ
- Impey R
- Irish-Tavares D
- Iturriza-Gomara M
- Izuagbe R
- Jackson B
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- Jones TR
- Joseph A
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- Kasipandian V
- Kay GL
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- Keating S
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- Keeley AJ
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- Kiy RT
- Klenerman P
- Knight BA
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- Kumziene-Summerhayes S
- Kwiatkowski D
- Lackenby A
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- Langford CF
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- Mantzouratou A
- Marchbank A
- Mariappan A
- Marsh L
- Martincorena I
- Martinez Nunez RT
- Maslen L
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- Matovu E
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- Mayhew M
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- McCafferty S
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- Papakonstantinou D
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- Torok ME
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- Twagira M
- Twohig KA
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- Vasylyeva TI
- Vattipally S
- Vernet G
- Vincent-Smith L
- Vipond BB
- Visuvanathan S
- Volz EM
- Vuylsteke A
- Waddy S
- Wai Ho AY
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- Walden A
- Walsh S
- Wang D
- Warne B
- Warwick-Dugdale J
- Wastnedge E
- Watkins J
- Watson LK
- Waugh S
- Webster HJ
- Weldon D
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- Welters I
- Westwick E
- Whalley T
- Wham M
- Wheeler H
- Whitehead M
- Whitehouse T
- Whiteley M
- Whittaker P
- Whittington A
- Whitwham A
- Wierzbicki C
- Wijesinghe M
- Wilcock E
- Willford NJ
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- Williams L-A
- Williams M
- Williams R
- Williams RJ
- Williams T
- Williamson KA
- Wilson L
- Wilson-Davies E
- Winchester S
- Wiselka M
- Witele E
- Withell KT
- Witney AA
- Wolverson A
- Wolverson P
- Wong N
- Wootton DG
- Workman A
- Workman T
- Wright DW
- Wright V
- Wrobel N
- Wyatt T
- Wyllie S
- xeine O'Toole
- Xu-McCrae L
- Yao X
- Yates B
- Yavus M
- Yaze G
- Yeats CA
- Yebra G
- Yew WC
- Ying Z
- Young GR
- Young J
- Young P
- Zambon M
- Zamudio ME
- Zarebski AE
- Zhang JE
- Zhang P
- Publication venue
- iScience
- Publication date
- 01/01/2021
- Field of study
We identify amino acid variants within dominant SARS-CoV-2 T cell epitopes by interrogating global sequence data. Several variants within nucleocapsid and ORF3a epitopes have arisen independently in multiple lineages and result in loss of recognition by epitope-specific T cells assessed by IFN-γ and cytotoxic killing assays. Complete loss of T cell responsiveness was seen due to Q213K in the A∗01:01-restricted CD8+ ORF3a epitope FTSDYYQLY207-215; due to P13L, P13S, and P13T in the B∗27:05-restricted CD8+ nucleocapsid epitope QRNAPRITF9-17; and due to T362I and P365S in the A∗03:01/A∗11:01-restricted CD8+ nucleocapsid epitope KTFPPTEPK361-369. CD8+ T cell lines unable to recognize variant epitopes have diverse T cell receptor repertoires. These data demonstrate the potential for T cell evasion and highlight the need for ongoing surveillance for variants capable of escaping T cell as well as humoral immunity.This work is supported by the UK Medical Research Council (MRC); Chinese Academy of Medical Sciences(CAMS) Innovation Fund for Medical Sciences (CIFMS), China; National Institute for Health Research (NIHR)Oxford Biomedical Research Centre, and UK Researchand Innovation (UKRI)/NIHR through the UK Coro-navirus Immunology Consortium (UK-CIC). Sequencing of SARS-CoV-2 samples and collation of data wasundertaken by the COG-UK CONSORTIUM. COG-UK is supported by funding from the Medical ResearchCouncil (MRC) part of UK Research & Innovation (UKRI),the National Institute of Health Research (NIHR),and Genome Research Limited, operating as the Wellcome Sanger Institute. T.I.d.S. is supported by a Well-come Trust Intermediate Clinical Fellowship (110058/Z/15/Z). L.T. is supported by the Wellcome Trust(grant number 205228/Z/16/Z) and by theUniversity of Liverpool Centre for Excellence in Infectious DiseaseResearch (CEIDR). S.D. is funded by an NIHR GlobalResearch Professorship (NIHR300791). L.T. and S.C.M.are also supported by the U.S. Food and Drug Administration Medical Countermeasures Initiative contract75F40120C00085 and the National Institute for Health Research Health Protection Research Unit (HPRU) inEmerging and Zoonotic Infections (NIHR200907) at University of Liverpool inpartnership with Public HealthEngland (PHE), in collaboration with Liverpool School of Tropical Medicine and the University of Oxford.L.T. is based at the University of Liverpool. M.D.P. is funded by the NIHR Sheffield Biomedical ResearchCentre (BRC – IS-BRC-1215-20017). ISARIC4C is supported by the MRC (grant no MC_PC_19059). J.C.K.is a Wellcome Investigator (WT204969/Z/16/Z) and supported by NIHR Oxford Biomedical Research Centreand CIFMS. The views expressed are those of the authors and not necessarily those of the NIHR or MRC
SARS-CoV-2 Omicron-B.1.1.529 leads to widespread escape from neutralizing antibody responses
- Author
- Adele S
- Adeniji K
- Agranoff D
- Agwuh K
- Ahmed KA
- Ail D
- Aldera EL
- Alegria A
- Alex B
- Aley PK
- Allen S
- Amini A
- Andrikopoulos P
- Angus B
- Armstrong JA
- Ashish A
- Ashworth M
- Asiimwe IG
- Assadi S
- Atkinson D
- Avinoam O
- Bach B
- Bahar M
- Baillie JK
- Baillie JK
- Baillie V
- Bakshi S
- Barclay WS
- Bari S
- Barlow G
- Barlow SL
- Barnass S
- Barnes E
- Barrett N
- Bassford C
- Basude S
- Baxter D
- Beadsworth M
- Bellass A
- Bernatoniene J
- Berridge J
- Berry C
- Best N
- Bogaert D
- Booth L
- Bothma P
- Brennan B
- Brittain-Long R
- Bullock K
- Bulteel N
- Burden T
- Burtenshaw A
- Carlucci N
- Carracedo AD
- Carroll MW
- Carson G
- Caruth V
- Cass E
- Catterall BWA
- Chadwick D
- Chadwick D
- Chambler D
- Chand M
- Chechi K
- Chee N
- Child J
- Chukkambotla S
- Clark JJ
- Clark R
- Clark T
- Clarke EA
- Clohisey S
- Cole S
- Cole S
- Collini P
- Conlon C
- Connor M
- Constantinides B
- Cooke GS
- Cooper L
- Cosgrove C
- Costa Clemens SA
- Coutts A
- Cox H
- Crook D
- Cupitt J
- Cutino-Moguel M-T
- da Silva Filipe A
- Da Silva K
- Dalton J
- Dark P
- Davis C
- Dawson C
- de Silva T
- Deeks AS
- Dejnirattisai W
- Dervisevic S
- Dijokaite A
- Dincarslan O
- Docherty AB
- Dold C
- Donegan C
- Donnelly L
- Donnison P
- Donohue C
- dos Santos Correia G
- Douthwaite S
- Drake TM
- Drummond A
- Dumas M-E
- Dunachie SJ
- Dunn C
- Dunning J
- DuRand I
- Dushianthan A
- Duyvesteyn HME
- Dyer P
- Dyer T
- Elliott A
- Evans A
- Evans C
- Eziefula C
- Fairfield CJ
- Fawkes A
- Fegan C
- Fernandes da Costa C
- Finch L
- Finn A
- Fisher LWS
- Flaherty L
- Flaxman A
- Fletcher T
- Foster T
- Frater J
- Frending L
- Fry EE
- Fullerton D
- Gamble C
- Garcia-Dorival I
- Gardiner S
- Garg A
- Garg S
- Garg S
- Gilchrist T
- Ginn HM
- Girvan M
- Gkrania-Klotsas E
- Godden J
- Goldsmith A
- Graham C
- Green CA
- Greenhalf W
- Griffin JL
- Griffiths F
- Gunning P
- Gupta RK
- Hafezi K
- Hall DR
- Halpin S
- Hardwick H
- Hardy E
- Harrison EM
- Harrison J
- Hartley C
- Hartshorn S
- Harvey D
- Havalda P
- Hawcutt DB
- Hendry R
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- Publication venue
- Elsevier BV
- Publication date
- 22/12/2021
- Field of study
On 24th November 2021, the sequence of a new SARS-CoV-2 viral isolate Omicron-B.1.1.529 was announced, containing far more mutations in Spike (S) than previously reported variants. Neutralization titers of Omicron by sera from vaccinees and convalescent subjects infected with early pandemic Alpha, Beta, Gamma, or Delta are substantially reduced, or the sera failed to neutralize. Titers against Omicron are boosted by third vaccine doses and are high in both vaccinated individuals and those infected by Delta. Mutations in Omicron knock out or substantially reduce neutralization by most of the large panel of potent monoclonal antibodies and antibodies under commercial development. Omicron S has structural changes from earlier viruses and uses mutations that confer tight binding to ACE2 to unleash evolution driven by immune escape. This leads to a large number of mutations in the ACE2 binding site and rebalances receptor affinity to that of earlier pandemic viruses
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- Takahashi T
- Takaku Y
- Takano K
- Takata T
- Takats Z
- Takayanagi N
- Takeda Y
- Takeuchi M
- Taki R
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- Tamm A
- Tanaka A
- Tanaka H
- Tanck A
- Taneski F
- Tanfoni M
- Tang L
- Tani M
- Tanianis-Hughes J
- Tanigawa Y
- Tanigawa Y
- Tanino Y
- Taniyama D
- Tanudjaja F
- Tariq A
- Task HGC
- Tateishi T
- Tateno H
- Tatham K
- Tatham KC
- Tavares S
- Tavecchia L
- Taylor A
- Taylor J
- Taylor M
- Taylor M
- Taylor M
- Team AC
- Team GHR
- Tebbutt J
- Tedder RS
- Teles A
- Tellez L
- Templeton M
- Tench H
- Tenesa A
- Tentorio P
- Terai H
- Terranova L
- Terron Arcos V
- Tetla D
- Teumer A
- Teunissen C
- Texeira J
- Thanasi M
- Thankachen M
- Thibeault C
- Thirlwall Y
- Thirumaran M
- Thomas A
- Thomas A
- Thomas B
- Thomas E
- Thomas H
- Thomas J
- Thomas J
- Thomas J
- Thomas M
- Thomas R
- Thomas V
- Thomis L
- Thompsom M
- Thompson AAR
- Thompson C
- Thompson C
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- Thompson R
- Thompson RC
- Thomson EC
- Thomson N
- Thonon R
- Thoral P
- Thornton D
- Thornton L
- Thorpe C
- Thorsteinsdottir U
- Thrasyvoulou L
- Thrush J
- Thwaites RS
- Thwaites V
- Thwaites V
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- Tibke C
- Tierney C
- Tilbey S
- Tilney E
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- Timlick E
- Ting L
- Tiseo G
- Tiseo G
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- Tivenan H
- Toapanta D
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- Togashi Y
- Tohda S
- Tokunaga K
- Tolson M
- Tomas AL
- Tommasi A
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- Torrents D
- Tran F
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- Trankiem A
- Tranter H
- Trembath RC
- Trembath RC
- Tridente A
- Tridente A
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- Trumper E
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- Tschopp J
- Tselios C
- Tsinaslanidis G
- Tsonas A
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- Turki S
- Turley P
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- Turner-Bone I
- Turney S
- Turtle LCW
- Turtle LCW
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- Twiss S
- Tyl D
- Tyler A
- Uchimura Y
- Uddin MJ
- Uddin MM
- Ueda S
- Ueda T
- Uellendahl-Werth F
- Uffelmann E
- Umeda A
- Underwood SJ
- Urrechaga E
- Ustianowski A
- Ustinova M
- Utrilla A
- Utsugi M
- Uwamino Y
- Vadgama N
- Vadla MS
- Vaghi M
- Valente S
- Valenti L
- Valentin Quiroga J
- Valentine J
- Valentino F
- Valino K
- Vallerga C
- Vallotton N
- Valsecchi MG
- van Agtmael M
- van Baarle F
- van Blokland I
- van de Beek D
- van den Berge M
- van der Poll T
- van der Valk M
- van Heel D
- van Heel DA
- van Heel DA
- van Koutrik L
- van Mourik N
- Van Singer M
- van Tonder L
- van Uffelen KWJ
- van Vugt M
- Vandernoot I
- Varghese M
- Vari MS
- Varnai R
- Vecchia M
- Vedage D
- Veelo D
- Veerapen K
- Veerapen K
- Veerapen K
- Vehreschild MJGT
- Velho M
- Venkatesh H
- Venturelli S
- Verdugo RA
- Vergori A
- Verlander M
- Verma A
- Verma SS
- Vertue M
- Vertue M
- Verula J
- Verzuri A
- Viala B
- Vigurs C
- Vincent R
- Vincent-Smith L
- Vincenti A
- Viollet RM
- Visuvanathan S
- Vitart V
- Vizcaychipi MP
- Vlaar APJ
- Vochin A
- Voide C
- Voide C
- Volland S
- Vollenweider P
- Vollenweider P
- Von Frenckell C
- von Hohenstaufen K
- von Mering C
- Vonk JM
- Voza A
- Vulesevic B
- Vuylsteke A
- Vuylsteke A
- Wacker EM
- Wackett T
- Wadams B
- Waddington N
- Waddy S
- Wagstaff V
- Waite AAC
- Wakabayashi A
- Wakahara K
- Wake R
- Wakefield P
- Wakinshaw F
- Walden A
- Waldron J
- Walker D
- Walker R
- Walker S
- Walker S
- Walker S
- Wall A
- Walsh T
- Walter J
- Walters RK
- Walton O
- Wang B
- Wang C
- Wang H
- Wang J
- Wang Q
- Wang X
- Wang X
- Ward G
- Ward K
- Ward L
- Ward M
- Warden S
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- Warren D
- Washington NL
- Wassall H
- Wasson C
- Watanabe H
- Watanabe K
- Watson E
- Watson G
- Watson J
- Watson N
- Watters M
- Waugh V
- Weaver J
- Webster A
- Webster D
- Webster K
- Wei S
- Weiss ST
- Weldon CH
- Wells C
- Welters I
- Welters ID
- Wendorff M
- Wendt FR
- Wery M
- Wesse T
- West J
- Weston H
- Wham M
- Wheeler M
- Whileman A
- Whitbread J
- White D
- White I
- White K
- White M
- White N
- White S
- Whitehouse T
- Whiteley S
- Whiteside J
- Whittaker P
- Whittington A
- Whittle H
- Whitton C
- Whyte C
- Wicks SJ
- Wienbrandt L
- Wiersinga WJ
- Wijesinghe M
- Wilby E
- Wilcock E
- Wilcox L
- Wilcox R
- Wild H
- Wild L
- Wild L
- Wilding L
- Wiles M
- Wilfling S
- Wilkin F
- Wilkins J
- Wilkinson A
- Wilkinson B
- Willer CJ
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- Williams A
- Williams A
- Williams D
- Williams F
- Williams G
- Williams H
- Williams K
- Williams M
- Williams M
- Williams P
- Williams S
- Williams T
- Willis H
- Wills M
- Willson J
- Wilson A
- Wilson DJ
- Wilson J
- Wilson JF
- Wilson L
- Winchester S
- Winnard S
- Winter-Goodwin B
- Wiselka M
- Wittig M
- Witzke O
- Wolf-Roberts R
- Wolford B
- Wolford B
- Wolterman RA
- Wolverson A
- Wong J
- Wood D
- Wood H-L
- Wood S
- Wood T
- Woodford C
- Woodruff M
- Woods L
- Woodyatt W
- Woolley AE
- Wooton DG
- Working UCLAHATLASDM
- Workman A
- Worner R
- Worsley L
- Wouters D
- Wozniak H
- Wray G
- Wren L
- Wright D
- Wright J
- Wright J
- Wright M
- Wrobel N
- Wrobel N
- Wu Y
- Wulandari R
- Wyllie DH
- Wynter I
- Xavier K
- Xue X
- Yadav A
- Yagi K
- Yamada M
- Yamada Y
- Yamagata K
- Yamasaki M
- Yang G
- Yang J
- Yang Z
- Yaspan B
- Yasui Y
- Yates B
- Yates B
- Yatomi M
- Ye C
- Yengo L
- Yermakovich D
- Yi X
- Yonekawa A
- Yoon H
- Yoon KJ
- Yoshida K
- Yoshida S
- Yoshida S
- Yoshida T
- Yoshihara T
- Yoshiya K
- Yoshiyama T
- Youlton N
- Younes SE
- Young P
- Yun N
- Zak A
- Zaki A
- Zambon M
- Zamikula J
- Zanella A
- Zanella I
- Zanelli G
- Zara F
- Zara F
- Zarate R
- Zarate R
- Zborowski AC
- Zeberg H
- Zechner M
- Zechner M
- Zguro K
- Zhai R
- Zhang JE
- Zhang M
- Zhao JH
- Zhen J
- Zheng C
- Zheng T
- Zhou W
- Zhou W
- Zhu W
- Zitter L
- Zlatopolsky M
- Zoller H
- Zollner S
- Zongo O
- zu Bentrup FM
- Zucchi P
- Zwinderman AHK
- Zyndorf M
- Publication venue
- Publication date
- 01/01/2021
- Field of study
The genetic make-up of an individual contributes to the susceptibility and response to viral infection. Although environmental, clinical and social factors have a role in the chance of exposure to SARS-CoV-2 and the severity of COVID-191,2, host genetics may also be important. Identifying host-specific genetic factors may reveal biological mechanisms of therapeutic relevance and clarify causal relationships of modifiable environmental risk factors for SARS-CoV-2 infection and outcomes. We formed a global network of researchers to investigate the role of human genetics in SARS-CoV-2 infection and COVID-19 severity. Here we describe the results of three genome-wide association meta-analyses that consist of up to 49,562 patients with COVID-19 from 46 studies across 19 countries. We report 13 genome-wide significant loci that are associated with SARS-CoV-2 infection or severe manifestations of COVID-19. Several of these loci correspond to previously documented associations to lung or autoimmune and inflammatory diseases3,4,5,6,7. They also represent potentially actionable mechanisms in response to infection. Mendelian randomization analyses support a causal role for smoking and body-mass index for severe COVID-19 although not for type II diabetes. The identification of novel host genetic factors associated with COVID-19 was made possible by the community of human genetics researchers coming together to prioritize the sharing of data, results, resources and analytical frameworks. This working model of international collaboration underscores what is possible for future genetic discoveries in emerging pandemics, or indeed for any complex human disease
Abdominal Trauma
- Author
- A Aitokallio-Tallberg
- A Chulu
- A Enk Van
- A Golan
- A Judich
- A Nilsson
- A Puri
- A Rudra
- A Schoenfeld
- A Steptoe
- A Welsh
- A Wise
- AA Guth
- AB Berenson
- ACOG Educational Bulletin
- AF Maxwell
- AH Haider
- AH Tyroch
- AJ Kobak
- AJ Shah
- AJ Taylor
- AL Franger
- AM Connolly
- American Academy of Pediatrics Committee on Fetus and Newborn
- American College of Obstetricians and Gynecologists
- American College of Obstetricians and Gynecologists
- American College of Surgeons
- American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care
- American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care
- AQ Tuggle
- AS Al Mulhim
- AS Khashan
- AT Fort
- AY Weintraub
- B Eckerling
- B Goff
- B Gonik
- B Parker
- B Schei
- B Webster
- BJ Tsuei
- C Bomken
- C Glantz
- C Passman
- C Rachana
- C Srinarmwong
- CB Sirlin
- CB Sirlin
- CD Matthews
- CE Haycock
- CH Wright
- CJ Vaizey
- CM Dunham
- CP Martins
- D Beversdorf
- D Bissell
- D Coutts
- D Hansen
- D Reinfurt
- D Rochester
- D Rothenberger
- DA Hall
- DA Nyberg
- DA Theodorou
- DC Astarita
- DC Schrinsky
- DD Herbert
- DE Nelson
- DG Ikossi
- DJ Begg
- DJ Dunlop
- DJ Rosen
- DK Kaye
- DL Hoyert
- DL Malone
- DL North
- DM Moorcroft
- DP Baker
- DP Kissinger
- DS Warner
- E Caldwell
- E Carlson
- E Connor
- E Kirkman
- E McDonnell
- E Yanikkerem
- EA Deitch
- EA Sandy 2nd
- EB Lerner
- EB Mendelson
- EB Parkinson
- EE Moore
- EK Osei
- EL Diamond
- EL Ormsby
- EM Biester
- EM Lazard
- EP Sakala
- F Fernandez
- FA Iliya
- FA Strigini
- FB Rogers
- FC Greiss
- FE Rubovits
- FJ Mercier
- G Dildy
- G Kelly
- G McGwin
- G McGwin Jr
- GA Rees
- GA Timberlake
- GC Stuart
- GV Bochicchio
- GV Poole Jr
- GW Kasten
- GW Shaftan
- H Amaro
- H Goodwin
- H Grimstad
- H Mighty
- H Sirin
- H Wilson
- HB Weiss
- HB Weiss
- HB Weiss
- HB Weiss
- HC Johnson
- HC Pape
- HH Stone
- HJ Buchbaum
- HJ Buchsbaum
- HJ Buchsbaum
- HJ Buchsbaum
- HJ Buschbaum
- HR Ward
- I Dawidson
- I Stabile
- IB Runnebaum
- ID Richards
- J Ali
- J Campbell
- J Damilakis
- J Donnez
- J Fildes
- J Fish
- J Gumbert
- J Halme
- J Jagoe
- J Johnson
- J Kulowski
- J Mancini
- J McFarlane
- J McFarlane
- J Novak
- J Shumway
- J Vivian-Taylor
- JA Carugno
- JA Davis
- JA Morris Jr
- Japan Automobile Federation (JAF)
- JB Holcomb
- JBA MacLeod
- JC Dornan
- JC Share
- JD Graham
- JD Iams
- JD Kuenssberg Von
- JE Chliaoutakis
- JE Nichols
- JF Beattie
- JF Greenblatt
- JF Kuebler
- JF Mercier
- JF Miller
- JG Parreira
- JJ DeMars
- JK Johnson
- JK Williams
- JL Crain
- JL Simpson
- JL Sperry
- JP Lavery
- JP Lavin Jr
- JP Marcin
- JP McGahan
- JP McGahan
- JP Stapp
- JR Evrard
- JR Richards
- JR Richards
- JR Richards
- JT Awwad
- JT Parer
- JW Davis
- JW Davis
- JW Garrett
- JW Hook Van
- JW Ritter
- K Bochner
- K Brohi
- K Browns
- K Dunning
- KA Mack
- KC Sihler
- KD Klinich
- KD Klinich
- KH Shah
- KL Mattox
- KM Devries
- KM Kuczkowski
- KM Kuczkowski
- KM Kuczkowski
- KM Kuczkowski
- KM Kuczkowski
- L Berlin
- L Bullock
- L Doan-Wiggins
- L Ketchum
- L Kvarnstrand
- L Suarez
- LA Fingerhut
- LF Beck
- LG Smith Jr
- LK Hyde
- LL Pak
- LW Hedin
- M Baethmann
- M Burtelow
- M Curry
- M Dahmus
- M Elliott
- M Fisher
- M Hack
- M Ichikawa
- M Jacobson
- M Mofidi
- M Rotondo
- M Schiff
- M Schiff
- M Sugrue
- M Sugrue
- M Whitten
- MA Borgman
- MA Brown
- MA Honein
- MA Meyers
- MA Schellpfeffer
- MA Schiff
- MA Schiff
- MA Schiff
- MA Schiff
- MA Schiff
- MA Schreiber
- MB Aboutanos
- MC Allen
- MD Pearlman
- MD Pearlman
- MD Pearlman
- MD Pearlman
- MD Pearlman
- MD Pearlman
- MD Pearlman
- MD Pearlman
- ME Mendelsohn
- ME Sugrue
- ME Wolf
- MG Harvey
- MH Fries
- MJ Curet
- MJ Milos
- MK Angele
- MM Adams
- MP Steinkampf
- MR Peyser
- MR Timms
- MT Coleman
- MT Miller
- MV Muench
- MV Muench
- MW Knoferl
- N Bowdler
- N Rezai
- NB Attico
- NB Grossman
- NL DePace
- NR Shah
- NS Geggie
- O Guneysel
- O Jansen
- OJ Ma
- OJ McAnena
- OL Gunter
- P Haapaniemi
- P Kaloo
- P O’Campo
- P Petrone
- PA Stafford
- PD Badia
- PE Steiner
- PF Agran
- PG Rose
- PG Whittaker
- PL Lane
- PL Mollison
- PM Reis
- PR Corsi
- PR John
- PR Koninckx
- PW Reginald
- R Aniulene
- R Depp
- R Doll
- R Haiti
- R Petersen
- R Schneider
- RA Griswold
- RA Knuppel
- RC Kessler
- RD Eden
- RD Kuhlmann
- RD Lister
- RE Leggon
- RJ Pepperell
- RJ Scorpio
- RL George
- S Ahmed
- S Jacob
- S Lindgren
- S Martin
- S Morris
- S Mukherjee
- S Rasmussen
- SA Rasmussen
- SB Zane
- SC Tinker
- SC Tinker
- SH Merchant
- SJ Barker
- SJ Patel
- SK Clarren
- SK Patterson
- SL Carmichael
- SL Carmichael
- SL Romney
- SM Duma
- SM Duma
- SM Goldman
- SO Henderson
- SZ Aboutanos
- T Dye
- T Goodwin
- T Loegters
- T Reck
- TA Amoroso
- TC Bost
- TE Nolan
- TF Drost
- TF Rowe
- TH Strong Jr
- TJ Esposito
- TJ Esposito
- TJ Esposito
- TJ Hodgetts
- TJ VanSante
- TL Hammond
- TL Vanden Hoek
- U Onwudiegwu
- U Rudlof
- V Brace
- V Cokkinides
- V Katz
- V Leroy-Malherbe
- VC Romero
- VL Katz
- WE MacKenzie
- WH White Jr
- WJ Howland
- WM Court Brown
- WM Crosby
- WM Crosby
- WM Crosby
- WN Friedman
- Working Party Association of Anaesthetists of Great Britain and Ireland (AAGBI)
- WS Hoff
- WS Pearl
- Y Baerga-Varela
- Y Kataoka
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study