These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

270 related articles for article (PubMed ID: 34043590)

  • 1. Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.
    Povysil G; Butler-Laporte G; Shang N; Wang C; Khan A; Alaamery M; Nakanishi T; Zhou S; Forgetta V; Eveleigh RJ; Bourgey M; Aziz N; Jones SJ; Knoppers B; Scherer SW; Strug LJ; Lepage P; Ragoussis J; Bourque G; Alghamdi J; Aljawini N; Albes N; Al-Afghani HM; Alghamdi B; Almutairi MS; Mahmoud ES; Abu-Safieh L; El Bardisy H; Harthi FSA; Alshareef A; Suliman BA; Alqahtani SA; Almalik A; Alrashed MM; Massadeh S; Mooser V; Lathrop M; Fawzy M; Arabi YM; Mbarek H; Saad C; Al-Muftah W; Jung J; Mangul S; Badji R; Thani AA; Ismail SI; Gharavi AG; Abedalthagafi MS; Richards JB; Goldstein DB; Kiryluk K
    J Clin Invest; 2021 Jul; 131(14):. PubMed ID: 34043590
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19.
    Zhang Q; Bastard P; Liu Z; Le Pen J; Moncada-Velez M; Chen J; Ogishi M; Sabli IKD; Hodeib S; Korol C; Rosain J; Bilguvar K; Ye J; Bolze A; Bigio B; Yang R; Arias AA; Zhou Q; Zhang Y; Onodi F; Korniotis S; Karpf L; Philippot Q; Chbihi M; Bonnet-Madin L; Dorgham K; Smith N; Schneider WM; Razooky BS; Hoffmann HH; Michailidis E; Moens L; Han JE; Lorenzo L; Bizien L; Meade P; Neehus AL; Ugurbil AC; Corneau A; Kerner G; Zhang P; Rapaport F; Seeleuthner Y; Manry J; Masson C; Schmitt Y; Schlüter A; Le Voyer T; Khan T; Li J; Fellay J; Roussel L; Shahrooei M; Alosaimi MF; Mansouri D; Al-Saud H; Al-Mulla F; Almourfi F; Al-Muhsen SZ; Alsohime F; Al Turki S; Hasanato R; van de Beek D; Biondi A; Bettini LR; D'Angio' M; Bonfanti P; Imberti L; Sottini A; Paghera S; Quiros-Roldan E; Rossi C; Oler AJ; Tompkins MF; Alba C; Vandernoot I; Goffard JC; Smits G; Migeotte I; Haerynck F; Soler-Palacin P; Martin-Nalda A; Colobran R; Morange PE; Keles S; Çölkesen F; Ozcelik T; Yasar KK; Senoglu S; Karabela ŞN; Rodríguez-Gallego C; Novelli G; Hraiech S; Tandjaoui-Lambiotte Y; Duval X; Laouénan C; ; ; ; ; ; ; ; ; Snow AL; Dalgard CL; Milner JD; Vinh DC; Mogensen TH; Marr N; Spaan AN; Boisson B; Boisson-Dupuis S; Bustamante J; Puel A; Ciancanelli MJ; Meyts I; Maniatis T; Soumelis V; Amara A; Nussenzweig M; García-Sastre A; Krammer F; Pujol A; Duffy D; Lifton RP; Zhang SY; Gorochov G; Béziat V; Jouanguy E; Sancho-Shimizu V; Rice CM; Abel L; Notarangelo LD; Cobat A; Su HC; Casanova JL
    Science; 2020 Oct; 370(6515):. PubMed ID: 32972995
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19.
    Povysil G; Butler-Laporte G; Shang N; Weng C; Khan A; Alaamery M; Nakanishi T; Zhou S; Forgetta V; Eveleigh R; Bourgey M; Aziz N; Jones S; Knoppers B; Scherer S; Strug L; Lepage P; Ragoussis J; Bourque G; Alghamdi J; Aljawini N; Albes N; Al-Afghani HM; Alghamdi B; Almutair M; Mahmoud ES; Safie LA; Bardisy HE; Al Harthi FS; Alshareef A; Suliman BA; Alqahtani S; AlMalik A; Alrashed MM; Massadeh S; Mooser V; Lathrop M; Arabi Y; Mbarek H; Saad C; Al-Muftah W; Badji R; Al Thani A; Ismail SI; Gharavi AG; Abedalthagafi MS; Richards JB; Goldstein DB; Kiryluk K
    medRxiv; 2020 Dec; ():. PubMed ID: 33398295
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.
    Matuozzo D; Talouarn E; Marchal A; Zhang P; Manry J; Seeleuthner Y; Zhang Y; Bolze A; Chaldebas M; Milisavljevic B; Gervais A; Bastard P; Asano T; Bizien L; Barzaghi F; Abolhassani H; Abou Tayoun A; Aiuti A; Alavi Darazam I; Allende LM; Alonso-Arias R; Arias AA; Aytekin G; Bergman P; Bondesan S; Bryceson YT; Bustos IG; Cabrera-Marante O; Carcel S; Carrera P; Casari G; Chaïbi K; Colobran R; Condino-Neto A; Covill LE; Delmonte OM; El Zein L; Flores C; Gregersen PK; Gut M; Haerynck F; Halwani R; Hancerli S; Hammarström L; Hatipoğlu N; Karbuz A; Keles S; Kyheng C; Leon-Lopez R; Franco JL; Mansouri D; Martinez-Picado J; Metin Akcan O; Migeotte I; Morange PE; Morelle G; Martin-Nalda A; Novelli G; Novelli A; Ozcelik T; Palabiyik F; Pan-Hammarström Q; de Diego RP; Planas-Serra L; Pleguezuelo DE; Prando C; Pujol A; Reyes LF; Rivière JG; Rodriguez-Gallego C; Rojas J; Rovere-Querini P; Schlüter A; Shahrooei M; Sobh A; Soler-Palacin P; Tandjaoui-Lambiotte Y; Tipu I; Tresoldi C; Troya J; van de Beek D; Zatz M; Zawadzki P; Al-Muhsen SZ; Alosaimi MF; Alsohime FM; Baris-Feldman H; Butte MJ; Constantinescu SN; Cooper MA; Dalgard CL; Fellay J; Heath JR; Lau YL; Lifton RP; Maniatis T; Mogensen TH; von Bernuth H; Lermine A; Vidaud M; Boland A; Deleuze JF; Nussbaum R; Kahn-Kirby A; Mentre F; Tubiana S; Gorochov G; Tubach F; Hausfater P; ; ; ; ; ; ; ; ; ; Meyts I; Zhang SY; Puel A; Notarangelo LD; Boisson-Dupuis S; Su HC; Boisson B; Jouanguy E; Casanova JL; Zhang Q; Abel L; Cobat A
    Genome Med; 2023 Apr; 15(1):22. PubMed ID: 37020259
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rare coding variants in genes encoding GABA
    May P; Girard S; Harrer M; Bobbili DR; Schubert J; Wolking S; Becker F; Lachance-Touchette P; Meloche C; Gravel M; Niturad CE; Knaus J; De Kovel C; Toliat M; Polvi A; Iacomino M; Guerrero-López R; Baulac S; Marini C; Thiele H; Altmüller J; Jabbari K; Ruppert AK; Jurkowski W; Lal D; Rusconi R; Cestèle S; Terragni B; Coombs ID; Reid CA; Striano P; Caglayan H; Siren A; Everett K; Møller RS; Hjalgrim H; Muhle H; Helbig I; Kunz WS; Weber YG; Weckhuysen S; Jonghe P; Sisodiya SM; Nabbout R; Franceschetti S; Coppola A; Vari MS; Kasteleijn-Nolst Trenité D; Baykan B; Ozbek U; Bebek N; Klein KM; Rosenow F; Nguyen DK; Dubeau F; Carmant L; Lortie A; Desbiens R; Clément JF; Cieuta-Walti C; Sills GJ; Auce P; Francis B; Johnson MR; Marson AG; Berghuis B; Sander JW; Avbersek A; McCormack M; Cavalleri GL; Delanty N; Depondt C; Krenn M; Zimprich F; Peter S; Nikanorova M; Kraaij R; van Rooij J; Balling R; Ikram MA; Uitterlinden AG; Avanzini G; Schorge S; Petrou S; Mantegazza M; Sander T; LeGuern E; Serratosa JM; Koeleman BPC; Palotie A; Lehesjoki AE; Nothnagel M; Nürnberg P; Maljevic S; Zara F; Cossette P; Krause R; Lerche H; ; ;
    Lancet Neurol; 2018 Aug; 17(8):699-708. PubMed ID: 30033060
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare Variants in Inborn Errors of Immunity Genes Associated With Covid-19 Severity.
    Liu P; Fang M; Luo Y; Zheng F; Jin Y; Cheng F; Zhu H; Jin X
    Front Cell Infect Microbiol; 2022; 12():888582. PubMed ID: 35694544
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clustering of predicted loss-of-function variants in genes linked with monogenic disease can explain incomplete penetrance.
    Beaumont RN; Hawkes G; Gunning AC; Wright CF
    Genome Med; 2024 Apr; 16(1):64. PubMed ID: 38671509
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Differentially expressed immune response genes in COVID-19 patients based on disease severity.
    Li S; Duan X; Li Y; Li M; Gao Y; Li T; Li S; Tan L; Shao T; Jeyarajan AJ; Chen L; Han M; Lin W; Li X
    Aging (Albany NY); 2021 Mar; 13(7):9265-9276. PubMed ID: 33780352
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.
    Kosmicki JA; Horowitz JE; Banerjee N; Lanche R; Marcketta A; Maxwell E; Bai X; Sun D; Backman JD; Sharma D; Kury FSP; Kang HM; O'Dushlaine C; Yadav A; Mansfield AJ; Li AH; Watanabe K; Gurski L; McCarthy SE; Locke AE; Khalid S; O'Keeffe S; Mbatchou J; Chazara O; Huang Y; Kvikstad E; O'Neill A; Nioi P; Parker MM; Petrovski S; Runz H; Szustakowski JD; Wang Q; Wong E; Cordova-Palomera A; Smith EN; Szalma S; Zheng X; Esmaeeli S; Davis JW; Lai YP; Chen X; Justice AE; Leader JB; Mirshahi T; Carey DJ; Verma A; Sirugo G; Ritchie MD; Rader DJ; Povysil G; Goldstein DB; Kiryluk K; Pairo-Castineira E; Rawlik K; Pasko D; Walker S; Meynert A; Kousathanas A; Moutsianas L; Tenesa A; Caulfield M; Scott R; Wilson JF; Baillie JK; Butler-Laporte G; Nakanishi T; Lathrop M; Richards JB; ; ; Jones M; Balasubramanian S; Salerno W; Shuldiner AR; Marchini J; Overton JD; Habegger L; Cantor MN; Reid JG; Baras A; Abecasis GR; Ferreira MAR
    Am J Hum Genet; 2021 Jul; 108(7):1350-1355. PubMed ID: 34115965
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association between polymorphisms in
    Braga M; Shiga MAS; Silva PES; Yamanaka AHU; Souza VH; Grava S; Simão ANC; Neves JSF; de Lima Neto QA; Zacarias JMV; Visentainer JEL
    Expert Rev Mol Diagn; 2024 Jun; 24(6):525-531. PubMed ID: 38864429
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interferon linked to COVID-19 severity.
    Carvalho T
    Nat Med; 2020 Dec; 26(12):1806. PubMed ID: 33288943
    [No Abstract]   [Full Text] [Related]  

  • 12. Upregulated type I interferon responses in asymptomatic COVID-19 infection are associated with improved clinical outcome.
    Masood KI; Yameen M; Ashraf J; Shahid S; Mahmood SF; Nasir A; Nasir N; Jamil B; Ghanchi NK; Khanum I; Razzak SA; Kanji A; Hussain R; E Rottenberg M; Hasan Z
    Sci Rep; 2021 Nov; 11(1):22958. PubMed ID: 34824360
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The role of host genetics in susceptibility to severe viral infections in humans and insights into host genetics of severe COVID-19: A systematic review.
    Elhabyan A; Elyaacoub S; Sanad E; Abukhadra A; Elhabyan A; Dinu V
    Virus Res; 2020 Nov; 289():198163. PubMed ID: 32918943
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Differential induction of type I and III interferon genes in the upper respiratory tract of patients with coronavirus disease 2019 (COVID-19).
    Scagnolari C; Pierangeli A; Frasca F; Bitossi C; Viscido A; Oliveto G; Scordio M; Mazzuti L; Di Carlo D; Gentile M; Solimini A; Ceccarelli G; Pugliese F; Mastroianni CM; d'Ettorre G; Turriziani O; Antonelli G;
    Virus Res; 2021 Apr; 295():198283. PubMed ID: 33418027
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity.
    Fallerini C; Picchiotti N; Baldassarri M; Zguro K; Daga S; Fava F; Benetti E; Amitrano S; Bruttini M; Palmieri M; Croci S; Lista M; Beligni G; Valentino F; Meloni I; Tanfoni M; Minnai F; Colombo F; Cabri E; Fratelli M; Gabbi C; Mantovani S; Frullanti E; Gori M; Crawley FP; Butler-Laporte G; Richards B; Zeberg H; Lipcsey M; Hultström M; Ludwig KU; Schulte EC; Pairo-Castineira E; Baillie JK; Schmidt A; Frithiof R; ; ; ; Mari F; Renieri A; Furini S
    Hum Genet; 2022 Jan; 141(1):147-173. PubMed ID: 34889978
    [TBL] [Abstract][Full Text] [Related]  

  • 16. IFIH1 loss of function predisposes to inflammatory and SARS-CoV-2-related infectious diseases.
    Najm R; Yavuz L; Jain R; El Naofal M; Ramaswamy S; Abuhammour W; Loney T; Nowotny N; Alsheikh-Ali A; Abou Tayoun A; Kandasamy RK
    Scand J Immunol; 2024 Aug; 100(2):e13373. PubMed ID: 38757311
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Loss-of-function mutations in IFNAR2 in COVID-19 severe infection susceptibility.
    Smieszek SP; Polymeropoulos VM; Xiao C; Polymeropoulos CM; Polymeropoulos MH
    J Glob Antimicrob Resist; 2021 Sep; 26():239-240. PubMed ID: 34273592
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.
    Butler-Laporte G; Povysil G; Kosmicki JA; Cirulli ET; Drivas T; Furini S; Saad C; Schmidt A; Olszewski P; Korotko U; Quinodoz M; Çelik E; Kundu K; Walter K; Jung J; Stockwell AD; Sloofman LG; Jordan DM; Thompson RC; Del Valle D; Simons N; Cheng E; Sebra R; Schadt EE; Kim-Schulze S; Gnjatic S; Merad M; Buxbaum JD; Beckmann ND; Charney AW; Przychodzen B; Chang T; Pottinger TD; Shang N; Brand F; Fava F; Mari F; Chwialkowska K; Niemira M; Pula S; Baillie JK; Stuckey A; Salas A; Bello X; Pardo-Seco J; Gómez-Carballa A; Rivero-Calle I; Martinón-Torres F; Ganna A; Karczewski KJ; Veerapen K; Bourgey M; Bourque G; Eveleigh RJ; Forgetta V; Morrison D; Langlais D; Lathrop M; Mooser V; Nakanishi T; Frithiof R; Hultström M; Lipcsey M; Marincevic-Zuniga Y; Nordlund J; Schiabor Barrett KM; Lee W; Bolze A; White S; Riffle S; Tanudjaja F; Sandoval E; Neveux I; Dabe S; Casadei N; Motameny S; Alaamery M; Massadeh S; Aljawini N; Almutairi MS; Arabi YM; Alqahtani SA; Al Harthi FS; Almutairi A; Alqubaishi F; Alotaibi S; Binowayn A; Alsolm EA; El Bardisy H; Fawzy M; Cai F; Soranzo N; Butterworth A; ; ; ; ; ; ; ; ; Geschwind DH; Arteaga S; Stephens A; Butte MJ; Boutros PC; Yamaguchi TN; Tao S; Eng S; Sanders T; Tung PJ; Broudy ME; Pan Y; Gonzalez A; Chavan N; Johnson R; Pasaniuc B; Yaspan B; Smieszek S; Rivolta C; Bibert S; Bochud PY; Dabrowski M; Zawadzki P; Sypniewski M; Kaja E; Chariyavilaskul P; Nilaratanakul V; Hirankarn N; Shotelersuk V; Pongpanich M; Phokaew C; Chetruengchai W; Tokunaga K; Sugiyama M; Kawai Y; Hasegawa T; Naito T; Namkoong H; Edahiro R; Kimura A; Ogawa S; Kanai T; Fukunaga K; Okada Y; Imoto S; Miyano S; Mangul S; Abedalthagafi MS; Zeberg H; Grzymski JJ; Washington NL; Ossowski S; Ludwig KU; Schulte EC; Riess O; Moniuszko M; Kwasniewski M; Mbarek H; Ismail SI; Verma A; Goldstein DB; Kiryluk K; Renieri A; Ferreira MAR; Richards JB
    PLoS Genet; 2022 Nov; 18(11):e1010367. PubMed ID: 36327219
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of Toll-like receptor 7 variants with life-threatening COVID-19 disease in males: findings from a nested case-control study.
    Fallerini C; Daga S; Mantovani S; Benetti E; Picchiotti N; Francisci D; Paciosi F; Schiaroli E; Baldassarri M; Fava F; Palmieri M; Ludovisi S; Castelli F; Quiros-Roldan E; Vaghi M; Rusconi S; Siano M; Bandini M; Spiga O; Capitani K; Furini S; Mari F; ; Renieri A; Mondelli MU; Frullanti E
    Elife; 2021 Mar; 10():. PubMed ID: 33650967
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of Rare Predicted Loss-of-Function Variants in Cellular Pathways with Sub-Phenotypes in Age-Related Macular Degeneration.
    Pietraszkiewicz A; van Asten F; Kwong A; Ratnapriya R; Abecasis G; Swaroop A; Chew EY
    Ophthalmology; 2018 Mar; 125(3):398-406. PubMed ID: 29224928
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.