학술논문

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
Document Type
Artikel
Author
Butler-Laporte, GPovysil, GKosmicki, JACirulli, ETDrivas, TFurini, SSaad, CSchmidt, AOlszewski, PKorotko, UQuinodoz, MCelik, EKundu, KWalter, KJung, JStockwell, ADSloofman, LGJordan, DMThompson, RCDel Valle, DSimons, NCheng, ESebra, RSchadt, EEKim-Schulze, SGnjatic, SMerad, MBuxbaum, JDBeckmann, NDCharney, AWPrzychodzen, BChang, TPottinger, TDShang, NBrand, FFava, FMari, FChwialkowska, KNiemira, MPula, SBaillie, JKStuckey, ASalas, ABello, XPardo-Seco, JGomez-Carballa, ARivero-Calle, IMartinon-Torres, FGanna, AKarczewski, KJVeerapen, KBourgey, MBourque, GEveleigh, RJForgetta, VMorrison, DLanglais, DLathrop, MMooser, VNakanishi, TFrithiof, RHultstrom, MLipcsey, MMarincevic-Zuniga, YNordlund, JBarrett, KMSLee, WBolze, AWhite, SRiffle, STanudjaja, FSandoval, ENeveux, IDabe, SCasadei, NMotameny, SAlaamery, MMassadeh, SAljawini, NAlmutairi, MSArabi, YMAlqahtani, SAAl Harthi, FSAlmutairi, AAlqubaishi, FAlotaibi, SBinowayn, AAlsolm, EAEl Bardisy, HFawzy, MCai, FSoranzo, NButterworth, AGeschwind, DHArteaga, SStephens, AButte, MJBoutros, PCYamaguchi, TNTao, SEng, SSanders, TTung, PJBroudy, MEPan, YGonzalez, AChavan, NJohnson, RPasaniuc, BYaspan, BSmieszek, SRivolta, CBibert, SBochud, PYDabrowski, MZawadzki, PSypniewski, MKaja, EChariyavilaskul, PNilaratanakul, VHirankarn, NShotelersuk, VPongpanich, MPhokaew, CChetruengchai, WTokunaga, KSugiyama, MKawai, YHasegawa, TNaito, TNamkoong, HEdahiro, RKimura, AOgawa, SKanai, TFukunaga, KOkada, YImoto, SMiyano, SMangul, SAbedalthagafi, MSZeberg, HGrzymski, JJWashington, NLOssowski, SLudwig, KUSchulte, ECRiess, OMoniuszko, MKwasniewski, MMbarek, HIsmail, SIVerma, AGoldstein, DBKiryluk, KRenieri, AFerreira, MARRichards, JB
Source
PLoS genetics. 18(11):e1010367
Subject
Medicin och hälsovetenskap
Language
English
English
ISSN
1553-7404