Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.
Authors :Kurki MI
, Karjalainen J
, Palta P
, Sipilä TP
, Kristiansson K
, Donner KM
, Reeve MP
, Laivuori H
, Aavikko M
, Kaunisto MA
, Loukola A
, Lahtela E
, Mattsson H
, Laiho P
, Della Briotta Parolo P
, Lehisto AA
, Kanai M
, Mars N
, Rämö J
, Kiiskinen T
, Heyne HO
, Veerapen K
, Rüeger S
, Lemmelä S
, Zhou W
, Ruotsalainen S
, Pärn K
, Hiekkalinna T
, Koskelainen S
, Paajanen T
, Llorens V
, Gracia-Tabuenca J
, Siirtola H
, Reis K
, Elnahas AG
, Sun B
, Foley CN
, Aalto-Setälä K
, Alasoo K
, Arvas M
, Auro K
, Biswas S
, Bizaki-Vallaskangas A
, Carpen O
, Chen CY
, Dada OA
, Ding Z
, Ehm MG
, Eklund K
, Färkkilä M
, Finucane H
, Ganna A
, Ghazal A
, Graham RR
, Green EM
, Hakanen A
, Hautalahti M
, Hedman ÅK
, Hiltunen M
, Hinttala R
, Hovatta I
, Hu X
, Huertas-Vazquez A
, Huilaja L
, Hunkapiller J
, Jacob H
, Jensen JN
, Joensuu H
, John S
, Julkunen V
, Jung M
, Junttila J
, Kaarniranta K
, Kähönen M
, Kajanne R
, Kallio L
, Kälviäinen R
, Kaprio J
, FinnGen
, Kerimov N
, Kettunen J
, Kilpeläinen E
, Kilpi T
, Klinger K
, Kosma VM
, Kuopio T
, Kurra V
, Laisk T
, Laukkanen J
, Lawless N
, Liu A
, Longerich S
, Mägi R
, Mäkelä J
, Mäkitie A
, Malarstig A
, Mannermaa A
, Maranville J
, Matakidou A
, Meretoja T
, Mozaffari SV
, Niemi MEK
, Niemi M
, Niiranen T
, O Donnell CJ
, Obeidat ME
, Okafo G
, Ollila HM
, Palomäki A
, Palotie T
, Partanen J
, Paul DS
, Pelkonen M
, Pendergrass RK
, Petrovski S
, Pitkäranta A
, Platt A
, Pulford D
, Punkka E
, Pussinen P
, Raghavan N
, Rahimov F
, Rajpal D
, Renaud NA
, Riley-Gillis B
, Rodosthenous R
, Saarentaus E
, Salminen A
, Salminen E
, Salomaa V
, Schleutker J
, Serpi R
, Shen HY
, Siegel R
, Silander K
, Siltanen S
, Soini S
, Soininen H
, Sul JH
, Tachmazidou I
, Tasanen K
, Tienari P
, Toppila-Salmi S
, Tukiainen T
, Tuomi T
, Turunen JA
, Ulirsch JC
, Vaura F
, Virolainen P
, Waring J
, Waterworth D
, Yang R
, Nelis M
, Reigo A
, Metspalu A
, Milani L
, Esko T
, Fox C
, Havulinna AS
, Perola M
, Ripatti S
, Jalanko A
, Laitinen T
, Mäkelä TP
, Plenge R
, McCarthy M
, Runz H
, Daly MJ
, Palotie A
Published On :2023 Mar
Published Erratum
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy.
Authors :Nascimento A
, Bruels CC
, Donkervoort S
, Foley AR
, Codina A
, Milisenda JC
, Estrella EA
, Li C
, Pijuan J
, Draper I
, Hu Y
, Stafki SA
, Pais LS
, Ganesh VS
, O'Donnell-Luria A
, Syeda SB
, Carrera-García L
, Expósito-Escudero J
, Yubero D
, Martorell L
, Pinal-Fernandez I
, Lidov HGW
, Mammen AL
, Grau-Junyent JM
, Ortez C
, Palau F
, Ghosh PS
, Darras BT
, Jou C
, Kunkel LM
, Hoenicka J
, Bönnemann CG
, Kang PB
, Natera-de Benito D
Published On :2023 Apr
Journal Article
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes.
Authors :Karczewski KJ
, Solomonson M
, Chao KR
, Goodrich JK
, Tiao G
, Lu W
, Riley-Gillis BM
, Tsai EA
, Kim HI
, Zheng X
, Rahimov F
, Esmaeeli S
, Grundstad AJ
, Reppell M
, Waring J
, Jacob H
, Sexton D
, Bronson PG
, Chen X
, Hu X
, Goldstein JI
, King D
, Vittal C
, Poterba T
, Palmer DS
, Churchhouse C
, Howrigan DP
, Zhou W
, Watts NA
, Nguyen K
, Nguyen H
, Mason C
, Farnham C
, Tolonen C
, Gauthier LD
, Gupta N
, MacArthur DG
, Rehm HL
, Seed C
, Philippakis AA
, Daly MJ
, Davis JW
, Runz H
, Miller MR
, Neale BM
Published On :2022 Sep 14
Journal Article