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23 matches for
Hall IP,
showing the first 20.
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Wain LV,
Shrine N,
Artigas MS,
Erzurumluoglu AM,
Noyvert B,
Bossini-Castillo L,
Obeidat M,
Henry AP,
Portelli MA,
Hall RJ,
Billington CK,
Rimington TL
and 94 more — show all
Fenech AG,
John C,
Blake T,
Jackson VE,
Allen RJ,
Prins BP,
Campbell A,
Porteous DJ,
Jarvelin MR,
Wielscher M,
James AL,
Hui J,
Wareham NJ,
Zhao JH,
Wilson JF,
Joshi PK,
Stubbe B,
Rawal R,
Schulz H,
Imboden M,
Probst-Hensch NM,
Karrasch S,
Gieger C,
Deary IJ,
Harris SE,
Marten J,
Rudan I,
Enroth S,
Gyllensten U,
Kerr SM,
Polasek O,
Kähönen M,
Surakka I,
Vitart V,
Hayward C,
Lehtimäki T,
Raitakari OT,
Evans DM,
Henderson AJ,
Pennell CE,
Wang CA,
Sly PD,
Wan ES,
Busch R,
Hobbs BD,
Litonjua AA,
Sparrow DW,
Gulsvik A,
Bakke PS,
Crapo JD,
Beaty TH,
Hansel NN,
Mathias RA,
Ruczinski I,
Barnes KC,
Bossé Y,
Joubert P,
van den Berge M,
Brandsma CA,
Paré PD,
Sin DD,
Nickle DC,
Hao K,
Gottesman O,
Dewey FE,
Bruse SE,
Carey DJ,
Kirchner HL,
Jonsson S,
Thorleifsson G,
Jonsdottir I,
Gislason T,
Stefansson K,
Schurmann C,
Nadkarni G,
Bottinger EP,
Loos RJ,
Walters RG,
Chen Z,
Millwood IY,
Vaucher J,
Kurmi OP,
Li L,
Hansell AL,
Brightling C,
Zeggini E,
Cho MH,
Silverman EK,
Sayers I,
Trynka G,
Morris AP,
Strachan DP,
Hall IP,
Tobin MD
Understanding Society Scientific Group · Geisinger-Regeneron DiscovEHR Collaboration
Nature genetics · 2017 · PMID 28166213 · open access
12 pages+
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Shrine N,
Guyatt AL,
Erzurumluoglu AM,
Jackson VE,
Hobbs BD,
Melbourne CA,
Batini C,
Fawcett KA,
Song K,
Sakornsakolpat P,
Li X,
Boxall R
and 99 more — show all
Reeve NF,
Obeidat M,
Zhao JH,
Wielscher M,
Weiss S,
Kentistou KA,
Kentistou KA,
Cook JP,
Sun BB,
Zhou J,
Hui J,
Karrasch S,
Imboden M,
Harris SE,
Marten J,
Enroth S,
Kerr SM,
Surakka I,
Vitart V,
Lehtimäki T,
Allen RJ,
Bakke PS,
Beaty TH,
Bleecker ER,
Bossé Y,
Brandsma CA,
Chen Z,
Crapo JD,
Danesh J,
DeMeo DL,
Dudbridge F,
Ewert R,
Gieger C,
Gulsvik A,
Hansell AL,
Hao K,
Hoffman JD,
Hokanson JE,
Homuth G,
Joshi PK,
Joubert P,
Langenberg C,
Li X,
Li L,
Lin K,
Lind L,
Locantore N,
Luan J,
Mahajan A,
Maranville JC,
Murray A,
Nickle DC,
Packer R,
Parker MM,
Paynton ML,
Porteous DJ,
Porteous DJ,
Prokopenko D,
Qiao D,
Rawal R,
Runz H,
Sayers I,
Sin DD,
Smith BH,
Soler Artigas M,
Sparrow D,
Tal-Singer R,
Timmers PRHJ,
Van den Berge M,
Whittaker JC,
Woodruff PG,
Yerges-Armstrong LM,
Troyanskaya OG,
Raitakari OT,
Kähönen M,
Polašek O,
Gyllensten U,
Rudan I,
Deary IJ,
Probst-Hensch NM,
Schulz H,
James AL,
Wilson JF,
Stubbe B,
Zeggini E,
Jarvelin MR,
Wareham N,
Silverman EK,
Hayward C,
Morris AP,
Butterworth AS,
Scott RA,
Walters RG,
Meyers DA,
Cho MH,
Strachan DP,
Hall IP,
Tobin MD,
Wain LV
Understanding Society Scientific Group
Nature genetics · 2019 · PMID 30804560 · open access
12 pages+
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
Sakornsakolpat P,
Prokopenko D,
Lamontagne M,
Reeve NF,
Guyatt AL,
Jackson VE,
Shrine N,
Qiao D,
Bartz TM,
Kim DK,
Lee MK,
Latourelle JC
and 42 more — show all
Li X,
Morrow JD,
Obeidat M,
Wyss AB,
Bakke P,
Barr RG,
Beaty TH,
Belinsky SA,
Brusselle GG,
Crapo JD,
de Jong K,
DeMeo DL,
Fingerlin TE,
Gharib SA,
Gulsvik A,
Hall IP,
Hokanson JE,
Kim WJ,
Lomas DA,
London SJ,
Meyers DA,
O'Connor GT,
Rennard SI,
Schwartz DA,
Sliwinski P,
Sparrow D,
Strachan DP,
Tal-Singer R,
Tesfaigzi Y,
Vestbo J,
Vonk JM,
Yim JJ,
Zhou X,
Bossé Y,
Manichaikul A,
Lahousse L,
Silverman EK,
Boezen HM,
Wain LV,
Tobin MD,
Hobbs BD,
Cho MH
SpiroMeta Consortium · International COPD Genetics Consortium
Nature genetics · 2019 · PMID 30804561 · open access
12 pages+
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Shrine N,
Izquierdo AG,
Chen J,
Packer R,
Hall RJ,
Guyatt AL,
Batini C,
Thompson RJ,
Pavuluri C,
Malik V,
Hobbs BD,
Moll M
and 136 more — show all
Kim W,
Tal-Singer R,
Bakke P,
Fawcett KA,
John C,
Coley K,
Piga NN,
Pozarickij A,
Lin K,
Millwood IY,
Chen Z,
Li L,
Wijnant SRA,
Lahousse L,
Brusselle G,
Uitterlinden AG,
Manichaikul A,
Oelsner EC,
Rich SS,
Barr RG,
Kerr SM,
Vitart V,
Brown MR,
Wielscher M,
Imboden M,
Jeong A,
Bartz TM,
Gharib SA,
Flexeder C,
Karrasch S,
Gieger C,
Peters A,
Stubbe B,
Hu X,
Ortega VE,
Meyers DA,
Bleecker ER,
Gabriel SB,
Gupta N,
Smith AV,
Luan J,
Zhao JH,
Hansen AF,
Langhammer A,
Willer C,
Bhatta L,
Porteous D,
Smith BH,
Campbell A,
Sofer T,
Lee J,
Daviglus ML,
Yu B,
Lim E,
Xu H,
O'Connor GT,
Thareja G,
Albagha OME,
Suhre K,
Granell R,
Faquih TO,
Hiemstra PS,
Slats AM,
Mullin BH,
Hui J,
James A,
Beilby J,
Patasova K,
Hysi P,
Koskela JT,
Wyss AB,
Jin J,
Sikdar S,
Lee M,
May-Wilson S,
Pirastu N,
Kentistou KA,
Joshi PK,
Timmers PRHJ,
Williams AT,
Free RC,
Wang X,
Morrison JL,
Gilliland FD,
Chen Z,
Wang CA,
Foong RE,
Harris SE,
Taylor A,
Redmond P,
Cook JP,
Mahajan A,
Lind L,
Palviainen T,
Lehtimäki T,
Raitakari OT,
Kaprio J,
Rantanen T,
Pietiläinen KH,
Cox SR,
Pennell CE,
Hall GL,
Gauderman WJ,
Brightling C,
Wilson JF,
Vasankari T,
Laitinen T,
Salomaa V,
Mook-Kanamori DO,
Timpson NJ,
Zeggini E,
Dupuis J,
Hayward C,
Brumpton B,
Langenberg C,
Weiss S,
Homuth G,
Schmidt CO,
Probst-Hensch N,
Jarvelin MR,
Morrison AC,
Polasek O,
Rudan I,
Lee JH,
Sayers I,
Rawlins EL,
Dudbridge F,
Silverman EK,
Strachan DP,
Walters RG,
Morris AP,
London SJ,
Cho MH,
Wain LV,
Hall IP,
Tobin MD
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation
Soler Artigas M,
Wain LV,
Miller S,
Kheirallah AK,
Huffman JE,
Ntalla I,
Shrine N,
Obeidat M,
Trochet H,
McArdle WL,
Alves AC,
Hui J
and 78 more — show all
Zhao JH,
Joshi PK,
Teumer A,
Albrecht E,
Imboden M,
Rawal R,
Lopez LM,
Marten J,
Enroth S,
Surakka I,
Polasek O,
Lyytikäinen LP,
Granell R,
Hysi PG,
Flexeder C,
Mahajan A,
Beilby J,
Bossé Y,
Brandsma CA,
Campbell H,
Gieger C,
Gläser S,
González JR,
Grallert H,
Hammond CJ,
Harris SE,
Hartikainen AL,
Heliövaara M,
Henderson J,
Hocking L,
Horikoshi M,
Hutri-Kähönen N,
Ingelsson E,
Johansson Å,
Kemp JP,
Kolcic I,
Kumar A,
Lind L,
Melén E,
Musk AW,
Navarro P,
Nickle DC,
Padmanabhan S,
Raitakari OT,
Ried JS,
Ripatti S,
Schulz H,
Scott RA,
Sin DD,
Starr JM,
Viñuela A,
Völzke H,
Wild SH,
Wright AF,
Zemunik T,
Jarvis DL,
Spector TD,
Evans DM,
Lehtimäki T,
Vitart V,
Kähönen M,
Gyllensten U,
Rudan I,
Deary IJ,
Karrasch S,
Probst-Hensch NM,
Heinrich J,
Stubbe B,
Wilson JF,
Wareham NJ,
James AL,
Morris AP,
Jarvelin MR,
Hayward C,
Sayers I,
Strachan DP,
Hall IP,
Tobin MD
UK BiLEVE
Nature communications · 2015 · PMID 26635082 · open access
8 pages
Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study
Shrine N,
Portelli MA,
John C,
Soler Artigas M,
Bennett N,
Hall R,
Lewis J,
Henry AP,
Billington CK,
Ahmad A,
Packer RJ,
Shaw D
and 31 more — show all
Pogson ZEK,
Fogarty A,
McKeever TM,
Singapuri A,
Heaney LG,
Mansur AH,
Chaudhuri R,
Thomson NC,
Holloway JW,
Lockett GA,
Howarth PH,
Djukanovic R,
Hankinson J,
Niven R,
Simpson A,
Chung KF,
Sterk PJ,
Blakey JD,
Adcock IM,
Hu S,
Guo Y,
Obeidat M,
Sin DD,
van den Berge M,
Nickle DC,
Bossé Y,
Tobin MD,
Hall IP,
Brightling CE,
Wain LV,
Sayers I
The Lancet. Respiratory medicine · 2019 · PMID 30552067 · open access
7 pages
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Erzurumluoglu AM,
Liu M,
Jackson VE,
Barnes DR,
Datta G,
Melbourne CA,
Young R,
Batini C,
Surendran P,
Jiang T,
Adnan SD,
Afaq S
and 164 more — show all
Agrawal A,
Altmaier E,
Antoniou AC,
Asselbergs FW,
Baumbach C,
Bierut L,
Bertelsen S,
Boehnke M,
Bots ML,
Brazel DM,
Chambers JC,
Chang-Claude J,
Chen C,
Corley J,
Chou YL,
David SP,
de Boer RA,
de Leeuw CA,
Dennis JG,
Dominiczak AF,
Dunning AM,
Easton DF,
Eaton C,
Elliott P,
Evangelou E,
Faul JD,
Foroud T,
Goate A,
Gong J,
Grabe HJ,
Haessler J,
Haiman C,
Hallmans G,
Hammerschlag AR,
Harris SE,
Hattersley A,
Heath A,
Hsu C,
Iacono WG,
Kanoni S,
Kapoor M,
Kaprio J,
Kardia SL,
Karpe F,
Kontto J,
Kooner JS,
Kooperberg C,
Kuulasmaa K,
Laakso M,
Lai D,
Langenberg C,
Le N,
Lettre G,
Loukola A,
Luan J,
Madden PAF,
Mangino M,
Marioni RE,
Marouli E,
Marten J,
Martin NG,
McGue M,
Michailidou K,
Mihailov E,
Moayyeri A,
Moitry M,
Müller-Nurasyid M,
Naheed A,
Nauck M,
Neville MJ,
Nielsen SF,
North K,
Perola M,
Pharoah PDP,
Pistis G,
Polderman TJ,
Posthuma D,
Poulter N,
Qaiser B,
Rasheed A,
Reiner A,
Renström F,
Rice J,
Rohde R,
Rolandsson O,
Samani NJ,
Samuel M,
Schlessinger D,
Scholte SH,
Scott RA,
Sever P,
Shao Y,
Shrine N,
Smith JA,
Starr JM,
Stirrups K,
Stram D,
Stringham HM,
Tachmazidou I,
Tardif JC,
Thompson DJ,
Tindle HA,
Tragante V,
Trompet S,
Turcot V,
Tyrrell J,
Vaartjes I,
van der Leij AR,
van der Meer P,
Varga TV,
Verweij N,
Völzke H,
Wareham NJ,
Warren HR,
Weir DR,
Weiss S,
Wetherill L,
Yaghootkar H,
Yavas E,
Jiang Y,
Chen F,
Zhan X,
Zhang W,
Zhao W,
Zhao W,
Zhou K,
Amouyel P,
Blankenberg S,
Caulfield MJ,
Chowdhury R,
Cucca F,
Deary IJ,
Deloukas P,
Di Angelantonio E,
Ferrario M,
Ferrières J,
Franks PW,
Frayling TM,
Frossard P,
Hall IP,
Hayward C,
Jansson JH,
Jukema JW,
Kee F,
Männistö S,
Metspalu A,
Munroe PB,
Nordestgaard BG,
Palmer CNA,
Salomaa V,
Sattar N,
Spector T,
Strachan DP,
van der Harst P,
Zeggini E,
Saleheen D,
Butterworth AS,
Wain LV,
Abecasis GR,
Danesh J,
Tobin MD,
Vrieze S,
Liu DJ,
Howson JMM
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
Wain LV,
Shrine N,
Miller S,
Jackson VE,
Ntalla I,
Soler Artigas M,
Billington CK,
Kheirallah AK,
Allen R,
Cook JP,
Probert K,
Obeidat M
and 27 more — show all
Bossé Y,
Hao K,
Postma DS,
Paré PD,
Ramasamy A,
Mägi R,
Mihailov E,
Reinmaa E,
Melén E,
O'Connell J,
Frangou E,
Delaneau O,
Freeman C,
Petkova D,
McCarthy M,
Sayers I,
Deloukas P,
Hubbard R,
Pavord I,
Hansell AL,
Thomson NC,
Zeggini E,
Morris AP,
Marchini J,
Strachan DP,
Tobin MD,
Hall IP
UK Brain Expression Consortium (UKBEC) · OxGSK Consortium
The Lancet. Respiratory medicine · 2015 · PMID 26423011 · open access
6 pages
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
Soler Artigas M,
Loth DW,
Wain LV,
Gharib SA,
Obeidat M,
Tang W,
Zhai G,
Zhao JH,
Smith AV,
Huffman JE,
Albrecht E,
Jackson CM
and 158 more — show all
Evans DM,
Cadby G,
Fornage M,
Manichaikul A,
Lopez LM,
Johnson T,
Aldrich MC,
Aspelund T,
Barroso I,
Campbell H,
Cassano PA,
Couper DJ,
Eiriksdottir G,
Franceschini N,
Garcia M,
Gieger C,
Gislason GK,
Grkovic I,
Hammond CJ,
Hancock DB,
Harris TB,
Ramasamy A,
Heckbert SR,
Heliövaara M,
Homuth G,
Hysi PG,
James AL,
James AL,
Jankovic S,
Joubert BR,
Karrasch S,
Klopp N,
Koch B,
Kritchevsky SB,
Launer LJ,
Liu Y,
Loehr LR,
Lohman K,
Loos RJ,
Lumley T,
Al Balushi KA,
Ang WQ,
Barr RG,
Beilby J,
Blakey JD,
Boban M,
Boraska V,
Brisman J,
Britton JR,
Brusselle GG,
Cooper C,
Curjuric I,
Dahgam S,
Deary IJ,
Ebrahim S,
Eijgelsheim M,
Francks C,
Gaysina D,
Granell R,
Gu X,
Hankinson JL,
Hardy R,
Harris SE,
Henderson J,
Henry A,
Hingorani AD,
Hofman A,
Holt PG,
Hui J,
Hunter ML,
Imboden M,
Jameson KA,
Kerr SM,
Kolcic I,
Kronenberg F,
Liu JZ,
Marchini J,
McKeever T,
Morris AD,
Olin AC,
Porteous DJ,
Postma DS,
Rich SS,
Ring SM,
Rivadeneira F,
Rochat T,
Sayer AA,
Sayers I,
Sly PD,
Smith GD,
Sood A,
Starr JM,
Uitterlinden AG,
Vonk JM,
Wannamethee SG,
Whincup PH,
Wijmenga C,
Williams OD,
Wong A,
Mangino M,
Marciante KD,
McArdle WL,
Meibohm B,
Morrison AC,
North KE,
Omenaas E,
Palmer LJ,
Pietiläinen KH,
Pin I,
Pola Sbreve Ek O,
Pouta A,
Psaty BM,
Hartikainen AL,
Rantanen T,
Ripatti S,
Rotter JI,
Rudan I,
Rudnicka AR,
Schulz H,
Shin SY,
Spector TD,
Surakka I,
Vitart V,
Völzke H,
Wareham NJ,
Warrington NM,
Wichmann HE,
Wild SH,
Wilk JB,
Wjst M,
Wright AF,
Zgaga L,
Zemunik T,
Pennell CE,
Nyberg F,
Kuh D,
Holloway JW,
Boezen HM,
Lawlor DA,
Morris RW,
Probst-Hensch N,
Kaprio J,
Wilson JF,
Hayward C,
Kähönen M,
Heinrich J,
Musk AW,
Jarvis DL,
Gläser S,
Järvelin MR,
Ch Stricker BH,
Elliott P,
O'Connor GT,
Strachan DP,
London SJ,
Hall IP,
Gudnason V,
Tobin MD
International Lung Cancer Consortium · GIANT consortium
Nature genetics · 2011 · PMID 21946350 · open access
4 pages
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Loth DW,
Soler Artigas M,
Gharib SA,
Wain LV,
Franceschini N,
Koch B,
Pottinger TD,
Smith AV,
Duan Q,
Oldmeadow C,
Lee MK,
Strachan DP
and 148 more — show all
James AL,
Huffman JE,
Vitart V,
Ramasamy A,
Wareham NJ,
Kaprio J,
Wang XQ,
Trochet H,
Kähönen M,
Flexeder C,
Albrecht E,
Lopez LM,
de Jong K,
Thyagarajan B,
Alves AC,
Enroth S,
Omenaas E,
Joshi PK,
Fall T,
Viñuela A,
Launer LJ,
Loehr LR,
Fornage M,
Li G,
Wilk JB,
Tang W,
Manichaikul A,
Lahousse L,
Harris TB,
North KE,
Rudnicka AR,
Hui J,
Gu X,
Lumley T,
Wright AF,
Hastie ND,
Campbell S,
Kumar R,
Pin I,
Scott RA,
Pietiläinen KH,
Surakka I,
Liu Y,
Holliday EG,
Schulz H,
Heinrich J,
Davies G,
Vonk JM,
Wojczynski M,
Pouta A,
Johansson A,
Wild SH,
Ingelsson E,
Rivadeneira F,
Völzke H,
Hysi PG,
Eiriksdottir G,
Morrison AC,
Rotter JI,
Gao W,
Postma DS,
White WB,
Rich SS,
Hofman A,
Aspelund T,
Couper D,
Smith LJ,
Psaty BM,
Lohman K,
Burchard EG,
Uitterlinden AG,
Garcia M,
Joubert BR,
McArdle WL,
Musk AB,
Hansel N,
Heckbert SR,
Zgaga L,
van Meurs JB,
Navarro P,
Rudan I,
Oh YM,
Redline S,
Jarvis DL,
Zhao JH,
Rantanen T,
O'Connor GT,
Ripatti S,
Scott RJ,
Karrasch S,
Grallert H,
Gaddis NC,
Starr JM,
Wijmenga C,
Minster RL,
Lederer DJ,
Pekkanen J,
Gyllensten U,
Campbell H,
Morris AP,
Gläser S,
Hammond CJ,
Burkart KM,
Beilby J,
Kritchevsky SB,
Gudnason V,
Hancock DB,
Williams OD,
Polasek O,
Zemunik T,
Kolcic I,
Petrini MF,
Wjst M,
Kim WJ,
Porteous DJ,
Scotland G,
Smith BH,
Viljanen A,
Heliövaara M,
Attia JR,
Sayers I,
Hampel R,
Gieger C,
Deary IJ,
Boezen HM,
Newman A,
Jarvelin MR,
Wilson JF,
Lind L,
Stricker BH,
Teumer A,
Spector TD,
Melén E,
Peters MJ,
Lange LA,
Barr RG,
Bracke KR,
Verhamme FM,
Sung J,
Hiemstra PS,
Cassano PA,
Sood A,
Hayward C,
Dupuis J,
Hall IP,
Brusselle GG,
Tobin MD,
London SJ
Nature genetics · 2014 · PMID 24929828
4 pages
A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary disease
Moll M,
Jackson VE,
Yu B,
Grove ML,
London SJ,
Gharib SA,
Bartz TM,
Sitlani CM,
Dupuis J,
O'Connor GT,
Xu H,
Cassano PA
and 21 more — show all
Patchen BK,
Kim WJ,
Park J,
Kim KH,
Han B,
Barr RG,
Manichaikul A,
Nguyen JN,
Rich SS,
Lahousse L,
Terzikhan N,
Brusselle G,
Sakornsakolpat P,
Liu J,
Benway CJ,
Hall IP,
Tobin MD,
Wain LV,
Silverman EK,
Cho MH,
Hobbs BD
American journal of physiology. Lung cellular and molecular physiology · 2021 · PMID 33909500
4 pages
Genome-wide association study identifies five loci associated with lung function
Repapi E,
Sayers I,
Wain LV,
Burton PR,
Johnson T,
Obeidat M,
Zhao JH,
Ramasamy A,
Zhai G,
Vitart V,
Huffman JE,
Igl W
and 83 more — show all
Albrecht E,
Deloukas P,
Henderson J,
Granell R,
McArdle WL,
Rudnicka AR,
Barroso I,
Loos RJ,
Wareham NJ,
Mustelin L,
Rantanen T,
Surakka I,
Imboden M,
Wichmann HE,
Grkovic I,
Jankovic S,
Zgaga L,
Hartikainen AL,
Peltonen L,
Gyllensten U,
Johansson A,
Zaboli G,
Campbell H,
Wild SH,
Wilson JF,
Gläser S,
Homuth G,
Völzke H,
Mangino M,
Soranzo N,
Spector TD,
Polasek O,
Rudan I,
Wright AF,
Heliövaara M,
Ripatti S,
Pouta A,
Naluai AT,
Olin AC,
Torén K,
Cooper MN,
James AL,
James AL,
Palmer LJ,
Hingorani AD,
Wannamethee SG,
Whincup PH,
Smith GD,
Ebrahim S,
McKeever TM,
Pavord ID,
MacLeod AK,
Morris AD,
Porteous DJ,
Cooper C,
Dennison E,
Shaheen S,
Karrasch S,
Schnabel E,
Schulz H,
Grallert H,
Bouatia-Naji N,
Delplanque J,
Froguel P,
Blakey JD,
Britton JR,
Morris RW,
Holloway JW,
Lawlor DA,
Hui J,
Nyberg F,
Jarvelin MR,
Jackson C,
Kähönen M,
Kaprio J,
Probst-Hensch NM,
Koch B,
Hayward C,
Evans DM,
Elliott P,
Strachan DP,
Hall IP,
Tobin MD
Wellcome Trust Case Control Consortium · NSHD Respiratory Study Team
Nature genetics · 2010 · PMID 20010834
3 pages
Genome-wide association study of preserved ratio impaired spirometry (PRISm)
Higbee DH,
Lirio A,
Hamilton F,
Granell R,
Wyss AB,
London SJ,
Bartz TM,
Gharib SA,
Cho MH,
Wan E,
Silverman E,
Crapo JD
and 33 more — show all
Lominchar JVT,
Hansen T,
Grarup N,
Dantoft T,
Kårhus L,
Linneberg A,
O'Connor GT,
Dupuis J,
Xu H,
De Vries MM,
Hu X,
Rich SS,
Barr RG,
Manichaikul A,
Wijnant SRA,
Brusselle GG,
Lahousse L,
Li X,
Hernández Cordero AI,
Obeidat M,
Sin DD,
Harris SE,
Redmond P,
Taylor AM,
Cox SR,
Williams AT,
Shrine N,
John C,
Guyatt AL,
Hall IP,
Davey Smith G,
Tobin MD,
Dodd JW
The European respiratory journal · 2024 · PMID 38097206 · open access
3 pages
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
Gudbjartsson DF,
Bjornsdottir US,
Halapi E,
Helgadottir A,
Sulem P,
Jonsdottir GM,
Thorleifsson G,
Helgadottir H,
Steinthorsdottir V,
Stefansson H,
Williams C,
Hui J
and 61 more — show all
Beilby J,
Warrington NM,
James A,
Palmer LJ,
Koppelman GH,
Heinzmann A,
Krueger M,
Boezen HM,
Wheatley A,
Altmuller J,
Shin HD,
Uh ST,
Cheong HS,
Jonsdottir B,
Gislason D,
Park CS,
Rasmussen LM,
Porsbjerg C,
Hansen JW,
Backer V,
Werge T,
Janson C,
Jönsson UB,
Ng MC,
Chan J,
So WY,
Ma R,
Shah SH,
Granger CB,
Quyyumi AA,
Levey AI,
Vaccarino V,
Reilly MP,
Rader DJ,
Williams MJ,
van Rij AM,
Jones GT,
Trabetti E,
Malerba G,
Pignatti PF,
Boner A,
Pescollderungg L,
Girelli D,
Olivieri O,
Martinelli N,
Ludviksson BR,
Ludviksdottir D,
Eyjolfsson GI,
Arnar D,
Thorgeirsson G,
Deichmann K,
Thompson PJ,
Wjst M,
Hall IP,
Postma DS,
Gislason T,
Gulcher J,
Kong A,
Jonsdottir I,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2009 · PMID 19198610
2 pages
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function
Hancock DB,
Soler Artigas M,
Gharib SA,
Henry A,
Manichaikul A,
Ramasamy A,
Loth DW,
Imboden M,
Koch B,
McArdle WL,
Smith AV,
Smolonska J
and 78 more — show all
Sood A,
Tang W,
Wilk JB,
Zhai G,
Zhao JH,
Aschard H,
Burkart KM,
Curjuric I,
Eijgelsheim M,
Elliott P,
Gu X,
Harris TB,
Janson C,
Homuth G,
Hysi PG,
Liu JZ,
Loehr LR,
Lohman K,
Loos RJ,
Manning AK,
Marciante KD,
Obeidat M,
Postma DS,
Aldrich MC,
Brusselle GG,
Chen TH,
Eiriksdottir G,
Franceschini N,
Heinrich J,
Rotter JI,
Wijmenga C,
Williams OD,
Bentley AR,
Hofman A,
Laurie CC,
Lumley T,
Morrison AC,
Joubert BR,
Rivadeneira F,
Couper DJ,
Kritchevsky SB,
Liu Y,
Wjst M,
Wain LV,
Vonk JM,
Uitterlinden AG,
Rochat T,
Rich SS,
Psaty BM,
O'Connor GT,
North KE,
Mirel DB,
Meibohm B,
Launer LJ,
Khaw KT,
Hartikainen AL,
Hammond CJ,
Gläser S,
Marchini J,
Kraft P,
Wareham NJ,
Völzke H,
Stricker BH,
Spector TD,
Probst-Hensch NM,
Jarvis D,
Jarvelin MR,
Heckbert SR,
Gudnason V,
Boezen HM,
Barr RG,
Cassano PA,
Strachan DP,
Fornage M,
Hall IP,
Dupuis J,
Tobin MD,
London SJ
PLoS genetics · 2012 · PMID 23284291 · open access
2 pages
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis
Hobbs BD,
de Jong K,
Lamontagne M,
Bossé Y,
Shrine N,
Artigas MS,
Wain LV,
Hall IP,
Jackson VE,
Wyss AB,
London SJ,
North KE
and 64 more — show all
Franceschini N,
Strachan DP,
Beaty TH,
Hokanson JE,
Crapo JD,
Castaldi PJ,
Chase RP,
Bartz TM,
Heckbert SR,
Psaty BM,
Gharib SA,
Zanen P,
Lammers JW,
Oudkerk M,
Groen HJ,
Locantore N,
Tal-Singer R,
Rennard SI,
Vestbo J,
Timens W,
Paré PD,
Latourelle JC,
Dupuis J,
O'Connor GT,
Wilk JB,
Kim WJ,
Lee MK,
Oh YM,
Vonk JM,
de Koning HJ,
Leng S,
Belinsky SA,
Tesfaigzi Y,
Manichaikul A,
Wang XQ,
Rich SS,
Barr RG,
Sparrow D,
Litonjua AA,
Bakke P,
Gulsvik A,
Lahousse L,
Brusselle GG,
Stricker BH,
Uitterlinden AG,
Ampleford EJ,
Bleecker ER,
Woodruff PG,
Meyers DA,
Qiao D,
Lomas DA,
Yim JJ,
Kim DK,
Hawrylkiewicz I,
Sliwinski P,
Hardin M,
Fingerlin TE,
Schwartz DA,
Postma DS,
MacNee W,
Tobin MD,
Silverman EK,
Boezen HM,
Cho MH
COPDGene Investigators · ECLIPSE Investigators and 5 more consortia
Nature genetics · 2017 · PMID 28166215
2 pages
Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study
Allen RJ,
Porte J,
Braybrooke R,
Flores C,
Fingerlin TE,
Oldham JM,
Guillen-Guio B,
Ma SF,
Okamoto T,
John AE,
Obeidat M,
Yang IV
and 31 more — show all
Henry A,
Hubbard RB,
Navaratnam V,
Saini G,
Thompson N,
Booth HL,
Hart SP,
Hill MR,
Hirani N,
Maher TM,
McAnulty RJ,
Millar AB,
Molyneaux PL,
Parfrey H,
Rassl DM,
Whyte MKB,
Fahy WA,
Marshall RP,
Oballa E,
Bossé Y,
Nickle DC,
Sin DD,
Timens W,
Shrine N,
Sayers I,
Hall IP,
Noth I,
Schwartz DA,
Tobin MD,
Wain LV,
Jenkins RG
The Lancet. Respiratory medicine · 2017 · PMID 29066090 · open access
2 pages
Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis
Allen RJ,
Guillen-Guio B,
Oldham JM,
Ma SF,
Dressen A,
Paynton ML,
Kraven LM,
Obeidat M,
Li X,
Ng M,
Braybrooke R,
Molina-Molina M
and 54 more — show all
Hobbs BD,
Putman RK,
Sakornsakolpat P,
Booth HL,
Fahy WA,
Hart SP,
Hill MR,
Hirani N,
Hubbard RB,
McAnulty RJ,
Millar AB,
Navaratnam V,
Oballa E,
Parfrey H,
Saini G,
Whyte MKB,
Zhang Y,
Kaminski N,
Adegunsoye A,
Strek ME,
Neighbors M,
Sheng XR,
Gudmundsson G,
Gudnason V,
Hatabu H,
Lederer DJ,
Manichaikul A,
Newell JD Jr,
O'Connor GT,
Ortega VE,
Xu H,
Fingerlin TE,
Bossé Y,
Hao K,
Joubert P,
Nickle DC,
Sin DD,
Timens W,
Furniss D,
Morris AP,
Zondervan KT,
Hall IP,
Sayers I,
Tobin MD,
Maher TM,
Cho MH,
Hunninghake GM,
Schwartz DA,
Yaspan BL,
Molyneaux PL,
Flores C,
Noth I,
Jenkins RG,
Wain LV
American journal of respiratory and critical care medicine · 2020 · PMID 31710517 · open access
2 pages
Genetic Associations and Architecture of Asthma-COPD Overlap
John C,
Guyatt AL,
Shrine N,
Packer R,
Olafsdottir TA,
Liu J,
Hayden LP,
Chu SH,
Koskela JT,
Luan J,
Li X,
Terzikhan N
and 42 more — show all
Xu H,
Bartz TM,
Petersen H,
Leng S,
Belinsky SA,
Cepelis A,
Hernández Cordero AI,
Obeidat M,
Thorleifsson G,
Meyers DA,
Bleecker ER,
Sakoda LC,
Iribarren C,
Tesfaigzi Y,
Gharib SA,
Dupuis J,
Brusselle G,
Lahousse L,
Ortega VE,
Jonsdottir I,
Sin DD,
Bossé Y,
van den Berge M,
Nickle D,
Quint JK,
Sayers I,
Hall IP,
Langenberg C,
Ripatti S,
Laitinen T,
Wu AC,
Lasky-Su J,
Bakke P,
Gulsvik A,
Hersh CP,
Hayward C,
Langhammer A,
Brumpton B,
Stefansson K,
Cho MH,
Wain LV,
Tobin MD
Chest · 2022 · PMID 35104449 · open access
2 pages
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction
Wilk JB,
Shrine NR,
Loehr LR,
Zhao JH,
Manichaikul A,
Lopez LM,
Smith AV,
Heckbert SR,
Smolonska J,
Tang W,
Loth DW,
Curjuric I
and 67 more — show all
Hui J,
Cho MH,
Latourelle JC,
Henry AP,
Aldrich M,
Bakke P,
Beaty TH,
Bentley AR,
Borecki IB,
Brusselle GG,
Burkart KM,
Chen TH,
Couper D,
Crapo JD,
Davies G,
Dupuis J,
Franceschini N,
Gulsvik A,
Hancock DB,
Harris TB,
Hofman A,
Imboden M,
James AL,
Khaw KT,
Lahousse L,
Launer LJ,
Litonjua A,
Liu Y,
Lohman KK,
Lomas DA,
Lumley T,
Marciante KD,
McArdle WL,
Meibohm B,
Morrison AC,
Musk AW,
Myers RH,
North KE,
Postma DS,
Psaty BM,
Rich SS,
Rivadeneira F,
Rochat T,
Rotter JI,
Soler Artigas M,
Starr JM,
Uitterlinden AG,
Wareham NJ,
Wijmenga C,
Zanen P,
Province MA,
Silverman EK,
Deary IJ,
Palmer LJ,
Cassano PA,
Gudnason V,
Barr RG,
Loos RJ,
Strachan DP,
London SJ,
Boezen HM,
Probst-Hensch N,
Gharib SA,
Hall IP,
O'Connor GT,
Tobin MD,
Stricker BH
American journal of respiratory and critical care medicine · 2012 · PMID 22837378
1 page
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