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2,661 papers hold this site up. Every variant and condition page names
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11 matches for
Jackson VE.
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+
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function
Wyss AB,
Sofer T,
Lee MK,
Terzikhan N,
Nguyen JN,
Lahousse L,
Latourelle JC,
Smith AV,
Bartz TM,
Feitosa MF,
Gao W,
Ahluwalia TS
and 91 more — show all
Tang W,
Oldmeadow C,
Duan Q,
de Jong K,
Wojczynski MK,
Wang XQ,
Noordam R,
Hartwig FP,
Jackson VE,
Wang T,
Obeidat M,
Hobbs BD,
Huan T,
Gui H,
Parker MM,
Hu D,
Mogil LS,
Kichaev G,
Jin J,
Graff M,
Harris TB,
Kalhan R,
Heckbert SR,
Paternoster L,
Burkart KM,
Liu Y,
Holliday EG,
Wilson JG,
Vonk JM,
Sanders JL,
Barr RG,
de Mutsert R,
Menezes AMB,
Adams HHH,
van den Berge M,
Joehanes R,
Levin AM,
Liberto J,
Launer LJ,
Morrison AC,
Sitlani CM,
Celedón JC,
Kritchevsky SB,
Scott RJ,
Christensen K,
Rotter JI,
Bonten TN,
Wehrmeister FC,
Bossé Y,
Xiao S,
Oh S,
Franceschini N,
Brody JA,
Kaplan RC,
Lohman K,
McEvoy M,
Province MA,
Rosendaal FR,
Taylor KD,
Nickle DC,
Williams LK,
Burchard EG,
Wheeler HE,
Wheeler HE,
Sin DD,
Gudnason V,
North KE,
Fornage M,
Psaty BM,
Myers RH,
O'Connor G,
Hansen T,
Laurie CC,
Cassano PA,
Sung J,
Kim WJ,
Attia JR,
Lange L,
Boezen HM,
Thyagarajan B,
Rich SS,
Mook-Kanamori DO,
Horta BL,
Uitterlinden AG,
Im HK,
Cho MH,
Brusselle GG,
Gharib SA,
Dupuis J,
Manichaikul A,
London SJ
Nature communications · 2018 · PMID 30061609 · 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-omic spatial effects on high-resolution AI-derived retinal thickness
Jackson VE,
Wu Y,
Bonelli R,
Owen JP,
Scott LW,
Farashi S,
Kihara Y,
Gantner ML,
Egan C,
Williams KM,
Ansell BRE,
Tufail A
and 2 more — show all
Nature communications · 2025 · PMID 39904976 · open access
12 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
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
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
Meta-analysis of exome array data identifies six novel genetic loci for lung function
Jackson VE,
Latourelle JC,
Wain LV,
Smith AV,
Grove ML,
Bartz TM,
Obeidat M,
Province MA,
Gao W,
Qaiser B,
Porteous DJ,
Cassano PA
and 95 more — show all
Ahluwalia TS,
Grarup N,
Li J,
Altmaier E,
Marten J,
Harris SE,
Manichaikul A,
Pottinger TD,
Li-Gao R,
Lind-Thomsen A,
Mahajan A,
Lahousse L,
Imboden M,
Teumer A,
Prins B,
Lyytikäinen LP,
Eiriksdottir G,
Franceschini N,
Sitlani CM,
Brody JA,
Bossé Y,
Timens W,
Kraja A,
Loukola A,
Tang W,
Liu Y,
Bork-Jensen J,
Justesen JM,
Linneberg A,
Lange LA,
Rawal R,
Karrasch S,
Huffman JE,
Smith BH,
Davies G,
Burkart KM,
Mychaleckyj JC,
Bonten TN,
Enroth S,
Lind L,
Brusselle GG,
Kumar A,
Stubbe B,
Kähönen M,
Wyss AB,
Psaty BM,
Heckbert SR,
Hao K,
Rantanen T,
Kritchevsky SB,
Lohman K,
Skaaby T,
Pisinger C,
Hansen T,
Schulz H,
Polasek O,
Campbell A,
Starr JM,
Rich SS,
Mook-Kanamori DO,
Johansson Å,
Ingelsson E,
Uitterlinden AG,
Weiss S,
Raitakari OT,
Gudnason V,
North KE,
Gharib SA,
Sin DD,
Taylor KD,
O'Connor GT,
Kaprio J,
Harris TB,
Pederson O,
Vestergaard H,
Wilson JG,
Strauch K,
Hayward C,
Kerr S,
Deary IJ,
Barr RG,
de Mutsert R,
Gyllensten U,
Morris AP,
Ikram MA,
Probst-Hensch N,
Gläser S,
Zeggini E,
Lehtimäki T,
Strachan DP,
Dupuis J,
Morrison AC,
Hall IP,
Tobin MD,
London SJ
Understanding Society Scientific Group
Wellcome open research · 2018 · PMID 30175238 · open access
1 page
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.