For researchers
Is your paper here?
2,660 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
12 matches for
Brusselle GG.
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Demenais F,
Margaritte-Jeannin P,
Barnes KC,
Cookson WOC,
Altmüller J,
Ang W,
Barr RG,
Beaty TH,
Becker AB,
Beilby J,
Bisgaard H,
Bjornsdottir US
and 163 more — show all
Bleecker E,
Bønnelykke K,
Boomsma DI,
Bouzigon E,
Brightling CE,
Brossard M,
Brusselle GG,
Burchard E,
Burkart KM,
Bush A,
Chan-Yeung M,
Chung KF,
Couto Alves A,
Curtin JA,
Custovic A,
Daley D,
de Jongste JC,
Del-Rio-Navarro BE,
Donohue KM,
Duijts L,
Eng C,
Eriksson JG,
Farrall M,
Fedorova Y,
Feenstra B,
Ferreira MA,
Freidin MB,
Gajdos Z,
Gauderman J,
Gehring U,
Geller F,
Genuneit J,
Gharib SA,
Gilliland F,
Granell R,
Graves PE,
Gudbjartsson DF,
Haahtela T,
Heckbert SR,
Heederik D,
Heinrich J,
Heliövaara M,
Henderson J,
Himes BE,
Hirose H,
Hirschhorn JN,
Hofman A,
Holt P,
Hottenga J,
Hudson TJ,
Hui J,
Imboden M,
Ivanov V,
Jaddoe VWV,
James A,
Janson C,
Jarvelin MR,
Jarvis D,
Jones G,
Jonsdottir I,
Jousilahti P,
Kabesch M,
Kähönen M,
Kantor DB,
Karunas AS,
Khusnutdinova E,
Koppelman GH,
Kozyrskyj AL,
Kreiner E,
Kubo M,
Kumar R,
Kumar A,
Kuokkanen M,
Lahousse L,
Laitinen T,
Laprise C,
Lathrop M,
Lau S,
Lee YA,
Lehtimäki T,
Letort S,
Levin AM,
Li G,
Liang L,
Loehr LR,
London SJ,
Loth DW,
Manichaikul A,
Marenholz I,
Martinez FJ,
Matheson MC,
Mathias RA,
Matsumoto K,
Mbarek H,
McArdle WL,
Melbye M,
Melén E,
Meyers D,
Michel S,
Mohamdi H,
Musk AW,
Myers RA,
Nieuwenhuis MAE,
Noguchi E,
O'Connor GT,
Ogorodova LM,
Palmer CD,
Palotie A,
Park JE,
Pennell CE,
Pershagen G,
Polonikov A,
Postma DS,
Probst-Hensch N,
Puzyrev VP,
Raby BA,
Raitakari OT,
Ramasamy A,
Rich SS,
Robertson CF,
Romieu I,
Salam MT,
Salomaa V,
Schlünssen V,
Scott R,
Selivanova PA,
Sigsgaard T,
Simpson A,
Siroux V,
Smith LJ,
Solodilova M,
Standl M,
Stefansson K,
Strachan DP,
Stricker BH,
Takahashi A,
Thompson PJ,
Thorleifsson G,
Thorsteinsdottir U,
Tiesler CMT,
Torgerson DG,
Tsunoda T,
Uitterlinden AG,
van der Valk RJP,
Vaysse A,
Vedantam S,
von Berg A,
von Mutius E,
Vonk JM,
Waage J,
Wareham NJ,
Weiss ST,
White WB,
Wickman M,
Widén E,
Willemsen G,
Williams LK,
Wouters IM,
Yang JJ,
Zhao JH,
Moffatt MF,
Ober C,
Nicolae DL
Australian Asthma Genetics Consortium (AAGC) collaborators
Nature genetics · 2018 · PMID 29273806 · 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+
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+
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function
Hancock DB,
Eijgelsheim M,
Wilk JB,
Gharib SA,
Loehr LR,
Marciante KD,
Franceschini N,
van Durme YM,
Chen TH,
Barr RG,
Schabath MB,
Couper DJ
and 16 more — show all
Brusselle GG,
Psaty BM,
van Duijn CM,
Rotter JI,
Uitterlinden AG,
Hofman A,
Punjabi NM,
Rivadeneira F,
Morrison AC,
Enright PL,
North KE,
Heckbert SR,
Lumley T,
Stricker BH,
O'Connor GT,
London SJ
Nature genetics · 2010 · PMID 20010835
5 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
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
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
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
Heritability and genome-wide association study of diffusing capacity of the lung
Terzikhan N,
Sun F,
Verhamme FM,
Adams HHH,
Loth D,
Bracke KR,
Stricker BHC,
Lahousse L,
Dupuis J,
Brusselle GG,
O'Connor GT
The European respiratory journal · 2018 · PMID 30049742
1 page
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.