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2,646 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.
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9 matches for
Lu C.
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels
Dehghan A,
Dupuis J,
Barbalic M,
Bis JC,
Eiriksdottir G,
Lu C,
Pellikka N,
Wallaschofski H,
Kettunen J,
Henneman P,
Baumert J,
Strachan DP
and 102 more — show all
Fuchsberger C,
Vitart V,
Wilson JF,
Paré G,
Naitza S,
Rudock ME,
Surakka I,
de Geus EJ,
Alizadeh BZ,
Guralnik J,
Shuldiner A,
Tanaka T,
Zee RY,
Schnabel RB,
Nambi V,
Kavousi M,
Ripatti S,
Nauck M,
Smith NL,
Smith AV,
Sundvall J,
Scheet P,
Liu Y,
Ruokonen A,
Rose LM,
Larson MG,
Hoogeveen RC,
Freimer NB,
Teumer A,
Tracy RP,
Launer LJ,
Buring JE,
Yamamoto JF,
Folsom AR,
Sijbrands EJ,
Pankow J,
Elliott P,
Keaney JF,
Sun W,
Sarin AP,
Fontes JD,
Badola S,
Astor BC,
Hofman A,
Pouta A,
Werdan K,
Greiser KH,
Kuss O,
Meyer zu Schwabedissen HE,
Thiery J,
Jamshidi Y,
Nolte IM,
Soranzo N,
Spector TD,
Völzke H,
Parker AN,
Aspelund T,
Bates D,
Young L,
Tsui K,
Siscovick DS,
Guo X,
Rotter JI,
Uda M,
Schlessinger D,
Rudan I,
Hicks AA,
Penninx BW,
Thorand B,
Gieger C,
Coresh J,
Willemsen G,
Harris TB,
Uitterlinden AG,
Järvelin MR,
Rice K,
Radke D,
Salomaa V,
Willems van Dijk K,
Boerwinkle E,
Vasan RS,
Ferrucci L,
Gibson QD,
Bandinelli S,
Snieder H,
Boomsma DI,
Xiao X,
Campbell H,
Hayward C,
Pramstaller PP,
van Duijn CM,
Peltonen L,
Psaty BM,
Gudnason V,
Ridker PM,
Homuth G,
Koenig W,
Ballantyne CM,
Witteman JC,
Benjamin EJ,
Perola M,
Chasman DI
Circulation · 2011 · PMID 21300955
9 pages
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling
Ho JE,
Chen WY,
Chen MH,
Larson MG,
McCabe EL,
Cheng S,
Ghorbani A,
Coglianese E,
Emilsson V,
Johnson AD,
Walter S,
Franceschini N
and 12 more — show all
O'Donnell CJ,
Dehghan A,
Lu C,
Levy D,
Newton-Cheh C,
Lin H,
Felix JF,
Schreiter ER,
Vasan RS,
Januzzi JL,
Lee RT,
Wang TJ
CARDIoGRAM Consortium · CHARGE Inflammation Working Group and 1 more consortia
The Journal of clinical investigation · 2013 · PMID 23999434
9 pages
Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions
Wu C,
Kraft P,
Zhai K,
Chang J,
Wang Z,
Li Y,
Hu Z,
He Z,
Jia W,
Abnet CC,
Liang L,
Hu N
and 24 more — show all
Miao X,
Zhou Y,
Liu Z,
Zhan Q,
Liu Y,
Qiao Y,
Zhou Y,
Jin G,
Guo C,
Lu C,
Yang H,
Fu J,
Yu D,
Freedman ND,
Ding T,
Tan W,
Goldstein AM,
Wu T,
Shen H,
Ke Y,
Zeng Y,
Chanock SJ,
Taylor PR,
Lin D
Nature genetics · 2012 · PMID 22960999
3 pages
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Lu Y,
Day FR,
Gustafsson S,
Buchkovich ML,
Na J,
Bataille V,
Cousminer DL,
Dastani Z,
Drong AW,
Esko T,
Evans DM,
Falchi M
and 247 more — show all
Feitosa MF,
Ferreira T,
Hedman ÅK,
Haring R,
Hysi PG,
Iles MM,
Justice AE,
Kanoni S,
Lagou V,
Li R,
Li X,
Locke A,
Lu C,
Mägi R,
Perry JR,
Pers TH,
Qi Q,
Sanna M,
Schmidt EM,
Scott WR,
Shungin D,
Teumer A,
Vinkhuyzen AA,
Walker RW,
Westra HJ,
Zhang M,
Zhang W,
Zhao JH,
Zhu Z,
Afzal U,
Ahluwalia TS,
Bakker SJ,
Bellis C,
Bonnefond A,
Borodulin K,
Buchman AS,
Cederholm T,
Choh AC,
Choi HJ,
Curran JE,
de Groot LC,
De Jager PL,
Dhonukshe-Rutten RA,
Enneman AW,
Eury E,
Evans DS,
Forsen T,
Friedrich N,
Fumeron F,
Garcia ME,
Gärtner S,
Han BG,
Havulinna AS,
Hayward C,
Hernandez D,
Hillege H,
Ittermann T,
Kent JW,
Kolcic I,
Laatikainen T,
Lahti J,
Mateo Leach I,
Lee CG,
Lee JY,
Liu T,
Liu Y,
Lobbens S,
Loh M,
Lyytikäinen LP,
Medina-Gomez C,
Michaëlsson K,
Nalls MA,
Nielson CM,
Oozageer L,
Pascoe L,
Paternoster L,
Polašek O,
Ripatti S,
Sarzynski MA,
Shin CS,
Narančić NS,
Spira D,
Srikanth P,
Steinhagen-Thiessen E,
Sung YJ,
Swart KM,
Taittonen L,
Tanaka T,
Tikkanen E,
van der Velde N,
van Schoor NM,
Verweij N,
Wright AF,
Yu L,
Zmuda JM,
Eklund N,
Forrester T,
Grarup N,
Jackson AU,
Kristiansson K,
Kuulasmaa T,
Kuusisto J,
Lichtner P,
Luan J,
Mahajan A,
Männistö S,
Palmer CD,
Ried JS,
Scott RA,
Stancáková A,
Wagner PJ,
Demirkan A,
Döring A,
Gudnason V,
Kiel DP,
Kühnel B,
Mangino M,
Mcknight B,
Menni C,
O'Connell JR,
Oostra BA,
Shuldiner AR,
Song K,
Vandenput L,
van Duijn CM,
Vollenweider P,
White CC,
Boehnke M,
Boettcher Y,
Cooper RS,
Forouhi NG,
Gieger C,
Grallert H,
Hingorani A,
Jørgensen T,
Jousilahti P,
Kivimaki M,
Kumari M,
Laakso M,
Langenberg C,
Linneberg A,
Luke A,
Mckenzie CA,
Palotie A,
Pedersen O,
Peters A,
Strauch K,
Tayo BO,
Wareham NJ,
Bennett DA,
Bertram L,
Blangero J,
Blüher M,
Bouchard C,
Campbell H,
Cho NH,
Cummings SR,
Czerwinski SA,
Demuth I,
Eckardt R,
Eriksson JG,
Ferrucci L,
Franco OH,
Froguel P,
Gansevoort RT,
Hansen T,
Harris TB,
Hastie N,
Heliövaara M,
Hofman A,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Knekt PB,
Koskinen S,
Kovacs P,
Lehtimäki T,
Lind L,
Liu Y,
Orwoll ES,
Osmond C,
Perola M,
Pérusse L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Rivadeneira F,
Rudan I,
Salomaa V,
Sørensen TI,
Stumvoll M,
Tönjes A,
Towne B,
Tranah GJ,
Tremblay A,
Uitterlinden AG,
van der Harst P,
Vartiainen E,
Viikari JS,
Vitart V,
Vohl MC,
Völzke H,
Walker M,
Wallaschofski H,
Wild S,
Wilson JF,
Yengo L,
Bishop DT,
Borecki IB,
Chambers JC,
Cupples LA,
Dehghan A,
Deloukas P,
Fatemifar G,
Fox C,
Furey TS,
Franke L,
Han J,
Hunter DJ,
Karjalainen J,
Karpe F,
Kaplan RC,
Kooner JS,
McCarthy MI,
Murabito JM,
Morris AP,
Bishop JA,
North KE,
Ohlsson C,
Ong KK,
Prokopenko I,
Richards JB,
Schadt EE,
Spector TD,
Widén E,
Willer CJ,
Yang J,
Ingelsson E,
Mohlke KL,
Hirschhorn JN,
Pospisilik JA,
Zillikens MC,
Lindgren C,
Kilpeläinen TO,
Loos RJ
Nature communications · 2016 · PMID 26833246 · open access
3 pages
Environmental and genetic predictors of human cardiovascular ageing
Shah M,
de A Inácio MH,
Lu C,
Schiratti PR,
Zheng SL,
Clement A,
de Marvao A,
Bai W,
King AP,
Ware JS,
Wilkins MR,
Mielke J
and 6 more — show all
Nature communications · 2023 · PMID 37604819 · open access
3 pages
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies
Grallert H,
Dupuis J,
Bis JC,
Dehghan A,
Barbalic M,
Baumert J,
Lu C,
Smith NL,
Uitterlinden AG,
Roberts R,
Khuseyinova N,
Schnabel RB
and 33 more — show all
Rice KM,
Rivadeneira F,
Hoogeveen RC,
Fontes JD,
Meisinger C,
Keaney JF Jr,
Lemaitre R,
Aulchenko YS,
Vasan RS,
Ellis S,
Hazen SL,
van Duijn CM,
Nelson JJ,
März W,
Schunkert H,
McPherson RM,
Stirnadel-Farrant HA,
Psaty BM,
Gieger C,
Siscovick D,
Hofman A,
Illig T,
Cushman M,
Yamamoto JF,
Rotter JI,
Larson MG,
Stewart AF,
Boerwinkle E,
Witteman JC,
Tracy RP,
Koenig W,
Benjamin EJ,
Ballantyne CM
European heart journal · 2012 · PMID 22003152
2 pages
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic
Han F,
Faraco J,
Dong XS,
Ollila HM,
Lin L,
Li J,
An P,
Wang S,
Jiang KW,
Gao ZC,
Zhao L,
Yan H
and 13 more — show all
Liu YN,
Li QH,
Zhang XZ,
Hu Y,
Wang JY,
Lu YH,
Lu CJ,
Zhou W,
Hallmayer J,
Huang YS,
Strohl KP,
Pollmächer T,
Mignot E
PLoS genetics · 2013 · PMID 24204295 · open access
2 pages
Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels
Barbalic M,
Dupuis J,
Dehghan A,
Bis JC,
Hoogeveen RC,
Schnabel RB,
Nambi V,
Bretler M,
Smith NL,
Peters A,
Lu C,
Tracy RP
and 20 more — show all
Aleksic N,
Heeriga J,
Keaney JF Jr,
Rice K,
Lip GY,
Vasan RS,
Glazer NL,
Larson MG,
Uitterlinden AG,
Yamamoto J,
Durda P,
Haritunians T,
Psaty BM,
Boerwinkle E,
Hofman A,
Koenig W,
Jenny NS,
Witteman JC,
Ballantyne C,
Benjamin EJ
Human molecular genetics · 2010 · PMID 20167578
1 page
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
Ahluwalia TS,
Prins BP,
Abdollahi M,
Armstrong NJ,
Aslibekyan S,
Bain L,
Jefferis B,
Baumert J,
Beekman M,
Ben-Shlomo Y,
Bis JC,
Mitchell BD
and 114 more — show all
de Geus E,
Delgado GE,
Marek D,
Eriksson J,
Kajantie E,
Kanoni S,
Kemp JP,
Lu C,
Marioni RE,
McLachlan S,
Milaneschi Y,
Nolte IM,
Petrelis AM,
Porcu E,
Sabater-Lleal M,
Naderi E,
Seppälä I,
Shah T,
Singhal G,
Standl M,
Teumer A,
Thalamuthu A,
Thiering E,
Trompet S,
Ballantyne CM,
Benjamin EJ,
Casas JP,
Toben C,
Dedoussis G,
Deelen J,
Durda P,
Engmann J,
Feitosa MF,
Grallert H,
Hammarstedt A,
Harris SE,
Homuth G,
Hottenga JJ,
Jalkanen S,
Jamshidi Y,
Jawahar MC,
Jess T,
Kivimaki M,
Kleber ME,
Lahti J,
Liu Y,
Marques-Vidal P,
Mellström D,
Mooijaart SP,
Müller-Nurasyid M,
Penninx B,
Revez JA,
Rossing P,
Räikkönen K,
Sattar N,
Scharnagl H,
Sennblad B,
Silveira A,
Pourcain BS,
Timpson NJ,
Trollor J,
van Dongen J,
Van Heemst D,
Visvikis-Siest S,
Vollenweider P,
Völker U,
Waldenberger M,
Willemsen G,
Zabaneh D,
Morris RW,
Arnett DK,
Baune BT,
Boomsma DI,
Chang YC,
Deary IJ,
Deloukas P,
Eriksson JG,
Evans DM,
Ferreira MA,
Gaunt T,
Gudnason V,
Hamsten A,
Heinrich J,
Hingorani A,
Humphries SE,
Jukema JW,
Koenig W,
Kumari M,
Kutalik Z,
Lawlor DA,
Lehtimäki T,
März W,
Mather KA,
Naitza S,
Nauck M,
Ohlsson C,
Price JF,
Raitakari O,
Rice K,
Sachdev PS,
Slagboom E,
Sørensen TIA,
Spector T,
Stacey D,
Stathopoulou MG,
Tanaka T,
Wannamethee SG,
Whincup P,
Rotter JI,
Dehghan A,
Boerwinkle E,
Psaty BM,
Snieder H,
Alizadeh BZ
CHARGE Inflammation Working Group
Human molecular genetics · 2021 · PMID 33517400 · open access
1 page
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Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
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Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
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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
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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.
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