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2,663 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.
5 matches for
Lin WY.
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits
Tachmazidou I,
Süveges D,
Min JL,
Ritchie GRS,
Steinberg J,
Walter K,
Iotchkova V,
Schwartzentruber J,
Huang J,
Memari Y,
McCarthy S,
Crawford AA
and 91 more — show all
Bombieri C,
Cocca M,
Farmaki AE,
Gaunt TR,
Jousilahti P,
Kooijman MN,
Lehne B,
Malerba G,
Männistö S,
Matchan A,
Medina-Gomez C,
Metrustry SJ,
Nag A,
Ntalla I,
Paternoster L,
Rayner NW,
Sala C,
Scott WR,
Shihab HA,
Southam L,
St Pourcain B,
Traglia M,
Trajanoska K,
Zaza G,
Zhang W,
Artigas MS,
Bansal N,
Benn M,
Chen Z,
Danecek P,
Lin WY,
Locke A,
Luan J,
Manning AK,
Mulas A,
Sidore C,
Tybjaerg-Hansen A,
Varbo A,
Zoledziewska M,
Finan C,
Hatzikotoulas K,
Hendricks AE,
Kemp JP,
Moayyeri A,
Panoutsopoulou K,
Szpak M,
Wilson SG,
Boehnke M,
Cucca F,
Di Angelantonio E,
Langenberg C,
Lindgren C,
McCarthy MI,
Morris AP,
Nordestgaard BG,
Scott RA,
Tobin MD,
Wareham NJ,
Burton P,
Chambers JC,
Smith GD,
Dedoussis G,
Felix JF,
Franco OH,
Gambaro G,
Gasparini P,
Hammond CJ,
Hofman A,
Jaddoe VWV,
Kleber M,
Kooner JS,
Perola M,
Relton C,
Ring SM,
Rivadeneira F,
Salomaa V,
Spector TD,
Stegle O,
Toniolo D,
Uitterlinden AG,
Barroso I,
Greenwood CMT,
Perry JRB,
Walker BR,
Butterworth AS,
Xue Y,
Durbin R,
Small KS,
Soranzo N,
Timpson NJ,
Zeggini E
SpiroMeta Consortium · GoT2D Consortium and 3 more consortia
American journal of human genetics · 2017 · PMID 28552196 · open access
12 pages+
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Evangelou E,
Warren HR,
Mosen-Ansorena D,
Mifsud B,
Pazoki R,
Gao H,
Ntritsos G,
Dimou N,
Cabrera CP,
Karaman I,
Ng FL,
Evangelou M
and 268 more — show all
Witkowska K,
Tzanis E,
Hellwege JN,
Giri A,
Velez Edwards DR,
Sun YV,
Cho K,
Gaziano JM,
Wilson PWF,
Tsao PS,
Kovesdy CP,
Esko T,
Mägi R,
Milani L,
Almgren P,
Boutin T,
Debette S,
Ding J,
Giulianini F,
Holliday EG,
Jackson AU,
Li-Gao R,
Lin WY,
Luan J,
Mangino M,
Oldmeadow C,
Prins BP,
Qian Y,
Sargurupremraj M,
Shah N,
Surendran P,
Thériault S,
Verweij N,
Willems SM,
Zhao JH,
Amouyel P,
Connell J,
de Mutsert R,
Doney ASF,
Farrall M,
Menni C,
Morris AD,
Noordam R,
Paré G,
Poulter NR,
Shields DC,
Stanton A,
Thom S,
Abecasis G,
Amin N,
Arking DE,
Ayers KL,
Barbieri CM,
Batini C,
Bis JC,
Blake T,
Bochud M,
Boehnke M,
Boerwinkle E,
Boomsma DI,
Bottinger EP,
Braund PS,
Brumat M,
Campbell A,
Campbell H,
Chakravarti A,
Chambers JC,
Chauhan G,
Ciullo M,
Cocca M,
Collins F,
Cordell HJ,
Davies G,
de Borst MH,
de Geus EJ,
Deary IJ,
Deelen J,
Del Greco M F,
Demirkale CY,
Dörr M,
Ehret GB,
Elosua R,
Enroth S,
Erzurumluoglu AM,
Ferreira T,
Frånberg M,
Franco OH,
Gandin I,
Gasparini P,
Giedraitis V,
Gieger C,
Girotto G,
Goel A,
Gow AJ,
Gudnason V,
Guo X,
Gyllensten U,
Hamsten A,
Harris TB,
Harris SE,
Hartman CA,
Havulinna AS,
Hicks AA,
Hofer E,
Hofman A,
Hottenga JJ,
Huffman JE,
Hwang SJ,
Ingelsson E,
James A,
Jansen R,
Jarvelin MR,
Joehanes R,
Johansson Å,
Johnson AD,
Joshi PK,
Jousilahti P,
Jukema JW,
Jula A,
Kähönen M,
Kathiresan S,
Keavney BD,
Khaw KT,
Knekt P,
Knight J,
Kolcic I,
Kooner JS,
Koskinen S,
Kristiansson K,
Kutalik Z,
Laan M,
Larson M,
Launer LJ,
Lehne B,
Lehtimäki T,
Liewald DCM,
Lin L,
Lind L,
Lindgren CM,
Liu Y,
Loos RJF,
Lopez LM,
Lu Y,
Lyytikäinen LP,
Mahajan A,
Mamasoula C,
Marrugat J,
Marten J,
Milaneschi Y,
Morgan A,
Morris AP,
Morrison AC,
Munson PJ,
Nalls MA,
Nandakumar P,
Nelson CP,
Niiranen T,
Nolte IM,
Nutile T,
Oldehinkel AJ,
Oostra BA,
O'Reilly PF,
Org E,
Padmanabhan S,
Palmas W,
Palotie A,
Pattie A,
Penninx BWJH,
Perola M,
Peters A,
Polasek O,
Pramstaller PP,
Nguyen QT,
Raitakari OT,
Ren M,
Rettig R,
Rice K,
Ridker PM,
Ried JS,
Riese H,
Ripatti S,
Robino A,
Rose LM,
Rotter JI,
Rudan I,
Ruggiero D,
Saba Y,
Sala CF,
Salomaa V,
Samani NJ,
Sarin AP,
Schmidt R,
Schmidt H,
Shrine N,
Siscovick D,
Smith AV,
Snieder H,
Sõber S,
Sorice R,
Starr JM,
Stott DJ,
Strachan DP,
Strawbridge RJ,
Sundström J,
Swertz MA,
Taylor KD,
Teumer A,
Tobin MD,
Tomaszewski M,
Toniolo D,
Traglia M,
Trompet S,
Tuomilehto J,
Tzourio C,
Uitterlinden AG,
Vaez A,
van der Most PJ,
van Duijn CM,
Vergnaud AC,
Verwoert GC,
Vitart V,
Völker U,
Vollenweider P,
Vuckovic D,
Watkins H,
Wild SH,
Willemsen G,
Wilson JF,
Wright AF,
Yao J,
Zemunik T,
Zhang W,
Attia JR,
Butterworth AS,
Chasman DI,
Conen D,
Cucca F,
Danesh J,
Hayward C,
Howson JMM,
Laakso M,
Lakatta EG,
Langenberg C,
Melander O,
Mook-Kanamori DO,
Palmer CNA,
Risch L,
Scott RA,
Scott RJ,
Sever P,
Spector TD,
van der Harst P,
Wareham NJ,
Zeggini E,
Levy D,
Munroe PB,
Newton-Cheh C,
Brown MJ,
Metspalu A,
Hung AM,
O'Donnell CJ,
Edwards TL,
Psaty BM,
Tzoulaki I,
Barnes MR,
Wain LV,
Elliott P,
Caulfield MJ
Million Veteran Program
Nature genetics · 2018 · PMID 30224653
12 pages+
Genome-wide association study identifies susceptibility loci for acute myeloid leukemia
Lin WY,
Fordham SE,
Hungate E,
Sunter NJ,
Elstob C,
Xu Y,
Park C,
Quante A,
Strauch K,
Gieger C,
Skol A,
Rahman T
and 71 more — show all
Sucheston-Campbell L,
Wang J,
Hahn T,
Clay-Gilmour AI,
Jones GL,
Marr HJ,
Jackson GH,
Menne T,
Collin M,
Ivey A,
Hills RK,
Burnett AK,
Russell NH,
Fitzgibbon J,
Larson RA,
Le Beau MM,
Stock W,
Heidenreich O,
Alharbi A,
Allsup DJ,
Houlston RS,
Norden J,
Dickinson AM,
Douglas E,
Lendrem C,
Daly AK,
Palm L,
Piechocki K,
Jeffries S,
Bornhäuser M,
Röllig C,
Altmann H,
Ruhnke L,
Kunadt D,
Wagenführ L,
Cordell HJ,
Darlay R,
Andersen MK,
Fontana MC,
Martinelli G,
Marconi G,
Sanz MA,
Cervera J,
Gómez-Seguí I,
Cluzeau T,
Moreilhon C,
Raynaud S,
Sill H,
Voso MT,
Lo-Coco F,
Dombret H,
Cheok M,
Preudhomme C,
Gale RE,
Linch D,
Gaal-Wesinger J,
Masszi A,
Nowak D,
Hofmann WK,
Gilkes A,
Porkka K,
Milosevic Feenstra JD,
Kralovics R,
Grimwade D,
Meggendorfer M,
Haferlach T,
Krizsán S,
Bödör C,
Stölzel F,
Onel K,
Allan JM
Nature communications · 2021 · PMID 34716350 · open access
1 page
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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.