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2,657 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.
6 matches for
Tang CS.
Seventy-five genetic loci influencing the human red blood cell
van der Harst P,
Zhang W,
Mateo Leach I,
Rendon A,
Verweij N,
Sehmi J,
Paul DS,
Elling U,
Allayee H,
Li X,
Radhakrishnan A,
Tan ST
and 183 more — show all
Voss K,
Weichenberger CX,
Albers CA,
Al-Hussani A,
Asselbergs FW,
Ciullo M,
Danjou F,
Dina C,
Esko T,
Evans DM,
Franke L,
Gögele M,
Hartiala J,
Hersch M,
Holm H,
Hottenga JJ,
Kanoni S,
Kleber ME,
Lagou V,
Langenberg C,
Lopez LM,
Lyytikäinen LP,
Melander O,
Murgia F,
Nolte IM,
O'Reilly PF,
Padmanabhan S,
Parsa A,
Pirastu N,
Porcu E,
Portas L,
Prokopenko I,
Ried JS,
Shin SY,
Tang CS,
Teumer A,
Traglia M,
Ulivi S,
Westra HJ,
Yang J,
Zhao JH,
Anni F,
Abdellaoui A,
Attwood A,
Balkau B,
Bandinelli S,
Bastardot F,
Benyamin B,
Boehm BO,
Cookson WO,
Das D,
de Bakker PI,
de Boer RA,
de Geus EJ,
de Moor MH,
Dimitriou M,
Domingues FS,
Döring A,
Engström G,
Eyjolfsson GI,
Ferrucci L,
Fischer K,
Galanello R,
Garner SF,
Genser B,
Gibson QD,
Girotto G,
Gudbjartsson DF,
Harris SE,
Hartikainen AL,
Hastie CE,
Hedblad B,
Illig T,
Jolley J,
Kähönen M,
Kema IP,
Kemp JP,
Liang L,
Lloyd-Jones H,
Loos RJ,
Meacham S,
Medland SE,
Meisinger C,
Memari Y,
Mihailov E,
Miller K,
Moffatt MF,
Nauck M,
Novatchkova M,
Nutile T,
Olafsson I,
Onundarson PT,
Parracciani D,
Penninx BW,
Perseu L,
Piga A,
Pistis G,
Pouta A,
Puc U,
Raitakari O,
Ring SM,
Robino A,
Ruggiero D,
Ruokonen A,
Saint-Pierre A,
Sala C,
Salumets A,
Sambrook J,
Schepers H,
Schmidt CO,
Silljé HH,
Sladek R,
Smit JH,
Starr JM,
Stephens J,
Sulem P,
Tanaka T,
Thorsteinsdottir U,
Tragante V,
van Gilst WH,
van Pelt LJ,
van Veldhuisen DJ,
Völker U,
Whitfield JB,
Willemsen G,
Winkelmann BR,
Wirnsberger G,
Algra A,
Cucca F,
d'Adamo AP,
Danesh J,
Deary IJ,
Dominiczak AF,
Elliott P,
Fortina P,
Froguel P,
Gasparini P,
Greinacher A,
Hazen SL,
Jarvelin MR,
Khaw KT,
Lehtimäki T,
Maerz W,
Martin NG,
Metspalu A,
Mitchell BD,
Montgomery GW,
Moore C,
Navis G,
Pirastu M,
Pramstaller PP,
Ramirez-Solis R,
Schadt E,
Scott J,
Shuldiner AR,
Smith GD,
Smith JG,
Snieder H,
Sorice R,
Spector TD,
Stefansson K,
Stumvoll M,
Tang WH,
Toniolo D,
Tönjes A,
Visscher PM,
Vollenweider P,
Wareham NJ,
Wolffenbuttel BH,
Boomsma DI,
Beckmann JS,
Dedoussis GV,
Deloukas P,
Ferreira MA,
Sanna S,
Uda M,
Hicks AA,
Penninger JM,
Gieger C,
Kooner JS,
Ouwehand WH,
Soranzo N,
Chambers JC
Nature · 2012 · PMID 23222517
12 pages+
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype
Ferreira MA,
Matheson MC,
Tang CS,
Granell R,
Ang W,
Hui J,
Kiefer AK,
Duffy DL,
Baltic S,
Danoy P,
Bui M,
Price L
and 22 more — show all
Sly PD,
Eriksson N,
Madden PA,
Abramson MJ,
Holt PG,
Heath AC,
Hunter M,
Musk B,
Robertson CF,
Le Souëf P,
Montgomery GW,
Henderson AJ,
Tung JY,
Dharmage SC,
Brown MA,
James A,
Thompson PJ,
Pennell C,
Martin NG,
Evans DM,
Hinds DA,
Hopper JL
Australian Asthma Genetics Consortium Collaborators
The Journal of allergy and clinical immunology · 2014 · PMID 24388013
8 pages
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization
Bønnelykke K,
Matheson MC,
Pers TH,
Granell R,
Strachan DP,
Alves AC,
Linneberg A,
Curtin JA,
Warrington NM,
Standl M,
Kerkhof M,
Jonsdottir I
and 58 more — show all
Bukvic BK,
Kaakinen M,
Sleimann P,
Thorleifsson G,
Thorsteinsdottir U,
Schramm K,
Baltic S,
Kreiner-Møller E,
Simpson A,
St Pourcain B,
Coin L,
Hui J,
Walters EH,
Tiesler CMT,
Duffy DL,
Jones G,
Ring SM,
McArdle WL,
Price L,
Robertson CF,
Pekkanen J,
Pekkanen J,
Tang CS,
Thiering E,
Montgomery GW,
Hartikainen AL,
Dharmage SC,
Husemoen LL,
Herder C,
Kemp JP,
Elliot P,
James A,
Waldenberger M,
Abramson MJ,
Fairfax BP,
Knight JC,
Knight JC,
Gupta R,
Thompson PJ,
Holt P,
Sly P,
Hirschhorn JN,
Blekic M,
Weidinger S,
Hakonarsson H,
Stefansson K,
Heinrich J,
Postma DS,
Custovic A,
Pennell CE,
Pennell CE,
Jarvelin MR,
Koppelman GH,
Timpson N,
Ferreira MA,
Ferreira MA,
Bisgaard H,
Henderson AJ
AAGC
Nature genetics · 2013 · PMID 23817571
7 pages
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease
Tang CS,
Gui H,
Kapoor A,
Kim JH,
Luzón-Toro B,
Pelet A,
Burzynski G,
Lantieri F,
So MT,
Berrios C,
Shin HD,
Fernández RM
and 20 more — show all
Le TL,
Verheij JB,
Matera I,
Cherny SS,
Nandakumar P,
Cheong HS,
Antiñolo G,
Amiel J,
Seo JM,
Kim DY,
Oh JT,
Lyonnet S,
Borrego S,
Ceccherini I,
Hofstra RM,
Chakravarti A,
Kim HY,
Sham PC,
Tam PK,
Garcia-Barceló MM
Human molecular genetics · 2016 · PMID 27702942
3 pages
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease
Garcia-Barcelo MM,
Tang CS,
Ngan ES,
Lui VC,
Chen Y,
So MT,
Leon TY,
Miao XP,
Shum CK,
Liu FQ,
Yeung MY,
Yuan ZW
and 12 more — show all
Guo WH,
Liu L,
Sun XB,
Huang LM,
Tou JF,
Song YQ,
Chan D,
Cheung KM,
Wong KK,
Cherny SS,
Sham PC,
Tam PK
Proceedings of the National Academy of Sciences of the United States of America · 2009 · PMID 19196962
2 pages
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2
Garcia-Barceló MM,
Yeung MY,
Miao XP,
Tang CS,
Cheng G,
So MT,
Ngan ES,
Lui VC,
Chen Y,
Liu XL,
Hui KJ,
Li L
and 13 more — show all
Guo WH,
Sun XB,
Tou JF,
Chan KW,
Wu XZ,
Song YQ,
Chan D,
Cheung K,
Chung PH,
Wong KK,
Sham PC,
Cherny SS,
Tam PK
Human molecular genetics · 2010 · PMID 20460270
2 pages
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.