For researchers
Is your paper here?
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.
7 matches for
Tsui K.
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Elks CE,
Perry JR,
Sulem P,
Chasman DI,
Franceschini N,
He C,
Lunetta KL,
Visser JA,
Byrne EM,
Cousminer DL,
Gudbjartsson DF,
Esko T
and 162 more — show all
Feenstra B,
Hottenga JJ,
Koller DL,
Kutalik Z,
Lin P,
Mangino M,
Marongiu M,
McArdle PF,
Smith AV,
Stolk L,
van Wingerden SH,
Zhao JH,
Albrecht E,
Corre T,
Ingelsson E,
Hayward C,
Magnusson PK,
Smith EN,
Ulivi S,
Warrington NM,
Zgaga L,
Alavere H,
Amin N,
Aspelund T,
Bandinelli S,
Barroso I,
Berenson GS,
Bergmann S,
Blackburn H,
Boerwinkle E,
Buring JE,
Busonero F,
Campbell H,
Chanock SJ,
Chen W,
Cornelis MC,
Couper D,
Coviello AD,
d'Adamo P,
de Faire U,
de Geus EJ,
Deloukas P,
Döring A,
Smith GD,
Easton DF,
Eiriksdottir G,
Emilsson V,
Eriksson J,
Ferrucci L,
Folsom AR,
Foroud T,
Garcia M,
Gasparini P,
Geller F,
Gieger C,
Gudnason V,
Hall P,
Hankinson SE,
Ferreli L,
Heath AC,
Hernandez DG,
Hofman A,
Hu FB,
Illig T,
Järvelin MR,
Johnson AD,
Karasik D,
Khaw KT,
Kiel DP,
Kilpeläinen TO,
Kolcic I,
Kraft P,
Launer LJ,
Laven JS,
Li S,
Liu J,
Levy D,
Martin NG,
McArdle WL,
Melbye M,
Mooser V,
Murray JC,
Murray SS,
Nalls MA,
Navarro P,
Nelis M,
Ness AR,
Northstone K,
Oostra BA,
Peacock M,
Palmer LJ,
Palotie A,
Paré G,
Parker AN,
Pedersen NL,
Peltonen L,
Pennell CE,
Pharoah P,
Polasek O,
Plump AS,
Pouta A,
Porcu E,
Rafnar T,
Rice JP,
Ring SM,
Rivadeneira F,
Rudan I,
Sala C,
Salomaa V,
Sanna S,
Schlessinger D,
Schork NJ,
Scuteri A,
Segrè AV,
Shuldiner AR,
Soranzo N,
Sovio U,
Srinivasan SR,
Strachan DP,
Tammesoo ML,
Tikkanen E,
Toniolo D,
Tsui K,
Tryggvadottir L,
Tyrer J,
Uda M,
van Dam RM,
van Meurs JB,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Weedon MN,
Wichmann HE,
Willemsen G,
Wilson JF,
Wright AF,
Young L,
Zhai G,
Zhuang WV,
Bierut LJ,
Boomsma DI,
Boyd HA,
Crisponi L,
Demerath EW,
van Duijn CM,
Econs MJ,
Harris TB,
Hunter DJ,
Loos RJ,
Metspalu A,
Montgomery GW,
Ridker PM,
Spector TD,
Streeten EA,
Stefansson K,
Thorsteinsdottir U,
Uitterlinden AG,
Widen E,
Murabito JM,
Ong KK,
Murray A
GIANT Consortium
Nature genetics · 2010 · PMID 21102462
11 pages
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
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
Stolk L,
Perry JR,
Chasman DI,
He C,
Mangino M,
Sulem P,
Barbalic M,
Broer L,
Byrne EM,
Ernst F,
Esko T,
Franceschini N
and 167 more — show all
Gudbjartsson DF,
Hottenga JJ,
Kraft P,
McArdle PF,
Porcu E,
Shin SY,
Smith AV,
van Wingerden S,
Zhai G,
Zhuang WV,
Albrecht E,
Alizadeh BZ,
Aspelund T,
Bandinelli S,
Lauc LB,
Beckmann JS,
Boban M,
Boerwinkle E,
Broekmans FJ,
Burri A,
Campbell H,
Chanock SJ,
Chen C,
Cornelis MC,
Corre T,
Coviello AD,
d'Adamo P,
Davies G,
de Faire U,
de Geus EJ,
Deary IJ,
Dedoussis GV,
Deloukas P,
Ebrahim S,
Eiriksdottir G,
Emilsson V,
Eriksson JG,
Fauser BC,
Ferreli L,
Ferrucci L,
Fischer K,
Folsom AR,
Garcia ME,
Gasparini P,
Gieger C,
Glazer N,
Grobbee DE,
Hall P,
Haller T,
Hankinson SE,
Hass M,
Hayward C,
Heath AC,
Hofman A,
Ingelsson E,
Janssens AC,
Johnson AD,
Karasik D,
Kardia SL,
Keyzer J,
Kiel DP,
Kolcic I,
Kutalik Z,
Lahti J,
Lai S,
Laisk T,
Laven JS,
Lawlor DA,
Liu J,
Lopez LM,
Louwers YV,
Magnusson PK,
Marongiu M,
Martin NG,
Klaric IM,
Masciullo C,
McKnight B,
Medland SE,
Melzer D,
Mooser V,
Navarro P,
Newman AB,
Nyholt DR,
Onland-Moret NC,
Palotie A,
Paré G,
Parker AN,
Pedersen NL,
Peeters PH,
Pistis G,
Plump AS,
Polasek O,
Pop VJ,
Psaty BM,
Räikkönen K,
Rehnberg E,
Rotter JI,
Rudan I,
Sala C,
Salumets A,
Scuteri A,
Singleton A,
Smith JA,
Snieder H,
Soranzo N,
Stacey SN,
Starr JM,
Stathopoulou MG,
Stirrups K,
Stolk RP,
Styrkarsdottir U,
Sun YV,
Tenesa A,
Thorand B,
Toniolo D,
Tryggvadottir L,
Tsui K,
Ulivi S,
van Dam RM,
van der Schouw YT,
van Gils CH,
van Nierop P,
Vink JM,
Visscher PM,
Voorhuis M,
Waeber G,
Wallaschofski H,
Wichmann HE,
Widen E,
Wijnands-van Gent CJ,
Willemsen G,
Wilson JF,
Wolffenbuttel BH,
Wright AF,
Yerges-Armstrong LM,
Zemunik T,
Zgaga L,
Zillikens MC,
Zygmunt M,
Arnold AM,
Boomsma DI,
Buring JE,
Crisponi L,
Demerath EW,
Gudnason V,
Harris TB,
Hu FB,
Hunter DJ,
Launer LJ,
Metspalu A,
Montgomery GW,
Oostra BA,
Ridker PM,
Sanna S,
Schlessinger D,
Spector TD,
Stefansson K,
Streeten EA,
Thorsteinsdottir U,
Uda M,
Uitterlinden AG,
van Duijn CM,
Völzke H,
Murray A,
Murabito JM,
Visser JA,
Lunetta KL
LifeLines Cohort Study
Nature genetics · 2012 · PMID 22267201 · open access
8 pages
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
Khor CC,
Miyake M,
Chen LJ,
Shi Y,
Barathi VA,
Qiao F,
Nakata I,
Yamashiro K,
Zhou X,
Tam PO,
Cheng CY,
Tai ES
and 14 more — show all
Vithana EN,
Aung T,
Teo YY,
Wong TY,
Moriyama M,
Ohno-Matsui K,
Mochizuki M,
Matsuda F,
Yong RY,
Yap EP,
Yang Z,
Pang CP,
Saw SM,
Yoshimura N
Nagahama Study Group
Human molecular genetics · 2013 · PMID 23933737
1 page
CCDC102B confers risk of low vision and blindness in high myopia
Hosoda Y,
Yoshikawa M,
Miyake M,
Tabara Y,
Shimada N,
Zhao W,
Oishi A,
Nakanishi H,
Hata M,
Akagi T,
Ooto S,
Nagaoka N
and 8 more — show all
Nagahama Study group
Nature communications · 2018 · PMID 29725004 · open access
1 page
A genome-wide association study on adherence to low-carbohydrate diets in Japanese
Nakamura Y,
Tamura T,
Narita A,
Shimizu A,
Sutoh Y,
Takashima N,
Matsui K,
Miyagawa N,
Kadota A,
Miura K,
Otonari J,
Ikezaki H
and 24 more — show all
Hishida A,
Nagayoshi M,
Okada R,
Kubo Y,
Tanaka K,
Shimanoe C,
Ibusuki R,
Nishimoto D,
Oze I,
Ito H,
Ozaki E,
Matsui D,
Mikami H,
Kusakabe M,
Suzuki S,
Watanabe M,
Arisawa K,
Katsuura-Kamano S,
Kuriki K,
Nakatochi M,
Momozawa Y,
Kubo M,
Takeuchi K,
Wakai K
J-MICC Research Group Consortium
European journal of clinical nutrition · 2022 · PMID 35132194
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.