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2,657 papers hold this site up. Every variant and condition page names
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4 matches for
Kwan T.
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Lango Allen H,
Estrada K,
Lettre G,
Berndt SI,
Weedon MN,
Rivadeneira F,
Willer CJ,
Jackson AU,
Vedantam S,
Raychaudhuri S,
Ferreira T,
Wood AR
and 281 more — show all
Weyant RJ,
Segrè AV,
Speliotes EK,
Wheeler E,
Soranzo N,
Park JH,
Yang J,
Gudbjartsson D,
Heard-Costa NL,
Randall JC,
Qi L,
Vernon Smith A,
Mägi R,
Pastinen T,
Liang L,
Heid IM,
Luan J,
Thorleifsson G,
Winkler TW,
Goddard ME,
Sin Lo K,
Palmer C,
Workalemahu T,
Aulchenko YS,
Johansson A,
Zillikens MC,
Feitosa MF,
Esko T,
Johnson T,
Ketkar S,
Kraft P,
Mangino M,
Prokopenko I,
Absher D,
Albrecht E,
Ernst F,
Glazer NL,
Hayward C,
Hottenga JJ,
Jacobs KB,
Knowles JW,
Kutalik Z,
Monda KL,
Polasek O,
Preuss M,
Rayner NW,
Robertson NR,
Steinthorsdottir V,
Tyrer JP,
Voight BF,
Wiklund F,
Xu J,
Zhao JH,
Nyholt DR,
Pellikka N,
Perola M,
Perry JR,
Surakka I,
Tammesoo ML,
Altmaier EL,
Amin N,
Aspelund T,
Bhangale T,
Boucher G,
Chasman DI,
Chen C,
Coin L,
Cooper MN,
Dixon AL,
Gibson Q,
Grundberg E,
Hao K,
Juhani Junttila M,
Kaplan LM,
Kettunen J,
König IR,
Kwan T,
Lawrence RW,
Levinson DF,
Lorentzon M,
McKnight B,
Morris AP,
Müller M,
Suh Ngwa J,
Purcell S,
Rafelt S,
Salem RM,
Salvi E,
Sanna S,
Shi J,
Sovio U,
Thompson JR,
Turchin MC,
Vandenput L,
Verlaan DJ,
Vitart V,
White CC,
Ziegler A,
Almgren P,
Balmforth AJ,
Campbell H,
Citterio L,
De Grandi A,
Dominiczak A,
Duan J,
Elliott P,
Elosua R,
Eriksson JG,
Freimer NB,
Geus EJ,
Glorioso N,
Haiqing S,
Hartikainen AL,
Havulinna AS,
Hicks AA,
Hui J,
Igl W,
Illig T,
Jula A,
Kajantie E,
Kilpeläinen TO,
Koiranen M,
Kolcic I,
Koskinen S,
Kovacs P,
Laitinen J,
Liu J,
Lokki ML,
Marusic A,
Maschio A,
Meitinger T,
Mulas A,
Paré G,
Parker AN,
Peden JF,
Petersmann A,
Pichler I,
Pietiläinen KH,
Pouta A,
Ridderstråle M,
Rotter JI,
Sambrook JG,
Sanders AR,
Schmidt CO,
Sinisalo J,
Smit JH,
Stringham HM,
Bragi Walters G,
Widen E,
Wild SH,
Willemsen G,
Zagato L,
Zgaga L,
Zitting P,
Alavere H,
Farrall M,
McArdle WL,
Nelis M,
Peters MJ,
Ripatti S,
van Meurs JB,
Aben KK,
Ardlie KG,
Beckmann JS,
Beilby JP,
Bergman RN,
Bergmann S,
Collins FS,
Cusi D,
den Heijer M,
Eiriksdottir G,
Gejman PV,
Hall AS,
Hamsten A,
Huikuri HV,
Iribarren C,
Kähönen M,
Kaprio J,
Kathiresan S,
Kiemeney L,
Kocher T,
Launer LJ,
Lehtimäki T,
Melander O,
Mosley TH Jr,
Musk AW,
Nieminen MS,
O'Donnell CJ,
Ohlsson C,
Oostra B,
Palmer LJ,
Raitakari O,
Ridker PM,
Rioux JD,
Rissanen A,
Rivolta C,
Schunkert H,
Shuldiner AR,
Siscovick DS,
Stumvoll M,
Tönjes A,
Tuomilehto J,
van Ommen GJ,
Viikari J,
Heath AC,
Martin NG,
Montgomery GW,
Province MA,
Kayser M,
Arnold AM,
Atwood LD,
Boerwinkle E,
Chanock SJ,
Deloukas P,
Gieger C,
Grönberg H,
Hall P,
Hattersley AT,
Hengstenberg C,
Hoffman W,
Lathrop GM,
Salomaa V,
Schreiber S,
Uda M,
Waterworth D,
Wright AF,
Assimes TL,
Barroso I,
Hofman A,
Mohlke KL,
Boomsma DI,
Caulfield MJ,
Cupples LA,
Erdmann J,
Fox CS,
Gudnason V,
Gyllensten U,
Harris TB,
Hayes RB,
Jarvelin MR,
Mooser V,
Munroe PB,
Ouwehand WH,
Penninx BW,
Pramstaller PP,
Quertermous T,
Rudan I,
Samani NJ,
Spector TD,
Völzke H,
Watkins H,
Wilson JF,
Groop LC,
Haritunians T,
Hu FB,
Kaplan RC,
Metspalu A,
North KE,
Schlessinger D,
Wareham NJ,
Hunter DJ,
O'Connell JR,
Strachan DP,
Wichmann HE,
Borecki IB,
van Duijn CM,
Schadt EE,
Thorsteinsdottir U,
Peltonen L,
Uitterlinden AG,
Visscher PM,
Chatterjee N,
Loos RJ,
Boehnke M,
McCarthy MI,
Ingelsson E,
Lindgren CM,
Abecasis GR,
Stefansson K,
Frayling TM,
Hirschhorn JN
Nature · 2010 · PMID 20881960 · open access
12 pages+
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Astle WJ,
Elding H,
Jiang T,
Allen D,
Ruklisa D,
Mann AL,
Mead D,
Bouman H,
Riveros-Mckay F,
Kostadima MA,
Lambourne JJ,
Sivapalaratnam S
and 62 more — show all
Downes K,
Kundu K,
Bomba L,
Berentsen K,
Bradley JR,
Daugherty LC,
Delaneau O,
Freson K,
Garner SF,
Grassi L,
Guerrero J,
Haimel M,
Janssen-Megens EM,
Kaan A,
Kamat M,
Kim B,
Mandoli A,
Marchini J,
Martens JHA,
Meacham S,
Megy K,
O'Connell J,
Petersen R,
Sharifi N,
Sheard SM,
Staley JR,
Tuna S,
van der Ent M,
Walter K,
Wang SY,
Wheeler E,
Wilder SP,
Iotchkova V,
Moore C,
Sambrook J,
Stunnenberg HG,
Di Angelantonio E,
Kaptoge S,
Kuijpers TW,
Carrillo-de-Santa-Pau E,
Juan D,
Rico D,
Valencia A,
Chen L,
Ge B,
Vasquez L,
Kwan T,
Garrido-Martín D,
Watt S,
Yang Y,
Guigo R,
Beck S,
Paul DS,
Pastinen T,
Bujold D,
Bourque G,
Frontini M,
Danesh J,
Roberts DJ,
Ouwehand WH,
Butterworth AS,
Soranzo N
Cell · 2016 · PMID 27863252 · open access
12 pages+
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Estrada K,
Styrkarsdottir U,
Evangelou E,
Hsu YH,
Duncan EL,
Ntzani EE,
Oei L,
Albagha OM,
Amin N,
Kemp JP,
Koller DL,
Li G
and 170 more — show all
Liu CT,
Minster RL,
Moayyeri A,
Vandenput L,
Willner D,
Xiao SM,
Yerges-Armstrong LM,
Zheng HF,
Alonso N,
Eriksson J,
Kammerer CM,
Kaptoge SK,
Leo PJ,
Thorleifsson G,
Wilson SG,
Wilson JF,
Aalto V,
Alen M,
Aragaki AK,
Aspelund T,
Center JR,
Dailiana Z,
Duggan DJ,
Garcia M,
Garcia-Giralt N,
Giroux S,
Hallmans G,
Hocking LJ,
Husted LB,
Jameson KA,
Khusainova R,
Kim GS,
Kooperberg C,
Koromila T,
Kruk M,
Laaksonen M,
Lacroix AZ,
Lee SH,
Leung PC,
Lewis JR,
Masi L,
Mencej-Bedrac S,
Nguyen TV,
Nogues X,
Nogues X,
Patel MS,
Prezelj J,
Rose LM,
Scollen S,
Siggeirsdottir K,
Smith AV,
Svensson O,
Trompet S,
Trummer O,
van Schoor NM,
Woo J,
Zhu K,
Balcells S,
Brandi ML,
Buckley BM,
Cheng S,
Christiansen C,
Cooper C,
Dedoussis G,
Ford I,
Frost M,
Goltzman D,
González-Macías J,
Kähönen M,
Karlsson M,
Khusnutdinova E,
Koh JM,
Kollia P,
Langdahl BL,
Leslie WD,
Lips P,
Ljunggren Ö,
Lorenc RS,
Marc J,
Mellström D,
Obermayer-Pietsch B,
Olmos JM,
Pettersson-Kymmer U,
Reid DM,
Riancho JA,
Ridker PM,
Rousseau F,
Slagboom PE,
Tang NL,
Urreizti R,
Van Hul W,
Viikari J,
Zarrabeitia MT,
Aulchenko YS,
Castano-Betancourt M,
Grundberg E,
Herrera L,
Ingvarsson T,
Johannsdottir H,
Kwan T,
Li R,
Luben R,
Medina-Gómez C,
Palsson ST,
Reppe S,
Rotter JI,
Sigurdsson G,
van Meurs JB,
Verlaan D,
Williams FM,
Wood AR,
Zhou Y,
Gautvik KM,
Pastinen T,
Raychaudhuri S,
Cauley JA,
Chasman DI,
Clark GR,
Cummings SR,
Danoy P,
Dennison EM,
Eastell R,
Eisman JA,
Gudnason V,
Hofman A,
Jackson RD,
Jones G,
Jukema JW,
Khaw KT,
Lehtimäki T,
Liu Y,
Lorentzon M,
McCloskey E,
Mitchell BD,
Nandakumar K,
Nicholson GC,
Oostra BA,
Peacock M,
Pols HA,
Prince RL,
Raitakari O,
Reid IR,
Robbins J,
Sambrook PN,
Sham PC,
Shuldiner AR,
Tylavsky FA,
van Duijn CM,
Wareham NJ,
Cupples LA,
Econs MJ,
Evans DM,
Harris TB,
Kung AW,
Psaty BM,
Reeve J,
Spector TD,
Streeten EA,
Zillikens MC,
Thorsteinsdottir U,
Ohlsson C,
Karasik D,
Richards JB,
Brown MA,
Stefansson K,
Uitterlinden AG,
Ralston SH,
Ioannidis JP,
Kiel DP,
Rivadeneira F
Nature genetics · 2012 · PMID 22504420 · open access
7 pages
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture
Zheng HF,
Forgetta V,
Hsu YH,
Estrada K,
Rosello-Diez A,
Leo PJ,
Dahia CL,
Park-Min KH,
Tobias JH,
Kooperberg C,
Kleinman A,
Styrkarsdottir U
and 146 more — show all
Liu CT,
Uggla C,
Evans DS,
Nielson CM,
Walter K,
Pettersson-Kymmer U,
McCarthy S,
Eriksson J,
Kwan T,
Jhamai M,
Trajanoska K,
Memari Y,
Min J,
Huang J,
Danecek P,
Wilmot B,
Li R,
Chou WC,
Mokry LE,
Moayyeri A,
Claussnitzer M,
Cheng CH,
Cheung W,
Medina-Gómez C,
Ge B,
Chen SH,
Choi K,
Oei L,
Fraser J,
Kraaij R,
Hibbs MA,
Gregson CL,
Paquette D,
Hofman A,
Wibom C,
Tranah GJ,
Marshall M,
Gardiner BB,
Cremin K,
Auer P,
Hsu L,
Ring S,
Tung JY,
Thorleifsson G,
Enneman AW,
van Schoor NM,
de Groot LC,
van der Velde N,
Melin B,
Kemp JP,
Christiansen C,
Sayers A,
Zhou Y,
Calderari S,
van Rooij J,
Carlson C,
Peters U,
Berlivet S,
Dostie J,
Uitterlinden AG,
Williams SR,
Farber C,
Grinberg D,
LaCroix AZ,
Haessler J,
Chasman DI,
Giulianini F,
Rose LM,
Ridker PM,
Eisman JA,
Nguyen TV,
Center JR,
Nogues X,
Nogues X,
Garcia-Giralt N,
Launer LL,
Gudnason V,
Mellström D,
Vandenput L,
Amin N,
van Duijn CM,
Karlsson MK,
Ljunggren Ö,
Svensson O,
Hallmans G,
Rousseau F,
Giroux S,
Bussière J,
Arp PP,
Koromani F,
Prince RL,
Lewis JR,
Langdahl BL,
Hermann AP,
Jensen JE,
Kaptoge S,
Khaw KT,
Reeve J,
Formosa MM,
Xuereb-Anastasi A,
Åkesson K,
McGuigan FE,
Garg G,
Olmos JM,
Zarrabeitia MT,
Riancho JA,
Ralston SH,
Alonso N,
Jiang X,
Goltzman D,
Pastinen T,
Grundberg E,
Gauguier D,
Orwoll ES,
Karasik D,
Davey-Smith G,
Smith AV,
Smith AV,
Siggeirsdottir K,
Harris TB,
Zillikens MC,
van Meurs JB,
Thorsteinsdottir U,
Maurano MT,
Timpson NJ,
Soranzo N,
Durbin R,
Wilson SG,
Ntzani EE,
Brown MA,
Stefansson K,
Hinds DA,
Spector T,
Cupples LA,
Ohlsson C,
Greenwood CM,
Jackson RD,
Rowe DW,
Loomis CA,
Evans DM,
Ackert-Bicknell CL,
Joyner AL,
Duncan EL,
Kiel DP,
Rivadeneira F,
Richards JB
AOGC Consortium · UK10K Consortium
Nature · 2015 · PMID 26367794
7 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
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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
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