For researchers
Is your paper here?
2,677 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.
4 matches for
Kleinman A.
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
Lee JJ,
Wedow R,
Okbay A,
Kong E,
Maghzian O,
Zacher M,
Nguyen-Viet TA,
Bowers P,
Sidorenko J,
Karlsson Linnér R,
Fontana MA,
Kundu T
and 65 more — show all
Lee C,
Li H,
Li R,
Royer R,
Timshel PN,
Walters RK,
Willoughby EA,
Yengo L,
Alver M,
Bao Y,
Clark DW,
Day FR,
Furlotte NA,
Joshi PK,
Kemper KE,
Kleinman A,
Langenberg C,
Mägi R,
Trampush JW,
Verma SS,
Wu Y,
Lam M,
Zhao JH,
Zheng Z,
Boardman JD,
Campbell H,
Freese J,
Harris KM,
Hayward C,
Herd P,
Kumari M,
Lencz T,
Luan J,
Malhotra AK,
Metspalu A,
Milani L,
Ong KK,
Perry JRB,
Porteous DJ,
Ritchie MD,
Smart MC,
Smith BH,
Tung JY,
Wareham NJ,
Wilson JF,
Beauchamp JP,
Conley DC,
Esko T,
Lehrer SF,
Magnusson PKE,
Oskarsson S,
Pers TH,
Robinson MR,
Thom K,
Watson C,
Chabris CF,
Meyer MN,
Laibson DI,
Yang J,
Johannesson M,
Koellinger PD,
Turley P,
Visscher PM,
Benjamin DJ,
Cesarini D
23andMe Research Team · COGENT (Cognitive Genomics Consortium) and 1 more consortia
Nature genetics · 2018 · PMID 30038396
12 pages+
An atlas of genetic influences on osteoporosis in humans and mice
Morris JA,
Kemp JP,
Youlten SE,
Laurent L,
Logan JG,
Chai RC,
Vulpescu NA,
Forgetta V,
Kleinman A,
Mohanty ST,
Sergio CM,
Quinn J
and 47 more — show all
Nguyen-Yamamoto L,
Luco AL,
Vijay J,
Simon MM,
Pramatarova A,
Medina-Gomez C,
Trajanoska K,
Ghirardello EJ,
Butterfield NC,
Curry KF,
Leitch VD,
Sparkes PC,
Adoum AT,
Mannan NS,
Komla-Ebri DSK,
Pollard AS,
Dewhurst HF,
Hassall TAD,
Beltejar MG,
Adams DJ,
Vaillancourt SM,
Kaptoge S,
Baldock P,
Cooper C,
Reeve J,
Ntzani EE,
Evangelou E,
Ohlsson C,
Karasik D,
Rivadeneira F,
Kiel DP,
Tobias JH,
Gregson CL,
Harvey NC,
Grundberg E,
Goltzman D,
Adams DJ,
Lelliott CJ,
Hinds DA,
Ackert-Bicknell CL,
Hsu YH,
Maurano MT,
Croucher PI,
Williams GR,
Bassett JHD,
Evans DM,
Richards JB
23andMe Research Team
Nature genetics · 2019 · PMID 30598549 · open access
12 pages+
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
Karlsson Linnér R,
Biroli P,
Kong E,
Meddens SFW,
Wedow R,
Fontana MA,
Lebreton M,
Tino SP,
Abdellaoui A,
Hammerschlag AR,
Nivard MG,
Okbay A
and 80 more — show all
Rietveld CA,
Timshel PN,
Trzaskowski M,
Vlaming R,
Zünd CL,
Bao Y,
Buzdugan L,
Caplin AH,
Chen CY,
Eibich P,
Fontanillas P,
Gonzalez JR,
Joshi PK,
Karhunen V,
Kleinman A,
Levin RZ,
Lill CM,
Meddens GA,
Muntané G,
Sanchez-Roige S,
Rooij FJV,
Taskesen E,
Wu Y,
Zhang F,
Auton A,
Boardman JD,
Clark DW,
Conlin A,
Dolan CC,
Fischbacher U,
Groenen PJF,
Harris KM,
Hasler G,
Hofman A,
Ikram MA,
Jain S,
Karlsson R,
Kessler RC,
Kooyman M,
MacKillop J,
Männikkö M,
Morcillo-Suarez C,
McQueen MB,
Schmidt KM,
Smart MC,
Sutter M,
Thurik AR,
Uitterlinden AG,
White J,
Wit H,
Yang J,
Bertram L,
Boomsma DI,
Esko T,
Fehr E,
Hinds DA,
Johannesson M,
Kumari M,
Laibson D,
Magnusson PKE,
Meyer MN,
Navarro A,
Palmer AA,
Pers TH,
Posthuma D,
Schunk D,
Stein MB,
Svento R,
Tiemeier H,
Timmers PRHJ,
Turley P,
Ursano RJ,
Wagner GG,
Wilson JF,
Gratten J,
Lee JJ,
Cesarini D,
Benjamin DJ,
Koellinger PD,
Beauchamp JP
23and Me Research Team · eQTLgen Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30643258
12 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
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.