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2 matches for
Arnlöv J.
Defining the role of common variation in the genomic and biological architecture of adult human height
Wood AR,
Esko T,
Yang J,
Vedantam S,
Pers TH,
Gustafsson S,
Chu AY,
Estrada K,
Luan J,
Kutalik Z,
Amin N,
Buchkovich ML
and 433 more — show all
Croteau-Chonka DC,
Day FR,
Duan Y,
Fall T,
Fehrmann R,
Ferreira T,
Jackson AU,
Karjalainen J,
Lo KS,
Locke AE,
Mägi R,
Mihailov E,
Porcu E,
Randall JC,
Scherag A,
Vinkhuyzen AA,
Westra HJ,
Winkler TW,
Workalemahu T,
Zhao JH,
Absher D,
Albrecht E,
Anderson D,
Baron J,
Beekman M,
Demirkan A,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Fraser RM,
Goel A,
Gong J,
Justice AE,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Lui JC,
Mangino M,
Mateo Leach I,
Medina-Gomez C,
Nalls MA,
Nyholt DR,
Palmer CD,
Pasko D,
Pechlivanis S,
Prokopenko I,
Ried JS,
Ripke S,
Shungin D,
Stancáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Afzal U,
Arnlöv J,
Arscott GM,
Bandinelli S,
Barrett A,
Bellis C,
Bennett AJ,
Berne C,
Blüher M,
Bolton JL,
Böttcher Y,
Boyd HA,
Bruinenberg M,
Buckley BM,
Buyske S,
Caspersen IH,
Chines PS,
Clarke R,
Claudi-Boehm S,
Cooper M,
Daw EW,
De Jong PA,
Deelen J,
Delgado G,
Denny JC,
Dhonukshe-Rutten R,
Dimitriou M,
Doney AS,
Dörr M,
Eklund N,
Eury E,
Folkersen L,
Garcia ME,
Geller F,
Giedraitis V,
Go AS,
Grallert H,
Grammer TB,
Gräßler J,
Grönberg H,
de Groot LC,
Groves CJ,
Haessler J,
Hall P,
Haller T,
Hallmans G,
Hannemann A,
Hartman CA,
Hassinen M,
Hayward C,
Heard-Costa NL,
Helmer Q,
Hemani G,
Henders AK,
Hillege HL,
Hlatky MA,
Hoffmann W,
Hoffmann P,
Holmen O,
Houwing-Duistermaat JJ,
Illig T,
Isaacs A,
James AL,
Jeff J,
Johansen B,
Johansson Å,
Jolley J,
Juliusdottir T,
Junttila J,
Kho AN,
Kinnunen L,
Klopp N,
Kocher T,
Kratzer W,
Lichtner P,
Lind L,
Lindström J,
Lobbens S,
Lorentzon M,
Lu Y,
Lyssenko V,
Magnusson PK,
Mahajan A,
Maillard M,
McArdle WL,
McKenzie CA,
McLachlan S,
McLaren PJ,
Menni C,
Merger S,
Milani L,
Moayyeri A,
Monda KL,
Morken MA,
Müller G,
Müller-Nurasyid M,
Musk AW,
Narisu N,
Nauck M,
Nolte IM,
Nöthen MM,
Oozageer L,
Pilz S,
Rayner NW,
Renstrom F,
Robertson NR,
Rose LM,
Roussel R,
Sanna S,
Scharnagl H,
Scholtens S,
Schumacher FR,
Schunkert H,
Scott RA,
Sehmi J,
Seufferlein T,
Shi J,
Silventoinen K,
Smit JH,
Smith AV,
Smolonska J,
Stanton AV,
Stirrups K,
Stott DJ,
Stringham HM,
Sundström J,
Swertz MA,
Syvänen AC,
Tayo BO,
Thorleifsson G,
Tyrer JP,
van Dijk S,
van Schoor NM,
van der Velde N,
van Heemst D,
van Oort FV,
Vermeulen SH,
Verweij N,
Vonk JM,
Waite LL,
Waldenberger M,
Wennauer R,
Wilkens LR,
Willenborg C,
Wilsgaard T,
Wojczynski MK,
Wong A,
Wright AF,
Zhang Q,
Arveiler D,
Bakker SJ,
Beilby J,
Bergman RN,
Bergmann S,
Biffar R,
Blangero J,
Boomsma DI,
Bornstein SR,
Bovet P,
Brambilla P,
Brown MJ,
Campbell H,
Caulfield MJ,
Chakravarti A,
Collins R,
Collins FS,
Crawford DC,
Cupples LA,
Danesh J,
de Faire U,
den Ruijter HM,
Erbel R,
Erdmann J,
Eriksson JG,
Farrall M,
Ferrannini E,
Ferrières J,
Ford I,
Forouhi NG,
Forrester T,
Gansevoort RT,
Gejman PV,
Gieger C,
Golay A,
Gottesman O,
Gudnason V,
Gyllensten U,
Haas DW,
Hall AS,
Harris TB,
Hattersley AT,
Heath AC,
Hengstenberg C,
Hicks AA,
Hindorff LA,
Hingorani AD,
Hofman A,
Hovingh GK,
Humphries SE,
Hunt SC,
Hypponen E,
Jacobs KB,
Jarvelin MR,
Jousilahti P,
Jula AM,
Kaprio J,
Kastelein JJ,
Kayser M,
Kee F,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Kooner JS,
Kooperberg C,
Koskinen S,
Kovacs P,
Kraja AT,
Kumari M,
Kuusisto J,
Lakka TA,
Langenberg C,
Le Marchand L,
Lehtimäki T,
Lupoli S,
Madden PA,
Männistö S,
Manunta P,
Marette A,
Matise TC,
McKnight B,
Meitinger T,
Moll FL,
Montgomery GW,
Morris AD,
Morris AP,
Murray JC,
Nelis M,
Ohlsson C,
Oldehinkel AJ,
Ong KK,
Ouwehand WH,
Pasterkamp G,
Peters A,
Pramstaller PP,
Price JF,
Qi L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Ritchie M,
Rudan I,
Salomaa V,
Samani NJ,
Saramies J,
Sarzynski MA,
Schwarz PE,
Sebert S,
Sever P,
Shuldiner AR,
Sinisalo J,
Steinthorsdottir V,
Stolk RP,
Tardif JC,
Tönjes A,
Tremblay A,
Tremoli E,
Virtamo J,
Vohl MC,
Amouyel P,
Asselbergs FW,
Assimes TL,
Bochud M,
Boehm BO,
Boerwinkle E,
Bottinger EP,
Bouchard C,
Cauchi S,
Chambers JC,
Chanock SJ,
Cooper RS,
de Bakker PI,
Dedoussis G,
Ferrucci L,
Franks PW,
Froguel P,
Groop LC,
Haiman CA,
Hamsten A,
Hayes MG,
Hui J,
Hunter DJ,
Hveem K,
Jukema JW,
Kaplan RC,
Kivimaki M,
Kuh D,
Laakso M,
Liu Y,
Martin NG,
März W,
Melbye M,
Moebus S,
Munroe PB,
Njølstad I,
Oostra BA,
Palmer CN,
Pedersen NL,
Perola M,
Pérusse L,
Peters U,
Powell JE,
Power C,
Quertermous T,
Rauramaa R,
Reinmaa E,
Ridker PM,
Rivadeneira F,
Rotter JI,
Saaristo TE,
Saleheen D,
Schlessinger D,
Slagboom PE,
Snieder H,
Spector TD,
Strauch K,
Stumvoll M,
Tuomilehto J,
Uusitupa M,
van der Harst P,
Völzke H,
Walker M,
Wareham NJ,
Watkins H,
Wichmann HE,
Wilson JF,
Zanen P,
Deloukas P,
Heid IM,
Lindgren CM,
Mohlke KL,
Speliotes EK,
Thorsteinsdottir U,
Barroso I,
Fox CS,
North KE,
Strachan DP,
Beckmann JS,
Berndt SI,
Boehnke M,
Borecki IB,
McCarthy MI,
Metspalu A,
Stefansson K,
Uitterlinden AG,
van Duijn CM,
Franke L,
Willer CJ,
Price AL,
Lettre G,
Loos RJ,
Weedon MN,
Ingelsson E,
O'Connell JR,
Abecasis GR,
Chasman DI,
Goddard ME,
Visscher PM,
Hirschhorn JN,
Frayling TM
Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25282103 · open access
12 pages+
CUBN is a gene locus for albuminuria
Böger CA,
Chen MH,
Tin A,
Olden M,
Köttgen A,
de Boer IH,
Fuchsberger C,
O'Seaghdha CM,
Pattaro C,
Teumer A,
Liu CT,
Glazer NL
and 103 more — show all
Li M,
O'Connell JR,
Tanaka T,
Peralta CA,
Kutalik Z,
Luan J,
Zhao JH,
Hwang SJ,
Akylbekova E,
Kramer H,
van der Harst P,
Smith AV,
Lohman K,
de Andrade M,
Hayward C,
Kollerits B,
Tönjes A,
Aspelund T,
Ingelsson E,
Eiriksdottir G,
Launer LJ,
Harris TB,
Shuldiner AR,
Mitchell BD,
Arking DE,
Franceschini N,
Boerwinkle E,
Egan J,
Hernandez D,
Reilly M,
Townsend RR,
Lumley T,
Siscovick DS,
Psaty BM,
Kestenbaum B,
Haritunians T,
Bergmann S,
Vollenweider P,
Waeber G,
Mooser V,
Waterworth D,
Johnson AD,
Florez JC,
Meigs JB,
Lu X,
Turner ST,
Atkinson EJ,
Leak TS,
Aasarød K,
Skorpen F,
Syvänen AC,
Illig T,
Baumert J,
Koenig W,
Krämer BK,
Devuyst O,
Mychaleckyj JC,
Minelli C,
Bakker SJ,
Kedenko L,
Paulweber B,
Coassin S,
Endlich K,
Kroemer HK,
Biffar R,
Stracke S,
Völzke H,
Stumvoll M,
Mägi R,
Campbell H,
Vitart V,
Hastie ND,
Gudnason V,
Kardia SL,
Liu Y,
Polasek O,
Curhan G,
Kronenberg F,
Prokopenko I,
Rudan I,
Arnlöv J,
Hallan S,
Navis G,
Parsa A,
Ferrucci L,
Coresh J,
Shlipak MG,
Bull SB,
Paterson NJ,
Wichmann HE,
Wareham NJ,
Loos RJ,
Rotter JI,
Pramstaller PP,
Cupples LA,
Beckmann JS,
Yang Q,
Heid IM,
Rettig R,
Dreisbach AW,
Bochud M,
Fox CS,
Kao WH
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
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.