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Wood AR,
showing the first 20.
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Morris AP,
Voight BF,
Teslovich TM,
Ferreira T,
Segrè AV,
Steinthorsdottir V,
Strawbridge RJ,
Khan H,
Grallert H,
Mahajan A,
Prokopenko I,
Kang HM
and 192 more — show all
Dina C,
Esko T,
Fraser RM,
Kanoni S,
Kumar A,
Lagou V,
Langenberg C,
Luan J,
Lindgren CM,
Müller-Nurasyid M,
Pechlivanis S,
Rayner NW,
Scott LJ,
Wiltshire S,
Yengo L,
Kinnunen L,
Rossin EJ,
Raychaudhuri S,
Johnson AD,
Dimas AS,
Loos RJ,
Vedantam S,
Chen H,
Florez JC,
Fox C,
Liu CT,
Rybin D,
Couper DJ,
Kao WH,
Li M,
Cornelis MC,
Kraft P,
Sun Q,
van Dam RM,
Stringham HM,
Chines PS,
Fischer K,
Fontanillas P,
Holmen OL,
Hunt SE,
Jackson AU,
Kong A,
Lawrence R,
Meyer J,
Perry JR,
Platou CG,
Potter S,
Rehnberg E,
Robertson N,
Sivapalaratnam S,
Stančáková A,
Stirrups K,
Thorleifsson G,
Tikkanen E,
Wood AR,
Almgren P,
Atalay M,
Benediktsson R,
Bonnycastle LL,
Burtt N,
Carey J,
Charpentier G,
Crenshaw AT,
Doney AS,
Dorkhan M,
Edkins S,
Emilsson V,
Eury E,
Forsen T,
Gertow K,
Gigante B,
Grant GB,
Groves CJ,
Guiducci C,
Herder C,
Hreidarsson AB,
Hui J,
James A,
Jonsson A,
Rathmann W,
Klopp N,
Kravic J,
Krjutškov K,
Langford C,
Leander K,
Lindholm E,
Lobbens S,
Männistö S,
Mirza G,
Mühleisen TW,
Musk B,
Parkin M,
Rallidis L,
Saramies J,
Sennblad B,
Shah S,
Sigurðsson G,
Silveira A,
Steinbach G,
Thorand B,
Trakalo J,
Veglia F,
Wennauer R,
Winckler W,
Zabaneh D,
Campbell H,
van Duijn C,
Uitterlinden AG,
Hofman A,
Sijbrands E,
Abecasis GR,
Owen KR,
Zeggini E,
Trip MD,
Forouhi NG,
Syvänen AC,
Eriksson JG,
Peltonen L,
Nöthen MM,
Balkau B,
Palmer CN,
Lyssenko V,
Tuomi T,
Isomaa B,
Hunter DJ,
Qi L,
Shuldiner AR,
Roden M,
Barroso I,
Wilsgaard T,
Beilby J,
Hovingh K,
Price JF,
Wilson JF,
Rauramaa R,
Lakka TA,
Lind L,
Dedoussis G,
Njølstad I,
Pedersen NL,
Khaw KT,
Wareham NJ,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Korpi-Hyövälti E,
Saltevo J,
Laakso M,
Kuusisto J,
Metspalu A,
Collins FS,
Mohlke KL,
Bergman RN,
Tuomilehto J,
Boehm BO,
Gieger C,
Hveem K,
Cauchi S,
Froguel P,
Baldassarre D,
Tremoli E,
Humphries SE,
Saleheen D,
Danesh J,
Ingelsson E,
Ripatti S,
Salomaa V,
Erbel R,
Jöckel KH,
Moebus S,
Peters A,
Illig T,
de Faire U,
Hamsten A,
Morris AD,
Donnelly PJ,
Frayling TM,
Hattersley AT,
Boerwinkle E,
Melander O,
Kathiresan S,
Nilsson PM,
Deloukas P,
Thorsteinsdottir U,
Groop LC,
Stefansson K,
Hu F,
Pankow JS,
Dupuis J,
Meigs JB,
Altshuler D,
Boehnke M,
McCarthy MI
Wellcome Trust Case Control Consortium · Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Investigators and 4 more consortia
Nature genetics · 2012 · PMID 22885922 · open access
10 pages
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Mahajan A,
Go MJ,
Zhang W,
Below JE,
Gaulton KJ,
Ferreira T,
Horikoshi M,
Johnson AD,
Ng MC,
Prokopenko I,
Saleheen D,
Wang X
and 322 more — show all
Zeggini E,
Abecasis GR,
Adair LS,
Almgren P,
Atalay M,
Aung T,
Baldassarre D,
Balkau B,
Bao Y,
Barnett AH,
Barroso I,
Basit A,
Been LF,
Beilby J,
Bell GI,
Benediktsson R,
Bergman RN,
Boehm BO,
Boerwinkle E,
Bonnycastle LL,
Burtt N,
Cai Q,
Campbell H,
Carey J,
Cauchi S,
Caulfield M,
Chan JC,
Chang LC,
Chang TJ,
Chang YC,
Charpentier G,
Chen CH,
Chen H,
Chen YT,
Chia KS,
Chidambaram M,
Chines PS,
Cho NH,
Cho YM,
Chuang LM,
Chuang LM,
Collins FS,
Cornelis MC,
Couper DJ,
Crenshaw AT,
van Dam RM,
Danesh J,
Das D,
de Faire U,
Dedoussis G,
Deloukas P,
Dimas AS,
Dina C,
Doney AS,
Donnelly PJ,
Dorkhan M,
van Duijn C,
Dupuis J,
Edkins S,
Elliott P,
Emilsson V,
Erbel R,
Eriksson JG,
Escobedo J,
Esko T,
Eury E,
Florez JC,
Fontanillas P,
Forouhi NG,
Forsen T,
Fox C,
Fraser RM,
Frayling TM,
Froguel P,
Frossard P,
Gao Y,
Gertow K,
Gieger C,
Gigante B,
Grallert H,
Grant GB,
Grrop LC,
Groves CJ,
Grundberg E,
Guiducci C,
Hamsten A,
Han BG,
Hara K,
Hassanali N,
Hattersley AT,
Hayward C,
Hedman AK,
Herder C,
Hofman A,
Holmen OL,
Hovingh K,
Hreidarsson AB,
Hu C,
Hu FB,
Hui J,
Humphries SE,
Hunt SE,
Hunter DJ,
Hveem K,
Hydrie ZI,
Ikegami H,
Illig T,
Ingelsson E,
Islam M,
Isomaa B,
Jackson AU,
Jafar T,
James A,
Jia W,
Jöckel KH,
Jonsson A,
Jowett JB,
Kadowaki T,
Kang HM,
Kanoni S,
Kao WH,
Kathiresan S,
Kato N,
Katulanda P,
Keinanen-Kiukaanniemi KM,
Kelly AM,
Khan H,
Khaw KT,
Khor CC,
Kim HL,
Kim S,
Kim YJ,
Kinnunen L,
Klopp N,
Kong A,
Korpi-Hyövälti E,
Kowlessur S,
Kraft P,
Kravic J,
Kristensen MM,
Krithika S,
Kumar A,
Kumate J,
Kuusisto J,
Kwak SH,
Laakso M,
Lagou V,
Lakka TA,
Langenberg C,
Langford C,
Lawrence R,
Leander K,
Lee JM,
Lee NR,
Li M,
Li X,
Li Y,
Liang J,
Liju S,
Lim WY,
Lind L,
Lindgren CM,
Lindholm E,
Liu CT,
Liu JJ,
Lobbens S,
Long J,
Loos RJ,
Lu W,
Luan J,
Lyssenko V,
Ma RC,
Maeda S,
Mägi R,
Männisto S,
Matthews DR,
Meigs JB,
Melander O,
Metspalu A,
Meyer J,
Mirza G,
Mihailov E,
Moebus S,
Mohan V,
Mohlke KL,
Morris AD,
Mühleisen TW,
Müller-Nurasyid M,
Musk B,
Nakamura J,
Nakashima E,
Navarro P,
Ng PK,
Nica AC,
Nilsson PM,
Njølstad I,
Nöthen MM,
Ohnaka K,
Ong TH,
Owen KR,
Palmer CN,
Pankow JS,
Park KS,
Parkin M,
Pechlivanis S,
Pedersen NL,
Peltonen L,
Perry JR,
Peters A,
Pinidiyapathirage JM,
Platou CG,
Potter S,
Price JF,
Qi L,
Radha V,
Rallidis L,
Rasheed A,
Rathman W,
Rauramaa R,
Raychaudhuri S,
Rayner NW,
Rees SD,
Rehnberg E,
Ripatti S,
Robertson N,
Roden M,
Rossin EJ,
Rudan I,
Rybin D,
Saaristo TE,
Salomaa V,
Saltevo J,
Samuel M,
Sanghera DK,
Saramies J,
Scott J,
Scott LJ,
Scott RA,
Segrè AV,
Sehmi J,
Sennblad B,
Shah N,
Shah S,
Shera AS,
Shu XO,
Shuldiner AR,
Sigurđsson G,
Sijbrands E,
Silveira A,
Sim X,
Sivapalaratnam S,
Small KS,
So WY,
Stančáková A,
Stefansson K,
Steinbach G,
Steinthorsdottir V,
Stirrups K,
Strawbridge RJ,
Stringham HM,
Sun Q,
Suo C,
Syvänen AC,
Takayanagi R,
Takeuchi F,
Tay WT,
Teslovich TM,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tikkanen E,
Trakalo J,
Tremoli E,
Trip MD,
Tsai FJ,
Tuomi T,
Tuomilehto J,
Uitterlinden AG,
Valladares-Salgado A,
Vedantam S,
Veglia F,
Voight BF,
Wang C,
Wareham NJ,
Wennauer R,
Wickremasinghe AR,
Wilsgaard T,
Wilson JF,
Wiltshire S,
Winckler W,
Wong TY,
Wood AR,
Wu JY,
Wu Y,
Yamamoto K,
Yamauchi T,
Yang M,
Yengo L,
Yokota M,
Young R,
Zabaneh D,
Zhang F,
Zhang R,
Zheng W,
Zheng W,
Zimmet PZ,
Altshuler D,
Bowden DW,
Cho YS,
Cox NJ,
Cruz M,
Hanis CL,
Kooner J,
Lee JY,
Seielstad M,
Teo YY,
Boehnke M,
Parra EJ,
Chambers JC,
Tai ES,
McCarthy MI,
Morris AP
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 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
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Kanoni S,
Graham SE,
Wang Y,
Surakka I,
Ramdas S,
Zhu X,
Clarke SL,
Bhatti KF,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
and 527 more — show all
Zajac GJM,
Wu KH,
Ntalla I,
Hui Q,
Klarin D,
Hilliard AT,
Wang Z,
Xue C,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Hwang MY,
Han S,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Havulinna AS,
Veturi Y,
Pacheco JA,
Rosenthal EA,
Lingren T,
Feng Q,
Kullo IJ,
Narita A,
Takayama J,
Martin HC,
Hunt KA,
Trivedi B,
Haessler J,
Giulianini F,
Bradford Y,
Miller JE,
Campbell A,
Lin K,
Millwood IY,
Rasheed A,
Hindy G,
Faul JD,
Zhao W,
Weir DR,
Turman C,
Huang H,
Graff M,
Choudhury A,
Sengupta D,
Mahajan A,
Brown MR,
Zhang W,
Yu K,
Schmidt EM,
Pandit A,
Gustafsson S,
Yin X,
Luan J,
Zhao JH,
Matsuda F,
Jang HM,
Yoon K,
Medina-Gomez C,
Pitsillides A,
Hottenga JJ,
Wood AR,
Ji Y,
Gao Z,
Haworth S,
Yousri NA,
Mitchell RE,
Chai JF,
Aadahl M,
Bjerregaard AA,
Yao J,
Manichaikul A,
Hwu CM,
Hung YJ,
Warren HR,
Ramirez J,
Bork-Jensen J,
Kårhus LL,
Goel A,
Sabater-Lleal M,
Noordam R,
Mauro P,
Matteo F,
McDaid AF,
Marques-Vidal P,
Wielscher M,
Trompet S,
Sattar N,
Møllehave LT,
Munz M,
Zeng L,
Huang J,
Yang B,
Poveda A,
Kurbasic A,
Lamina C,
Forer L,
Scholz M,
Galesloot TE,
Bradfield JP,
Ruotsalainen SE,
Daw E,
Zmuda JM,
Mitchell JS,
Fuchsberger C,
Christensen H,
Brody JA,
Vazquez-Moreno M,
Feitosa MF,
Wojczynski MK,
Wang Z,
Preuss MH,
Mangino M,
Christofidou P,
Verweij N,
Benjamins JW,
Engmann J,
Tsao NL,
Verma A,
Slieker RC,
Lo KS,
Zilhao NR,
Le P,
Kleber ME,
Delgado GE,
Huo S,
Ikeda DD,
Iha H,
Yang J,
Liu J,
Demirkan A,
Leonard HL,
Marten J,
Frank M,
Schmidt B,
Smyth LJ,
Cañadas-Garre M,
Wang C,
Nakatochi M,
Wong A,
Hutri-Kähönen N,
Sim X,
Xia R,
Huerta-Chagoya A,
Fernandez-Lopez JC,
Lyssenko V,
Nongmaithem SS,
Bayyana S,
Stringham HM,
Irvin MR,
Oldmeadow C,
Kim HN,
Ryu S,
Timmers PRHJ,
Arbeeva L,
Dorajoo R,
Lange LA,
Prasad G,
Lorés-Motta L,
Pauper M,
Long J,
Li X,
Theusch E,
Takeuchi F,
Spracklen CN,
Loukola A,
Bollepalli S,
Warner SC,
Wang YX,
Wei WB,
Nutile T,
Ruggiero D,
Sung YJ,
Chen S,
Liu F,
Yang J,
Kentistou KA,
Banas B,
Nardone GG,
Meidtner K,
Bielak LF,
Smith JA,
Hebbar P,
Farmaki AE,
Hofer E,
Lin M,
Concas MP,
Vaccargiu S,
van der Most PJ,
Pitkänen N,
Cade BE,
van der Laan SW,
Chitrala KN,
Weiss S,
Bentley AR,
Doumatey AP,
Adeyemo AA,
Lee JY,
Petersen ERB,
Nielsen AA,
Choi HS,
Nethander M,
Freitag-Wolf S,
Southam L,
Rayner NW,
Wang CA,
Lin SY,
Wang JS,
Couture C,
Lyytikäinen LP,
Nikus K,
Cuellar-Partida G,
Vestergaard H,
Hidalgo B,
Giannakopoulou O,
Cai Q,
Obura MO,
van Setten J,
Li X,
Liang J,
Tang H,
Terzikhan N,
Shin JH,
Jackson RD,
Reiner AP,
Martin LW,
Chen Z,
Li L,
Kawaguchi T,
Thiery J,
Bis JC,
Launer LJ,
Li H,
Nalls MA,
Raitakari OT,
Ichihara S,
Wild SH,
Nelson CP,
Campbell H,
Jäger S,
Nabika T,
Al-Mulla F,
Niinikoski H,
Braund PS,
Kolcic I,
Kovacs P,
Giardoglou T,
Katsuya T,
de Kleijn D,
de Borst GJ,
Kim EK,
Adams HHH,
Ikram MA,
Zhu X,
Asselbergs FW,
Kraaijeveld AO,
Beulens JWJ,
Shu XO,
Rallidis LS,
Pedersen O,
Hansen T,
Mitchell P,
Hewitt AW,
Kähönen M,
Pérusse L,
Bouchard C,
Tönjes A,
Chen YI,
Pennell CE,
Mori TA,
Lieb W,
Franke A,
Ohlsson C,
Mellström D,
Cho YS,
Lee H,
Yuan JM,
Koh WP,
Rhee SY,
Woo JT,
Heid IM,
Stark KJ,
Zimmermann ME,
Völzke H,
Homuth G,
Evans MK,
Zonderman AB,
Polasek O,
Pasterkamp G,
Hoefer IE,
Redline S,
Pahkala K,
Oldehinkel AJ,
Snieder H,
Biino G,
Schmidt R,
Schmidt H,
Bandinelli S,
Dedoussis G,
Thanaraj TA,
Kardia SLR,
Peyser PA,
Kato N,
Schulze MB,
Girotto G,
Böger CA,
Jung B,
Joshi PK,
Bennett DA,
De Jager PL,
Lu X,
Mamakou V,
Brown M,
Caulfield MJ,
Munroe PB,
Guo X,
Ciullo M,
Jonas JB,
Samani NJ,
Kaprio J,
Pajukanta P,
Tusié-Luna T,
Aguilar-Salinas CA,
Adair LS,
Bechayda SA,
de Silva HJ,
Wickremasinghe AR,
Krauss RM,
Wu JY,
Zheng W,
Hollander AI,
Bharadwaj D,
Correa A,
Wilson JG,
Lind L,
Heng CK,
Nelson AE,
Golightly YM,
Wilson JF,
Penninx B,
Kim HL,
Attia J,
Scott RJ,
Rao DC,
Arnett DK,
Hunt SC,
Walker M,
Koistinen HA,
Chandak GR,
Mercader JM,
Costanzo MC,
Jang D,
Burtt NP,
Villalpando CG,
Orozco L,
Fornage M,
Tai E,
van Dam RM,
Lehtimäki T,
Chaturvedi N,
Yokota M,
Liu J,
Reilly DF,
McKnight AJ,
Kee F,
Jöckel KH,
McCarthy MI,
Palmer CNA,
Vitart V,
Hayward C,
Simonsick E,
van Duijn CM,
Jin ZB,
Qu J,
Hishigaki H,
Lin X,
März W,
Gudnason V,
Tardif JC,
Lettre G,
Hart LM',
Elders PJM,
Damrauer SM,
Kumari M,
Kivimaki M,
van der Harst P,
Spector TD,
Loos RJF,
Province MA,
Parra EJ,
Cruz M,
Psaty BM,
Brandslund I,
Pramstaller PP,
Rotimi CN,
Christensen K,
Ripatti S,
Widén E,
Hakonarson H,
Grant SFA,
Kiemeney LALM,
de Graaf J,
Loeffler M,
Kronenberg F,
Gu D,
Erdmann J,
Schunkert H,
Franks PW,
Linneberg A,
Jukema JW,
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Hayes MG,
Frayling TM,
Hivert MF,
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Hyppönen E,
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Early Growth Genetics (EGG) Consortium
Human molecular genetics · 2018 · PMID 29309628 · open access
1 page
Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms
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Gut · 2019 · PMID 30661054
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Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour
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Ruth KS,
Tuke MA,
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Harrison JW,
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Nature communications · 2019 · PMID 30952852 · open access
1 page
A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin-creatinine ratio
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Human molecular genetics · 2019 · PMID 31630189 · open access
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.