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8 matches for
Glahn DC.
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Davies G,
Lam M,
Harris SE,
Trampush JW,
Luciano M,
Hill WD,
Hagenaars SP,
Ritchie SJ,
Marioni RE,
Fawns-Ritchie C,
Liewald DCM,
Okely JA
and 212 more — show all
Ahola-Olli AV,
Barnes CLK,
Bertram L,
Bis JC,
Burdick KE,
Christoforou A,
DeRosse P,
Djurovic S,
Espeseth T,
Giakoumaki S,
Giddaluru S,
Gustavson DE,
Hayward C,
Hofer E,
Ikram MA,
Karlsson R,
Knowles E,
Lahti J,
Leber M,
Li S,
Mather KA,
Melle I,
Morris D,
Oldmeadow C,
Palviainen T,
Payton A,
Pazoki R,
Petrovic K,
Reynolds CA,
Sargurupremraj M,
Scholz M,
Smith JA,
Smith AV,
Terzikhan N,
Thalamuthu A,
Trompet S,
van der Lee SJ,
Ware EB,
Windham BG,
Wright MJ,
Yang J,
Yu J,
Ames D,
Amin N,
Amouyel P,
Andreassen OA,
Armstrong NJ,
Assareh AA,
Attia JR,
Attix D,
Avramopoulos D,
Bennett DA,
Böhmer AC,
Boyle PA,
Brodaty H,
Campbell H,
Cannon TD,
Cirulli ET,
Congdon E,
Conley ED,
Corley J,
Cox SR,
Dale AM,
Dehghan A,
Dick D,
Dickinson D,
Eriksson JG,
Evangelou E,
Faul JD,
Ford I,
Freimer NA,
Gao H,
Giegling I,
Gillespie NA,
Gordon SD,
Gottesman RF,
Griswold ME,
Gudnason V,
Harris TB,
Hartmann AM,
Hatzimanolis A,
Heiss G,
Holliday EG,
Joshi PK,
Kähönen M,
Kardia SLR,
Karlsson I,
Kleineidam L,
Knopman DS,
Kochan NA,
Konte B,
Kwok JB,
Le Hellard S,
Lee T,
Lehtimäki T,
Li SC,
Lill CM,
Liu T,
Koini M,
London E,
Longstreth WT Jr,
Lopez OL,
Loukola A,
Luck T,
Lundervold AJ,
Lundquist A,
Lyytikäinen LP,
Martin NG,
Montgomery GW,
Murray AD,
Need AC,
Noordam R,
Nyberg L,
Ollier W,
Papenberg G,
Pattie A,
Polasek O,
Poldrack RA,
Psaty BM,
Reppermund S,
Riedel-Heller SG,
Rose RJ,
Rotter JI,
Roussos P,
Rovio SP,
Saba Y,
Sabb FW,
Sachdev PS,
Satizabal CL,
Satizabal CL,
Schmid M,
Scott RJ,
Scult MA,
Simino J,
Slagboom PE,
Smyrnis N,
Soumaré A,
Stefanis NC,
Stott DJ,
Straub RE,
Sundet K,
Taylor AM,
Taylor KD,
Tzoulaki I,
Tzourio C,
Uitterlinden A,
Vitart V,
Voineskos AN,
Kaprio J,
Wagner M,
Wagner H,
Weinhold L,
Wen KH,
Widen E,
Yang Q,
Zhao W,
Adams HHH,
Arking DE,
Bilder RM,
Bitsios P,
Boerwinkle E,
Chiba-Falek O,
Corvin A,
De Jager PL,
Debette S,
Donohoe G,
Elliott P,
Fitzpatrick AL,
Gill M,
Glahn DC,
Hägg S,
Hansell NK,
Hariri AR,
Ikram MK,
Jukema JW,
Jukema JW,
Vuoksimaa E,
Keller MC,
Kremen WS,
Launer L,
Lindenberger U,
Palotie A,
Pedersen NL,
Pendleton N,
Porteous DJ,
Räikkönen K,
Raitakari OT,
Ramirez A,
Reinvang I,
Rudan I,
Dan Rujescu,
Schmidt R,
Schmidt H,
Schofield PW,
Schofield PR,
Starr JM,
Steen VM,
Trollor JN,
Turner ST,
Van Duijn CM,
Villringer A,
Weinberger DR,
Weir DR,
Wilson JF,
Malhotra A,
McIntosh AM,
Gale CR,
Seshadri S,
Mosley TH Jr,
Bressler J,
Lencz T,
Deary IJ
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Savage JE,
Jansen PR,
Stringer S,
Watanabe K,
Bryois J,
de Leeuw CA,
Nagel M,
Awasthi S,
Barr PB,
Coleman JRI,
Grasby KL,
Hammerschlag AR
and 105 more — show all
Kaminski JA,
Karlsson R,
Krapohl E,
Lam M,
Nygaard M,
Reynolds CA,
Trampush JW,
Young H,
Zabaneh D,
Hägg S,
Hansell NK,
Karlsson IK,
Linnarsson S,
Montgomery GW,
Muñoz-Manchado AB,
Quinlan EB,
Schumann G,
Skene NG,
Webb BT,
White T,
Arking DE,
Avramopoulos D,
Bilder RM,
Bitsios P,
Burdick KE,
Cannon TD,
Chiba-Falek O,
Christoforou A,
Cirulli ET,
Congdon E,
Corvin A,
Davies G,
Deary IJ,
DeRosse P,
Dickinson D,
Djurovic S,
Donohoe G,
Conley ED,
Eriksson JG,
Espeseth T,
Freimer NA,
Giakoumaki S,
Giegling I,
Gill M,
Glahn DC,
Hariri AR,
Hatzimanolis A,
Keller MC,
Knowles E,
Koltai D,
Konte B,
Lahti J,
Le Hellard S,
Lencz T,
Liewald DC,
London E,
Lundervold AJ,
Malhotra AK,
Melle I,
Morris D,
Need AC,
Ollier W,
Palotie A,
Payton A,
Pendleton N,
Poldrack RA,
Räikkönen K,
Reinvang I,
Roussos P,
Rujescu D,
Sabb FW,
Scult MA,
Smeland OB,
Smyrnis N,
Starr JM,
Steen VM,
Stefanis NC,
Straub RE,
Sundet K,
Tiemeier H,
Voineskos AN,
Weinberger DR,
Widen E,
Yu J,
Abecasis G,
Andreassen OA,
Breen G,
Christiansen L,
Debrabant B,
Dick DM,
Heinz A,
Hjerling-Leffler J,
Ikram MA,
Kendler KS,
Martin NG,
Medland SE,
Pedersen NL,
Plomin R,
Polderman TJC,
Ripke S,
van der Sluis S,
Sullivan PF,
Vrieze SI,
Wright MJ,
Posthuma D
Nature genetics · 2018 · PMID 29942086
12 pages+
The genetic architecture of the human cerebral cortex
Grasby KL,
Jahanshad N,
Painter JN,
Colodro-Conde L,
Bralten J,
Hibar DP,
Lind PA,
Pizzagalli F,
Ching CRK,
McMahon MAB,
Shatokhina N,
Zsembik LCP
and 348 more — show all
Thomopoulos SI,
Zhu AH,
Strike LT,
Agartz I,
Alhusaini S,
Almeida MAA,
Alnæs D,
Amlien IK,
Andersson M,
Ard T,
Armstrong NJ,
Ashley-Koch A,
Atkins JR,
Bernard M,
Brouwer RM,
Buimer EEL,
Bülow R,
Bürger C,
Cannon DM,
Chakravarty M,
Chen Q,
Cheung JW,
Couvy-Duchesne B,
Dale AM,
Dalvie S,
de Araujo TK,
de Zubicaray GI,
de Zwarte SMC,
den Braber A,
Doan NT,
Dohm K,
Ehrlich S,
Engelbrecht HR,
Erk S,
Fan CC,
Fedko IO,
Foley SF,
Ford JM,
Fukunaga M,
Garrett ME,
Ge T,
Giddaluru S,
Goldman AL,
Green MJ,
Groenewold NA,
Grotegerd D,
Gurholt TP,
Gutman BA,
Hansell NK,
Harris MA,
Harrison MB,
Haswell CC,
Hauser M,
Herms S,
Heslenfeld DJ,
Ho NF,
Hoehn D,
Hoffmann P,
Holleran L,
Hoogman M,
Hottenga JJ,
Ikeda M,
Janowitz D,
Jansen IE,
Jia T,
Jockwitz C,
Kanai R,
Karama S,
Kasperaviciute D,
Kaufmann T,
Kelly S,
Kikuchi M,
Klein M,
Knapp M,
Knodt AR,
Krämer B,
Lam M,
Lancaster TM,
Lee PH,
Lett TA,
Lewis LB,
Lopes-Cendes I,
Luciano M,
Macciardi F,
Marquand AF,
Mathias SR,
Melzer TR,
Milaneschi Y,
Mirza-Schreiber N,
Moreira JCV,
Mühleisen TW,
Müller-Myhsok B,
Najt P,
Nakahara S,
Nho K,
Olde Loohuis LM,
Orfanos DP,
Pearson JF,
Pitcher TL,
Pütz B,
Quidé Y,
Ragothaman A,
Rashid FM,
Reay WR,
Redlich R,
Reinbold CS,
Repple J,
Richard G,
Riedel BC,
Risacher SL,
Rocha CS,
Mota NR,
Salminen L,
Saremi A,
Saykin AJ,
Schlag F,
Schmaal L,
Schofield PR,
Secolin R,
Shapland CY,
Shen L,
Shin J,
Shumskaya E,
Sønderby IE,
Sprooten E,
Tansey KE,
Teumer A,
Thalamuthu A,
Tordesillas-Gutiérrez D,
Turner JA,
Uhlmann A,
Vallerga CL,
van der Meer D,
van Donkelaar MMJ,
van Eijk L,
van Erp TGM,
van Haren NEM,
van Rooij D,
van Tol MJ,
Veldink JH,
Verhoef E,
Walton E,
Wang M,
Wang Y,
Wardlaw JM,
Wen W,
Westlye LT,
Whelan CD,
Witt SH,
Wittfeld K,
Wolf C,
Wolfers T,
Wu JQ,
Yasuda CL,
Zaremba D,
Zhang Z,
Zwiers MP,
Artiges E,
Assareh AA,
Ayesa-Arriola R,
Belger A,
Brandt CL,
Brown GG,
Cichon S,
Curran JE,
Davies GE,
Degenhardt F,
Dennis MF,
Dietsche B,
Djurovic S,
Doherty CP,
Espiritu R,
Garijo D,
Gil Y,
Gowland PA,
Green RC,
Häusler AN,
Heindel W,
Ho BC,
Hoffmann WU,
Holsboer F,
Homuth G,
Hosten N,
Jack CR Jr,
Jang M,
Jansen A,
Kimbrel NA,
Kolskår K,
Koops S,
Krug A,
Lim KO,
Luykx JJ,
Mathalon DH,
Mather KA,
Mattay VS,
Matthews S,
Mayoral Van Son J,
McEwen SC,
Melle I,
Morris DW,
Mueller BA,
Nauck M,
Nordvik JE,
Nöthen MM,
O'Leary DS,
Opel N,
Martinot MP,
Pike GB,
Preda A,
Quinlan EB,
Rasser PE,
Ratnakar V,
Reppermund S,
Steen VM,
Tooney PA,
Torres FR,
Veltman DJ,
Voyvodic JT,
Whelan R,
White T,
Yamamori H,
Adams HHH,
Bis JC,
Debette S,
Decarli C,
Fornage M,
Gudnason V,
Hofer E,
Ikram MA,
Launer L,
Longstreth WT,
Lopez OL,
Mazoyer B,
Mosley TH,
Roshchupkin GV,
Satizabal CL,
Schmidt R,
Seshadri S,
Yang Q,
Alvim MKM,
Ames D,
Anderson TJ,
Andreassen OA,
Arias-Vasquez A,
Bastin ME,
Baune BT,
Beckham JC,
Blangero J,
Boomsma DI,
Brodaty H,
Brunner HG,
Buckner RL,
Buitelaar JK,
Bustillo JR,
Cahn W,
Cairns MJ,
Calhoun V,
Carr VJ,
Caseras X,
Caspers S,
Cavalleri GL,
Cendes F,
Corvin A,
Crespo-Facorro B,
Dalrymple-Alford JC,
Dannlowski U,
de Geus EJC,
Deary IJ,
Delanty N,
Depondt C,
Desrivières S,
Donohoe G,
Espeseth T,
Fernández G,
Fisher SE,
Flor H,
Forstner AJ,
Francks C,
Franke B,
Glahn DC,
Gollub RL,
Grabe HJ,
Gruber O,
Håberg AK,
Hariri AR,
Hartman CA,
Hashimoto R,
Heinz A,
Henskens FA,
Hillegers MHJ,
Hoekstra PJ,
Holmes AJ,
Hong LE,
Hopkins WD,
Hulshoff Pol HE,
Jernigan TL,
Jönsson EG,
Kahn RS,
Kennedy MA,
Kircher TTJ,
Kochunov P,
Kwok JBJ,
Le Hellard S,
Loughland CM,
Martin NG,
Martinot JL,
McDonald C,
McMahon KL,
Meyer-Lindenberg A,
Michie PT,
Morey RA,
Mowry B,
Nyberg L,
Oosterlaan J,
Ophoff RA,
Pantelis C,
Paus T,
Pausova Z,
Penninx BWJH,
Polderman TJC,
Posthuma D,
Rietschel M,
Roffman JL,
Rowland LM,
Sachdev PS,
Sämann PG,
Schall U,
Schumann G,
Scott RJ,
Sim K,
Sisodiya SM,
Smoller JW,
Sommer IE,
St Pourcain B,
Stein DJ,
Toga AW,
Trollor JN,
Van der Wee NJA,
van 't Ent D,
Völzke H,
Walter H,
Weber B,
Weinberger DR,
Wright MJ,
Zhou J,
Stein JL,
Thompson PM,
Medland SE
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
Genetic diversity fuels gene discovery for tobacco and alcohol use
Saunders GRB,
Wang X,
Chen F,
Jang SK,
Liu M,
Wang C,
Gao S,
Jiang Y,
Khunsriraksakul C,
Otto JM,
Addison C,
Akiyama M
and 205 more — show all
Albert CM,
Aliev F,
Alonso A,
Arnett DK,
Ashley-Koch AE,
Ashrani AA,
Barnes KC,
Barr RG,
Bartz TM,
Becker DM,
Bielak LF,
Benjamin EJ,
Bis JC,
Bjornsdottir G,
Blangero J,
Bleecker ER,
Boardman JD,
Boerwinkle E,
Boomsma DI,
Boorgula MP,
Bowden DW,
Brody JA,
Cade BE,
Chasman DI,
Chavan S,
Chen YI,
Chen Z,
Cheng I,
Cho MH,
Choquet H,
Cole JW,
Cornelis MC,
Cucca F,
Curran JE,
de Andrade M,
Dick DM,
Docherty AR,
Duggirala R,
Eaton CB,
Ehringer MA,
Esko T,
Faul JD,
Fernandes Silva L,
Fiorillo E,
Fornage M,
Freedman BI,
Gabrielsen ME,
Garrett ME,
Gharib SA,
Gieger C,
Gillespie N,
Glahn DC,
Gordon SD,
Gu CC,
Gu D,
Gudbjartsson DF,
Guo X,
Haessler J,
Hall ME,
Haller T,
Harris KM,
He J,
Herd P,
Hewitt JK,
Hickie I,
Hidalgo B,
Hokanson JE,
Hopfer C,
Hottenga J,
Hou L,
Huang H,
Hung YJ,
Hunter DJ,
Hveem K,
Hwang SJ,
Hwu CM,
Iacono W,
Irvin MR,
Jee YH,
Johnson EO,
Joo YY,
Jorgenson E,
Justice AE,
Kamatani Y,
Kaplan RC,
Kaprio J,
Kardia SLR,
Keller MC,
Kelly TN,
Kooperberg C,
Korhonen T,
Kraft P,
Krauter K,
Kuusisto J,
Laakso M,
Lasky-Su J,
Lee WJ,
Lee JJ,
Levy D,
Li L,
Li K,
Li Y,
Lin K,
Lind PA,
Liu C,
Lloyd-Jones DM,
Lutz SM,
Ma J,
Mägi R,
Manichaikul A,
Martin NG,
Mathur R,
Matoba N,
McArdle PF,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Meyers DA,
Millwood IY,
Mitchell BD,
Mohlke KL,
Moll M,
Montasser ME,
Morrison AC,
Mulas A,
Nielsen JB,
North KE,
Oelsner EC,
Okada Y,
Orrù V,
Palmer ND,
Palviainen T,
Pandit A,
Park SL,
Peters U,
Peters A,
Peyser PA,
Polderman TJC,
Rafaels N,
Redline S,
Reed RM,
Reiner AP,
Rice JP,
Rich SS,
Richmond NE,
Roan C,
Rotter JI,
Rueschman MN,
Runarsdottir V,
Saccone NL,
Schwartz DA,
Shadyab AH,
Shi J,
Shringarpure SS,
Sicinski K,
Skogholt AH,
Smith JA,
Smith NL,
Sotoodehnia N,
Stallings MC,
Stefansson H,
Stefansson K,
Stitzel JA,
Sun X,
Syed M,
Tal-Singer R,
Taylor AE,
Taylor KD,
Telen MJ,
Thai KK,
Tiwari H,
Turman C,
Tyrfingsson T,
Wall TL,
Walters RG,
Weir DR,
Weiss ST,
White WB,
Whitfield JB,
Wiggins KL,
Willemsen G,
Willer CJ,
Winsvold BS,
Xu H,
Yanek LR,
Yin J,
Young KL,
Young KA,
Yu B,
Zhao W,
Zhou W,
Zöllner S,
Zuccolo L,
Batini C,
Bergen AW,
Bierut LJ,
David SP,
Gagliano Taliun SA,
Hancock DB,
Jiang B,
Munafò MR,
Thorgeirsson TE,
Liu DJ,
Vrieze S
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative
Little A,
Hu Y,
Sun Q,
Jain D,
Broome J,
Chen MH,
Thibord F,
McHugh C,
Surendran P,
Blackwell TW,
Brody JA,
Bhan A
and 55 more — show all
Chami N,
de Vries PS,
Ekunwe L,
Heard-Costa N,
Hobbs BD,
Manichaikul A,
Moon JY,
Preuss MH,
Ryan K,
Wang Z,
Wheeler M,
Yanek LR,
Abecasis GR,
Almasy L,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Choquet H,
Correa A,
Curran JE,
Faraday N,
Fornage M,
Glahn DC,
Hou L,
Jorgenson E,
Kooperberg C,
Lewis JP,
Lloyd-Jones DM,
Loos RJF,
Min YI,
Mitchell BD,
Morrison AC,
Nickerson DA,
North KE,
O'Connell JR,
Pankratz N,
Psaty BM,
Vasan RS,
Rich SS,
Rotter JI,
Smith AV,
Smith NL,
Tang H,
Tracy RP,
Conomos MP,
Laurie CA,
Mathias RA,
Li Y,
Auer PL,
Thornton T,
Reiner AP,
Johnson AD,
Raffield LM
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Human molecular genetics · 2022 · PMID 34553764
2 pages
Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes
Carless MA,
Glahn DC,
Johnson MP,
Curran JE,
Bozaoglu K,
Dyer TD,
Winkler AM,
Cole SA,
Almasy L,
MacCluer JW,
Duggirala R,
Moses EK
and 2 more — show all
Molecular psychiatry · 2011 · PMID 21483430 · open access
1 page
Identification of common variants associated with human hippocampal and intracranial volumes
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Senstad RE,
Winkler AM,
Toro R,
Appel K,
Bartecek R,
Bergmann Ø,
Bernard M,
Brown AA
and 190 more — show all
Cannon DM,
Chakravarty MM,
Christoforou A,
Domin M,
Grimm O,
Hollinshead M,
Holmes AJ,
Homuth G,
Hottenga JJ,
Langan C,
Lopez LM,
Hansell NK,
Hwang KS,
Kim S,
Laje G,
Lee PH,
Liu X,
Loth E,
Lourdusamy A,
Mattingsdal M,
Mohnke S,
Maniega SM,
Nho K,
Nugent AC,
O'Brien C,
Papmeyer M,
Pütz B,
Ramasamy A,
Rasmussen J,
Rijpkema M,
Risacher SL,
Roddey JC,
Rose EJ,
Ryten M,
Shen L,
Sprooten E,
Strengman E,
Teumer A,
Trabzuni D,
Turner J,
van Eijk K,
van Erp TG,
van Tol MJ,
Wittfeld K,
Wolf C,
Woudstra S,
Aleman A,
Alhusaini S,
Almasy L,
Binder EB,
Brohawn DG,
Cantor RM,
Carless MA,
Corvin A,
Czisch M,
Curran JE,
Davies G,
de Almeida MA,
Delanty N,
Depondt C,
Duggirala R,
Dyer TD,
Erk S,
Fagerness J,
Fox PT,
Freimer NB,
Gill M,
Göring HH,
Hagler DJ,
Hoehn D,
Holsboer F,
Hoogman M,
Hosten N,
Jahanshad N,
Johnson MP,
Kasperaviciute D,
Kent JW Jr,
Kochunov P,
Lancaster JL,
Lawrie SM,
Liewald DC,
Mandl R,
Matarin M,
Mattheisen M,
Meisenzahl E,
Melle I,
Moses EK,
Mühleisen TW,
Nauck M,
Nöthen MM,
Olvera RL,
Pandolfo M,
Pike GB,
Puls R,
Reinvang I,
Rentería ME,
Rietschel M,
Roffman JL,
Royle NA,
Rujescu D,
Savitz J,
Schnack HG,
Schnell K,
Seiferth N,
Smith C,
Steen VM,
Valdés Hernández MC,
Van den Heuvel M,
van der Wee NJ,
Van Haren NE,
Veltman JA,
Völzke H,
Walker R,
Westlye LT,
Whelan CD,
Agartz I,
Boomsma DI,
Cavalleri GL,
Dale AM,
Djurovic S,
Drevets WC,
Hagoort P,
Hall J,
Heinz A,
Jack CR Jr,
Foroud TM,
Le Hellard S,
Macciardi F,
Montgomery GW,
Poline JB,
Porteous DJ,
Sisodiya SM,
Starr JM,
Sussmann J,
Toga AW,
Veltman DJ,
Walter H,
Weiner MW,
Bis JC,
Ikram MA,
Smith AV,
Gudnason V,
Tzourio C,
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Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium and 4 more consortia
Nature genetics · 2012 · PMID 22504417
1 page
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
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NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
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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.