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23 matches for
McMahon G,
showing the first 20.
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Perry JR,
Day F,
Elks CE,
Sulem P,
Thompson DJ,
Ferreira T,
He C,
Chasman DI,
Esko T,
Thorleifsson G,
Albrecht E,
Ang WQ
and 186 more — show all
Corre T,
Cousminer DL,
Feenstra B,
Franceschini N,
Ganna A,
Johnson AD,
Kjellqvist S,
Lunetta KL,
McMahon G,
Nolte IM,
Paternoster L,
Porcu E,
Smith AV,
Stolk L,
Teumer A,
Tšernikova N,
Tikkanen E,
Ulivi S,
Wagner EK,
Amin N,
Bierut LJ,
Byrne EM,
Hottenga JJ,
Koller DL,
Mangino M,
Pers TH,
Yerges-Armstrong LM,
Zhao JH,
Andrulis IL,
Anton-Culver H,
Atsma F,
Bandinelli S,
Beckmann MW,
Benitez J,
Blomqvist C,
Bojesen SE,
Bolla MK,
Bonanni B,
Brauch H,
Brenner H,
Buring JE,
Chang-Claude J,
Chanock S,
Chen J,
Chenevix-Trench G,
Collée JM,
Couch FJ,
Couper D,
Coveillo AD,
Cox A,
Czene K,
D'adamo AP,
Smith GD,
De Vivo I,
Demerath EW,
Dennis J,
Devilee P,
Dieffenbach AK,
Dunning AM,
Eiriksdottir G,
Eriksson JG,
Fasching PA,
Ferrucci L,
Flesch-Janys D,
Flyger H,
Foroud T,
Franke L,
Garcia ME,
García-Closas M,
Geller F,
de Geus EE,
Giles GG,
Gudbjartsson DF,
Gudnason V,
Guénel P,
Guo S,
Hall P,
Hamann U,
Haring R,
Hartman CA,
Heath AC,
Hofman A,
Hooning MJ,
Hopper JL,
Hu FB,
Hunter DJ,
Karasik D,
Kiel DP,
Knight JA,
Kosma VM,
Kutalik Z,
Lai S,
Lambrechts D,
Lindblom A,
Mägi R,
Magnusson PK,
Mannermaa A,
Martin NG,
Masson G,
McArdle PF,
McArdle WL,
Melbye M,
Michailidou K,
Mihailov E,
Milani L,
Milne RL,
Nevanlinna H,
Neven P,
Nohr EA,
Oldehinkel AJ,
Oostra BA,
Palotie A,
Peacock M,
Pedersen NL,
Peterlongo P,
Peto J,
Pharoah PD,
Postma DS,
Pouta A,
Pylkäs K,
Radice P,
Ring S,
Rivadeneira F,
Robino A,
Rose LM,
Rudolph A,
Salomaa V,
Sanna S,
Schlessinger D,
Schmidt MK,
Southey MC,
Sovio U,
Stampfer MJ,
Stöckl D,
Storniolo AM,
Timpson NJ,
Tyrer J,
Visser JA,
Vollenweider P,
Völzke H,
Waeber G,
Waldenberger M,
Wallaschofski H,
Wang Q,
Willemsen G,
Winqvist R,
Wolffenbuttel BH,
Wright MJ,
Boomsma DI,
Econs MJ,
Khaw KT,
Loos RJ,
McCarthy MI,
Montgomery GW,
Rice JP,
Streeten EA,
Thorsteinsdottir U,
van Duijn CM,
Alizadeh BZ,
Bergmann S,
Boerwinkle E,
Boyd HA,
Crisponi L,
Gasparini P,
Gieger C,
Harris TB,
Ingelsson E,
Järvelin MR,
Kraft P,
Lawlor D,
Metspalu A,
Pennell CE,
Ridker PM,
Snieder H,
Sørensen TI,
Spector TD,
Strachan DP,
Uitterlinden AG,
Wareham NJ,
Widen E,
Zygmunt M,
Murray A,
Easton DF,
Stefansson K,
Murabito JM,
Ong KK
Australian Ovarian Cancer Study · GENICA Network and 4 more consortia
Nature · 2014 · PMID 25231870 · open access
12 pages+
Genome-wide association study identifies 74 loci associated with educational attainment
Okbay A,
Beauchamp JP,
Fontana MA,
Lee JJ,
Pers TH,
Rietveld CA,
Turley P,
Chen GB,
Emilsson V,
Meddens SF,
Oskarsson S,
Pickrell JK
and 243 more — show all
Thom K,
Timshel P,
de Vlaming R,
Abdellaoui A,
Ahluwalia TS,
Bacelis J,
Baumbach C,
Bjornsdottir G,
Brandsma JH,
Pina Concas M,
Derringer J,
Furlotte NA,
Galesloot TE,
Girotto G,
Gupta R,
Hall LM,
Harris SE,
Hofer E,
Horikoshi M,
Huffman JE,
Kaasik K,
Kalafati IP,
Karlsson R,
Kong A,
Lahti J,
van der Lee SJ,
deLeeuw C,
Lind PA,
Lindgren KO,
Liu T,
Mangino M,
Marten J,
Mihailov E,
Miller MB,
van der Most PJ,
Oldmeadow C,
Payton A,
Pervjakova N,
Peyrot WJ,
Qian Y,
Raitakari O,
Rueedi R,
Salvi E,
Schmidt B,
Schraut KE,
Shi J,
Smith AV,
Poot RA,
St Pourcain B,
Teumer A,
Thorleifsson G,
Verweij N,
Vuckovic D,
Wellmann J,
Westra HJ,
Yang J,
Zhao W,
Zhu Z,
Alizadeh BZ,
Amin N,
Bakshi A,
Baumeister SE,
Biino G,
Bønnelykke K,
Boyle PA,
Campbell H,
Cappuccio FP,
Davies G,
De Neve JE,
Deloukas P,
Demuth I,
Ding J,
Eibich P,
Eisele L,
Eklund N,
Evans DM,
Faul JD,
Feitosa MF,
Forstner AJ,
Gandin I,
Gunnarsson B,
Halldórsson BV,
Harris TB,
Heath AC,
Hocking LJ,
Holliday EG,
Homuth G,
Horan MA,
Hottenga JJ,
de Jager PL,
Joshi PK,
Jugessur A,
Kaakinen MA,
Kähönen M,
Kanoni S,
Keltigangas-Järvinen L,
Kiemeney LA,
Kolcic I,
Koskinen S,
Kraja AT,
Kroh M,
Kutalik Z,
Latvala A,
Launer LJ,
Lebreton MP,
Levinson DF,
Lichtenstein P,
Lichtner P,
Liewald DC,
Loukola A,
Madden PA,
Mägi R,
Mäki-Opas T,
Marioni RE,
Marques-Vidal P,
Meddens GA,
McMahon G,
Meisinger C,
Meitinger T,
Milaneschi Y,
Milani L,
Montgomery GW,
Myhre R,
Nelson CP,
Nyholt DR,
Ollier WE,
Palotie A,
Paternoster L,
Pedersen NL,
Petrovic KE,
Porteous DJ,
Räikkönen K,
Ring SM,
Robino A,
Rostapshova O,
Rudan I,
Rustichini A,
Salomaa V,
Sanders AR,
Sarin AP,
Schmidt H,
Scott RJ,
Smith BH,
Smith JA,
Staessen JA,
Steinhagen-Thiessen E,
Strauch K,
Terracciano A,
Tobin MD,
Ulivi S,
Vaccargiu S,
Quaye L,
van Rooij FJ,
Venturini C,
Vinkhuyzen AA,
Völker U,
Völzke H,
Vonk JM,
Vozzi D,
Waage J,
Ware EB,
Willemsen G,
Attia JR,
Bennett DA,
Berger K,
Bertram L,
Bisgaard H,
Boomsma DI,
Borecki IB,
Bültmann U,
Chabris CF,
Cucca F,
Cusi D,
Deary IJ,
Dedoussis GV,
van Duijn CM,
Eriksson JG,
Franke B,
Franke L,
Gasparini P,
Gejman PV,
Gieger C,
Grabe HJ,
Gratten J,
Groenen PJ,
Gudnason V,
van der Harst P,
Hayward C,
Hinds DA,
Hoffmann W,
Hyppönen E,
Iacono WG,
Jacobsson B,
Järvelin MR,
Jöckel KH,
Kaprio J,
Kardia SL,
Lehtimäki T,
Lehrer SF,
Magnusson PK,
Martin NG,
McGue M,
Metspalu A,
Pendleton N,
Penninx BW,
Perola M,
Pirastu N,
Pirastu M,
Polasek O,
Posthuma D,
Power C,
Province MA,
Samani NJ,
Schlessinger D,
Schmidt R,
Sørensen TI,
Spector TD,
Stefansson K,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tiemeier H,
Tung JY,
Uitterlinden AG,
Vitart V,
Vollenweider P,
Weir DR,
Wilson JF,
Wright AF,
Conley DC,
Krueger RF,
Davey Smith G,
Hofman A,
Laibson DI,
Medland SE,
Meyer MN,
Yang J,
Johannesson M,
Visscher PM,
Esko T,
Koellinger PD,
Cesarini D,
Benjamin DJ
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
12 pages+
Genome-wide associations for birth weight and correlations with adult disease
Horikoshi M,
Beaumont RN,
Day FR,
Warrington NM,
Kooijman MN,
Fernandez-Tajes J,
Feenstra B,
van Zuydam NR,
Gaulton KJ,
Grarup N,
Bradfield JP,
Strachan DP
and 157 more — show all
Li-Gao R,
Ahluwalia TS,
Kreiner E,
Rueedi R,
Lyytikäinen LP,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Hottenga JJ,
Vilor-Tejedor N,
Joshi PK,
Boh ETH,
Ntalla I,
Pitkänen N,
Mahajan A,
van Leeuwen EM,
Joro R,
Lagou V,
Nodzenski M,
Diver LA,
Zondervan KT,
Bustamante M,
Marques-Vidal P,
Mercader JM,
Bennett AJ,
Rahmioglu N,
Nyholt DR,
Ma RCW,
Tam CHT,
Tam WH,
Ganesh SK,
van Rooij FJ,
Jones SE,
Loh PR,
Ruth KS,
Tuke MA,
Tyrrell J,
Wood AR,
Yaghootkar H,
Scholtens DM,
Paternoster L,
Prokopenko I,
Kovacs P,
Atalay M,
Willems SM,
Panoutsopoulou K,
Wang X,
Carstensen L,
Geller F,
Schraut KE,
Murcia M,
van Beijsterveldt CE,
Willemsen G,
Appel EVR,
Fonvig CE,
Trier C,
Tiesler CM,
Standl M,
Kutalik Z,
Bonas-Guarch S,
Hougaard DM,
Sánchez F,
Torrents D,
Waage J,
Hollegaard MV,
de Haan HG,
Rosendaal FR,
Medina-Gomez C,
Ring SM,
Hemani G,
McMahon G,
Robertson NR,
Groves CJ,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Mentch FD,
MacKenzie SM,
Reynolds RM,
Lowe WL Jr,
Tönjes A,
Stumvoll M,
Lindi V,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Sørensen TI,
Niinikoski H,
Pahkala K,
Raitakari OT,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Melbye M,
Campbell H,
Wilson JF,
Vrijheid M,
de Geus EJ,
Boomsma DI,
Kadarmideen HN,
Holm JC,
Holm JC,
Hansen T,
Sebert S,
Hattersley AT,
Beilin LJ,
Newnham JP,
Newnham JP,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Kähönen M,
Viikari JS,
Lehtimäki T,
Vollenweider P,
Vollenweider P,
Bønnelykke K,
Bisgaard H,
Mook-Kanamori DO,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Pisinger C,
Pisinger C,
Pedersen O,
Power C,
Hyppönen E,
Wareham NJ,
Hakonarson H,
Davies E,
Walker BR,
Jaddoe VW,
Jarvelin MR,
Grant SF,
Vaag AA,
Lawlor DA,
Frayling TM,
Frayling TM,
Davey Smith G,
Morris AP,
Ong KK,
Felix JF,
Timpson NJ,
Perry JR,
Evans DM,
McCarthy MI,
McCarthy MI,
Freathy RM
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
12 pages+
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Liu M,
Jiang Y,
Wedow R,
Li Y,
Brazel DM,
Chen F,
Datta G,
Davila-Velderrain J,
McGuire D,
Tian C,
Zhan X,
Choquet H
and 111 more — show all
Docherty AR,
Faul JD,
Foerster JR,
Fritsche LG,
Gabrielsen ME,
Gordon SD,
Haessler J,
Hottenga JJ,
Huang H,
Jang SK,
Jansen PR,
Ling Y,
Mägi R,
Matoba N,
McMahon G,
Mulas A,
Orrù V,
Palviainen T,
Pandit A,
Reginsson GW,
Skogholt AH,
Smith JA,
Taylor AE,
Turman C,
Willemsen G,
Young H,
Young KA,
Zajac GJM,
Zhao W,
Zhou W,
Bjornsdottir G,
Boardman JD,
Boehnke M,
Boomsma DI,
Chen C,
Cucca F,
Davies GE,
Eaton CB,
Ehringer MA,
Esko T,
Fiorillo E,
Gillespie NA,
Gudbjartsson DF,
Haller T,
Harris KM,
Heath AC,
Hewitt JK,
Hickie IB,
Hokanson JE,
Hopfer CJ,
Hunter DJ,
Iacono WG,
Johnson EO,
Kamatani Y,
Kardia SLR,
Keller MC,
Kellis M,
Kooperberg C,
Kraft P,
Krauter KS,
Laakso M,
Lind PA,
Loukola A,
Lutz SM,
Madden PAF,
Martin NG,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Mohlke KL,
Nielsen JB,
Okada Y,
Peters U,
Polderman TJC,
Posthuma D,
Reiner AP,
Rice JP,
Rimm E,
Rose RJ,
Runarsdottir V,
Stallings MC,
Stančáková A,
Stefansson H,
Thai KK,
Tindle HA,
Tyrfingsson T,
Wall TL,
Weir DR,
Weisner C,
Whitfield JB,
Winsvold BS,
Yin J,
Zuccolo L,
Bierut LJ,
Hveem K,
Lee JJ,
Munafò MR,
Saccone NL,
Willer CJ,
Cornelis MC,
David SP,
Hinds DA,
Jorgenson E,
Kaprio J,
Stitzel JA,
Stefansson K,
Thorgeirsson TE,
Abecasis G,
Liu DJ,
Vrieze S
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
12 pages+
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Fan Q,
Verhoeven VJ,
Wojciechowski R,
Barathi VA,
Hysi PG,
Guggenheim JA,
Höhn R,
Vitart V,
Khawaja AP,
Yamashiro K,
Hosseini SM,
Lehtimäki T
and 142 more — show all
Lu Y,
Haller T,
Xie J,
Delcourt C,
Pirastu M,
Wedenoja J,
Gharahkhani P,
Venturini C,
Miyake M,
Hewitt AW,
Guo X,
Mazur J,
Huffman JE,
Williams KM,
Polasek O,
Campbell H,
Rudan I,
Vatavuk Z,
Wilson JF,
Joshi PK,
McMahon G,
St Pourcain B,
Evans DM,
Simpson CL,
Schwantes-An TH,
Igo RP,
Mirshahi A,
Cougnard-Gregoire A,
Bellenguez C,
Blettner M,
Raitakari O,
Kähönen M,
Seppala I,
Zeller T,
Meitinger T,
Ried JS,
Gieger C,
Portas L,
van Leeuwen EM,
Amin N,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
Vingerling JR,
Wang YX,
Wang X,
Tai-Hui Boh E,
Ikram MK,
Sabanayagam C,
Gupta P,
Tan V,
Zhou L,
Ho CE,
Lim W,
Beuerman RW,
Siantar R,
Tai ES,
Vithana E,
Mihailov E,
Khor CC,
Hayward C,
Luben RN,
Foster PJ,
Klein BE,
Klein R,
Wong HS,
Mitchell P,
Metspalu A,
Aung T,
Young TL,
He M,
Pärssinen O,
van Duijn CM,
Jin Wang J,
Williams C,
Jonas JB,
Teo YY,
Mackey DA,
Oexle K,
Yoshimura N,
Paterson AD,
Pfeiffer N,
Wong TY,
Baird PN,
Stambolian D,
Wilson JE,
Cheng CY,
Hammond CJ,
Klaver CC,
Saw SM,
Rahi JS,
Korobelnik JF,
Kemp JP,
Timpson NJ,
Smith GD,
Craig JE,
Burdon KP,
Fogarty RD,
Iyengar SK,
Chew E,
Janmahasatian S,
Martin NG,
MacGregor S,
Xu L,
Schache M,
Nangia V,
Panda-Jonas S,
Wright AF,
Fondran JR,
Lass JH,
Feng S,
Zhao JH,
Khaw KT,
Wareham NJ,
Rantanen T,
Kaprio J,
Pang CP,
Chen LJ,
Tam PO,
Jhanji V,
Young AL,
Döring A,
Raffel LJ,
Cotch MF,
Li X,
Yip SP,
Yap MK,
Biino G,
Vaccargiu S,
Fossarello M,
Fleck B,
Yazar S,
Tideman JW,
Tedja M,
Deangelis MM,
Morrison M,
Farrer L,
Zhou X,
Chen W,
Mizuki N,
Meguro A,
Mäkelä KM
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
10 pages
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
Hysi PG,
Valdes AM,
Liu F,
Furlotte NA,
Evans DM,
Bataille V,
Visconti A,
Hemani G,
McMahon G,
Ring SM,
Smith GD,
Duffy DL
and 32 more — show all
Zhu G,
Gordon SD,
Medland SE,
Lin BD,
Willemsen G,
Jan Hottenga J,
Vuckovic D,
Girotto G,
Gandin I,
Sala C,
Concas MP,
Brumat M,
Gasparini P,
Toniolo D,
Cocca M,
Robino A,
Yazar S,
Hewitt AW,
Chen Y,
Zeng C,
Uitterlinden AG,
Ikram MA,
Hamer MA,
van Duijn CM,
Nijsten T,
Mackey DA,
Falchi M,
Boomsma DI,
Martin NG,
Hinds DA,
Kayser M,
Spector TD
International Visible Trait Genetics Consortium
Nature genetics · 2018 · PMID 29662168 · open access
10 pages
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
Gormley P,
Anttila V,
Winsvold BS,
Palta P,
Esko T,
Pers TH,
Farh KH,
Cuenca-Leon E,
Muona M,
Furlotte NA,
Kurth T,
Ingason A
and 95 more — show all
McMahon G,
Ligthart L,
Terwindt GM,
Kallela M,
Freilinger TM,
Ran C,
Gordon SG,
Stam AH,
Steinberg S,
Borck G,
Koiranen M,
Quaye L,
Adams HH,
Lehtimäki T,
Sarin AP,
Wedenoja J,
Hinds DA,
Buring JE,
Schürks M,
Ridker PM,
Hrafnsdottir MG,
Stefansson H,
Ring SM,
Hottenga JJ,
Penninx BW,
Färkkilä M,
Artto V,
Kaunisto M,
Vepsäläinen S,
Malik R,
Heath AC,
Madden PA,
Martin NG,
Montgomery GW,
Kurki MI,
Kals M,
Mägi R,
Pärn K,
Hämäläinen E,
Huang H,
Byrnes AE,
Franke L,
Huang J,
Stergiakouli E,
Lee PH,
Sandor C,
Webber C,
Cader Z,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Eriksson JG,
Salomaa V,
Heikkilä K,
Loehrer E,
Uitterlinden AG,
Hofman A,
van Duijn CM,
Cherkas L,
Pedersen LM,
Stubhaug A,
Nielsen CS,
Männikkö M,
Mihailov E,
Milani L,
Göbel H,
Esserlind AL,
Christensen AF,
Hansen TF,
Werge T,
Kaprio J,
Aromaa AJ,
Raitakari O,
Ikram MA,
Spector T,
Järvelin MR,
Metspalu A,
Kubisch C,
Strachan DP,
Ferrari MD,
Belin AC,
Dichgans M,
Wessman M,
van den Maagdenberg AM,
Zwart JA,
Boomsma DI,
Smith GD,
Stefansson K,
Eriksson N,
Daly MJ,
Neale BM,
Olesen J,
Chasman DI,
Nyholt DR,
Palotie A
International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
9 pages
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index
Felix JF,
Bradfield JP,
Monnereau C,
van der Valk RJ,
Stergiakouli E,
Chesi A,
Gaillard R,
Feenstra B,
Thiering E,
Kreiner-Møller E,
Mahajan A,
Pitkänen N
and 99 more — show all
Joro R,
Cavadino A,
Huikari V,
Franks S,
Groen-Blokhuis MM,
Cousminer DL,
Marsh JA,
Lehtimäki T,
Curtin JA,
Vioque J,
Ahluwalia TS,
Myhre R,
Price TS,
Vilor-Tejedor N,
Yengo L,
Grarup N,
Ntalla I,
Ang W,
Atalay M,
Bisgaard H,
Blakemore AI,
Bonnefond A,
Carstensen L,
Eriksson J,
Flexeder C,
Franke L,
Geller F,
Geserick M,
Hartikainen AL,
Haworth CM,
Hirschhorn JN,
Hofman A,
Holm JC,
Horikoshi M,
Hottenga JJ,
Huang J,
Kadarmideen HN,
Kähönen M,
Kiess W,
Lakka HM,
Lakka TA,
Lewin AM,
Liang L,
Lyytikäinen LP,
Ma B,
Magnus P,
McCormack SE,
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Nature genetics · 2013 · PMID 23396134
6 pages
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Human molecular genetics · 2013 · PMID 23720494
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Nature genetics · 2013 · PMID 23817569 · open access
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Science (New York, N.Y.) · 2013 · PMID 23722424
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North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
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BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
3 pages
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Cheng CY,
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Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group and 2 more consortia
American journal of human genetics · 2013 · PMID 24144296
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Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position
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Common variants at 12q15 and 12q24 are associated with infant head circumference
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Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and 1 more consortia
Nature genetics · 2012 · PMID 22504419
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A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor α gene as a quantitative trait locus for eye size in white Europeans
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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.