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184 matches for
Ell C,
showing the first 20.
Genomics and phenomics of body mass index reveals a complex disease network
Huang J,
Huffman JE,
Huang Y,
Do Valle Í,
Assimes TL,
Raghavan S,
Voight BF,
Liu C,
Barabási AL,
Huang RDL,
Hui Q,
Nguyen XT
and 26 more — show all
Ho YL,
Djousse L,
Lynch JA,
Vujkovic M,
Tcheandjieu C,
Tang H,
Damrauer SM,
Reaven PD,
Miller D,
Phillips LS,
Ng MCY,
Graff M,
Haiman CA,
Loos RJF,
North KE,
Yengo L,
Smith GD,
Saleheen D,
Gaziano JM,
Rader DJ,
Tsao PS,
Cho K,
Chang KM,
Wilson PWF,
Sun YV,
O'Donnell CJ
VA Million Veteran Program
Nature communications · 2022 · PMID 36581621 · open access
12 pages+
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Shrine N,
Izquierdo AG,
Chen J,
Packer R,
Hall RJ,
Guyatt AL,
Batini C,
Thompson RJ,
Pavuluri C,
Malik V,
Hobbs BD,
Moll M
and 136 more — show all
Kim W,
Tal-Singer R,
Bakke P,
Fawcett KA,
John C,
Coley K,
Piga NN,
Pozarickij A,
Lin K,
Millwood IY,
Chen Z,
Li L,
Wijnant SRA,
Lahousse L,
Brusselle G,
Uitterlinden AG,
Manichaikul A,
Oelsner EC,
Rich SS,
Barr RG,
Kerr SM,
Vitart V,
Brown MR,
Wielscher M,
Imboden M,
Jeong A,
Bartz TM,
Gharib SA,
Flexeder C,
Karrasch S,
Gieger C,
Peters A,
Stubbe B,
Hu X,
Ortega VE,
Meyers DA,
Bleecker ER,
Gabriel SB,
Gupta N,
Smith AV,
Luan J,
Zhao JH,
Hansen AF,
Langhammer A,
Willer C,
Bhatta L,
Porteous D,
Smith BH,
Campbell A,
Sofer T,
Lee J,
Daviglus ML,
Yu B,
Lim E,
Xu H,
O'Connor GT,
Thareja G,
Albagha OME,
Suhre K,
Granell R,
Faquih TO,
Hiemstra PS,
Slats AM,
Mullin BH,
Hui J,
James A,
Beilby J,
Patasova K,
Hysi P,
Koskela JT,
Wyss AB,
Jin J,
Sikdar S,
Lee M,
May-Wilson S,
Pirastu N,
Kentistou KA,
Joshi PK,
Timmers PRHJ,
Williams AT,
Free RC,
Wang X,
Morrison JL,
Gilliland FD,
Chen Z,
Wang CA,
Foong RE,
Harris SE,
Taylor A,
Redmond P,
Cook JP,
Mahajan A,
Lind L,
Palviainen T,
Lehtimäki T,
Raitakari OT,
Kaprio J,
Rantanen T,
Pietiläinen KH,
Cox SR,
Pennell CE,
Hall GL,
Gauderman WJ,
Brightling C,
Wilson JF,
Vasankari T,
Laitinen T,
Salomaa V,
Mook-Kanamori DO,
Timpson NJ,
Zeggini E,
Dupuis J,
Hayward C,
Brumpton B,
Langenberg C,
Weiss S,
Homuth G,
Schmidt CO,
Probst-Hensch N,
Jarvelin MR,
Morrison AC,
Polasek O,
Rudan I,
Lee JH,
Sayers I,
Rawlins EL,
Dudbridge F,
Silverman EK,
Strachan DP,
Walters RG,
Morris AP,
London SJ,
Cho MH,
Wain LV,
Hall IP,
Tobin MD
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
Pairo-Castineira E,
Rawlik K,
Bretherick AD,
Qi T,
Wu Y,
Nassiri I,
McConkey GA,
Zechner M,
Klaric L,
Griffiths F,
Oosthuyzen W,
Kousathanas A
and 43 more — show all
Richmond A,
Millar J,
Russell CD,
Malinauskas T,
Thwaites R,
Morrice K,
Keating S,
Maslove D,
Nichol A,
Semple MG,
Knight J,
Shankar-Hari M,
Summers C,
Hinds C,
Horby P,
Ling L,
McAuley D,
Montgomery H,
Openshaw PJM,
Begg C,
Walsh T,
Tenesa A,
Flores C,
Riancho JA,
Rojas-Martinez A,
Lapunzina P,
Yang J,
Ponting CP,
Wilson JF,
Vitart V,
Abedalthagafi M,
Luchessi AD,
Parra EJ,
Cruz R,
Carracedo A,
Fawkes A,
Murphy L,
Rowan K,
Pereira AC,
Law A,
Fairfax B,
Hendry SC,
Baillie JK
GenOMICC Investigators · SCOURGE Consortium and 2 more consortia
Nature · 2023 · PMID 37198478 · open access
12 pages+
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
Budu-Aggrey A,
Kilanowski A,
Sobczyk MK,
Shringarpure SS,
Mitchell R,
Reis K,
Reigo A,
Mägi R,
Nelis M,
Tanaka N,
Brumpton BM,
Thomas LF
and 120 more — show all
Sole-Navais P,
Flatley C,
Espuela-Ortiz A,
Herrera-Luis E,
Lominchar JVT,
Bork-Jensen J,
Marenholz I,
Arnau-Soler A,
Jeong A,
Fawcett KA,
Baurecht H,
Rodriguez E,
Alves AC,
Kumar A,
Sleiman PM,
Chang X,
Medina-Gomez C,
Hu C,
Xu CJ,
Qi C,
El-Heis S,
Titcombe P,
Antoun E,
Fadista J,
Wang CA,
Thiering E,
Wu B,
Kress S,
Kothalawala DM,
Kadalayil L,
Duan J,
Zhang H,
Hadebe S,
Hoffmann T,
Jorgenson E,
Choquet H,
Risch N,
Njølstad P,
Andreassen OA,
Johansson S,
Almqvist C,
Gong T,
Ullemar V,
Karlsson R,
Magnusson PKE,
Szwajda A,
Burchard EG,
Thyssen JP,
Hansen T,
Kårhus LL,
Dantoft TM,
Jeanrenaud ACSN,
Ghauri A,
Arnold A,
Homuth G,
Lau S,
Nöthen MM,
Hübner N,
Imboden M,
Visconti A,
Falchi M,
Bataille V,
Hysi P,
Ballardini N,
Boomsma DI,
Hottenga JJ,
Müller-Nurasyid M,
Ahluwalia TS,
Stokholm J,
Chawes B,
Schoos AM,
Esplugues A,
Bustamante M,
Raby B,
Arshad S,
German C,
Esko T,
Milani LA,
Metspalu A,
Terao C,
Abuabara K,
Løset M,
Hveem K,
Jacobsson B,
Pino-Yanes M,
Strachan DP,
Grarup N,
Linneberg A,
Lee YA,
Probst-Hensch N,
Weidinger S,
Jarvelin MR,
Melén E,
Hakonarson H,
Irvine AD,
Jarvis D,
Nijsten T,
Duijts L,
Vonk JM,
Koppelmann GH,
Godfrey KM,
Barton SJ,
Feenstra B,
Pennell CE,
Sly PD,
Holt PG,
Williams LK,
Bisgaard H,
Bønnelykke K,
Curtin J,
Simpson A,
Murray C,
Schikowski T,
Bunyavanich S,
Weiss ST,
Holloway JW,
Min JL,
Brown SJ,
Standl M,
Paternoster L
23andMe Research Team · Estonian Biobank Research Team
Nature communications · 2023 · PMID 37794016 · open access
12 pages+
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Keaton JM,
Kamali Z,
Xie T,
Vaez A,
Williams A,
Goleva SB,
Ani A,
Evangelou E,
Hellwege JN,
Yengo L,
Young WJ,
Traylor M
and 135 more — show all
Giri A,
Zheng Z,
Zeng J,
Chasman DI,
Morris AP,
Caulfield MJ,
Hwang SJ,
Kooner JS,
Conen D,
Attia JR,
Morrison AC,
Loos RJF,
Kristiansson K,
Schmidt R,
Hicks AA,
Pramstaller PP,
Nelson CP,
Samani NJ,
Risch L,
Gyllensten U,
Melander O,
Riese H,
Wilson JF,
Campbell H,
Rich SS,
Psaty BM,
Lu Y,
Rotter JI,
Guo X,
Rice KM,
Vollenweider P,
Sundström J,
Langenberg C,
Tobin MD,
Giedraitis V,
Luan J,
Tuomilehto J,
Kutalik Z,
Ripatti S,
Salomaa V,
Girotto G,
Trompet S,
Jukema JW,
van der Harst P,
Ridker PM,
Giulianini F,
Vitart V,
Goel A,
Watkins H,
Harris SE,
Deary IJ,
van der Most PJ,
Oldehinkel AJ,
Keavney BD,
Hayward C,
Campbell A,
Boehnke M,
Scott LJ,
Boutin T,
Mamasoula C,
Järvelin MR,
Peters A,
Gieger C,
Lakatta EG,
Cucca F,
Hui J,
Knekt P,
Enroth S,
De Borst MH,
Polašek O,
Concas MP,
Catamo E,
Cocca M,
Li-Gao R,
Hofer E,
Schmidt H,
Spedicati B,
Waldenberger M,
Strachan DP,
Laan M,
Teumer A,
Dörr M,
Gudnason V,
Cook JP,
Ruggiero D,
Kolcic I,
Boerwinkle E,
Traglia M,
Lehtimäki T,
Raitakari OT,
Johnson AD,
Newton-Cheh C,
Brown MJ,
Dominiczak AF,
Sever PJ,
Poulter N,
Chambers JC,
Elosua R,
Siscovick D,
Esko T,
Metspalu A,
Strawbridge RJ,
Laakso M,
Hamsten A,
Hottenga JJ,
de Geus E,
Morris AD,
Palmer CNA,
Nolte IM,
Milaneschi Y,
Marten J,
Wright A,
Zeggini E,
Howson JMM,
O'Donnell CJ,
Spector T,
Nalls MA,
Simonsick EM,
Liu Y,
van Duijn CM,
Butterworth AS,
Danesh JN,
Menni C,
Wareham NJ,
Khaw KT,
Sun YV,
Wilson PWF,
Cho K,
Visscher PM,
Denny JC,
Levy D,
Edwards TL,
Munroe PB,
Snieder H,
Warren HR
Million Veteran Program · Lifelines Cohort Study and 2 more consortia
Nature genetics · 2024 · PMID 38689001 · open access
12 pages+
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Verma A,
Huffman JE,
Rodriguez A,
Conery M,
Liu M,
Ho YL,
Kim Y,
Heise DA,
Guare L,
Panickan VA,
Garcon H,
Linares F
and 59 more — show all
Costa L,
Goethert I,
Tipton R,
Honerlaw J,
Davies L,
Whitbourne S,
Cohen J,
Posner DC,
Sangar R,
Murray M,
Wang X,
Dochtermann DR,
Devineni P,
Shi Y,
Nandi TN,
Assimes TL,
Brunette CA,
Carroll RJ,
Clifford R,
Duvall S,
Gelernter J,
Hung A,
Iyengar SK,
Joseph J,
Kember R,
Kranzler H,
Kripke CM,
Levey D,
Luoh SW,
Merritt VC,
Overstreet C,
Deak JD,
Grant SFA,
Polimanti R,
Roussos P,
Shakt G,
Sun YV,
Tsao N,
Venkatesh S,
Voloudakis G,
Justice A,
Begoli E,
Ramoni R,
Tourassi G,
Pyarajan S,
Tsao P,
O'Donnell CJ,
Muralidhar S,
Moser J,
Casas JP,
Bick AG,
Zhou W,
Cai T,
Voight BF,
Cho K,
Gaziano JM,
Madduri RK,
Damrauer S,
Liao KP
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
12 pages+
Novel risk loci for COVID-19 hospitalization among admixed American populations
Diz-de Almeida S,
Cruz R,
Luchessi AD,
Lorenzo-Salazar JM,
de Heredia ML,
Quintela I,
González-Montelongo R,
Nogueira Silbiger V,
Porras MS,
Tenorio Castaño JA,
Nevado J,
Aguado JM
and 109 more — show all
Aguilar C,
Aguilera-Albesa S,
Almadana V,
Almoguera B,
Alvarez N,
Andreu-Bernabeu Á,
Arana-Arri E,
Arango C,
Arranz MJ,
Artiga MJ,
Baptista-Rosas RC,
Barreda-Sánchez M,
Belhassen-Garcia M,
Bezerra JF,
Bezerra MAC,
Boix-Palop L,
Brion M,
Brugada R,
Bustos M,
Calderón EJ,
Carbonell C,
Castano L,
Castelao JE,
Conde-Vicente R,
Cordero-Lorenzana ML,
Cortes-Sanchez JL,
Corton M,
Darnaude MT,
De Martino-Rodríguez A,
Del Campo-Pérez V,
de Bustamante AD,
Domínguez-Garrido E,
Eirós R,
Fariñas MC,
Fernandez-Nestosa MJ,
Fernández-Robelo U,
Fernández-Rodríguez A,
Fernández-Villa T,
Gago-Dominguez M,
Gil-Fournier B,
Gómez-Arrue J,
Álvarez BG,
Bernaldo de Quirós FG,
González-Neira A,
González-Peñas J,
Gutiérrez-Bautista JF,
Herrero MJ,
Herrero-Gonzalez A,
Jimenez-Sousa MA,
Lattig MC,
Borja AL,
Lopez-Rodriguez R,
Mancebo E,
Martín-López C,
Martín V,
Martinez-Nieto O,
Martinez-Lopez I,
Martinez-Resendez MF,
Martinez-Perez A,
Mazzeu JF,
Macías EM,
Minguez P,
Cuerda VM,
Oliveira SF,
Ortega-Paino E,
Parellada M,
Paz-Artal E,
Santos NPC,
Pérez-Matute P,
Perez P,
Pérez-Tomás ME,
Perucho T,
Pinsach-Abuin M,
Pita G,
Pompa-Mera EN,
Porras-Hurtado GL,
Pujol A,
León SR,
Resino S,
Fernandes MR,
Rodríguez-Ruiz E,
Rodriguez-Artalejo F,
Rodriguez-Garcia JA,
Ruiz-Cabello F,
Ruiz-Hornillos J,
Ryan P,
Soria JM,
Souto JC,
Tamayo E,
Tamayo-Velasco A,
Taracido-Fernandez JC,
Teper A,
Torres-Tobar L,
Urioste M,
Valencia-Ramos J,
Yáñez Z,
Zarate R,
de Rojas I,
Ruiz A,
Sánchez P,
Real LM,
Guillen-Navarro E,
Ayuso C,
Parra E,
Riancho JA,
Rojas-Martinez A,
Flores C,
Lapunzina P,
Carracedo Á
SCOURGE Cohort Group
eLife · 2024 · PMID 39361370 · open access
12 pages+
Novel loci and biomedical consequences of iron homoeostasis variation
Allara E,
Bell S,
Smith R,
Keene SJ,
Gill D,
Gaziano L,
Morselli Gysi D,
Wang F,
Tragante V,
Mason A,
Karthikeyan S,
Lumbers RT
and 60 more — show all
Bonglack E,
Ouwehand W,
Roberts DJ,
Dowsett J,
Ostrowski SR,
Larsen MH,
Ullum H,
Pedersen OB,
Brunak S,
Banasik K,
Erikstrup C,
Mitchell J,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Girelli D,
Arvas M,
Toivonen J,
Molnos S,
Peters A,
Polasek O,
Rudan I,
Hayward C,
McDonnell C,
Pirastu N,
Wilson JF,
van den Hurk K,
Quee F,
Ferrucci L,
Bandinelli S,
Tanaka T,
Girotto G,
Concas MP,
Pecori A,
Verweij N,
van der Harst P,
van de Vegte YJ,
Kiemeney LA,
Sweep FC,
Galesloot TE,
Sulem P,
Gudbjartsson D,
Ferkingstad E,
Djousse L,
Cho K,
Inouye M,
Burgess S,
Benyamin B,
Oexle K,
Swinkels D,
Stefansson K,
Magnusson M,
Ganna A,
Gaziano M,
Ivey K,
Danesh J,
Pereira A,
Wood AM,
Butterworth AS,
Di Angelantonio E
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
12 pages+
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Small AM,
Yang TY,
Itoh S,
Thériault S,
Dufresne L,
Kurosawa R,
Komuro I,
Matsuda K,
Vy HMT,
Farber-Eger EH,
Shaffer LL,
Boulier KM
and 89 more — show all
Corey KM,
Ramaker ME,
Laporte F,
Schott JJ,
Le Scouarnec S,
Singh SA,
Sonawane AR,
Smith HA,
Rafaels N,
Ghouse J,
Raja AA,
Ostrowski SR,
Sørensen E,
Mikkelsen C,
Pedersen OB,
Erikstrup C,
Ullum H,
Sveinbjornsson G,
Gudbjartsson DF,
Abner E,
Lee J,
Ganna A,
Nowak-Göttl U,
Finer S,
Schumacher J,
Maj C,
Al-Kassou B,
Nickenig G,
Trenkwalder T,
Dreβen M,
Krane M,
Nöthen MM,
Moksnes MR,
Brumpton BM,
Knight S,
Knowlton KU,
Nadauld L,
Debiec R,
Musameh MD,
Braund PS,
Nelson CP,
Czuba T,
Melander O,
Selvaraj MS,
Koyama S,
Bhukar R,
Ruan Y,
Ljungberg J,
Damrauer SM,
Levin MG,
Franke A,
Berger K,
Ruff CT,
Melloni GEM,
Kamanu FK,
Ito K,
Do R,
Loos RJF,
Schunkert H,
Wells QS,
Shah SH,
Le Tourneau T,
Messika-Zeitoun D,
Gignoux C,
Bundgaard H,
Larsson SC,
Michaëlsson K,
Holm H,
Helgadottir A,
Esko T,
van Heel DA,
Mathieu P,
Samani NJ,
Smith JG,
Söderberg S,
Rader DJ,
Marston NA,
Sabatine MS,
Pasaniuc B,
Cho K,
Wilson PWF,
O'Donnell CJ,
Stefansson K,
Bossé Y,
Aikawa E,
Engert JC,
Peloso GM,
Natarajan P,
Thanassoulis G
Colorado Center for Personalized Medicine · DBDS Genomic Consortium and 2 more consortia
Nature genetics · 2026 · PMID 41419686 · open access
12 pages+
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
White SL,
Brasher MS,
Pattee J,
Zhou W,
Chapman S,
Jee YH,
Bell CC,
Jamil TL,
Barrio M,
Arehart CH,
Evans LM,
Hirbo J
and 73 more — show all
Cox NJ,
Straub P,
Namba S,
Bertucci-Richter E,
Guare L,
Edris A,
Morris S,
Mulford AJ,
Zhang H,
Fennessy B,
Tobin MD,
Chen J,
Williams AT,
John C,
van Heel DA,
Mathur R,
Finer S,
Moksnes MR,
Brumpton BM,
Åsvold BO,
Peculis R,
Rovite V,
Konrade I,
Wang Y,
Crooks K,
Chavan S,
Fisher MJ,
Rafaels N,
Lin M,
Shortt JA,
Sanders AR,
Whiteman DC,
MacGregor S,
Medland SE,
Thorsteinsdóttir U,
Stefánsson K,
Karaderi T,
Egan KM,
Bocklage T,
McCrary HC,
Riedlinger G,
Salhia B,
Shriver C,
Phan MD,
Farlow JL,
Edge S,
Kaur V,
Churchman ML,
Rounbehler RJ,
Brock PL,
Ringel MD,
Pividori M,
Schweppe R,
Raeburn CD,
Walters RG,
Chen Z,
Li L,
Matsuda K,
Okada Y,
Zöllner S,
Verma A,
Preuss MH,
Kenny E,
Hendricks AE,
Fishbein L,
Kraft P,
Daly MJ,
Neale BM,
Martin AR,
Cole JB,
Haugen BR,
Gignoux CR,
Pozdeyev N
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium and 4 more consortia
Nature genetics · 2026 · PMID 41644669 · open access
12 pages+
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Speliotes EK,
Willer CJ,
Berndt SI,
Monda KL,
Thorleifsson G,
Jackson AU,
Lango Allen H,
Lindgren CM,
Luan J,
Mägi R,
Randall JC,
Vedantam S
and 366 more — show all
Winkler TW,
Qi L,
Workalemahu T,
Heid IM,
Steinthorsdottir V,
Stringham HM,
Weedon MN,
Wheeler E,
Wood AR,
Ferreira T,
Weyant RJ,
Segrè AV,
Estrada K,
Liang L,
Nemesh J,
Park JH,
Gustafsson S,
Kilpeläinen TO,
Yang J,
Bouatia-Naji N,
Esko T,
Feitosa MF,
Kutalik Z,
Mangino M,
Raychaudhuri S,
Scherag A,
Smith AV,
Welch R,
Zhao JH,
Aben KK,
Absher DM,
Amin N,
Dixon AL,
Fisher E,
Glazer NL,
Goddard ME,
Heard-Costa NL,
Hoesel V,
Hottenga JJ,
Johansson A,
Johnson T,
Ketkar S,
Lamina C,
Li S,
Moffatt MF,
Myers RH,
Narisu N,
Perry JR,
Peters MJ,
Preuss M,
Ripatti S,
Rivadeneira F,
Sandholt C,
Scott LJ,
Timpson NJ,
Tyrer JP,
van Wingerden S,
Watanabe RM,
White CC,
Wiklund F,
Barlassina C,
Chasman DI,
Cooper MN,
Jansson JO,
Lawrence RW,
Pellikka N,
Prokopenko I,
Shi J,
Thiering E,
Alavere H,
Alibrandi MT,
Almgren P,
Arnold AM,
Aspelund T,
Atwood LD,
Balkau B,
Balmforth AJ,
Bennett AJ,
Ben-Shlomo Y,
Bergman RN,
Bergmann S,
Biebermann H,
Blakemore AI,
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NEIGHBOR Consortium
Nature genetics · 2013 · PMID 23291589
10 pages
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
Bao EL,
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Li B
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Emdin C,
Codd V,
Nelson CP,
Walker CJ,
Churchhouse C,
de la Chapelle A,
Klein DE,
Nilsson B,
Wilson PWF,
Cho K,
Pyarajan S,
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Regev A,
Palotie A,
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Kathiresan S,
Sankaran VG
FinnGen · 23andMe Research Team
Nature · 2020 · PMID 33057200 · open access
10 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.