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16 matches for
Scheet P.
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
Purdue MP,
Dutta D,
Machiela MJ,
Gorman BR,
Winter T,
Okuhara D,
Cleland S,
Ferreiro-Iglesias A,
Scheet P,
Liu A,
Wu C,
Antwi SO
and 120 more — show all
Larkin J,
Zequi SC,
Sun M,
Hikino K,
Hajiran A,
Lawson KA,
Cárcano F,
Blanchet O,
Shuch B,
Nepple KG,
Margue G,
Sundi D,
Diver WR,
Folgueira MAAK,
van Bokhoven A,
Neffa F,
Brown KM,
Hofmann JN,
Rhee J,
Yeager M,
Cole NR,
Hicks BD,
Manning MR,
Hutchinson AA,
Rothman N,
Huang WY,
Linehan WM,
Lori A,
Ferragu M,
Zidane-Marinnes M,
Serrano SV,
Magnabosco WJ,
Vilas A,
Decia R,
Carusso F,
Graham LS,
Anderson K,
Bilen MA,
Arciero C,
Pellegrin I,
Ricard S,
Scelo G,
Banks RE,
Vasudev NS,
Soomro N,
Stewart GD,
Adeyoju A,
Bromage S,
Hrouda D,
Gibbons N,
Patel P,
Sullivan M,
Protheroe A,
Nugent FI,
Fournier MJ,
Zhang X,
Martin LJ,
Komisarenko M,
Eisen T,
Cunningham SA,
Connolly DC,
Uzzo RG,
Zaridze D,
Mukeria A,
Holcatova I,
Hornakova A,
Foretova L,
Janout V,
Mates D,
Jinga V,
Rascu S,
Mijuskovic M,
Savic S,
Milosavljevic S,
Gaborieau V,
Abedi-Ardekani B,
McKay J,
Johansson M,
Phouthavongsy L,
Hayman L,
Li J,
Lungu I,
Bezerra SM,
Souza AG,
Sares CTG,
Reis RB,
Gallucci FP,
Cordeiro MD,
Pomerantz M,
Lee GM,
Freedman ML,
Jeong A,
Greenberg SE,
Sanchez A,
Thompson RH,
Sharma V,
Thiel DD,
Ball CT,
Abreu D,
Lam ET,
Nahas WC,
Master VA,
Patel AV,
Bernhard JC,
Freedman ND,
Bigot P,
Reis RM,
Colli LM,
Finelli A,
Manley BJ,
Terao C,
Choueiri TK,
Carraro DM,
Houlston R,
Eckel-Passow JE,
Abbosh PH,
Ganna A,
Brennan P,
Gu J,
Chanock SJ
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
Common variants at 30 loci contribute to polygenic dyslipidemia
Kathiresan S,
Willer CJ,
Peloso GM,
Demissie S,
Musunuru K,
Schadt EE,
Kaplan L,
Bennett D,
Li Y,
Tanaka T,
Voight BF,
Bonnycastle LL
and 49 more — show all
Jackson AU,
Crawford G,
Surti A,
Guiducci C,
Burtt NP,
Parish S,
Clarke R,
Zelenika D,
Kubalanza KA,
Morken MA,
Scott LJ,
Stringham HM,
Galan P,
Swift AJ,
Kuusisto J,
Bergman RN,
Sundvall J,
Laakso M,
Ferrucci L,
Scheet P,
Sanna S,
Uda M,
Yang Q,
Lunetta KL,
Dupuis J,
de Bakker PI,
O'Donnell CJ,
Chambers JC,
Kooner JS,
Hercberg S,
Meneton P,
Lakatta EG,
Scuteri A,
Schlessinger D,
Tuomilehto J,
Collins FS,
Groop L,
Altshuler D,
Collins R,
Lathrop GM,
Melander O,
Salomaa V,
Peltonen L,
Orho-Melander M,
Ordovas JM,
Boehnke M,
Abecasis GR,
Mohlke KL,
Cupples LA
Nature genetics · 2009 · PMID 19060906
9 pages
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels
Dehghan A,
Dupuis J,
Barbalic M,
Bis JC,
Eiriksdottir G,
Lu C,
Pellikka N,
Wallaschofski H,
Kettunen J,
Henneman P,
Baumert J,
Strachan DP
and 102 more — show all
Fuchsberger C,
Vitart V,
Wilson JF,
Paré G,
Naitza S,
Rudock ME,
Surakka I,
de Geus EJ,
Alizadeh BZ,
Guralnik J,
Shuldiner A,
Tanaka T,
Zee RY,
Schnabel RB,
Nambi V,
Kavousi M,
Ripatti S,
Nauck M,
Smith NL,
Smith AV,
Sundvall J,
Scheet P,
Liu Y,
Ruokonen A,
Rose LM,
Larson MG,
Hoogeveen RC,
Freimer NB,
Teumer A,
Tracy RP,
Launer LJ,
Buring JE,
Yamamoto JF,
Folsom AR,
Sijbrands EJ,
Pankow J,
Elliott P,
Keaney JF,
Sun W,
Sarin AP,
Fontes JD,
Badola S,
Astor BC,
Hofman A,
Pouta A,
Werdan K,
Greiser KH,
Kuss O,
Meyer zu Schwabedissen HE,
Thiery J,
Jamshidi Y,
Nolte IM,
Soranzo N,
Spector TD,
Völzke H,
Parker AN,
Aspelund T,
Bates D,
Young L,
Tsui K,
Siscovick DS,
Guo X,
Rotter JI,
Uda M,
Schlessinger D,
Rudan I,
Hicks AA,
Penninx BW,
Thorand B,
Gieger C,
Coresh J,
Willemsen G,
Harris TB,
Uitterlinden AG,
Järvelin MR,
Rice K,
Radke D,
Salomaa V,
Willems van Dijk K,
Boerwinkle E,
Vasan RS,
Ferrucci L,
Gibson QD,
Bandinelli S,
Snieder H,
Boomsma DI,
Xiao X,
Campbell H,
Hayward C,
Pramstaller PP,
van Duijn CM,
Peltonen L,
Psaty BM,
Gudnason V,
Ridker PM,
Homuth G,
Koenig W,
Ballantyne CM,
Witteman JC,
Benjamin EJ,
Perola M,
Chasman DI
Circulation · 2011 · PMID 21300955
9 pages
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes
Miller FW,
Chen W,
O'Hanlon TP,
Cooper RG,
Vencovsky J,
Rider LG,
Danko K,
Wedderburn LR,
Lundberg IE,
Pachman LM,
Reed AM,
Ytterberg SR
and 13 more — show all
Padyukov L,
Selva-O'Callaghan A,
Radstake TR,
Isenberg DA,
Chinoy H,
Ollier WE,
Scheet P,
Peng B,
Lee A,
Byun J,
Lamb JA,
Gregersen PK,
Amos CI
Myositis Genetics Consortium
Genes and immunity · 2015 · PMID 26291516
9 pages
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
Dastani Z,
Hivert MF,
Timpson N,
Perry JR,
Yuan X,
Scott RA,
Henneman P,
Heid IM,
Kizer JR,
Lyytikäinen LP,
Fuchsberger C,
Tanaka T
and 548 more — show all
Morris AP,
Small K,
Isaacs A,
Beekman M,
Coassin S,
Lohman K,
Qi L,
Kanoni S,
Pankow JS,
Uh HW,
Wu Y,
Bidulescu A,
Rasmussen-Torvik LJ,
Greenwood CM,
Ladouceur M,
Grimsby J,
Manning AK,
Liu CT,
Kooner J,
Mooser VE,
Vollenweider P,
Kapur KA,
Chambers J,
Wareham NJ,
Langenberg C,
Frants R,
Willems-Vandijk K,
Oostra BA,
Willems SM,
Lamina C,
Winkler TW,
Psaty BM,
Tracy RP,
Brody J,
Chen I,
Viikari J,
Kähönen M,
Pramstaller PP,
Evans DM,
St Pourcain B,
Sattar N,
Wood AR,
Bandinelli S,
Carlson OD,
Egan JM,
Böhringer S,
van Heemst D,
Kedenko L,
Kristiansson K,
Nuotio ML,
Loo BM,
Harris T,
Garcia M,
Kanaya A,
Haun M,
Klopp N,
Wichmann HE,
Deloukas P,
Katsareli E,
Couper DJ,
Duncan BB,
Kloppenburg M,
Adair LS,
Borja JB,
Wilson JG,
Musani S,
Guo X,
Johnson T,
Semple R,
Teslovich TM,
Allison MA,
Redline S,
Buxbaum SG,
Mohlke KL,
Meulenbelt I,
Ballantyne CM,
Dedoussis GV,
Hu FB,
Liu Y,
Paulweber B,
Spector TD,
Slagboom PE,
Ferrucci L,
Jula A,
Perola M,
Raitakari O,
Florez JC,
Salomaa V,
Eriksson JG,
Frayling TM,
Hicks AA,
Lehtimäki T,
Smith GD,
Siscovick DS,
Kronenberg F,
van Duijn C,
Loos RJ,
Waterworth DM,
Meigs JB,
Dupuis J,
Richards JB,
Voight BF,
Scott LJ,
Steinthorsdottir V,
Dina C,
Welch RP,
Zeggini E,
Huth C,
Aulchenko YS,
Thorleifsson G,
McCulloch LJ,
Ferreira T,
Grallert H,
Amin N,
Wu G,
Willer CJ,
Raychaudhuri S,
McCarroll SA,
Hofmann OM,
Segrè AV,
van Hoek M,
Navarro P,
Ardlie K,
Balkau B,
Benediktsson R,
Bennett AJ,
Blagieva R,
Boerwinkle E,
Bonnycastle LL,
Boström KB,
Bravenboer B,
Bumpstead S,
Burtt NP,
Charpentier G,
Chines PS,
Cornelis M,
Crawford G,
Doney AS,
Elliott KS,
Elliott AL,
Erdos MR,
Fox CS,
Franklin CS,
Ganser M,
Gieger C,
Grarup N,
Green T,
Griffin S,
Groves CJ,
Guiducci C,
Hadjadj S,
Hassanali N,
Herder C,
Isomaa B,
Jackson AU,
Johnson PR,
Jørgensen T,
Kao WH,
Kong A,
Kraft P,
Kuusisto J,
Lauritzen T,
Li M,
Lieverse A,
Lindgren CM,
Lyssenko V,
Marre M,
Meitinger T,
Midthjell K,
Morken MA,
Narisu N,
Nilsson P,
Owen KR,
Payne F,
Petersen AK,
Platou C,
Proença C,
Prokopenko I,
Rathmann W,
Rayner NW,
Robertson NR,
Rocheleau G,
Roden M,
Sampson MJ,
Saxena R,
Shields BM,
Shrader P,
Sigurdsson G,
Sparsø T,
Strassburger K,
Stringham HM,
Sun Q,
Swift AJ,
Thorand B,
Tichet J,
Tuomi T,
van Dam RM,
van Haeften TW,
van Herpt T,
van Vliet-Ostaptchouk JV,
Walters GB,
Weedon MN,
Wijmenga C,
Witteman J,
Bergman RN,
Cauchi S,
Collins FS,
Gloyn AL,
Gyllensten U,
Hansen T,
Hide WA,
Hitman GA,
Hofman A,
Hunter DJ,
Hveem K,
Laakso M,
Morris AD,
Palmer CN,
Rudan I,
Sijbrands E,
Stein LD,
Tuomilehto J,
Uitterlinden A,
Walker M,
Watanabe RM,
Abecasis GR,
Boehm BO,
Campbell H,
Daly MJ,
Hattersley AT,
Pedersen O,
Barroso I,
Groop L,
Sladek R,
Thorsteinsdottir U,
Wilson JF,
Illig T,
Froguel P,
van Duijn CM,
Stefansson K,
Altshuler D,
Boehnke M,
McCarthy MI,
Soranzo N,
Wheeler E,
Glazer NL,
Bouatia-Naji N,
Mägi R,
Randall J,
Elliott P,
Rybin D,
Dehghan A,
Hottenga JJ,
Song K,
Goel A,
Lajunen T,
Doney A,
Cavalcanti-Proença C,
Kumari M,
Timpson NJ,
Zabena C,
Ingelsson E,
An P,
O'Connell J,
Luan J,
Elliott A,
McCarroll SA,
Roccasecca RM,
Pattou F,
Sethupathy P,
Ariyurek Y,
Barter P,
Beilby JP,
Ben-Shlomo Y,
Bergmann S,
Bochud M,
Bonnefond A,
Borch-Johnsen K,
Böttcher Y,
Brunner E,
Bumpstead SJ,
Chen YD,
Chines P,
Clarke R,
Coin LJ,
Cooper MN,
Crisponi L,
Day IN,
de Geus EJ,
Delplanque J,
Fedson AC,
Fischer-Rosinsky A,
Forouhi NG,
Franzosi MG,
Galan P,
Goodarzi MO,
Graessler J,
Grundy S,
Gwilliam R,
Hallmans G,
Hammond N,
Han X,
Hartikainen AL,
Hayward C,
Heath SC,
Hercberg S,
Hillman DR,
Hingorani AD,
Hui J,
Hung J,
Kaakinen M,
Kaprio J,
Kesaniemi YA,
Kivimaki M,
Knight B,
Koskinen S,
Kovacs P,
Kyvik KO,
Lathrop GM,
Lawlor DA,
Le Bacquer O,
Lecoeur C,
Li Y,
Mahley R,
Mangino M,
Martínez-Larrad MT,
McAteer JB,
McPherson R,
Meisinger C,
Melzer D,
Meyre D,
Mitchell BD,
Mukherjee S,
Naitza S,
Neville MJ,
Orrù M,
Pakyz R,
Paolisso G,
Pattaro C,
Pearson D,
Peden JF,
Pedersen NL,
Pfeiffer AF,
Pichler I,
Polasek O,
Posthuma D,
Potter SC,
Pouta A,
Province MA,
Rayner NW,
Rice K,
Ripatti S,
Rivadeneira F,
Rolandsson O,
Sandbaek A,
Sandhu M,
Sanna S,
Sayer AA,
Scheet P,
Seedorf U,
Sharp SJ,
Shields B,
Sigurðsson G,
Sijbrands EJ,
Silveira A,
Simpson L,
Singleton A,
Smith NL,
Sovio U,
Swift A,
Syddall H,
Syvänen AC,
Tönjes A,
Uitterlinden AG,
van Dijk KW,
Varma D,
Visvikis-Siest S,
Vitart V,
Vogelzangs N,
Waeber G,
Wagner PJ,
Walley A,
Ward KL,
Watkins H,
Wild SH,
Willemsen G,
Witteman JC,
Yarnell JW,
Zelenika D,
Zethelius B,
Zhai G,
Zhao JH,
Zillikens MC,
Borecki IB,
Meneton P,
Magnusson PK,
Nathan DM,
Williams GH,
Silander K,
Bornstein SR,
Schwarz P,
Spranger J,
Karpe F,
Shuldiner AR,
Cooper C,
Serrano-Ríos M,
Lind L,
Palmer LJ,
Hu FB 1st,
Franks PW,
Ebrahim S,
Marmot M,
Kao WH,
Pramstaller PP,
Wright AF,
Stumvoll M,
Hamsten A,
Buchanan TA,
Valle TT,
Rotter JI,
Penninx BW,
Boomsma DI,
Cao A,
Scuteri A,
Schlessinger D,
Uda M,
Ruokonen A,
Jarvelin MR,
Peltonen L,
Mooser V,
Sladek R,
Musunuru K,
Smith AV,
Edmondson AC,
Stylianou IM,
Koseki M,
Pirruccello JP,
Chasman DI,
Johansen CT,
Fouchier SW,
Peloso GM,
Barbalic M,
Ricketts SL,
Bis JC,
Feitosa MF,
Orho-Melander M,
Melander O,
Li X,
Li M,
Cho YS,
Go MJ,
Kim YJ,
Lee JY,
Park T,
Kim K,
Sim X,
Ong RT,
Croteau-Chonka DC,
Lange LA,
Smith JD,
Ziegler A,
Zhang W,
Zee RY,
Whitfield JB,
Thompson JR,
Surakka I,
Spector TD,
Smit JH,
Sinisalo J,
Scott J,
Saharinen J,
Sabatti C,
Rose LM,
Roberts R,
Rieder M,
Parker AN,
Pare G,
O'Donnell CJ,
Nieminen MS,
Nickerson DA,
Montgomery GW,
McArdle W,
Masson D,
Martin NG,
Marroni F,
Lucas G,
Luben R,
Lokki ML,
Lettre G,
Launer LJ,
Lakatta EG,
Laaksonen R,
Kyvik KO,
König IR,
Khaw KT,
Kaplan LM,
Johansson Å,
Janssens AC,
Igl W,
Hovingh GK,
Hengstenberg C,
Havulinna AS,
Hastie ND,
Harris TB,
Haritunians T,
Hall AS,
Groop LC,
Gonzalez E,
Freimer NB,
Erdmann J,
Ejebe KG,
Döring A,
Dominiczak AF,
Demissie S,
Deloukas P,
de Faire U,
Crawford G,
Chen YD,
Caulfield MJ,
Boekholdt SM,
Assimes TL,
Quertermous T,
Seielstad M,
Wong TY,
Tai ES,
Feranil AB,
Kuzawa CW,
Taylor HA Jr,
Gabriel SB,
Holm H,
Gudnason V,
Krauss RM,
Ordovas JM,
Munroe PB,
Kooner JS,
Tall AR,
Hegele RA,
Kastelein JJ,
Schadt EE,
Strachan DP,
Reilly MP,
Samani NJ,
Schunkert H,
Cupples LA,
Sandhu MS,
Ridker PM,
Rader DJ,
Kathiresan S
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
Willer CJ,
Sanna S,
Jackson AU,
Scuteri A,
Bonnycastle LL,
Clarke R,
Heath SC,
Timpson NJ,
Najjar SS,
Stringham HM,
Strait J,
Duren WL
and 38 more — show all
Maschio A,
Busonero F,
Mulas A,
Albai G,
Swift AJ,
Morken MA,
Narisu N,
Bennett D,
Parish S,
Shen H,
Galan P,
Meneton P,
Hercberg S,
Zelenika D,
Chen WM,
Li Y,
Scott LJ,
Scheet PA,
Sundvall J,
Watanabe RM,
Nagaraja R,
Ebrahim S,
Lawlor DA,
Ben-Shlomo Y,
Davey-Smith G,
Shuldiner AR,
Collins R,
Bergman RN,
Uda M,
Tuomilehto J,
Cao A,
Collins FS,
Lakatta E,
Lathrop GM,
Boehnke M,
Schlessinger D,
Mohlke KL,
Abecasis GR
Nature genetics · 2008 · PMID 18193043
5 pages
Genome-wide association study identifies eight loci associated with blood pressure
Newton-Cheh C,
Johnson T,
Gateva V,
Tobin MD,
Bochud M,
Coin L,
Najjar SS,
Zhao JH,
Heath SC,
Eyheramendy S,
Papadakis K,
Voight BF
and 147 more — show all
Scott LJ,
Zhang F,
Farrall M,
Tanaka T,
Wallace C,
Chambers JC,
Khaw KT,
Nilsson P,
van der Harst P,
Polidoro S,
Grobbee DE,
Onland-Moret NC,
Bots ML,
Wain LV,
Elliott KS,
Teumer A,
Luan J,
Lucas G,
Kuusisto J,
Burton PR,
Hadley D,
McArdle WL,
Brown M,
Dominiczak A,
Newhouse SJ,
Samani NJ,
Webster J,
Zeggini E,
Beckmann JS,
Bergmann S,
Lim N,
Song K,
Vollenweider P,
Waeber G,
Waterworth DM,
Yuan X,
Groop L,
Orho-Melander M,
Allione A,
Di Gregorio A,
Guarrera S,
Panico S,
Ricceri F,
Romanazzi V,
Sacerdote C,
Vineis P,
Barroso I,
Sandhu MS,
Luben RN,
Crawford GJ,
Jousilahti P,
Perola M,
Boehnke M,
Bonnycastle LL,
Collins FS,
Jackson AU,
Mohlke KL,
Stringham HM,
Valle TT,
Willer CJ,
Bergman RN,
Morken MA,
Döring A,
Gieger C,
Illig T,
Meitinger T,
Org E,
Org E,
Pfeufer A,
Wichmann HE,
Kathiresan S,
Marrugat J,
O'Donnell CJ,
Schwartz SM,
Siscovick DS,
Subirana I,
Freimer NB,
Hartikainen AL,
McCarthy MI,
O'Reilly PF,
Peltonen L,
Pouta A,
de Jong PE,
Snieder H,
van Gilst WH,
Clarke R,
Goel A,
Hamsten A,
Peden JF,
Seedorf U,
Syvänen AC,
Tognoni G,
Lakatta EG,
Sanna S,
Scheet P,
Schlessinger D,
Scuteri A,
Dörr M,
Ernst F,
Felix SB,
Homuth G,
Lorbeer R,
Reffelmann T,
Rettig R,
Völker U,
Galan P,
Gut IG,
Hercberg S,
Lathrop GM,
Zelenika D,
Deloukas P,
Soranzo N,
Williams FM,
Zhai G,
Salomaa V,
Laakso M,
Elosua R,
Forouhi NG,
Völzke H,
Uiterwaal CS,
van der Schouw YT,
Numans ME,
Matullo G,
Navis G,
Berglund G,
Bingham SA,
Kooner JS,
Connell JM,
Bandinelli S,
Ferrucci L,
Watkins H,
Spector TD,
Tuomilehto J,
Altshuler D,
Strachan DP,
Laan M,
Meneton P,
Wareham NJ,
Uda M,
Jarvelin MR,
Mooser V,
Melander O,
Loos RJ,
Elliott P,
Abecasis GR,
Caulfield M,
Munroe PB
Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19430483 · open access
4 pages
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Dupuis J,
Langenberg C,
Prokopenko I,
Saxena R,
Soranzo N,
Jackson AU,
Wheeler E,
Glazer NL,
Bouatia-Naji N,
Gloyn AL,
Lindgren CM,
Mägi R
and 292 more — show all
Morris AP,
Randall J,
Johnson T,
Elliott P,
Rybin D,
Thorleifsson G,
Steinthorsdottir V,
Henneman P,
Grallert H,
Dehghan A,
Hottenga JJ,
Franklin CS,
Navarro P,
Song K,
Goel A,
Perry JR,
Egan JM,
Lajunen T,
Grarup N,
Sparsø T,
Doney A,
Voight BF,
Stringham HM,
Li M,
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Karol SE,
Yang W,
Van Driest SL,
Chang TY,
Kaste S,
Bowton E,
Basford M,
Bastarache L,
Roden DM,
Denny JC,
Larsen E,
Winick N
and 16 more — show all
Carroll WL,
Cheng C,
Pei D,
Fernandez CA,
Liu C,
Smith C,
Loh ML,
Raetz EA,
Hunger SP,
Scheet P,
Jeha S,
Pui CH,
Evans WE,
Devidas M,
Mattano LA Jr,
Relling MV
Blood · 2015 · PMID 26265699
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.