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61 matches for
He M,
showing the first 20.
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
He M,
Xu M,
Zhang B,
Liang J,
Chen P,
Lee JY,
Johnson TA,
Li H,
Yang X,
Dai J,
Liang L,
Gui L
and 79 more — show all
Qi Q,
Huang J,
Li Y,
Adair LS,
Aung T,
Cai Q,
Cheng CY,
Cho MC,
Cho YS,
Chu M,
Cui B,
Gao YT,
Go MJ,
Gu D,
Gu W,
Guo H,
Hao Y,
Hong J,
Hu Z,
Hu Y,
Huang J,
Hwang JY,
Ikram MK,
Jin G,
Kang DH,
Khor CC,
Kim BJ,
Kim HT,
Kubo M,
Lee J,
Lee J,
Lee NR,
Li R,
Li J,
Liu J,
Longe J,
Lu W,
Lu X,
Miao X,
Okada Y,
Ong RT,
Qiu G,
Seielstad M,
Sim X,
Song H,
Takeuchi F,
Tanaka T,
Taylor PR,
Wang L,
Wang W,
Wang Y,
Wu C,
Wu Y,
Xiang YB,
Yamamoto K,
Yang H,
Liao M,
Yokota M,
Young T,
Zhang X,
Kato N,
Wang QK,
Zheng W,
Zheng W,
Hu FB,
Lin D,
Shen H,
Teo YY,
Mo Z,
Wong TY,
Lin X,
Mohlke KL,
Ning G,
Tsunoda T,
Han BG,
Shu XO,
Tai ES,
Wu T,
Qi L
Human molecular genetics · 2015 · PMID 25429064
12 pages+
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Spracklen CN,
Chen P,
Kim YJ,
Wang X,
Cai H,
Li S,
Long J,
Wu Y,
Wang YX,
Takeuchi F,
Wu JY,
Jung KJ
and 103 more — show all
Hu C,
Akiyama K,
Zhang Y,
Moon S,
Johnson TA,
Li H,
Dorajoo R,
He M,
Cannon ME,
Roman TS,
Salfati E,
Lin KH,
Guo X,
Sheu WHH,
Absher D,
Adair LS,
Assimes TL,
Aung T,
Cai Q,
Chang LC,
Chen CH,
Chien LH,
Chuang LM,
Chuang SC,
Du S,
Fan Q,
Fann CSJ,
Feranil AB,
Friedlander Y,
Gordon-Larsen P,
Gu D,
Gui L,
Guo Z,
Heng CK,
Hixson J,
Hou X,
Hsiung CA,
Hu Y,
Hwang MY,
Hwu CM,
Isono M,
Juang JJ,
Khor CC,
Kim YK,
Koh WP,
Kubo M,
Lee IT,
Lee SJ,
Lee WJ,
Liang KW,
Lim B,
Lim SH,
Liu J,
Nabika T,
Pan WH,
Peng H,
Quertermous T,
Sabanayagam C,
Sandow K,
Shi J,
Sun L,
Tan PC,
Tan SP,
Taylor KD,
Teo YY,
Toh SA,
Tsunoda T,
van Dam RM,
Wang A,
Wang F,
Wang J,
Wei WB,
Xiang YB,
Yao J,
Yuan JM,
Zhang R,
Zhao W,
Chen YI,
Rich SS,
Rotter JI,
Wang TD,
Wu T,
Lin X,
Han BG,
Tanaka T,
Cho YS,
Katsuya T,
Jia W,
Jee SH,
Chen YT,
Kato N,
Jonas JB,
Cheng CY,
Shu XO,
He J,
Zheng W,
Zheng W,
Wong TY,
Huang W,
Kim BJ,
Tai ES,
Mohlke KL,
Sim X
Human molecular genetics · 2017 · PMID 28334899
12 pages+
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
Feitosa MF,
Kraja AT,
Chasman DI,
Sung YJ,
Winkler TW,
Ntalla I,
Guo X,
Franceschini N,
Cheng CY,
Sim X,
Vojinovic D,
Marten J
and 261 more — show all
Musani SK,
Li C,
Bentley AR,
Brown MR,
Schwander K,
Richard MA,
Noordam R,
Aschard H,
Bartz TM,
Bielak LF,
Dorajoo R,
Fisher V,
Hartwig FP,
Horimoto ARVR,
Lohman KK,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Wojczynski MK,
Alver M,
Boissel M,
Cai Q,
Campbell A,
Chai JF,
Chen X,
Divers J,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
He M,
Hsu FC,
Jackson AU,
Kähönen M,
Kasturiratne A,
Komulainen P,
Kühnel B,
Laguzzi F,
Luan J,
Matoba N,
Nolte IM,
Padmanabhan S,
Riaz M,
Rueedi R,
Robino A,
Said MA,
Scott RA,
Sofer T,
Stančáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Vitart V,
Wang Y,
Ware EB,
Warren HR,
Weiss S,
Wen W,
Yanek LR,
Zhang W,
Zhao JH,
Afaq S,
Amin N,
Amini M,
Arking DE,
Aung T,
Boerwinkle E,
Borecki I,
Broeckel U,
Brown M,
Brumat M,
Burke GL,
Canouil M,
Chakravarti A,
Charumathi S,
Ida Chen YD,
Connell JM,
Correa A,
de las Fuentes L,
de Mutsert R,
de Silva HJ,
Deng X,
Ding J,
Duan Q,
Eaton CB,
Ehret G,
Eppinga RN,
Evangelou E,
Faul JD,
Felix SB,
Forouhi NG,
Forrester T,
Franco OH,
Friedlander Y,
Gandin I,
Gao H,
Ghanbari M,
Gigante B,
Gu CC,
Gu D,
Hagenaars SP,
Hallmans G,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hirata M,
Howard BV,
Ikram MA,
John U,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Lin S,
Liu J,
Liu J,
Loh M,
Louie T,
Mägi R,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Momozawa Y,
Nalls MA,
Nelson CP,
Sotoodehnia N,
Norris JM,
O'Connell JR,
Palmer ND,
Perls T,
Pedersen NL,
Peters A,
Peyser PA,
Poulter N,
Raffel LJ,
Raitakari OT,
Roll K,
Rose LM,
Rosendaal FR,
Rotter JI,
Schmidt CO,
Schreiner PJ,
Schupf N,
Scott WR,
Sever PS,
Shi Y,
Sidney S,
Sims M,
Sitlani CM,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Stringham HM,
Tan NYQ,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Turner ST,
Uitterlinden AG,
Vollenweider P,
Waldenberger M,
Wang L,
Wang YX,
Wei WB,
Williams C,
Yao J,
Yu C,
Yuan JM,
Zhao W,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Deary IJ,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Jonas JB,
Kamatani Y,
Kato N,
Kooner JS,
Kutalik Z,
Laakso M,
Laurie CC,
Leander K,
Lehtimäki T,
Study LC,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Polasek O,
Porteous DJ,
Rauramaa R,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zheng W,
Bouchard C,
Christensen K,
Evans MK,
Gudnason V,
Horta BL,
Kardia SLR,
Liu Y,
Pereira AC,
Psaty BM,
Ridker PM,
van Dam RM,
Gauderman WJ,
Zhu X,
Mook-Kanamori DO,
Fornage M,
Rotimi CN,
Cupples LA,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Kooperberg C,
Palmas W,
Rice K,
Morrison AC,
Elliott P,
Caulfield MJ,
Munroe PB,
Rao DC,
Province MA,
Levy D
InterAct Consortium
PloS one · 2018 · PMID 29912962 · open access
12 pages+
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Klarin D,
Damrauer SM,
Cho K,
Sun YV,
Teslovich TM,
Honerlaw J,
Gagnon DR,
DuVall SL,
Li J,
Peloso GM,
Chaffin M,
Small AM
and 33 more — show all
Huang J,
Tang H,
Lynch JA,
Ho YL,
Liu DJ,
Emdin CA,
Li AH,
Huffman JE,
Lee JS,
Natarajan P,
Chowdhury R,
Saleheen D,
Vujkovic M,
Baras A,
Pyarajan S,
Di Angelantonio E,
Neale BM,
Naheed A,
Khera AV,
Danesh J,
Chang KM,
Abecasis G,
Willer C,
Dewey FE,
Carey DJ,
Concato J,
Gaziano JM,
O'Donnell CJ,
Tsao PS,
Kathiresan S,
Rader DJ,
Wilson PWF,
Assimes TL
Global Lipids Genetics Consortium · Myocardial Infarction Genetics (MIGen) Consortium and 2 more consortia
Nature genetics · 2018 · PMID 30275531 · open access
12 pages+
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Kilpeläinen TO,
Bentley AR,
Noordam R,
Sung YJ,
Schwander K,
Winkler TW,
Jakupović H,
Chasman DI,
Manning A,
Ntalla I,
Aschard H,
Brown MR
and 217 more — show all
de las Fuentes L,
Franceschini N,
Guo X,
Vojinovic D,
Aslibekyan S,
Feitosa MF,
Kho M,
Musani SK,
Richard M,
Wang H,
Wang Z,
Bartz TM,
Bielak LF,
Campbell A,
Dorajoo R,
Fisher V,
Hartwig FP,
Horimoto ARVR,
Li C,
Lohman KK,
Marten J,
Sim X,
Smith AV,
Tajuddin SM,
Alver M,
Amini M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Graff M,
Harris SE,
He M,
Hsu FC,
Jackson AU,
Zhao JH,
Kraja AT,
Kühnel B,
Laguzzi F,
Lyytikäinen LP,
Nolte IM,
Rauramaa R,
Riaz M,
Robino A,
Rueedi R,
Stringham HM,
Takeuchi F,
van der Most PJ,
Varga TV,
Verweij N,
Ware EB,
Wen W,
Li X,
Yanek LR,
Amin N,
Arnett DK,
Boerwinkle E,
Brumat M,
Cade B,
Canouil M,
Chen YI,
Concas MP,
Connell J,
de Mutsert R,
de Silva HJ,
de Vries PS,
Demirkan A,
Ding J,
Eaton CB,
Faul JD,
Friedlander Y,
Gabriel KP,
Ghanbari M,
Giulianini F,
Gu CC,
Gu D,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hunt SC,
Ikram MA,
Jonas JB,
Koh WP,
Komulainen P,
Krieger JE,
Kritchevsky SB,
Kutalik Z,
Kuusisto J,
Langefeld CD,
Langenberg C,
Launer LJ,
Leander K,
Lemaitre RN,
Lewis CE,
Liang J,
Liu J,
Mägi R,
Manichaikul A,
Meitinger T,
Metspalu A,
Milaneschi Y,
Mohlke KL,
Mosley TH Jr,
Murray AD,
Nalls MA,
Nang EK,
Nelson CP,
Nona S,
Norris JM,
Nwuba CV,
O'Connell J,
Palmer ND,
Papanicolau GJ,
Pazoki R,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Porteous DJ,
Poveda A,
Raitakari OT,
Rich SS,
Risch N,
Robinson JG,
Rose LM,
Rudan I,
Schreiner PJ,
Scott RA,
Sidney SS,
Sims M,
Smith JA,
Snieder H,
Sofer T,
Starr JM,
Sternfeld B,
Strauch K,
Tang H,
Taylor KD,
Tsai MY,
Tuomilehto J,
Uitterlinden AG,
van der Ende MY,
van Heemst D,
Voortman T,
Waldenberger M,
Wennberg P,
Wilson G,
Xiang YB,
Yao J,
Yu C,
Yuan JM,
Zhao W,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
de Faire U,
Deary IJ,
Elliott P,
Esko T,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Kato N,
Laakso M,
Lakka TA,
Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Samani NJ,
Shu XO,
van der Harst P,
Van Vliet-Ostaptchouk JV,
Vollenweider P,
Wagenknecht LE,
Wang YX,
Wareham NJ,
Weir DR,
Wu T,
Zheng W,
Zhu X,
Evans MK,
Franks PW,
Gudnason V,
Hayward C,
Horta BL,
Kelly TN,
Liu Y,
North KE,
Pereira AC,
Ridker PM,
Tai ES,
van Dam RM,
Fox ER,
Kardia SLR,
Liu CT,
Mook-Kanamori DO,
Province MA,
Redline S,
van Duijn CM,
Rotter JI,
Kooperberg CB,
Gauderman WJ,
Psaty BM,
Rice K,
Munroe PB,
Fornage M,
Cupples LA,
Rotimi CN,
Morrison AC,
Rao DC,
Loos RJF
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error
Fan Q,
Pozarickij A,
Tan NYQ,
Guo X,
Verhoeven VJM,
Vitart V,
Guggenheim JA,
Miyake M,
Tideman JWL,
Khawaja AP,
Zhang L,
MacGregor S
and 46 more — show all
Höhn R,
Chen P,
Biino G,
Wedenoja J,
Saffari SE,
Tedja MS,
Xie J,
Lanca C,
Wang YX,
Sahebjada S,
Mazur J,
Mirshahi A,
Martin NG,
Yazar S,
Pennell CE,
Yap M,
Haarman AEG,
Enthoven CA,
Polling J,
Hewitt AW,
Jaddoe VWV,
van Duijn CM,
Hayward C,
Polasek O,
Tai ES,
Yoshikatsu H,
Hysi PG,
Young TL,
Tsujikawa A,
Wang JJ,
Mitchell P,
Pfeiffer N,
Pärssinen O,
Foster PJ,
Fossarello M,
Yip SP,
Williams C,
Hammond CJ,
Jonas JB,
He M,
Mackey DA,
Wong TY,
Klaver CCW,
Saw SM,
Baird PN,
Cheng CY
Consortium for Refractive Error and Myopia (CREAM) · UK Biobank Eye and Vision Consortium
Communications biology · 2020 · PMID 32193507 · 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+
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Sawcer S,
Hellenthal G,
Pirinen M,
Spencer CC,
Patsopoulos NA,
Moutsianas L,
Dilthey A,
Su Z,
Freeman C,
Hunt SE,
Edkins S,
Gray E
and 230 more — show all
Booth DR,
Potter SC,
Goris A,
Band G,
Oturai AB,
Strange A,
Saarela J,
Bellenguez C,
Fontaine B,
Gillman M,
Hemmer B,
Gwilliam R,
Zipp F,
Jayakumar A,
Martin R,
Leslie S,
Hawkins S,
Giannoulatou E,
D'alfonso S,
Blackburn H,
Martinelli Boneschi F,
Liddle J,
Harbo HF,
Perez ML,
Spurkland A,
Waller MJ,
Mycko MP,
Ricketts M,
Comabella M,
Hammond N,
Kockum I,
McCann OT,
Ban M,
Whittaker P,
Kemppinen A,
Weston P,
Hawkins C,
Widaa S,
Zajicek J,
Dronov S,
Robertson N,
Bumpstead SJ,
Barcellos LF,
Ravindrarajah R,
Abraham R,
Alfredsson L,
Ardlie K,
Aubin C,
Baker A,
Baker K,
Baranzini SE,
Bergamaschi L,
Bergamaschi R,
Bernstein A,
Berthele A,
Boggild M,
Bradfield JP,
Brassat D,
Broadley SA,
Buck D,
Butzkueven H,
Capra R,
Carroll WM,
Cavalla P,
Celius EG,
Cepok S,
Chiavacci R,
Clerget-Darpoux F,
Clysters K,
Comi G,
Cossburn M,
Cournu-Rebeix I,
Cox MB,
Cozen W,
Cree BA,
Cross AH,
Cusi D,
Daly MJ,
Davis E,
de Bakker PI,
Debouverie M,
D'hooghe MB,
Dixon K,
Dobosi R,
Dubois B,
Ellinghaus D,
Elovaara I,
Esposito F,
Fontenille C,
Foote S,
Franke A,
Galimberti D,
Ghezzi A,
Glessner J,
Gomez R,
Gout O,
Graham C,
Grant SF,
Guerini FR,
Hakonarson H,
Hall P,
Hamsten A,
Hartung HP,
Heard RN,
Heath S,
Hobart J,
Hoshi M,
Infante-Duarte C,
Ingram G,
Ingram W,
Islam T,
Jagodic M,
Kabesch M,
Kermode AG,
Kilpatrick TJ,
Kim C,
Klopp N,
Koivisto K,
Larsson M,
Lathrop M,
Lechner-Scott JS,
Leone MA,
Leppä V,
Liljedahl U,
Bomfim IL,
Lincoln RR,
Link J,
Liu J,
Lorentzen AR,
Lupoli S,
Macciardi F,
Mack T,
Marriott M,
Martinelli V,
Mason D,
McCauley JL,
Mentch F,
Mero IL,
Mihalova T,
Montalban X,
Mottershead J,
Myhr KM,
Naldi P,
Ollier W,
Page A,
Palotie A,
Pelletier J,
Piccio L,
Pickersgill T,
Piehl F,
Pobywajlo S,
Quach HL,
Ramsay PP,
Reunanen M,
Reynolds R,
Rioux JD,
Rodegher M,
Roesner S,
Rubio JP,
Rückert IM,
Salvetti M,
Salvi E,
Santaniello A,
Schaefer CA,
Schreiber S,
Schulze C,
Scott RJ,
Sellebjerg F,
Selmaj KW,
Sexton D,
Shen L,
Simms-Acuna B,
Skidmore S,
Sleiman PM,
Smestad C,
Sørensen PS,
Søndergaard HB,
Stankovich J,
Strange RC,
Sulonen AM,
Sundqvist E,
Syvänen AC,
Taddeo F,
Taylor B,
Blackwell JM,
Tienari P,
Bramon E,
Tourbah A,
Brown MA,
Tronczynska E,
Casas JP,
Tubridy N,
Corvin A,
Vickery J,
Jankowski J,
Villoslada P,
Markus HS,
Wang K,
Mathew CG,
Wason J,
Palmer CN,
Wichmann HE,
Plomin R,
Willoughby E,
Rautanen A,
Winkelmann J,
Wittig M,
Trembath RC,
Yaouanq J,
Viswanathan AC,
Zhang H,
Wood NW,
Zuvich R,
Deloukas P,
Langford C,
Duncanson A,
Oksenberg JR,
Pericak-Vance MA,
Haines JL,
Olsson T,
Hillert J,
Ivinson AJ,
De Jager PL,
Peltonen L,
Stewart GJ,
Hafler DA,
Hauser SL,
McVean G,
Donnelly P,
Compston A
International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium 2
Nature · 2011 · PMID 21833088 · open access
11 pages
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Ripke S,
O'Dushlaine C,
Chambert K,
Moran JL,
Kähler AK,
Akterin S,
Bergen SE,
Collins AL,
Crowley JJ,
Fromer M,
Kim Y,
Lee SH
and 176 more — show all
Lee SH,
Magnusson PK,
Sanchez N,
Stahl EA,
Williams S,
Wray NR,
Xia K,
Bettella F,
Borglum AD,
Bulik-Sullivan BK,
Cormican P,
Craddock N,
de Leeuw C,
Durmishi N,
Gill M,
Golimbet V,
Hamshere ML,
Holmans P,
Hougaard DM,
Kendler KS,
Lin K,
Morris DW,
Mors O,
Mortensen PB,
Neale BM,
O'Neill FA,
Owen MJ,
Milovancevic MP,
Posthuma D,
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Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
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Genetic dissection of stool frequency implicates vitamin B1 metabolism and other actionable pathways in the modulation of gut motility
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Genome-wide meta-analysis across East Asian and European populations provides insights into the molecular basis of lung cancer
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Genome medicine · 2026 · PMID 42152146 · open access
6 pages
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension
Lu X,
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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.