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44 matches for
Ma H,
showing the first 20.
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels
Draisma HHM,
Pool R,
Kobl M,
Jansen R,
Petersen AK,
Vaarhorst AAM,
Yet I,
Haller T,
Demirkan A,
Esko T,
Zhu G,
Böhringer S
and 36 more — show all
Beekman M,
van Klinken JB,
Römisch-Margl W,
Prehn C,
Adamski J,
de Craen AJM,
van Leeuwen EM,
Amin N,
Dharuri H,
Westra HJ,
Franke L,
de Geus EJC,
Hottenga JJ,
Willemsen G,
Henders AK,
Montgomery GW,
Nyholt DR,
Whitfield JB,
Penninx BW,
Spector TD,
Metspalu A,
Slagboom PE,
van Dijk KW,
't Hoen PAC,
Strauch K,
Martin NG,
van Ommen GB,
Illig T,
Bell JT,
Mangino M,
Suhre K,
McCarthy MI,
Gieger C,
Isaacs A,
van Duijn CM,
Boomsma DI
Nature communications · 2015 · PMID 26068415
3 pages
Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies
Wang Z,
Dai J,
Hu N,
Miao X,
Abnet CC,
Yang M,
Freedman ND,
Chen J,
Burdette L,
Zhu X,
Chung CC,
Ren C
and 35 more — show all
Dawsey SM,
Wang M,
Ding T,
Du J,
Gao YT,
Zhong R,
Giffen C,
Pan W,
Koh WP,
Dai N,
Liao LM,
Yan C,
Qiao YL,
Jiang Y,
Shu XO,
Chen J,
Wang C,
Ma H,
Su H,
Zhang Z,
Wang L,
Wu C,
Xiang YB,
Hu Z,
Yuan JM,
Xie L,
Zheng W,
Zheng W,
Lin D,
Chanock SJ,
Shi Y,
Goldstein AM,
Jin G,
Taylor PR,
Shen H
Gut · 2017 · PMID 26701879 · open access
3 pages
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA
Kettunen J,
Demirkan A,
Würtz P,
Draisma HH,
Haller T,
Rawal R,
Vaarhorst A,
Kangas AJ,
Lyytikäinen LP,
Pirinen M,
Pool R,
Sarin AP
and 38 more — show all
Soininen P,
Tukiainen T,
Wang Q,
Tiainen M,
Tynkkynen T,
Amin N,
Zeller T,
Beekman M,
Deelen J,
van Dijk KW,
Esko T,
Hottenga JJ,
van Leeuwen EM,
Lehtimäki T,
Mihailov E,
Rose RJ,
de Craen AJ,
Gieger C,
Kähönen M,
Perola M,
Blankenberg S,
Savolainen MJ,
Verhoeven A,
Viikari J,
Willemsen G,
Boomsma DI,
van Duijn CM,
Eriksson J,
Jula A,
Järvelin MR,
Kaprio J,
Metspalu A,
Raitakari O,
Salomaa V,
Slagboom PE,
Waldenberger M,
Ripatti S,
Ala-Korpela M
Nature communications · 2016 · PMID 27005778 · open access
3 pages
Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma
Shiraishi K,
Okada Y,
Takahashi A,
Kamatani Y,
Momozawa Y,
Ashikawa K,
Kunitoh H,
Matsumoto S,
Takano A,
Shimizu K,
Goto A,
Tsuta K
and 34 more — show all
Watanabe SI,
Ohe Y,
Watanabe Y,
Goto Y,
Nokihara H,
Furuta K,
Yoshida A,
Goto K,
Hishida T,
Tsuboi M,
Tsuchihara K,
Miyagi Y,
Nakayama H,
Yokose T,
Tanaka K,
Nagashima T,
Ohtaki Y,
Maeda D,
Imai K,
Minamiya Y,
Sakamoto H,
Saito A,
Shimada Y,
Sunami K,
Saito M,
Inazawa J,
Nakamura Y,
Yoshida T,
Yokota J,
Matsuda F,
Matsuo K,
Daigo Y,
Kubo M,
Kohno T
Nature communications · 2016 · PMID 27501781 · open access
3 pages
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes
Nakayama A,
Nakaoka H,
Yamamoto K,
Sakiyama M,
Shaukat A,
Toyoda Y,
Okada Y,
Kamatani Y,
Nakamura T,
Takada T,
Inoue K,
Yasujima T
and 34 more — show all
Yuasa H,
Shirahama Y,
Nakashima H,
Shimizu S,
Higashino T,
Kawamura Y,
Ogata H,
Kawaguchi M,
Ohkawa Y,
Danjoh I,
Tokumasu A,
Ooyama K,
Ito T,
Kondo T,
Wakai K,
Stiburkova B,
Pavelka K,
Stamp LK,
Dalbeth N,
Sakurai Y,
Suzuki H,
Hosoyamada M,
Fujimori S,
Yokoo T,
Hosoya T,
Inoue I,
Takahashi A,
Kubo M,
Ooyama H,
Shimizu T,
Ichida K,
Shinomiya N,
Merriman TR,
Matsuo H
Eurogout Consortium · Eurogout Consortium
Annals of the rheumatic diseases · 2017 · PMID 27899376 · open access
3 pages
Development and evaluation of a polygenic risk score for lung cancer in never-smoking women: A large-scale prospective Chinese cohort study
Wei X,
Sun D,
Gao J,
Zhang J,
Zhu M,
Yu C,
Ma Z,
Fu Y,
Ji C,
Pei P,
Yang L,
Millwood IY
and 10 more — show all
International journal of cancer · 2024 · PMID 37846649
3 pages
Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese
Jin G,
Ma H,
Wu C,
Dai J,
Zhang R,
Shi Y,
Lu J,
Miao X,
Wang M,
Zhou Y,
Chen J,
Li H
and 21 more — show all
Pan S,
Chu M,
Lu F,
Yu D,
Jiang Y,
Dong J,
Hu L,
Chen Y,
Xu L,
Shu Y,
Pan S,
Tan W,
Zhou B,
Lu D,
Wu T,
Zhang Z,
Chen F,
Wang X,
Hu Z,
Lin D,
Shen H
American journal of human genetics · 2012 · PMID 23103227
2 pages
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese
Dong J,
Jin G,
Wu C,
Guo H,
Zhou B,
Lv J,
Lu D,
Shi Y,
Shu Y,
Xu L,
Chu M,
Wang C
and 37 more — show all
Zhang R,
Dai J,
Jiang Y,
Yu D,
Ma H,
Zhao X,
Yin Z,
Yang L,
Li Z,
Deng Q,
Cao S,
Qin Z,
Gong J,
Sun C,
Wang J,
Wu W,
Zhou G,
Chen H,
Guan P,
Chen Y,
Liu X,
Liu L,
Xu P,
Han B,
Bai C,
Zhao Y,
Zhang H,
Yan Y,
Liu J,
Amos CI,
Chen F,
Tan W,
Jin L,
Wu T,
Hu Z,
Lin D,
Shen H
PLoS genetics · 2013 · PMID 23341777 · open access
2 pages
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Kato N,
Loh M,
Takeuchi F,
Verweij N,
Wang X,
Zhang W,
Kelly TN,
Saleheen D,
Lehne B,
Leach IM,
Drong AW,
Abbott J
and 233 more — show all
Wahl S,
Tan ST,
Scott WR,
Campanella G,
Chadeau-Hyam M,
Afzal U,
Ahluwalia TS,
Bonder MJ,
Chen P,
Dehghan A,
Edwards TL,
Esko T,
Go MJ,
Harris SE,
Hartiala J,
Kasela S,
Kasturiratne A,
Khor CC,
Kleber ME,
Li H,
Yu Mok Z,
Nakatochi M,
Sapari NS,
Saxena R,
Stewart AFR,
Stolk L,
Tabara Y,
Teh AL,
Wu Y,
Wu JY,
Zhang Y,
Aits I,
Da Silva Couto Alves A,
Das S,
Dorajoo R,
Hopewell JC,
Kim YK,
Koivula RW,
Luan J,
Lyytikäinen LP,
Nguyen QN,
Pereira MA,
Postmus I,
Raitakari OT,
Scannell Bryan M,
Scott RA,
Sorice R,
Tragante V,
Traglia M,
White J,
Yamamoto K,
Zhang Y,
Adair LS,
Ahmed A,
Akiyama K,
Asif R,
Aung T,
Barroso I,
Bjonnes A,
Braun TR,
Cai H,
Chang LC,
Chen CH,
Cheng CY,
Chong YS,
Collins R,
Courtney R,
Davies G,
Delgado G,
Do LD,
Doevendans PA,
Gansevoort RT,
Gao YT,
Grammer TB,
Grarup N,
Grewal J,
Gu D,
Wander GS,
Hartikainen AL,
Hazen SL,
He J,
Heng CK,
Hixson JE,
Hofman A,
Hsu C,
Huang W,
Husemoen LLN,
Hwang JY,
Ichihara S,
Igase M,
Isono M,
Justesen JM,
Katsuya T,
Kibriya MG,
Kim YJ,
Kishimoto M,
Koh WP,
Kohara K,
Kumari M,
Kwek K,
Lee NR,
Lee J,
Liao J,
Lieb W,
Liewald DCM,
Matsubara T,
Matsushita Y,
Meitinger T,
Mihailov E,
Milani L,
Mills R,
Mononen N,
Müller-Nurasyid M,
Nabika T,
Nakashima E,
Ng HK,
Nikus K,
Nutile T,
Ohkubo T,
Ohnaka K,
Parish S,
Paternoster L,
Peng H,
Peters A,
Pham ST,
Pinidiyapathirage MJ,
Rahman M,
Rakugi H,
Rolandsson O,
Ann Rozario M,
Ruggiero D,
Sala CF,
Sarju R,
Shimokawa K,
Snieder H,
Sparsø T,
Spiering W,
Starr JM,
Stott DJ,
Stram DO,
Sugiyama T,
Szymczak S,
Tang WHW,
Tong L,
Trompet S,
Turjanmaa V,
Ueshima H,
Uitterlinden AG,
Umemura S,
Vaarasmaki M,
van Dam RM,
van Gilst WH,
van Veldhuisen DJ,
Viikari JS,
Waldenberger M,
Wang Y,
Wang A,
Wilson R,
Wong TY,
Xiang YB,
Yamaguchi S,
Ye X,
Young RD,
Young TL,
Yuan JM,
Zhou X,
Asselbergs FW,
Ciullo M,
Clarke R,
Deloukas P,
Franke A,
Franks PW,
Franks S,
Friedlander Y,
Gross MD,
Guo Z,
Hansen T,
Jarvelin MR,
Jørgensen T,
Jukema JW,
Kähönen M,
Kajio H,
Kivimaki M,
Lee JY,
Lehtimäki T,
Linneberg A,
Miki T,
Pedersen O,
Samani NJ,
Sørensen TIA,
Takayanagi R,
Toniolo D,
Ahsan H,
Allayee H,
Chen YT,
Danesh J,
Deary IJ,
Franco OH,
Franke L,
Heijman BT,
Holbrook JD,
Isaacs A,
Kim BJ,
Lin X,
Liu J,
März W,
Metspalu A,
Mohlke KL,
Sanghera DK,
Shu XO,
van Meurs JBJ,
Vithana E,
Wickremasinghe AR,
Wijmenga C,
Wolffenbuttel BHW,
Yokota M,
Zheng W,
Zheng W,
Zhu D,
Vineis P,
Kyrtopoulos SA,
Kleinjans JCS,
McCarthy MI,
Soong R,
Gieger C,
Scott J,
Teo YY,
He J,
Elliott P,
Tai ES,
van der Harst P,
Kooner JS,
Chambers JC
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
Hu Z,
Wu C,
Shi Y,
Guo H,
Zhao X,
Yin Z,
Yang L,
Dai J,
Hu L,
Tan W,
Li Z,
Deng Q
and 33 more — show all
Wang J,
Wu W,
Jin G,
Jiang Y,
Yu D,
Zhou G,
Chen H,
Guan P,
Chen Y,
Shu Y,
Xu L,
Liu X,
Liu L,
Xu P,
Han B,
Bai C,
Zhao Y,
Zhang H,
Yan Y,
Ma H,
Chen J,
Chu M,
Lu F,
Zhang Z,
Chen F,
Wang X,
Jin L,
Lu J,
Zhou B,
Lu D,
Wu T,
Lin D,
Shen H
Nature genetics · 2011 · PMID 21725308
1 page
Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review
Molodecky NA,
Soon IS,
Rabi DM,
Ghali WA,
Ferris M,
Chernoff G,
Benchimol EI,
Panaccione R,
Ghosh S,
Barkema HW,
Kaplan GG
Gastroenterology · 2012 · PMID 22001864
1 page
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
Voight BF,
Peloso GM,
Orho-Melander M,
Frikke-Schmidt R,
Barbalic M,
Jensen MK,
Hindy G,
Hólm H,
Ding EL,
Johnson T,
Schunkert H,
Samani NJ
and 114 more — show all
Clarke R,
Hopewell JC,
Thompson JF,
Li M,
Thorleifsson G,
Newton-Cheh C,
Musunuru K,
Pirruccello JP,
Saleheen D,
Chen L,
Stewart A,
Schillert A,
Thorsteinsdottir U,
Thorgeirsson G,
Anand S,
Engert JC,
Morgan T,
Spertus J,
Stoll M,
Berger K,
Martinelli N,
Girelli D,
McKeown PP,
Patterson CC,
Epstein SE,
Devaney J,
Burnett MS,
Mooser V,
Ripatti S,
Surakka I,
Nieminen MS,
Sinisalo J,
Lokki ML,
Perola M,
Havulinna A,
de Faire U,
Gigante B,
Ingelsson E,
Zeller T,
Wild P,
de Bakker PI,
Klungel OH,
Maitland-van der Zee AH,
Peters BJ,
de Boer A,
Grobbee DE,
Kamphuisen PW,
Deneer VH,
Elbers CC,
Onland-Moret NC,
Hofker MH,
Wijmenga C,
Verschuren WM,
Boer JM,
van der Schouw YT,
Rasheed A,
Frossard P,
Demissie S,
Willer C,
Do R,
Ordovas JM,
Abecasis GR,
Boehnke M,
Mohlke KL,
Daly MJ,
Guiducci C,
Burtt NP,
Surti A,
Gonzalez E,
Purcell S,
Gabriel S,
Marrugat J,
Peden J,
Erdmann J,
Diemert P,
Willenborg C,
König IR,
Fischer M,
Hengstenberg C,
Ziegler A,
Buysschaert I,
Lambrechts D,
Van de Werf F,
Fox KA,
El Mokhtari NE,
Rubin D,
Schrezenmeir J,
Schreiber S,
Schäfer A,
Danesh J,
Blankenberg S,
Roberts R,
McPherson R,
Watkins H,
Hall AS,
Overvad K,
Rimm E,
Boerwinkle E,
Tybjaerg-Hansen A,
Cupples LA,
Reilly MP,
Melander O,
Mannucci PM,
Ardissino D,
Siscovick D,
Elosua R,
Stefansson K,
O'Donnell CJ,
Salomaa V,
Rader DJ,
Peltonen L,
Schwartz SM,
Altshuler D,
Kathiresan S
Lancet (London, England) · 2012 · PMID 22607825 · open access
1 page
Common variants on chromosome 9p21 are associated with normal tension glaucoma
Takamoto M,
Kaburaki T,
Mabuchi A,
Araie M,
Amano S,
Aihara M,
Tomidokoro A,
Iwase A,
Mabuchi F,
Kashiwagi K,
Shirato S,
Yasuda N
and 6 more — show all
PloS one · 2012 · PMID 22792221 · open access
1 page
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations
Hu Z,
Shi Y,
Mo X,
Xu J,
Zhao B,
Lin Y,
Yang S,
Xu Z,
Dai J,
Pan S,
Da M,
Wang X
and 15 more — show all
Qian B,
Wen Y,
Wen J,
Xing J,
Guo X,
Xia Y,
Ma H,
Jin G,
Yu S,
Liu J,
Zhou Z,
Wang X,
Chen Y,
Sha J,
Shen H
Nature genetics · 2013 · PMID 23708190
1 page
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Wang Z,
Seow WJ,
Shiraishi K,
Hsiung CA,
Matsuo K,
Liu J,
Chen K,
Yamji T,
Yang Y,
Chang IS,
Wu C,
Hong YC
and 138 more — show all
Burdett L,
Wyatt K,
Chung CC,
Li SA,
Yeager M,
Hutchinson A,
Hu W,
Caporaso N,
Landi MT,
Chatterjee N,
Song M,
Fraumeni JF Jr,
Kohno T,
Yokota J,
Kunitoh H,
Ashikawa K,
Momozawa Y,
Daigo Y,
Mitsudomi T,
Yatabe Y,
Hida T,
Hu Z,
Dai J,
Ma H,
Jin G,
Song B,
Wang Z,
Cheng S,
Yin Z,
Li X,
Ren Y,
Guan P,
Chang J,
Tan W,
Chen CJ,
Chang GC,
Tsai YH,
Su WC,
Chen KY,
Huang MS,
Chen YM,
Zheng H,
Li H,
Cui P,
Guo H,
Xu P,
Liu L,
Iwasaki M,
Shimazu T,
Tsugane S,
Zhu J,
Jiang G,
Fei K,
Park JY,
Kim YH,
Sung JS,
Park KH,
Kim YT,
Jung YJ,
Kang CH,
Park IK,
Kim HN,
Jeon HS,
Choi JE,
Choi YY,
Kim JH,
Oh IJ,
Kim YC,
Sung SW,
Kim JS,
Yoon HI,
Kweon SS,
Shin MH,
Seow A,
Chen Y,
Lim WY,
Liu J,
Wong MP,
Lee VH,
Bassig BA,
Tucker M,
Berndt SI,
Chow WH,
Ji BT,
Wang J,
Xu J,
Sihoe AD,
Ho JC,
Chan JK,
Wang JC,
Lu D,
Zhao X,
Zhao Z,
Wu J,
Chen H,
Jin L,
Wei F,
Wu G,
An SJ,
Zhang XC,
Su J,
Wu YL,
Gao YT,
Xiang YB,
He X,
Li J,
Zheng W,
Shu XO,
Cai Q,
Klein R,
Pao W,
Lawrence C,
Hosgood HD 3rd,
Hsiao CF,
Chien LH,
Chen YH,
Chen CH,
Wang WC,
Chen CY,
Wang CL,
Yu CJ,
Chen HL,
Su YC,
Tsai FY,
Chen YS,
Li YJ,
Yang TY,
Lin CC,
Yang PC,
Wu T,
Lin D,
Zhou B,
Yu J,
Shen H,
Kubo M,
Chanock SJ,
Rothman N,
Lan Q
Human molecular genetics · 2016 · PMID 26732429
1 page
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Wen W,
Kato N,
Hwang JY,
Guo X,
Tabara Y,
Li H,
Dorajoo R,
Yang X,
Tsai FJ,
Li S,
Wu Y,
Wu T
and 64 more — show all
Kim S,
Guo X,
Liang J,
Shungin D,
Adair LS,
Akiyama K,
Allison M,
Cai Q,
Chang LC,
Chen CH,
Chen YT,
Cho YS,
Choi BY,
Gao Y,
Go MJ,
Gu D,
Han BG,
He M,
Hixson JE,
Hu Y,
Huang T,
Isono M,
Jung KJ,
Kang D,
Kim YJ,
Kita Y,
Lee J,
Lee NR,
Lee J,
Wang Y,
Liu JJ,
Long J,
Moon S,
Nakamura Y,
Nakatochi M,
Ohnaka K,
Rao D,
Shi J,
Sull JW,
Tan A,
Ueshima H,
Wu C,
Xiang YB,
Yamamoto K,
Yao J,
Ye X,
Yokota M,
Zhang X,
Zheng Y,
Qi L,
Rotter JI,
Jee SH,
Lin D,
Mohlke KL,
He J,
Mo Z,
Wu JY,
Tai ES,
Lin X,
Miki T,
Kim BJ,
Takeuchi F,
Zheng W,
Shu XO
Scientific reports · 2016 · PMID 26785701 · open access
1 page
Splicing variant of <i>WDFY4</i> augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis
Kochi Y,
Kamatani Y,
Kondo Y,
Suzuki A,
Kawakami E,
Hiwa R,
Momozawa Y,
Fujimoto M,
Jinnin M,
Tanaka Y,
Kanda T,
Cooper RG
and 36 more — show all
Chinoy H,
Rothwell S,
Lamb JA,
Vencovský J,
Mann H,
Ohmura K,
Myouzen K,
Ishigaki K,
Nakashima R,
Hosono Y,
Tsuboi H,
Kawasumi H,
Iwasaki Y,
Kajiyama H,
Horita T,
Ogawa-Momohara M,
Takamura A,
Tsunoda S,
Shimizu J,
Fujio K,
Amano H,
Mimori A,
Kawakami A,
Umehara H,
Takeuchi T,
Sano H,
Muro Y,
Atsumi T,
Mimura T,
Kawaguchi Y,
Mimori T,
Takahashi A,
Kubo M,
Kohsaka H,
Sumida T,
Yamamoto K
Annals of the rheumatic diseases · 2018 · PMID 29331962
1 page
A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia
Miyagawa T,
Khor SS,
Toyoda H,
Kanbayashi T,
Imanishi A,
Sagawa Y,
Kotorii N,
Kotorii T,
Ariyoshi Y,
Hashizume Y,
Ogi K,
Hiejima H
and 46 more — show all
Kamei Y,
Hida A,
Miyamoto M,
Ikegami A,
Wada Y,
Takami M,
Higashiyama Y,
Miyake R,
Kondo H,
Fujimura Y,
Tamura Y,
Taniyama Y,
Omata N,
Tanaka Y,
Moriya S,
Furuya H,
Kato M,
Kawamura Y,
Otowa T,
Miyashita A,
Kojima H,
Saji H,
Shimada M,
Yamasaki M,
Kobayashi T,
Misawa R,
Shigematsu Y,
Kuwano R,
Sasaki T,
Ishigooka J,
Wada Y,
Tsuruta K,
Chiba S,
Tanaka F,
Yamada N,
Okawa M,
Kuroda K,
Kume K,
Hirata K,
Uchimura N,
Shimizu T,
Inoue Y,
Honda Y,
Mishima K,
Honda M,
Tokunaga K
Journal of human genetics · 2018 · PMID 30266950
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.