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11 matches for
Petty LE.
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Mahajan A,
Taliun D,
Thurner M,
Robertson NR,
Torres JM,
Rayner NW,
Payne AJ,
Steinthorsdottir V,
Scott RA,
Grarup N,
Cook JP,
Schmidt EM
and 103 more — show all
Wuttke M,
Sarnowski C,
Mägi R,
Nano J,
Gieger C,
Trompet S,
Lecoeur C,
Preuss MH,
Prins BP,
Guo X,
Bielak LF,
Below JE,
Bowden DW,
Chambers JC,
Kim YJ,
Ng MCY,
Petty LE,
Sim X,
Zhang W,
Bennett AJ,
Bork-Jensen J,
Brummett CM,
Canouil M,
Ec Kardt KU,
Fischer K,
Kardia SLR,
Kronenberg F,
Läll K,
Liu CT,
Locke AE,
Luan J,
Ntalla I,
Nylander V,
Schönherr S,
Schurmann C,
Yengo L,
Bottinger EP,
Brandslund I,
Christensen C,
Dedoussis G,
Florez JC,
Ford I,
Franco OH,
Frayling TM,
Giedraitis V,
Hackinger S,
Hattersley AT,
Herder C,
Ikram MA,
Ingelsson M,
Jørgensen ME,
Jørgensen T,
Kriebel J,
Kuusisto J,
Ligthart S,
Lindgren CM,
Linneberg A,
Lyssenko V,
Mamakou V,
Meitinger T,
Mohlke KL,
Morris AD,
Nadkarni G,
Pankow JS,
Peters A,
Sattar N,
Stančáková A,
Strauch K,
Taylor KD,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tuomilehto J,
Witte DR,
Dupuis J,
Peyser PA,
Zeggini E,
Loos RJF,
Froguel P,
Ingelsson E,
Lind L,
Groop L,
Laakso M,
Collins FS,
Jukema JW,
Palmer CNA,
Grallert H,
Metspalu A,
Dehghan A,
Köttgen A,
Abecasis GR,
Meigs JB,
Rotter JI,
Marchini J,
Pedersen O,
Hansen T,
Langenberg C,
Wareham NJ,
Stefansson K,
Gloyn AL,
Morris AP,
Boehnke M,
McCarthy MI
Nature genetics · 2018 · PMID 30297969
12 pages+
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Spracklen CN,
Horikoshi M,
Kim YJ,
Lin K,
Bragg F,
Moon S,
Suzuki K,
Tam CHT,
Tabara Y,
Kwak SH,
Takeuchi F,
Long J
and 101 more — show all
Lim VJY,
Chai JF,
Chen CH,
Nakatochi M,
Yao J,
Choi HS,
Iyengar AK,
Perrin HJ,
Brotman SM,
van de Bunt M,
Gloyn AL,
Below JE,
Boehnke M,
Bowden DW,
Chambers JC,
Mahajan A,
McCarthy MI,
Ng MCY,
Petty LE,
Zhang W,
Morris AP,
Adair LS,
Akiyama M,
Bian Z,
Chan JCN,
Chang LC,
Chee ML,
Chen YI,
Chen YT,
Chen Z,
Chuang LM,
Du S,
Gordon-Larsen P,
Gross M,
Guo X,
Guo Y,
Han S,
Howard AG,
Huang W,
Hung YJ,
Hwang MY,
Hwu CM,
Ichihara S,
Isono M,
Jang HM,
Jiang G,
Jonas JB,
Kamatani Y,
Katsuya T,
Kawaguchi T,
Khor CC,
Kohara K,
Lee MS,
Lee NR,
Li L,
Liu J,
Luk AO,
Lv J,
Okada Y,
Pereira MA,
Sabanayagam C,
Shi J,
Shin DM,
So WY,
Takahashi A,
Tomlinson B,
Tsai FJ,
van Dam RM,
Xiang YB,
Yamamoto K,
Yamauchi T,
Yoon K,
Yu C,
Yuan JM,
Zhang L,
Zheng W,
Zheng W,
Igase M,
Cho YS,
Rotter JI,
Wang YX,
Sheu WHH,
Yokota M,
Wu JY,
Cheng CY,
Wong TY,
Shu XO,
Kato N,
Park KS,
Tai ES,
Matsuda F,
Koh WP,
Ma RCW,
Maeda S,
Millwood IY,
Lee J,
Kadowaki T,
Walters RG,
Kim BJ,
Mohlke KL,
Sim X
Nature · 2020 · PMID 32499647 · open access
12 pages+
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
Mahajan A,
Spracklen CN,
Zhang W,
Ng MCY,
Petty LE,
Kitajima H,
Yu GZ,
Rüeger S,
Speidel L,
Kim YJ,
Horikoshi M,
Mercader JM
and 337 more — show all
Taliun D,
Moon S,
Kwak SH,
Robertson NR,
Rayner NW,
Loh M,
Kim BJ,
Chiou J,
Miguel-Escalada I,
Della Briotta Parolo P,
Lin K,
Bragg F,
Preuss MH,
Takeuchi F,
Nano J,
Guo X,
Lamri A,
Nakatochi M,
Scott RA,
Lee JJ,
Huerta-Chagoya A,
Graff M,
Chai JF,
Parra EJ,
Yao J,
Bielak LF,
Tabara Y,
Hai Y,
Steinthorsdottir V,
Cook JP,
Kals M,
Grarup N,
Schmidt EM,
Pan I,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Long J,
Sun M,
Tong L,
Chen WM,
Ahmad M,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Lecoeur C,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Jensen RA,
Tajuddin S,
Kabagambe EK,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
Flanagan J,
Abaitua F,
Adair LS,
Adeyemo A,
Aguilar-Salinas CA,
Akiyama M,
Anand SS,
Bertoni A,
Bian Z,
Bork-Jensen J,
Brandslund I,
Brody JA,
Brummett CM,
Buchanan TA,
Canouil M,
Chan JCN,
Chang LC,
Chee ML,
Chen J,
Chen SH,
Chen YT,
Chen Z,
Chuang LM,
Cushman M,
Das SK,
de Silva HJ,
Dedoussis G,
Dimitrov L,
Doumatey AP,
Du S,
Duan Q,
Eckardt KU,
Emery LS,
Evans DS,
Evans MK,
Fischer K,
Floyd JS,
Ford I,
Fornage M,
Franco OH,
Frayling TM,
Freedman BI,
Fuchsberger C,
Genter P,
Gerstein HC,
Giedraitis V,
González-Villalpando C,
González-Villalpando ME,
Goodarzi MO,
Gordon-Larsen P,
Gorkin D,
Gross M,
Guo Y,
Hackinger S,
Han S,
Hattersley AT,
Herder C,
Howard AG,
Hsueh W,
Huang M,
Huang W,
Hung YJ,
Hwang MY,
Hwu CM,
Ichihara S,
Ikram MA,
Ingelsson M,
Islam MT,
Isono M,
Jang HM,
Jasmine F,
Jiang G,
Jonas JB,
Jørgensen ME,
Jørgensen T,
Kamatani Y,
Kandeel FR,
Kasturiratne A,
Katsuya T,
Kaur V,
Kawaguchi T,
Keaton JM,
Kho AN,
Khor CC,
Kibriya MG,
Kim DH,
Kohara K,
Kriebel J,
Kronenberg F,
Kuusisto J,
Läll K,
Lange LA,
Lee MS,
Lee NR,
Leong A,
Li L,
Li Y,
Li-Gao R,
Ligthart S,
Lindgren CM,
Linneberg A,
Liu CT,
Liu J,
Locke AE,
Louie T,
Luan J,
Luk AO,
Luo X,
Lv J,
Lyssenko V,
Mamakou V,
Mani KR,
Meitinger T,
Metspalu A,
Morris AD,
Nadkarni GN,
Nadler JL,
Nalls MA,
Nayak U,
Nongmaithem SS,
Ntalla I,
Okada Y,
Orozco L,
Patel SR,
Pereira MA,
Peters A,
Pirie FJ,
Porneala B,
Prasad G,
Preissl S,
Rasmussen-Torvik LJ,
Reiner AP,
Roden M,
Rohde R,
Roll K,
Sabanayagam C,
Sander M,
Sandow K,
Sattar N,
Schönherr S,
Schurmann C,
Shahriar M,
Shi J,
Shin DM,
Shriner D,
Smith JA,
So WY,
Stančáková A,
Stilp AM,
Strauch K,
Suzuki K,
Takahashi A,
Taylor KD,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tomlinson B,
Torres JM,
Tsai FJ,
Tuomilehto J,
Tusie-Luna T,
Udler MS,
Valladares-Salgado A,
van Dam RM,
van Klinken JB,
Varma R,
Vujkovic M,
Wacher-Rodarte N,
Wheeler E,
Whitsel EA,
Wickremasinghe AR,
van Dijk KW,
Witte DR,
Yajnik CS,
Yamamoto K,
Yamauchi T,
Yengo L,
Yoon K,
Yu C,
Yuan JM,
Yusuf S,
Zhang L,
Zheng W,
Raffel LJ,
Igase M,
Ipp E,
Redline S,
Cho YS,
Lind L,
Province MA,
Hanis CL,
Peyser PA,
Ingelsson E,
Zonderman AB,
Psaty BM,
Wang YX,
Rotimi CN,
Becker DM,
Matsuda F,
Liu Y,
Zeggini E,
Yokota M,
Rich SS,
Kooperberg C,
Pankow JS,
Engert JC,
Chen YI,
Froguel P,
Wilson JG,
Sheu WHH,
Kardia SLR,
Wu JY,
Hayes MG,
Ma RCW,
Wong TY,
Groop L,
Mook-Kanamori DO,
Chandak GR,
Collins FS,
Bharadwaj D,
Paré G,
Sale MM,
Ahsan H,
Motala AA,
Shu XO,
Park KS,
Jukema JW,
Cruz M,
McKean-Cowdin R,
Grallert H,
Cheng CY,
Bottinger EP,
Dehghan A,
Tai ES,
Dupuis J,
Kato N,
Laakso M,
Köttgen A,
Koh WP,
Palmer CNA,
Liu S,
Abecasis G,
Kooner JS,
Loos RJF,
North KE,
Haiman CA,
Florez JC,
Saleheen D,
Hansen T,
Pedersen O,
Mägi R,
Langenberg C,
Wareham NJ,
Maeda S,
Kadowaki T,
Lee J,
Millwood IY,
Walters RG,
Stefansson K,
Myers SR,
Ferrer J,
Gaulton KJ,
Meigs JB,
Mohlke KL,
Gloyn AL,
Bowden DW,
Below JE,
Chambers JC,
Sim X,
Boehnke M,
Rotter JI,
McCarthy MI,
Morris AP
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Suzuki K,
Hatzikotoulas K,
Southam L,
Taylor HJ,
Yin X,
Lorenz KM,
Mandla R,
Huerta-Chagoya A,
Melloni GEM,
Kanoni S,
Rayner NW,
Bocher O
and 351 more — show all
Arruda AL,
Sonehara K,
Namba S,
Lee SSK,
Preuss MH,
Petty LE,
Schroeder P,
Vanderwerff B,
Kals M,
Bragg F,
Lin K,
Guo X,
Zhang W,
Yao J,
Kim YJ,
Graff M,
Takeuchi F,
Nano J,
Lamri A,
Nakatochi M,
Moon S,
Scott RA,
Cook JP,
Lee JJ,
Pan I,
Taliun D,
Parra EJ,
Chai JF,
Bielak LF,
Tabara Y,
Hai Y,
Thorleifsson G,
Grarup N,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Kwak SH,
Long J,
Sun M,
Tong L,
Chen WM,
Nongmaithem SS,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Brody JA,
Kabagambe E,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
Broadaway KA,
Williamson A,
Kamali Z,
Cui J,
Thangam M,
Adair LS,
Adeyemo A,
Aguilar-Salinas CA,
Ahluwalia TS,
Anand SS,
Bertoni A,
Bork-Jensen J,
Brandslund I,
Buchanan TA,
Burant CF,
Butterworth AS,
Canouil M,
Chan JCN,
Chang LC,
Chee ML,
Chen J,
Chen SH,
Chen YT,
Chen Z,
Chuang LM,
Cushman M,
Danesh J,
Das SK,
de Silva HJ,
Dedoussis G,
Dimitrov L,
Doumatey AP,
Du S,
Duan Q,
Eckardt KU,
Emery LS,
Evans DS,
Evans MK,
Fischer K,
Floyd JS,
Ford I,
Franco OH,
Frayling TM,
Freedman BI,
Genter P,
Gerstein HC,
Giedraitis V,
González-Villalpando C,
González-Villalpando ME,
Gordon-Larsen P,
Gross M,
Guare LA,
Hackinger S,
Hakaste L,
Han S,
Hattersley AT,
Herder C,
Horikoshi M,
Howard AG,
Hsueh W,
Huang M,
Huang W,
Hung YJ,
Hwang MY,
Hwu CM,
Ichihara S,
Ikram MA,
Ingelsson M,
Islam MT,
Isono M,
Jang HM,
Jasmine F,
Jiang G,
Jonas JB,
Jørgensen T,
Kamanu FK,
Kandeel FR,
Kasturiratne A,
Katsuya T,
Kaur V,
Kawaguchi T,
Keaton JM,
Kho AN,
Khor CC,
Kibriya MG,
Kim DH,
Kronenberg F,
Kuusisto J,
Läll K,
Lange LA,
Lee KM,
Lee MS,
Lee NR,
Leong A,
Li L,
Li Y,
Li-Gao R,
Ligthart S,
Lindgren CM,
Linneberg A,
Liu CT,
Liu J,
Locke AE,
Louie T,
Luan J,
Luk AO,
Luo X,
Lv J,
Lynch JA,
Lyssenko V,
Maeda S,
Mamakou V,
Mansuri SR,
Matsuda K,
Meitinger T,
Melander O,
Metspalu A,
Mo H,
Morris AD,
Moura FA,
Nadler JL,
Nalls MA,
Nayak U,
Ntalla I,
Okada Y,
Orozco L,
Patel SR,
Patil S,
Pei P,
Pereira MA,
Peters A,
Pirie FJ,
Polikowsky HG,
Porneala B,
Prasad G,
Rasmussen-Torvik LJ,
Reiner AP,
Roden M,
Rohde R,
Roll K,
Sabanayagam C,
Sandow K,
Sankareswaran A,
Sattar N,
Schönherr S,
Shahriar M,
Shen B,
Shi J,
Shin DM,
Shojima N,
Smith JA,
So WY,
Stančáková A,
Steinthorsdottir V,
Stilp AM,
Strauch K,
Taylor KD,
Thorand B,
Thorsteinsdottir U,
Tomlinson B,
Tran TC,
Tsai FJ,
Tuomilehto J,
Tusie-Luna T,
Udler MS,
Valladares-Salgado A,
van Dam RM,
van Klinken JB,
Varma R,
Wacher-Rodarte N,
Wheeler E,
Wickremasinghe AR,
van Dijk KW,
Witte DR,
Yajnik CS,
Yamamoto K,
Yamamoto K,
Yoon K,
Yu C,
Yuan JM,
Yusuf S,
Zawistowski M,
Zhang L,
Zheng W,
Raffel LJ,
Igase M,
Ipp E,
Redline S,
Cho YS,
Lind L,
Province MA,
Fornage M,
Hanis CL,
Ingelsson E,
Zonderman AB,
Psaty BM,
Wang YX,
Rotimi CN,
Becker DM,
Matsuda F,
Liu Y,
Yokota M,
Kardia SLR,
Peyser PA,
Pankow JS,
Engert JC,
Bonnefond A,
Froguel P,
Wilson JG,
Sheu WHH,
Wu JY,
Hayes MG,
Ma RCW,
Wong TY,
Mook-Kanamori DO,
Tuomi T,
Chandak GR,
Collins FS,
Bharadwaj D,
Paré G,
Sale MM,
Ahsan H,
Motala AA,
Shu XO,
Park KS,
Jukema JW,
Cruz M,
Chen YI,
Rich SS,
McKean-Cowdin R,
Grallert H,
Cheng CY,
Ghanbari M,
Tai ES,
Dupuis J,
Kato N,
Laakso M,
Köttgen A,
Koh WP,
Bowden DW,
Palmer CNA,
Kooner JS,
Kooperberg C,
Liu S,
North KE,
Saleheen D,
Hansen T,
Pedersen O,
Wareham NJ,
Lee J,
Kim BJ,
Millwood IY,
Walters RG,
Stefansson K,
Ahlqvist E,
Goodarzi MO,
Mohlke KL,
Langenberg C,
Haiman CA,
Loos RJF,
Florez JC,
Rader DJ,
Ritchie MD,
Zöllner S,
Mägi R,
Marston NA,
Ruff CT,
van Heel DA,
Finer S,
Denny JC,
Yamauchi T,
Kadowaki T,
Chambers JC,
Ng MCY,
Sim X,
Below JE,
Tsao PS,
Chang KM,
McCarthy MI,
Meigs JB,
Mahajan A,
Spracklen CN,
Mercader JM,
Boehnke M,
Rotter JI,
Vujkovic M,
Voight BF,
Morris AP,
Zeggini E
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits
Petty LE,
Chen HH,
Frankel EG,
Zhu W,
Downie CG,
Graff M,
Lin P,
Sharma P,
Zhang X,
Scartozzi AC,
Roshani R,
Landman JM
and 80 more — show all
Boehnke M,
Bowden DW,
Chambers JC,
Mahajan A,
McCarthy MI,
Ng MCY,
Sim X,
Spracklen CN,
Zhang W,
Preuss M,
Bottinger EP,
Nadkarni GN,
Loos RJF,
Chen YI,
Tan J,
Ipp E,
Genter P,
Emery LS,
Louie T,
Sofer T,
Stilp AM,
Taylor KD,
Xiang AH,
Buchanan TA,
Roll K,
Gao C,
Palmer ND,
Norris JM,
Wagenknecht LE,
Nousome D,
Varma R,
McKean-Cowdin R,
Guo X,
Hai Y,
Hsueh W,
Sandow K,
Parra EJ,
Cruz M,
Valladares-Salgado A,
Wacher-Rodarte N,
Rotter JI,
Goodarzi MO,
Rich SS,
Bertoni A,
Raffel LJ,
Nadler JL,
Kandeel FR,
Duggirala R,
Blangero J,
Lehman DM,
DeFronzo RA,
Thameem F,
Wang Y,
Gahagan S,
Blanco E,
Burrows R,
Huerta-Chagoya A,
Florez JC,
Tusie-Luna T,
González-Villalpando C,
Orozco L,
Haiman CA,
Hanis CL,
Rohde R,
Whitsel EA,
Reiner AP,
Kooperberg C,
Li Y,
Duan Q,
Lee M,
Correa-Burrows P,
Fried SK,
North KE,
McCormick JB,
Fisher-Hoch SP,
Gamazon ER,
Morris AP,
Mercader JM,
Highland HM,
Below JE
DIAMANTE Hispanic/Latino Consortium · Global Hispanic Lipids Consortium
Nature communications · 2025 · PMID 40210677 · open access
12 pages+
Large-scale genome-wide analyses of stuttering
Polikowsky HG,
Scartozzi AC,
Shaw DM,
Pruett DG,
Chen HH,
Petty LE,
Petty AS,
Lowther EJ,
Cho SH,
Yu Y,
Mozaffari S,
Avery CL
and 9 more — show all
23andMe Research Team
Nature genetics · 2025 · PMID 40721530 · open access
12 pages+
GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals
Méndez-Giráldez R,
Gogarten SM,
Below JE,
Yao J,
Seyerle AA,
Highland HM,
Kooperberg C,
Soliman EZ,
Rotter JI,
Kerr KF,
Ryckman KK,
Taylor KD
and 13 more — show all
Petty LE,
Shah SJ,
Conomos MP,
Sotoodehnia N,
Cheng S,
Heckbert SR,
Sofer T,
Guo X,
Whitsel EA,
Lin HJ,
Hanis CL,
Laurie CC,
Avery CL
Scientific reports · 2017 · PMID 29213071 · open access
7 pages
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Noordam R,
Wang W,
Nagarajan P,
Wang H,
Brown MR,
Bentley AR,
Hui Q,
Kraja AT,
Morrison JL,
O'Connel JR,
Lee S,
Schwander K
and 137 more — show all
Bartz TM,
de Las Fuentes L,
Feitosa MF,
Guo X,
Hanfei X,
Harris SE,
Huang Z,
Kals M,
Lefevre C,
Mangino M,
Milaneschi Y,
van der Most PJ,
Pacheco NL,
Palmer ND,
Rao V,
Rauramaa R,
Sun Q,
Tabara Y,
Vojinovic D,
Wang Y,
Weiss S,
Yang Q,
Zhao W,
Zhu W,
Ansari MAY,
Aschard H,
Anugu P,
Assimes TL,
Attia J,
Baker LD,
Ballantyne C,
Bazzano L,
Boerwinkle E,
Cade B,
Chen HH,
Chen W,
Ida Chen YD,
Chen Z,
Cho K,
De Anda-Duran I,
Dimitrov L,
Do A,
Edwards T,
Faquih T,
Hingorani A,
Fisher-Hoch SP,
Gaziano JM,
Gharib SA,
Giri A,
Ghanbari M,
Grabe HJ,
Graff M,
Charles Gu C,
He J,
Heikkinen S,
Hixson J,
Ho YL,
Hood MM,
Houghton SC,
Karvonen-Gutierrez CA,
Kawaguchi T,
Kilpeläinen TO,
Komulainen P,
Lin HJ,
Linchangco GV Jr,
Luik AI,
Ma J,
Meigs JB,
McCormick JB,
Menni C,
Nolte IM,
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Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
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GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations
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Communications biology · 2022 · PMID 35393509 · open access
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A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A<sub>1c</sub> With Implications for Glycemic Status in U.S. Hispanics/Latinos
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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.