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11 matches for
Leonard H.
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls MA,
Blauwendraat C,
Vallerga CL,
Heilbron K,
Bandres-Ciga S,
Chang D,
Tan M,
Kia DA,
Noyce AJ,
Xue A,
Bras J,
Young E
and 39 more — show all
von Coelln R,
Simón-Sánchez J,
Schulte C,
Sharma M,
Krohn L,
Pihlstrøm L,
Siitonen A,
Iwaki H,
Leonard H,
Faghri F,
Gibbs JR,
Hernandez DG,
Scholz SW,
Botia JA,
Martinez M,
Corvol JC,
Lesage S,
Jankovic J,
Shulman LM,
Sutherland M,
Tienari P,
Majamaa K,
Toft M,
Andreassen OA,
Bangale T,
Brice A,
Yang J,
Gan-Or Z,
Gasser T,
Heutink P,
Shulman JM,
Wood NW,
Hinds DA,
Hardy JA,
Morris HR,
Gratten J,
Visscher PM,
Graham RR,
Singleton AB
23andMe Research Team · System Genomics of Parkinson's Disease Consortium and 1 more consortia
The Lancet. Neurology · 2019 · PMID 31701892
12 pages+
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
Graff M,
Justice AE,
Young KL,
Marouli E,
Zhang X,
Fine RS,
Lim E,
Buchanan V,
Rand K,
Feitosa MF,
Wojczynski MK,
Yanek LR
and 213 more — show all
Shao Y,
Rohde R,
Adeyemo AA,
Aldrich MC,
Allison MA,
Ambrosone CB,
Ambs S,
Amos C,
Arnett DK,
Atwood L,
Bandera EV,
Bartz T,
Becker DM,
Berndt SI,
Bernstein L,
Bielak LF,
Blot WJ,
Bottinger EP,
Bowden DW,
Bradfield JP,
Brody JA,
Broeckel U,
Burke G,
Cade BE,
Cai Q,
Caporaso N,
Carlson C,
Carpten J,
Casey G,
Chanock SJ,
Chen G,
Chen M,
Chen YI,
Chen WM,
Chesi A,
Chiang CWK,
Chu L,
Coetzee GA,
Conti DV,
Cooper RS,
Cushman M,
Demerath E,
Deming SL,
Dimitrov L,
Ding J,
Diver WR,
Duan Q,
Evans MK,
Falusi AG,
Faul JD,
Fornage M,
Fox C,
Freedman BI,
Garcia M,
Gillanders EM,
Goodman P,
Gottesman O,
Grant SFA,
Guo X,
Hakonarson H,
Haritunians T,
Harris TB,
Harris CC,
Henderson BE,
Hennis A,
Hernandez DG,
Hirschhorn JN,
McNeill LH,
Howard TD,
Howard B,
Hsing AW,
Hsu YH,
Hu JJ,
Huff CD,
Huo D,
Ingles SA,
Irvin MR,
John EM,
Johnson KC,
Jordan JM,
Kabagambe EK,
Kang SJ,
Kardia SL,
Keating BJ,
Kittles RA,
Klein EA,
Kolb S,
Kolonel LN,
Kooperberg C,
Kuller L,
Kutlar A,
Lange L,
Langefeld CD,
Le Marchand L,
Leonard H,
Lettre G,
Levin AM,
Li Y,
Li J,
Liu Y,
Liu Y,
Liu S,
Lohman K,
Lotay V,
Lu Y,
Maixner W,
Manson JE,
McKnight B,
Meng Y,
Monda KL,
Monroe K,
Moore JH,
Mosley TH,
Mudgal P,
Murphy AB,
Nadukuru R,
Nalls MA,
Nathanson KL,
Nayak U,
N'Diaye A,
Nemesure B,
Neslund-Dudas C,
Neuhouser ML,
Nyante S,
Ochs-Balcom H,
Ogundiran TO,
Ogunniyi A,
Ojengbede O,
Okut H,
Olopade OI,
Olshan A,
Padhukasahasram B,
Palmer J,
Palmer CD,
Palmer ND,
Papanicolaou G,
Patel SR,
Pettaway CA,
Peyser PA,
Press MF,
Rao DC,
Rasmussen-Torvik LJ,
Redline S,
Reiner AP,
Rhie SK,
Rodriguez-Gil JL,
Rotimi CN,
Rotter JI,
Ruiz-Narvaez EA,
Rybicki BA,
Salako B,
Sale MM,
Sanderson M,
Schadt E,
Schreiner PJ,
Schurmann C,
Schwartz AG,
Shriner DA,
Signorello LB,
Singleton AB,
Siscovick DS,
Smith JA,
Smith S,
Speliotes E,
Spitz M,
Stanford JL,
Stevens VL,
Stram A,
Strom SS,
Sucheston L,
Sun YV,
Tajuddin SM,
Taylor H,
Taylor K,
Tayo BO,
Thun MJ,
Tucker MA,
Vaidya D,
Van Den Berg DJ,
Vedantam S,
Vitolins M,
Wang Z,
Ware EB,
Wassertheil-Smoller S,
Weir DR,
Wiencke JK,
Williams SM,
Williams LK,
Wilson JG,
Witte JS,
Wrensch M,
Wu X,
Yao J,
Zakai N,
Zanetti K,
Zemel BS,
Zhao W,
Zhao JH,
Zheng W,
Zhi D,
Zhou J,
Zhu X,
Ziegler RG,
Zmuda J,
Zonderman AB,
Psaty BM,
Borecki IB,
Cupples LA,
Liu CT,
Haiman CA,
Loos R,
Ng MCY,
North KE
American journal of human genetics · 2021 · PMID 33713608
12 pages+
The power of genetic diversity in genome-wide association studies of lipids
Graham SE,
Clarke SL,
Wu KH,
Kanoni S,
Zajac GJM,
Ramdas S,
Surakka I,
Ntalla I,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
and 523 more — show all
Hwang MY,
Han S,
Narita A,
Choudhury A,
Bentley AR,
Ekoru K,
Verma A,
Trivedi B,
Martin HC,
Hunt KA,
Hui Q,
Klarin D,
Zhu X,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Ruotsalainen SE,
Havulinna AS,
Veturi Y,
Feng Q,
Rosenthal EA,
Lingren T,
Pacheco JA,
Pendergrass SA,
Haessler J,
Giulianini F,
Bradford Y,
Miller JE,
Campbell A,
Lin K,
Millwood IY,
Hindy G,
Rasheed A,
Faul JD,
Zhao W,
Weir DR,
Turman C,
Huang H,
Graff M,
Mahajan A,
Brown MR,
Zhang W,
Yu K,
Schmidt EM,
Pandit A,
Gustafsson S,
Yin X,
Luan J,
Zhao JH,
Matsuda F,
Jang HM,
Yoon K,
Medina-Gomez C,
Pitsillides A,
Hottenga JJ,
Willemsen G,
Wood AR,
Ji Y,
Gao Z,
Haworth S,
Mitchell RE,
Chai JF,
Aadahl M,
Yao J,
Manichaikul A,
Warren HR,
Ramirez J,
Bork-Jensen J,
Kårhus LL,
Goel A,
Sabater-Lleal M,
Noordam R,
Sidore C,
Fiorillo E,
McDaid AF,
Marques-Vidal P,
Wielscher M,
Trompet S,
Sattar N,
Møllehave LT,
Thuesen BH,
Munz M,
Zeng L,
Huang J,
Yang B,
Poveda A,
Kurbasic A,
Lamina C,
Forer L,
Scholz M,
Galesloot TE,
Bradfield JP,
Daw EW,
Zmuda JM,
Mitchell JS,
Fuchsberger C,
Christensen H,
Brody JA,
Feitosa MF,
Wojczynski MK,
Preuss M,
Mangino M,
Christofidou P,
Verweij N,
Benjamins JW,
Engmann J,
Kember RL,
Slieker RC,
Lo KS,
Zilhao NR,
Le P,
Kleber ME,
Delgado GE,
Huo S,
Ikeda DD,
Iha H,
Yang J,
Liu J,
Leonard HL,
Marten J,
Schmidt B,
Arendt M,
Smyth LJ,
Cañadas-Garre M,
Wang C,
Nakatochi M,
Wong A,
Hutri-Kähönen N,
Sim X,
Xia R,
Huerta-Chagoya A,
Fernandez-Lopez JC,
Lyssenko V,
Ahmed M,
Jackson AU,
Yousri NA,
Irvin MR,
Oldmeadow C,
Kim HN,
Ryu S,
Timmers PRHJ,
Arbeeva L,
Dorajoo R,
Lange LA,
Chai X,
Prasad G,
Lorés-Motta L,
Pauper M,
Long J,
Li X,
Theusch E,
Takeuchi F,
Spracklen CN,
Loukola A,
Bollepalli S,
Warner SC,
Wang YX,
Wei WB,
Nutile T,
Ruggiero D,
Sung YJ,
Hung YJ,
Chen S,
Liu F,
Yang J,
Yang J,
Kentistou KA,
Gorski M,
Brumat M,
Meidtner K,
Bielak LF,
Smith JA,
Hebbar P,
Farmaki AE,
Hofer E,
Lin M,
Lin M,
Xue C,
Zhang J,
Concas MP,
Vaccargiu S,
van der Most PJ,
Pitkänen N,
Cade BE,
Lee J,
van der Laan SW,
Chitrala KN,
Weiss S,
Zimmermann ME,
Lee JY,
Choi HS,
Nethander M,
Freitag-Wolf S,
Southam L,
Rayner NW,
Wang CA,
Lin SY,
Wang JS,
Couture C,
Lyytikäinen LP,
Nikus K,
Cuellar-Partida G,
Vestergaard H,
Hildalgo B,
Giannakopoulou O,
Cai Q,
Obura MO,
van Setten J,
Li X,
Schwander K,
Terzikhan N,
Shin JH,
Jackson RD,
Reiner AP,
Martin LW,
Chen Z,
Li L,
Highland HM,
Young KL,
Kawaguchi T,
Thiery J,
Bis JC,
Nadkarni GN,
Launer LJ,
Li H,
Nalls MA,
Raitakari OT,
Ichihara S,
Wild SH,
Nelson CP,
Campbell H,
Jäger S,
Nabika T,
Al-Mulla F,
Niinikoski H,
Braund PS,
Kolcic I,
Kovacs P,
Kovacs P,
Giardoglou T,
Katsuya T,
Bhatti KF,
de Kleijn D,
de Borst GJ,
Kim EK,
Adams HHH,
Ikram MA,
Zhu X,
Asselbergs FW,
Kraaijeveld AO,
Beulens JWJ,
Shu XO,
Rallidis LS,
Pedersen O,
Hansen T,
Mitchell P,
Hewitt AW,
Hewitt AW,
Kähönen M,
Pérusse L,
Bouchard C,
Tönjes A,
Chen YI,
Pennell CE,
Mori TA,
Lieb W,
Franke A,
Ohlsson C,
Mellström D,
Cho YS,
Lee H,
Yuan JM,
Koh WP,
Rhee SY,
Woo JT,
Heid IM,
Stark KJ,
Völzke H,
Homuth G,
Evans MK,
Zonderman AB,
Zonderman AB,
Polasek O,
Pasterkamp G,
Hoefer IE,
Redline S,
Pahkala K,
Oldehinkel AJ,
Snieder H,
Biino G,
Schmidt R,
Schmidt H,
Chen YE,
Bandinelli S,
Dedoussis G,
Thanaraj TA,
Kardia SLR,
Kato N,
Schulze MB,
Girotto G,
Jung B,
Böger CA,
Joshi PK,
Bennett DA,
De Jager PL,
Lu X,
Mamakou V,
Brown M,
Caulfield MJ,
Munroe PB,
Guo X,
Ciullo M,
Jonas JB,
Samani NJ,
Kaprio J,
Pajukanta P,
Adair LS,
Bechayda SA,
de Silva HJ,
Wickremasinghe AR,
Krauss RM,
Wu JY,
Zheng W,
den Hollander AI,
Bharadwaj D,
Correa A,
Wilson JG,
Lind L,
Heng CK,
Nelson AE,
Golightly YM,
Wilson JF,
Penninx B,
Kim HL,
Attia J,
Scott RJ,
Rao DC,
Arnett DK,
Hunt SC,
Walker M,
Koistinen HA,
Chandak GR,
Yajnik CS,
Mercader JM,
Tusié-Luna T,
Aguilar-Salinas CA,
Villalpando CG,
Orozco L,
Fornage M,
Tai ES,
van Dam RM,
Lehtimäki T,
Chaturvedi N,
Yokota M,
Liu J,
Reilly DF,
McKnight AJ,
Kee F,
Jöckel KH,
McCarthy MI,
Palmer CNA,
Vitart V,
Hayward C,
Simonsick E,
van Duijn CM,
Lu F,
Qu J,
Hishigaki H,
Lin X,
März W,
Parra EJ,
Parra EJ,
Cruz M,
Gudnason V,
Tardif JC,
Lettre G,
't Hart LM,
Elders PJM,
Damrauer SM,
Kumari M,
Kivimaki M,
van der Harst P,
Spector TD,
Loos RJF,
Province MA,
Province MA,
Psaty BM,
Brandslund I,
Pramstaller PP,
Christensen K,
Ripatti S,
Widén E,
Hakonarson H,
Grant SFA,
Kiemeney LALM,
de Graaf J,
Loeffler M,
Kronenberg F,
Gu D,
Erdmann J,
Schunkert H,
Franks PW,
Linneberg A,
Jukema JW,
Khera AV,
Männikkö M,
Jarvelin MR,
Kutalik Z,
Cucca F,
Mook-Kanamori DO,
van Dijk KW,
Watkins H,
Strachan DP,
Grarup N,
Sever P,
Poulter N,
Rotter JI,
Dantoft TM,
Karpe F,
Karpe F,
Neville MJ,
Timpson NJ,
Cheng CY,
Wong TY,
Khor CC,
Sabanayagam C,
Peters A,
Gieger C,
Hattersley AT,
Pedersen NL,
Magnusson PKE,
Boomsma DI,
de Geus EJC,
Cupples LA,
van Meurs JBJ,
Ghanbari M,
Gordon-Larsen P,
Huang W,
Kim YJ,
Kim YJ,
Tabara Y,
Wareham NJ,
Langenberg C,
Zeggini E,
Kuusisto J,
Laakso M,
Ingelsson E,
Abecasis G,
Chambers JC,
Kooner JS,
de Vries PS,
Morrison AC,
North KE,
Daviglus M,
Kraft P,
Martin NG,
Whitfield JB,
Abbas S,
Saleheen D,
Walters RG,
Holmes MV,
Black C,
Smith BH,
Justice AE,
Baras A,
Buring JE,
Ridker PM,
Chasman DI,
Kooperberg C,
Wei WQ,
Jarvik GP,
Namjou B,
Hayes MG,
Ritchie MD,
Jousilahti P,
Salomaa V,
Hveem K,
Åsvold BO,
Kubo M,
Kamatani Y,
Okada Y,
Murakami Y,
Thorsteinsdottir U,
Stefansson K,
Ho YL,
Lynch JA,
Rader DJ,
Tsao PS,
Chang KM,
Cho K,
O'Donnell CJ,
Gaziano JM,
Wilson P,
Rotimi CN,
Hazelhurst S,
Ramsay M,
Trembath RC,
van Heel DA,
Tamiya G,
Yamamoto M,
Kim BJ,
Mohlke KL,
Frayling TM,
Hirschhorn JN,
Kathiresan S,
Boehnke M,
Natarajan P,
Peloso GM,
Brown CD,
Morris AP,
Assimes TL,
Deloukas P,
Sun YV,
Willer CJ
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Trpchevska N,
Freidin MB,
Broer L,
Oosterloo BC,
Yao S,
Zhou Y,
Vona B,
Bishop C,
Bizaki-Vallaskangas A,
Canlon B,
Castellana F,
Chasman DI
and 54 more — show all
Cherny S,
Christensen K,
Concas MP,
Correa A,
Elkon R,
Mengel-From J,
Gao Y,
Giersch ABS,
Girotto G,
Gudjonsson A,
Gudnason V,
Heard-Costa NL,
Hertzano R,
Hjelmborg JVB,
Hjerling-Leffler J,
Hoffman HJ,
Kaprio J,
Kettunen J,
Krebs K,
Kähler AK,
Lallemend F,
Launer LJ,
Lee IM,
Leonard H,
Li CM,
Lowenheim H,
Magnusson PKE,
van Meurs J,
Milani L,
Morton CC,
Mäkitie A,
Nalls MA,
Nardone GG,
Nygaard M,
Palviainen T,
Pratt S,
Quaranta N,
Rämö J,
Saarentaus E,
Sardone R,
Satizabal CL,
Schweinfurth JM,
Seshadri S,
Shiroma E,
Shulman E,
Simonsick E,
Spankovich C,
Tropitzsch A,
Lauschke VM,
Sullivan PF,
Goedegebure A,
Cederroth CR,
Williams FMK,
Nagtegaal AP
Estonian Biobank Research Team
American journal of human genetics · 2022 · PMID 35580588 · open access
12 pages+
A saturated map of common genetic variants associated with human height
Yengo L,
Vedantam S,
Marouli E,
Sidorenko J,
Bartell E,
Sakaue S,
Graff M,
Eliasen AU,
Jiang Y,
Raghavan S,
Miao J,
Arias JD
and 610 more — show all
Graham SE,
Mukamel RE,
Spracklen CN,
Yin X,
Chen SH,
Ferreira T,
Highland HH,
Ji Y,
Karaderi T,
Lin K,
Lüll K,
Malden DE,
Medina-Gomez C,
Machado M,
Moore A,
Rüeger S,
Sim X,
Vrieze S,
Ahluwalia TS,
Akiyama M,
Allison MA,
Alvarez M,
Andersen MK,
Ani A,
Appadurai V,
Arbeeva L,
Bhaskar S,
Bielak LF,
Bollepalli S,
Bonnycastle LL,
Bork-Jensen J,
Bradfield JP,
Bradford Y,
Braund PS,
Brody JA,
Burgdorf KS,
Cade BE,
Cai H,
Cai Q,
Campbell A,
Cañadas-Garre M,
Catamo E,
Chai JF,
Chai X,
Chang LC,
Chang YC,
Chen CH,
Chesi A,
Choi SH,
Chung RH,
Cocca M,
Concas MP,
Couture C,
Cuellar-Partida G,
Danning R,
Daw EW,
Degenhard F,
Delgado GE,
Delitala A,
Demirkan A,
Deng X,
Devineni P,
Dietl A,
Dimitriou M,
Dimitrov L,
Dorajoo R,
Ekici AB,
Engmann JE,
Fairhurst-Hunter Z,
Farmaki AE,
Faul JD,
Fernandez-Lopez JC,
Forer L,
Francescatto M,
Freitag-Wolf S,
Fuchsberger C,
Galesloot TE,
Gao Y,
Gao Z,
Geller F,
Giannakopoulou O,
Giulianini F,
Gjesing AP,
Goel A,
Gordon SD,
Gorski M,
Grove J,
Guo X,
Gustafsson S,
Haessler J,
Hansen TF,
Havulinna AS,
Haworth SJ,
He J,
Heard-Costa N,
Hebbar P,
Hindy G,
Ho YA,
Hofer E,
Holliday E,
Horn K,
Hornsby WE,
Hottenga JJ,
Huang H,
Huang J,
Huerta-Chagoya A,
Huffman JE,
Hung YJ,
Huo S,
Hwang MY,
Iha H,
Ikeda DD,
Isono M,
Jackson AU,
Jäger S,
Jansen IE,
Johansson I,
Jonas JB,
Jonsson A,
Jørgensen T,
Kalafati IP,
Kanai M,
Kanoni S,
Kårhus LL,
Kasturiratne A,
Katsuya T,
Kawaguchi T,
Kember RL,
Kentistou KA,
Kim HN,
Kim YJ,
Kleber ME,
Knol MJ,
Kurbasic A,
Lauzon M,
Le P,
Lea R,
Lee JY,
Leonard HL,
Li SA,
Li X,
Li X,
Liang J,
Lin H,
Lin SY,
Liu J,
Liu X,
Lo KS,
Long J,
Lores-Motta L,
Luan J,
Lyssenko V,
Lyytikäinen LP,
Mahajan A,
Mamakou V,
Mangino M,
Manichaikul A,
Marten J,
Mattheisen M,
Mavarani L,
McDaid AF,
Meidtner K,
Melendez TL,
Mercader JM,
Milaneschi Y,
Miller JE,
Millwood IY,
Mishra PP,
Mitchell RE,
Møllehave LT,
Morgan A,
Mucha S,
Munz M,
Nakatochi M,
Nelson CP,
Nethander M,
Nho CW,
Nielsen AA,
Nolte IM,
Nongmaithem SS,
Noordam R,
Ntalla I,
Nutile T,
Pandit A,
Christofidou P,
Pärna K,
Pauper M,
Petersen ERB,
Petersen LV,
Pitkänen N,
Polašek O,
Poveda A,
Preuss MH,
Pyarajan S,
Raffield LM,
Rakugi H,
Ramirez J,
Rasheed A,
Raven D,
Rayner NW,
Riveros C,
Rohde R,
Ruggiero D,
Ruotsalainen SE,
Ryan KA,
Sabater-Lleal M,
Saxena R,
Scholz M,
Sendamarai A,
Shen B,
Shi J,
Shin JH,
Sidore C,
Sitlani CM,
Slieker RC,
Smit RAJ,
Smith AV,
Smith JA,
Smyth LJ,
Southam L,
Steinthorsdottir V,
Sun L,
Takeuchi F,
Tallapragada DSP,
Taylor KD,
Tayo BO,
Tcheandjieu C,
Terzikhan N,
Tesolin P,
Teumer A,
Theusch E,
Thompson DJ,
Thorleifsson G,
Timmers PRHJ,
Trompet S,
Turman C,
Vaccargiu S,
van der Laan SW,
van der Most PJ,
van Klinken JB,
van Setten J,
Verma SS,
Verweij N,
Veturi Y,
Wang CA,
Wang C,
Wang L,
Wang Z,
Warren HR,
Bin Wei W,
Wickremasinghe AR,
Wielscher M,
Wiggins KL,
Winsvold BS,
Wong A,
Wu Y,
Wuttke M,
Xia R,
Xie T,
Yamamoto K,
Yang J,
Yao J,
Young H,
Yousri NA,
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Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease
Lake J,
Warly Solsberg C,
Kim JJ,
Acosta-Uribe J,
Makarious MB,
Li Z,
Levine K,
Heutink P,
Alvarado CX,
Vitale D,
Kang S,
Gim J
and 8 more — show all
Molecular psychiatry · 2023 · PMID 37198259 · open access
3 pages
Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits
Gouveia MH,
Bentley AR,
Leonard H,
Meeks KAC,
Ekoru K,
Chen G,
Nalls MA,
Simonsick EM,
Tarazona-Santos E,
Lima-Costa MF,
Adeyemo A,
Shriner D
and 1 more — show all
Scientific reports · 2021 · PMID 33603002 · open access
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.