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Torres M.
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Arking DE,
Pulit SL,
Crotti L,
van der Harst P,
Munroe PB,
Koopmann TT,
Sotoodehnia N,
Rossin EJ,
Morley M,
Wang X,
Johnson AD,
Lundby A
and 218 more — show all
Gudbjartsson DF,
Noseworthy PA,
Eijgelsheim M,
Bradford Y,
Tarasov KV,
Dörr M,
Müller-Nurasyid M,
Lahtinen AM,
Nolte IM,
Smith AV,
Bis JC,
Isaacs A,
Newhouse SJ,
Evans DS,
Post WS,
Waggott D,
Lyytikäinen LP,
Hicks AA,
Eisele L,
Ellinghaus D,
Hayward C,
Navarro P,
Ulivi S,
Tanaka T,
Tester DJ,
Chatel S,
Gustafsson S,
Kumari M,
Morris RW,
Naluai ÅT,
Padmanabhan S,
Kluttig A,
Strohmer B,
Panayiotou AG,
Torres M,
Knoflach M,
Hubacek JA,
Slowikowski K,
Raychaudhuri S,
Kumar RD,
Harris TB,
Launer LJ,
Shuldiner AR,
Alonso A,
Bader JS,
Ehret G,
Huang H,
Kao WH,
Strait JB,
Macfarlane PW,
Brown M,
Caulfield MJ,
Samani NJ,
Kronenberg F,
Willeit J,
Smith JG,
Greiser KH,
Meyer Zu Schwabedissen H,
Werdan K,
Carella M,
Zelante L,
Heckbert SR,
Psaty BM,
Rotter JI,
Kolcic I,
Polašek O,
Wright AF,
Griffin M,
Daly MJ,
Arnar DO,
Hólm H,
Thorsteinsdottir U,
Denny JC,
Roden DM,
Zuvich RL,
Emilsson V,
Plump AS,
Larson MG,
O'Donnell CJ,
Yin X,
Bobbo M,
D'Adamo AP,
Iorio A,
Sinagra G,
Carracedo A,
Cummings SR,
Nalls MA,
Jula A,
Kontula KK,
Marjamaa A,
Oikarinen L,
Perola M,
Porthan K,
Erbel R,
Hoffmann P,
Jöckel KH,
Kälsch H,
Nöthen MM,
den Hoed M,
Loos RJ,
Thelle DS,
Gieger C,
Meitinger T,
Perz S,
Peters A,
Prucha H,
Sinner MF,
Waldenberger M,
de Boer RA,
Franke L,
van der Vleuten PA,
Beckmann BM,
Martens E,
Bardai A,
Hofman N,
Wilde AA,
Behr ER,
Dalageorgou C,
Giudicessi JR,
Medeiros-Domingo A,
Barc J,
Kyndt F,
Probst V,
Ghidoni A,
Insolia R,
Hamilton RM,
Scherer SW,
Brandimarto J,
Margulies K,
Moravec CE,
del Greco M F,
Fuchsberger C,
O'Connell JR,
Lee WK,
Watt GC,
Campbell H,
Wild SH,
El Mokhtari NE,
Frey N,
Asselbergs FW,
Mateo Leach I,
Navis G,
van den Berg MP,
van Veldhuisen DJ,
Kellis M,
Krijthe BP,
Franco OH,
Hofman A,
Kors JA,
Uitterlinden AG,
Witteman JC,
Kedenko L,
Lamina C,
Oostra BA,
Abecasis GR,
Lakatta EG,
Mulas A,
Orrú M,
Schlessinger D,
Uda M,
Markus MR,
Völker U,
Snieder H,
Spector TD,
Ärnlöv J,
Lind L,
Sundström J,
Syvänen AC,
Kivimaki M,
Kähönen M,
Mononen N,
Raitakari OT,
Viikari JS,
Adamkova V,
Kiechl S,
Brion M,
Nicolaides AN,
Paulweber B,
Haerting J,
Dominiczak AF,
Nyberg F,
Whincup PH,
Hingorani AD,
Schott JJ,
Bezzina CR,
Ingelsson E,
Ferrucci L,
Gasparini P,
Wilson JF,
Rudan I,
Franke A,
Mühleisen TW,
Pramstaller PP,
Lehtimäki TJ,
Paterson AD,
Parsa A,
Liu Y,
van Duijn CM,
Siscovick DS,
Gudnason V,
Jamshidi Y,
Salomaa V,
Felix SB,
Sanna S,
Ritchie MD,
Stricker BH,
Stefansson K,
Boyer LA,
Cappola TP,
Olsen JV,
Lage K,
Schwartz PJ,
Kääb S,
Chakravarti A,
Ackerman MJ,
Pfeufer A,
de Bakker PI,
Newton-Cheh C
CARe Consortium · COGENT Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24952745 · open access
12 pages+
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
Justice AE,
Karaderi T,
Highland HM,
Young KL,
Graff M,
Lu Y,
Turcot V,
Auer PL,
Fine RS,
Guo X,
Schurmann C,
Lempradl A
and 268 more — show all
Marouli E,
Mahajan A,
Winkler TW,
Winkler TW,
Locke AE,
Medina-Gomez C,
Esko T,
Vedantam S,
Giri A,
Lo KS,
Alfred T,
Mudgal P,
Ng MCY,
Heard-Costa NL,
Feitosa MF,
Manning AK,
Willems SM,
Sivapalaratnam S,
Abecasis G,
Alam DS,
Allison M,
Amouyel P,
Arzumanyan Z,
Balkau B,
Bastarache L,
Bergmann S,
Bielak LF,
Blüher M,
Boehnke M,
Boeing H,
Boerwinkle E,
Böger CA,
Bork-Jensen J,
Bottinger EP,
Bowden DW,
Brandslund I,
Broer L,
Burt AA,
Butterworth AS,
Caulfield MJ,
Cesana G,
Chambers JC,
Chasman DI,
Chen YI,
Chowdhury R,
Christensen C,
Chu AY,
Collins FS,
Cook JP,
Cox AJ,
Crosslin DS,
Danesh J,
de Bakker PIW,
Denus S,
Mutsert R,
Dedoussis G,
Demerath EW,
Dennis JG,
Denny JC,
Di Angelantonio E,
Dörr M,
Drenos F,
Dubé MP,
Dunning AM,
Easton DF,
Elliott P,
Evangelou E,
Farmaki AE,
Feng S,
Ferrannini E,
Ferrieres J,
Florez JC,
Fornage M,
Fox CS,
Franks PW,
Friedrich N,
Gan W,
Gandin I,
Gasparini P,
Giedraitis V,
Girotto G,
Gorski M,
Grallert H,
Grarup N,
Grove ML,
Gustafsson S,
Haessler J,
Hansen T,
Hattersley AT,
Hayward C,
Heid IM,
Holmen OL,
Hovingh GK,
Howson JMM,
Hu Y,
Hung YJ,
Hveem K,
Ikram MA,
Ingelsson E,
Jackson AU,
Jarvik GP,
Jia Y,
Jørgensen T,
Jousilahti P,
Justesen JM,
Kahali B,
Karaleftheri M,
Kardia SLR,
Karpe F,
Kee F,
Kitajima H,
Komulainen P,
Kooner JS,
Kovacs P,
Krämer BK,
Kuulasmaa K,
Kuusisto J,
Laakso M,
Lakka TA,
Lamparter D,
Lange LA,
Langenberg C,
Larson EB,
Lee NR,
Lee WJ,
Lehtimäki T,
Lewis CE,
Li H,
Li J,
Li-Gao R,
Lin LA,
Lin X,
Lind L,
Lindström J,
Linneberg A,
Liu CT,
Liu DJ,
Luan J,
Lyytikäinen LP,
MacGregor S,
Mägi R,
Männistö S,
Marenne G,
Marten J,
Masca NGD,
McCarthy MI,
Meidtner K,
Mihailov E,
Moilanen L,
Moitry M,
Mook-Kanamori DO,
Morgan A,
Morris AP,
Müller-Nurasyid M,
Munroe PB,
Narisu N,
Nelson CP,
Neville M,
Ntalla I,
O'Connell JR,
Owen KR,
Pedersen O,
Peloso GM,
Pennell CE,
Perola M,
Perry JA,
Perry JRB,
Pers TH,
Ewing A,
Polasek O,
Raitakari OT,
Rasheed A,
Raulerson CK,
Rauramaa R,
Reilly DF,
Reiner AP,
Ridker PM,
Rivas MA,
Robertson NR,
Robino A,
Rudan I,
Ruth KS,
Saleheen D,
Salomaa V,
Samani NJ,
Schreiner PJ,
Schulze MB,
Scott RA,
Segura-Lepe M,
Sim X,
Slater AJ,
Small KS,
Smith BH,
Smith JA,
Southam L,
Spector TD,
Speliotes EK,
Stefansson K,
Steinthorsdottir V,
Stirrups KE,
Strauch K,
Stringham HM,
Stumvoll M,
Sun L,
Surendran P,
Swart KMA,
Tardif JC,
Taylor KD,
Teumer A,
Thompson DJ,
Thorleifsson G,
Thorsteinsdottir U,
Thuesen BH,
Tönjes A,
Torres M,
Tsafantakis E,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van Duijn CM,
Vanhala M,
Varma R,
Vermeulen SH,
Vestergaard H,
Vitart V,
Vogt TF,
Vuckovic D,
Wagenknecht LE,
Walker M,
Wallentin L,
Wang F,
Wang CA,
Wang S,
Wareham NJ,
Warren HR,
Waterworth DM,
Wessel J,
White HD,
Willer CJ,
Wilson JG,
Wood AR,
Wu Y,
Yaghootkar H,
Yao J,
Yerges-Armstrong LM,
Young R,
Zeggini E,
Zhan X,
Zhang W,
Zhao JH,
Zhao W,
Zheng H,
Zhou W,
Zillikens MC,
Rivadeneira F,
Borecki IB,
Pospisilik JA,
Deloukas P,
Frayling TM,
Lettre G,
Mohlke KL,
Rotter JI,
Kutalik Z,
Hirschhorn JN,
Cupples LA,
Loos RJF,
North KE,
Lindgren CM
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Conti DV,
Darst BF,
Moss LC,
Saunders EJ,
Sheng X,
Chou A,
Schumacher FR,
Olama AAA,
Benlloch S,
Dadaev T,
Brook MN,
Sahimi A
and 220 more — show all
Hoffmann TJ,
Takahashi A,
Matsuda K,
Momozawa Y,
Fujita M,
Muir K,
Lophatananon A,
Wan P,
Le Marchand L,
Wilkens LR,
Stevens VL,
Gapstur SM,
Carter BD,
Schleutker J,
Tammela TLJ,
Sipeky C,
Auvinen A,
Giles GG,
Southey MC,
MacInnis RJ,
Cybulski C,
Wokołorczyk D,
Lubiński J,
Neal DE,
Donovan JL,
Hamdy FC,
Martin RM,
Nordestgaard BG,
Nielsen SF,
Weischer M,
Bojesen SE,
Røder MA,
Iversen P,
Batra J,
Chambers S,
Moya L,
Horvath L,
Clements JA,
Tilley W,
Risbridger GP,
Gronberg H,
Aly M,
Szulkin R,
Eklund M,
Nordström T,
Pashayan N,
Dunning AM,
Ghoussaini M,
Travis RC,
Key TJ,
Riboli E,
Park JY,
Sellers TA,
Lin HY,
Albanes D,
Weinstein SJ,
Mucci LA,
Giovannucci E,
Lindstrom S,
Kraft P,
Hunter DJ,
Penney KL,
Turman C,
Tangen CM,
Goodman PJ,
Thompson IM Jr,
Hamilton RJ,
Fleshner NE,
Finelli A,
Parent MÉ,
Stanford JL,
Ostrander EA,
Geybels MS,
Koutros S,
Freeman LEB,
Stampfer M,
Wolk A,
Håkansson N,
Andriole GL,
Hoover RN,
Machiela MJ,
Sørensen KD,
Borre M,
Blot WJ,
Zheng W,
Zheng W,
Yeboah ED,
Mensah JE,
Lu YJ,
Zhang HW,
Feng N,
Mao X,
Wu Y,
Zhao SC,
Sun Z,
Thibodeau SN,
McDonnell SK,
Schaid DJ,
West CML,
Burnet N,
Barnett G,
Maier C,
Schnoeller T,
Luedeke M,
Kibel AS,
Drake BF,
Cussenot O,
Cancel-Tassin G,
Menegaux F,
Truong T,
Koudou YA,
John EM,
Grindedal EM,
Maehle L,
Khaw KT,
Ingles SA,
Stern MC,
Vega A,
Gómez-Caamaño A,
Fachal L,
Rosenstein BS,
Kerns SL,
Ostrer H,
Teixeira MR,
Paulo P,
Brandão A,
Watya S,
Lubwama A,
Bensen JT,
Fontham ETH,
Mohler J,
Taylor JA,
Kogevinas M,
Llorca J,
Castaño-Vinyals G,
Cannon-Albright L,
Teerlink CC,
Huff CD,
Strom SS,
Multigner L,
Blanchet P,
Brureau L,
Kaneva R,
Slavov C,
Mitev V,
Leach RJ,
Weaver B,
Brenner H,
Cuk K,
Holleczek B,
Saum KU,
Klein EA,
Hsing AW,
Kittles RA,
Murphy AB,
Logothetis CJ,
Kim J,
Neuhausen SL,
Steele L,
Ding YC,
Isaacs WB,
Nemesure B,
Hennis AJM,
Carpten J,
Pandha H,
Michael A,
De Ruyck K,
De Meerleer G,
Ost P,
Xu J,
Razack A,
Lim J,
Teo SH,
Newcomb LF,
Lin DW,
Fowke JH,
Neslund-Dudas C,
Rybicki BA,
Gamulin M,
Lessel D,
Kulis T,
Usmani N,
Singhal S,
Parliament M,
Claessens F,
Joniau S,
Van den Broeck T,
Gago-Dominguez M,
Castelao JE,
Martinez ME,
Larkin S,
Townsend PA,
Aukim-Hastie C,
Bush WS,
Aldrich MC,
Crawford DC,
Srivastava S,
Cullen JC,
Petrovics G,
Casey G,
Roobol MJ,
Jenster G,
van Schaik RHN,
Hu JJ,
Sanderson M,
Varma R,
McKean-Cowdin R,
Torres M,
Mancuso N,
Berndt SI,
Van Den Eeden SK,
Easton DF,
Chanock SJ,
Cook MB,
Wiklund F,
Nakagawa H,
Witte JS,
Eeles RA,
Kote-Jarai Z,
Haiman CA
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Wang A,
Shen J,
Rodriguez AA,
Saunders EJ,
Chen F,
Janivara R,
Darst BF,
Sheng X,
Xu Y,
Chou AJ,
Benlloch S,
Dadaev T
and 279 more — show all
Brook MN,
Plym A,
Sahimi A,
Hoffman TJ,
Takahashi A,
Matsuda K,
Momozawa Y,
Fujita M,
Laisk T,
Figuerêdo J,
Muir K,
Ito S,
Liu X,
Uchio Y,
Kubo M,
Kamatani Y,
Lophatananon A,
Wan P,
Andrews C,
Lori A,
Choudhury PP,
Schleutker J,
Tammela TLJ,
Sipeky C,
Auvinen A,
Giles GG,
Southey MC,
MacInnis RJ,
Cybulski C,
Wokolorczyk D,
Lubinski J,
Rentsch CT,
Cho K,
Mcmahon BH,
Neal DE,
Donovan JL,
Hamdy FC,
Martin RM,
Nordestgaard BG,
Nielsen SF,
Weischer M,
Bojesen SE,
Røder A,
Stroomberg HV,
Batra J,
Chambers S,
Horvath L,
Clements JA,
Tilly W,
Risbridger GP,
Gronberg H,
Aly M,
Szulkin R,
Eklund M,
Nordstrom T,
Pashayan N,
Dunning AM,
Ghoussaini M,
Travis RC,
Key TJ,
Riboli E,
Park JY,
Sellers TA,
Lin HY,
Albanes D,
Weinstein S,
Cook MB,
Mucci LA,
Giovannucci E,
Lindstrom S,
Kraft P,
Hunter DJ,
Penney KL,
Turman C,
Tangen CM,
Goodman PJ,
Thompson IM Jr,
Hamilton RJ,
Fleshner NE,
Finelli A,
Parent MÉ,
Stanford JL,
Ostrander EA,
Koutros S,
Beane Freeman LE,
Stampfer M,
Wolk A,
Håkansson N,
Andriole GL,
Hoover RN,
Machiela MJ,
Sørensen KD,
Borre M,
Blot WJ,
Zheng W,
Yeboah ED,
Mensah JE,
Lu YJ,
Zhang HW,
Feng N,
Mao X,
Wu Y,
Zhao SC,
Sun Z,
Thibodeau SN,
McDonnell SK,
Schaid DJ,
West CML,
Barnett G,
Maier C,
Schnoeller T,
Luedeke M,
Kibel AS,
Drake BF,
Cussenot O,
Cancel-Tassin G,
Menegaux F,
Truong T,
Koudou YA,
John EM,
Grindedal EM,
Maehle L,
Khaw KT,
Ingles SA,
Stern MC,
Vega A,
Gómez-Caamaño A,
Fachal L,
Rosenstein BS,
Kerns SL,
Ostrer H,
Teixeira MR,
Paulo P,
Brandão A,
Watya S,
Lubwama A,
Bensen JT,
Butler EN,
Mohler JL,
Taylor JA,
Kogevinas M,
Dierssen-Sotos T,
Castaño-Vinyals G,
Cannon-Albright L,
Teerlink CC,
Huff CD,
Pilie P,
Yu Y,
Bohlender RJ,
Gu J,
Strom SS,
Multigner L,
Blanchet P,
Brureau L,
Kaneva R,
Slavov C,
Mitev V,
Leach RJ,
Brenner H,
Chen X,
Holleczek B,
Schöttker B,
Klein EA,
Hsing AW,
Kittles RA,
Murphy AB,
Logothetis CJ,
Kim J,
Neuhausen SL,
Steele L,
Ding YC,
Isaacs WB,
Nemesure B,
Hennis AJM,
Carpten J,
Pandha H,
Michael A,
De Ruyck K,
De Meerleer G,
Ost P,
Xu J,
Razack A,
Lim J,
Teo SH,
Newcomb LF,
Lin DW,
Fowke JH,
Neslund-Dudas CM,
Rybicki BA,
Gamulin M,
Lessel D,
Kulis T,
Usmani N,
Abraham A,
Singhal S,
Parliament M,
Claessens F,
Joniau S,
Van den Broeck T,
Gago-Dominguez M,
Castelao JE,
Martinez ME,
Larkin S,
Townsend PA,
Aukim-Hastie C,
Bush WS,
Aldrich MC,
Crawford DC,
Srivastava S,
Cullen J,
Petrovics G,
Casey G,
Wang Y,
Tettey Y,
Lachance J,
Tang W,
Biritwum RB,
Adjei AA,
Tay E,
Truelove A,
Niwa S,
Yamoah K,
Govindasami K,
Chokkalingam AP,
Keaton JM,
Hellwege JN,
Clark PE,
Jalloh M,
Gueye SM,
Niang L,
Ogunbiyi O,
Shittu O,
Amodu O,
Adebiyi AO,
Aisuodionoe-Shadrach OI,
Ajibola HO,
Jamda MA,
Oluwole OP,
Nwegbu M,
Adusei B,
Mante S,
Darkwa-Abrahams A,
Diop H,
Gundell SM,
Roobol MJ,
Jenster G,
van Schaik RHN,
Hu JJ,
Sanderson M,
Kachuri L,
Varma R,
McKean-Cowdin R,
Torres M,
Preuss MH,
Loos RJF,
Zawistowski M,
Zöllner S,
Lu Z,
Van Den Eeden SK,
Easton DF,
Ambs S,
Edwards TL,
Mägi R,
Rebbeck TR,
Fritsche L,
Chanock SJ,
Berndt SI,
Wiklund F,
Nakagawa H,
Witte JS,
Gaziano JM,
Justice AC,
Mancuso N,
Terao C,
Eeles RA,
Kote-Jarai Z,
Madduri RK,
Conti DV,
Haiman CA
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos
Ko A,
Cantor RM,
Weissglas-Volkov D,
Nikkola E,
Reddy PM,
Sinsheimer JS,
Pasaniuc B,
Brown R,
Alvarez M,
Rodriguez A,
Rodriguez-Guillen R,
Bautista IC
and 19 more — show all
Arellano-Campos O,
Muñoz-Hernández LL,
Salomaa V,
Kaprio J,
Jula A,
Jauhiainen M,
Heliövaara M,
Raitakari O,
Lehtimäki T,
Eriksson JG,
Perola M,
Lohmueller KE,
Matikainen N,
Taskinen MR,
Rodriguez-Torres M,
Riba L,
Tusie-Luna T,
Aguilar-Salinas CA,
Pajukanta P
Nature communications · 2014 · PMID 24886709 · open access
5 pages
Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos
Gao X,
Nannini DR,
Corrao K,
Torres M,
Chen YI,
Fan BJ,
Wiggs JL,
Taylor KD,
Gauderman WJ,
Rotter JI,
Varma R
International Glaucoma Genetics Consortium
Human molecular genetics · 2016 · PMID 28171582
1 page
A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 Diabetes
Mercader JM,
Liao RG,
Bell AD,
Dymek Z,
Estrada K,
Tukiainen T,
Huerta-Chagoya A,
Moreno-Macías H,
Jablonski KA,
Hanson RL,
Walford GA,
Moran I
and 66 more — show all
Chen L,
Agarwala V,
Ordoñez-Sánchez ML,
Rodríguez-Guillen R,
Rodríguez-Torres M,
Segura-Kato Y,
García-Ortiz H,
Centeno-Cruz F,
Barajas-Olmos F,
Caulkins L,
Puppala S,
Fontanillas P,
Williams AL,
Bonàs-Guarch S,
Hartl C,
Ripke S,
Tooley K,
Lane J,
Zerrweck C,
Martínez-Hernández A,
Córdova EJ,
Mendoza-Caamal E,
Contreras-Cubas C,
González-Villalpando ME,
Cruz-Bautista I,
Muñoz-Hernández L,
Gómez-Velasco D,
Alvirde U,
Henderson BE,
Wilkens LR,
Le Marchand L,
Arellano-Campos O,
Riba L,
Harden M,
Gabriel S,
Abboud HE,
Cortes ML,
Revilla-Monsalve C,
Islas-Andrade S,
Soberon X,
Curran JE,
Jenkinson CP,
DeFronzo RA,
Lehman DM,
Hanis CL,
Bell GI,
Boehnke M,
Blangero J,
Duggirala R,
Saxena R,
MacArthur D,
Ferrer J,
McCarroll SA,
Torrents D,
Knowler WC,
Baier LJ,
Burtt N,
González-Villalpando C,
Haiman CA,
Aguilar-Salinas CA,
Tusié-Luna T,
Flannick J,
Jacobs SBR,
Orozco L,
Altshuler D,
Florez JC
Diabetes Prevention Program Research Group · Broad Genomics Platform and 2 more consortia
Diabetes · 2017 · PMID 28838971 · 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.