For researchers
Is your paper here?
2,682 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
11 matches for
Perz S.
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+
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
Christophersen IE,
Rienstra M,
Roselli C,
Yin X,
Geelhoed B,
Barnard J,
Lin H,
Arking DE,
Smith AV,
Albert CM,
Chaffin M,
Tucker NR
and 150 more — show all
Li M,
Klarin D,
Bihlmeyer NA,
Low SK,
Weeke PE,
Müller-Nurasyid M,
Smith JG,
Brody JA,
Niemeijer MN,
Dörr M,
Trompet S,
Huffman J,
Gustafsson S,
Schurmann C,
Kleber ME,
Lyytikäinen LP,
Seppälä I,
Malik R,
Horimoto ARVR,
Perez M,
Sinisalo J,
Aeschbacher S,
Thériault S,
Yao J,
Radmanesh F,
Weiss S,
Teumer A,
Choi SH,
Weng LC,
Clauss S,
Deo R,
Rader DJ,
Shah SH,
Sun A,
Hopewell JC,
Debette S,
Chauhan G,
Yang Q,
Worrall BB,
Paré G,
Kamatani Y,
Hagemeijer YP,
Verweij N,
Siland JE,
Kubo M,
Smith JD,
Van Wagoner DR,
Bis JC,
Perz S,
Psaty BM,
Ridker PM,
Magnani JW,
Harris TB,
Launer LJ,
Shoemaker MB,
Padmanabhan S,
Haessler J,
Bartz TM,
Waldenberger M,
Lichtner P,
Arendt M,
Krieger JE,
Kähönen M,
Risch L,
Mansur AJ,
Peters A,
Smith BH,
Lind L,
Scott SA,
Lu Y,
Bottinger EB,
Hernesniemi J,
Lindgren CM,
Wong JA,
Huang J,
Eskola M,
Morris AP,
Ford I,
Reiner AP,
Delgado G,
Chen LY,
Chen YI,
Sandhu RK,
Li M,
Boerwinkle E,
Eisele L,
Lannfelt L,
Rost N,
Anderson CD,
Taylor KD,
Campbell A,
Magnusson PK,
Porteous D,
Hocking LJ,
Vlachopoulou E,
Pedersen NL,
Nikus K,
Orho-Melander M,
Hamsten A,
Heeringa J,
Denny JC,
Kriebel J,
Darbar D,
Newton-Cheh C,
Shaffer C,
Macfarlane PW,
Heilmann-Heimbach S,
Almgren P,
Huang PL,
Sotoodehnia N,
Soliman EZ,
Uitterlinden AG,
Hofman A,
Franco OH,
Völker U,
Jöckel KH,
Sinner MF,
Lin HJ,
Guo X,
Dichgans M,
Ingelsson E,
Kooperberg C,
Melander O,
Loos RJF,
Laurikka J,
Conen D,
Rosand J,
van der Harst P,
Lokki ML,
Kathiresan S,
Pereira A,
Jukema JW,
Hayward C,
Rotter JI,
März W,
Lehtimäki T,
Stricker BH,
Chung MK,
Felix SB,
Gudnason V,
Alonso A,
Roden DM,
Kääb S,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Tanaka T,
Lunetta KL,
Lubitz SA,
Ellinor PT
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium and 1 more consortia
Nature genetics · 2017 · PMID 28416818
12 pages+
Genome-wide association study of PR interval
Pfeufer A,
van Noord C,
Marciante KD,
Arking DE,
Larson MG,
Smith AV,
Tarasov KV,
Müller M,
Sotoodehnia N,
Sinner MF,
Verwoert GC,
Li M
and 53 more — show all
Kao WH,
Köttgen A,
Coresh J,
Bis JC,
Psaty BM,
Rice K,
Rotter JI,
Rivadeneira F,
Hofman A,
Kors JA,
Stricker BH,
Uitterlinden AG,
van Duijn CM,
Beckmann BM,
Sauter W,
Gieger C,
Lubitz SA,
Newton-Cheh C,
Wang TJ,
Magnani JW,
Schnabel RB,
Chung MK,
Barnard J,
Smith JD,
Van Wagoner DR,
Vasan RS,
Aspelund T,
Eiriksdottir G,
Harris TB,
Launer LJ,
Najjar SS,
Lakatta E,
Schlessinger D,
Uda M,
Abecasis GR,
Müller-Myhsok B,
Ehret GB,
Boerwinkle E,
Chakravarti A,
Soliman EZ,
Lunetta KL,
Perz S,
Wichmann HE,
Meitinger T,
Levy D,
Gudnason V,
Ellinor PT,
Sanna S,
Kääb S,
Witteman JC,
Alonso A,
Benjamin EJ,
Heckbert SR
Nature genetics · 2010 · PMID 20062060 · open access
6 pages
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
Nolte IM,
Munoz ML,
Tragante V,
Amare AT,
Jansen R,
Vaez A,
von der Heyde B,
Avery CL,
Bis JC,
Dierckx B,
van Dongen J,
Gogarten SM
and 153 more — show all
Goyette P,
Hernesniemi J,
Huikari V,
Hwang SJ,
Jaju D,
Kerr KF,
Kluttig A,
Krijthe BP,
Kumar J,
van der Laan SW,
Lyytikäinen LP,
Maihofer AX,
Minassian A,
van der Most PJ,
Müller-Nurasyid M,
Nivard M,
Salvi E,
Stewart JD,
Thayer JF,
Verweij N,
Wong A,
Zabaneh D,
Zafarmand MH,
Abdellaoui A,
Albarwani S,
Albert C,
Alonso A,
Ashar F,
Auvinen J,
Axelsson T,
Baker DG,
de Bakker PIW,
Barcella M,
Bayoumi R,
Bieringa RJ,
Boomsma D,
Boucher G,
Britton AR,
Christophersen I,
Dietrich A,
Ehret GB,
Ellinor PT,
Eskola M,
Felix JF,
Floras JS,
Franco OH,
Friberg P,
Gademan MGJ,
Geyer MA,
Giedraitis V,
Hartman CA,
Hemerich D,
Hofman A,
Hottenga JJ,
Huikuri H,
Hutri-Kähönen N,
Jouven X,
Junttila J,
Juonala M,
Kiviniemi AM,
Kors JA,
Kumari M,
Kuznetsova T,
Kuznetsova T,
Laurie CC,
Lefrandt JD,
Li Y,
Li Y,
Liao D,
Limacher MC,
Lin HJ,
Lindgren CM,
Lubitz SA,
Mahajan A,
McKnight B,
Zu Schwabedissen HM,
Milaneschi Y,
Mononen N,
Morris AP,
Nalls MA,
Navis G,
Neijts M,
Nikus K,
North KE,
O'Connor DT,
Ormel J,
Perz S,
Peters A,
Psaty BM,
Raitakari OT,
Risbrough VB,
Sinner MF,
Siscovick D,
Smit JH,
Smith NL,
Soliman EZ,
Sotoodehnia N,
Staessen JA,
Stein PK,
Stilp AM,
Stolarz-Skrzypek K,
Strauch K,
Sundström J,
Swenne CA,
Syvänen AC,
Tardif JC,
Taylor KD,
Teumer A,
Thornton TA,
Tinker LE,
Uitterlinden AG,
van Setten J,
Voss A,
Waldenberger M,
Wilhelmsen KC,
Willemsen G,
Wong Q,
Zhang ZM,
Zonderman AB,
Cusi D,
Evans MK,
Greiser HK,
van der Harst P,
Hassan M,
Ingelsson E,
Järvelin MR,
Kääb S,
Kähönen M,
Kivimaki M,
Kooperberg C,
Kuh D,
Lehtimäki T,
Lind L,
Nievergelt CM,
O'Donnell CJ,
Oldehinkel AJ,
Penninx B,
Reiner AP,
Riese H,
van Roon AM,
Rioux JD,
Rotter JI,
Sofer T,
Stricker BH,
Tiemeier H,
Vrijkotte TGM,
Asselbergs FW,
Brundel BJJM,
Heckbert SR,
Whitsel EA,
den Hoed M,
Snieder H,
de Geus EJC
Nature communications · 2017 · PMID 28613276 · open access
6 pages
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Sotoodehnia N,
Isaacs A,
de Bakker PI,
Dörr M,
Newton-Cheh C,
Nolte IM,
van der Harst P,
Müller M,
Eijgelsheim M,
Alonso A,
Hicks AA,
Padmanabhan S
and 91 more — show all
Hayward C,
Smith AV,
Polasek O,
Giovannone S,
Fu J,
Magnani JW,
Marciante KD,
Pfeufer A,
Gharib SA,
Teumer A,
Li M,
Bis JC,
Rivadeneira F,
Aspelund T,
Köttgen A,
Johnson T,
Rice K,
Sie MP,
Wang YA,
Klopp N,
Fuchsberger C,
Wild SH,
Mateo Leach I,
Estrada K,
Völker U,
Wright AF,
Asselbergs FW,
Qu J,
Chakravarti A,
Sinner MF,
Kors JA,
Petersmann A,
Harris TB,
Soliman EZ,
Munroe PB,
Psaty BM,
Oostra BA,
Cupples LA,
Perz S,
de Boer RA,
Uitterlinden AG,
Völzke H,
Spector TD,
Liu FY,
Boerwinkle E,
Dominiczak AF,
Rotter JI,
van Herpen G,
Levy D,
Wichmann HE,
van Gilst WH,
Witteman JC,
Kroemer HK,
Kao WH,
Heckbert SR,
Meitinger T,
Hofman A,
Campbell H,
Folsom AR,
van Veldhuisen DJ,
Schwienbacher C,
O'Donnell CJ,
Volpato CB,
Caulfield MJ,
Connell JM,
Launer L,
Lu X,
Franke L,
Fehrmann RS,
te Meerman G,
Groen HJ,
Weersma RK,
van den Berg LH,
Wijmenga C,
Ophoff RA,
Navis G,
Rudan I,
Snieder H,
Wilson JF,
Pramstaller PP,
Siscovick DS,
Wang TJ,
Gudnason V,
van Duijn CM,
Felix SB,
Fishman GI,
Jamshidi Y,
Stricker BH,
Samani NJ,
Kääb S,
Arking DE
Nature genetics · 2010 · PMID 21076409 · open access
5 pages
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Pfeufer A,
Sanna S,
Arking DE,
Müller M,
Gateva V,
Fuchsberger C,
Ehret GB,
Orrú M,
Pattaro C,
Köttgen A,
Perz S,
Usala G
and 32 more — show all
Barbalic M,
Li M,
Pütz B,
Scuteri A,
Prineas RJ,
Sinner MF,
Gieger C,
Najjar SS,
Kao WH,
Mühleisen TW,
Dei M,
Happle C,
Möhlenkamp S,
Crisponi L,
Erbel R,
Jöckel KH,
Naitza S,
Steinbeck G,
Marroni F,
Hicks AA,
Lakatta E,
Müller-Myhsok B,
Pramstaller PP,
Wichmann HE,
Schlessinger D,
Boerwinkle E,
Meitinger T,
Uda M,
Coresh J,
Kääb S,
Abecasis GR,
Chakravarti A
Nature genetics · 2009 · PMID 19305409
4 pages
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Ellinor PT,
Lunetta KL,
Albert CM,
Glazer NL,
Ritchie MD,
Smith AV,
Arking DE,
Müller-Nurasyid M,
Krijthe BP,
Lubitz SA,
Bis JC,
Chung MK
and 77 more — show all
Dörr M,
Ozaki K,
Roberts JD,
Smith JG,
Pfeufer A,
Sinner MF,
Lohman K,
Ding J,
Smith NL,
Smith JD,
Rienstra M,
Rice KM,
Van Wagoner DR,
Magnani JW,
Wakili R,
Clauss S,
Rotter JI,
Steinbeck G,
Launer LJ,
Davies RW,
Borkovich M,
Harris TB,
Lin H,
Völker U,
Völzke H,
Milan DJ,
Hofman A,
Boerwinkle E,
Chen LY,
Soliman EZ,
Voight BF,
Li G,
Chakravarti A,
Kubo M,
Tedrow UB,
Rose LM,
Ridker PM,
Conen D,
Tsunoda T,
Furukawa T,
Sotoodehnia N,
Xu S,
Kamatani N,
Levy D,
Nakamura Y,
Parvez B,
Mahida S,
Furie KL,
Rosand J,
Muhammad R,
Psaty BM,
Meitinger T,
Perz S,
Wichmann HE,
Witteman JC,
Kao WH,
Kathiresan S,
Roden DM,
Uitterlinden AG,
Rivadeneira F,
McKnight B,
Sjögren M,
Newman AB,
Liu Y,
Gollob MH,
Melander O,
Tanaka T,
Stricker BH,
Felix SB,
Alonso A,
Darbar D,
Barnard J,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Gudnason V,
Kääb S
Nature genetics · 2012 · PMID 22544366
3 pages
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Benjamin EJ,
Rice KM,
Arking DE,
Pfeufer A,
van Noord C,
Smith AV,
Schnabel RB,
Bis JC,
Boerwinkle E,
Sinner MF,
Dehghan A,
Lubitz SA
and 44 more — show all
D'Agostino RB Sr,
Lumley T,
Ehret GB,
Heeringa J,
Aspelund T,
Newton-Cheh C,
Larson MG,
Marciante KD,
Soliman EZ,
Rivadeneira F,
Wang TJ,
Eiríksdottir G,
Levy D,
Psaty BM,
Li M,
Chamberlain AM,
Hofman A,
Vasan RS,
Harris TB,
Rotter JI,
Kao WH,
Agarwal SK,
Stricker BH,
Wang K,
Launer LJ,
Smith NL,
Chakravarti A,
Uitterlinden AG,
Wolf PA,
Sotoodehnia N,
Köttgen A,
van Duijn CM,
Meitinger T,
Mueller M,
Perz S,
Steinbeck G,
Wichmann HE,
Lunetta KL,
Heckbert SR,
Gudnason V,
Alonso A,
Kääb S,
Ellinor PT,
Witteman JC
Nature genetics · 2009 · PMID 19597492 · open access
1 page
Common variants in KCNN3 are associated with lone atrial fibrillation
Ellinor PT,
Lunetta KL,
Glazer NL,
Pfeufer A,
Alonso A,
Chung MK,
Sinner MF,
de Bakker PI,
Mueller M,
Lubitz SA,
Fox E,
Darbar D
and 50 more — show all
Smith NL,
Smith JD,
Schnabel RB,
Soliman EZ,
Rice KM,
Van Wagoner DR,
Beckmann BM,
van Noord C,
Wang K,
Ehret GB,
Rotter JI,
Hazen SL,
Steinbeck G,
Smith AV,
Launer LJ,
Harris TB,
Makino S,
Nelis M,
Milan DJ,
Perz S,
Esko T,
Köttgen A,
Moebus S,
Newton-Cheh C,
Li M,
Möhlenkamp S,
Wang TJ,
Kao WH,
Vasan RS,
Nöthen MM,
MacRae CA,
Stricker BH,
Hofman A,
Uitterlinden AG,
Levy D,
Boerwinkle E,
Metspalu A,
Topol EJ,
Chakravarti A,
Gudnason V,
Psaty BM,
Roden DM,
Meitinger T,
Wichmann HE,
Witteman JC,
Barnard J,
Arking DE,
Benjamin EJ,
Heckbert SR,
Kääb S
Nature genetics · 2010 · PMID 20173747 · open access
1 page
Genome-wide association analysis identifies multiple loci related to resting heart rate
Eijgelsheim M,
Newton-Cheh C,
Sotoodehnia N,
de Bakker PI,
Müller M,
Morrison AC,
Smith AV,
Isaacs A,
Sanna S,
Dörr M,
Navarro P,
Fuchsberger C
and 62 more — show all
Nolte IM,
de Geus EJ,
Estrada K,
Hwang SJ,
Bis JC,
Rückert IM,
Alonso A,
Launer LJ,
Hottenga JJ,
Rivadeneira F,
Noseworthy PA,
Rice KM,
Perz S,
Arking DE,
Spector TD,
Kors JA,
Aulchenko YS,
Tarasov KV,
Homuth G,
Wild SH,
Marroni F,
Gieger C,
Licht CM,
Prineas RJ,
Hofman A,
Rotter JI,
Hicks AA,
Ernst F,
Najjar SS,
Wright AF,
Peters A,
Fox ER,
Oostra BA,
Kroemer HK,
Couper D,
Völzke H,
Campbell H,
Meitinger T,
Uda M,
Witteman JC,
Psaty BM,
Wichmann HE,
Harris TB,
Kääb S,
Siscovick DS,
Jamshidi Y,
Uitterlinden AG,
Folsom AR,
Larson MG,
Wilson JF,
Penninx BW,
Snieder H,
Pramstaller PP,
van Duijn CM,
Lakatta EG,
Felix SB,
Gudnason V,
Pfeufer A,
Heckbert SR,
Stricker BH,
Boerwinkle E,
O'Donnell CJ
Human molecular genetics · 2010 · PMID 20639392
1 page
ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals
Bihlmeyer NA,
Brody JA,
Smith AV,
Warren HR,
Lin H,
Isaacs A,
Liu CT,
Marten J,
Radmanesh F,
Hall LM,
Grarup N,
Mei H
and 88 more — show all
Müller-Nurasyid M,
Huffman JE,
Verweij N,
Guo X,
Yao J,
Li-Gao R,
van den Berg M,
Weiss S,
Prins BP,
van Setten J,
Haessler J,
Lyytikäinen LP,
Li M,
Alonso A,
Soliman EZ,
Bis JC,
Austin T,
Chen YI,
Psaty BM,
Harrris TB,
Launer LJ,
Padmanabhan S,
Dominiczak A,
Huang PL,
Xie Z,
Ellinor PT,
Kors JA,
Campbell A,
Murray AD,
Nelson CP,
Tobin MD,
Bork-Jensen J,
Hansen T,
Pedersen O,
Linneberg A,
Sinner MF,
Peters A,
Waldenberger M,
Meitinger T,
Perz S,
Kolcic I,
Rudan I,
de Boer RA,
van der Meer P,
Lin HJ,
Taylor KD,
de Mutsert R,
Trompet S,
Jukema JW,
Maan AC,
Stricker BHC,
Rivadeneira F,
Uitterlinden A,
Völker U,
Homuth G,
Völzke H,
Felix SB,
Mangino M,
Spector TD,
Bots ML,
Perez M,
Raitakari OT,
Kähönen M,
Mononen N,
Gudnason V,
Munroe PB,
Lubitz SA,
van Duijn CM,
Newton-Cheh CH,
Hayward C,
Rosand J,
Samani NJ,
Kanters JK,
Wilson JG,
Kääb S,
Polasek O,
van der Harst P,
Heckbert SR,
Rotter JI,
Mook-Kanamori DO,
Eijgelsheim M,
Dörr M,
Jamshidi Y,
Asselbergs FW,
Kooperberg C,
Lehtimäki T,
Arking DE,
Sotoodehnia N
Circulation. Genomic and precision medicine · 2018 · PMID 29874175 · 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.