For researchers
Is your paper here?
2,662 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.
7 matches for
Chouraki V.
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Pattaro C,
Teumer A,
Gorski M,
Chu AY,
Li M,
Mijatovic V,
Garnaas M,
Tin A,
Sorice R,
Li Y,
Taliun D,
Olden M
and 240 more — show all
Foster M,
Yang Q,
Chen MH,
Pers TH,
Johnson AD,
Ko YA,
Fuchsberger C,
Tayo B,
Nalls M,
Feitosa MF,
Isaacs A,
Dehghan A,
d'Adamo P,
Adeyemo A,
Dieffenbach AK,
Zonderman AB,
Nolte IM,
van der Most PJ,
Wright AF,
Shuldiner AR,
Morrison AC,
Hofman A,
Smith AV,
Dreisbach AW,
Franke A,
Uitterlinden AG,
Metspalu A,
Tonjes A,
Lupo A,
Robino A,
Johansson Å,
Demirkan A,
Kollerits B,
Freedman BI,
Ponte B,
Oostra BA,
Paulweber B,
Krämer BK,
Mitchell BD,
Buckley BM,
Peralta CA,
Hayward C,
Helmer C,
Rotimi CN,
Shaffer CM,
Müller C,
Sala C,
van Duijn CM,
Saint-Pierre A,
Ackermann D,
Shriner D,
Ruggiero D,
Toniolo D,
Lu Y,
Cusi D,
Czamara D,
Ellinghaus D,
Siscovick DS,
Ruderfer D,
Gieger C,
Grallert H,
Rochtchina E,
Atkinson EJ,
Holliday EG,
Boerwinkle E,
Salvi E,
Bottinger EP,
Murgia F,
Rivadeneira F,
Ernst F,
Kronenberg F,
Hu FB,
Navis GJ,
Curhan GC,
Ehret GB,
Homuth G,
Coassin S,
Thun GA,
Pistis G,
Gambaro G,
Malerba G,
Montgomery GW,
Eiriksdottir G,
Jacobs G,
Li G,
Wichmann HE,
Campbell H,
Schmidt H,
Wallaschofski H,
Völzke H,
Brenner H,
Kroemer HK,
Kramer H,
Lin H,
Leach IM,
Ford I,
Guessous I,
Rudan I,
Prokopenko I,
Borecki I,
Heid IM,
Kolcic I,
Persico I,
Jukema JW,
Wilson JF,
Felix JF,
Divers J,
Lambert JC,
Stafford JM,
Gaspoz JM,
Smith JA,
Faul JD,
Wang JJ,
Ding J,
Hirschhorn JN,
Attia J,
Whitfield JB,
Chalmers J,
Viikari J,
Coresh J,
Denny JC,
Karjalainen J,
Fernandes JK,
Endlich K,
Butterbach K,
Keene KL,
Lohman K,
Portas L,
Launer LJ,
Lyytikäinen LP,
Yengo L,
Franke L,
Ferrucci L,
Rose LM,
Kedenko L,
Rao M,
Struchalin M,
Kleber ME,
Cavalieri M,
Haun M,
Cornelis MC,
Ciullo M,
Pirastu M,
de Andrade M,
McEvoy MA,
Woodward M,
Adam M,
Cocca M,
Nauck M,
Imboden M,
Waldenberger M,
Pruijm M,
Metzger M,
Stumvoll M,
Evans MK,
Sale MM,
Kähönen M,
Boban M,
Bochud M,
Rheinberger M,
Verweij N,
Bouatia-Naji N,
Martin NG,
Hastie N,
Probst-Hensch N,
Soranzo N,
Devuyst O,
Raitakari O,
Gottesman O,
Franco OH,
Polasek O,
Gasparini P,
Munroe PB,
Ridker PM,
Mitchell P,
Muntner P,
Meisinger C,
Smit JH,
Kovacs P,
Wild PS,
Froguel P,
Rettig R,
Mägi R,
Biffar R,
Schmidt R,
Middelberg RP,
Carroll RJ,
Penninx BW,
Scott RJ,
Katz R,
Sedaghat S,
Wild SH,
Kardia SL,
Ulivi S,
Hwang SJ,
Enroth S,
Kloiber S,
Trompet S,
Stengel B,
Hancock SJ,
Turner ST,
Rosas SE,
Stracke S,
Harris TB,
Zeller T,
Zemunik T,
Lehtimäki T,
Illig T,
Aspelund T,
Nikopensius T,
Esko T,
Tanaka T,
Gyllensten U,
Völker U,
Emilsson V,
Vitart V,
Aalto V,
Gudnason V,
Chouraki V,
Chen WM,
Igl W,
März W,
Koenig W,
Lieb W,
Loos RJ,
Liu Y,
Snieder H,
Pramstaller PP,
Parsa A,
O'Connell JR,
Susztak K,
Hamet P,
Tremblay J,
de Boer IH,
Böger CA,
Goessling W,
Chasman DI,
Köttgen A,
Kao WH,
Fox CS
ICBP Consortium · AGEN Consortium and 3 more consortia
Nature communications · 2016 · PMID 26831199 · open access
12 pages+
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI
Verhaaren BF,
Debette S,
Bis JC,
Smith JA,
Ikram MK,
Adams HH,
Beecham AH,
Rajan KB,
Lopez LM,
Barral S,
van Buchem MA,
van der Grond J
and 90 more — show all
Smith AV,
Hegenscheid K,
Aggarwal NT,
de Andrade M,
Atkinson EJ,
Beekman M,
Beiser AS,
Blanton SH,
Boerwinkle E,
Brickman AM,
Bryan RN,
Chauhan G,
Chen CP,
Chouraki V,
de Craen AJ,
Crivello F,
Deary IJ,
Deelen J,
De Jager PL,
Dufouil C,
Elkind MS,
Evans DA,
Freudenberger P,
Gottesman RF,
Guðnason V,
Habes M,
Heckbert SR,
Heiss G,
Hilal S,
Hofer E,
Hofman A,
Ibrahim-Verbaas CA,
Knopman DS,
Lewis CE,
Liao J,
Liewald DC,
Luciano M,
van der Lugt A,
Martinez OO,
Mayeux R,
Mazoyer B,
Nalls M,
Nauck M,
Niessen WJ,
Oostra BA,
Psaty BM,
Rice KM,
Rotter JI,
von Sarnowski B,
Schmidt H,
Schreiner PJ,
Schuur M,
Sidney SS,
Sigurdsson S,
Slagboom PE,
Stott DJ,
van Swieten JC,
Teumer A,
Töglhofer AM,
Traylor M,
Trompet S,
Turner ST,
Tzourio C,
Uh HW,
Uitterlinden AG,
Vernooij MW,
Wang JJ,
Wong TY,
Wardlaw JM,
Windham BG,
Wittfeld K,
Wolf C,
Wright CB,
Yang Q,
Zhao W,
Zijdenbos A,
Jukema JW,
Sacco RL,
Kardia SL,
Amouyel P,
Mosley TH,
Longstreth WT Jr,
DeCarli CC,
van Duijn CM,
Schmidt R,
Launer LJ,
Grabe HJ,
Seshadri SS,
Ikram MA,
Fornage M
Circulation. Cardiovascular genetics · 2015 · PMID 25663218
4 pages
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function
Gorski M,
van der Most PJ,
Teumer A,
Chu AY,
Li M,
Mijatovic V,
Nolte IM,
Cocca M,
Taliun D,
Gomez F,
Li Y,
Tayo B
and 114 more — show all
Tin A,
Feitosa MF,
Aspelund T,
Attia J,
Biffar R,
Bochud M,
Boerwinkle E,
Borecki I,
Bottinger EP,
Chen MH,
Chouraki V,
Ciullo M,
Coresh J,
Cornelis MC,
Curhan GC,
d'Adamo AP,
Dehghan A,
Dengler L,
Ding J,
Eiriksdottir G,
Endlich K,
Enroth S,
Esko T,
Franco OH,
Gasparini P,
Gieger C,
Girotto G,
Gottesman O,
Gudnason V,
Gyllensten U,
Hancock SJ,
Harris TB,
Helmer C,
Höllerer S,
Hofer E,
Hofman A,
Holliday EG,
Homuth G,
Hu FB,
Huth C,
Hutri-Kähönen N,
Hwang SJ,
Imboden M,
Johansson Å,
Kähönen M,
König W,
Kramer H,
Krämer BK,
Kumar A,
Kutalik Z,
Lambert JC,
Launer LJ,
Lehtimäki T,
de Borst M,
Navis G,
Swertz M,
Liu Y,
Lohman K,
Loos RJF,
Lu Y,
Lyytikäinen LP,
McEvoy MA,
Meisinger C,
Meitinger T,
Metspalu A,
Metzger M,
Mihailov E,
Mitchell P,
Nauck M,
Oldehinkel AJ,
Olden M,
Wjh Penninx B,
Pistis G,
Pramstaller PP,
Probst-Hensch N,
Raitakari OT,
Rettig R,
Ridker PM,
Rivadeneira F,
Robino A,
Rosas SE,
Ruderfer D,
Ruggiero D,
Saba Y,
Sala C,
Schmidt H,
Schmidt R,
Scott RJ,
Sedaghat S,
Smith AV,
Sorice R,
Stengel B,
Stracke S,
Strauch K,
Toniolo D,
Uitterlinden AG,
Ulivi S,
Viikari JS,
Völker U,
Vollenweider P,
Völzke H,
Vuckovic D,
Waldenberger M,
Jin Wang J,
Yang Q,
Chasman DI,
Tromp G,
Snieder H,
Heid IM,
Fox CS,
Köttgen A,
Pattaro C,
Böger CA,
Fuchsberger C
Scientific reports · 2017 · PMID 28452372 · open access
4 pages
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Bis JC,
DeCarli C,
Smith AV,
van der Lijn F,
Crivello F,
Fornage M,
Debette S,
Shulman JM,
Schmidt H,
Srikanth V,
Schuur M,
Yu L
and 71 more — show all
Choi SH,
Sigurdsson S,
Verhaaren BF,
DeStefano AL,
Lambert JC,
Jack CR Jr,
Struchalin M,
Stankovich J,
Ibrahim-Verbaas CA,
Fleischman D,
Zijdenbos A,
den Heijer T,
Mazoyer B,
Coker LH,
Enzinger C,
Danoy P,
Amin N,
Arfanakis K,
van Buchem MA,
de Bruijn RF,
Beiser A,
Dufouil C,
Huang J,
Cavalieri M,
Thomson R,
Niessen WJ,
Chibnik LB,
Gislason GK,
Hofman A,
Pikula A,
Pikula A,
Amouyel P,
Freeman KB,
Phan TG,
Oostra BA,
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Wright MJ,
Franke B,
Martin NG,
Thompson PM,
Nalls MA,
Uitterlinden AG,
Au R,
Elbaz A,
Beare RJ,
van Swieten JC,
Lopez OL,
Harris TB,
Chouraki V,
Breteler MM,
De Jager PL,
Becker JT,
Vernooij MW,
Knopman D,
Fazekas F,
Wolf PA,
van der Lugt A,
Gudnason V,
Longstreth WT Jr,
Brown MA,
Bennett DA,
van Duijn CM,
Mosley TH,
Schmidt R,
Tzourio C,
Launer LJ,
Ikram MA,
Seshadri S
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
2 pages
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Lambert JC,
Ibrahim-Verbaas CA,
Harold D,
Naj AC,
Sims R,
Bellenguez C,
DeStafano AL,
Bis JC,
Beecham GW,
Grenier-Boley B,
Russo G,
Thorton-Wells TA
and 160 more — show all
Jones N,
Smith AV,
Chouraki V,
Thomas C,
Ikram MA,
Zelenika D,
Vardarajan BN,
Kamatani Y,
Lin CF,
Gerrish A,
Gerrish A,
Schmidt H,
Kunkle B,
Dunstan ML,
Ruiz A,
Bihoreau MT,
Choi SH,
Reitz C,
Pasquier F,
Cruchaga C,
Craig D,
Amin N,
Berr C,
Lopez OL,
De Jager PL,
Deramecourt V,
Johnston JA,
Evans D,
Lovestone S,
Letenneur L,
Morón FJ,
Rubinsztein DC,
Eiriksdottir G,
Sleegers K,
Goate AM,
Fiévet N,
Huentelman MW,
Gill M,
Brown K,
Kamboh MI,
Keller L,
Barberger-Gateau P,
McGuiness B,
Larson EB,
Green R,
Myers AJ,
Dufouil C,
Todd S,
Wallon D,
Love S,
Rogaeva E,
Gallacher J,
St George-Hyslop P,
Clarimon J,
Lleo A,
Bayer A,
Tsuang DW,
Yu L,
Tsolaki M,
Bossù P,
Spalletta G,
Proitsi P,
Collinge J,
Sorbi S,
Sanchez-Garcia F,
Fox NC,
Hardy J,
Deniz Naranjo MC,
Bosco P,
Clarke R,
Brayne C,
Galimberti D,
Mancuso M,
Matthews F,
Moebus S,
Mecocci P,
Del Zompo M,
Maier W,
Hampel H,
Pilotto A,
Bullido M,
Panza F,
Caffarra P,
Nacmias B,
Gilbert JR,
Mayhaus M,
Lannefelt L,
Hakonarson H,
Pichler S,
Carrasquillo MM,
Ingelsson M,
Beekly D,
Alvarez V,
Zou F,
Valladares O,
Younkin SG,
Coto E,
Hamilton-Nelson KL,
Gu W,
Razquin C,
Pastor P,
Mateo I,
Owen MJ,
Faber KM,
Jonsson PV,
Combarros O,
O'Donovan MC,
Cantwell LB,
Soininen H,
Blacker D,
Mead S,
Mosley TH Jr,
Bennett DA,
Harris TB,
Fratiglioni L,
Holmes C,
de Bruijn RF,
Passmore P,
Montine TJ,
Bettens K,
Rotter JI,
Brice A,
Morgan K,
Foroud TM,
Kukull WA,
Hannequin D,
Powell JF,
Nalls MA,
Ritchie K,
Lunetta KL,
Kauwe JS,
Boerwinkle E,
Riemenschneider M,
Boada M,
Hiltuenen M,
Martin ER,
Schmidt R,
Rujescu D,
Wang LS,
Dartigues JF,
Mayeux R,
Tzourio C,
Hofman A,
Nöthen MM,
Graff C,
Psaty BM,
Jones L,
Haines JL,
Holmans PA,
Lathrop M,
Pericak-Vance MA,
Launer LJ,
Farrer LA,
van Duijn CM,
Van Broeckhoven C,
Moskvina V,
Seshadri S,
Williams J,
Schellenberg GD,
Amouyel P
European Alzheimer's Disease Initiative (EADI) · Genetic and Environmental Risk in Alzheimer's Disease and 2 more consortia
Nature genetics · 2013 · PMID 24162737
1 page
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Sims R,
van der Lee SJ,
Naj AC,
Bellenguez C,
Badarinarayan N,
Jakobsdottir J,
Kunkle BW,
Boland A,
Raybould R,
Bis JC,
Martin ER,
Grenier-Boley B
and 437 more — show all
Heilmann-Heimbach S,
Chouraki V,
Kuzma AB,
Sleegers K,
Vronskaya M,
Ruiz A,
Graham RR,
Olaso R,
Hoffmann P,
Grove ML,
Vardarajan BN,
Hiltunen M,
Nöthen MM,
White CC,
Hamilton-Nelson KL,
Epelbaum J,
Maier W,
Choi SH,
Beecham GW,
Dulary C,
Herms S,
Smith AV,
Funk CC,
Derbois C,
Forstner AJ,
Ahmad S,
Li H,
Bacq D,
Harold D,
Satizabal CL,
Valladares O,
Squassina A,
Thomas R,
Brody JA,
Qu L,
Sánchez-Juan P,
Morgan T,
Wolters FJ,
Zhao Y,
Garcia FS,
Denning N,
Fornage M,
Malamon J,
Naranjo MCD,
Majounie E,
Mosley TH,
Dombroski B,
Wallon D,
Lupton MK,
Dupuis J,
Whitehead P,
Fratiglioni L,
Medway C,
Jian X,
Mukherjee S,
Keller L,
Brown K,
Lin H,
Cantwell LB,
Panza F,
McGuinness B,
Moreno-Grau S,
Burgess JD,
Solfrizzi V,
Proitsi P,
Adams HH,
Allen M,
Seripa D,
Pastor P,
Cupples LA,
Price ND,
Hannequin D,
Frank-García A,
Levy D,
Chakrabarty P,
Caffarra P,
Giegling I,
Beiser AS,
Giedraitis V,
Hampel H,
Garcia ME,
Wang X,
Lannfelt L,
Mecocci P,
Eiriksdottir G,
Crane PK,
Pasquier F,
Boccardi V,
Henández I,
Barber RC,
Scherer M,
Tarraga L,
Adams PM,
Leber M,
Chen Y,
Albert MS,
Riedel-Heller S,
Emilsson V,
Beekly D,
Braae A,
Schmidt R,
Blacker D,
Masullo C,
Schmidt H,
Doody RS,
Spalletta G,
Longstreth WT Jr,
Fairchild TJ,
Bossù P,
Lopez OL,
Frosch MP,
Sacchinelli E,
Ghetti B,
Yang Q,
Huebinger RM,
Jessen F,
Li S,
Kamboh MI,
Morris J,
Sotolongo-Grau O,
Katz MJ,
Corcoran C,
Dunstan M,
Braddel A,
Thomas C,
Meggy A,
Marshall R,
Gerrish A,
Chapman J,
Aguilar M,
Taylor S,
Hill M,
Fairén MD,
Hodges A,
Vellas B,
Soininen H,
Kloszewska I,
Daniilidou M,
Uphill J,
Patel Y,
Hughes JT,
Lord J,
Turton J,
Hartmann AM,
Cecchetti R,
Fenoglio C,
Serpente M,
Arcaro M,
Caltagirone C,
Orfei MD,
Ciaramella A,
Pichler S,
Mayhaus M,
Gu W,
Lleó A,
Fortea J,
Blesa R,
Barber IS,
Brookes K,
Cupidi C,
Maletta RG,
Carrell D,
Sorbi S,
Moebus S,
Urbano M,
Pilotto A,
Kornhuber J,
Bosco P,
Todd S,
Craig D,
Johnston J,
Gill M,
Lawlor B,
Lynch A,
Fox NC,
Hardy J,
Albin RL,
Apostolova LG,
Arnold SE,
Asthana S,
Atwood CS,
Baldwin CT,
Barnes LL,
Barral S,
Beach TG,
Becker JT,
Bigio EH,
Bird TD,
Boeve BF,
Bowen JD,
Boxer A,
Burke JR,
Burns JM,
Buxbaum JD,
Cairns NJ,
Cao C,
Carlson CS,
Carlsson CM,
Carney RM,
Carrasquillo MM,
Carroll SL,
Diaz CC,
Chui HC,
Clark DG,
Cribbs DH,
Crocco EA,
DeCarli C,
Dick M,
Duara R,
Evans DA,
Faber KM,
Fallon KB,
Fardo DW,
Farlow MR,
Ferris S,
Foroud TM,
Galasko DR,
Gearing M,
Geschwind DH,
Gilbert JR,
Graff-Radford NR,
Green RC,
Growdon JH,
Hamilton RL,
Harrell LE,
Honig LS,
Huentelman MJ,
Hulette CM,
Hyman BT,
Jarvik GP,
Abner E,
Jin LW,
Jun G,
Karydas A,
Kaye JA,
Kim R,
Kowall NW,
Kramer JH,
LaFerla FM,
Lah JJ,
Leverenz JB,
Levey AI,
Li G,
Lieberman AP,
Lunetta KL,
Lyketsos CG,
Marson DC,
Martiniuk F,
Mash DC,
Masliah E,
McCormick WC,
McCurry SM,
McDavid AN,
McKee AC,
Mesulam M,
Miller BL,
Miller CA,
Miller JW,
Morris JC,
Murrell JR,
Myers AJ,
O'Bryant S,
Olichney JM,
Pankratz VS,
Parisi JE,
Paulson HL,
Perry W,
Peskind E,
Pierce A,
Poon WW,
Potter H,
Quinn JF,
Raj A,
Raskind M,
Reisberg B,
Reitz C,
Ringman JM,
Roberson ED,
Rogaeva E,
Rosen HJ,
Rosenberg RN,
Sager MA,
Saykin AJ,
Schneider JA,
Schneider LS,
Seeley WW,
Smith AG,
Sonnen JA,
Spina S,
Stern RA,
Swerdlow RH,
Tanzi RE,
Thornton-Wells TA,
Trojanowski JQ,
Troncoso JC,
Van Deerlin VM,
Van Eldik LJ,
Vinters HV,
Vonsattel JP,
Weintraub S,
Welsh-Bohmer KA,
Wilhelmsen KC,
Williamson J,
Wingo TS,
Woltjer RL,
Wright CB,
Yu CE,
Yu L,
Garzia F,
Golamaully F,
Septier G,
Engelborghs S,
Vandenberghe R,
De Deyn PP,
Fernadez CM,
Benito YA,
Thonberg H,
Forsell C,
Lilius L,
Kinhult-Stählbom A,
Kilander L,
Brundin R,
Concari L,
Helisalmi S,
Koivisto AM,
Haapasalo A,
Dermecourt V,
Fievet N,
Hanon O,
Dufouil C,
Brice A,
Ritchie K,
Dubois B,
Himali JJ,
Keene CD,
Tschanz J,
Fitzpatrick AL,
Kukull WA,
Norton M,
Aspelund T,
Larson EB,
Munger R,
Rotter JI,
Lipton RB,
Bullido MJ,
Hofman A,
Montine TJ,
Coto E,
Boerwinkle E,
Petersen RC,
Alvarez V,
Rivadeneira F,
Reiman EM,
Gallo M,
O'Donnell CJ,
Reisch JS,
Bruni AC,
Royall DR,
Dichgans M,
Sano M,
Galimberti D,
St George-Hyslop P,
Scarpini E,
Tsuang DW,
Mancuso M,
Bonuccelli U,
Winslow AR,
Daniele A,
Wu CK,
Peters O,
Nacmias B,
Riemenschneider M,
Heun R,
Brayne C,
Rubinsztein DC,
Bras J,
Guerreiro R,
Al-Chalabi A,
Shaw CE,
Collinge J,
Mann D,
Tsolaki M,
Clarimón J,
Sussams R,
Lovestone S,
O'Donovan MC,
Owen MJ,
Behrens TW,
Mead S,
Goate AM,
Uitterlinden AG,
Holmes C,
Cruchaga C,
Ingelsson M,
Bennett DA,
Powell J,
Golde TE,
Graff C,
De Jager PL,
Morgan K,
Ertekin-Taner N,
Combarros O,
Psaty BM,
Passmore P,
Younkin SG,
Berr C,
Gudnason V,
Rujescu D,
Dickson DW,
Dartigues JF,
DeStefano AL,
Ortega-Cubero S,
Hakonarson H,
Campion D,
Boada M,
Kauwe JK,
Farrer LA,
Van Broeckhoven C,
Ikram MA,
Jones L,
Haines JL,
Tzourio C,
Launer LJ,
Escott-Price V,
Mayeux R,
Deleuze JF,
Amin N,
Holmans PA,
Pericak-Vance MA,
Amouyel P,
van Duijn CM,
Ramirez A,
Wang LS,
Lambert JC,
Seshadri S,
Williams J,
Schellenberg GD
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels
Sarnowski C,
Ghanbari M,
Bis JC,
Logue M,
Fornage M,
Mishra A,
Ahmad S,
Beiser AS,
Boerwinkle E,
Bouteloup V,
Chouraki V,
Cupples LA
and 24 more — show all
Damotte V,
DeCarli CS,
DeStefano AL,
Djoussé L,
Fohner AE,
Franz CE,
Kautz TF,
Lambert JC,
Lyons MJ,
Mosley TH,
Mukamal KJ,
Pase MP,
Portilla Fernandez EC,
Rissman RA,
Satizabal CL,
Vasan RS,
Yaqub A,
Debette S,
Dufouil C,
Launer LJ,
Kremen WS,
Longstreth WT,
Ikram MA,
Seshadri S
Communications biology · 2022 · PMID 35396452 · 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.