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15 matches for
Ikram MK.
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
He M,
Xu M,
Zhang B,
Liang J,
Chen P,
Lee JY,
Johnson TA,
Li H,
Yang X,
Dai J,
Liang L,
Gui L
and 79 more — show all
Qi Q,
Huang J,
Li Y,
Adair LS,
Aung T,
Cai Q,
Cheng CY,
Cho MC,
Cho YS,
Chu M,
Cui B,
Gao YT,
Go MJ,
Gu D,
Gu W,
Guo H,
Hao Y,
Hong J,
Hu Z,
Hu Y,
Huang J,
Hwang JY,
Ikram MK,
Jin G,
Kang DH,
Khor CC,
Kim BJ,
Kim HT,
Kubo M,
Lee J,
Lee J,
Lee NR,
Li R,
Li J,
Liu J,
Longe J,
Lu W,
Lu X,
Miao X,
Okada Y,
Ong RT,
Qiu G,
Seielstad M,
Sim X,
Song H,
Takeuchi F,
Tanaka T,
Taylor PR,
Wang L,
Wang W,
Wang Y,
Wu C,
Wu Y,
Xiang YB,
Yamamoto K,
Yang H,
Liao M,
Yokota M,
Young T,
Zhang X,
Kato N,
Wang QK,
Zheng W,
Zheng W,
Hu FB,
Lin D,
Shen H,
Teo YY,
Mo Z,
Wong TY,
Lin X,
Mohlke KL,
Ning G,
Tsunoda T,
Han BG,
Shu XO,
Tai ES,
Wu T,
Qi L
Human molecular genetics · 2015 · PMID 25429064
12 pages+
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Davies G,
Lam M,
Harris SE,
Trampush JW,
Luciano M,
Hill WD,
Hagenaars SP,
Ritchie SJ,
Marioni RE,
Fawns-Ritchie C,
Liewald DCM,
Okely JA
and 212 more — show all
Ahola-Olli AV,
Barnes CLK,
Bertram L,
Bis JC,
Burdick KE,
Christoforou A,
DeRosse P,
Djurovic S,
Espeseth T,
Giakoumaki S,
Giddaluru S,
Gustavson DE,
Hayward C,
Hofer E,
Ikram MA,
Karlsson R,
Knowles E,
Lahti J,
Leber M,
Li S,
Mather KA,
Melle I,
Morris D,
Oldmeadow C,
Palviainen T,
Payton A,
Pazoki R,
Petrovic K,
Reynolds CA,
Sargurupremraj M,
Scholz M,
Smith JA,
Smith AV,
Terzikhan N,
Thalamuthu A,
Trompet S,
van der Lee SJ,
Ware EB,
Windham BG,
Wright MJ,
Yang J,
Yu J,
Ames D,
Amin N,
Amouyel P,
Andreassen OA,
Armstrong NJ,
Assareh AA,
Attia JR,
Attix D,
Avramopoulos D,
Bennett DA,
Böhmer AC,
Boyle PA,
Brodaty H,
Campbell H,
Cannon TD,
Cirulli ET,
Congdon E,
Conley ED,
Corley J,
Cox SR,
Dale AM,
Dehghan A,
Dick D,
Dickinson D,
Eriksson JG,
Evangelou E,
Faul JD,
Ford I,
Freimer NA,
Gao H,
Giegling I,
Gillespie NA,
Gordon SD,
Gottesman RF,
Griswold ME,
Gudnason V,
Harris TB,
Hartmann AM,
Hatzimanolis A,
Heiss G,
Holliday EG,
Joshi PK,
Kähönen M,
Kardia SLR,
Karlsson I,
Kleineidam L,
Knopman DS,
Kochan NA,
Konte B,
Kwok JB,
Le Hellard S,
Lee T,
Lehtimäki T,
Li SC,
Lill CM,
Liu T,
Koini M,
London E,
Longstreth WT Jr,
Lopez OL,
Loukola A,
Luck T,
Lundervold AJ,
Lundquist A,
Lyytikäinen LP,
Martin NG,
Montgomery GW,
Murray AD,
Need AC,
Noordam R,
Nyberg L,
Ollier W,
Papenberg G,
Pattie A,
Polasek O,
Poldrack RA,
Psaty BM,
Reppermund S,
Riedel-Heller SG,
Rose RJ,
Rotter JI,
Roussos P,
Rovio SP,
Saba Y,
Sabb FW,
Sachdev PS,
Satizabal CL,
Satizabal CL,
Schmid M,
Scott RJ,
Scult MA,
Simino J,
Slagboom PE,
Smyrnis N,
Soumaré A,
Stefanis NC,
Stott DJ,
Straub RE,
Sundet K,
Taylor AM,
Taylor KD,
Tzoulaki I,
Tzourio C,
Uitterlinden A,
Vitart V,
Voineskos AN,
Kaprio J,
Wagner M,
Wagner H,
Weinhold L,
Wen KH,
Widen E,
Yang Q,
Zhao W,
Adams HHH,
Arking DE,
Bilder RM,
Bitsios P,
Boerwinkle E,
Chiba-Falek O,
Corvin A,
De Jager PL,
Debette S,
Donohoe G,
Elliott P,
Fitzpatrick AL,
Gill M,
Glahn DC,
Hägg S,
Hansell NK,
Hariri AR,
Ikram MK,
Jukema JW,
Jukema JW,
Vuoksimaa E,
Keller MC,
Kremen WS,
Launer L,
Lindenberger U,
Palotie A,
Pedersen NL,
Pendleton N,
Porteous DJ,
Räikkönen K,
Raitakari OT,
Ramirez A,
Reinvang I,
Rudan I,
Dan Rujescu,
Schmidt R,
Schmidt H,
Schofield PW,
Schofield PR,
Starr JM,
Steen VM,
Trollor JN,
Turner ST,
Van Duijn CM,
Villringer A,
Weinberger DR,
Weir DR,
Wilson JF,
Malhotra A,
McIntosh AM,
Gale CR,
Seshadri S,
Mosley TH Jr,
Bressler J,
Lencz T,
Deary IJ
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Fan Q,
Verhoeven VJ,
Wojciechowski R,
Barathi VA,
Hysi PG,
Guggenheim JA,
Höhn R,
Vitart V,
Khawaja AP,
Yamashiro K,
Hosseini SM,
Lehtimäki T
and 142 more — show all
Lu Y,
Haller T,
Xie J,
Delcourt C,
Pirastu M,
Wedenoja J,
Gharahkhani P,
Venturini C,
Miyake M,
Hewitt AW,
Guo X,
Mazur J,
Huffman JE,
Williams KM,
Polasek O,
Campbell H,
Rudan I,
Vatavuk Z,
Wilson JF,
Joshi PK,
McMahon G,
St Pourcain B,
Evans DM,
Simpson CL,
Schwantes-An TH,
Igo RP,
Mirshahi A,
Cougnard-Gregoire A,
Bellenguez C,
Blettner M,
Raitakari O,
Kähönen M,
Seppala I,
Zeller T,
Meitinger T,
Ried JS,
Gieger C,
Portas L,
van Leeuwen EM,
Amin N,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
Vingerling JR,
Wang YX,
Wang X,
Tai-Hui Boh E,
Ikram MK,
Sabanayagam C,
Gupta P,
Tan V,
Zhou L,
Ho CE,
Lim W,
Beuerman RW,
Siantar R,
Tai ES,
Vithana E,
Mihailov E,
Khor CC,
Hayward C,
Luben RN,
Foster PJ,
Klein BE,
Klein R,
Wong HS,
Mitchell P,
Metspalu A,
Aung T,
Young TL,
He M,
Pärssinen O,
van Duijn CM,
Jin Wang J,
Williams C,
Jonas JB,
Teo YY,
Mackey DA,
Oexle K,
Yoshimura N,
Paterson AD,
Pfeiffer N,
Wong TY,
Baird PN,
Stambolian D,
Wilson JE,
Cheng CY,
Hammond CJ,
Klaver CC,
Saw SM,
Rahi JS,
Korobelnik JF,
Kemp JP,
Timpson NJ,
Smith GD,
Craig JE,
Burdon KP,
Fogarty RD,
Iyengar SK,
Chew E,
Janmahasatian S,
Martin NG,
MacGregor S,
Xu L,
Schache M,
Nangia V,
Panda-Jonas S,
Wright AF,
Fondran JR,
Lass JH,
Feng S,
Zhao JH,
Khaw KT,
Wareham NJ,
Rantanen T,
Kaprio J,
Pang CP,
Chen LJ,
Tam PO,
Jhanji V,
Young AL,
Döring A,
Raffel LJ,
Cotch MF,
Li X,
Yip SP,
Yap MK,
Biino G,
Vaccargiu S,
Fossarello M,
Fleck B,
Yazar S,
Tideman JW,
Tedja M,
Deangelis MM,
Morrison M,
Farrer L,
Zhou X,
Chen W,
Mizuki N,
Meguro A,
Mäkelä KM
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
10 pages
Genetic architecture of subcortical brain structures in 38,851 individuals
Satizabal CL,
Adams HHH,
Hibar DP,
White CC,
Knol MJ,
Stein JL,
Scholz M,
Sargurupremraj M,
Jahanshad N,
Roshchupkin GV,
Smith AV,
Bis JC
and 277 more — show all
Jian X,
Luciano M,
Hofer E,
Teumer A,
van der Lee SJ,
Yang J,
Yanek LR,
Lee TV,
Li S,
Hu Y,
Koh JY,
Eicher JD,
Desrivières S,
Arias-Vasquez A,
Chauhan G,
Athanasiu L,
Rentería ME,
Kim S,
Hoehn D,
Armstrong NJ,
Chen Q,
Holmes AJ,
den Braber A,
Kloszewska I,
Andersson M,
Espeseth T,
Grimm O,
Abramovic L,
Alhusaini S,
Milaneschi Y,
Papmeyer M,
Axelsson T,
Ehrlich S,
Roiz-Santiañez R,
Kraemer B,
Håberg AK,
Jones HJ,
Pike GB,
Stein DJ,
Stevens A,
Bralten J,
Vernooij MW,
Harris TB,
Filippi I,
Witte AV,
Guadalupe T,
Wittfeld K,
Mosley TH,
Becker JT,
Doan NT,
Hagenaars SP,
Saba Y,
Cuellar-Partida G,
Amin N,
Hilal S,
Nho K,
Mirza-Schreiber N,
Arfanakis K,
Becker DM,
Ames D,
Goldman AL,
Lee PH,
Boomsma DI,
Lovestone S,
Giddaluru S,
Le Hellard S,
Mattheisen M,
Bohlken MM,
Kasperaviciute D,
Schmaal L,
Lawrie SM,
Agartz I,
Walton E,
Tordesillas-Gutierrez D,
Davies GE,
Shin J,
Ipser JC,
Vinke LN,
Hoogman M,
Jia T,
Burkhardt R,
Klein M,
Crivello F,
Janowitz D,
Carmichael O,
Haukvik UK,
Aribisala BS,
Schmidt H,
Strike LT,
Cheng CY,
Risacher SL,
Pütz B,
Fleischman DA,
Assareh AA,
Mattay VS,
Buckner RL,
Mecocci P,
Dale AM,
Cichon S,
Boks MP,
Matarin M,
Penninx BWJH,
Calhoun VD,
Chakravarty MM,
Marquand AF,
Macare C,
Kharabian Masouleh S,
Oosterlaan J,
Amouyel P,
Hegenscheid K,
Rotter JI,
Schork AJ,
Liewald DCM,
de Zubicaray GI,
Wong TY,
Shen L,
Sämann PG,
Brodaty H,
Roffman JL,
de Geus EJC,
Tsolaki M,
Erk S,
van Eijk KR,
Cavalleri GL,
van der Wee NJA,
McIntosh AM,
Gollub RL,
Bulayeva KB,
Bernard M,
Richards JS,
Himali JJ,
Loeffler M,
Rommelse N,
Hoffmann W,
Westlye LT,
Valdés Hernández MC,
Hansell NK,
van Erp TGM,
Wolf C,
Kwok JBJ,
Vellas B,
Heinz A,
Olde Loohuis LM,
Delanty N,
Ho BC,
Ching CRK,
Shumskaya E,
Singh B,
Hofman A,
van der Meer D,
Homuth G,
Psaty BM,
Bastin ME,
Montgomery GW,
Foroud TM,
Reppermund S,
Hottenga JJ,
Simmons A,
Meyer-Lindenberg A,
Cahn W,
Whelan CD,
van Donkelaar MMJ,
Yang Q,
Hosten N,
Green RC,
Thalamuthu A,
Mohnke S,
Hulshoff Pol HE,
Lin H,
Jack CR Jr,
Schofield PR,
Mühleisen TW,
Maillard P,
Potkin SG,
Wen W,
Fletcher E,
Toga AW,
Gruber O,
Huentelman M,
Davey Smith G,
Launer LJ,
Nyberg L,
Jönsson EG,
Crespo-Facorro B,
Koen N,
Greve DN,
Uitterlinden AG,
Weinberger DR,
Steen VM,
Fedko IO,
Groenewold NA,
Niessen WJ,
Toro R,
Tzourio C,
Longstreth WT Jr,
Ikram MK,
Smoller JW,
van Tol MJ,
Sussmann JE,
Paus T,
Lemaître H,
Schroeter ML,
Mazoyer B,
Andreassen OA,
Holsboer F,
Depondt C,
Veltman DJ,
Turner JA,
Pausova Z,
Schumann G,
van Rooij D,
Djurovic S,
Deary IJ,
McMahon KL,
Müller-Myhsok B,
Brouwer RM,
Soininen H,
Pandolfo M,
Wassink TH,
Cheung JW,
Wolfers T,
Martinot JL,
Zwiers MP,
Nauck M,
Melle I,
Martin NG,
Kanai R,
Westman E,
Kahn RS,
Sisodiya SM,
White T,
Saremi A,
van Bokhoven H,
Brunner HG,
Völzke H,
Wright MJ,
van 't Ent D,
Nöthen MM,
Ophoff RA,
Buitelaar JK,
Fernández G,
Sachdev PS,
Rietschel M,
van Haren NEM,
Fisher SE,
Beiser AS,
Francks C,
Saykin AJ,
Mather KA,
Romanczuk-Seiferth N,
Hartman CA,
DeStefano AL,
Heslenfeld DJ,
Weiner MW,
Walter H,
Hoekstra PJ,
Nyquist PA,
Franke B,
Bennett DA,
Grabe HJ,
Johnson AD,
Chen C,
van Duijn CM,
Lopez OL,
Fornage M,
Wardlaw JM,
Schmidt R,
DeCarli C,
De Jager PL,
Villringer A,
Debette S,
Gudnason V,
Medland SE,
Shulman JM,
Thompson PM,
Seshadri S,
Ikram MA
Nature genetics · 2019 · PMID 31636452
9 pages
A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology
de Vries PS,
Sabater-Lleal M,
Huffman JE,
Marten J,
Song C,
Pankratz N,
Bartz TM,
de Haan HG,
Delgado GE,
Eicher JD,
Martinez-Perez A,
Ward-Caviness CK
and 33 more — show all
Brody JA,
Chen MH,
de Maat MPM,
Frånberg M,
Gill D,
Kleber ME,
Rivadeneira F,
Soria JM,
Tang W,
Tofler GH,
Uitterlinden AG,
van Hylckama Vlieg A,
Seshadri S,
Boerwinkle E,
Davies NM,
Giese AK,
Ikram MK,
Kittner SJ,
McKnight B,
Psaty BM,
Reiner AP,
Sargurupremraj M,
Taylor KD,
Fornage M,
Hamsten A,
März W,
Rosendaal FR,
Souto JC,
Dehghan A,
Johnson AD,
Morrison AC,
O'Donnell CJ,
Smith NL
INVENT Consortium · MEGASTROKE Consortium of the International Stroke Genetics Consortium
Blood · 2019 · PMID 30642921
8 pages
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Verhoeven VJ,
Hysi PG,
Wojciechowski R,
Fan Q,
Guggenheim JA,
Höhn R,
MacGregor S,
Hewitt AW,
Nag A,
Cheng CY,
Yonova-Doing E,
Zhou X
and 96 more — show all
Ikram MK,
Buitendijk GH,
McMahon G,
Kemp JP,
Pourcain BS,
Simpson CL,
Mäkelä KM,
Lehtimäki T,
Kähönen M,
Paterson AD,
Hosseini SM,
Wong HS,
Xu L,
Jonas JB,
Pärssinen O,
Wedenoja J,
Yip SP,
Ho DW,
Pang CP,
Chen LJ,
Burdon KP,
Craig JE,
Klein BE,
Klein R,
Haller T,
Metspalu A,
Khor CC,
Tai ES,
Aung T,
Vithana E,
Tay WT,
Barathi VA,
Chen P,
Li R,
Liao J,
Zheng Y,
Ong RT,
Döring A,
Evans DM,
Timpson NJ,
Verkerk AJ,
Meitinger T,
Raitakari O,
Hawthorne F,
Spector TD,
Karssen LC,
Pirastu M,
Murgia F,
Ang W,
Mishra A,
Montgomery GW,
Pennell CE,
Cumberland PM,
Cotlarciuc I,
Mitchell P,
Wang JJ,
Schache M,
Janmahasatian S,
Igo RP Jr,
Lass JH,
Chew E,
Iyengar SK,
Gorgels TG,
Rudan I,
Hayward C,
Wright AF,
Polasek O,
Vatavuk Z,
Wilson JF,
Fleck B,
Zeller T,
Mirshahi A,
Müller C,
Uitterlinden AG,
Rivadeneira F,
Vingerling JR,
Hofman A,
Oostra BA,
Amin N,
Bergen AA,
Teo YY,
Rahi JS,
Vitart V,
Williams C,
Baird PN,
Wong TY,
Oexle K,
Pfeiffer N,
Mackey DA,
Young TL,
van Duijn CM,
Saw SM,
Bailey-Wilson JE,
Stambolian D,
Klaver CC,
Hammond CJ
Consortium for Refractive Error and Myopia (CREAM) · Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and 2 more consortia
Nature genetics · 2013 · PMID 23396134
6 pages
A genome-wide association study of optic disc parameters
Ramdas WD,
van Koolwijk LM,
Ikram MK,
Jansonius NM,
de Jong PT,
Bergen AA,
Isaacs A,
Amin N,
Aulchenko YS,
Wolfs RC,
Hofman A,
Rivadeneira F
and 8 more — show all
PLoS genetics · 2010 · PMID 20548946 · open access
5 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
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25
Hysi PG,
Young TL,
Mackey DA,
Andrew T,
Fernández-Medarde A,
Solouki AM,
Hewitt AW,
Macgregor S,
Vingerling JR,
Li YJ,
Ikram MK,
Fai LY
and 13 more — show all
Sham PC,
Manyes L,
Porteros A,
Lopes MC,
Carbonaro F,
Fahy SJ,
Martin NG,
van Duijn CM,
Spector TD,
Rahi JS,
Santos E,
Klaver CC,
Hammond CJ
Nature genetics · 2010 · PMID 20835236
2 pages
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14
Solouki AM,
Verhoeven VJ,
van Duijn CM,
Verkerk AJ,
Ikram MK,
Hysi PG,
Despriet DD,
van Koolwijk LM,
Ho L,
Ramdas WD,
Czudowska M,
Kuijpers RW
and 23 more — show all
Amin N,
Struchalin M,
Aulchenko YS,
van Rij G,
Riemslag FC,
Young TL,
Mackey DA,
Spector TD,
Gorgels TG,
Willemse-Assink JJ,
Isaacs A,
Kramer R,
Swagemakers SM,
Bergen AA,
van Oosterhout AA,
Oostra BA,
Rivadeneira F,
Uitterlinden AG,
Hofman A,
de Jong PT,
Hammond CJ,
Vingerling JR,
Klaver CC
Nature genetics · 2010 · PMID 20835239
2 pages
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo
Ikram MK,
Sim X,
Jensen RA,
Cotch MF,
Hewitt AW,
Ikram MA,
Wang JJ,
Klein R,
Klein BE,
Breteler MM,
Cheung N,
Liew G
and 45 more — show all
Mitchell P,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
de Jong PT,
van Duijn CM,
Kao L,
Cheng CY,
Smith AV,
Glazer NL,
Lumley T,
McKnight B,
Psaty BM,
Jonasson F,
Eiriksdottir G,
Aspelund T,
Harris TB,
Launer LJ,
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Xi Q,
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Mackey DA,
Macgregor S,
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Young TL,
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Hammond CJ,
Andrew T,
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Attia J,
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Islam FM,
Rotter JI,
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Wong TY
Global BPgen Consortium
PLoS genetics · 2010 · PMID 21060863 · open access
2 pages
Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism
Fan Q,
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Cheng CY,
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Tay WT,
Li YJ,
Ong RT,
Suo C,
Cornes B,
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and 10 more — show all
PLoS genetics · 2011 · PMID 22144915 · open access
2 pages
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Cheng CY,
Schache M,
Ikram MK,
Young TL,
Guggenheim JA,
Vitart V,
MacGregor S,
Verhoeven VJ,
Barathi VA,
Liao J,
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Bailey-Wilson JE
and 96 more — show all
St Pourcain B,
Kemp JP,
McMahon G,
Timpson NJ,
Evans DM,
Montgomery GW,
Mishra A,
Wang YX,
Wang JJ,
Rochtchina E,
Polasek O,
Wright AF,
Amin N,
van Leeuwen EM,
Wilson JF,
Pennell CE,
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Mackey DA,
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Baird PN
Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group and 2 more consortia
American journal of human genetics · 2013 · PMID 24144296
2 pages
CMPK1 and RBP3 are associated with corneal curvature in Asian populations
Chen P,
Miyake M,
Fan Q,
Liao J,
Yamashiro K,
Ikram MK,
Chew M,
Vithana EN,
Khor CC,
Aung T,
Tai ES,
Wong TY
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Human molecular genetics · 2014 · PMID 24963161
2 pages
Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population
de Haan A,
Ahmadizar F,
van der Most PJ,
Thio CHL,
Kamali Z,
Ani A,
Ghanbari M,
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and 6 more — show all
Frontiers in cardiovascular medicine · 2021 · PMID 35097025 · 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.