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5 matches for
Linge J.
The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition
van der Meer D,
Gurholt TP,
Sønderby IE,
Shadrin AA,
Hindley G,
Rahman Z,
de Lange AG,
Frei O,
Leinhard OD,
Linge J,
Simon R,
Beck D
and 6 more — show all
Communications biology · 2022 · PMID 36402844 · open access
10 pages
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
Jones E,
Hummerich H,
Viré E,
Uphill J,
Dimitriadis A,
Speedy H,
Campbell T,
Norsworthy P,
Quinn L,
Whitfield J,
Linehan J,
Jaunmuktane Z
and 53 more — show all
Brandner S,
Jat P,
Nihat A,
How Mok T,
Ahmed P,
Collins S,
Stehmann C,
Sarros S,
Kovacs GG,
Geschwind MD,
Golubjatnikov A,
Frontzek K,
Budka H,
Aguzzi A,
Karamujić-Čomić H,
van der Lee SJ,
Ibrahim-Verbaas CA,
van Duijn CM,
Sikorska B,
Golanska E,
Liberski PP,
Calero M,
Calero O,
Sanchez-Juan P,
Salas A,
Martinón-Torres F,
Bouaziz-Amar E,
Haïk S,
Laplanche JL,
Brandel JP,
Amouyel P,
Lambert JC,
Parchi P,
Bartoletti-Stella A,
Capellari S,
Poleggi A,
Ladogana A,
Pocchiari M,
Aneli S,
Matullo G,
Knight R,
Zafar S,
Zerr I,
Booth S,
Coulthart MB,
Jansen GH,
Glisic K,
Blevins J,
Gambetti P,
Safar J,
Appleby B,
Collinge J,
Mead S
The Lancet. Neurology · 2020 · PMID 32949544
2 pages
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study
Mead S,
Poulter M,
Uphill J,
Beck J,
Whitfield J,
Webb TE,
Campbell T,
Adamson G,
Deriziotis P,
Tabrizi SJ,
Hummerich H,
Verzilli C
and 3 more — show all
The Lancet. Neurology · 2009 · PMID 19081515 · open access
1 page
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
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.