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2,665 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.
2 matches for
Adams L.
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Henry A,
Mo X,
Finan C,
Chaffin MD,
Speed D,
Issa H,
Denaxas S,
Ware JS,
Zheng SL,
Malarstig A,
Gratton J,
Bond I
and 169 more — show all
Roselli C,
Miller D,
Chopade S,
Schmidt AF,
Abner E,
Adams L,
Andersson C,
Aragam KG,
Ärnlöv J,
Asselin G,
Raja AA,
Backman JD,
Bartz TM,
Biddinger KJ,
Biggs ML,
Bloom HL,
Boersma E,
Brandimarto J,
Brown MR,
Brunak S,
Bruun MT,
Buckbinder L,
Bundgaard H,
Carey DJ,
Chasman DI,
Chen X,
Cook JP,
Czuba T,
de Denus S,
Dehghan A,
Delgado GE,
Doney AS,
Dörr M,
Dowsett J,
Dudley SC,
Engström G,
Erikstrup C,
Esko T,
Farber-Eger EH,
Felix SB,
Finer S,
Ford I,
Ghanbari M,
Ghasemi S,
Ghouse J,
Giedraitis V,
Giulianini F,
Gottdiener JS,
Gross S,
Guðbjartsson DF,
Gui H,
Gutmann R,
Hägg S,
Haggerty CM,
Hedman ÅK,
Helgadottir A,
Hemingway H,
Hillege H,
Hyde CL,
Aagaard Jensen B,
Jukema JW,
Kardys I,
Karra R,
Kavousi M,
Kizer JR,
Kleber ME,
Køber L,
Koekemoer A,
Kuchenbaecker K,
Lai YP,
Lanfear D,
Langenberg C,
Lin H,
Lind L,
Lindgren CM,
Liu PP,
London B,
Lowery BD,
Luan J,
Lubitz SA,
Magnusson P,
Margulies KB,
Marston NA,
Martin H,
März W,
Melander O,
Mordi IR,
Morley MP,
Morris AP,
Morrison AC,
Morton L,
Nagle MW,
Nelson CP,
Niessner A,
Niiranen T,
Noordam R,
Nowak C,
O'Donoghue ML,
Ostrowski SR,
Owens AT,
Palmer CNA,
Paré G,
Pedersen OB,
Perola M,
Pigeyre M,
Psaty BM,
Rice KM,
Ridker PM,
Romaine SPR,
Rotter JI,
Ruff CT,
Sabatine MS,
Sallah N,
Salomaa V,
Sattar N,
Shalaby AA,
Shekhar A,
Smelser DT,
Smith NL,
Sørensen E,
Srinivasan S,
Stefansson K,
Sveinbjörnsson G,
Svensson P,
Tammesoo ML,
Tardif JC,
Teder-Laving M,
Teumer A,
Thorgeirsson G,
Thorsteinsdottir U,
Torp-Pedersen C,
Tragante V,
Trompet S,
Uitterlinden AG,
Ullum H,
van der Harst P,
van Heel D,
van Setten J,
van Vugt M,
Veluchamy A,
Verschuuren M,
Verweij N,
Vissing CR,
Völker U,
Voors AA,
Wallentin L,
Wang Y,
Weeke PE,
Wiggins KL,
Williams LK,
Yang Y,
Yu B,
Zannad F,
Zheng C,
Asselbergs FW,
Cappola TP,
Dubé MP,
Dunn ME,
Lang CC,
Samani NJ,
Shah S,
Vasan RS,
Smith JG,
Holm H,
Shah S,
Ellinor PT,
Hingorani AD,
Wells Q,
Lumbers RT
Genes & Health Research Team · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2025 · PMID 40038546 · open access
12 pages+
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Rajabli F,
Benchek P,
Tosto G,
Kushch N,
Sha J,
Bazemore K,
Zhu C,
Lee WP,
Haut J,
Hamilton-Nelson KL,
Wheeler NR,
Zhao Y
and 274 more — show all
Farrell JJ,
Grunin MA,
Leung YY,
Kuksa PP,
Li D,
da Fonseca EL,
Mez JB,
Palmer EL,
Pillai J,
Sherva RM,
Song YE,
Zhang X,
Ikeuchi T,
Iqbal T,
Pathak O,
Valladares O,
Reyes-Dumeyer D,
Kuzma AB,
Abner E,
Adams LD,
Adams PM,
Aguirre A,
Albert MS,
Albin RL,
Allen M,
Alvarez L,
Apostolova LG,
Arnold SE,
Asthana S,
Atwood CS,
Auerbach S,
Ayres G,
Baldwin CT,
Barber RC,
Barnes LL,
Barral S,
Beach TG,
Becker JT,
Beecham GW,
Beekly D,
Benitez BA,
Bennett D,
Bertelson J,
Bird TD,
Blacker D,
Boeve BF,
Bowen JD,
Boxer A,
Brewer J,
Burke JR,
Burns JM,
Buxbaum JD,
Cairns NJ,
Cantwell LB,
Cao C,
Carlson CS,
Carlsson CM,
Carney RM,
Carrasquillo MM,
Chasse S,
Chesselet MF,
Chin NA,
Chui HC,
Chung J,
Craft S,
Crane PK,
Cribbs DH,
Crocco EA,
Cruchaga C,
Cuccaro ML,
Cullum M,
Darby E,
Davis B,
De Jager PL,
DeCarli C,
DeToledo J,
Dick M,
Dickson DW,
Dombroski BA,
Doody RS,
Duara R,
Ertekin-Taner N,
Evans DA,
Faber KM,
Fairchild TJ,
Fallon KB,
Fardo DW,
Farlow MR,
Fernandez-Hernandez V,
Ferris S,
Friedland RP,
Foroud TM,
Frosch MP,
Fulton-Howard B,
Galasko DR,
Gamboa A,
Gearing M,
Geschwind DH,
Ghetti B,
Gilbert JR,
Go RCP,
Goate AM,
Grabowski TJ,
Graff-Radford NR,
Green RC,
Growdon JH,
Hakonarson H,
Hall J,
Hamilton RL,
Harari O,
Hardy J,
Harrell LE,
Head E,
Henderson VW,
Hernandez M,
Hohman T,
Honig LS,
Huebinger RM,
Huentelman MJ,
Hulette CM,
Hyman BT,
Hynan LS,
Ibanez L,
Jarvik GP,
Jayadev S,
Jin LW,
Johnson K,
Johnson L,
Kamboh MI,
Karydas AM,
Katz MJ,
Kauwe JS,
Kaye JA,
Keene CD,
Khaleeq A,
Kikuchi M,
Kim R,
Knebl J,
Kowall NW,
Kramer JH,
Kukull WA,
LaFerla FM,
Lah JJ,
Larson EB,
Lerner A,
Leverenz JB,
Levey AI,
Lieberman AP,
Lipton RB,
Logue M,
Lopez OL,
Lunetta KL,
Lyketsos CG,
Mains D,
Margaret FE,
Marson DC,
Martin ER,
Martiniuk F,
Mash DC,
Masliah E,
Massman P,
Masurkar A,
McCormick WC,
McCurry SM,
McDavid AN,
McDonough S,
McKee AC,
Mesulam M,
Miller BL,
Miller CA,
Miller JW,
Montine TJ,
Monuki ES,
Morris JC,
Mukherjee S,
Myers AJ,
Nguyen T,
Obisesan T,
O'Bryant S,
Olichney JM,
Ory M,
Palmer R,
Parisi JE,
Paulson HL,
Pavlik V,
Paydarfar D,
Perez V,
Peskind E,
Petersen RC,
Petrovitch H,
Pierce A,
Polk M,
Poon WW,
Potter H,
Qu L,
Quiceno M,
Quinn JF,
Raj A,
Raskind M,
Reiman EM,
Reisberg B,
Reisch JS,
Ringman JM,
Roberson ED,
Rodriguear M,
Rogaeva E,
Rosen HJ,
Rosenberg RN,
Royall DR,
Sabbagh M,
Sadovnick AD,
Sager MA,
Sano M,
Saykin AJ,
Schneider JA,
Schneider LS,
Seeley WW,
Slifer SH,
Small S,
Smith AG,
Smith JP,
Sonnen JA,
Spina S,
George-Hyslop PS,
Starks TD,
Stern RA,
Stevens AB,
Strittmatter SM,
Sultzer D,
Swerdlow RH,
Tanzi RE,
Tilson JL,
Trojanowski JQ,
Troncoso JC,
Tsolaki M,
Tsuang DW,
Van Deerlin VM,
van Eldik LJ,
Vance JM,
Vardarajan BN,
Vassar R,
Vinters HV,
Vonsattel JP,
Weintraub S,
Welsh-Bohmer KA,
Whitehead PL,
Wijsman EM,
Wilhelmsen KC,
Williams B,
Williamson J,
Wilms H,
Wingo TS,
Wisniewski T,
Woltjer RL,
Woon M,
Wright CB,
Wu CK,
Younkin SG,
Yu CE,
Yu L,
Zhu X,
Kunkle BW,
Bush WS,
Miyashita A,
Byrd GS,
Wang LS,
Farrer LA,
Haines JL,
Mayeux R,
Pericak-Vance MA,
Schellenberg GD,
Jun GR,
Reitz C,
Naj AC
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
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.