For researchers
Is your paper here?
2,657 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.
4 matches for
Budoff M.
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Vujkovic M,
Ramdas S,
Lorenz KM,
Guo X,
Darlay R,
Cordell HJ,
He J,
Gindin Y,
Chung C,
Myers RP,
Schneider CV,
Park J
and 78 more — show all
Lee KM,
Serper M,
Carr RM,
Kaplan DE,
Haas ME,
MacLean MT,
Witschey WR,
Zhu X,
Tcheandjieu C,
Kember RL,
Kranzler HR,
Verma A,
Giri A,
Klarin DM,
Sun YV,
Huang J,
Huffman JE,
Creasy KT,
Hand NJ,
Liu CT,
Long MT,
Yao J,
Budoff M,
Tan J,
Li X,
Lin HJ,
Chen YI,
Taylor KD,
Chang RK,
Krauss RM,
Vilarinho S,
Brancale J,
Nielsen JB,
Locke AE,
Jones MB,
Verweij N,
Baras A,
Reddy KR,
Neuschwander-Tetri BA,
Schwimmer JB,
Sanyal AJ,
Chalasani N,
Ryan KA,
Mitchell BD,
Gill D,
Wells AD,
Manduchi E,
Saiman Y,
Mahmud N,
Miller DR,
Reaven PD,
Phillips LS,
Muralidhar S,
DuVall SL,
Lee JS,
Assimes TL,
Pyarajan S,
Cho K,
Edwards TL,
Damrauer SM,
Wilson PW,
Gaziano JM,
O'Donnell CJ,
Khera AV,
Grant SFA,
Brown CD,
Tsao PS,
Saleheen D,
Lotta LA,
Bastarache L,
Anstee QM,
Daly AK,
Meigs JB,
Rotter JI,
Lynch JA,
Rader DJ,
Voight BF,
Chang KM
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study
Manichaikul A,
Hoffman EA,
Smolonska J,
Gao W,
Cho MH,
Baumhauer H,
Budoff M,
Austin JH,
Washko GR,
Carr JJ,
Kaufman JD,
Pottinger T
and 22 more — show all
Powell CA,
Wijmenga C,
Zanen P,
Groen HJ,
Postma DS,
Wanner A,
Rouhani FN,
Brantly ML,
Powell R,
Smith BM,
Rabinowitz D,
Raffel LJ,
Hinckley Stukovsky KD,
Crapo JD,
Beaty TH,
Hokanson JE,
Silverman EK,
Dupuis J,
O'Connor GT,
Boezen HM,
Rich SS,
Barr RG
American journal of respiratory and critical care medicine · 2014 · PMID 24383474
2 pages
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Kavousi M,
Bos MM,
Barnes HJ,
Lino Cardenas CL,
Wong D,
Lu H,
Hodonsky CJ,
Landsmeer LPL,
Turner AW,
Kho M,
Hasbani NR,
de Vries PS
and 77 more — show all
Bowden DW,
Chopade S,
Deelen J,
Benavente ED,
Guo X,
Hofer E,
Hwang SJ,
Lutz SM,
Lyytikäinen LP,
Slenders L,
Smith AV,
Stanislawski MA,
van Setten J,
Wong Q,
Yanek LR,
Becker DM,
Beekman M,
Budoff MJ,
Feitosa MF,
Finan C,
Hilliard AT,
Kardia SLR,
Kovacic JC,
Kral BG,
Langefeld CD,
Launer LJ,
Malik S,
Hoesein FAAM,
Mokry M,
Schmidt R,
Smith JA,
Taylor KD,
Terry JG,
van der Grond J,
van Meurs J,
Vliegenthart R,
Xu J,
Young KA,
Zilhão NR,
Zweiker R,
Assimes TL,
Becker LC,
Bos D,
Carr JJ,
Cupples LA,
de Kleijn DPV,
de Winther M,
den Ruijter HM,
Fornage M,
Freedman BI,
Gudnason V,
Hingorani AD,
Hokanson JE,
Ikram MA,
Išgum I,
Jacobs DR Jr,
Kähönen M,
Lange LA,
Lehtimäki T,
Pasterkamp G,
Raitakari OT,
Schmidt H,
Slagboom PE,
Uitterlinden AG,
Vernooij MW,
Bis JC,
Franceschini N,
Psaty BM,
Post WS,
Rotter JI,
Björkegren JLM,
O'Donnell CJ,
Bielak LF,
Peyser PA,
Malhotra R,
van der Laan SW,
Miller CL
Nature genetics · 2023 · PMID 37770635
2 pages
Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease
Chen Y,
Du X,
Kuppa A,
Feitosa MF,
Bielak LF,
O'Connell JR,
Musani SK,
Guo X,
Kahali B,
Chen VL,
Smith AV,
Ryan KA
and 25 more — show all
Eirksdottir G,
Allison MA,
Bowden DW,
Budoff MJ,
Carr JJ,
Chen YI,
Taylor KD,
Oliveri A,
Correa A,
Crudup BF,
Kardia SLR,
Mosley TH Jr,
Norris JM,
Terry JG,
Rotter JI,
Wagenknecht LE,
Halligan BD,
Young KA,
Hokanson JE,
Washko GR,
Gudnason V,
Province MA,
Peyser PA,
Palmer ND,
Speliotes EK
Nature genetics · 2023 · PMID 37709864
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.