For researchers
Is your paper here?
2,645 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
Kripke CM.
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Verma A,
Huffman JE,
Rodriguez A,
Conery M,
Liu M,
Ho YL,
Kim Y,
Heise DA,
Guare L,
Panickan VA,
Garcon H,
Linares F
and 59 more — show all
Costa L,
Goethert I,
Tipton R,
Honerlaw J,
Davies L,
Whitbourne S,
Cohen J,
Posner DC,
Sangar R,
Murray M,
Wang X,
Dochtermann DR,
Devineni P,
Shi Y,
Nandi TN,
Assimes TL,
Brunette CA,
Carroll RJ,
Clifford R,
Duvall S,
Gelernter J,
Hung A,
Iyengar SK,
Joseph J,
Kember R,
Kranzler H,
Kripke CM,
Levey D,
Luoh SW,
Merritt VC,
Overstreet C,
Deak JD,
Grant SFA,
Polimanti R,
Roussos P,
Shakt G,
Sun YV,
Tsao N,
Venkatesh S,
Voloudakis G,
Justice A,
Begoli E,
Ramoni R,
Tourassi G,
Pyarajan S,
Tsao P,
O'Donnell CJ,
Muralidhar S,
Moser J,
Casas JP,
Bick AG,
Zhou W,
Cai T,
Voight BF,
Cho K,
Gaziano JM,
Madduri RK,
Damrauer S,
Liao KP
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
12 pages+
Cross-definition GWAS of IBS in 2.8 million individuals reveals cardiometabolic and triglyceride-linked mechanisms
Di Lorenzo B,
Camargo Tavares L,
Díaz-Muñoz C,
Heredia-Fernández F,
Bozzarelli I,
Esteban Blanco C,
Wang Z,
Smit RAJ,
Loos RJF,
Hirbo J,
Cox NJ,
Straub P
and 57 more — show all
Favé MJ,
Awadalla P,
Pozdeyev N,
Gignoux CR,
Gudbjartsson DF,
Thorleifsson G,
Jonsdottir I,
Stefansson K,
Abner E,
Palta P,
Williams AT,
Coley K,
Sze G,
John C,
Richmond A,
McCartney D,
Hayward C,
Mulford AJ,
Sanders AR,
Peculis R,
Rovite V,
Dombrovska MS,
Capasso M,
Lo Faro V,
Sinha T,
Lopera Maya EA,
Zhernakova A,
Wang Y,
Martin A,
Vanderwerff B,
Zöllner S,
Ferolito BR,
Pereira AC,
Gaziano JM,
Cho K,
Caruth L,
Guare L,
Kripke CM,
Rader DJ,
Verma SS,
Verma A,
Saad C,
Mbarek H,
Chao PY,
Chen TT,
Lin YF,
Feng YA,
Challa PK,
Khalili H,
Andries A,
Ness-Jensen E,
Brumpton BM,
Grover M,
Lemmelä S,
Sanna S,
Bonfiglio F,
D'Amato M
Colorado Center for Personalized Medicine · Estonian Biobank Research Team and 3 more consortia
Gut · 2026 · PMID 42425734
3 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.