For researchers
Is your paper here?
2,662 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
Karalis K.
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes
Akbari P,
Sosina OA,
Bovijn J,
Landheer K,
Nielsen JB,
Kim M,
Aykul S,
De T,
Haas ME,
Hindy G,
Lin N,
Dinsmore IR
and 48 more — show all
Luo JZ,
Hectors S,
Geraghty B,
Germino M,
Panagis L,
Parasoglou P,
Walls JR,
Halasz G,
Atwal GS,
Jones M,
LeBlanc MG,
Still CD,
Carey DJ,
Giontella A,
Orho-Melander M,
Berumen J,
Kuri-Morales P,
Alegre-Díaz J,
Torres JM,
Emberson JR,
Collins R,
Rader DJ,
Zambrowicz B,
Murphy AJ,
Balasubramanian S,
Overton JD,
Reid JG,
Shuldiner AR,
Cantor M,
Abecasis GR,
Ferreira MAR,
Sleeman MW,
Gusarova V,
Altarejos J,
Harris C,
Economides AN,
Idone V,
Karalis K,
Della Gatta G,
Mirshahi T,
Yancopoulos GD,
Melander O,
Marchini J,
Tapia-Conyer R,
Locke AE,
Baras A,
Verweij N,
Lotta LA
Regeneron Genetics Center · DiscovEHR Collaboration
Nature communications · 2022 · PMID 35999217 · open access
2 pages
Genetic risk factors for COVID-19 and influenza are largely distinct
Kosmicki JA,
Marcketta A,
Sharma D,
Di Gioia SA,
Batista S,
Yang XM,
Tzoneva G,
Martinez H,
Sidore C,
Kessler MD,
Horowitz JE,
Roberts GHL
and 43 more — show all
Justice AE,
Banerjee N,
Coignet MV,
Leader JB,
Park DS,
Lanche R,
Maxwell E,
Knight SC,
Bai X,
Guturu H,
Baltzell A,
Girshick AR,
McCurdy SR,
Partha R,
Mansfield AJ,
Turissini DA,
Zhang M,
Mbatchou J,
Watanabe K,
Verma A,
Sirugo G,
Ritchie MD,
Salerno WJ,
Shuldiner AR,
Rader DJ,
Mirshahi T,
Marchini J,
Overton JD,
Carey DJ,
Habegger L,
Reid JG,
Economides A,
Kyratsous C,
Karalis K,
Baum A,
Cantor MN,
Rand KA,
Hong EL,
Ball CA,
Siminovitch K,
Baras A,
Abecasis GR,
Ferreira MAR
Colorado Center for Precision Medicine · Mayo Clinic Project Generation and 2 more consortia
Nature genetics · 2024 · PMID 39103650 · 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.