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.
8 matches for
Sekula P.
Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms
Li Y,
Sekula P,
Wuttke M,
Wahrheit J,
Hausknecht B,
Schultheiss UT,
Gronwald W,
Schlosser P,
Tucci S,
Ekici AB,
Spiekerkoetter U,
Kronenberg F
and 3 more — show all
GCKD Investigators
Journal of the American Society of Nephrology : JASN · 2018 · PMID 29545352
12 pages+
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans
Schlosser P,
Li Y,
Sekula P,
Raffler J,
Grundner-Culemann F,
Pietzner M,
Cheng Y,
Wuttke M,
Steinbrenner I,
Schultheiss UT,
Kotsis F,
Kacprowski T
and 14 more — show all
Forer L,
Hausknecht B,
Ekici AB,
Nauck M,
Völker U,
Walz G,
Oefner PJ,
Kronenberg F,
Mohney RP,
Köttgen M,
Suhre K,
Eckardt KU,
Kastenmüller G,
Köttgen A
GCKD Investigators
Nature genetics · 2020 · PMID 31959995
12 pages+
Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine
Schlosser P,
Scherer N,
Grundner-Culemann F,
Monteiro-Martins S,
Haug S,
Steinbrenner I,
Uluvar B,
Wuttke M,
Cheng Y,
Ekici AB,
Gyimesi G,
Karoly ED
and 20 more — show all
Kotsis F,
Mielke J,
Gomez MF,
Yu B,
Grams ME,
Coresh J,
Boerwinkle E,
Köttgen M,
Kronenberg F,
Meiselbach H,
Mohney RP,
Akilesh S,
Schmidts M,
Hediger MA,
Schultheiss UT,
Eckardt KU,
Oefner PJ,
Sekula P,
Li Y,
Köttgen A
GCKD Investigators
Nature genetics · 2023 · PMID 37277652 · open access
12 pages+
Genetic screens of imaging-derived kidney volumes identify genes linked to kidney function
Monteiro-Martins S,
Li Y,
Borisov O,
Khan A,
Reichardt W,
Haug S,
Kellner E,
Buechert M,
Ott E,
Russe MF,
Bamberg F,
Kiryluk K
and 3 more — show all
Kidney international · 2026 · PMID 41077127 · open access
12 pages+
Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases
Li Y,
Cheng Y,
Consolato F,
Schiano G,
Chong MR,
Pietzner M,
Nguyen NQH,
Scherer N,
Biggs ML,
Kleber ME,
Haug S,
Göçmen B
and 31 more — show all
Pigeyre M,
Sekula P,
Steinbrenner I,
Schlosser P,
Joseph CB,
Brody JA,
Grams ME,
Hayward C,
Schultheiss UT,
Krämer BK,
Kronenberg F,
Peters A,
Seissler J,
Steubl D,
Then C,
Wuttke M,
März W,
Eckardt KU,
Gieger C,
Boerwinkle E,
Psaty BM,
Coresh J,
Oefner PJ,
Pare G,
Langenberg C,
Scherberich JE,
Yu B,
Akilesh S,
Devuyst O,
Rampoldi L,
Köttgen A
JCI insight · 2022 · PMID 35446786 · open access
4 pages
Genetics of osteopontin in patients with chronic kidney disease: The German Chronic Kidney Disease study
Cheng Y,
Li Y,
Scherer N,
Grundner-Culemann F,
Lehtimäki T,
Mishra BH,
Raitakari OT,
Nauck M,
Eckardt KU,
Sekula P,
Schultheiss UT
GCKD investigators
PLoS genetics · 2022 · PMID 35385482 · open access
1 page
Meta-GWAS on PCSK9 concentrations reveals associations of novel loci outside the PCSK9 locus in White populations
Kheirkhah A,
Schachtl-Riess JF,
Lamina C,
Di Maio S,
Koller A,
Schönherr S,
Coassin S,
Forer L,
Sekula P,
Gieger C,
Peters A,
Köttgen A
and 2 more — show all
Atherosclerosis · 2023 · PMID 37989062
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.