For researchers
Is your paper here?
2,661 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.
9 matches for
Raffler J.
Human metabolic individuality in biomedical and pharmaceutical research
Suhre K,
Shin SY,
Petersen AK,
Mohney RP,
Meredith D,
Wägele B,
Altmaier E,
Deloukas P,
Erdmann J,
Grundberg E,
Hammond CJ,
de Angelis MH
and 21 more — show all
Kastenmüller G,
Köttgen A,
Kronenberg F,
Mangino M,
Meisinger C,
Meitinger T,
Mewes HW,
Milburn MV,
Prehn C,
Raffler J,
Ried JS,
Römisch-Margl W,
Samani NJ,
Small KS,
Wichmann HE,
Zhai G,
Illig T,
Spector TD,
Adamski J,
Soranzo N,
Gieger C
CARDIoGRAM
Nature · 2011 · PMID 21886157
12 pages+
Connecting genetic risk to disease end points through the human blood plasma proteome
Suhre K,
Arnold M,
Bhagwat AM,
Cotton RJ,
Engelke R,
Raffler J,
Sarwath H,
Thareja G,
Wahl A,
DeLisle RK,
Gold L,
Pezer M
and 12 more — show all
Lauc G,
El-Din Selim MA,
Mook-Kanamori DO,
Al-Dous EK,
Mohamoud YA,
Malek J,
Strauch K,
Grallert H,
Peters A,
Kastenmüller G,
Gieger C,
Graumann J
Nature communications · 2017 · PMID 28240269 · open access
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+
A cross-platform approach identifies genetic regulators of human metabolism and health
Lotta LA,
Pietzner M,
Stewart ID,
Wittemans LBL,
Li C,
Bonelli R,
Raffler J,
Biggs EK,
Oliver-Williams C,
Auyeung VPW,
Luan J,
Wheeler E
and 22 more — show all
Paige E,
Surendran P,
Michelotti GA,
Scott RA,
Burgess S,
Zuber V,
Sanderson E,
Koulman A,
Imamura F,
Forouhi NG,
Khaw KT,
Griffin JL,
Wood AM,
Kastenmüller G,
Danesh J,
Butterworth AS,
Gribble FM,
Reimann F,
Bahlo M,
Fauman E,
Wareham NJ,
Langenberg C
MacTel Consortium
Nature genetics · 2021 · PMID 33414548
12 pages+
Mapping the proteo-genomic convergence of human diseases
Pietzner M,
Wheeler E,
Carrasco-Zanini J,
Cortes A,
Koprulu M,
Wörheide MA,
Oerton E,
Cook J,
Stewart ID,
Kerrison ND,
Luan J,
Raffler J
and 9 more — show all
Science (New York, N.Y.) · 2021 · PMID 34648354
12 pages+
Rare and common genetic determinants of metabolic individuality and their effects on human health
Surendran P,
Stewart ID,
Au Yeung VPW,
Pietzner M,
Raffler J,
Wörheide MA,
Li C,
Smith RF,
Wittemans LBL,
Bomba L,
Menni C,
Zierer J
and 24 more — show all
Rossi N,
Sheridan PA,
Watkins NA,
Mangino M,
Hysi PG,
Di Angelantonio E,
Falchi M,
Spector TD,
Soranzo N,
Michelotti GA,
Arlt W,
Lotta LA,
Denaxas S,
Hemingway H,
Gamazon ER,
Howson JMM,
Wood AM,
Danesh J,
Wareham NJ,
Kastenmüller G,
Fauman EB,
Suhre K,
Butterworth AS,
Langenberg C
Nature medicine · 2022 · PMID 36357675 · open access
12 pages+
Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality
Raffler J,
Friedrich N,
Arnold M,
Kacprowski T,
Rueedi R,
Altmaier E,
Bergmann S,
Budde K,
Gieger C,
Homuth G,
Pietzner M,
Römisch-Margl W
and 8 more — show all
PLoS genetics · 2015 · PMID 26352407 · open access
5 pages
A genome-wide association study of metabolic traits in human urine
Suhre K,
Wallaschofski H,
Raffler J,
Friedrich N,
Haring R,
Michael K,
Wasner C,
Krebs A,
Kronenberg F,
Chang D,
Meisinger C,
Wichmann HE
and 12 more — show all
Hoffmann W,
Völzke H,
Völker U,
Teumer A,
Biffar R,
Kocher T,
Felix SB,
Illig T,
Kroemer HK,
Gieger C,
Römisch-Margl W,
Nauck M
Nature genetics · 2011 · PMID 21572414
3 pages
Genome-wide scan identifies novel genetic loci regulating salivary metabolite levels
Nag A,
Kurushima Y,
Bowyer RCE,
Wells PM,
Weiss S,
Pietzner M,
Kocher T,
Raffler J,
Völker U,
Mangino M,
Spector TD,
Milburn MV
and 5 more — show all
Human molecular genetics · 2020 · PMID 31960908 · 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.