For researchers
Is your paper here?
2,663 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.
5 matches for
Saut N.
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Thibord F,
Klarin D,
Brody JA,
Chen MH,
Levin MG,
Chasman DI,
Goode EL,
Hveem K,
Teder-Laving M,
Martinez-Perez A,
Aïssi D,
Daian-Bacq D
and 76 more — show all
Ito K,
Natarajan P,
Lutsey PL,
Nadkarni GN,
de Vries PS,
Cuellar-Partida G,
Wolford BN,
Pattee JW,
Kooperberg C,
Braekkan SK,
Li-Gao R,
Saut N,
Sept C,
Germain M,
Judy RL,
Wiggins KL,
Ko D,
O'Donnell CJ,
Taylor KD,
Giulianini F,
De Andrade M,
Nøst TH,
Boland A,
Empana JP,
Koyama S,
Gilliland T,
Do R,
Huffman JE,
Wang X,
Wang X,
Zhou W,
Manuel Soria J,
Carlos Souto J,
Pankratz N,
Haessler J,
Hindberg K,
Rosendaal FR,
Turman C,
Olaso R,
Kember RL,
Bartz TM,
Lynch JA,
Heckbert SR,
Armasu SM,
Brumpton B,
Smadja DM,
Jouven X,
Komuro I,
Clapham KR,
Loos RJF,
Willer CJ,
Sabater-Lleal M,
Pankow JS,
Reiner AP,
Morelli VM,
Ridker PM,
Vlieg AVH,
Deleuze JF,
Kraft P,
Rader DJ,
Min Lee K,
Psaty BM,
Heidi Skogholt A,
Emmerich J,
Suchon P,
Rich SS,
Vy HMT,
Tang W,
Jackson RD,
Hansen JB,
Morange PE,
Kabrhel C,
Trégouët DA,
Damrauer SM,
Johnson AD,
Smith NL
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
Molecular determinants of thrombosis recurrence risk across venous thromboembolism subtypes
Munsch G,
Thibord F,
Bezerra OC,
Brody JA,
van Hylckama Vlieg A,
Gourhant L,
Chen MH,
Samaria F,
Germain M,
Caro I,
Suchon P,
Olaso R
and 22 more — show all
Wiggins KL,
Saut N,
Besse C,
Goumidi L,
Bacq D,
Harrington LB,
Boland A,
Emmerich J,
Smadja DM,
Lemarié CA,
Danckwardt S,
Debette S,
Deleuze JF,
Jacqmin-Gadda H,
Rodger MA,
Gagnon F,
Rosendaal FR,
Johnson AD,
Smith NL,
Couturaud F,
Morange PE,
Trégouët DA
Blood · 2025 · PMID 40811855
4 pages
Genetics of venous thrombosis: insights from a new genome wide association study
Germain M,
Saut N,
Greliche N,
Dina C,
Lambert JC,
Perret C,
Cohen W,
Oudot-Mellakh T,
Antoni G,
Alessi MC,
Zelenika D,
Cambien F
and 9 more — show all
PloS one · 2011 · PMID 21980494 · open access
2 pages
A meta-analysis of genome-wide association studies identifies ORM1 as a novel gene controlling thrombin generation potential
Rocanin-Arjo A,
Cohen W,
Carcaillon L,
Frère C,
Saut N,
Letenneur L,
Alhenc-Gelas M,
Dupuy AM,
Bertrand M,
Alessi MC,
Germain M,
Wild PS
and 7 more — show all
CardioGenics Consortium
Blood · 2014 · PMID 24357727
2 pages
C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies
Buil A,
Trégouët DA,
Souto JC,
Saut N,
Germain M,
Rotival M,
Tiret L,
Cambien F,
Lathrop M,
Zeller T,
Alessi MC,
Rodriguez de Cordoba S
and 9 more — show all
Blood · 2010 · PMID 20212171
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.