For researchers
Is your paper here?
2,673 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.
6 matches for
Djousse L.
Genomics and phenomics of body mass index reveals a complex disease network
Huang J,
Huffman JE,
Huang Y,
Do Valle Í,
Assimes TL,
Raghavan S,
Voight BF,
Liu C,
Barabási AL,
Huang RDL,
Hui Q,
Nguyen XT
and 26 more — show all
Ho YL,
Djousse L,
Lynch JA,
Vujkovic M,
Tcheandjieu C,
Tang H,
Damrauer SM,
Reaven PD,
Miller D,
Phillips LS,
Ng MCY,
Graff M,
Haiman CA,
Loos RJF,
North KE,
Yengo L,
Smith GD,
Saleheen D,
Gaziano JM,
Rader DJ,
Tsao PS,
Cho K,
Chang KM,
Wilson PWF,
Sun YV,
O'Donnell CJ
VA Million Veteran Program
Nature communications · 2022 · PMID 36581621 · open access
12 pages+
Novel loci and biomedical consequences of iron homoeostasis variation
Allara E,
Bell S,
Smith R,
Keene SJ,
Gill D,
Gaziano L,
Morselli Gysi D,
Wang F,
Tragante V,
Mason A,
Karthikeyan S,
Lumbers RT
and 60 more — show all
Bonglack E,
Ouwehand W,
Roberts DJ,
Dowsett J,
Ostrowski SR,
Larsen MH,
Ullum H,
Pedersen OB,
Brunak S,
Banasik K,
Erikstrup C,
Mitchell J,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Girelli D,
Arvas M,
Toivonen J,
Molnos S,
Peters A,
Polasek O,
Rudan I,
Hayward C,
McDonnell C,
Pirastu N,
Wilson JF,
van den Hurk K,
Quee F,
Ferrucci L,
Bandinelli S,
Tanaka T,
Girotto G,
Concas MP,
Pecori A,
Verweij N,
van der Harst P,
van de Vegte YJ,
Kiemeney LA,
Sweep FC,
Galesloot TE,
Sulem P,
Gudbjartsson D,
Ferkingstad E,
Djousse L,
Cho K,
Inouye M,
Burgess S,
Benyamin B,
Oexle K,
Swinkels D,
Stefansson K,
Magnusson M,
Ganna A,
Gaziano M,
Ivey K,
Danesh J,
Pereira A,
Wood AM,
Butterworth AS,
Di Angelantonio E
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
12 pages+
Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium
Guan W,
Steffen BT,
Lemaitre RN,
Wu JHY,
Tanaka T,
Manichaikul A,
Foy M,
Rich SS,
Wang L,
Nettleton JA,
Tang W,
Gu X
and 12 more — show all
Bandinelli S,
King IB,
McKnight B,
Psaty BM,
Siscovick D,
Djousse L,
Chen YI,
Ferrucci L,
Fornage M,
Mozafarrian D,
Tsai MY,
Steffen LM
Circulation. Cardiovascular genetics · 2014 · PMID 24823311
5 pages
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium
Lemaitre RN,
Tanaka T,
Tang W,
Manichaikul A,
Foy M,
Kabagambe EK,
Nettleton JA,
King IB,
Weng LC,
Bhattacharya S,
Bandinelli S,
Bis JC
and 23 more — show all
Rich SS,
Jacobs DR Jr,
Cherubini A,
McKnight B,
Liang S,
Gu X,
Rice K,
Laurie CC,
Lumley T,
Browning BL,
Psaty BM,
Chen YD,
Friedlander Y,
Djousse L,
Wu JH,
Siscovick DS,
Uitterlinden AG,
Arnett DK,
Ferrucci L,
Fornage M,
Tsai MY,
Mozaffarian D,
Steffen LM
PLoS genetics · 2011 · PMID 21829377 · open access
2 pages
Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium
Wu JH,
Lemaitre RN,
Manichaikul A,
Guan W,
Tanaka T,
Foy M,
Kabagambe EK,
Djousse L,
Siscovick D,
Fretts AM,
Johnson C,
King IB
and 16 more — show all
Psaty BM,
McKnight B,
Rich SS,
Chen YD,
Nettleton JA,
Tang W,
Bandinelli S,
Jacobs DR Jr,
Browning BL,
Laurie CC,
Gu X,
Tsai MY,
Steffen LM,
Ferrucci L,
Fornage M,
Mozaffarian D
Circulation. Cardiovascular genetics · 2013 · PMID 23362303
2 pages
Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program
Huang RDL,
Nguyen XT,
Peloso GM,
Trinder M,
Posner DC,
Aragam KG,
Ho YL,
Lynch JA,
Damrauer SM,
Chang KM,
Tsao PS,
Natarajan P
and 7 more — show all
Veterans Affairs’ Million Veteran Program
PloS one · 2022 · PMID 35613103 · 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.