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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.
5 matches for
Song J.
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
Sabater-Lleal M,
Huang J,
Chasman D,
Naitza S,
Dehghan A,
Johnson AD,
Teumer A,
Reiner AP,
Folkersen L,
Basu S,
Rudnicka AR,
Trompet S
and 133 more — show all
Mälarstig A,
Baumert J,
Bis JC,
Guo X,
Hottenga JJ,
Shin SY,
Lopez LM,
Lahti J,
Tanaka T,
Yanek LR,
Oudot-Mellakh T,
Wilson JF,
Navarro P,
Huffman JE,
Zemunik T,
Redline S,
Mehra R,
Pulanic D,
Rudan I,
Wright AF,
Kolcic I,
Polasek O,
Wild SH,
Campbell H,
Curb JD,
Wallace R,
Liu S,
Eaton CB,
Becker DM,
Becker LC,
Bandinelli S,
Räikkönen K,
Widen E,
Palotie A,
Fornage M,
Green D,
Gross M,
Davies G,
Harris SE,
Liewald DC,
Starr JM,
Williams FM,
Grant PJ,
Spector TD,
Strawbridge RJ,
Silveira A,
Sennblad B,
Rivadeneira F,
Uitterlinden AG,
Franco OH,
Hofman A,
van Dongen J,
Willemsen G,
Boomsma DI,
Yao J,
Swords Jenny N,
Haritunians T,
McKnight B,
Lumley T,
Taylor KD,
Rotter JI,
Psaty BM,
Peters A,
Gieger C,
Illig T,
Grotevendt A,
Homuth G,
Völzke H,
Kocher T,
Goel A,
Franzosi MG,
Seedorf U,
Clarke R,
Steri M,
Tarasov KV,
Sanna S,
Schlessinger D,
Stott DJ,
Sattar N,
Buckley BM,
Rumley A,
Lowe GD,
McArdle WL,
Chen MH,
Tofler GH,
Song J,
Boerwinkle E,
Folsom AR,
Rose LM,
Franco-Cereceda A,
Teichert M,
Ikram MA,
Mosley TH,
Bevan S,
Dichgans M,
Rothwell PM,
Sudlow CL,
Hopewell JC,
Chambers JC,
Saleheen D,
Kooner JS,
Danesh J,
Nelson CP,
Erdmann J,
Reilly MP,
Kathiresan S,
Schunkert H,
Morange PE,
Ferrucci L,
Eriksson JG,
Jacobs D,
Deary IJ,
Soranzo N,
Witteman JC,
de Geus EJ,
Tracy RP,
Hayward C,
Koenig W,
Cucca F,
Jukema JW,
Eriksson P,
Seshadri S,
Markus HS,
Watkins H,
Samani NJ,
Wallaschofski H,
Smith NL,
Tregouet D,
Ridker PM,
Tang W,
Strachan DP,
Hamsten A,
O'Donnell CJ
VTE Consortium · STROKE Consortium and 3 more consortia
Circulation · 2013 · PMID 23969696
9 pages
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder
Hou L,
Bergen SE,
Akula N,
Song J,
Hultman CM,
Landén M,
Adli M,
Alda M,
Ardau R,
Arias B,
Aubry JM,
Backlund L
and 127 more — show all
Badner JA,
Barrett TB,
Bauer M,
Baune BT,
Bellivier F,
Benabarre A,
Bengesser S,
Berrettini WH,
Bhattacharjee AK,
Biernacka JM,
Birner A,
Bloss CS,
Brichant-Petitjean C,
Bui ET,
Byerley W,
Cervantes P,
Chillotti C,
Cichon S,
Colom F,
Coryell W,
Craig DW,
Cruceanu C,
Czerski PM,
Davis T,
Dayer A,
Degenhardt F,
Del Zompo M,
DePaulo JR,
Edenberg HJ,
Étain B,
Falkai P,
Foroud T,
Forstner AJ,
Frisén L,
Frye MA,
Fullerton JM,
Gard S,
Garnham JS,
Gershon ES,
Goes FS,
Greenwood TA,
Grigoroiu-Serbanescu M,
Hauser J,
Heilbronner U,
Heilmann-Heimbach S,
Herms S,
Hipolito M,
Hitturlingappa S,
Hoffmann P,
Hofmann A,
Jamain S,
Jiménez E,
Kahn JP,
Kassem L,
Kelsoe JR,
Kittel-Schneider S,
Kliwicki S,
Koller DL,
König B,
Lackner N,
Laje G,
Lang M,
Lavebratt C,
Lawson WB,
Leboyer M,
Leckband SG,
Liu C,
Maaser A,
Mahon PB,
Maier W,
Maj M,
Manchia M,
Martinsson L,
McCarthy MJ,
McElroy SL,
McInnis MG,
McKinney R,
Mitchell PB,
Mitjans M,
Mondimore FM,
Monteleone P,
Mühleisen TW,
Nievergelt CM,
Nöthen MM,
Novák T,
Nurnberger JI Jr,
Nwulia EA,
Ösby U,
Pfennig A,
Potash JB,
Propping P,
Reif A,
Reininghaus E,
Rice J,
Rietschel M,
Rouleau GA,
Rybakowski JK,
Schalling M,
Scheftner WA,
Schofield PR,
Schork NJ,
Schulze TG,
Schumacher J,
Schweizer BW,
Severino G,
Shekhtman T,
Shilling PD,
Simhandl C,
Slaney CM,
Smith EN,
Squassina A,
Stamm T,
Stopkova P,
Streit F,
Strohmaier J,
Szelinger S,
Tighe SK,
Tortorella A,
Turecki G,
Vieta E,
Volkert J,
Witt SH,
Wright A,
Zandi PP,
Zhang P,
Zollner S,
McMahon FJ
Human molecular genetics · 2016 · PMID 27329760
2 pages
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder
Song J,
Bergen SE,
Di Florio A,
Karlsson R,
Charney A,
Ruderfer DM,
Stahl EA,
Chambert KD,
Moran JL,
Gordon-Smith K,
Forty L,
Green EK
and 39 more — show all
Jones I,
Jones L,
Scolnick EM,
Sklar P,
Smoller JW,
Lichtenstein P,
Hultman C,
Craddock N,
Landén M,
Smoller JW,
Perlis RH,
Lee PH,
Castro VM,
Hoffnagle AG,
Sklar P,
Stahl EA,
Purcell SM,
Ruderfer DM,
Charney AW,
Roussos P,
Michele Pato CP,
Medeiros H,
Sobel J,
Craddock N,
Jones I,
Forty L,
Florio AD,
Green E,
Jones L,
Gordon-Smith K,
Landen M,
Hultman C,
Jureus A,
Bergen S,
McCarroll S,
Moran J,
Smoller JW,
Chambert K,
Belliveau RA
Members of the International Cohort Collection for Bipolar Disorder (ICCBD)
Molecular psychiatry · 2016 · PMID 26503763 · open access
1 page
Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population
Bai H,
Song M,
Lei S,
Jiao L,
Hu X,
Wu T,
Song J,
Liu T,
Peng W,
Zhao Z,
Meng Z,
Ying B
MedComm · 2023 · PMID 37009413 · 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.