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.
3 matches for
Louie TL.
Discovery of common and rare genetic risk variants for colorectal cancer
Huyghe JR,
Bien SA,
Harrison TA,
Kang HM,
Chen S,
Schmit SL,
Conti DV,
Qu C,
Jeon J,
Edlund CK,
Greenside P,
Wainberg M
and 188 more — show all
Schumacher FR,
Smith JD,
Levine DM,
Nelson SC,
Sinnott-Armstrong NA,
Albanes D,
Alonso MH,
Anderson K,
Arnau-Collell C,
Arndt V,
Bamia C,
Banbury BL,
Baron JA,
Berndt SI,
Bézieau S,
Bishop DT,
Boehm J,
Boeing H,
Brenner H,
Brezina S,
Buch S,
Buchanan DD,
Burnett-Hartman A,
Butterbach K,
Caan BJ,
Campbell PT,
Carlson CS,
Castellví-Bel S,
Chan AT,
Chang-Claude J,
Chanock SJ,
Chirlaque MD,
Cho SH,
Connolly CM,
Cross AJ,
Cuk K,
Curtis KR,
de la Chapelle A,
Doheny KF,
Duggan D,
Easton DF,
Elias SG,
Elliott F,
English DR,
Feskens EJM,
Figueiredo JC,
Fischer R,
FitzGerald LM,
Forman D,
Gala M,
Gallinger S,
Gauderman WJ,
Giles GG,
Gillanders E,
Gong J,
Goodman PJ,
Grady WM,
Grove JS,
Gsur A,
Gunter MJ,
Haile RW,
Hampe J,
Hampel H,
Harlid S,
Hayes RB,
Hofer P,
Hoffmeister M,
Hopper JL,
Hsu WL,
Huang WY,
Hudson TJ,
Hunter DJ,
Ibañez-Sanz G,
Idos GE,
Ingersoll R,
Jackson RD,
Jacobs EJ,
Jenkins MA,
Joshi AD,
Joshu CE,
Keku TO,
Key TJ,
Kim HR,
Kobayashi E,
Kolonel LN,
Kooperberg C,
Kühn T,
Küry S,
Kweon SS,
Larsson SC,
Laurie CA,
Le Marchand L,
Leal SM,
Lee SC,
Lejbkowicz F,
Lemire M,
Li CI,
Li L,
Lieb W,
Lin Y,
Lindblom A,
Lindor NM,
Ling H,
Louie TL,
Männistö S,
Markowitz SD,
Martín V,
Masala G,
McNeil CE,
Melas M,
Milne RL,
Moreno L,
Murphy N,
Myte R,
Naccarati A,
Newcomb PA,
Offit K,
Ogino S,
Onland-Moret NC,
Pardini B,
Parfrey PS,
Pearlman R,
Perduca V,
Pharoah PDP,
Pinchev M,
Platz EA,
Prentice RL,
Pugh E,
Raskin L,
Rennert G,
Rennert HS,
Riboli E,
Rodríguez-Barranco M,
Romm J,
Sakoda LC,
Schafmayer C,
Schoen RE,
Seminara D,
Shah M,
Shelford T,
Shin MH,
Shulman K,
Sieri S,
Slattery ML,
Southey MC,
Stadler ZK,
Stegmaier C,
Su YR,
Tangen CM,
Thibodeau SN,
Thomas DC,
Thomas SS,
Toland AE,
Trichopoulou A,
Ulrich CM,
Van Den Berg DJ,
van Duijnhoven FJB,
Van Guelpen B,
van Kranen H,
Vijai J,
Visvanathan K,
Vodicka P,
Vodickova L,
Vymetalkova V,
Weigl K,
Weinstein SJ,
White E,
Win AK,
Wolf CR,
Wolk A,
Woods MO,
Wu AH,
Zaidi SH,
Zanke BW,
Zhang Q,
Zheng W,
Zheng W,
Scacheri PC,
Potter JD,
Bassik MC,
Kundaje A,
Casey G,
Moreno V,
Abecasis GR,
Nickerson DA,
Gruber SB,
Hsu L,
Peters U
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration
Scammell BH,
Tchio C,
Song Y,
Nishiyama T,
Louie TL,
Dashti HS,
Nakatochi M,
Zee PC,
Daghlas I,
Momozawa Y,
Cai J,
Ollila HM
and 6 more — show all
Human molecular genetics · 2023 · PMID 37384397
11 pages
A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A<sub>1c</sub> With Implications for Glycemic Status in U.S. Hispanics/Latinos
Moon JY,
Louie TL,
Jain D,
Sofer T,
Schurmann C,
Below JE,
Lai CQ,
Aviles-Santa ML,
Talavera GA,
Smith CE,
Petty LE,
Bottinger EP
and 13 more — show all
Chen YI,
Taylor KD,
Daviglus ML,
Cai J,
Wang T,
Tucker KL,
Ordovás JM,
Hanis CL,
Loos RJF,
Schneiderman N,
Rotter JI,
Kaplan RC,
Qi Q
Diabetes care · 2019 · PMID 31213470
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.