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.
10 matches for
Abel L.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts
Rashkin SR,
Graff RE,
Kachuri L,
Thai KK,
Alexeeff SE,
Blatchins MA,
Cavazos TB,
Corley DA,
Emami NC,
Hoffman JD,
Jorgenson E,
Kushi LH
and 7 more — show all
Nature communications · 2020 · PMID 32887889 · open access
12 pages+
Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci
Chen H,
Fan S,
Stone J,
Thompson DJ,
Douglas J,
Li S,
Scott C,
Bolla MK,
Wang Q,
Dennis J,
Michailidou K,
Li C
and 44 more — show all
Peters U,
Hopper JL,
Southey MC,
Nguyen-Dumont T,
Nguyen TL,
Fasching PA,
Behrens A,
Cadby G,
Murphy RA,
Aronson K,
Howell A,
Astley S,
Couch F,
Olson J,
Milne RL,
Giles GG,
Haiman CA,
Maskarinec G,
Winham S,
John EM,
Kurian A,
Eliassen H,
Andrulis I,
Evans DG,
Newman WG,
Hall P,
Czene K,
Swerdlow A,
Jones M,
Pollan M,
Fernandez-Navarro P,
McConnell DS,
Kristensen VN,
Rothstein JH,
Wang P,
Habel LA,
Sieh W,
Dunning AM,
Pharoah PDP,
Easton DF,
Gierach GL,
Tamimi RM,
Vachon CM,
Lindström S
NBCS Investigators
Breast cancer research : BCR · 2022 · PMID 35414113 · open access
12 pages+
Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer
Hoffmann TJ,
Passarelli MN,
Graff RE,
Emami NC,
Sakoda LC,
Jorgenson E,
Habel LA,
Shan J,
Ranatunga DK,
Quesenberry CP,
Chao CR,
Ghai NR
and 17 more — show all
Aaronson D,
Presti J,
Nordström T,
Wang Z,
Berndt SI,
Chanock SJ,
Mosley JD,
Klein RJ,
Middha M,
Lilja H,
Melander O,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Van Den Eeden SK,
Witte JS
Nature communications · 2017 · PMID 28139693 · open access
5 pages
A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences
Hoffmann TJ,
Van Den Eeden SK,
Sakoda LC,
Jorgenson E,
Habel LA,
Graff RE,
Passarelli MN,
Cario CL,
Emami NC,
Chao CR,
Ghai NR,
Shan J
and 23 more — show all
Ranatunga DK,
Quesenberry CP,
Aaronson D,
Presti J,
Wang Z,
Berndt SI,
Chanock SJ,
McDonnell SK,
French AJ,
Schaid DJ,
Thibodeau SN,
Li Q,
Freedman ML,
Penney KL,
Mucci LA,
Haiman CA,
Henderson BE,
Seminara D,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Witte JS
Cancer discovery · 2015 · PMID 26034056
3 pages
Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk
Sieh W,
Rothstein JH,
Klein RJ,
Alexeeff SE,
Sakoda LC,
Jorgenson E,
McBride RB,
Graff RE,
McGuire V,
Achacoso N,
Acton L,
Liang RY
and 8 more — show all
Nature communications · 2020 · PMID 33037222 · open access
3 pages
Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection
Patin E,
Kutalik Z,
Guergnon J,
Bibert S,
Nalpas B,
Jouanguy E,
Munteanu M,
Bousquet L,
Argiro L,
Halfon P,
Boland A,
Müllhaupt B
and 24 more — show all
Semela D,
Dufour JF,
Heim MH,
Moradpour D,
Cerny A,
Malinverni R,
Hirsch H,
Martinetti G,
Suppiah V,
Stewart G,
Booth DR,
George J,
Casanova JL,
Bréchot C,
Rice CM,
Talal AH,
Jacobson IM,
Bourlière M,
Theodorou I,
Poynard T,
Negro F,
Pol S,
Bochud PY,
Abel L
Swiss Hepatitis C Cohort Study Group, International Hepatitis C Genetics Consortium · French ANRS HC EP 26 Genoscan Study Group
Gastroenterology · 2012 · PMID 22841784
2 pages
Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines
Scepanovic P,
Alanio C,
Hammer C,
Hodel F,
Hodel F,
Bergstedt J,
Patin E,
Thorball CW,
Chaturvedi N,
Charbit B,
Abel L,
Quintana-Murci L
and 3 more — show all
Milieu Intérieur Consortium
Genome medicine · 2018 · PMID 30053915 · open access
1 page
Family-based genome-wide association study of leprosy in Vietnam
Gzara C,
Dallmann-Sauer M,
Orlova M,
Van Thuc N,
Thai VH,
Fava VM,
Bihoreau MT,
Boland A,
Abel L,
Alcaïs A,
Schurr E,
Cobat A
PLoS pathogens · 2020 · PMID 32421744 · open access
1 page
A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility
Emami NC,
Cavazos TB,
Rashkin SR,
Cario CL,
Graff RE,
Tai CG,
Mefford JA,
Kachuri L,
Wan E,
Wong S,
Aaronson D,
Presti J
and 14 more — show all
Habel LA,
Shan J,
Ranatunga DK,
Chao CR,
Ghai NR,
Jorgenson E,
Sakoda LC,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Hoffmann TJ,
Van Den Eeden SK,
Witte JS
Cancer research · 2021 · PMID 33293427
1 page
Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations
Quistrebert J,
Orlova M,
Kerner G,
Ton LT,
Luong NT,
Danh NT,
Vincent QB,
Jabot-Hanin F,
Seeleuthner Y,
Bustamante J,
Boisson-Dupuis S,
Huong NT
and 10 more — show all
PLoS genetics · 2021 · PMID 33661925 · 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.