For researchers
Is your paper here?
2,661 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.
1 match for
Schoof N.
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Michailidou K,
Hall P,
Gonzalez-Neira A,
Ghoussaini M,
Dennis J,
Milne RL,
Schmidt MK,
Chang-Claude J,
Bojesen SE,
Bolla MK,
Wang Q,
Dicks E
and 208 more — show all
Lee A,
Turnbull C,
Rahman N,
Fletcher O,
Peto J,
Gibson L,
Dos Santos Silva I,
Nevanlinna H,
Muranen TA,
Aittomäki K,
Blomqvist C,
Czene K,
Irwanto A,
Liu J,
Waisfisz Q,
Meijers-Heijboer H,
Adank M,
van der Luijt RB,
Hein R,
Dahmen N,
Beckman L,
Meindl A,
Schmutzler RK,
Müller-Myhsok B,
Lichtner P,
Hopper JL,
Southey MC,
Makalic E,
Schmidt DF,
Uitterlinden AG,
Hofman A,
Hunter DJ,
Chanock SJ,
Vincent D,
Bacot F,
Tessier DC,
Canisius S,
Wessels LF,
Haiman CA,
Shah M,
Luben R,
Brown J,
Luccarini C,
Schoof N,
Humphreys K,
Li J,
Nordestgaard BG,
Nielsen SF,
Flyger H,
Couch FJ,
Wang X,
Vachon C,
Stevens KN,
Lambrechts D,
Moisse M,
Paridaens R,
Christiaens MR,
Rudolph A,
Nickels S,
Flesch-Janys D,
Johnson N,
Aitken Z,
Aaltonen K,
Heikkinen T,
Broeks A,
Veer LJ,
van der Schoot CE,
Guénel P,
Truong T,
Laurent-Puig P,
Menegaux F,
Marme F,
Schneeweiss A,
Sohn C,
Burwinkel B,
Zamora MP,
Perez JI,
Pita G,
Alonso MR,
Cox A,
Brock IW,
Cross SS,
Reed MW,
Sawyer EJ,
Tomlinson I,
Kerin MJ,
Miller N,
Henderson BE,
Schumacher F,
Le Marchand L,
Andrulis IL,
Knight JA,
Glendon G,
Mulligan AM,
Lindblom A,
Margolin S,
Hooning MJ,
Hollestelle A,
van den Ouweland AM,
Jager A,
Bui QM,
Stone J,
Dite GS,
Apicella C,
Tsimiklis H,
Giles GG,
Severi G,
Baglietto L,
Fasching PA,
Haeberle L,
Ekici AB,
Beckmann MW,
Brenner H,
Müller H,
Arndt V,
Stegmaier C,
Swerdlow A,
Ashworth A,
Orr N,
Jones M,
Figueroa J,
Lissowska J,
Brinton L,
Goldberg MS,
Labrèche F,
Dumont M,
Winqvist R,
Pylkäs K,
Jukkola-Vuorinen A,
Grip M,
Brauch H,
Hamann U,
Brüning T,
Radice P,
Peterlongo P,
Manoukian S,
Bonanni B,
Devilee P,
Tollenaar RA,
Seynaeve C,
van Asperen CJ,
Jakubowska A,
Lubinski J,
Jaworska K,
Durda K,
Mannermaa A,
Kataja V,
Kosma VM,
Hartikainen JM,
Bogdanova NV,
Antonenkova NN,
Dörk T,
Kristensen VN,
Anton-Culver H,
Slager S,
Toland AE,
Edge S,
Fostira F,
Kang D,
Yoo KY,
Noh DY,
Matsuo K,
Ito H,
Iwata H,
Sueta A,
Wu AH,
Tseng CC,
Van Den Berg D,
Stram DO,
Shu XO,
Lu W,
Gao YT,
Cai H,
Teo SH,
Yip CH,
Phuah SY,
Cornes BK,
Hartman M,
Miao H,
Lim WY,
Sng JH,
Muir K,
Lophatananon A,
Stewart-Brown S,
Siriwanarangsan P,
Shen CY,
Hsiung CN,
Wu PE,
Ding SL,
Sangrajrang S,
Gaborieau V,
Brennan P,
McKay J,
Blot WJ,
Signorello LB,
Cai Q,
Zheng W,
Zheng W,
Deming-Halverson S,
Shrubsole M,
Long J,
Simard J,
Garcia-Closas M,
Pharoah PD,
Chenevix-Trench G,
Dunning AM,
Benitez J,
Easton DF
Breast and Ovarian Cancer Susceptibility Collaboration · Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON) and 3 more consortia
Nature genetics · 2013 · PMID 23535729
12 pages+
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.