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Is your paper here?
2,876 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
Ligtenberg MJ.
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk
Couch FJ,
Wang X,
McGuffog L,
Lee A,
Olswold C,
Kuchenbaecker KB,
Soucy P,
Fredericksen Z,
Barrowdale D,
Dennis J,
Gaudet MM,
Dicks E
and 250 more — show all
Kosel M,
Healey S,
Sinilnikova OM,
Lee A,
Bacot F,
Vincent D,
Hogervorst FB,
Peock S,
Stoppa-Lyonnet D,
Jakubowska A,
Radice P,
Schmutzler RK,
Domchek SM,
Piedmonte M,
Singer CF,
Friedman E,
Thomassen M,
Hansen TV,
Neuhausen SL,
Szabo CI,
Blanco I,
Greene MH,
Karlan BY,
Garber J,
Phelan CM,
Weitzel JN,
Montagna M,
Olah E,
Andrulis IL,
Godwin AK,
Yannoukakos D,
Goldgar DE,
Caldes T,
Nevanlinna H,
Osorio A,
Terry MB,
Daly MB,
van Rensburg EJ,
Hamann U,
Ramus SJ,
Toland AE,
Caligo MA,
Olopade OI,
Tung N,
Claes K,
Beattie MS,
Southey MC,
Imyanitov EN,
Tischkowitz M,
Janavicius R,
John EM,
Kwong A,
Diez O,
Balmaña J,
Barkardottir RB,
Arun BK,
Rennert G,
Teo SH,
Ganz PA,
Campbell I,
van der Hout AH,
van Deurzen CH,
Seynaeve C,
Gómez Garcia EB,
van Leeuwen FE,
Meijers-Heijboer HE,
Gille JJ,
Ausems MG,
Blok MJ,
Ligtenberg MJ,
Rookus MA,
Devilee P,
Verhoef S,
van Os TA,
Wijnen JT,
Frost D,
Ellis S,
Fineberg E,
Platte R,
Evans DG,
Izatt L,
Eeles RA,
Adlard J,
Eccles DM,
Cook J,
Brewer C,
Douglas F,
Hodgson S,
Morrison PJ,
Side LE,
Donaldson A,
Houghton C,
Rogers MT,
Dorkins H,
Eason J,
Gregory H,
McCann E,
Murray A,
Calender A,
Hardouin A,
Berthet P,
Delnatte C,
Nogues C,
Lasset C,
Houdayer C,
Leroux D,
Rouleau E,
Prieur F,
Damiola F,
Sobol H,
Coupier I,
Venat-Bouvet L,
Castera L,
Gauthier-Villars M,
Léoné M,
Pujol P,
Mazoyer S,
Bignon YJ,
Złowocka-Perłowska E,
Gronwald J,
Lubinski J,
Durda K,
Jaworska K,
Huzarski T,
Spurdle AB,
Viel A,
Peissel B,
Bonanni B,
Melloni G,
Ottini L,
Papi L,
Varesco L,
Tibiletti MG,
Peterlongo P,
Volorio S,
Manoukian S,
Pensotti V,
Arnold N,
Engel C,
Deissler H,
Gadzicki D,
Gehrig A,
Kast K,
Rhiem K,
Meindl A,
Niederacher D,
Ditsch N,
Plendl H,
Preisler-Adams S,
Engert S,
Sutter C,
Varon-Mateeva R,
Wappenschmidt B,
Weber BH,
Arver B,
Stenmark-Askmalm M,
Loman N,
Rosenquist R,
Einbeigi Z,
Nathanson KL,
Rebbeck TR,
Blank SV,
Cohn DE,
Rodriguez GC,
Small L,
Friedlander M,
Bae-Jump VL,
Fink-Retter A,
Rappaport C,
Gschwantler-Kaulich D,
Pfeiler G,
Tea MK,
Lindor NM,
Kaufman B,
Shimon Paluch S,
Laitman Y,
Skytte AB,
Gerdes AM,
Pedersen IS,
Moeller ST,
Kruse TA,
Jensen UB,
Vijai J,
Sarrel K,
Robson M,
Kauff N,
Mulligan AM,
Glendon G,
Ozcelik H,
Ejlertsen B,
Nielsen FC,
Jønson L,
Andersen MK,
Ding YC,
Steele L,
Foretova L,
Teulé A,
Lazaro C,
Brunet J,
Pujana MA,
Mai PL,
Loud JT,
Walsh C,
Lester J,
Orsulic S,
Narod SA,
Herzog J,
Sand SR,
Tognazzo S,
Agata S,
Vaszko T,
Weaver J,
Stavropoulou AV,
Buys SS,
Romero A,
de la Hoya M,
Aittomäki K,
Muranen TA,
Duran M,
Chung WK,
Lasa A,
Dorfling CM,
Miron A,
Benitez J,
Senter L,
Huo D,
Chan SB,
Sokolenko AP,
Chiquette J,
Tihomirova L,
Friebel TM,
Agnarsson BA,
Lu KH,
Lejbkowicz F,
James PA,
Hall P,
Dunning AM,
Tessier D,
Cunningham J,
Slager SL,
Wang C,
Hart S,
Stevens K,
Simard J,
Pastinen T,
Pankratz VS,
Offit K,
Easton DF,
Chenevix-Trench G,
Antoniou AC
kConFab Investigators · SWE-BRCA and 6 more consortia
PLoS genetics · 2013 · PMID 23544013 · 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.