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2,660 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.
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2 matches for
Białkowska K.
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Coignard J,
Lush M,
Beesley J,
O'Mara TA,
Dennis J,
Tyrer JP,
Barnes DR,
McGuffog L,
Leslie G,
Bolla MK,
Adank MA,
Agata S
and 207 more — show all
Ahearn T,
Aittomäki K,
Andrulis IL,
Anton-Culver H,
Arndt V,
Arnold N,
Aronson KJ,
Arun BK,
Augustinsson A,
Azzollini J,
Barrowdale D,
Baynes C,
Becher H,
Bermisheva M,
Bernstein L,
Białkowska K,
Blomqvist C,
Bojesen SE,
Bonanni B,
Borg A,
Brauch H,
Brenner H,
Burwinkel B,
Buys SS,
Caldés T,
Caligo MA,
Campa D,
Carter BD,
Castelao JE,
Chang-Claude J,
Chanock SJ,
Chung WK,
Claes KBM,
Clarke CL,
Collée JM,
Conroy DM,
Czene K,
Daly MB,
Devilee P,
Diez O,
Ding YC,
Domchek SM,
Dörk T,
Dos-Santos-Silva I,
Dunning AM,
Dwek M,
Eccles DM,
Eliassen AH,
Engel C,
Eriksson M,
Evans DG,
Fasching PA,
Flyger H,
Fostira F,
Friedman E,
Fritschi L,
Frost D,
Gago-Dominguez M,
Gapstur SM,
Garber J,
Garcia-Barberan V,
García-Closas M,
García-Sáenz JA,
Gaudet MM,
Gayther SA,
Gehrig A,
Georgoulias V,
Giles GG,
Godwin AK,
Goldberg MS,
Goldgar DE,
González-Neira A,
Greene MH,
Guénel P,
Haeberle L,
Hahnen E,
Haiman CA,
Håkansson N,
Hall P,
Hamann U,
Harrington PA,
Hart SN,
He W,
Hogervorst FBL,
Hollestelle A,
Hopper JL,
Horcasitas DJ,
Hulick PJ,
Hunter DJ,
Imyanitov EN,
Jager A,
Jakubowska A,
James PA,
Jensen UB,
John EM,
Jones ME,
Kaaks R,
Kapoor PM,
Karlan BY,
Keeman R,
Khusnutdinova E,
Kiiski JI,
Ko YD,
Kosma VM,
Kraft P,
Kurian AW,
Laitman Y,
Lambrechts D,
Le Marchand L,
Lester J,
Lesueur F,
Lindstrom T,
Lopez-Fernández A,
Loud JT,
Luccarini C,
Mannermaa A,
Manoukian S,
Margolin S,
Martens JWM,
Mebirouk N,
Meindl A,
Miller A,
Milne RL,
Montagna M,
Nathanson KL,
Neuhausen SL,
Nevanlinna H,
Nielsen FC,
O'Brien KM,
Olopade OI,
Olson JE,
Olsson H,
Osorio A,
Ottini L,
Park-Simon TW,
Parsons MT,
Pedersen IS,
Peshkin B,
Peterlongo P,
Peto J,
Pharoah PDP,
Phillips KA,
Polley EC,
Poppe B,
Presneau N,
Pujana MA,
Punie K,
Radice P,
Rantala J,
Rashid MU,
Rennert G,
Rennert HS,
Robson M,
Romero A,
Rossing M,
Saloustros E,
Sandler DP,
Santella R,
Scheuner MT,
Schmidt MK,
Schmidt G,
Scott C,
Sharma P,
Soucy P,
Southey MC,
Spinelli JJ,
Steinsnyder Z,
Stone J,
Stoppa-Lyonnet D,
Swerdlow A,
Tamimi RM,
Tapper WJ,
Taylor JA,
Terry MB,
Teulé A,
Thull DL,
Tischkowitz M,
Toland AE,
Torres D,
Trainer AH,
Truong T,
Tung N,
Vachon CM,
Vega A,
Vijai J,
Wang Q,
Wappenschmidt B,
Weinberg CR,
Weitzel JN,
Wendt C,
Wolk A,
Yadav S,
Yang XR,
Yannoukakos D,
Zheng W,
Ziogas A,
Zorn KK,
Park SK,
Thomassen M,
Offit K,
Schmutzler RK,
Couch FJ,
Simard J,
Chenevix-Trench G,
Easton DF,
Andrieu N,
Antoniou AC
GEMO Study Collaborators · EMBRACE Collaborators and 3 more consortia
Nature communications · 2021 · PMID 33597508 · open access
5 pages
Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer
Barnes DR,
Tyrer JP,
Dennis J,
Leslie G,
Bolla MK,
Lush M,
Aeilts AM,
Aittomäki K,
Andrieu N,
Andrulis IL,
Anton-Culver H,
Arason A
and 156 more — show all
Arun BK,
Balmaña J,
Bandera EV,
Barkardottir RB,
Berger LPV,
Berrington de Gonzalez A,
Berthet P,
Białkowska K,
Bjørge L,
Blanco AM,
Blok MJ,
Bobolis KA,
Bogdanova NV,
Brenton JD,
Butz H,
Buys SS,
Caligo MA,
Campbell I,
Castillo C,
Claes KBM,
Colonna SV,
Cook LS,
Daly MB,
Dansonka-Mieszkowska A,
de la Hoya M,
deFazio A,
DePersia A,
Ding YC,
Doherty JA,
Domchek SM,
Dörk T,
Einbeigi Z,
Engel C,
Evans DG,
Foretova L,
Fortner RT,
Fostira F,
Foti MC,
Friedman E,
Frone MN,
Ganz PA,
Gentry-Maharaj A,
Glendon G,
Godwin AK,
González-Neira A,
Greene MH,
Gronwald J,
Guerrieri-Gonzaga A,
Hamann U,
Hansen TVO,
Harris HR,
Hauke J,
Heitz F,
Hogervorst FBL,
Hooning MJ,
Hopper JL,
Huff CD,
Huntsman DG,
Imyanitov EN,
Izatt L,
Jakubowska A,
James PA,
Janavicius R,
John EM,
Kar S,
Karlan BY,
Kennedy CJ,
Kiemeney LALM,
Konstantopoulou I,
Kupryjanczyk J,
Laitman Y,
Lavie O,
Lawrenson K,
Lester J,
Lesueur F,
Lopez-Pleguezuelos C,
Mai PL,
Manoukian S,
May T,
McNeish IA,
Menon U,
Milne RL,
Modugno F,
Mongiovi JM,
Montagna M,
Moysich KB,
Neuhausen SL,
Nielsen FC,
Noguès C,
Oláh E,
Olopade OI,
Osorio A,
Papi L,
Pathak H,
Pearce CL,
Pedersen IS,
Peixoto A,
Pejovic T,
Peng PC,
Peshkin BN,
Peterlongo P,
Powell CB,
Prokofyeva D,
Pujana MA,
Radice P,
Rashid MU,
Rennert G,
Richenberg G,
Sandler DP,
Sasamoto N,
Setiawan VW,
Sharma P,
Sieh W,
Singer CF,
Snape K,
Sokolenko AP,
Soucy P,
Southey MC,
Stoppa-Lyonnet D,
Sutphen R,
Sutter C,
Tan YY,
Teixeira MR,
Terry KL,
Thomsen LCV,
Tischkowitz M,
Toland AE,
Van Gorp T,
Vega A,
Velez Edwards DR,
Webb PM,
Weitzel JN,
Wentzensen N,
Whittemore AS,
Winham SJ,
Wu AH,
Yadav S,
Yu Y,
Ziogas A,
Berchuck A,
Couch FJ,
Goode EL,
Goodman MT,
Monteiro AN,
Offit K,
Ramus SJ,
Risch HA,
Schildkraut JM,
Thomassen M,
Simard J,
Easton DF,
Jones MR,
Chenevix-Trench G,
Gayther SA,
Antoniou AC,
Pharoah PDP
NPJ genomic medicine · 2025 · PMID 41266372 · open access
4 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.