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2,663 papers hold this site up. Every variant and condition page names
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3 matches for
Maranian M.
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Michailidou K,
Beesley J,
Lindstrom S,
Canisius S,
Dennis J,
Lush MJ,
Maranian MJ,
Bolla MK,
Wang Q,
Shah M,
Perkins BJ,
Czene K
and 232 more — show all
Eriksson M,
Darabi H,
Brand JS,
Bojesen SE,
Nordestgaard BG,
Flyger H,
Nielsen SF,
Rahman N,
Turnbull C,
Fletcher O,
Peto J,
Gibson L,
dos-Santos-Silva I,
Chang-Claude J,
Flesch-Janys D,
Rudolph A,
Eilber U,
Behrens S,
Nevanlinna H,
Muranen TA,
Aittomäki K,
Blomqvist C,
Khan S,
Aaltonen K,
Ahsan H,
Kibriya MG,
Whittemore AS,
John EM,
Malone KE,
Gammon MD,
Santella RM,
Ursin G,
Makalic E,
Schmidt DF,
Casey G,
Hunter DJ,
Gapstur SM,
Gaudet MM,
Diver WR,
Haiman CA,
Schumacher F,
Henderson BE,
Le Marchand L,
Berg CD,
Chanock SJ,
Figueroa J,
Hoover RN,
Lambrechts D,
Neven P,
Wildiers H,
van Limbergen E,
Schmidt MK,
Broeks A,
Verhoef S,
Cornelissen S,
Couch FJ,
Olson JE,
Hallberg E,
Vachon C,
Waisfisz Q,
Meijers-Heijboer H,
Adank MA,
van der Luijt RB,
Li J,
Liu J,
Humphreys K,
Kang D,
Choi JY,
Park SK,
Yoo KY,
Matsuo K,
Ito H,
Iwata H,
Tajima K,
Guénel P,
Truong T,
Mulot C,
Sanchez M,
Burwinkel B,
Marme F,
Surowy H,
Sohn C,
Wu AH,
Tseng CC,
Van Den Berg D,
Stram DO,
González-Neira A,
Benitez J,
Zamora MP,
Perez JI,
Shu XO,
Lu W,
Gao YT,
Cai H,
Cox A,
Cross SS,
Reed MW,
Andrulis IL,
Knight JA,
Glendon G,
Mulligan AM,
Sawyer EJ,
Tomlinson I,
Kerin MJ,
Miller N,
Lindblom A,
Margolin S,
Teo SH,
Yip CH,
Taib NA,
Tan GH,
Hooning MJ,
Hollestelle A,
Martens JW,
Collée JM,
Blot W,
Signorello LB,
Cai Q,
Hopper JL,
Southey MC,
Tsimiklis H,
Apicella C,
Shen CY,
Hsiung CN,
Wu PE,
Hou MF,
Kristensen VN,
Nord S,
Alnaes GI,
Giles GG,
Milne RL,
McLean C,
Canzian F,
Trichopoulos D,
Peeters P,
Lund E,
Sund M,
Khaw KT,
Gunter MJ,
Palli D,
Mortensen LM,
Dossus L,
Huerta JM,
Meindl A,
Schmutzler RK,
Sutter C,
Yang R,
Muir K,
Lophatananon A,
Stewart-Brown S,
Siriwanarangsan P,
Hartman M,
Miao H,
Chia KS,
Chan CW,
Fasching PA,
Hein A,
Beckmann MW,
Haeberle L,
Brenner H,
Dieffenbach AK,
Arndt V,
Stegmaier C,
Ashworth A,
Orr N,
Schoemaker MJ,
Swerdlow AJ,
Brinton L,
Garcia-Closas M,
Zheng W,
Zheng W,
Halverson SL,
Shrubsole M,
Long J,
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,
Bernard L,
Bogdanova NV,
Dörk T,
Mannermaa A,
Kataja V,
Kosma VM,
Hartikainen JM,
Devilee P,
Tollenaar RA,
Seynaeve C,
Van Asperen CJ,
Jakubowska A,
Lubinski J,
Jaworska K,
Huzarski T,
Sangrajrang S,
Gaborieau V,
Brennan P,
McKay J,
Slager S,
Toland AE,
Ambrosone CB,
Yannoukakos D,
Kabisch M,
Torres D,
Neuhausen SL,
Anton-Culver H,
Luccarini C,
Baynes C,
Ahmed S,
Healey CS,
Tessier DC,
Vincent D,
Bacot F,
Pita G,
Alonso MR,
Álvarez N,
Herrero D,
Simard J,
Pharoah PP,
Kraft P,
Dunning AM,
Chenevix-Trench G,
Hall P,
Easton DF
BOCS · kConFab Investigators and 3 more consortia
Nature genetics · 2015 · PMID 25751625 · open access
12 pages+
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
Eeles RA,
Olama AA,
Benlloch S,
Saunders EJ,
Leongamornlert DA,
Tymrakiewicz M,
Ghoussaini M,
Luccarini C,
Dennis J,
Jugurnauth-Little S,
Dadaev T,
Neal DE
and 132 more — show all
Hamdy FC,
Donovan JL,
Muir K,
Giles GG,
Severi G,
Wiklund F,
Gronberg H,
Haiman CA,
Schumacher F,
Henderson BE,
Le Marchand L,
Lindstrom S,
Kraft P,
Hunter DJ,
Gapstur S,
Chanock SJ,
Berndt SI,
Albanes D,
Andriole G,
Schleutker J,
Weischer M,
Canzian F,
Riboli E,
Key TJ,
Travis RC,
Campa D,
Ingles SA,
John EM,
Hayes RB,
Pharoah PD,
Pashayan N,
Khaw KT,
Stanford JL,
Ostrander EA,
Signorello LB,
Thibodeau SN,
Schaid D,
Maier C,
Vogel W,
Kibel AS,
Cybulski C,
Lubinski J,
Cannon-Albright L,
Brenner H,
Park JY,
Kaneva R,
Batra J,
Spurdle AB,
Clements JA,
Teixeira MR,
Dicks E,
Lee A,
Dunning AM,
Baynes C,
Conroy D,
Maranian MJ,
Ahmed S,
Govindasami K,
Guy M,
Wilkinson RA,
Sawyer EJ,
Morgan A,
Dearnaley DP,
Horwich A,
Huddart RA,
Khoo VS,
Parker CC,
Van As NJ,
Woodhouse CJ,
Thompson A,
Dudderidge T,
Ogden C,
Cooper CS,
Lophatananon A,
Cox A,
Southey MC,
Hopper JL,
English DR,
Aly M,
Adolfsson J,
Xu J,
Zheng SL,
Yeager M,
Kaaks R,
Diver WR,
Gaudet MM,
Stern MC,
Corral R,
Joshi AD,
Shahabi A,
Wahlfors T,
Tammela TL,
Auvinen A,
Virtamo J,
Klarskov P,
Nordestgaard BG,
Røder MA,
Nielsen SF,
Bojesen SE,
Siddiq A,
Fitzgerald LM,
Kolb S,
Kwon EM,
Karyadi DM,
Blot WJ,
Zheng W,
Cai Q,
McDonnell SK,
Rinckleb AE,
Drake B,
Colditz G,
Wokolorczyk D,
Stephenson RA,
Teerlink C,
Muller H,
Rothenbacher D,
Sellers TA,
Lin HY,
Slavov C,
Mitev V,
Lose F,
Srinivasan S,
Maia S,
Paulo P,
Lange E,
Cooney KA,
Antoniou AC,
Vincent D,
Bacot F,
Tessier DC,
Kote-Jarai Z,
Easton DF
COGS–Cancer Research UK GWAS–ELLIPSE (part of GAME-ON) Initiative · Australian Prostate Cancer Bioresource and 3 more consortia
Nature genetics · 2013 · PMID 23535732
7 pages
Genome-wide association study identifies five new breast cancer susceptibility loci
Turnbull C,
Ahmed S,
Morrison J,
Pernet D,
Renwick A,
Maranian M,
Seal S,
Ghoussaini M,
Hines S,
Healey CS,
Hughes D,
Warren-Perry M
and 14 more — show all
Tapper W,
Eccles D,
Evans DG,
Hooning M,
Schutte M,
van den Ouweland A,
Houlston R,
Ross G,
Langford C,
Pharoah PD,
Stratton MR,
Dunning AM,
Rahman N,
Easton DF
Breast Cancer Susceptibility Collaboration (UK)
Nature genetics · 2010 · PMID 20453838
3 pages
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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.