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2,657 papers hold this site up. Every variant and condition page names
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3 matches for
Santella R.
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+
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
Effect of selenium and vitamin E on risk of prostate cancer and other cancers: the Selenium and Vitamin E Cancer Prevention Trial (SELECT)
Lippman SM,
Klein EA,
Goodman PJ,
Lucia MS,
Thompson IM,
Ford LG,
Parnes HL,
Minasian LM,
Gaziano JM,
Hartline JA,
Parsons JK,
Bearden JD 3rd
and 21 more — show all
Crawford ED,
Goodman GE,
Claudio J,
Winquist E,
Cook ED,
Karp DD,
Walther P,
Lieber MM,
Kristal AR,
Darke AK,
Arnold KB,
Ganz PA,
Santella RM,
Albanes D,
Taylor PR,
Probstfield JL,
Jagpal TJ,
Crowley JJ,
Meyskens FL Jr,
Baker LH,
Coltman CA Jr
JAMA · 2009 · PMID 19066370
1 page
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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.