For researchers
Is your paper here?
2,663 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.
47 matches for
Giles GG,
showing the first 7.
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
Siddiq A,
Couch FJ,
Chen GK,
Lindström S,
Eccles D,
Millikan RC,
Michailidou K,
Stram DO,
Beckmann L,
Rhie SK,
Ambrosone CB,
Aittomäki K
and 129 more — show all
Amiano P,
Apicella C,
Baglietto L,
Bandera EV,
Beckmann MW,
Berg CD,
Bernstein L,
Blomqvist C,
Brauch H,
Brinton L,
Bui QM,
Buring JE,
Buys SS,
Campa D,
Carpenter JE,
Chasman DI,
Chang-Claude J,
Chen C,
Clavel-Chapelon F,
Cox A,
Cross SS,
Czene K,
Deming SL,
Diasio RB,
Diver WR,
Dunning AM,
Durcan L,
Ekici AB,
Fasching PA,
Feigelson HS,
Fejerman L,
Figueroa JD,
Fletcher O,
Flesch-Janys D,
Gaudet MM,
Gerty SM,
Rodriguez-Gil JL,
Giles GG,
van Gils CH,
Godwin AK,
Graham N,
Greco D,
Hall P,
Hankinson SE,
Hartmann A,
Hein R,
Heinz J,
Hoover RN,
Hopper JL,
Hu JJ,
Huntsman S,
Ingles SA,
Irwanto A,
Isaacs C,
Jacobs KB,
John EM,
Justenhoven C,
Kaaks R,
Kolonel LN,
Coetzee GA,
Lathrop M,
Le Marchand L,
Lee AM,
Lee IM,
Lesnick T,
Lichtner P,
Liu J,
Lund E,
Makalic E,
Martin NG,
McLean CA,
Meijers-Heijboer H,
Meindl A,
Miron P,
Monroe KR,
Montgomery GW,
Müller-Myhsok B,
Nickels S,
Nyante SJ,
Olswold C,
Overvad K,
Palli D,
Park DJ,
Palmer JR,
Pathak H,
Peto J,
Pharoah P,
Rahman N,
Rivadeneira F,
Schmidt DF,
Schmutzler RK,
Slager S,
Southey MC,
Stevens KN,
Sinn HP,
Press MF,
Ross E,
Riboli E,
Ridker PM,
Schumacher FR,
Severi G,
Dos Santos Silva I,
Stone J,
Sund M,
Tapper WJ,
Thun MJ,
Travis RC,
Turnbull C,
Uitterlinden AG,
Waisfisz Q,
Wang X,
Wang Z,
Weaver J,
Schulz-Wendtland R,
Wilkens LR,
Van Den Berg D,
Zheng W,
Zheng W,
Ziegler RG,
Ziv E,
Nevanlinna H,
Easton DF,
Hunter DJ,
Henderson BE,
Chanock SJ,
Garcia-Closas M,
Kraft P,
Haiman CA,
Vachon CM
Australian Breast Cancer Tissue Bank Investigators · Familial Breast Cancer Study and 1 more consortia
Human molecular genetics · 2012 · PMID 22976474
1 page
A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease
Amin Al Olama A,
Kote-Jarai Z,
Schumacher FR,
Wiklund F,
Berndt SI,
Benlloch S,
Giles GG,
Severi G,
Neal DE,
Hamdy FC,
Donovan JL,
Hunter DJ
and 135 more — show all
Henderson BE,
Thun MJ,
Gaziano M,
Giovannucci EL,
Siddiq A,
Travis RC,
Cox DG,
Canzian F,
Riboli E,
Key TJ,
Andriole G,
Albanes D,
Hayes RB,
Schleutker J,
Auvinen A,
Tammela TL,
Weischer M,
Stanford JL,
Ostrander EA,
Cybulski C,
Lubinski J,
Thibodeau SN,
Schaid DJ,
Sorensen KD,
Batra J,
Clements JA,
Chambers S,
Aitken J,
Gardiner RA,
Maier C,
Vogel W,
Dörk T,
Brenner H,
Habuchi T,
Ingles S,
John EM,
Dickinson JL,
Cannon-Albright L,
Teixeira MR,
Kaneva R,
Zhang HW,
Lu YJ,
Park JY,
Cooney KA,
Muir KR,
Leongamornlert DA,
Saunders E,
Tymrakiewicz M,
Mahmud N,
Guy M,
Govindasami K,
O'Brien LT,
Wilkinson RA,
Hall AL,
Sawyer EJ,
Dadaev T,
Morrison J,
Dearnaley DP,
Horwich A,
Huddart RA,
Khoo VS,
Parker CC,
Van As N,
Woodhouse CJ,
Thompson A,
Dudderidge T,
Ogden C,
Cooper CS,
Lophatonanon A,
Southey MC,
Hopper JL,
English D,
Virtamo J,
Le Marchand L,
Campa D,
Kaaks R,
Lindstrom S,
Diver WR,
Gapstur S,
Yeager M,
Cox A,
Stern MC,
Corral R,
Aly M,
Isaacs W,
Adolfsson J,
Xu J,
Zheng SL,
Wahlfors T,
Taari K,
Kujala P,
Klarskov P,
Nordestgaard BG,
Røder MA,
Frikke-Schmidt R,
Bojesen SE,
FitzGerald LM,
Kolb S,
Kwon EM,
Karyadi DM,
Orntoft TF,
Borre M,
Rinckleb A,
Luedeke M,
Herkommer K,
Meyer A,
Serth J,
Marthick JR,
Patterson B,
Wokolorczyk D,
Spurdle A,
Lose F,
McDonnell SK,
Joshi AD,
Shahabi A,
Pinto P,
Santos J,
Ray A,
Sellers TA,
Lin HY,
Stephenson RA,
Teerlink C,
Muller H,
Rothenbacher D,
Tsuchiya N,
Narita S,
Cao GW,
Slavov C,
Mitev V,
Chanock S,
Gronberg H,
Haiman CA,
Kraft P,
Easton DF,
Eeles RA
UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology · UK ProtecT Study Collaborators and 2 more consortia
Human molecular genetics · 2013 · PMID 23065704
1 page
Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk
Lindström S,
Thompson DJ,
Paterson AD,
Li J,
Gierach GL,
Scott C,
Stone J,
Douglas JA,
dos-Santos-Silva I,
Fernandez-Navarro P,
Verghase J,
Smith P
and 33 more — show all
Brown J,
Luben R,
Wareham NJ,
Loos RJ,
Heit JA,
Pankratz VS,
Norman A,
Goode EL,
Cunningham JM,
deAndrade M,
Vierkant RA,
Czene K,
Fasching PA,
Baglietto L,
Southey MC,
Giles GG,
Shah KP,
Chan HP,
Helvie MA,
Beck AH,
Knoblauch NW,
Hazra A,
Hunter DJ,
Kraft P,
Pollan M,
Figueroa JD,
Couch FJ,
Hopper JL,
Hall P,
Easton DF,
Boyd NF,
Vachon CM,
Tamimi RM
Nature communications · 2014 · PMID 25342443 · open access
1 page
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
Thompson DJ,
Helgason H,
Chasman DI,
Finucane H,
Sulem P,
Ruth KS,
Whalen S,
Sarkar AK,
Albrecht E,
Altmaier E,
Amini M
and 204 more — show all
Barbieri CM,
Boutin T,
Campbell A,
Demerath E,
Giri A,
He C,
Hottenga JJ,
Karlsson R,
Kolcic I,
Loh PR,
Lunetta KL,
Mangino M,
Marco B,
McMahon G,
Medland SE,
Nolte IM,
Noordam R,
Nutile T,
Paternoster L,
Perjakova N,
Porcu E,
Rose LM,
Schraut KE,
Segrè AV,
Smith AV,
Stolk L,
Teumer A,
Andrulis IL,
Bandinelli S,
Beckmann MW,
Benitez J,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Brand JS,
Brauch H,
Brenner H,
Broer L,
Brüning T,
Buring JE,
Campbell H,
Catamo E,
Chanock S,
Chenevix-Trench G,
Corre T,
Couch FJ,
Cousminer DL,
Cox A,
Crisponi L,
Czene K,
Davey Smith G,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Dennis J,
Devilee P,
Dos-Santos-Silva I,
Dunning AM,
Eriksson JG,
Fasching PA,
Fernández-Rhodes L,
Ferrucci L,
Flesch-Janys D,
Franke L,
Gabrielson M,
Gandin I,
Giles GG,
Grallert H,
Gudbjartsson DF,
Guénel P,
Hall P,
Hallberg E,
Hamann U,
Harris TB,
Hartman CA,
Heiss G,
Hooning MJ,
Hopper JL,
Hu F,
Hunter DJ,
Ikram MA,
Im HK,
Järvelin MR,
Joshi PK,
Karasik D,
Kellis M,
Kutalik Z,
LaChance G,
Lambrechts D,
Langenberg C,
Launer LJ,
Laven JSE,
Lenarduzzi S,
Li J,
Lind PA,
Lindstrom S,
Liu Y,
Luan J,
Mägi R,
Mannermaa A,
Mbarek H,
McCarthy MI,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Michailidou K,
Milani L,
Milne RL,
Montgomery GW,
Mulligan AM,
Nalls MA,
Navarro P,
Nevanlinna H,
Nyholt DR,
Oldehinkel AJ,
O'Mara TA,
Padmanabhan S,
Palotie A,
Pedersen N,
Peters A,
Peto J,
Pharoah PDP,
Pouta A,
Radice P,
Rahman I,
Ring SM,
Robino A,
Rosendaal FR,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Schmidt MK,
Scott RA,
Shah M,
Sorice R,
Southey MC,
Sovio U,
Stampfer M,
Steri M,
Strauch K,
Tanaka T,
Tikkanen E,
Timpson NJ,
Traglia M,
Truong T,
Tyrer JP,
Uitterlinden AG,
Edwards DRV,
Vitart V,
Völker U,
Vollenweider P,
Wang Q,
Widen E,
van Dijk KW,
Willemsen G,
Winqvist R,
Wolffenbuttel BHR,
Zhao JH,
Zoledziewska M,
Zygmunt M,
Alizadeh BZ,
Boomsma DI,
Ciullo M,
Cucca F,
Esko T,
Franceschini N,
Gieger C,
Gudnason V,
Hayward C,
Kraft P,
Lawlor DA,
Magnusson PKE,
Martin NG,
Mook-Kanamori DO,
Nohr EA,
Polasek O,
Porteous D,
Price AL,
Ridker PM,
Snieder H,
Spector TD,
Stöckl D,
Toniolo D,
Ulivi S,
Visser JA,
Völzke H,
Wareham NJ,
Wilson JF,
Spurdle AB,
Thorsteindottir U,
Pollard KS,
Easton DF,
Tung JY,
Chang-Claude J,
Hinds D,
Murray A,
Murabito JM,
Stefansson K,
Ong KK,
Perry JRB
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
1 page
Sex specific associations in genome wide association analysis of renal cell carcinoma
Laskar RS,
Muller DC,
Li P,
Machiela MJ,
Ye Y,
Gaborieau V,
Foll M,
Hofmann JN,
Colli L,
Sampson JN,
Wang Z,
Bacq-Daian D
and 96 more — show all
Boland A,
Abedi-Ardekani B,
Durand G,
Le Calvez-Kelm F,
Robinot N,
Blanche H,
Prokhortchouk E,
Skryabin KG,
Burdett L,
Yeager M,
Radojevic-Skodric S,
Savic S,
Foretova L,
Holcatova I,
Janout V,
Mates D,
Rascu S,
Mukeria A,
Zaridze D,
Bencko V,
Cybulski C,
Fabianova E,
Jinga V,
Lissowska J,
Lubinski J,
Navratilova M,
Rudnai P,
Świątkowska B,
Benhamou S,
Cancel-Tassin G,
Cussenot O,
Trichopoulou A,
Riboli E,
Overvad K,
Panico S,
Ljungberg B,
Sitaram RT,
Giles GG,
Milne RL,
Severi G,
Bruinsma F,
Fletcher T,
Koppova K,
Larsson SC,
Wolk A,
Banks RE,
Selby PJ,
Easton DF,
Pharoah P,
Andreotti G,
Beane Freeman LE,
Koutros S,
Albanes D,
Männistö S,
Weinstein S,
Clark PE,
Edwards TL,
Lipworth L,
Carol H,
Freedman ML,
Pomerantz MM,
Cho E,
Kraft P,
Preston MA,
Wilson KM,
Michael Gaziano J,
Sesso HD,
Black A,
Freedman ND,
Huang WY,
Anema JG,
Kahnoski RJ,
Lane BR,
Noyes SL,
Petillo D,
Teh BT,
Peters U,
White E,
Anderson GL,
Johnson L,
Luo J,
Chow WH,
Moore LE,
Choueiri TK,
Wood C,
Johansson M,
McKay JD,
Brown KM,
Rothman N,
Lathrop MG,
Deleuze JF,
Wu X,
Brennan P,
Chanock SJ,
Purdue MP,
Scelo G
European journal of human genetics : EJHG · 2019 · PMID 31231134
1 page
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes
Din L,
Sheikh M,
Kosaraju N,
Smedby KE,
Bernatsky S,
Berndt SI,
Skibola CF,
Nieters A,
Wang S,
McKay JD,
Cocco P,
Maynadié M
and 80 more — show all
Foretová L,
Staines A,
Mack TM,
de Sanjosé S,
Vyse TJ,
Padyukov L,
Monnereau A,
Arslan AA,
Moore A,
Brooks-Wilson AR,
Novak AJ,
Glimelius B,
Birmann BM,
Link BK,
Stewart C,
Vajdic CM,
Haioun C,
Magnani C,
Conti DV,
Cox DG,
Casabonne D,
Albanes D,
Kane E,
Roman E,
Muzi G,
Salles G,
Giles GG,
Adami HO,
Ghesquières H,
De Vivo I,
Clavel J,
Cerhan JR,
Spinelli JJ,
Hofmann J,
Vijai J,
Curtin K,
Costenbader KH,
Onel K,
Offit K,
Teras LR,
Morton L,
Conde L,
Miligi L,
Melbye M,
Ennas MG,
Liebow M,
Purdue MP,
Glenn M,
Southey MC,
Din M,
Rothman N,
Camp NJ,
Wong Doo N,
Becker N,
Pradhan N,
Bracci PM,
Boffetta P,
Vineis P,
Brennan P,
Kraft P,
Lan Q,
Severson RK,
Vermeulen RCH,
Milne RL,
Kaaks R,
Travis RC,
Weinstein SJ,
Chanock SJ,
Ansell SM,
Slager SL,
Zheng T,
Zhang Y,
Benavente Y,
Taub Z,
Madireddy L,
Gourraud PA,
Oksenberg JR,
Cozen W,
Hjalgrim H,
Khankhanian P
Genetic epidemiology · 2019 · PMID 31407831
1 page
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Berndt SI,
Vijai J,
Benavente Y,
Camp NJ,
Nieters A,
Wang Z,
Smedby KE,
Kleinstern G,
Hjalgrim H,
Besson C,
Skibola CF,
Morton LM
and 128 more — show all
Brooks-Wilson AR,
Teras LR,
Breeze C,
Arias J,
Adami HO,
Albanes D,
Anderson KC,
Ansell SM,
Bassig B,
Becker N,
Bhatti P,
Birmann BM,
Boffetta P,
Bracci PM,
Brennan P,
Brown EE,
Burdett L,
Cannon-Albright LA,
Chang ET,
Chiu BCH,
Chung CC,
Clavel J,
Cocco P,
Colditz G,
Conde L,
Conti DV,
Cox DG,
Curtin K,
Casabonne D,
De Vivo I,
Diepstra A,
Diver WR,
Dogan A,
Edlund CK,
Foretova L,
Fraumeni JF Jr,
Gabbas A,
Ghesquières H,
Giles GG,
Glaser S,
Glenn M,
Glimelius B,
Gu J,
Habermann TM,
Haiman CA,
Haioun C,
Hofmann JN,
Holford TR,
Holly EA,
Hutchinson A,
Izhar A,
Jackson RD,
Jarrett RF,
Kaaks R,
Kane E,
Kolonel LN,
Kong Y,
Kraft P,
Kricker A,
Lake A,
Lan Q,
Lawrence C,
Li D,
Liebow M,
Link BK,
Magnani C,
Maynadie M,
McKay J,
Melbye M,
Miligi L,
Milne RL,
Molina TJ,
Monnereau A,
Montalvan R,
North KE,
Novak AJ,
Onel K,
Purdue MP,
Rand KA,
Riboli E,
Riby J,
Roman E,
Salles G,
Sborov DW,
Severson RK,
Shanafelt TD,
Smith MT,
Smith A,
Song KW,
Song L,
Southey MC,
Spinelli JJ,
Staines A,
Stephens D,
Sutherland HJ,
Tkachuk K,
Thompson CA,
Tilly H,
Tinker LF,
Travis RC,
Turner J,
Vachon CM,
Vajdic CM,
Van Den Berg A,
Van Den Berg DJ,
Vermeulen RCH,
Vineis P,
Wang SS,
Weiderpass E,
Weiner GJ,
Weinstein S,
Doo NW,
Ye Y,
Yeager M,
Yu K,
Zeleniuch-Jacquotte A,
Zhang Y,
Zheng T,
Ziv E,
Sampson J,
Chatterjee N,
Offit K,
Cozen W,
Wu X,
Cerhan JR,
Chanock SJ,
Slager SL,
Rothman N
Leukemia · 2022 · PMID 36273105
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.