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2,657 papers hold this site up. Every variant and condition page names
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6 matches for
Irwanto A.
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Michailidou K,
Hall P,
Gonzalez-Neira A,
Ghoussaini M,
Dennis J,
Milne RL,
Schmidt MK,
Chang-Claude J,
Bojesen SE,
Bolla MK,
Wang Q,
Dicks E
and 208 more — show all
Lee A,
Turnbull C,
Rahman N,
Fletcher O,
Peto J,
Gibson L,
Dos Santos Silva I,
Nevanlinna H,
Muranen TA,
Aittomäki K,
Blomqvist C,
Czene K,
Irwanto A,
Liu J,
Waisfisz Q,
Meijers-Heijboer H,
Adank M,
van der Luijt RB,
Hein R,
Dahmen N,
Beckman L,
Meindl A,
Schmutzler RK,
Müller-Myhsok B,
Lichtner P,
Hopper JL,
Southey MC,
Makalic E,
Schmidt DF,
Uitterlinden AG,
Hofman A,
Hunter DJ,
Chanock SJ,
Vincent D,
Bacot F,
Tessier DC,
Canisius S,
Wessels LF,
Haiman CA,
Shah M,
Luben R,
Brown J,
Luccarini C,
Schoof N,
Humphreys K,
Li J,
Nordestgaard BG,
Nielsen SF,
Flyger H,
Couch FJ,
Wang X,
Vachon C,
Stevens KN,
Lambrechts D,
Moisse M,
Paridaens R,
Christiaens MR,
Rudolph A,
Nickels S,
Flesch-Janys D,
Johnson N,
Aitken Z,
Aaltonen K,
Heikkinen T,
Broeks A,
Veer LJ,
van der Schoot CE,
Guénel P,
Truong T,
Laurent-Puig P,
Menegaux F,
Marme F,
Schneeweiss A,
Sohn C,
Burwinkel B,
Zamora MP,
Perez JI,
Pita G,
Alonso MR,
Cox A,
Brock IW,
Cross SS,
Reed MW,
Sawyer EJ,
Tomlinson I,
Kerin MJ,
Miller N,
Henderson BE,
Schumacher F,
Le Marchand L,
Andrulis IL,
Knight JA,
Glendon G,
Mulligan AM,
Lindblom A,
Margolin S,
Hooning MJ,
Hollestelle A,
van den Ouweland AM,
Jager A,
Bui QM,
Stone J,
Dite GS,
Apicella C,
Tsimiklis H,
Giles GG,
Severi G,
Baglietto L,
Fasching PA,
Haeberle L,
Ekici AB,
Beckmann MW,
Brenner H,
Müller H,
Arndt V,
Stegmaier C,
Swerdlow A,
Ashworth A,
Orr N,
Jones M,
Figueroa J,
Lissowska J,
Brinton L,
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,
Bonanni B,
Devilee P,
Tollenaar RA,
Seynaeve C,
van Asperen CJ,
Jakubowska A,
Lubinski J,
Jaworska K,
Durda K,
Mannermaa A,
Kataja V,
Kosma VM,
Hartikainen JM,
Bogdanova NV,
Antonenkova NN,
Dörk T,
Kristensen VN,
Anton-Culver H,
Slager S,
Toland AE,
Edge S,
Fostira F,
Kang D,
Yoo KY,
Noh DY,
Matsuo K,
Ito H,
Iwata H,
Sueta A,
Wu AH,
Tseng CC,
Van Den Berg D,
Stram DO,
Shu XO,
Lu W,
Gao YT,
Cai H,
Teo SH,
Yip CH,
Phuah SY,
Cornes BK,
Hartman M,
Miao H,
Lim WY,
Sng JH,
Muir K,
Lophatananon A,
Stewart-Brown S,
Siriwanarangsan P,
Shen CY,
Hsiung CN,
Wu PE,
Ding SL,
Sangrajrang S,
Gaborieau V,
Brennan P,
McKay J,
Blot WJ,
Signorello LB,
Cai Q,
Zheng W,
Zheng W,
Deming-Halverson S,
Shrubsole M,
Long J,
Simard J,
Garcia-Closas M,
Pharoah PD,
Chenevix-Trench G,
Dunning AM,
Benitez J,
Easton DF
Breast and Ovarian Cancer Susceptibility Collaboration · Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON) and 3 more consortia
Nature genetics · 2013 · PMID 23535729
12 pages+
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
Fehringer G,
Kraft P,
Pharoah PD,
Eeles RA,
Chatterjee N,
Schumacher FR,
Schildkraut JM,
Lindström S,
Brennan P,
Bickeböller H,
Houlston RS,
Landi MT
and 121 more — show all
Caporaso N,
Risch A,
Amin Al Olama A,
Berndt SI,
Giovannucci EL,
Grönberg H,
Kote-Jarai Z,
Ma J,
Muir K,
Stampfer MJ,
Stevens VL,
Wiklund F,
Willett WC,
Goode EL,
Permuth JB,
Risch HA,
Reid BM,
Bezieau S,
Brenner H,
Chan AT,
Chang-Claude J,
Hudson TJ,
Kocarnik JK,
Newcomb PA,
Schoen RE,
Slattery ML,
White E,
Adank MA,
Ahsan H,
Aittomäki K,
Baglietto L,
Blomquist C,
Canzian F,
Czene K,
Dos-Santos-Silva I,
Eliassen AH,
Figueroa JD,
Flesch-Janys D,
Fletcher O,
Garcia-Closas M,
Gaudet MM,
Johnson N,
Hall P,
Hazra A,
Hein R,
Hofman A,
Hopper JL,
Irwanto A,
Johansson M,
Kaaks R,
Kibriya MG,
Lichtner P,
Liu J,
Lund E,
Makalic E,
Meindl A,
Müller-Myhsok B,
Muranen TA,
Nevanlinna H,
Peeters PH,
Peto J,
Prentice RL,
Rahman N,
Sanchez MJ,
Schmidt DF,
Schmutzler RK,
Southey MC,
Tamimi R,
Travis RC,
Turnbull C,
Uitterlinden AG,
Wang Z,
Whittemore AS,
Yang XR,
Zheng W,
Zheng W,
Buchanan DD,
Casey G,
Conti DV,
Edlund CK,
Gallinger S,
Haile RW,
Jenkins M,
Le Marchand L,
Li L,
Lindor NM,
Schmit SL,
Thibodeau SN,
Woods MO,
Rafnar T,
Gudmundsson J,
Stacey SN,
Stefansson K,
Sulem P,
Chen YA,
Tyrer JP,
Christiani DC,
Wei Y,
Shen H,
Hu Z,
Shu XO,
Shiraishi K,
Takahashi A,
Bossé Y,
Obeidat M,
Nickle D,
Timens W,
Freedman ML,
Li Q,
Seminara D,
Chanock SJ,
Gong J,
Peters U,
Gruber SB,
Amos CI,
Sellers TA,
Easton DF,
Hunter DJ,
Haiman CA,
Henderson BE,
Hung RJ
Ovarian Cancer Association Consortium (OCAC) · PRACTICAL Consortium and 3 more consortia
Cancer research · 2016 · PMID 27197191
6 pages
Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy
Liu H,
Irwanto A,
Fu X,
Yu G,
Yu Y,
Sun Y,
Wang C,
Wang Z,
Okada Y,
Low H,
Li Y,
Liany H
and 20 more — show all
Chen M,
Bao F,
Li J,
You J,
Zhang Q,
Liu J,
Chu T,
Andiappan AK,
Wang N,
Niu G,
Liu D,
Yu X,
Zhang L,
Tian H,
Zhou G,
Rotzschke O,
Chen S,
Zhang X,
Liu J,
Zhang F
Nature genetics · 2015 · PMID 25642632
5 pages
A large-scale genome-wide association and meta-analysis identified four novel susceptibility loci for leprosy
Wang Z,
Sun Y,
Fu X,
Yu G,
Wang C,
Bao F,
Yue Z,
Li J,
Sun L,
Irwanto A,
Yu Y,
Chen M
and 21 more — show all
Mi Z,
Wang H,
Huai P,
Li Y,
Du T,
Yu W,
Xia Y,
Xiao H,
You J,
Li J,
Yang Q,
Wang N,
Shang P,
Niu G,
Chi X,
Wang X,
Cao J,
Cheng X,
Liu H,
Liu J,
Zhang F
Nature communications · 2016 · PMID 27976721 · open access
3 pages
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
Haiman CA,
Chen GK,
Vachon CM,
Canzian F,
Dunning A,
Millikan RC,
Wang X,
Ademuyiwa F,
Ahmed S,
Ambrosone CB,
Baglietto L,
Balleine R
and 119 more — show all
Bandera EV,
Beckmann MW,
Berg CD,
Bernstein L,
Blomqvist C,
Blot WJ,
Brauch H,
Buring JE,
Carey LA,
Carpenter JE,
Chang-Claude J,
Chanock SJ,
Chasman DI,
Clarke CL,
Cox A,
Cross SS,
Deming SL,
Diasio RB,
Dimopoulos AM,
Driver WR,
Dünnebier T,
Durcan L,
Eccles D,
Edlund CK,
Ekici AB,
Fasching PA,
Feigelson HS,
Flesch-Janys D,
Fostira F,
Försti A,
Fountzilas G,
Gerty SM,
Giles GG,
Godwin AK,
Goodfellow P,
Graham N,
Greco D,
Hamann U,
Hankinson SE,
Hartmann A,
Hein R,
Heinz J,
Holbrook A,
Hoover RN,
Hu JJ,
Hunter DJ,
Ingles SA,
Irwanto A,
Ivanovich J,
John EM,
Johnson N,
Jukkola-Vuorinen A,
Kaaks R,
Ko YD,
Kolonel LN,
Konstantopoulou I,
Kosma VM,
Kulkarni S,
Lambrechts D,
Lee AM,
Marchand LL,
Lesnick T,
Liu J,
Lindstrom S,
Mannermaa A,
Margolin S,
Martin NG,
Miron P,
Montgomery GW,
Nevanlinna H,
Nickels S,
Nyante S,
Olswold C,
Palmer J,
Pathak H,
Pectasides D,
Perou CM,
Peto J,
Pharoah PD,
Pooler LC,
Press MF,
Pylkäs K,
Rebbeck TR,
Rodriguez-Gil JL,
Rosenberg L,
Ross E,
Rüdiger T,
Silva Idos S,
Sawyer E,
Schmidt MK,
Schulz-Wendtland R,
Schumacher F,
Severi G,
Sheng X,
Signorello LB,
Sinn HP,
Stevens KN,
Southey MC,
Tapper WJ,
Tomlinson I,
Hogervorst FB,
Wauters E,
Weaver J,
Wildiers H,
Winqvist R,
Van Den Berg D,
Wan P,
Xia LY,
Yannoukakos D,
Zheng W,
Zheng W,
Ziegler RG,
Siddiq A,
Slager SL,
Stram DO,
Easton D,
Kraft P,
Henderson BE,
Couch FJ
Gene Environment Interaction and Breast Cancer in Germany (GENICA) Consortium
Nature genetics · 2011 · PMID 22037553
1 page
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
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.