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6 matches for
Lund E.
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+
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
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
Saevarsdottir S,
Stefansdottir L,
Sulem P,
Thorleifsson G,
Ferkingstad E,
Rutsdottir G,
Glintborg B,
Westerlind H,
Grondal G,
Loft IC,
Sorensen SB,
Lie BA
and 66 more — show all
Brink M,
Ärlestig L,
Arnthorsson AO,
Baecklund E,
Banasik K,
Bank S,
Bjorkman LI,
Ellingsen T,
Erikstrup C,
Frei O,
Gjertsson I,
Gudbjartsson DF,
Gudjonsson SA,
Halldorsson GH,
Hendricks O,
Hillert J,
Hogdall E,
Jacobsen S,
Jensen DV,
Jonsson H,
Kastbom A,
Kockum I,
Kristensen S,
Kristjansdottir H,
Larsen MH,
Linauskas A,
Hauge EM,
Loft AG,
Ludviksson BR,
Lund SH,
Markusson T,
Masson G,
Melsted P,
Moore KHS,
Munk H,
Nielsen KR,
Norddahl GL,
Oddsson A,
Olafsdottir TA,
Olason PI,
Olsson T,
Ostrowski SR,
Hørslev-Petersen K,
Rognvaldsson S,
Sanner H,
Silberberg GN,
Stefansson H,
Sørensen E,
Sørensen IJ,
Turesson C,
Bergman T,
Alfredsson L,
Kvien TK,
Brunak S,
Steinsson K,
Andersen V,
Andreassen OA,
Rantapää-Dahlqvist S,
Hetland ML,
Klareskog L,
Askling J,
Padyukov L,
Pedersen OB,
Thorsteinsdottir U,
Jonsdottir I,
Stefansson K
Members of the DBDS Genomic Consortium · Danish RA Genetics Working Group and 1 more consortia
Annals of the rheumatic diseases · 2022 · PMID 35470158 · open access
3 pages
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
Hung RJ,
McKay JD,
Gaborieau V,
Boffetta P,
Hashibe M,
Zaridze D,
Mukeria A,
Szeszenia-Dabrowska N,
Lissowska J,
Rudnai P,
Fabianova E,
Mates D
and 53 more — show all
Bencko V,
Foretova L,
Janout V,
Chen C,
Goodman G,
Field JK,
Liloglou T,
Xinarianos G,
Cassidy A,
McLaughlin J,
Liu G,
Narod S,
Krokan HE,
Skorpen F,
Elvestad MB,
Hveem K,
Vatten L,
Linseisen J,
Clavel-Chapelon F,
Vineis P,
Bueno-de-Mesquita HB,
Lund E,
Martinez C,
Bingham S,
Rasmuson T,
Hainaut P,
Riboli E,
Ahrens W,
Benhamou S,
Lagiou P,
Trichopoulos D,
Holcátová I,
Merletti F,
Kjaerheim K,
Agudo A,
Macfarlane G,
Talamini R,
Simonato L,
Lowry R,
Conway DI,
Znaor A,
Healy C,
Zelenika D,
Boland A,
Delepine M,
Foglio M,
Lechner D,
Matsuda F,
Blanche H,
Gut I,
Heath S,
Lathrop M,
Brennan P
Nature · 2008 · PMID 18385738
2 pages
Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis
Lotta LA,
Scott RA,
Sharp SJ,
Burgess S,
Luan J,
Tillin T,
Schmidt AF,
Imamura F,
Stewart ID,
Perry JR,
Marney L,
Koulman A
and 16 more — show all
Karoly ED,
Forouhi NG,
Sjögren RJ,
Näslund E,
Zierath JR,
Krook A,
Savage DB,
Griffin JL,
Chaturvedi N,
Hingorani AD,
Khaw KT,
Barroso I,
McCarthy MI,
O'Rahilly S,
Wareham NJ,
Langenberg C
PLoS medicine · 2016 · PMID 27898682 · open access
2 pages
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
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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?
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