Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer (English)
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In:
Nature Genetics
;
41
, 9
;
986-990
;
2009
-
ISSN:
- Article (Journal) / Electronic Resource
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Title:Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
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Contributors:Amundadottir, Laufey ( author ) / Kraft, Peter ( author ) / Stolzenberg-Solomon, Rachael Z ( author ) / Fuchs, Charles S ( author ) / Petersen, Gloria M ( author ) / Arslan, Alan A ( author ) / Bueno-de-Mesquita, H Bas ( author ) / Gross, Myron ( author ) / Helzlsouer, Kathy ( author ) / Jacobs, Eric J ( author )
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Published in:Nature Genetics ; 41, 9 ; 986-990
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Publisher:
- New search for: Nature Publishing Group
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Publication date:2009-09-01
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Size:5 pages
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ISSN:
-
DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 41, Issue 9
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 953
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Twelve lords a-leaping| 2009
- 954
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CLCN2 variants in idiopathic generalized epilepsyKleefuß-Lie, Ailing / Friedl, Waltraut / Cichon, Sven / Haug, Karsten / Warnstedt, Maike / Alekov, Alexi / Sander, Thomas / Ramirez, Alfredo / Poser, Barbara / Maljevic, Snezana et al. | 2009
- 957
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Inherited susceptibility to pediatric acute lymphoblastic leukemiaLevine, Ross L et al. | 2009
- 958
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Closing the gap between genotype and phenotypeGregersen, Peter K et al. | 2009
- 960
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An uphill battle toward pluripotencyGraf, Thomas et al. | 2009
- 962
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Research Highlights| 2009
- 965
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Genomic privacy and limits of individual detection in a poolSankararaman, Sriram / Obozinski, Guillaume / Jordan, Michael I / Halperin, Eran et al. | 2009
- 968
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Differentiation stage determines potential of hematopoietic cells for reprogramming into induced pluripotent stem cellsEminli, Sarah / Foudi, Adlen / Stadtfeld, Matthias / Maherali, Nimet / Ahfeldt, Tim / Mostoslavsky, Gustavo / Hock, Hanno / Hochedlinger, Konrad et al. | 2009
- 977
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Posterior malformations in Dact1 mutant mice arise through misregulated Vangl2 at the primitive streakSuriben, Rowena / Kivimäe, Saul / Fisher, Daniel A C / Moon, Randall T / Cheyette, Benjamin N R et al. | 2009
- 986
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Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancerAmundadottir, Laufey / Kraft, Peter / Stolzenberg-Solomon, Rachael Z / Fuchs, Charles S / Petersen, Gloria M / Arslan, Alan A / Bueno-de-Mesquita, H Bas / Gross, Myron / Helzlsouer, Kathy / Jacobs, Eric J et al. | 2009
- 991
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Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancerWu, Xifeng / Ye, Yuanqing / Kiemeney, Lambertus A / Sulem, Patrick / Rafnar, Thorunn / Matullo, Giuseppe / Seminara, Daniela / Yoshida, Teruhiko / Saeki, Norihisa / Andrew, Angeline S et al. | 2009
- 996
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A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2Song, Honglin / Ramus, Susan J / Tyrer, Jonathan / Bolton, Kelly L / Gentry-Maharaj, Aleksandra / Wozniak, Eva / Anton-Culver, Hoda / Chang-Claude, Jenny / Cramer, Daniel W / DiCioccio, Richard et al. | 2009
- 1001
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Germline genomic variants associated with childhood acute lymphoblastic leukemiaTreviño, Lisa R / Yang, Wenjian / French, Deborah / Hunger, Stephen P / Carroll, William L / Devidas, Meenakshi / Willman, Cheryl / Neale, Geoffrey / Downing, James / Raimondi, Susana C et al. | 2009
- 1006
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Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemiaPapaemmanuil, Elli / Hosking, Fay J / Vijayakrishnan, Jayaram / Price, Amy / Olver, Bianca / Sheridan, Eammon / Kinsey, Sally E / Lightfoot, Tracy / Roman, Eve / Irving, Julie A E et al. | 2009
- 1011
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Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresourceDendrou, Calliope A / Plagnol, Vincent / Fung, Erik / Yang, Jennie H M / Downes, Kate / Cooper, Jason D / Nutland, Sarah / Coleman, Gillian / Himsworth, Matthew / Hardy, Matthew et al. | 2009
- 1016
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Mutations in PYCR1 cause cutis laxa with progeroid featuresReversade, Bruno / Escande-Beillard, Nathalie / Dimopoulou, Aikaterini / Fischer, Björn / Chng, Serene C / Li, Yun / Shboul, Mohammad / Tham, Puay-Yoke / Kayserili, Hülya / Al-Gazali, Lihadh et al. | 2009
- 1022
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Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hairCordeddu, Viviana / Di Schiavi, Elia / Pennacchio, Len A / Ma'ayan, Avi / Sarkozy, Anna / Fodale, Valentina / Cecchetti, Serena / Cardinale, Alessio / Martin, Joel / Schackwitz, Wendy et al. | 2009
- 1027
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INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouseJacoby, Monique / Cox, James J / Gayral, Stéphanie / Hampshire, Daniel J / Ayub, Mohammed / Blockmans, Marianne / Pernot, Eileen / Kisseleva, Marina V / Compère, Philippe / Schiffmann, Serge N et al. | 2009
- 1032
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Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathiesBielas, Stephanie L / Silhavy, Jennifer L / Brancati, Francesco / Kisseleva, Marina V / Al-Gazali, Lihadh / Sztriha, Laszlo / Bayoumi, Riad A / Zaki, Maha S / Abdel-Aleem, Alice / Rosti, Rasim Ozgur et al. | 2009
- 1037
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FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformationAldinger, Kimberly A / Lehmann, Ordan J / Hudgins, Louanne / Chizhikov, Victor V / Bassuk, Alexander G / Ades, Lesley C / Krantz, Ian D / Dobyns, William B / Millen, Kathleen J et al. | 2009