Items where authors include "Zheng, W."

Article

Siebert, M.R. orcid.org/0000-0003-2445-3891, Kwok, L.A. orcid.org/0000-0003-3108-1328, Johansson, J. orcid.org/0000-0001-5975-290X et al. (79 more authors) (2023) Ground-based and JWST observations of SN 2022pul. I. Unusual signatures of carbon, oxygen, and circumstellar interaction in a peculiar type Ia supernova. The Astrophysical Journal, 960 (1). 88. ISSN 0004-637X

Ho, A.Y.Q., Perley, D.A., Chen, P. et al. (74 more authors) (2023) Minutes-duration optical flares with supernova luminosities. Nature. ISSN 0028-0836

Wichert, K. orcid.org/0000-0001-7708-7843, Hoppe, R., Ickstadt, K. et al. (45 more authors) (2023) Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer. European Journal of Epidemiology, 38. pp. 1053-1068. ISSN 0393-2990

Thomas, M. orcid.org/0000-0001-9337-7015, Su, Y.-R., Rosenthal, E.A. orcid.org/0000-0001-6042-4487 et al. (126 more authors) (2023) Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations. Nature Communications, 14. 6147. ISSN 2041-1723

Middha, P., Wang, X., Behrens, S. et al. (129 more authors) (2023) A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry. Breast Cancer Research, 25. 93.

Levi, H., Carmi, S., Rosset, S. et al. (135 more authors) (2023) Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel. Journal of Medical Genetics. ISSN 0022-2593

Shi, J. orcid.org/0000-0001-8606-4707, Shiraishi, K. orcid.org/0000-0002-5821-7400, Choi, J. orcid.org/0000-0002-0955-2384 et al. (219 more authors) (2023) Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population. Nature Communications, 14 (1). 3043. ISSN 2041-1723

Dixon-Suen, S.C. orcid.org/0000-0003-3714-8386, Lewis, S.J., Martin, R.M. et al. (155 more authors) (2022) Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study. British Journal of Sports Medicine, 56 (20). pp. 1157-1170. ISSN 0306-3674

Perley, D.A., Sollerman, J., Schulze, S. et al. (32 more authors) (2022) The type Icn SN 2021csp: implications for the origins of the fastest supernovae and the fates of Wolf–Rayet stars. The Astrophysical Journal, 927 (2). 180. ISSN 0004-637X

Patra, K.C., Yang (杨轶), Y., Brink, T.G. et al. (12 more authors) (2022) Spectropolarimetry of the Type Ia SN 2019ein rules out significant global asphericity of the ejecta. Monthly Notices of the Royal Astronomical Society, 509 (3). pp. 4058-4070. ISSN 0035-8711

Dyk, S.D.V., Zheng, W., Maund, J.R. et al. (31 more authors) (2019) The type II-plateau supernova 2017eaw in NGC 6946 and its red supergiant progenitor. Astrophysical Journal, 875 (2). 136. ISSN 0004-637X

O'Mara, T.A. orcid.org/0000-0002-5436-3232, Glubb, D.M. orcid.org/0000-0002-2184-7708, Amant, F. et al. (122 more authors) (2018) Identification of nine new susceptibility loci for endometrial cancer. Nature Communications, 9. 3166.

Wu, L., Shi, W., Long, J. et al. (3 more authors) (2018) A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer. Nature Genetics, 50. pp. 968-978. ISSN 1061-4036

Martynov, S., Zheng, W., Mahgerefteh, H. et al. (4 more authors) (2018) Computational and experimental study of solid phase formation during the decompression of high-pressure CO2 pipelines. Industrial & Engineering Chemistry Research, 57 (20). pp. 7054-7063. ISSN 0888-5885

Colombo, M., Lopez-Perolio, I., Meeks, H.D. et al. (112 more authors) (2018) The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity. Human Mutation, 39 (5). pp. 729-741. ISSN 1059-7794

Guo, Q., Burgess, S., Turman, C. et al. (132 more authors) (2017) Body mass index and breast cancer survival: a Mendelian randomization analysis. International Journal of Epidemiology, 46 (6). pp. 1814-1822. ISSN 0300-5771

Jiao, X., Aravidis, C., Marikkannu, R. et al. (103 more authors) (2017) PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1. Oncotarget, 8. pp. 102769-102782. ISSN 1949-2553

Zheng, W., Mahgerefteh, H., Martynov, S. et al. (1 more author) (2017) Modeling of CO2 Decompression across the Triple Point. Industrial & Engineering Chemistry Research, 56 (37). pp. 10491-10499. ISSN 0888-5885

Shimelis, H., Mesman, R.L.S., Von Nicolai, C. et al. (130 more authors) (2017) BRCA2 hypomorphic missense variants confer moderate risks of breast cancer. Cancer Research, 77 (11). pp. 2789-2799. ISSN 0008-5472

Ghoussaini, M, French, J.D., Michailidou, K. et al. (122 more authors) (2016) Evidence that the 5p12 variant rs10941679 confers susceptibility to estrogen receptor positive breast cancer through FGF10 and MRPS30 regulation. American Journal of Human Genetics, 99 (4). pp. 903-911. ISSN 0002-9297

Shi, J., Zhang, Y., Zheng, W. et al. (125 more authors) (2016) Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer. International Journal of Cancer, 139 (6). pp. 1303-1317. ISSN 0020-7136

Darabi, H., Beesley, J., Droit, A. et al. (111 more authors) (2016) Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs). Scientific Reports, 6. p. 32512. ISSN 2045-2322

Horne, H.N., Chung, C.E., Zhang, H. et al. (112 more authors) (2016) Fine-mapping of the 1p11.2 breast cancer susceptibility locus. PLoS One, 11 (8). e0160316. ISSN 1932-6203

Guo, Y., Warren Andersen, S., Shu, X.O. et al. (108 more authors) (2016) Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent. PLoS Medicine, 13 (8). e1002105. ISSN 1549-1277

Wyszynski, A., Hong, C.C., Lam, K. et al. (107 more authors) (2016) An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression. Human Molecular Genetics , 25 (17). pp. 3863-3876. ISSN 0964-6906

Zeng, C., Guo, X., Long, J. et al. (234 more authors) (2016) Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus. Breast Cancer Research, 18 (1). 64. ISSN 1465-542X

Zheng, W., Mahgerefteh, H., Brown, S. orcid.org/0000-0001-8229-8004 et al. (1 more author) (2016) Integral Multiphase Turbulence Compressible Jet Expansion Model for Accidental Releases from Pressurized Containments. Industrial & Engineering Chemistry Research, 55 (27). pp. 7558-7568. ISSN 0888-5885

Hierons, R.M. orcid.org/0000-0002-4771-1446, Li, M., Liu, X. et al. (2 more authors) (2016) SIP: Optimal Product Selection from Feature Models Using Many-Objective Evolutionary Optimization. ACM Transactions on Software Engineering and Methodology, 25 (2). 17. ISSN 1049-331X

Hollestelle, A., van der Baan, F.H., Berchuck, A. et al. (355 more authors) (2016) No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer. Gynecologic Oncology, 141 (2). pp. 386-401. ISSN 0090-8258

Zhao, Z., Wen, W., Michailidou, K. et al. (115 more authors) (2016) Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry. Cancer Causes and Control. pp. 1-15. ISSN 0957-5243

Dunning, A.M., Michailidou, K., Kuchenbaecker, K.B. et al. (245 more authors) (2016) Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170. Nature Genetics. ISSN 1061-4036

Easton, D.F., Lesueur, F., Decker, B. et al. (126 more authors) (2016) No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. Journal of Medical Genetics . ISSN 0022-2593

Lei, J., Rudolph, A., Moysich, K.B. et al. (67 more authors) (2016) Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium. Human Genetics, 135 (1). pp. 137-154. ISSN 0340-6717

Hamdi, Y., Soucy, P., Adoue, V. et al. (93 more authors) (2016) Association of Breast Cancer Risk with Genetic Variants Showing Differential Allelic Expression: Identification of a Novel Breast Cancer Susceptibility Locus at 4q21. Oncotarget, 7. pp. 80140-80163. ISSN 1949-2553

Guo, X., Long, J., Zeng, C. et al. (112 more authors) (2015) Fine-Scale Mapping of the 4q24 Locus Identifies Two Independent Loci Associated with Breast Cancer Risk. Cancer Epidemiology, Biomarkers and Prevention, 24 (11). pp. 1680-1691. ISSN 1055-9965

Orr, N., Dudbridge, F., Dryden, N. et al. (213 more authors) (2015) Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2. Human Molecular Genetics, 24 (10). 2966 - 2984. ISSN 0964-6906

Mavaddat, N., Pharoah, P.D.P., Michailidou, K. et al. (209 more authors) (2015) Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants. JNCI-Journal of the National Cancer Institute, 107 (5). ISSN 0027-8874

Michailidou, K., Beesley, J., Lindstrom, S. et al. (245 more authors) (2015) Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. Nature Genetics, 47. pp. 373-380. ISSN 1061-4036

Painter, J.N., O'Mara, T.A., Batra, J. et al. (116 more authors) (2015) Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics, 24 (5). pp. 1478-1492. ISSN 0964-6906

Milne, R.L., Burwinkel, B., Michailidou, K. et al. (178 more authors) (2014) Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium. Human Molecular Genetics, 23 (22). pp. 6096-6111. ISSN 0964-6906

Ng, M.C.Y., Shriner, D., Chen, B.H. et al. (83 more authors) (2014) Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes. PLoS Genetics, 10 (8). e1004517. ISSN 1553-7390

Johnson, N., Dudbridge, F., Orr, N. et al. (182 more authors) (2014) Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study. Breast Cancer Research , 16 (3). R51. ISSN 1465-5411

Agarwal, D., Pineda, S., Michailidou, K. et al. (179 more authors) (2014) FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium. British Journal of Cancer, 110 (4). pp. 1088-1100. ISSN 0007-0920

Zheng, W., Su, T., Zhang, H. et al. (3 more authors) (2013) Distributed power optimization for spectrum-sharing femtocell networks: A fictitious game approach. Journal of Network and Computer Applications, 37. pp. 315-322. ISSN 1084-8045

Zheng, W., Zhang, H., Chu, X. et al. (1 more author) (2013) Mobility robustness optimization in self-organizing LTE femtocell networks. EURASIP Journal on Wireless Communications and Networking (EURASIP JWCN), 27. ISSN 1687-1472

Proceedings Paper

Zhang, H., Zheng, W., Wen, X. et al. (1 more author) (2012) Interference-aware resource allocation in co-channel deployment of OFDMA femtocells. In: IEEE International Conference on Communications. Communications (ICC), 2012 IEEE International Conference on , 10-15 Jun 2012, Ottawa, ON . , 4663 - 4667. ISBN 978-1-4577-2052-9

Zhang, H., Zheng, W., Wen, X. et al. (4 more authors) (2012) Joint subchannel and power allocation in interference-limited OFDMA femtocells with heterogeneous QoS guarantee. In: GLOBECOM - IEEE Global Telecommunications Conference. Global Communications Conference (GLOBECOM), 2012 IEEE , 03-07 Dec 2012, Anaheim, CA . , 4572 - 4577. ISBN 978-1-4673-0920-2

Zhang, H., Zheng, W., Wen, X. et al. (3 more authors) (2012) Secure resource allocation for OFDMA two-way relay networks. In: GLOBECOM - IEEE Global Telecommunications Conference. Global Communications Conference (GLOBECOM), 2012 IEEE , 03-07 Dec 2012, Anaheim, CA . , 3649 - 3654.