Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Kimberly A Zuhlke"'
Autor:
Ethan M Lange, Anna M Johnson, Yunfei Wang, Kimberly A Zuhlke, Yurong Lu, Jessica V Ribado, Gregory R Keele, Jin Li, Qing Duan, Ge Li, Zhengrong Gao, Yun Li, Jianfeng Xu, William B Isaacs, Siqun Zheng, Kathleen A Cooney
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e93436 (2014)
Prostate cancer is the most common non-skin cancer and the second leading cause of cancer related mortality for men in the United States. There is strong empirical and epidemiological evidence supporting a stronger role of genetics in early-onset pro
Externí odkaz:
https://doaj.org/article/98d573dd13d54d61b2bd7817179e867d
Autor:
Anna Johnson, Daniel R. Liesman, Kimberly A. Zuhlke, Kathleen A. Cooney, Jennifer L. Beebe-Dimmer
Publikováno v:
The Prostate. 78(5)
BACKGROUND: African Americans have both a higher incidence of prostate cancer and greater disease-specific mortality compared with non-Hispanic whites. Historically, the investigation of the contribution of rare genetic variants to prostate cancer in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab4740d5bcf9410b2a16ec9502216117
https://pubmed.ncbi.nlm.nih.gov/29356034
https://pubmed.ncbi.nlm.nih.gov/29356034
Autor:
Kimberly A. Zuhlke, Anna Johnson, Shannon K. McDonnell, Daniel J. Schaid, Chris Plotts, Shaun M. Riska, Kathleen A. Cooney, Julie A. Douglas, Stephen N. Thibodeau, Sumit Middha
Publikováno v:
The Prostate. 74:1371-1378
BACKGROUND Family history is a major risk factor for prostate cancer (PCa), suggesting a genetic component to the disease. However, traditional linkage and association studies have failed to fully elucidate the underlying genetic basis of familial PC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac9cdcb3e6e54ddc12d30cf7c7c08ccd
https://doi.org/10.1002/pros.22849
https://doi.org/10.1002/pros.22849
Autor:
Kimberly A. Zuhlke, Scott A. Tomlins, John D. Carpten, Kathleen A. Cooney, Nallasivam Palanisamy, Anna Johnson, William B. Isaacs, Ethan M. Lange
Publikováno v:
The Prostate. 74:983-990
BACKGROUND Family history of prostate cancer is a well-recognized risk factor. Previous linkage studies have reported a putative prostate cancer susceptibility locus at chromosome 17q21–22. SPOP (Speckle-type POZ protein) maps to the 17q21–22 can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5f2690f6db4c57cc45ebd0a95bca62c
https://doi.org/10.1002/pros.22818
https://doi.org/10.1002/pros.22818
Autor:
Javed Siddiqui, Arul M. Chinnaiyan, Anna Johnson, Steven C. Smith, Nallasivam Palanisamy, Kathleen A. Cooney, Scott A. Tomlins, Lakshmi P. Kunju, Kimberly A. Zuhlke
Publikováno v:
American Journal of Surgical Pathology. 38:615-626
Recent genetic epidemiologic studies identified a germline mutation in the homeobox transcription factor, HOXB13 G84E, which is associated with markedly increased risk for prostate cancer, particularly early-onset hereditary prostate cancer. The hist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdb216888925b3aefb53b6fc8e81927f
https://doi.org/10.1097/pas.0000000000000090
https://doi.org/10.1097/pas.0000000000000090
Autor:
Anna Johnson, James E. Montie, William B. Isaacs, Kathleen A. Cooney, Kimberly A. Zuhlke, Charles E. Ewing, Cecilia Yee, Elizabeth B. Humphreys, Sarah D. Isaacs, Jennifer L. Beebe-Dimmer, Patrick C. Walsh, Wasim H. Chowdhury
Publikováno v:
BJU International. 113:830-835
Objective To determine the prevalence and clinical correlates of the G84E mutation in the homeobox transcription factor, or HOXB13, gene using DNA samples from 9559 men with prostate cancer undergoing radical prostatectomy. Patients and Methods DNA s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f60d072b7b638cc6cd2752cac2e56ecd
https://doi.org/10.1111/bju.12522
https://doi.org/10.1111/bju.12522
Autor:
Craig C. Teerlink, Christiane Maier, Graham G. Giles, Jianfeng Xu, Douglas F. Easton, Kathleen E. Wiley, Christophe Egrot, William J. Catalona, John D. Carpten, Zsofia Kote-Jarai, Stephen N. Thibodeau, Fredrik Wiklund, Kimberly A. Zuhlke, Nicola J. Camp, Guangfu Jin, Tiina Wahlfors, Michelle Guy, Elaine A. Ostrander, Johanna Schleutker, S. Lilly Zheng, Ros Eeles, Teuvo L.J. Tammela, Monica Emanuelsson, Lisa A. Cannon-Albright, Sarah D. Isaacs, John L. Hopper, Walther Vogel, Ethan M. Lange, Patrick C. Walsh, Antje E. Rinckleb, William D. Foulkes, Lingyi Lu, Ingrid Oakley-Girvan, Geraldine Cancel-Tassin, Daniel J. Schaid, Olivier Cussenot, William B. Isaacs, Liesel M. FitzGerald, Alice S. Whittemore, Kathleen A. Cooney, Shannon K. McDonnell, Gianluca Severi, Joan E. Bailey-Wilson, Janet L. Stanford, Chih-Lin Hsieh, Anna M. Ray, Henrik Grönberg
Publikováno v:
Human Genetics. 133:347-356
Previous GWAS studies have reported significant associations between various common SNPs and prostate cancer risk using cases unselected for family history. How these variants influence risk in familial prostate cancer is not well studied. Here, we a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b102cbee2190b227efec5f354dde2ea
https://doi.org/10.1007/s00439-013-1384-2
https://doi.org/10.1007/s00439-013-1384-2
Autor:
Nicola J. Camp, Ros Eeles, Graham G. Giles, Kathleen E. Wiley, Kimberly A. Zuhlke, Gianluca Severi, Johanna Schleutker, Henrik Grönberg, Doug Easton, Stephen N. Thibodeau, Sarah D. Isaacs, William J. Catalona, Fredrik Wiklund, Melissa S. DeRycke, Craig C. Teerlink, Walther Vogel, Lisa A. Cannon-Albright, Manuel Luedeke, Siqun L. Zheng, Alice S. Whittemore, Teuvo L.J. Tammela, Olivier Cussenot, Joan E. Bailey-Wilson, Chih-Lin Hsieh, Isaac J. Powell, William B. Isaacs, Pål Møller, Shannon K. McDonnell, Elaine A. Ostrander, Ethan M. Lange, Nancy Hamel, Anna Johnson, Patrick C. Walsh, Tiina Wahlfors, Lovise Mahle, John L. Hopper, Diptasri Mandal, William D. Foulkes, Zsofia Kote-Jarai, Elisa M. Ledet, Christiane Maier, Daniel J. Schaid, Geraldine Cancel-Tassin, Lingyi Lu, Janet L. Stanford, John D. Carpten, Kathleen A. Cooney, Jianfeng Xu, Daniela Seminara, Zhong Wang
Publikováno v:
Human Genetics; Vol 132
Human Genetics
Human Genetics
Prostate cancer has a strong familial component but uncovering the molecular basis for inherited susceptibility for this disease has been challenging. Recently, a rare, recurrent mutation (G84E) in HOXB13 was reported to be associated with prostate c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61612efdfc1c9a6af91f1adbe459d270
Autor:
Kimberly A. Zuhlke, Anna Johnson, Zhengrong Gao, Jessica V. Ribado, Gregory R. Keele, S. Lilly Zheng, Qing Duan, Jianfeng Xu, Yun Li, Ge Li, Jin Li, Ethan M. Lange, Yunfei Wang, Kathleen A. Cooney
Background: We assessed the evidence for association between 23 recently reported prostate cancer variants and early-onset prostate cancer and the aggregate value of 63 prostate cancer variants for predicting early-onset disease using 931 unrelated m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d2d5cb45e267ba7ae9979cbe51a8b8a
https://europepmc.org/articles/PMC4873425/
https://europepmc.org/articles/PMC4873425/
Autor:
Kimberly A. Zuhlke, Yunfei Wang, Ethan M. Lange, Anna M. Ray, Emilie K. Johnson, Kathleen A. Cooney
Publikováno v:
The Prostate. 71:225-231
BACKGROUND. Prostate cancer is the most commonly diagnosed non-skin cancer in men in the United States and the second leading cause of cancer-related mortality. African American men have substantially increased risk of both being diagnosed and dying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb8d29fbe4e0c35509b334ae3665b589
https://doi.org/10.1002/pros.21234
https://doi.org/10.1002/pros.21234