Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Neoplasms and LDLR[original query] |
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| Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia. Clinical chemistry and laboratory medicine : CCLM / FESCC 2002 May 40 (5): 441-5. Salazar Luis A, Hirata Mario H, Hirata Rosario D |
| Polymorphisms of genes in the lipid metabolism pathway and risk of biliary tract cancers and stones: a population-based case-control study in Shanghai, China. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008 Mar 17 (3): 525-34. Andreotti Gabriella, Chen Jinbo, Gao Yu-Tang, Rashid Asif, Chen Bingshu E, Rosenberg Philip, Sakoda Lori C, Deng Jie, Shen Ming-Chang, Wang Bing-Sheng, Han Tian-Quan, Zhang Bai-He, Yeager Meredith, Welch Robert, Chanock Stephen, Fraumeni Joseph F, Hsing Ann |
| Genetic variation and reproductive timing: African American women from the Population Architecture using Genomics and Epidemiology (PAGE) Study. PloS one 2013 8 (2): e55258. Spencer Kylee L, Malinowski Jennifer, Carty Cara L, Franceschini Nora, Fernández-Rhodes Lindsay, Young Alicia, Cheng Iona, Ritchie Marylyn D, Haiman Christopher A, Wilkens Lynne, Chunyuanwu , Matise Tara C, Carlson Christopher S, Brennan Kathleen, Park Amy, Rajkovic Aleksandar, Hindorff Lucia A, Buyske Steven, Crawford Dana |
| Functional variants in the low-density lipoprotein receptor gene are associated with clear cell renal cell carcinoma susceptibility. Carcinogenesis 2017 Sep . Zhang Gui-Ming, Wang Meng-Yun, Liu Ya-Nan, Zhu Yao, Wan Fang-Ning, Wei Qing-Yi, Ye Ding-W |
| Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients. Human genetics 2020 7 140 (2): 321-331. Horiuchi Yasue, Matsubayashi Hiroyuki, Kiyozumi Yoshimi, Nishimura Seiichiro, Higashigawa Satomi, Kado Nobuhiro, Nagashima Takeshi, Mizuguchi Maki, Ohnami Sumiko, Arai Makoto, Urakami Kenichi, Kusuhara Masatoshi, Yamaguchi K |
| Low Density Lipoprotein Receptor (LDLR) and 3-Hydroxy-3-Methylglutaryl Coenzyme a Reductase (HMGCR) Expression are Associated with Platinum-Resistance and Prognosis in Ovarian Carcinoma Patients. Cancer management and research 2021 12 13 9015-9024. Huang Xueyao, Wei Xuan, Qiao Sijing, Zhang Xue, Li Rui, Hu Shunxue, Mao Hongluan, Liu Peis |
| Whole-exome sequencing reveals a comprehensive germline mutation landscape and identifies twelve novel predisposition genes in Chinese prostate cancer patients. PLoS genetics 2022 Sep 18 (9): e1010373. Liang Yonghao, Chiu Peter Ka-Fung, Zhu Yao, Wong Christine Yim-Ping, Xiong Qing, Wang Lin, Teoh Jeremy Yuen-Chun, Cao Qin, Wei Yu, Ye Ding-Wei, Tsui Stephen Kwok-Wing, Ng Chi-F |
| Long-term cancer risk in heterozygous familial hypercholesterolemia relatives: a 25-year cohort study. Lipids in health and disease 2022 7 21 (1): 56. Kjærgaard Kasper Aalbæk, Harborg Sixten, Jensen Henrik Kjærulf, Borgquist Sig |
| Germline and somatic genetic variability of oxysterol-related genes in breast cancer patients with early disease of the luminal subtype. Biochimie 2022 Aug 199 158-169. Holý Petr, Hlavá? Viktor, Ostašov Pavel, Brynychová Veronika, Koževnikovová Renata, Trnková Markéta, Kope?ková Kate?ina, M?š?áková So?a, Mrhalová Marcela, Sou?ek Pav |
| Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia. Journal of lipid research 2022 4 63 (6): 100209. Dong Weilai, Wong Karen H Y, Liu Youbin, Levy-Sakin Michal, Hung Wei-Chien, Li Mo, Li Boyang, Jin Sheng Chih, Choi Jungmin, Lopez-Giraldez Francesc, Vaka Dedeepya, Poon Annie, Chu Catherine, Lao Richard, Balamir Melek, Movsesyan Irina, Malloy Mary J, Zhao Hongyu, Kwok Pui-Yan, Kane John P, Lifton Richard P, Pullinger Clive |
| Loss of STK11 Suppresses Lipid Metabolism and Attenuates KRAS-Induced Immunogenicity in Patients with Non-Small Cell Lung Cancer. Cancer research communications 2024 8 . Daniel R Principe, Mary M Pasquinelli, Ryan H Nguyen, Hidayatullah G Munshi, Alicia Hulbert, Alexandre F Aissa, Frank Weinbe |
| Mayo Clinic Tapestry Study: A Large-Scale Decentralized Whole Exome Sequencing Study for Clinical Practice, Research Discovery, and Genomic Education. Mayo Clinic proceedings 2024 12 . Lorelei A Bandel, Robert A Vierkant, Teresa M Kruisselbrink, Michelle L Bublitz, Tammy A Wilson, Sebastian M Armasu, Jan B Egan, Richard J Presutti, Niloy Jewel J Samadder, Aleksandar Sekulic, Rory J Olson, Jennifer Tan-Arroyo, Joel A Morales-Rosado, Eric W Klee, Matthew J Ferber, Jennifer L Kemppainen, Jennifer L Anderson, Jessa S Bidwell, Joseph J Wick, Victor E Ortega, William V Bobo, Pavel N Pichurin, Jessica M Mcmillan, DeAnna M Weaver, Douglas L Riegert-Johnson, Alanna M Cera, Lauren M Boucher, Iftikhar J Kullo, Sarah K Mantia, Matthew T Jones, Nicholas B Larson, Tony C Luehrs, Jon W Leitzke, Hugues Sicotte, Shulan Tian, Jennifer R Stavlund, Joel E Pacyna, Richard R Sharp, Akwasi A Asabere, James Lu, Tammy M McAllister, T'Nita S Walker, A Keith Stewart, Gianrico Farrugia, Konstantinos N Lazarid |
| Rare copy-number variants as modulators of common disease susceptibility. Genome medicine 2024 1 16 (1): 5. Chiara Auwerx, Maarja Jõeloo, Marie C Sadler, Nicolò Tesio, Sven Ojavee, Charlie J Clark, Reedik Mägi, , Alexandre Reymond, Zoltán Kutal |
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