Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 32 Records) |
| Query Trace: Disease and WRN[original query] |
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| WRN gene 1367 Arg allele protects against development of type 2 diabetes mellitus. Diabetes research and clinical practice 2005 Sep 69 (3): 287-92. Hirai Masashi, Suzuki Susumu, Hinokio Yoshinori, Yamada Takahiro, Yoshizumi Shinsuke, Suzuki Chitose, Satoh Jo, Oka Yoshito |
| Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma. Clinical and experimental medicine 2005 Dec 5 (4): 161-8. Khayat A S, Lobo Gatti L, Moura Lima E, de Assumpção P P, Nascimento Motta F J, Harada M L, Casartelli C, Marques Payão S L, Cardoso Smith M A, Burbano R |
Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.
BMC medical genetics 2007 8 Suppl 1 S2. Vasan Ramachandran S, Larson Martin G, Aragam Jayashri, Wang Thomas J, Mitchell Gary F, Kathiresan Sekar, Newton-Cheh Christopher, Vita Joseph A, Keyes Michelle J, O'Donnell Christopher J, Levy Daniel, Benjamin Emelia |
| WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brazil. Journal of neuro-oncology 2008 Dec 90 (3): 253-8. Pinto Giovanny R, Yoshioka France K N, Clara Carlos A, Santos Marcelo J, Almeida José R W, Burbano Rommel R, Rey Juan A, Casartelli Cacil |
| WRN polymorphisms affect expression levels of plasminogen activator inhibitor type 1 in cultured fibroblasts. BMC cardiovascular disorders 2008 8 (1): 5. Castro Elena, Oviedo-Rodríguez Vladimir, Angel-Chávez Luis |
| Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936. Genes, brain, and behavior 2009 Mar 8 (2): 238-47. Houlihan L M, Harris S E, Luciano M, Gow A J, Starr J M, Visscher P M, Deary I |
| Association of candidate gene polymorphisms with chronic kidney disease in Japanese individuals with hypertension. Hypertension research : official journal of the Japanese Society of Hypertension 2009 Mar . Yoshida T, Kato K, Yokoi K, Watanabe S, Metoki N, Satoh K, Aoyagi Y, Nishigaki Y, Nozawa Y, Yamada Y |
| Lack of association of the WRN C1367T polymorphism with senile cataract in the Israeli population. Molecular vision 2010 16 1771-5. Ehrenberg M, Dratviman-Storobinsky O, Avraham-Lubin B R, Goldenberg-Cohen |
| Applying and testing the conveniently optimized enzyme mismatch cleavage method to clinical DNA diagnosis. Molecular genetics and metabolism 2012 Nov 107 (3): 580-5. Niida Yo, Kuroda Mondo, Mitani Yusuke, Okumura Akiko, Yokoi Aya |
| Polymorphisms of the WRN gene and DNA damage of peripheral lymphocytes in age-related cataract in a Han Chinese population. Age (Dordrecht, Netherlands) 2013 Dec 35 (6): 2435-44. Jiang Shengqun, Hu Nan, Zhou Jing, Zhang Junfang, Gao Ruifang, Hu Jianyan, Guan Huaij |
| The associations between single nucleotide polymorphisms of DNA repair genes, DNA damage, and age-related cataract: Jiangsu Eye Study. Investigative ophthalmology & visual science 2013 Feb 54 (2): 1201-7. Su Shu, Yao Yong, Zhu Rongrong, Liang Congkai, Jiang Shengqun, Hu Nan, Zhou Jing, Yang Mei, Xing Qian, Guan Huaij |
| WRN Cys1367Arg polymorphism is not associated with skull base chordoma. Biomedical reports 2014 Jul 2 (4): 521-524. Wang Ke, Wang Liang, Feng Jie, Hao Shuyu, Tian Kaibing, Wu Zhen, Zhang Liwei, Jia Guijun, Wan Hong, Zhang Junti |
| Predictive impact of genetic polymorphisms in DNA repair genes on susceptibility and therapeutic outcomes to colorectal cancer patients. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Mar 36 (3): 1549-59. Sun Kang, Gong Aixia, Liang P |
| Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data. Genes, brain, and behavior 2015 Sep . Saad M, Brkanac Z, Wijsman E |
| Warfarin-related nephropathy: possible role for the warfarin pharmacogenetic profile. Clinical kidney journal 2014 Dec 7 (6): 605-8. Di Maso Vittorio, Carraro Michele, Bevilacqua Elena, Bucconi Sergio, Artero Mary Louise, Boscutti Giulia |
| A missense single nucleotide polymorphism, V114I of the Werner syndrome gene, is associated with risk of osteoporosis and femoral fracture in the Japanese population. Journal of bone and mineral metabolism 2015 Jan . Zhou Heying, Mori Seijiro, Tanaka Masashi, Sawabe Motoji, Arai Tomio, Muramatsu Masaaki, Mieno Makiko Naka, Shinkai Shoji, Yamada Yoshiji, Miyachi Motohiko, Murakami Haruka, Sanada Kiyoshi, Ito Hide |
| Association of the rs1346044 Polymorphism of the Werner Syndrome Gene RECQL2 with Increased Risk and Premature Onset of Breast Cancer. International journal of molecular sciences 2015 16 (12): 29643-53. Zins Karin, Frech Barbara, Taubenschuss Eva, Schneeberger Christian, Abraham Dietmar, Schreiber Mart |
| Candidate gene analysis of BRCA1/2 mutation-negative high-risk Russian breast cancer patients. Cancer letters 2015 Apr 359 (2): 259-61. Sokolenko Anna P, Preobrazhenskaya Elena V, Aleksakhina Svetlana N, Iyevleva Aglaya G, Mitiushkina Natalia V, Zaitseva Olga A, Yatsuk Olga S, Tiurin Vladislav I, Strelkova Tatiana N, Togo Alexandr V, Imyanitov Evgeny |
| Determining the frequency of pathogenic germline variants from exome sequencing in patients with castrate-resistant prostate cancer. BMJ open 2016 6 (4): e010332. Hart Steven N, Ellingson Marissa S, Schahl Kim, Vedell Peter T, Carlson Rachel E, Sinnwell Jason P, Barman Poulami, Sicotte Hugues, Eckel-Passow Jeanette E, Wang Liguo, Kalari Krishna R, Qin Rui, Kruisselbrink Teresa M, Jimenez Rafael E, Bryce Alan H, Tan Winston, Weinshilboum Richard, Wang Liewei, Kohli Mani |
| Targeted exome sequencing of Korean triple-negative breast cancer reveals homozygous deletions associated with poor prognosis of adjuvant chemotherapy-treated patients. Oncotarget 2017 Sep 8 (37): 61538-61550. Jeong Hae Min, Kim Ryong Nam, Kwon Mi Jeong, Oh Ensel, Han Jinil, Lee Se Kyung, Choi Jong-Sun, Park Sara, Nam Seok Jin, Gong Gyung Yup, Nam Jin Wu, Choi Doo Ho, Lee Hannah, Nam Byung-Ho, Choi Yoon-La, Shin Young K |
| Genetic variation in WRN and ischemic stroke: General population studies and meta-analyses. Experimental gerontology 2017 03 89 69-77. Christoffersen Mette, Frikke-Schmidt Ruth, Nordestgaard Børge G, Tybjærg-Hansen An |
| Mutation Spectrum of Cancer-Associated Genes in Patients With Early Onset of Colorectal Cancer. Frontiers in oncology 2019 8 9 673. Zhunussova Gulnur, Afonin Georgiy, Abdikerim Saltanat, Jumanov Abai, Perfilyeva Anastassiya, Kaidarova Dilyara, Djansugurova Ley |
| Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients. Scientific reports 2019 12 9 (1): 19986. Jarhelle Elisabeth, Riise Stensland Hilde Monica Frostad, Hansen Geir Åsmund Myge, Skarsfjord Siri, Jonsrud Christoffer, Ingebrigtsen Monica, Strømsvik Nina, Van Ghelue Marij |
| Polymorphisms in DNA repair pathway genes and ABCG2 gene in advanced colorectal cancer: correlation with tumor characteristics and clinical outcome in oxaliplatin-based chemotherapy. Cancer management and research 2019 11 285-297. Hu Xiaoyun, Qin Wenyan, Li Shanqiong, He Miao, Wang Yilin, Guan Shu, Zhao Haishan, Yao Weifan, Wei Minjie, Liu Mingyan, Wu Huiz |
| Gene Panel Testing in Hereditary Breast Cancer. Archives of Iranian medicine 2020 Mar 23 (3): 155-162. Rostami Parvin, Zendehdel Kazem, Shirkoohi Reza, Ebrahimi Elmira, Ataei Mitra, Imanian Hashem, Najmabadi Hossein, Akbari Mohammad Reza, Sanati Mohammad Hosse |
| The evaluation of gene mutation profiles by next-generation sequencing in diffuse large B-cell lymphoma. International journal of laboratory hematology 2022 12 . Özçal?ml? Azime, Erdo?du ?brahim Halil, Turgutkaya Atakan, Yava?o?lu ?rfan, Döger Füruzan Kaçar, Bolaman Ali Zah |
| Co-Occurrence of Germline Genomic Variants and Copy Number Variations in Hereditary Breast and Colorectal Cancer Patients. Genes 2023 8 14 (8): . Luiza Côrtes, Tatiane Ramos Basso, Rolando André Rios Villacis, Jeferson Dos Santos Souza, Mads Malik Aagaard Jørgensen, Maria Isabel Achatz, Silvia Regina Rogat |
| Presumed Pathogenic Germline and Somatic Variants in African American Thyroid Cancer. Thyroid : official journal of the American Thyroid Association 2023 12 . Zachary A Hurst, Sandya Liyanarachchi, Pamela Brock, Huiling He, Fadi Nabhan, Colleen Veloski, Amanda E Toland, Matthew D Ringel, Sissy M Jhia |
| Genetic predisposition to differentiated thyroid cancer among Polish population. Polish archives of internal medicine 2024 1 . Martyna Borowczyk, Mateusz Sypniewski, Joanna Szyda, Ma?gorzata Braszka, Katarzyna Ziemnicka, Marek Rucha?a, Michalina Oszywa, Zbigniew J Król, Paula Dobo |
| Novel FANCI and RAD54B Variants and the Observed Clinical Outcomes in a Hungarian Melanoma Cohort. International journal of molecular sciences 2025 1 26 (1): . Barbara Anna Bokor, Aliasgari Abdolreza, Flóra Kaptás, Margit Pál, Zita Battyani, Márta Széll, Nikoletta Na |
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