Last Posted: Jan 05, 2017
- Association between family history of diabetes and cardiovascular disease and lifestyle risk factors in the United States population: The 2009-2012 National Health and Nutrition Examination Survey.
Akhuemonkhan Eboselume et al. Preventive medicine 2016 Dec - Pharmacogenetic Optimization of Smoking Cessation Treatment.
Chenoweth Meghan J et al. Trends in pharmacological sciences 2017 Jan 38(1) 55-66 - Pharmacogenetic Optimization of Smoking Cessation Treatment
MJ Chenowetrh, Trends in Pharma Sciences, January 2017 - Study Finds No Safe Level of Smoking
NIH Director Blog, December 13, 2016 - Study Finds No Safe Level of Smoking
NIH Director Blog, December 13, 2016 - Genomic prediction of coronary heart disease.
Abraham Gad et al. European heart journal 2016 Sep - Genetic Risk, Smoking Behavior And The Question Of False Reassurance
R Green, Huffington Post, November 2016 - US Cancer Moonshot must strike a balance between research and prevention.
et al. Nature 2016 Nov 539(7630) 467 - Statin Use for the Primary Prevention of Cardiovascular Disease in Adults: US Preventive Services Task Force Recommendation Statement.
et al. JAMA 2016 Nov 316(19) 1997-2007 - DNA study lays bare devastating damage caused by smoking
The Guardian, November 3, 2016 - Every year of smoking causes DNA mutations that make cancer more likely
LA Times, November 3, 2016 - Every year of smoking causes DNA mutations that make cancer more likely
LA Times, November 3, 2016 - Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer
J Gong et al, PLOS Genetics, October 2016 - Familial hypercholesterolemia among unselected contemporary patients presenting with first myocardial infarction: Prevalence, risk factor burden, and impact on age at presentation.
Mortensen Martin Bødtker et al. Journal of clinical lipidology 10(5) 1145-1152.e1 - Smoking may affect DNA for more than 30 years
H Nichols, Medical News Today, September 21, 2016 - Implications of Personal Genomic Testing for Health Behaviors: The Case of Smoking.
Olfson Emily et al. Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco 2016 Jul
From CDC Information Database
This database includes general CDC public health information on specific diseases and health related topics. When available, the database displays genomic information from various CDC web pages. Users are also encouraged to conduct searches of CDC website for additional information.
- Make 2017 your year to quit
- Cancer and Tobacco Use
Tobacco use causes many cancers, CDC Vital Signs, November 2016 - Some racial, ethnic groups continue smoking cigarettes at higher rates
CDC press release, August 4, 2016 - Impact of first federally funded anti-smoking ad campaign remains strong after three years
- Smokers' Stories: Five Reasons to Quit
Tips from former smokers, 2016 - Smokers' Stories: Five Reasons to Quit
Tips from former smokers, 2016
From NIH National Cancer Institute Web Sites
From CDC-Authored Genomics Publication Database
This database contains CDC-authored publications in public health genomics including infectious diseases, newborn screening, reproductive health, genetic testing, cancer, chronic diseases, birth defects and developmental disabilities, environmental and occupational health as well as laboratory, bioinformatics and statistical methods.
- SHATTUCK LECTURE: The Future of Public Health.
Frieden Thomas R et al. The New England journal of medicine 2015 Oct (18) 1748-54 - Maternal smoking, xenobiotic metabolizing enzyme gene variants, and gastroschisis risk.
Jenkins Mary M et al. Am. J. Med. Genet. A 2014 Jun 164A(6) 1454-63 - A smoking-associated 7-gene signature for lung cancer diagnosis and prognosis.
Wan Ying-Wooi et al. Int. J. Oncol. 2012 Oct 41(4) 1387-96 - Varenicline for smoking cessation: nausea severity and variation in nicotinic receptor genes.
Swan G E et al. Pharmacogenomics J. 2012 Aug 12(4) 349-58
From Implementation Database
This database focuses on state and national activities that integrate genomics into public health programs and clinical practice
- WISEWOMAN
[Disease: Stroke|Familial Hypercholesterolemia|Heart Disease; Type: Program; State: Multiple States] - Addressing Familial Hypercholesterolemia
[Disease: Familial Hypercholesterolemia|Heart Disease|Stroke; Type: Education; State: West Virginia] - Cancer Genetics: Focus on BRCA1 and BRCA2 Mutations
[Disease: Breast Cancer|Ovarian Cancer; Type: Education; State: New York] - The Ohio Plan to Prevent Heart Disease and Stroke 2008-2012
[Disease: Heart Disease|Stroke|Familial Hypercholesterolemia; Type: Data|Policy|Program; State: Ohio] - Ohio Department of Health Heart Disease and Stroke Prevention Program Take Heart: Know Your Heart Disease and Stroke Family Health History
[Disease: Stroke|Heart Disease|Familial Hypercholesterolemia; Type: Education|Tools; State: Ohio]
From Guideline Database
This database contains updated guidelines, policies and recommendations on genomic research and practice, as provided by professional organizations, federal advisory groups, expert panels and policy groups.
- Appropriateness of newborn screening for [alpha]1-antitrypsin deficiency.
Published 2014 (Alpha-1 Foundation - Workshop Attendees) - Appropriateness of newborn screening for á1-antitrypsin deficiency.
Published 2014 (Alpha-1 Foundation) - Molecular testing guideline for selection of lung cancer patients for EGFR and ALK tyrosine kinase inhibitors: guideline from the College of American Pathologists, International Association for the Study of Lung Cancer, and Association for Molecular Pathology.
Published 2013 (College of American Pathologists) (International Association for the Study of Lung Cancer) (Association for Molecular Pathology)
From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations.
Human molecular genetics 2016 Dec .
Seow Wei Jie, Matsuo Keitaro, Hsiung Chao Agnes, Shiraishi Kouya, Song Minsun, Kim Hee Nam, Wong Maria Pik, Hong Yun-Chul, Dean Hosgood H, Wang Zhaoming, Chang I-Shou, Wang Jiu-Cun, Chatterjee Nilanjan, Tucker Margaret, Wei Hu, Mitsudomi Tetsuya, Zheng Wei, Kim Jin Hee, Zhou Baosen, Caporaso Neil E, Albanes Demetrius, Shin Min-Ho, Ping Chung Lap, An She-Juan, Wang Ping, Zheng Hong, Yatabe Yasushi, Zhang Xu-Chao, Kim Young Tae, Shu Xiao-Ou, Kim Young-Chul, Bassig Bryan A, Chang Jiang, Ho James Chung Man, Ji Bu-Tian, Kubo Michiaki, Daigo Yataro, Ito Hidemi, Momozawa Yukihide, Ashikawa Kyota, Kamatani Yoichiro, Honda Takayuki, Sakamoto Hiromi, Kunitoh Hideo, Tsuta Koji, Watanabe Shun-Ichi, Nokihara Hiroshi, Miyagi Yohei, Nakayama Haruhiko, Matsumoto Shingo, Tsuboi Masahiro, Goto Koichi, Yin Zhihua, Shi Jianxin, Takahashi Atsushi, Goto Akiteru, Minamiya Yoshihiro, Shimizu Kimihiro, Tanaka Kazumi, Wu Tangchun, Wei Fusheng, Wong Jason Y Y, Matsuda Fumihiko, Su Jian, Kim Yeul Hong, Oh In-Jae, Song Fengju, Lee Victor Ho Fun, Su Wu-Chou, Chen Yuh-Min, Chang Gee-Chen, Chen Kuan-Yu, Huang Ming-Shyan, Yang Pan-Chyr, Lin Hsien-Chih, Xiang Yong-Bing, Seow Adeline, Yong Park Jae, Kweon Sun-Seog, Chen Chien-Jen, Li Haixin, Gao Yu-Tang, Wu Chen, Qian Biyun, Lu Daru, Liu Jianjun, Jeon Hyo-Sung, Hsiao Chin-Fu, Sung Jae Sook, Tsai Ying-Huang, Jung Yoo Jin, Guo Huan, Hu Zhibin, Wang Wen-Chang, Chung Charles C, Lawrence Charles, Burdett Laurie, Yeager Meredith, Jacobs Kevin B, Hutchinson Amy, Berndt Sonja I, He Xingzhou, Wu Wei, Wang Junwen, Li Yuqing, Choi Jin Eun, Park Kyong Hwa, Sung Sook Whan, Liu Li, Kang Chang Hyun, Hu Lingmin, Chen Chung-Hsing, Yang Tsung-Ying, Xu Jun, Guan Peng, Tan Wen, Wang Chih-Liang, Sihoe Alan Dart Loon, Chen Ying, Choi Yi Young, Hung Jen-Yu, Kim Jun Suk, Yoon Ho-Il, Cai Qiuyin, Lin Chien-Chung, Park In Kyu, Xu Ping, Dong Jing, Kim Christopher, He Qincheng, Perng Reury-Perng, Chen Chih-Yi, Vermeulen Roel, Wu Junjie, Lim Wei-Yen, Chen Kun-Chieh, Chan John K C, Chu Minjie, Li Yao-Jen, Li Jihua, Chen Hongyan, Yu Chong-Jen, Jin Li, Lo Yen-Li, Chen Ying-Hsiang, Fraumeni Joseph F, Liu Jie, Yamaji Taiki, Yang Yang, Hicks Belynda, Wyatt Kathleen, Li Shengchao A, Dai Juncheng, Ma Hongxia, Jin Guangfu, Song Bao, Wang Zhehai, Cheng Sensen, Li Xuelian, Ren Yangwu, Cui Ping, Iwasaki Motoki, Shimazu Taichi, Tsugane Shoichiro, Zhu Junjie, Jiang Gening, Fei Ke, Wu Guoping, Chien Li-Hsin, Chen Hui-Ling, Su Yu-Chun, Tsai Fang-Yu, Chen Yi-Song, Yu Jinming, Stevens Victoria L, Laird-Offringa Ite A, Marconett Crystal N, Lin Dongxin, Chen Kexin, Wu Yi-Long, Landi Maria Teresa, Shen Hongbing, Rothman Nathaniel, Kohno Takashi, Chanock Stephen J, Lan Qi - Association of ZFHX3 gene variation with atrial fibrillation, cerebral infarction, and lung thromboembolism: An autopsy study.
Journal of cardiology 2016 Dec .
Zaw Khin Thet Thet, Sato Noriko, Ikeda Shinobu, Thu Kaung Si, Mieno Makiko Naka, Arai Tomio, Mori Seijiro, Furukawa Tetsushi, Sasano Tetsuo, Sawabe Motoji, Tanaka Masashi, Muramatsu Masaa - Genetic polymorphisms of vitamin D receptor (VDR), CYP27B1 and CYP24A1 genes and the risk of colorectal cancer.
The International journal of biological markers 2016 Dec 0.
Vidigal Verônica Marques, Silva Tiago Donizetti, de Oliveira Juliana, Pimenta Célia Aparecida Marques, Felipe Aledson Vitor, Forones Nora Manouki - Pilot Study on the Genetic Background of an Active Matrix Metalloproteinase (aMMP-8) Test in Finnish Adolescents.
Journal of periodontology 2016 Dec 1-10.
Heikkinen Anna Maria, Raivisto Teija, Kettunen Kaisa, Kovanen Leena, Haukka Jari, Esmaeili Elmira Pakbaznejad, Elg Jessica, Gieselmann Dirk-Rolf, Rathnayake Nilminie, Ruokonen Hellevi, Tervahartiala Taina, Sorsa Ti - The insertion/deletion polymorphism in the angiotensin-converting enzyme gene and nicotine dependence in schizophrenia patients.
Journal of neural transmission (Vienna, Austria : 1996) 2016 Dec .
Nadalin Sergej, Risti? Smiljana, Rebi? Jelena, Šendula Jengi? Vesna, Kapovi? Miljenko, Bureti?-Tomljanovi? Ale
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