Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: PCCB[original query] |
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Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.
Circulation. Cardiovascular genetics 2009 Apr 2 (2): 125-33. Dehghan Abbas, Yang Qiong, Peters Annette, Basu Saonli, Bis Joshua C, Rudnicka Alicja R, Kavousi Maryam, Chen Ming-Huei, Baumert Jens, Lowe Gordon D O, McKnight Barbara, Tang Weihong, de Maat Moniek, Larson Martin G, Eyhermendy Susana, McArdle Wendy L, Lumley Thomas, Pankow James S, Hofman Albert, Massaro Joseph M, Rivadeneira Fernando, Kolz Melanie, Taylor Kent D, van Duijn Cornelia M, Kathiresan Sekar, Illig Thomas, Aulchenko Yurii S, Volcik Kelly A, Johnson Andrew D, Uitterlinden Andre G, Tofler Geoffrey H, Gieger Christian, , Psaty Bruce M, Couper David J, Boerwinkle Eric, Koenig Wolfgang, O'Donnell Christopher J, Witteman Jacqueline C, Strachan David P, Smith Nicholas L, Folsom Aaron |
Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.
PLoS genetics 2009 Nov 5 (11): e1000730. Chasman Daniel I, Paré Guillaume, Mora Samia, Hopewell Jemma C, Peloso Gina, Clarke Robert, Cupples L Adrienne, Hamsten Anders, Kathiresan Sekar, Mälarstig Anders, Ordovas José M, Ripatti Samuli, Parker Alex N, Miletich Joseph P, Ridker Paul |
[Analysis of PCCA and PCCB gene mutations in patients with propionic acidemia]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 Feb 32 (1): 26-30. Chen Zhanling, Wen Pengqiang, Wang Guobing, Hu Yuhui, Liu Xiaohong, Chen Li, Chen Shuli, Wan Lisheng, Cui Dong, Shang Yue, Li Chengro |
Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.
BMC genomics 2016 17 (1): 443. Ligthart Symen, Vaez Ahmad, Hsu Yi-Hsiang, , , , Stolk Ronald, Uitterlinden André G, Hofman Albert, Alizadeh Behrooz Z, Franco Oscar H, Dehghan Abb |
Seventeen Novel Mutations in PCCA and PCCB Genes in Indian Propionic Acidemia Patients, and Their Outcomes. Genetic testing and molecular biomarkers 2016 May . Gupta Deepti, Bijarnia-Mahay Sunita, Kohli Sudha, Saxena Renu, Puri Ratna Dua, Shigematsu Yosuke, Yamaguchi Seiji, Sakamoto Osamu, Gupta Neerja, Kabra Madhulika, Thakur Seema, Deb Roumi, Verma Ishwar Chand |
Whole genome sequence study of cannabis dependence in two independent cohorts. Addiction biology 2017 Jan . Gizer Ian R, Bizon Chris, Gilder David A, Ehlers Cindy L, Wilhelmsen Kirk |
Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis. BMC medical genetics 2018 3 19 (1): 46. Prasad Aparna, Sdano Matthew A, Vanzo Rena J, Mowery-Rushton Patricia A, Serrano Moises A, Hensel Charles H, Wassman E Robe |
Spectrum of mutations underlying Propionic acidemia and further insight into a genotype-phenotype correlation for the common mutation in Saudi Arabia. Molecular genetics and metabolism reports 2019 2 18 22-29. Al-Hamed Mohamed H, Imtiaz Faiqa, Al-Hassnan Zuhair, Al-Owain Mohammed, Al-Zaidan Hamad, Alamoudi Mohamed S, Faqeih Eissa, Alfadhel Majid, Al-Asmari Ali, Saleh M M, Almutairi Fuad, Moghrabi Nabil, AlSayed Moeenalde |
Tandem Mass Spectrometry Screening for Inborn Errors of Metabolism in Newborns and High-Risk Infants in Southern China: Disease Spectrum and Genetic Characteristics in a Chinese Population. Frontiers in genetics 2021 8 12 631688. Tan Jianqiang, Chen Dayu, Chang Rongni, Pan Lizhen, Yang Jinling, Yuan Dejian, Huang Lihua, Yan Tizhen, Ning Haiping, Wei Jiangyan, Cai R |
Gene diagnosis and pedigree analysis of two Han ethnicity families with propionic acidemia in Fujian. Medicine 2021 3 100 (10): e24161. Chen Yao, Lin Xuehua, Lin Qingying, Zeng Yinglin, Qiu Xiaolong, Liu Guanghua, Zhu Wenb |
[Differential diagnosis of a Chinese pedigree with methylmalonic acidemia by next-generation sequencing]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 7 39 (7): 694-697. Zhao Ganye, Chen Chen, Zhao Xuechao, Liu Lina, Wang Conghui, Kong Xiangdo |
Analysis of the relationship between phenotypes and genotypes in 60 Chinese patients with propionic acidemia: a fourteen-year experience at a tertiary hospital. Orphanet journal of rare diseases 2022 3 17 (1): 135. Liu Yi, Chen Zhehui, Dong Hui, Ding Yuan, He Ruxuan, Kang Lulu, Li Dongxiao, Shen Ming, Jin Ying, Zhang Yao, Song Jinqing, Tian Yaping, Cao Yongtong, Liang Desheng, Yang Yanli |
Identification of genetic loci that overlap between schizophrenia and metabolic syndrome. Psychiatry research 2022 11 318 114947. Lv Honggang, Li Juan, Gao Kai, Zeng Lingsi, Xue Ranran, Liu Xia, Zhou Cong, Yue Weihua, Yu H |
Human forebrain organoid-based multi-omics analyses of PCCB as a schizophrenia associated gene linked to GABAergic pathways. Nature communications 2023 8 14 (1): 5176. Wendiao Zhang, Ming Zhang, Zhenhong Xu, Hongye Yan, Huimin Wang, Jiamei Jiang, Juan Wan, Beisha Tang, Chunyu Liu, Chao Chen, Qingtuan Me |
Identification of genetic variants associated with anterior cruciate ligament rupture and AKC standard coat color in the Labrador Retriever. BMC genomic data 2023 10 24 (1): 60. B T Lee, L A Baker, M Momen, H Terhaar, E E Binversie, S J Sample, Peter Mu |
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- Page last updated:Apr 29, 2024
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