Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: ACADS[original query] |
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A genome-wide perspective of genetic variation in human metabolism.
Nature genetics 2009 Dec . Illig Thomas, Gieger Christian, Zhai Guangju, Römisch-Margl Werner, Wang-Sattler Rui, Prehn Cornelia, Altmaier Elisabeth, Kastenmüller Gabi, Kato Bernet S, Mewes Hans-Werner, Meitinger Thomas, de Angelis Martin Hrabé, Kronenberg Florian, Soranzo Nicole, Wichmann H-Erich, Spector Tim D, Adamski Jerzy, Suhre Karst |
The minor C-allele of rs2014355 in ACADS is associated with reduced insulin release following an oral glucose load. BMC medical genetics 2011 12 4. Hornbak Malene, Banasik Karina, Justesen Johanne M, Krarup Nikolaj T, Sandholt Camilla H, Andersson Åsa, Sandbæk Annelli, Lauritzen Torsten, Pisinger Charlotta, Witte Daniel R, Sørensen Thorkild A A, Pedersen Oluf, Hansen Torb |
A genome-wide assessment of variability in human serum metabolism.
Human mutation 2012 Dec . Hong MG, Karlsson R, Magnusson PK, Lewis MR, Isaacs W, Zheng LS, Xu J, Grönberg H, Ingelsson E, Pawitan Y, Broeckling C, Prenni JE, Wiklund F, Prince JA |
Metabolic heritability at birth: implications for chronic disease research. Human genetics 2014 Aug 133 (8): 1049-57. Ryckman Kelli K, Smith Caitlin J, Jelliffe-Pawlowski Laura L, Momany Allison M, Berberich Stanton L, Murray Jeffrey |
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
Schizophrenia bulletin 2018 Oct . Ikeda Masashi, Takahashi Atsushi, Kamatani Yoichiro, Momozawa Yukihide, Saito Takeo, Kondo Kenji, Shimasaki Ayu, Kawase Kohei, Sakusabe Takaya, Iwayama Yoshimi, Toyota Tomoko, Wakuda Tomoyasu, Kikuchi Mitsuru, Kanahara Nobuhisa, Yamamori Hidenaga, Yasuda Yuka, Watanabe Yuichiro, Hoya Satoshi, Aleksic Branko, Kushima Itaru, Arai Heii, Takaki Manabu, Hattori Kotaro, Kunugi Hiroshi, Okahisa Yuko, Ohnuma Tohru, Ozaki Norio, Someya Toshiyuki, Hashimoto Ryota, Yoshikawa Takeo, Kubo Michiaki, Iwata Nak |
Expanded Newborn Screening for Inborn Errors of Metabolism by Tandem Mass Spectrometry in Suzhou, China: Disease Spectrum, Prevalence, Genetic Characteristics in a Chinese Population. Frontiers in genetics 2019 11 10 1052. Wang Ting, Ma Jun, Zhang Qin, Gao Ang, Wang Qi, Li Hong, Xiang Jingjing, Wang Benji |
Newborn screening and genetic characteristics of patients with short- and very long-chain acyl-CoA dehydrogenase deficiencies. Clinica chimica acta; international journal of clinical chemistry 2020 7 510 285-290. Lin Yiming, Zhang Weifeng, Chen Dongmei, Lin Chunmei, Zheng Zhenzhu, Fu Qingliu, Li Min, Peng Weil |
Effects of genetic variations in Acads gene on the risk of chronic obstructive pulmonary disease. IUBMB life 2020 6 72 (9): 1986-1996. Yuan Yiming, Yang Shanshan, Deng Dan, Chen Yulong, Zhang Caixia, Zhou Ruixue, Su Zhigua |
Detection of allele frequencies of common c. 511C>T and c.625G>A variants in the ACADS gene in the Turkish population. The Turkish journal of pediatrics 2020 62 (1): 19-23. K?l?ç Mustafa, Ergüner Bekir, Ko?ukçu Can, Özgül R?za Köks |
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 |
Variants in the ethylmalonyl-CoA decarboxylase (ECHDC1) gene: a novel player in ethylmalonic aciduria? Journal of inherited metabolic disease 2021 May . Fogh Sarah, Dipace Graziana, Bie Anne, Veiga-da-Cunha Maria, Hansen Jakob, Kjeldsen Margrethe, Mosegaard Signe, Ribes Antonia, Gregersen Niels, Aagaard Lars, Van Schaftingen Emile, Olsen Rikke K |
The minor C-allele of the rs2014355 variant in ACADS gene is associated with exercise-induced increase in HDL cholesterol levels in Taiwanese adults. Medicine 2021 Jan 100 (1): e23838. Yang Tzi-Peng, Shih Fen-Fen, Hsu Ming-Yi, Tsai Meng-Hsiun, Nfor Oswald Ndi, Chen Pei-Hsing, Ho Chien-Chang, Lin Chuan-Chao, Liaw Yung- |
Integrative Analysis of the Inflammatory Bowel Disease Serum Metabolome Improves Our Understanding of Genetic Etiology and Points to Novel Putative Therapeutic Targets.
Gastroenterology 2021 11 162 (3): 828-843.e11. Di'Narzo Antonio F, Houten Sander M, Kosoy Roman, Huang Ruiqi, Vaz Frédéric M, Hou Ruixue, Wei Gabrielle, Wang Wenhui, Comella Phillip H, Dodatko Tetyana, Rogatsky Eduard, Stojmirovic Aleksandar, Brodmerkel Carrie, Perrigoue Jacqueline, Hart Amy, Curran Mark, Friedman Joshua R, Zhu Jun, Agrawal Manasi, Cho Judy, Ungaro Ryan, Dubinsky Marla C, Sands Bruce E, Suárez-Fariñas Mayte, Schadt Eric E, Colombel Jean-Frédéric, Kasarskis Andrew, Hao Ke, Argmann Carm |
Identification of healthspan-promoting genes in Caenorhabditis elegans based on a human GWAS study.
Biogerontology 2022 6 23 (4): 431-452. Saul Nadine, Dhondt Ineke, Kuokkanen Mikko, Perola Markus, Verschuuren Clara, Wouters Brecht, von Chrzanowski Henrik, De Vos Winnok H, Temmerman Liesbet, Luyten Walter, Ze?i? Aleksandra, Loier Tim, Schmitz-Linneweber Christian, Braeckman Bart |
Analysis of genotypes and biochemical phenotypes of neonates with abnormal metabolism of butyrylcarnitine. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2023 12 1-8. Dingwen Wu, Rulai Yang, Kexin Fang, Chen Liu, Jiaming Tang, Meijun Yu, Zhengyan Zh |
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