Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Disease and CARS[original query] |
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| Impaired body movement representation in DYT1 mutation carriers. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology 2008 Aug 119 (8): 1864-9. Fiorio M, Gambarin M, Defazio G, Valente E M, Stanzani C, Moretto G, Loi M, Soliveri P, Nardocci N, Albanese A, Fiaschi A, Tinazzi |
| Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes. Diabetes 2009 Jun 58 (6): 1403-10. Pezzolesi Marcus G, Poznik G David, Mychaleckyj Josyf C, Paterson Andrew D, Barati Michelle T, Klein Jon B, Ng Daniel P K, Placha Grzegorz, Canani Luis H, Bochenski Jacek, Waggott Daryl, Merchant Michael L, Krolewski Bozena, Mirea Lucia, Wanic Krzysztof, Katavetin Pisut, Kure Masahiko, Wolkow Pawel, Dunn Jonathon S, Smiles Adam, Walker William H, Boright Andrew P, Bull Shelley B, , Doria Alessandro, Rogus John J, Rich Stephen S, Warram James H, Krolewski Andrzej |
| Genome-wide association study of alcohol dependence implicates a region on chromosome 11. Alcoholism, clinical and experimental research 2010 May 34 (5): 840-52. Edenberg Howard J, Koller Daniel L, Xuei Xiaoling, Wetherill Leah, McClintick Jeanette N, Almasy Laura, Bierut Laura J, Bucholz Kathleen K, Goate Alison, Aliev Fazil, Dick Danielle, Hesselbrock Victor, Hinrichs Anthony, Kramer John, Kuperman Sam, Nurnberger John I, Rice John P, Schuckit Marc A, Taylor Robert, Todd Webb B, Tischfield Jay A, Porjesz Bernice, Foroud Tatia |
| Genetic associations in diabetic nephropathy: a meta-analysis. Diabetologia 2010 Dec . Mooyaart AL, Valk EJ, van Es LA, Bruijn JA, de Heer E, Freedman BI, Dekkers OM, Baelde HJ |
| An intergenic region on chromosome 13q33.3 is associated with the susceptibility to kidney disease in type 1 and 2 diabetes. Kidney international 2011 Jul 80 (1): 105-11. Pezzolesi Marcus G, Poznik G David, Skupien Jan, Smiles Adam M, Mychaleckyj Josyf C, Rich Stephen S, Warram James H, Krolewski Andrzej |
| Evaluation of associations between single nucleotide polymorphisms in the FRMD3 and CARS genes and diabetic nephropathy in a Kuwaiti population. Genetics and molecular research : GMR 2016 Jan 15 (1): . Al-waheeb S, Alwohhaib M, Abdelghani A, Al-Sharrah S, Al-Shafey E, Al-Sahow A, Alyatama N, Dashti A A, Hussain |
| Clinical improvement following vitamin D3 supplementation in Autism Spectrum Disorder. Nutritional neuroscience 2016 Jan . Feng Junyan, Shan Ling, Du Lin, Wang Bing, Li Honghua, Wang Wei, Wang Tiantian, Dong Hanyu, Yue Xiaojing, Xu Zhida, Staal Wouter G, Jia Feiyo |
| The oxytocin receptor gene polymorphism -rs237902- is associated with the severity of autism spectrum disorder: A pilot study. Asian journal of psychiatry 2018 Jan . Ocako?lu Fevzi Tuna, Köse Sezen, Özbaran Burcu, Onay Hüsey |
| Association study between genetic variants in vitamin D metabolism related genes and childhood autism spectrum disorder. Metabolic brain disease 2020 Apr . Yu Hong, Zhang Zengyu, Liu Jun, Hu Pingfang, Liu Zh |
| Facial Emotion Recognition and Polymorphisms of Dopaminergic Pathway Genes in Children with ASD. Behavioural neurology 2020 2020 6376842. Liu Zhuo, Liu Jun, Zhang Zengyu, Yu Hong, Hu Fengp |
| Association between Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and Risk of Childhood Autism Spectrum Disorder. Behavioural neurology 2021 7 2021 4150926. Fang Fang, Ge Minxia, Liu Jun, Zhang Zengyu, Yu Hong, Zhu Shuilong, Xu Liwei, Shao Li |
| Association between autism spectrum disorder and polymorphisms in genes encoding serotine and dopamine receptors. Metabolic brain disease 2021 Mar . Liu Jun, Fu Huamei, Kong Jiangying, Yu Hong, Zhang Zeng |
| Genetic associated complications of type 2 diabetes mellitus. Panminerva medica 2021 10 64 (2): 274-288. Wong Yee H, Wong Shen H, Wong Xiao T, Yap Qiao Y, Yip Khar Y, Wong Liang Z, Chellappan Dinesh K, Bhattamisra Subrat K, Candasamy Mayur |
| Genomic signatures and prognosis of advanced stage Chinese pediatric T cell lymphoblastic lymphoma by whole exome sequencing. Frontiers in pediatrics 2023 9 11 1224966. Qinglin Liu, Xiang Yu, Jinquan Wen, Nange Yin, Xin Liao, Pinli Zou, Yuxia Guo, Lin Song, Jianwen Xi |
| A pilot study on glutamate receptor and carrier gene variants and risk of childhood autism spectrum. Metabolic brain disease 2023 8 . Jun Liu, Jing Yan, Fei Qu, Weiming Mo, Hong Yu, Pingfang Hu, Zengyu Zha |
| Mode of transport, genetic susceptibility, and incidence of coronary heart disease. The international journal of behavioral nutrition and physical activity 2023 7 20 (1): 79. Zhu Liduzi Jiesisibieke, Jenna Panter, Mengyao Wang, Shiu Lun Au Yeung, Shan Luo, Haeyoon Jang, Eric Yuk Fai Wan, Soren Brage, Youngwon K |
| "Predicting diabetic kidney disease in youth with type 1 diabetes: Insights from genetic risk assessment". Journal of diabetes and its complications 2024 9 38 (11): 108833. Ferda Evin, Tar?k K?rkgöz, Tahir Atik, Güne? Ak, Timur Köse, Caner Kabasakal, Behzat Özkan, Samim Özen, ?ükran Darcan, Damla Gök? |
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