Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: GSC[original query] |
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Association analysis between longevity in the Japanese population and polymorphic variants of genes involved in insulin and insulin-like growth factor 1 signaling pathways. Experimental gerontology 0 39 (11-12): 1595-8. Kojima Toshio, Kamei Hidehiko, Aizu Tomoyuki, Arai Yasumichi, Takayama Michiyo, Nakazawa Susumu, Ebihara Yoshinori, Inagaki Hiroki, Masui Yukie, Gondo Yasuyuki, Sakaki Yoshiyuki, Hirose Nobuyos |
Mitochondrial SNPs associated with Japanese centenarians, Alzheimer's patients, and Parkinson's patients. Computational biology and chemistry 2008 Oct 32 (5): 332-7. Takasaki Shige |
Environmental and genetic factors associated with congenital microtia: a case-control study in Jiangsu, China, 2004 to 2007. Plastic and reconstructive surgery 2009 Oct 124 (4): 1157-64. Zhang Qing-guo, Zhang Jiao, Yu Pei, Shen H |
A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose. Diabetes 2010 Feb 59 (2): 539-49. Paterson Andrew D, Waggott Daryl, Boright Andrew P, Hosseini S Mohsen, Shen Enqing, Sylvestre Marie-Pierre, Wong Isidro, Bharaj Bhupinder, Cleary Patricia A, Lachin John M, , Below Jennifer E, Nicolae Dan, Cox Nancy J, Canty Angelo J, Sun Lei, Bull Shelley B, |
Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study). BMC medical genetics 2011 12 (1): 20. Hertel Jens K, Johansson Stefan, Ræder Helge, Platou Carl G P, Midthjell Kristian, Hveem Kristian, Molven Anders, Njølstad Pål |
Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohort. The Journal of clinical endocrinology and metabolism 2013 Feb 98 (2): E346-54. Krone Nils, Rose Ian T, Willis Debbie S, Hodson James, Wild Sarah H, Doherty Emma J, Hahner Stefanie, Parajes Silvia, Stimson Roland H, Han Thang S, Carroll Paul V, Conway Gerry S, Walker Brian R, MacDonald Fiona, Ross Richard J, Arlt Wiebke, |
Elucidation of the genetic and epigenetic landscape alterations in RNA binding proteins in glioblastoma. Oncotarget 2016 12 8 (10): 16650-16668. Bhargava Shruti, Patil Vikas, Mahalingam Kulandaivelu, Somasundaram Kumarav |
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.
Nature communications 2017 Feb 8 14364. Yu Yanqin, Zuo Xianbo, He Miao, Gao Jinping, Fu Yuchuan, Qin Chuanqi, Meng Liuyan, Wang Wenjun, Song Yaling, Cheng Yong, Zhou Fusheng, Chen Gang, Zheng Xiaodong, Wang Xinhuan, Liang Bo, Zhu Zhengwei, Fu Xiazhou, Sheng Yujun, Hao Jiebing, Liu Zhongyin, Yan Hansong, Mangold Elisabeth, Ruczinski Ingo, Liu Jianjun, Marazita Mary L, Ludwig Kerstin U, Beaty Terri H, Zhang Xuejun, Sun Liangdan, Bian Zhu |
Mutational analysis of GSC, HOXA2 and PRKRA in 106 Chinese patients with microtia. International journal of pediatric otorhinolaryngology 2017 1 93 78-82. Hao Shaojuan, Jin Lei, Li Chenlong, Wang Huijun, Zheng Fengyun, Ma Duan, Zhang Tian |
Identification of Novel Loci Associated With Hip Shape: A Meta-Analysis of Genomewide Association Studies.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2019 Feb 34 (2): 241-251. Baird Denis A, Evans Daniel S, Kamanu Frederick K, Gregory Jennifer S, Saunders Fiona R, Giuraniuc Claudiu V, Barr Rebecca J, Aspden Richard M, Jenkins Deborah, Kiel Douglas P, Orwoll Eric S, Cummings Steven R, Lane Nancy E, Mullin Benjamin H, Williams Frances Mk, Richards J Brent, Wilson Scott G, Spector Tim D, Faber Benjamin G, Lawlor Deborah A, Grundberg Elin, Ohlsson Claes, Pettersson-Kymmer Ulrika, Capellini Terence D, Richard Daniel, Beck Thomas J, Evans David M, Paternoster Lavinia, Karasik David, Tobias Jonathan |
Low Prevalence of GSC Gene Mutations in a Large Cohort of Predominantly Caucasian Patients with Hidradenitis Suppurativa. The Journal of investigative dermatology 2020 3 140 (10): 2085-2088.e14. Duchatelet Sabine, Miskinyte Snaigune, Delage Maia, Ungeheuer Marie-Noëlle, Lam Thi, Benhadou Farida, Del Marmol Véronique, Vossen Allard R J V, Prens Errol P, Cogrel Olivier, Beylot-Barry Marie, Girard Céline, Vidil Julien, Join-Lambert Olivier, Parisot Mélanie, Nitschké Patrick, Hanein Sylvain, Fraitag Sylvie, Van der Zee Hessel H, Bessis Didier, Damiani Giovanni, Altomare Andrea, Liao Yi-Hua, Nikolakis Georgios, Zouboulis Christos C, Nassif Aude, Hovnanian Ala |
Demographic, radiographic, molecular and clinical characteristics of primary gliosarcoma and differences to glioblastoma. Clinical neurology and neurosurgery 2020 11 200 106348. Pierscianek Daniela, Ahmadipour Yahya, Michel Anna, Rauschenbach Laurèl, Darkwah Oppong Marvin, Deuschl Cornelius, Kebir Sied, Wrede Karsten H, Glas Martin, Stuschke Martin, Sure Ulrich, Jabbarli Ramaz |
Oncogene goosecoid is transcriptionally regulated by E2F1 and correlates with disease progression in prostate cancer. Chinese medical journal 2023 11 . Yue Ge, Sheng Ma, Qiang Zhou, Zezhong Xiong, Yanan Wang, Le Li, Zheng Chao, Junbiao Zhang, Tengfei Li, Zixi Wu, Yuan Gao, Guanyu Qu, Zirui Xi, Bo Liu, Xi Wu, Zhihua Wa |
Risk of malignancy in cytologically indeterminate thyroid nodules harboring thyroid stimulating hormone receptor mutations. Frontiers in endocrinology 2023 1 13 1073592. Whitmer Dorota, Phay John E, Holt Shelby, O'Donnell Benjamin, Nguyen Jay, Joseph Dennis, Chi Anthony, Wu Shuyang, Hao Yangyang, Huang Jing, Klopper Joshua P, Kloos Richard T, Kennedy Giulia C, Shin Joy |
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- Page last updated:Mar 18, 2024
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