Search Results - "Medical genetics

NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results - a pilot study by Kanika Singh, Sunita Bijarnia-Mahay, V. L. Ramprasad, Ratna Dua Puri, Sandhya Nair, Sheetal Sharda, Renu Saxena, Sudha Kohli, Samarth Kulshreshtha, Indrani Ganguli, Kanwal Gujral, Ishwar C. Verma

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Associations Between Genetically Predicted Plasma N-Glycans and Prostate Cancer Risk: Analysis of Over 140,000 European Descendants by Liu D, Zhu J, Zhao T, Sharapov S, Tiys E, Wu L

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Relationship Between Interleukin-6 −174G/C Genetic Variant and Efficacy of Methotrexate Treatment in Psoriatic Arthritis Patients by Sokolik R, Iwaszko M, Świerkot J, Wysoczańska B, Korman L, Wiland P, Bogunia-Kubik K

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A Newly Developed Web-Based Resource on Genetic Eye Disorders for Users With Visual Impairment (Gene.Vision): Usability Study by Yeong, Jian Lee, Thomas, Peter, Buller, James, Moosajee, Mariya

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Development of an Algorithm for Determining of Genetic Risk at the Primary Healthcare Level - A New Tool for Primary Prevention: A Study Protocol by Selič Polona, Klemenc-Ketiš Zalika, Zelko Erika, Kravos Andrej, Rifel Janez, Makivić Irena, Poplas Susič Antonija, Tevžič Špela, Cerovič Metka, Peterlin Borut, Kopčavar Guček Nena

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Frequency of Genetic Polymorphism of the Gene Encoding 16kDa Clara Cell Secretory Protein (CC16) in Shiraz, Iran by M Saadat, DD Farhud

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Analysis of genetic variation in human papillomavirus type 16 E1 and E2 in women with cervical infection in Xinjiang, China by Luyue Wang, Fang Wang, Shaowei Fu, Chunhe Zhang, Xiangyi Zhe, Hongtao Li, Dongmei Li, Renfu Shao, Zemin Pan

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Frequency of Genetic Polymorphism of the Gene Encoding 16kDa Clara Cell Secretory Protein (CC16) in Shiraz, Iran by M Saadat, DD Farhud

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Genetic investigation of 211 Chinese families expands the mutational and phenotypical spectra of hereditary retinopathy genes through targeted sequencing technology by Zhouxian Bai, Yanchuan Xie, Lina Liu, Jingzhi Shao, Yuying Liu, Xiangdong Kong

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Genetic variation in ACE A2350G: association with reduction in fasting blood glucose after fluoxetine therapy in depressed patients by Negar Firouzabadi, Mohammad Reza Hooshangi Shayesteh, Nasrollah Erfani, Ali Alavi Shoushtari

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Effects of <it>MCF2L2, ADIPOQ </it>and <it>SOX2 </it>genetic polymorphisms on the development of nephropathy in type 1 Diabetes Mellitus by Gu Harvest F, Brismar Kerstin, Efendic Suad, Zhang Dongying

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SNP-SNP interactions dominate the genetic architecture of candidate genes associated with left ventricular mass in african-americans of the GENOA study by Mosley Thomas H, Chu Jian, Meyers Kristin J, Kardia Sharon LR

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The Association between GSTM1, GSTT1 Genetic Variants and Gastric Carcinoma Susceptibility in Chinese: A Systematic Review Article by Dingyun YOU, Nanjia LU, Donghui DUAN, Hui LI, Wenhua XING

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Association of Genetic Polymorphisms in GSTP1, GSTM1, and GSTT1 Genes with Vesicoureteral Reflux Susceptibility in the Children of Southeast Iran by Sima SHAHROKHZADEH, Azam SOLEIMANI, Dor-Mohammad, Mohammad Hossein SANGTARASH, Omid NEJATI, Mohsen TAHERI

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A study of application effects of next-generation sequencing based preimplantation genetic testing for aneuploidies in advanced maternal age women by Yizhuo Yang, Xinmeng Guo, Ming Zhang, Hui Wang, Sha Mu, Hongmei Peng, Yuanqing Yao

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Disease Prevention, Genetic Selection, and Vaccination Based on BoLA-DRB3.2 Polymorphism: A Model for Immunogenetic Studies by Mohammad Mehdi Ranjbar, Ali Reza Yousefi, Mohammad Hasan Motedayen, Shima Molazadeh, Gholamreza Karimi

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Genetic factors in rotator cuff pathology: potential influence of col 5A1 polymorphism in outcomes of rotator cuff repair by Stefano Petrillo, Umile Giuseppe Longo, Katia Margiotti, Vincenzo Candela, Caterina Fusilli, Giacomo Rizzello, Alessandro De Luca, Vincenzo Denaro

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Genetic analyses of smoking initiation, persistence, quantity, and age-at-onset of regular cigarette use in Brazilian families: the Baependi Heart Study by Horimoto Andréa RVR, Oliveira Camila M, Giolo Suely R, Soler Júlia P, de Andrade Mariza, Krieger José E, Pereira Alexandre C

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PDX1 and MC4R genetic polymorphisms are associated with type 2 diabetes mellitus risk in the Chinese Han population by Ning Wang, Rui Tong, Jing Xu, Yanni Tian, Juan Pan, Jiaqi Cui, Huan Chen, Yanqi Peng, Sijia Fei, Shujun Yang, Lu Wang, Juanchuan Yao, Wei Cui

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Genetic variation in ACE A2350G: association with reduction in fasting blood glucose after fluoxetine therapy in depressed patients by Negar Firouzabadi, Mohammad Reza Hooshangi Shayesteh, Nasrollah Erfani, Ali Alavi Shoushtari

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