Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 129 Records) |
Query Trace: Syndrome and GC[original query] |
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Hereditary Diffuse Gastric Cancer: A Comparative Cohort Study According to Pathogenic Variant Status. Cancers 2020 12 12 (12): . Marwitz Tim, Hüneburg Robert, Spier Isabel, Lau Jan-Frederic, Kristiansen Glen, Lingohr Philipp, Kalff Jörg C, Aretz Stefan, Nattermann Jacob, Strassburg Christian |
Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome. Journal of neurology 2020 Nov . Jiménez-Jiménez Félix Javier, Amo Gemma, Alonso-Navarro Hortensia, Calleja Marisol, Díez-Fairén Mónica, Álvarez-Fernández Ignacio, Pastor Pau, Plaza-Nieto José Francisco, Navarro-Muñoz Santiago, Turpín-Fenoll Laura, Millán-Pascual Jorge, Recio-Bermejo Marta, García-Ruiz Rafael, García-Albea Esteban, Agúndez José A G, García-Martín Ele |
Children with Down syndrome: association of Bcl-I polymorphism of nuclear receptor subfamily 3 group C member 1 gene with obesity. Pediatric research 2021 8 92 (1): 216-224. Abo El-Fotoh Wafaa Moustafa M, Bahbah Hebatallah Mohammed Nasser, Elaithy Manal Abd El-Monem, Ahmed Rana Khairy Rashad, Bayomy Noha Rab |
Cancer predisposition and germline CTNNA1 variants. European journal of medical genetics 2021 8 64 (10): 104316. Lobo Silvana, Benusiglio Patrick R, Coulet Florence, Boussemart Lise, Golmard Lisa, Spier Isabel, Hüneburg Robert, Aretz Stefan, Colas Chrystelle, Oliveira Car |
Second Primary Cancers After Gastric Cancer, and Gastric Cancer as Second Primary Cancer. Clinical epidemiology 2021 7 13 515-525. Zheng Guoqiao, Sundquist Kristina, Sundquist Jan, Chen Tianhui, Försti Asta, Hemminki Akseli, Hemminki Ka |
Association of APOA1-75G/A and +83C/T polymorphic variation with acute coronary syndrome patients in Kashmir (India). Journal of cardiovascular and thoracic research 2021 7 13 (2): 109-115. Pandith Arshad A, Bhat Irfan Ahmad, Niyaz Iqra, Qasim Iqbal, Bhat Ina A, Manzoor Usma, Koul Aabid |
Polymorphism (-499C/G) in DDAH2 promoter may act as a protective factor for metabolic syndrome: A case-control study in Azar-Cohort population. Archives of endocrinology and metabolism 2021 Jul . Faramarzi Elnaz, Aftabi Younes, Ansarin Khalil, Somi Mohammad Hossein, Gilani Neda, Seyedrezazadeh Ensiy |
Untargeted Plasma Metabolomics Unravels a Metabolic Signature for Tissue Sensitivity to Glucocorticoids in Healthy Subjects: Its Implications in Dietary Planning for a Healthy Lifestyle. Nutrients 2021 7 13 (6): . Nicolaides Nicolas C, Ioannidi Maria-Konstantina, Koniari Eleni, Papageorgiou Ifigeneia, Bartzeliotou Anastasia, Sertedaki Amalia, Klapa Maria I, Charmandari Evangel |
Association of serum 25-hydroxyvitamin D with metabolic syndrome and type 2 diabetes: a one sample Mendelian randomization study. BMC geriatrics 2021 06 21 (1): 391. Xiao Jing, Lv Jingyi, Wang Shiyu, Zhou Yang, Chen Lunwen, Lu Juying, Zhang Xiaoyi, Wang Xiaojian, Gu Yunjuan, Lu Qingy |
Geographical Distribution of E-cadherin Germline Mutations in the Context of Diffuse Gastric Cancer: A Systematic Review. Cancers 2021 4 13 (6): . Corso Giovanni, Corso Federica, Bellerba Federica, Carneiro Patrícia, Seixas Susana, Cioffi Antonio, La Vecchia Carlo, Magnoni Francesca, Bonanni Bernardo, Veronesi Paolo, Gandini Sara, Figueiredo Joa |
CFH I62V as a Putative Genetic Marker for Posner-Schlossman Syndrome. Frontiers in immunology 2021 3 12 608723. Yang Ming Ming, Sun Hong Yan, Meng Ting, Qiu Shan Hu, Zeng Qi Qiao, Ng Tsz Kin, Jiang Li, Deng Ting Ming, Zeng Ai Neng, Wang Jun, Luo Xiao Li |
CDH1 germline mutations in healthy individuals from families with the hereditary diffuse gastric cancer syndrome. Journal of medical genetics 2021 12 59 (4): 313-317. Corso Giovanni, Magnoni Francesca, Massari Giulia, Trovato Cristina Maria, De Scalzi Alessandra Margherita, Vicini Elisa, Bonanni Bernardo, Veronesi Paolo, Galimberti Viviana, Bagnardi Vincen |
FMR1 allele frequencies in 51,000 newborns: a large-scale population study in China. World journal of pediatrics : WJP 2021 Nov . Zhang Jin-Yu, Wu Ding-Wen, Yang Ru-Lai, Zhu Lin, Jiang Meng-Yi, Wang Wen-Jun, Li Xue-Kun, Jiang Xiao-Ling, Tong Fan, Shu Qia |
Association Between Macrophage Migration Inhibitory Factor -173 G>C Gene Polymorphism and Childhood Idiopathic Nephrotic Syndrome: A Meta-Analysis. Frontiers in pediatrics 2021 9 724258. Ying Daojing, Jiang Mengjie, Rong Liping, Zhuang Hongjie, Chen Lizhi, Xu Yuanyuan, Jiang Xiaoy |
Unravelling the Contribution of the rs7041 and rs4588 Polymorphisms of the GC Gene and Serum VDBP Levels for Developing Metabolic Syndrome in the Mexican Population. International journal of molecular sciences 2022 Sep 23 (18): . Hidalgo-Bravo Alberto, Rivera-Paredez Berenice, León-Reyes Guadalupe, Patiño Nelly, Castillejos-López Manuel, Salmerón Jorge, Velázquez-Cruz Rafa |
The role of ERK-1 and ERK-2 gene polymorphisms in PCOS pathogenesis. Reproductive biology and endocrinology : RB&E 2022 6 20 (1): 95. Guney Gurhan, Ta?k?n Mine Islimye, Sener Nazli, Tolu Ezgi, Dodurga Yavuz, Elmas Levent, Cetin Orkun, Sarigul Ceng |
The FADS1 genotypes modify the effect of linoleic acid-enriched diet on adipose tissue inflammation via pro-inflammatory eicosanoid metabolism. European journal of nutrition 2022 Jun . Vaittinen Maija, Lankinen Maria A, Käkelä Pirjo, Ågren Jyrki, Wheelock Craig E, Laakso Markku, Schwab Ursula, Pihlajamäki Jus |
Association of Serum 25(OH)D with Metabolic Syndrome in Chinese Women of Childbearing Age. Nutrients 2022 May 14 (11): . Shan Xiaoyun, Zhao Xiayu, Li Siran, Song Pengkun, Man Qingqing, Liu Zhen, Hu Yichun, Yang Lich |
Extracolonic tumours in a pedigree with EPCAM-related Lynch Syndrome. European journal of medical genetics 2022 4 65 (5): 104479. Alves da Silva Joana, Castedo Sérgio, Pedroto Isabel, Marcos-Pinto Ricar |
The Single-Nucleotide Polymorphism of miR-27a rs895819 and the Expression of miR-27a in Helicobacter pylori-Related Diseases and the Correlation with the Traditional Chinese Medicine Syndrome. Evidence-based complementary and alternative medicine : eCAM 2022 3 2022 3086205. Zhang Ling, Huang Meng-Xin, Li Dan-Yan, Zhang Yun-Zhan, Lan Shao-Yang, Luo Qi, Dai Yun-Kai, Wu Yun-Bo, Ye Jin-Tong, Chen Wei-Jing, Li Ru-Liu, Hu Li |
Clinical and genetic characteristics of Chinese Duchenne/Becker muscular dystrophy patients with small mutations. Frontiers in neuroscience 2022 11 16 992546. Gan Siyi, Liu Shulei, Yang Haiyan, Wu Liw |
Genetic polymorphisms of IL6 gene -174G > C and -597G > A are associated with the risk of COVID-19 severity. International journal of immunogenetics 2022 11 50 (1): 5-11. Verma Shrikant, Verma Sushma, Khan Faizan Haider, Siddiqi Zeba, Raza Syed Tasleem, Abbas Mohammad, Mahdi Farza |
The Association Between GC Gene Polymorphisms and Metabolic Syndrome in Chinese Rural Population: A Case-Control Study. Diabetes, metabolic syndrome and obesity : targets and therapy 2022 15 165-174. Zhao Tong, Zhang Dongdong, Liu Yiming, Feng Mingming, Xu Ze, Huang Haoyue, Zhang Luoya, Li Wenjie, Li Xi |
Clinical implication of CDH1 mutations in genetic testing for diffuse gastric cancer patients. Oncology 2023 9 . Giovanni Corso, Cristina Maria Trovato, Salvatore Petitto, Antonia Girardi, Alessandra Margherita De Scalzi, Beatrice Bianchi, Francesca Magnoni, Antonio Cioffi, Viviana Galimberti, Paolo Veronesi, Giovanni Mazzarol, Patrick Maisonneu |
Clinical Predictive Value of Phospholipase A2 Receptor Gene Polymorphism Combined with Subclass of Immunoglobulin G in Renal Tissues for Membranous Nephropathy. Alternative therapies in health and medicine 2023 8 . Chunyang Ji, Qingqing Xu, Xueyan Bi |
Germline CDH1 variants in hereditary diffuse gastric cancer syndrome with focus on younger women. Journal of cancer research and clinical oncology 2023 8 . Giovanni Corso, Giovanni Comelli, Paolo Veronesi, Beatrice Bianchi, Salvatore Petitto, Andrea Polizzi, Antonia Girardi, Antonio Cioffi, Carlo La Vecchia, Vincenzo Bagnardi, Francesca Magno |
Serum Transforming Growth Factor ?1 and Its Genetic Variants Are Associated with Increased Macrophage Inflammatory Protein 1? and Susceptibility to Idiopathic Carpal Tunnel Syndrome. Journal of personalized medicine 2023 5 13 (5): . Shaimaa A Fattah, Mohamed S Selim, Maha A Abdel Fattah, Dina M Abo-Elmatty, Noha M Mesbah, Asmaa R Abdel-Ham |
Investigating Genetic Determinants of Plasma Inositol Status in Adult Humans.
The Journal of nutrition 2023 2 152 (11): 2333-2342. Weston Eleanor, Pangilinan Faith, Eaton Simon, Orford Michael, Leung Kit-Yi, Copp Andrew J, Mills James L, Molloy Anne M, Brody Lawrence C, Greene Nicholas |
Associations between Catechol-O-methyltransferase (COMT) polymorphisms and cognitive impairments, psychiatric symptoms and tardive dyskinesia in schizophrenia. Brain research 2023 12 148740. Jinghui Chi, Yanyan Ma, Menglei Shi, Chenghao Lu, Qiaona Jiang, Yanzhe Li, Xiaofei Zhang, Xiaomei Shi, Shen Li, Lili Wa |
Association between the genetic variant in the vitamin D pathway (rs2282679), circulating 25-hydroxyvitamin D levels, insulin resistance and metabolic syndrome criteria. Nutricion hospitalaria 2023 11 . Daniel de Luis Román, Olatz Izaola, David Primo Martín, Emilia Gómez Hoyos, Beatriz Torres, Juan José Lóp |
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