HuGE Literature Finder
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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 |
Polymorphism (-499C/G) in Archives of endocrinology and metabolism 2021 Jul . Faramarzi Elnaz, Aftabi Younes, Ansarin Khalil, Somi Mohammad Hossein, Gilani Neda, Seyedrezazadeh Ensiy |
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 |
Anthropometrics and metabolic syndrome in relation to glucocorticoid receptor polymorphisms in corticosteroid users. Neuroendocrinology 2020 Dec . Savas Mesut, Wester Vincent L, van der Voorn Bibian, Iyer Anand M, Koper Jan W, van den Akker Erica L T, van Rossum Elisabeth F |
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 |
Value of upper gastrointestinal endoscopy for gastric cancer surveillance in patients with Lynch syndrome. International journal of cancer 2020 Sep . Ladigan-Badura Swetlana, Vangala Deepak B, Engel Christoph, Bucksch Karolin, Hueneburg Robert, Perne Claudia, Nattermann Jacob, Steinke-Lange Verena, Rahner Nils, Schackert Hans K, Weitz Jürgen, Kloor Matthias, Kuhlkamp Judith, Nguyen Huu Phuc, Moeslein Gabriela, Strassburg Christian, Morak Monika, Holinski-Feder Elke, Buettner Reinhard, Aretz Stefan, Loeffler Markus, Schmiegel Wolff, Pox Christian, Schulmann Karsten, |
Genetic polymorphisms -137 (G?>?C) (rs187238) and -607 (C?>?A) (rs1946518) and serum level of interleukin 18 in Fars ethnic groups with metabolic syndrome in Northern Iran. Archives of physiology and biochemistry 2020 Jul 1-7. Aghajani Roja, Saeidi Mohsen, Amiriani Taghi, Marjani Majid, Amiriani Amir Hossein, Akhavan Tabib Atefeh, Marjani Abdoljal |
The genetic polymorphisms of XPR1 and SCL34A3 are associated with Fanconi syndrome in Chinese patients of tumor-induced osteomalacia. Journal of endocrinological investigation 2020 Jul . Jiang Y, Li X, Feng J, Li M, Wang O, Xing X-P, Xia W |
Association between melatonin receptor gene polymorphisms and polycystic ovarian syndrome: a systematic review and meta-analysis. Bioscience reports 2020 May . Yi Shiqi, Xu Jiawei, Shi Hao, Li Wenbo, Li Qian, Sun Ying |
Interleukin-18 promoter -137 G/C polymorphism (rs187238) is associated with biochemical markers of renal function and cardiovascular disease in type 2 diabetes patients. Clinical biochemistry 2020 Mar . Cavalcante Jânio Emanuel Andrade, de Sousa Ederson Laurindo Holanda, de Oliveira Rodrigues Raphael, de Almeida Viana Glautemberg, Duarte Gadelha Daniel, de Carvalho Manoela Montenegro Dias, Sousa Duaran Lopes, Silva Allysson Jordan Xavier, Filho Raimundo Rigoberto Barbosa Xavier, Fernandes Virgínia Oliveira, Montenegro Júnior Renan Magalhães, de Sousa Alves Renata, Meneses Gdayllon Cavalcante, Sampaio Tiago Lima, Queiroz Maria Goretti Rodrigu |
p53, Cyclin-D1, ß-catenin, APC and c-myc in Tumor Tissue from Colorectal and Gastric Cancer Patients with Suspected Lynch Syndrome by the Bethesda Criteria. Asian Pacific journal of cancer prevention : APJCP 2020 Feb 21 (2): 343-348. Marcolino Tais Fernanda, Pimenta Celia Aparecida Marques, Artigiani Neto Ricardo, Castelo Paula, Silva Marcelo Souza, Forones Nora Manoukian, Oshima Celina Tizuko Fujiya |
Interaction between Vascular Endothelial Growth Factor-A (rs2010963) Gene Polymorphisms and Dietary Diversity Score on Cardiovascular Risk Factors in Patients with Metabolic Syndrome. Lifestyle genomics 2019 Nov 1-10. Abbasalizad Farhangi Mahdieh, Vajdi Mahdi, Nikniaz Leila, Nikniaz Zein |
Genetic analyses supporting colorectal, gastric, and prostate cancer syndromes. Genes, chromosomes & cancer 2019 Jul . Wallander Karin, Liu Wen, von Holst Susanna, Thutkawkorapin Jessada, Kontham Vinaykumar, Forsberg Anna, Lindblom Annika, Lagerstedt-Robinson Kristi |
Macrophage Migration Inhibitory Factor -173 G>C Gene Polymorphism Is Associated with Increased Risk of Nephrotic Syndrome in Children. Iranian journal of kidney diseases 2019 Jul 13 (4): 232-236. Sadeghi-Bojd Simin, Falsafinejad Fariba, Danesh Hiva, Bizhani Fatemeh, Bahari Gholamreza, Hashemi Mohamm |
A new mutL homolog 1 c.1896+5G>A germline mutation detected in a Lynch syndrome-associated lung and gastric double primary cancer patient. Molecular genetics & genomic medicine 2019 Jun e787. Chen Xuyuan, Li Xiang, Liang Hongsen, Wei Lichun, Cui Qiang, Yao Ming, Wu |
Association between Interleukin-32 and Interleukin-17A Single Nucleotide Polymorphisms and Serum Levels with Polycystic Ovary Syndrome. Iranian journal of allergy, asthma, and immunology 2019 Feb 18 (1): 91-99. Hesampour Fateme, Namavar Jahromi Bahia, Tahmasebi Foroozan, Gharesi-Fard Behro |
Influence of K656N Polymorphism of the Leptin Receptor Gene on Obesity-Related Traits in Nondiabetic Afro-Caribbean Individuals. Metabolic syndrome and related disorders 2019 Feb . Foucan Lydia, Bassien-Capsa Valérie, Rambhojan Christine, Lacorte Jean-Marc, Larifla Laure |
Serum profile of cytokines and their genetic variants in metabolic syndrome and healthy subjects: a comparative study. Bioscience reports 2019 Jan . Zafar Uzma, Khaliq Saba, Ahmad Hafiz Usman, Lone Khalid Perva |
Association of 25-hydroxyvitamin D with cardiometabolic risk factors and metabolic syndrome: a mendelian randomization study. Nutrition journal 2019 10 18 (1): 61. Chen Chi, Chen Yi, Weng Pan, Xia Fangzhen, Li Qin, Zhai Hualing, Wang Ningjian, Lu Ying |
PRKCQ rs4750316 is associated with Vogt-Koyanagi-Harada syndrome in a Han Chinese population. Molecular vision 2019 25 834-842. Xu Lei, Zhao Tingting, Yuan Gangxiang, Hou Shengping, Zeng Wenxin, Chen Feil |
Association between rs1800795 polymorphism in the interleukin-6 gene and the risk of polycystic ovary syndrome: A meta-analysis. Medicine 2018 Jul 97 (29): e11558. Chen Linjie, Zhang Zhifen, Huang Jian, Jin Minju |
Association of CD28 and CTLA4 haplotypes with susceptibility to primary Sjögren's syndrome in Mexican population. Journal of clinical laboratory analysis 2018 Jul e22620. López-Villalobos Erika Fabiola, Carrillo-Ballesteros Francisco Josué, Muñoz-Valle José Francisco, Palafox-Sánchez Claudia Azucena, Valle Yeminia, Orozco-Barocio Gerardo, Oregon-Romero Edi |
Vitamin D-binding protein and its polymorphisms as a predictor for metabolic syndrome. Biomarkers in medicine 2018 Mar . Karuwanarint Piyaporn, Phonrat Benjaluck, Tungtrongchitr Anchalee, Suriyaprom Kanjana, Chuengsamarn Somlak, Schweigert Florian J, Tungtrongchitr Rungsu |
Men seeking counselling in a Breast Cancer Risk Evaluation Clinic. Ecancermedicalscience 2018 12 804. Freitas Ana Catarina, Opinião Ana, Fragoso Sofia, Nunes Hugo, Santos Madalena, Clara Ana, Bento Sandra, Luis Ana, Silva Jorge, Moura Cecília, Filipe Bruno, Machado Patrícia, Santos Sidónia, André Saudade, Rodrigues Paula, Parreira Joana, Vaz Fáti |
NBS1 rs2735383 polymorphism is associated with an increased risk of laryngeal carcinoma. BMC cancer 2018 02 18 (1): 175. Hu Xinmei, Liao Juan, Zhao Huiliu, Chen Feng, Zhu Xuefeng, Li Jiangheng, Nong Qingqi |
Cytokine Gene Polymorphism in Children With Idiopathic Nephrotic Syndrome. Iranian journal of kidney diseases 2017 Nov 11 (6): 414-421. Midan Dina Abdel Razek, Elhelbawy Nesreen Gamal, Habib Mona Salah El-Din, Ahmedy Iman Aly, Noreldin Rasha Ibrah |
MDR-1 and CYP3A5 Polymorphisms in Pediatric Idiopathic Nephrotic Syndrome: Impact on Susceptibility and Response to Steroids (Preliminary Results). Clinical laboratory 2017 Jul 63 (7): 1233-1242. Moussa Amira, Mabrouk Sameh, Hamdouni Haithem, Ajmi Maroua, Tfifha Miniar, Omezzine Asma, Abroug Saoussen, Bouslama A |
Correlation between Calpain-10 single-nucleotide polymorphisms and obstructive sleep apnea/hypopnoea syndrome with ischemic stroke in a Chinese population: A population-based study. Medicine 2017 Apr 96 (16): e6570. Zhang Wei, Zhao Zhi-Ru, Dai Chang-Fei, Zhang Rong, Chen Jie, Tian Hui-Juan, Wang Yun-Long, Sun Ji-Hong, Lian Qiu-Fa |
Decreased comfort food intake and allostatic load in adolescents carrying the A3669G variant of the glucocorticoid receptor gene. Appetite 2017 Apr . Rodrigues Danitsa Marcos, Reis Roberta Sena, Dalle Molle Roberta, Machado Tania Diniz, Mucellini Amanda Brondani, Bortoluzzi Andressa, Toazza Rudineia, Pérez Juliano Adams, Salum Giovanni Abrahão, Agranonik Marilyn, Minuzzi Luciano, Levitan Robert D, Buchweitz Augusto, Franco Alexandre Rosa, Manfro Gisele Gus, Silveira Patrícia Pelu |
Functional Analysis of the rs774872314, rs116171003, rs200231898 and rs201107751 Polymorphisms in the Human ROR?T Gene Promoter Region. Genes 2017 Apr 8 (4): . Ratajewski Marcin, Slomka Marcin, Karas Kaja, Sobalska-Kwapis Marta, Korycka-Machala Malgorzata, Salkowska Anna, Dziadek Jaroslaw, Strapagiel Dominik, Dastych Jarosl |
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- Page last updated:Jun 22, 2022
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