Human Genome Epidemiology Literature Finder
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Idiopathic infantile hypercalcemia in children with chronic kidney disease due to kidney hypodysplasia. Pediatric nephrology (Berlin, Germany) 2022 9 38 (4): 1067-1073. Gurevich Evgenia, Borovitz Yael, Levi Shelli, Perlman Sharon, Landau Dani |
Overcoming the Pitfalls of Next-Generation Sequencing-Based Molecular Diagnosis of Shwachman-Diamond Syndrome. The Journal of molecular diagnostics : JMD 2022 9 24 (12): 1240-1253. Peng Xiaomin, Dong Xinran, Wang Yaqiong, Wu Bingbing, Wang Huijun, Lu Wei, Xiao Feifan, Yang Lin, Li Gang, Zhou Wenhao, Liu Bo, Lu Yul |
Association of GAB2 with Quality of Life and Negative Emotions in Patients with Gastric Cancer after Postoperative Comprehensive Care. Evidence-based complementary and alternative medicine : eCAM 2022 2022 1732214. Zhuang Juping, Yu Jiejie, Yang Yanc |
How interactions between ADHD and schools affect educational achievement: a family-based genetically sensitive study. Journal of child psychology and psychiatry, and allied disciplines 2022 7 63 (10): 1174-1185. Cheesman Rosa, Eilertsen Espen M, Ayorech Ziada, Borgen Nicolai T, Andreassen Ole A, Larsson Henrik, Zachrisson Henrik, Torvik Fartein A, Ystrom Eivi |
Importance of Rare DPYD Genetic Polymorphisms for 5-Fluorouracil Therapy in the Japanese Population. Frontiers in pharmacology 2022 7 13 930470. Hishinuma Eiji, Narita Yoko, Obuchi Kai, Ueda Akiko, Saito Sakae, Tadaka Shu, Kinoshita Kengo, Maekawa Masamitsu, Mano Nariyasu, Hirasawa Noriyasu, Hiratsuka Masahi |
Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome. Italian journal of pediatrics 2022 7 48 (1): 121. Zhang Lu, Liu Xiaoliang, Zhao Yunjing, Wang Qingyi, Zhang Yuanyuan, Gao Haiming, Zhang Bijun, Cui Wanting, Zhao Yany |
Heterozygous NPR2 Variants in Idiopathic Short Stature. Genes 2022 6 13 (6): . Stavber Lana, Gaia Maria Joao, Hovnik Tinka, Jenko Bizjan Barbara, Debeljak Maruša, Kova? Jernej, Omladi? Jasna Šuput, Battelino Tadej, Kotnik Primož, Dov? Klem |
Green tea consumption and risk of depressive symptoms: Results from the TCLSIH Cohort Study. Journal of affective disorders 2022 4 310 183-188. Dong Xinrong, Gu Yeqing, Rayamajhi Sabina, Thapa Amrish, Meng Ge, Zhang Qing, Liu Li, Wu Hongmei, Zhang Shunming, Zhang Tingjing, Wang Xuena, Li Huiping, Zhang Juanjuan, Dong Jun, Zheng Xiaoxi, Cao Zhixia, Sun Shaomei, Wang Xing, Zhou Ming, Jia Qiyu, Song Kun, Chang Hong, Zheng Yunliang, Niu Kaij |
Clinical Characteristics of Short-Stature Patients With Collagen Gene Mutation and the Therapeutic Response to rhGH. Frontiers in endocrinology 2022 3 13 820001. Chen Meiping, Miao Hui, Liang Hanting, Ke Xiaoan, Yang Hongbo, Gong Fengying, Wang Linjie, Duan Lian, Chen Shi, Pan Hui, Zhu Huiju |
Familial early-onset obesity in Turkish children: variants and polymorphisms in the melanocortin-4 receptor (MC4R) gene. Journal of pediatric endocrinology & metabolism : JPEM 2022 3 35 (5): 657-662. K?rm?z?bekmez Heves, Kendir Demirkol Yasemin, Akgün Do?an Özlem, Seymen Gülcan, ?nan Balc? Elif, Atla P?nar, Dursun Fat |
Role of ZBTB38 Genotype and Expression in Growth and Response to Recombinant Human Growth Hormone Treatment. Journal of the Endocrine Society 2022 Mar 6 (3): bvac006. Parsons Samuel, Stevens Adam, Whatmore Andrew, Clayton Peter E, Murray Philip |
Delayed Puberty Phenotype Observed in Noonan Syndrome Is More Pronounced in Girls than Boys. Hormone research in paediatrics 2022 2 95 (1): 51-61. Rezende Raissa C, Noronha Renata Maria, Keselman Ana, Quedas Elisangela P S, Dantas Naiara C B, Andrade Nathalia L M, Bertola Debora R, Malaquias Alexsandra C, Jorge Alexander A |
Variability in Fetal Fraction Estimation: Comparing Fetal Fractions Reported by Noninvasive Prenatal Testing Providers Globally. Clinical chemistry 2022 12 69 (2): 160-167. Becking Ellis C, Linthorst Jasper, Patton Simon, Gutowska-Ding Weronika, Goodall Rebecca, Khawaja Farrah, Morgan Fiona, Deans Zandra, Chitty Lyn S, Bekker Mireille N, Scheffer Peter G, Sistermans Erik |
Genetic and phenotypic differences between sexes in congenital hypogonadotropic hypogonadism (CHH): Large cohort analysis from a single tertiary centre. Frontiers in endocrinology 2022 12 13 965074. Federici Silvia, Cangiano Biagio, Goggi Giovanni, Messetti Dario, Munari Elisabetta Veronica, Amer Myriam, Giovanelli Luca, Hrvat Faris, Vezzoli Valeria, Persani Luca, Bonomi Mar |
Phenotypic and genotypic characteristics of children with Bartter syndrome. The Turkish journal of pediatrics 2022 10 64 (5): 825-838. Güven Serçin, Gökçe ?brahim, Alavanda Ceren, Çiçek Neslihan, Demirci Ece Bodur, Sak Mehtap, Pul Serim, Türkkan Özde Nisa, Y?ld?z Nurdan, Ata P?nar, Alpay Hari |
The neuropeptide Y single-nucleotide polymorphism rs16147:T>C moderates the effect of alcohol dependence on depression in male Chinese Han population. Frontiers in psychiatry 2022 13 1012850. Wei Xiaojie, Cai Fangfang, Zhou Siyao, Zhang Jinjing, Xu Kewei, Shen Guanghui, Sun Huankun, Yang Fan, Hong Liuzhi, Zou Yang, Chen Yu-Hsin, Liu Yanlong, Chen Li, Wang Fan, Wang W |
A New Treatment Protocol of Combined High-Dose Levothyroxine and Repetitive Transcranial Magnetic Stimulation for the Treatment of Rapid-Cycling Bipolar Spectrum Disorders: A Cohort Evaluation of 55 Patients. Journal of clinical medicine 2022 10 11 (19): . Zamar Antonis C, Kouimtsidis Christos, Lulsegged Abbi, Roberts Robin, Koutsomitros Theodoros, Stahl Dani |
RETN gene polymorphisms interact with alcohol dependence in association with depression. Journal of clinical laboratory analysis 2023 6 e24933. Xiaoyan Xu, Zeping Xu, Fan Zhou, Lijing Chen, Huai Li, Michelle Niculescu, Guanghui Shen, Liujun Wu, Wei Wang, Li Chen, Yanlong Liu, Jue He, Fan Wang, Fan Ya |
An adult-based genetic risk score for liver fat associates with liver and plasma lipid traits in children and adolescents. Liver international : official journal of the International Association for the Study of the Liver 2023 5 . Yun Huang, Sara E Stinson, Helene Baek Juel, Morten A V Lund, Louise Aas Holm, Cilius E Fonvig, Trine Nielsen, Niels Grarup, Oluf Pedersen, Michael Christiansen, Elizaveta Chabanova, Henrik S Thomsen, Aleksander Krag, Stefan Stender, Jens-Christian Holm, Torben Hans |
Association of Dopamine Transporter Gene (DAT1) 40?bp 3' UTR VNTR Polymorphism (rs28363170) and Cannabis Use Disorder. Substance abuse : research and treatment 2023 4 17 11782218231163696. Olasore Holiness Sa, Osuntoki Akinniyi A, Magbagbeola Olubunmi A, Awesu Abdur-Rasheed B, Olashore Anthony |
Real life long-term efficacy and safety of rhGH therapy in children with SHOX deficiency. Endocrine connections 2023 4 . Bruzzi Patrizia, Vannelli Silvia, Scarano Emanuela, Di Iorgi Natascia, Parpagnoli Maria, Salerno Mariacarolina, Pitea Marco, Street Maria Elisabeth, Secco Andrea, Trettene Adolfo Andrea, Wasniewska Malgorzata, Corciulo Nicola, Tornese Gianluca, Faienza Maria Felicia, Delvecchio Maurizio, Madeo Simona Filomena, Iughetti Loren |
Metabolic Signatures of Youth Exposure to Mixtures of Per- and Polyfluoroalkyl Substances: A Multi-Cohort Study. Environmental health perspectives 2023 2 131 (2): 27005. Goodrich Jesse A, Walker Douglas I, He Jingxuan, Lin Xiangping, Baumert Brittney O, Hu Xin, Alderete Tanya L, Chen Zhanghua, Valvi Damaskini, Fuentes Zoe C, Rock Sarah, Wang Hongxu, Berhane Kiros, Gilliland Frank D, Goran Michael I, Jones Dean P, Conti David V, Chatzi Le |
Genetic background of idiopathic neurodevelopmental delay patients with significant brain deviation volume. Chinese medical journal 2023 2 . Chen Xiang, Chen Yuxi, Yan Kai, Chen Huiyao, Qin Qian, Yang Lin, Liu Bo, Cheng Guoqiang, Cao Yun, Wu Bingbing, Dong Xinran, Qiao Zhongwei, Zhou Wenh |
Distinguishing EGFR mutant subtypes in stage IA non-small cell lung cancer using the presence status of ground glass opacity and final histologic classification: a systematic review and meta-analysis. Frontiers in medicine 2023 12 10 1268846. Jianhao Qiu, Zheng Ma, Rongyang Li, Chenghao Qu, Kun Wang, Binyan Liu, Yu Tian, Hui Ti |
Molecular Mechanism of Vitamin D Receptor Modulating Wnt/?-catenin Signaling Pathway in Gastric Cancer. Journal of Cancer 2023 11 14 (17): 3285-3294. Ying Zhang, Yan Li, Yuzheng Wei, Lei Co |
Bone health in children with Angelman syndrome at the ENCORE Expertise Center. European journal of pediatrics 2023 10 . Karen G C B Bindels-de Heus, Doesjka A Hagenaar, Sabine E Mous, Ilonka Dekker, Daniëlle C M van der Kaay, Gerthe F Kerkhof, Ype Elgersma, Henriette A Moll, Marie-Claire Y de W |
Multicentric Italian case-control study on 25OH vitamin D levels in children and adolescents with Prader-Willi syndrome. Journal of endocrinological investigation 2023 1 . Panfili F M, Convertino A, Grugni G, Mazzitelli L, Bocchini S, Crinò A, Campana G, Cappa M, Delvecchio M, Faienza M F, Licenziati M R, Mariani M, Osimani S, Pajno R, Patti G, Rutigliano I, Sacco M, Scarano E, Fintini D, |
Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation. Journal of clinical research in pediatric endocrinology 2024 6 . Samim Özen, Damla Gök?en, Ferda Evin, Esra I??k, Hüseyin Onay, Bilça? Akgün, Aysun Ata, Tahir Atik, Füsun Düzcan, Ferda Özk?nay, ?ükran Darcan, Özgür Ço?u |
Association of ZBTB38 gene polymorphism (rs724016) with height and fetal hemoglobin in individuals with sickle cell anemia. Molecular genetics and metabolism reports 2024 5 39 101086. Domício Antônio Costa-Júnior, Thaisa N Souza Valente, André Rolim Belisário, Gisele Queiroz Carvalho, Miguel Madeira, Cibele Velloso-Rodrigu |
Role of IL-6, IL-10 and TNF? Gene Variants in Preterm Birth. Journal of clinical medicine 2024 4 13 (8): . Mirta Kadivnik, Deni Ple?ko, Kristina Kralik, Nena Arvaj, Jasenka Wagn |
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- Page last updated:Jun 11, 2024
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