Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 45 Records) |
| Query Trace: Disease and ABCC8[original query] |
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| Phenotypic heterogeneity in monogenic diabetes: the clinical and diagnostic utility of a gene panel-based next-generation sequencing approach. Molecular genetics and metabolism 2014 Dec 113 (4): 315-20. Alkorta-Aranburu G, Carmody D, Cheng Y W, Nelakuditi V, Ma L, Dickens Jazzmyne T, Das S, Greeley S A W, del Gaudio |
| Pharmacogenetics and individual responses to treatment of hyperglycemia in type 2 diabetes. Pharmacogenetics and genomics 2015 Oct 25 (10): 475-84. Engelbrechtsen Line, Andersson Ehm, Roepstorff Soeren, Hansen Torben, Vestergaard Henr |
| Replication of KCNJ11 (p.E23K) and ABCC8 (p.S1369A) Association in Russian Diabetes Mellitus 2 Type Cohort and Meta-Analysis. PloS one 2015 10 (5): e0124662. Sokolova Ekaterina Alekseevna, Bondar Irina Arkadievna, Shabelnikova Olesya Yurievna, Pyankova Olga Vladimirovna, Filipenko Maxim Leonidovi |
| Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients. Molecular genetics & genomic medicine 2015 Nov 3 (6): 526-36. Fan Zi-Chuan, Ni Jin-Wen, Yang Lin, Hu Li-Yuan, Ma Si-Min, Mei Mei, Sun Bi-Jun, Wang Hui-Jun, Zhou Wen-H |
| Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism. Journal of clinical research in pediatric endocrinology 2015 Dec . Güven Ayla, Cebeci Ay?e Nurcan, Ellard Sian, Flanagan Sarah |
| Both Low Blood Glucose and Insufficient Treatment Confer Risk of Neurodevelopmental Impairment in Congenital Hyperinsulinism: A Multinational Cohort Study. Frontiers in endocrinology 2017 7 8 156. Helleskov Annett, Melikyan Maria, Globa Evgenia, Shcherderkina Inna, Poertner Fani, Larsen Anna-Maria, Filipsen Karen, Brusgaard Klaus, Christiansen Charlotte Dahl, Hansen Lars Kjaersgaard, Christesen Henrik |
| Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals. BMC medicine 2017 12 15 (1): 213. Bansal Vikas, Gassenhuber Johann, Phillips Tierney, Oliveira Glenn, Harbaugh Rebecca, Villarasa Nikki, Topol Eric J, Seufferlein Thomas, Boehm Bernhard |
| CYP2C9*3 gene variant contributes independently to glycaemic control in patients with type 2 diabetes treated with glibenclamide. Journal of clinical pharmacy and therapeutics 2018 May . Castelán-Martínez O D, Hoyo-Vadillo C, Bazán-Soto T B, Cruz M, Tesoro-Cruz E, Valladares-Salgado |
| Pharmacogenetics and target identification in diabetes. Current opinion in genetics & development 2018 2 50 68-73. Pearson Ewan |
| Next generation sequencing targeted gene panel in Greek MODY patients increases diagnostic accuracy. Pediatric diabetes 2019 10 21 (1): 28-39. Tatsi Elizabeth B, Kanaka-Gantenbein Christina, Scorilas Andreas, Chrousos George P, Sertedaki Amal |
| Clinical and Genetic Characterization of 153 Patients with Persistent or Transient Congenital Hyperinsulinism. The Journal of clinical endocrinology and metabolism 2020 3 105 (4): . Männistö Jonna M E, Maria Maleeha, Raivo Joose, Kuulasmaa Teemu, Otonkoski Timo, Huopio Hanna, Laakso Mark |
| Role of Genetic Variation in ABC Transporters in Breast Cancer Prognosis and Therapy Response. International journal of molecular sciences 2020 Dec 21 (24): . Hlavác Viktor, Václavíková Radka, Brynychová Veronika, Koževnikovová Renata, Kopecková Katerina, Vrána David, Gatek Jirí, Soucek Pav |
| Genetic variants of ABCC8 and phenotypic features in Chinese early onset diabetes. Journal of diabetes 2020 Dec . Li Meng, Gong Siqian, Han Xueyao, Zhang Simin, Ren Qian, Cai Xiaoling, Luo Yingying, Zhou Lingli, Zhang Rui, Liu Wei, Zhu Yu, Zhou Xianghai, Sun Yanfang, Li Yufeng, Ma Yumin, Ji Lino |
| [Genetic analysis of a juvenile with maturity-onset diabetes of the young type 12]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 9 38 (9): 891-894. Luo Yue, Jin Jiahui, Li Liyi, Wu Huiping, Shan Xiao |
| Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience. Acta diabetologica 2021 8 58 (12): 1689-1700. Laimon Wafaa, El-Ziny Magdy, El-Hawary Amany, Elsharkawy Ashraf, Salem Nanees Abdel-Badie, Aboelenin Hadil Mohamed, Awad Mohammad Hosny, Flanagan Sarah E, De Franco Eli |
| Genotyping of ABCC8, KCNJ11, and HADH in Iranian Infants with Congenital Hyperinsulinism. Case reports in endocrinology 2021 5 2021 8826174. Hashemian Somayyeh, Esfehani Reza Jafarzadeh, Karimdadi Siroos, Ghaemi Nosrat, Eshraghi Peyman, Gonabadi Najmeh Malekzadeh, Sahebkar Amirhossein, Vakili Rahim, Abbaszadegan Mohammad Re |
| Clinical characteristics, outcome, and predictors of neurological sequelae of persistent congenital hyperinsulinism: A single tertiary center experience. Pediatric diabetes 2021 Feb . Laimon Wafaa, Aboelenin Hadil Mohamed, El Tantawi Noha |
| Polymorphisms in Genes of Lipid Metabolism Are Associated with Type 2 Diabetes Mellitus and Periodontitis, as Comorbidities, and with the Subjects' Periodontal, Glycemic, and Lipid Profiles. Journal of diabetes research 2021 11 2021 1049307. Nicchio Ingra G, Cirelli Thamiris, Nepomuceno Rafael, Hidalgo Marco A R, Rossa Carlos, Cirelli Joni A, Orrico Silvana R P, Barros Silvana P, Theodoro Letícia H, Scarel-Caminaga Raquel |
| Clinical and Genetic Characteristics of ABCC8 Nonneonatal Diabetes Mellitus: A Systematic Review. Journal of diabetes research 2021 10 2021 9479268. Li Meng, Han Xueyao, Ji Lino |
| Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience. Hormone research in paediatrics 2021 1 93 (7-8): 423-432. Abali Zehra Yavas, De Franco Elisa, Karakilic Ozturan Esin, Poyrazoglu Sukran, Bundak Ruveyde, Bas Firdevs, Flanagan Sarah E, Darendeliler Fey |
| Study of the frequency and clinical features of maturity-onset diabetes in the young in the pediatric and adolescent diabetes population in Iran. Journal of pediatric endocrinology & metabolism : JPEM 2022 9 35 (10): 1240-1249. Zamanfar Daniel, Ferdosipour Fatemeh, Ebrahimi Pirooz, Moghadam Mohamad, Amoli Mahsa M, Asadi Mojgan, Monajati Mahi |
| Early-onset diabetes involving three consecutive generations had different clinical features from age-matched type 2 diabetes without a family history in China. Endocrine 2022 Oct 78 (1): 47-56. Wang Da-Wei, Yuan Jing, Yang Fang-Yuan, Qiu Hai-Yan, Lu Jing, Yang Jin-K |
| Monogenic diabetes variants in Emirati women with gestational diabetes are associated with risk of non-autoimmune diabetes within 5 years after pregnancy. Metabolism open 2022 11 16 100213. Daggag Hinda, Gjesing Anette P, Mohammad Alshafi, Ängquist Lars, Shobi Bindu, Antony Suma, Haj Dalia, Al Tikriti Alia, Buckley Adam, Hansen Torben, Barakat Maha |
| Association of KCNJ11 and ABCC8 single-nucleotide polymorphisms with type 2 diabetes mellitus in a Kinh Vietnamese population. Medicine 2022 11 101 (46): e31653. Tran Nam Quang, Truong Steven D, Ma Phat Tung, Hoang Chi Khanh, Le Bao Hoang, Dinh Thang Tat Ngo, Van Tran Luong, Tran Thang Viet, Le Linh Hoang Gia, Le Khuong Thai, Nguyen Hien Thanh, Vu Hoang Anh, Mai Thao Phuong, Do Minh D |
| Polymorphisms in glucose homeostasis genes are associated with cardiovascular and renal parameters in patients with diabetic nephropathy. Annals of medicine 2022 10 54 (1): 3039-3051. Mota-Zamorano Sonia, González Luz M, Robles Nicolás R, Valdivielso José M, Arévalo-Lorido José C, López-Gómez Juan, Gervasini Guiller |
| MOLECULAR DIAGNOSIS IN PATIENTS WITH MONOGENIC DIABETES MELLITUS, AND DETECTION OF A NOVEL CANDIDATE GENE. Diabetes research and clinical practice 2023 10 110953. Damla Goksen, Ferda Evin, Esra Isik, Samim Ozen, Tahir Atik, Ferda Ozkinay, Nese Akcan, Behzat Ozkan, Muammer Buyukinan, Mehmet Nuri Ozbek, Sukran Darcan, Huseyin On |
| Clinical and genetic characteristics of congenital hyperinsulinism in Norway: A nationwide cohort study. The Journal of clinical endocrinology and metabolism 2024 7 . Christoffer Drabløs Velde, Janne Molnes, Siren Berland, Pål Rasmus Njølstad, Anders Molv |
| The obesity-related mutation gene on nonalcoholic fatty liver disease. Human genetics 2024 7 . Yen-Yu Chen, Chi-Sheng Chen, Jee-Fu Huang, Wen-Hsiu Su, Chia-Yang Li, Wei-Shiun Chen, En-Sheng Lin, Wan-Long Chuang, Ming-Lung Yu, Shu-Chi Wa |
| VARIATIONS IN MONOGENIC DIABETES AND DIABETES SUSCEPTIBILITY GENES IN PEDIATRIC CASES: SINGLE CENTER EXPERIENCE. Acta endocrinologica (Bucharest, Romania : 2005) 2024 6 19 (4): 512-522. I Arslano?lu, R Eröz, F Yavuzy?lmaz, M Do?an, S Bolu, S Kara |
| ABCC8 polymorphisms rs757110 and rs1801261 association with sulfonylurea therapy of Iraqi type 2 diabetics. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2024 12 77 (11): 2317-2325. Sarah H Shaalan, Muneer Khudhair, Noaman Ibadi Mohammed, Zubaida Falih Alzubai |
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