Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: SLC19A2[original query] |
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Analysis of slc19a2, on 1q23.3 encoding a thiamine transporter as a candidate gene for type 2 diabetes mellitus in pima indians. Molecular genetics and metabolism 2001 Apr 72 (4): 360-3. Thameem F, Wolford J K, Bogardus C, Prochazka |
A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.
Journal of thrombosis and haemostasis : JTH 2012 Aug 10 (8): 1521-31. Heit J A, Armasu S M, Asmann Y W, Cunningham J M, Matsumoto M E, Petterson T M, De Andrade |
A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array. European journal of human genetics : EJHG 2013 Jul 21 (7): 779-83. Gaunt Tom R, Lowe Gordon D O, Lawlor Debbie A, Casas Juan-Pablo, Day Ian N |
A three-step programmed method for the identification of causative gene mutations of maturity onset diabetes of the young (MODY). Gene 2016 May . Li Qian, Cao Xi, Qiu Hai-Yan, Lu Jing, Gao Rui, Liu Chao, Yuan Ming-Xia, Yang Guang-Ran, Yang Jin-K |
Genetic Analysis and Follow-Up of 25 Neonatal Diabetes Mellitus Patients in China. Journal of diabetes research 2016 2016 6314368. Cao Bingyan, Gong Chunxiu, Wu Di, Lu Chaoxia, Liu Fang, Liu Xiaojing, Zhang Yingxian, Gu Yi, Qi Zhan, Li Xiaoqiao, Liu Min, Li Wenjing, Su Chang, Liang Xuejun, Feng M |
Variation in SLC19A3 and Protection From Microvascular Damage in Type 1 Diabetes. Diabetes 2015 Dec . Porta Massimo, Toppila Iiro, Sandholm Niina, Hosseini S Mohsen, Forsblom Carol, Hietala Kustaa, Borio Lorenzo, Harjutsalo Valma, Klein Barbara E, Klein Ronald, Paterson Andrew D, , Groop Per-Henrik, |
Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome. Diabetologia 2018 2 61 (5): 1027-1036. Habeb Abdelhadi M, Flanagan Sarah E, Zulali Mohamed A, Abdullah Mohamed A, Pomaha?ová Renata, Boyadzhiev Veselin, Colindres Lesby E, Godoy Guillermo V, Vasanthi Thiruvengadam, Al Saif Ramlah, Setoodeh Aria, Haghighi Amirreza, Haghighi Alireza, Shaalan Yomna, , Hattersley Andrew T, Ellard Sian, De Franco Eli |
Type 1 diabetes genetic risk score discriminates between monogenic and Type 1 diabetes in children diagnosed at the age of <5 years in the Iranian population. Diabetic medicine : a journal of the British Diabetic Association 2019 7 36 (12): 1694-1702. Yaghootkar H, Abbasi F, Ghaemi N, Rabbani A, Wakeling M N, Eshraghi P, Enayati S, Vakili S, Heidari S, Patel K, Sayarifard F, Borhan-Dayani S, McDonald T J, Ellard S, Hattersley A T, Amoli M M, Vakili R, Colclough |
Genotype/phenotype correlations of childhood-onset congenital sideroblastic anaemia in a European cohort. British journal of haematology 2019 7 187 (4): 530-542. Fouquet Cyrielle, Le Rouzic Marie-Amelyne, Leblanc Thierry, Fouyssac Fanny, Leverger Guy, Hessissen Laila, Marlin Sandrine, Bourrat Emmanuelle, Fahd Mony, Raffoux Emmanuel, Vannier Jean-Pierre, Jäkel Nadja, Knoefler Ralf, Triolo Valerie, Pasquet Marlene, Bayart Sophie, Thuret Isabelle, Lutz Patrick, Vermylen Christiane, Touati Mohamed, Rose Christian, Matthes Thomas, Isidor Bertrand, Kannengiesser Caroline, Ducassou Stepha |
Whole-exome sequencing in Russian children with non-type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY-related and unrelated genes. Molecular medicine reports 2019 Oct . Glotov Oleg S, Serebryakova Elena A, Turkunova Mariia E, Efimova Olga A, Glotov Andrey S, Barbitoff Yury A, Nasykhova Yulia A, Predeus Alexander V, Polev Dmitrii E, Fedyakov Mikhail A, Polyakova Irina V, Ivashchenko Tatyana E, Shved Natalia Y, Shabanova Elena S, Tiselko Alena V, Romanova Olga V, Sarana Andrey M, Pendina Anna A, Scherbak Sergey G, Musina Ekaterina V, Petrovskaia-Kaminskaia Anastasiia V, Lonishin Liubov R, Ditkovskaya Liliya V, Zhelenina Liudmila ?, Tyrtova Ludmila V, Berseneva Olga S, Skitchenko Rostislav K, Suspitsin Evgenii N, Bashnina Elena B, Baranov Vladislav |
3'-UTR Polymorphisms of Vitamin B-Related Genes Are Associated with Osteoporosis and Osteoporotic Vertebral Compression Fractures (OVCFs) in Postmenopausal Women. Genes 2020 Jun 11 (6): . Ahn Tae-Keun, Kim Jung Oh, An Hui Jeong, Park Han Sung, Choi Un Yong, Sohn Seil, Kim Kyoung-Tae, Kim Nam Keun, Han In- |
Implications of venous thromboembolism GWAS reported genetic makeup in the clinical outcome of ovarian cancer patients. The pharmacogenomics journal 2020 Nov . Tavares Valéria, Pinto Ricardo, Assis Joana, Coelho Sara, Brandão Mariana, Alves Sara, Pereira Deolinda, Medeiros R |
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 |
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 |
Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt. Annals of pediatric endocrinology & metabolism 2022 2 27 (3): 214-222. Abdelmeguid Yasmine, Mowafy Ehsan Wafa, Marzouk Iman, Franco Elisa De, ElSayed Shaym |
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- Page last updated:Apr 29, 2024
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