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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Disease and SLC19A3[original query]
Folate network genetic variation, plasma homocysteine, and global genomic methylation content: a genetic association study.
BMC medical genetics 2011 12 (1): 150.
Wernimont Susan M, Clark Andrew G, Stover Patrick J, Wells Martin T, Litonjua Augusto A, Weiss Scott T, Gaziano J Michael, Tucker Katherine L, Baccarelli Andrea, Schwartz Joel, Bollati Valentina, Cassano Patricia
Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data.
Genes, brain, and behavior 2015 Sep .
Saad M, Brkanac Z, Wijsman E
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,
Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening.
Annals of clinical and translational neurology 2019 9 6 (10): 2097-2103.
Alfadhel Majid, Umair Muhammad, Almuzzaini Bader, Alsaif Saif, AlMohaimeed Sulaiman A, Almashary Maher A, Alharbi Wardah, Alayyar Latifah, Alasiri Abdulrahman, Ballow Mariam, AlAbdulrahman Abdulkareem, Alaujan Monira, Nashabat Marwan, Al-Odaib Ali, Altwaijri Waleed, Al-Rumayyan Ahmed, Alrifai Muhammad T, Alfares Ahmed, AlBalwi Mohammed, Tabarki Brah
[Identification of two novel SLC19A3 variants in a Chinese patient with Biotin-thiamine responsive basal ganglia disease].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 2 37 (2): 162-165.
Gao Min, Huang Yan, Zhang Kaihui, Lyu Yuqing, Dong Rui, Ma Jian, Wang Dong, Gai Zhongtao, Liu
SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population.
Human genetics 2021 11 141 (1): 81-99.
Mir Ali, Almudhry Montaha, Alghamdi Fouad, Albaradie Raidah, Ibrahim Mona, Aldurayhim Fatimah, Alhedaithy Abdullah, Alamr Mushari, Bawazir Maryam, Mohammad Sahar, Abdelhay Salma, Bashir Shahid, Housawi Yous
Exome-wide Analysis of De Novo and Rare Genetic Variants in Patients With Brain Arteriovenous Malformation.
Neurology 2022 3 98 (16): e1670-e1678.
Wang Kun, Zhao Sen, Xie Zhixin, Zhang Mingqi, Zhao Hengqiang, Cheng Xi, Zhang Yisen, Niu Yuchen, Liu Jian, Zhang Terry Jianguo, Zhang Ying, Wu Zhihong, Chu Junsheng, Yang Xinjian, Wu N
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia.
International journal of molecular sciences 2023 1 24 (2): .
Kistol Denis, Tsygankova Polina, Krylova Tatiana, Bychkov Igor, Itkis Yulia, Nikolaeva Ekaterina, Mikhailova Svetlana, Sumina Maria, Pechatnikova Natalia, Kurbatov Sergey, Bostanova Fatima, Migiaev Ochir, Zakharova Ekateri
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