Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 43 Records) |
Query Trace: HEXA[original query] |
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Simultaneous Genotyping of the rs4762 and rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR. Iranian journal of public health 2017 Jun 46 (6): 811-819. Khatami Mehri, Heidari Mohammad Mehdi, Hadadzadeh Mehdi, Scheiber-Mojdehkar Barbara, Bitaraf Sani Morteza, Houshmand Masso |
Evaluation of functional RAGE gene polymorphisms in childhood acute lymphoblastic leukemia-A case-control study from Iran. Nucleosides, nucleotides & nucleic acids 2017 Jan 1-11. Eskandari-Nasab Ebrahim, Hashemi Mohammad, Hasani Seyed-Shahab-Adin, Naderi Majid, Sadeghi-Bojd Simin, Taheri Mohs |
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. PLoS genetics 2018 5 14 (5): e1007329. Rivas Manuel A, Avila Brandon E, Koskela Jukka, Huang Hailiang, Stevens Christine, Pirinen Matti, Haritunians Talin, Neale Benjamin M, Kurki Mitja, Ganna Andrea, Graham Daniel, Glaser Benjamin, Peter Inga, Atzmon Gil, Barzilai Nir, Levine Adam P, Schiff Elena, Pontikos Nikolas, Weisburd Ben, Lek Monkol, Karczewski Konrad J, Bloom Jonathan, Minikel Eric V, Petersen Britt-Sabina, Beaugerie Laurent, Seksik Philippe, Cosnes Jacques, Schreiber Stefan, Bokemeyer Bernd, Bethge Johannes, , , , Heap Graham, Ahmad Tariq, Plagnol Vincent, Segal Anthony W, Targan Stephan, Turner Dan, Saavalainen Paivi, Farkkila Martti, Kontula Kimmo, Palotie Aarno, Brant Steven R, Duerr Richard H, Silverberg Mark S, Rioux John D, Weersma Rinse K, Franke Andre, Jostins Luke, Anderson Carl A, Barrett Jeffrey C, MacArthur Daniel G, Jalas Chaim, Sokol Harry, Xavier Ramnik J, Pulver Ann, Cho Judy H, McGovern Dermot P B, Daly Mark |
New Common and Rare Variants Influencing Metabolic Syndrome and Its Individual Components in a Korean Population.
Scientific reports 2018 Apr 8 (1): 5701. Lee Ho-Sun, Kim Yongkang, Park Taesu |
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients. PloS one 2018 2 13 (2): e0188869. Ji Haoran, Li Dongxiao, Wu Ye, Zhang Quanli, Gu Qiang, Xie Han, Ji Taoyun, Wang Huifang, Zhao Lu, Zhao Haijuan, Yang Yanling, Feng Hongchun, Xiong Hui, Ji Jinhua, Yang Zhixian, Kou Liping, Li Ming, Bao Xinhua, Chang Xingzhi, Zhang Yuehua, Li Li, Li Huijuan, Niu Zhengping, Wu Xiru, Xiao Jiangxi, Jiang Yuwu, Wang Jingm |
Genotype, phenotype and in silico pathogenicity analysis of HEXB mutations: Panel based sequencing for differential diagnosis of gangliosidosis. Clinical neurology and neurosurgery 2018 2 167 43-53. Mahdieh Nejat, Mikaeeli Sahar, Tavasoli Ali Reza, Rezaei Zahra, Maleki Majid, Rabbani Bahar |
Prenatal Diagnosis of Tay-Sachs Disease. Methods in molecular biology (Clifton, N.J.) 2018 12 1885 233-250. Zhang Jinglan, Chen Hongjie, Kornreich Ruth, Yu Chun |
Identification of novel variants in a large cohort of children with Tay-Sachs disease: An initiative of a multicentric task force on lysosomal storage disorders by Government of India. Journal of human genetics 2019 Aug . Mistri Mehul, Mehta Sanjeev, Solanki Dhaval, Kamate Mahesh, Gupta Neerja, Kabra Madhulika, Puri Ratna, Girisha Katta, Hariharan Sankar, Nampoothiri Sheela, Sheth Frenny, Sheth Jaye |
Identification of mutations in HEXA and HEXB in Sandhoff and Tay-Sachs diseases: a new large deletion caused by Alu elements in HEXA. Human genome variation 2019 8 5 18003. Dastsooz Hassan, Alipour Mohsen, Mohammadi Sanaz, Kamgarpour Fatemeh, Dehghanian Fatemeh, Fardaei Maj |
Association of BUD13-ZNF259-APOA5-APOA1-SIK3 cluster polymorphism in 11q23.3 and structure of APOA5 with increased plasma triglyceride levels in a Korean population. Scientific reports 2019 Jun 9 (1): 8296. Kim Han-Kyul, Anwar Muhammad Ayaz, Choi Sangd |
Amyotrophy, cerebellar impairment and psychiatric disease are the main symptoms in a cohort of 14 Czech patients with the late-onset form of Tay-Sachs disease. Journal of neurology 2019 5 266 (8): 1953-1959. Jahnová Helena, Poup?tová Helena, Jire?ková Jitka, Vlášková Hana, Koš?álová Eva, Mazanec Radim, Zumrová Alena, Me?í? Petr, Mušová Zuzana, Magner Mart |
Dietary Protein and Fat Intake Affects Diabetes Risk with CDKAL1 Genetic Variants in Korean Adults. International journal of molecular sciences 2020 8 21 (16): . Choi Woo Jeong, Jin Hyun-Seok, Kim Sung-Soo, Shin Daye |
Analyzing the Association between Hyperuricemia and Periodontitis: A Cross-Sectional Study Using KoGES HEXA Data. International journal of environmental research and public health 2020 7 17 (13): . Byun Soo-Hwan, Yoo Dae-Myoung, Lee Jung-Woo, Choi Hyo-Ge |
Identifying Interactions between Dietary Sodium, Potassium, Sodium-Potassium Ratios, and FGF5 rs16998073 Variants and Their Associated Risk for Hypertension in Korean Adults.
Nutrients 2020 Jul 12 (7): . Jeong Hyeyun, Jin Hyun-Seok, Kim Sung-Soo, Shin Daye |
Analysis of the Interaction between Polygenic Risk Score and Calorie Intake in Obesity in the Korean Population. Lifestyle genomics 2020 Dec 1-10. Lee Won-Jun, Lim Ji Eun, Jung Hae Un, Kang Ji-One, Park Taesung, Won Sungho, Rhee Sang Youl, Kim Mi Kyung, Kim Yeon-Jung, Oh Bermse |
A Transcriptome-Wide Association Study Identifies Novel Candidate Susceptibility Genes for Pancreatic Cancer. Journal of the National Cancer Institute 2020 Jan . Zhong Jun, Jermusyk Ashley, Wu Lang, Hoskins Jason W, Collins Irene, Mocci Evelina, Zhang Mingfeng, Song Lei, Chung Charles C, Zhang Tongwu, Xiao Wenming, Albanes Demetrius, Andreotti Gabriella, Arslan Alan A, Babic Ana, Bamlet William R, Beane-Freeman Laura, Berndt Sonja, Borgida Ayelet, Bracci Paige M, Brais Lauren, Brennan Paul, Bueno-de-Mesquita Bas, Buring Julie, Canzian Federico, Childs Erica J, Cotterchio Michelle, Du Mengmeng, Duell Eric J, Fuchs Charles, Gallinger Steven, Gaziano J Michael, Giles Graham G, Giovannucci Edward, Goggins Michael, Goodman Gary E, Goodman Phyllis J, Haiman Christopher, Hartge Patricia, Hasan Manal, Helzlsouer Kathy J, Holly Elizabeth A, Klein Eric A, Kogevinas Manolis, Kurtz Robert J, LeMarchand Loic, Malats Núria, Männistö Satu, Milne Roger, Neale Rachel E, Ng Kimmie, Obazee Ofure, Oberg Ann L, Orlow Irene, Patel Alpa V, Peters Ulrike, Porta Miquel, Rothman Nathaniel, Scelo Ghislaine, Sesso Howard D, Severi Gianluca, Sieri Sabina, Silverman Debra, Sund Malin, Tjønneland Anne, Thornquist Mark D, Tobias Geoffrey S, Trichopoulou Antonia, Van Den Eeden Stephen K, Visvanathan Kala, Wactawski-Wende Jean, Wentzensen Nicolas, White Emily, Yu Herbert, Yuan Chen, Zeleniuch-Jacquotte Anne, Hoover Robert, Brown Kevin, Kooperberg Charles, Risch Harvey A, Jacobs Eric J, Li Donghui, Yu Kai, Shu Xiao-Ou, Chanock Stephen J, Wolpin Brian M, Stolzenberg-Solomon Rachael Z, Chatterjee Nilanjan, Klein Alison P, Smith Jill P, Kraft Peter, Shi Jianxin, Petersen Gloria M, Zheng Wei, Amundadottir Laufey |
Analysis of the HEXA, HEXB, ARSA, and SMPD1 Genes in 68 Iranian Patients. Journal of molecular neuroscience : MN 2021 9 72 (3): 555-564. Abtahi Rezvan, Karimzadeh Parvaneh, Rezayi Alireza, Salehpour Shadab, Akbarzadeh Diba, Tonekaboni Seyed Hassan, Emameh Reza Zolfaghari, Houshmand Masso |
The Homocysteine and Metabolic Syndrome: A Mendelian Randomization Study. Nutrients 2021 8 13 (7): . Lee Ho-Sun, In Sanghwan, Park Taesu |
Analyses of the association between cervical cancer and osteoporosis/osteoporotic fracture: a cross-sectional study using KoGES HEXA data. International journal of clinical oncology 2021 6 26 (9): 1752-1758. Choi Hyo Geun, Lee Jung Woo, Min Chan Yang, Yoo Dae Myoung, Lee Suk W |
A Genome-Wide Association Study for Hypertensive Kidney Disease in Korean Men.
Genes 2021 May 12 (5): . Kim Hye-Rim, Jin Hyun-Seok, Eom Yong-B |
Analyses of the association between breast cancer and osteoporosis/fracture history: a cross-sectional study using KoGES HEXA data. Archives of osteoporosis 2021 6 16 (1): 98. Choi Hyo Geun, Suh Yong Joon, Lee Jung Woo, Min Chan Yang, Yoo Dae Myoung, Lee Suk W |
Synergistic effect between the KCNQ1 haplotype and alcohol consumption on the development of type 2 diabetes mellitus in Korean cohorts. Scientific reports 2021 Nov 11 (1): 21796. Park Ji Young, Yoo Min-Gyu, Yun Ji Ho, Lee Hye-Ja, Park Sang I |
Pontocerebellar atrophy is the hallmark neuroradiological finding in late-onset Tay-Sachs disease. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2021 11 43 (5): 3273-3281. Májovská Jitka, Hennig Anita, Nestrasil Igor, Schneider Susanne A, Jahnová Helena, Van??ková Manuela, Magner Martin, Dušek Pe |
Microsatellite Instability Is Rare in the Admixed Brazilian Population of Non-Small Cell Lung Cancer: A Cohort of 526 Cases. Pathobiology : journal of immunopathology, molecular and cellular biology 2021 Nov 1-6. De Marchi Pedro, Berardinelli Gustavo Noriz, Cavagna Rodrigo de Oliveira, Pinto Icaro Alves, da Silva Flavio Augusto Ferreira, Duval da Silva Vinicius, Santana Iara Viana Vidigal, da Silva Eduardo Caetano Albino, Ferro Leal Leticia, Reis Rui Manu |
The effect of the association between CETP variant type and alcohol consumption on cholesterol level differs according to the ALDH2 variant type. Scientific reports 2022 Sep 12 (1): 15129. Yoo Min-Gyu, Yun Ji Ho, Koo Soo Kyung, Lee Hye- |
The potential effects of HECTD4 variants on fasting glucose and triglyceride levels in relation to prevalence of type 2 diabetes based on alcohol intake. Archives of toxicology 2022 Jun . Lee Yoo Jeong, Lee Hansongyi, Jang Han Byul, Yoo Min-Gyu, Im Sumin, Koo Soo Kyung, Lee Hye- |
Gene-environment interaction in type 2 diabetes in Korean cohorts: Interaction of a type 2 diabetes polygenic risk score with triglyceride and cholesterol on fasting glucose levels. Genetic epidemiology 2022 4 46 (5-6): 285-302. Lim Ji Eun, Kang Ji-One, Ha Tae-Woong, Jung Hae-Un, Kim Dong Jun, Baek Eun Ju, Kim Han Kyul, Chung Ju Yeon, Rhee Sang Youl, Kim Mi Kyung, Kim Yeon-Jung, Park Taesung, Oh Bermse |
Development of a Polygenic Risk Score for BMI to Assess the Genetic Susceptibility to Obesity and Related Diseases in the Korean Population. International journal of molecular sciences 2023 7 24 (14): . Nara Yoon, Yoon Shin C |
Biochemical and mutational analyses of HEXA in a cohort of Egyptian patients with infantile Tay-Sachs disease. Expansion of the mutation spectrum. Orphanet journal of rare diseases 2023 3 18 (1): 52. Ibrahim Doaa M A, Ali Ola S M, Nasr Hala, Fateen Ekram, AbdelAleem Ali |
Influence of blood pressure polygenic risk scores and environmental factors on coronary artery disease in the Korean Genome and Epidemiology Study. Journal of human hypertension 2023 11 . Kyungsook Woo, Ji Eun Lim, Eun Young L |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
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