| For: | Dhillon BK, Das R, Garewal G, Chawla Y, Dhiman R, Das A, Duseja A, Chandak G. Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India. World J Gastroenterol 2007; 13(21): 2956-2959 [PMID: 17589946 DOI: 10.3748/wjg.v13.i21.2956] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v13/i21/2956.htm |
| Number | Citing Articles |
| 1 |
Dana Gabriková, Jarmila Bernasovská, Soňa Mačeková, Alexandra Bôžiková, Ivan Bernasovský, Alena Bališinová, Adriana Sovičová, Regína Behulová, Eva Petrejčíková, Miroslav Soták, Iveta Boroňová. Unique frequencies of HFE gene variants in Roma/Gypsies. Journal of Applied Genetics 2012; 53(2) doi: 10.1007/s13353-012-0088-y
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| 2 |
BARJINDERJIT KAUR DHILLON, SWAMI PRAKASH, G. R. CHANDAK, Y. K. CHAWLA, REENA DAS. H63D mutation in HFE gene is common in Indians and is associated with the European haplotype. Journal of Genetics 2012; 91(2) doi: 10.1007/s12041-012-0163-5
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| 3 |
Barjinderjit Kaur Dhillon, Gunjan Chopra, Manu Jamwal, Giri Raj Chandak, Ajay Duseja, Pankaj Malhotra, Yogesh Kumar Chawla, Gurjeewan Garewal, Reena Das. Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians. Blood Cells, Molecules, and Diseases 2018; 73 doi: 10.1016/j.bcmd.2018.08.003
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| 4 |
Sang Hyub Lee, Sook-Hyang Jeong, Donghun Lee, Jee Hye Lee, Sung Ho Hwang, Young Ae Cho, Young Soo Park, Jin-Hyeok Hwang, Jin-Wook Kim, Nayoung Kim, Dong Ho Lee, Weechang Kang. An Epidemiologic Study on the Incidence and Significance of HFE Mutations in a Korean Cohort With Nonalcoholic Fatty Liver Disease. Journal of Clinical Gastroenterology 2010; 44(7) doi: 10.1097/MCG.0b013e3181d347d9
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| 5 |
I. V. Paltsev, A. L. Kalinin. MUTATIONS OF GENE HFE AS A RISK FACTOR OF HEMOCHROMATOSIS DEVELOPMENT AT PATIENT WITH CHRONIC DIFFUSE LIVER DISEASES. Health and Ecology Issues 2010; (4) doi: 10.51523/2708-6011.2010-7-4-10
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| 6 |
Zahra Jowkar, Bita Geramizadeh, Mahmoud Shariat. Frequency of Two Common HFE Gene Mutations (C282Y and H63D) in a Group of Iranian Patients With Cryptogenic Cirrhosis. Hepatitis Monthly 2011; 11(11) doi: 10.5812/kowsar.1735143X.3749
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| 7 |
Qing Ye, Bao-Xin Qian, Wei-Li Yin, Feng-Mei Wang, Tao Han, Pavel Strnad. Association between the HFE C282Y, H63D Polymorphisms and the Risks of Non-Alcoholic Fatty Liver Disease, Liver Cirrhosis and Hepatocellular Carcinoma: An Updated Systematic Review and Meta-Analysis of 5,758 Cases and 14,741 Controls. PLOS ONE 2016; 11(9) doi: 10.1371/journal.pone.0163423
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| 8 |
Reena Das, Jasmina Ahluwalia, Man Updesh Singh Sachdeva. Hematological Practice in India. Hematology/Oncology Clinics of North America 2016; 30(2) doi: 10.1016/j.hoc.2015.11.009
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| 9 |
Abhishek Goyal, Bishav Mohan, Kavita Saggar, Gurpreet Singh Wander. Primary haemochromatosis resulting in dilated cardiomyopathy arising out of mutation in HJV gene in Indian patients: a rare scenario. BMJ Case Reports 2020; 13(9) doi: 10.1136/bcr-2020-235650
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| 10 |
Etiological Spectrum of Cirrhosis in India: A Systematic Review and Meta-analysis. Journal of Clinical and Experimental Hepatology 2024; 14(2) doi: 10.1016/j.jceh.2023.10.002
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| 11 |
Ling Nie, Lin Li, Lin Yang, Yue Zhang, Zhijian Xiao. HFE genotype and iron metabolism in Chinese patients with myelodysplastic syndromes and aplastic anemia. Annals of Hematology 2010; 89(12) doi: 10.1007/s00277-010-1016-z
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| 12 |
Darrell H. G. Crawford, Linda M. Fletcher, Kris V. Kowdley. Iron Physiology and Pathophysiology in Humans. 2012; doi: 10.1007/978-1-60327-485-2_22
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| 13 |
Bhuvana Selvaraj, Sangeetha Soundararajan, Shettu Narayanasamy, Ganesan Subramanian, Senthil Kumar Ramanathan. Frequency of hereditary hemochromatosis gene mutations and their effects on iron overload among beta thalassemia patients of Chennai residents. AIMS Molecular Science 2021; 8(4) doi: 10.3934/molsci.2021018
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| 14 |
Abraham Koshy, Roy J. Mukkada, Antony P. Chettupuzha, Jose V. Francis, Julio C. Kandathil, Pushpa Mahadevan. Hemochromatosis in India: First Report of Whole Exome Sequencing With Review of the Literature. Journal of Clinical and Experimental Hepatology 2020; 10(2) doi: 10.1016/j.jceh.2019.04.051
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| 15 |
Nihal Salah Ibrahim, Mohamed Menesy. Hemochromatosis gene mutations in chronic hepatitis “C” patients. Comparative Clinical Pathology 2016; 25(2) doi: 10.1007/s00580-015-2193-x
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| 16 |
Yoji Ishizu, Yoshiaki Katano, Takashi Honda, Kazuhiko Hayashi, Masatoshi Ishigami, Akihiro Itoh, Yoshiki Hirooka, Isao Nakano, Hidemi Goto. Clinical impact of HFE mutations in Japanese patients with chronic hepatitis C. Journal of Gastroenterology and Hepatology 2012; 27(6) doi: 10.1111/j.1440-1746.2011.06976.x
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| 17 |
Saumya Madushani Samarasinghe, Asanka Sudeshini Hewage, Rohan Chaminda Siriwardana, Kamani Hemamala Tennekoon, Madunil Anuk Niriella, Sumadee De Silva. Genetic and metabolic aspects of non-alcoholic fatty liver disease (NAFLD) pathogenicity. Egyptian Journal of Medical Human Genetics 2023; 24(1) doi: 10.1186/s43042-023-00433-x
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| 18 |
James E. Nelson, Heather Klintworth, Kris V. Kowdley. Iron Metabolism in Nonalcoholic Fatty Liver Disease. Current Gastroenterology Reports 2012; 14(1) doi: 10.1007/s11894-011-0234-4
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| 19 |
Yan-yan Xu, Yu-han Tang, Xiao-ping Guo, Jing Wang, Ping Yao. HFE genetic variability and risk of alcoholic liver disease: A meta-analysis. Journal of Huazhong University of Science and Technology [Medical Sciences] 2016; 36(5) doi: 10.1007/s11596-016-1637-0
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| 20 |
Reena Das, Giriraj Ratan Chandak. Obscure pathogenesis of primary iron overload in Indians warrants more focused research. Indian Journal of Gastroenterology 2011; 30(4) doi: 10.1007/s12664-011-0119-3
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| 21 |
Agustin Castiella. Iron Overload and HFE Mutations: Are They Relevant in Cryptogenic Cirrhosis?. Hepatitis Monthly 2012; 12(2) doi: 10.5812/hepatmon.4875
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| 22 |
Rekha Athiyarath, Alok Srivastava, Eunice Sindhuvi Edison. Molecular basis of primary iron overload in India and the role of serum-derived factors in hepcidin regulation. Annals of Hematology 2013; 92(6) doi: 10.1007/s00277-012-1621-0
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| 23 |
Prachi S. Patil, K. M. Mohandas. Primary iron overload and HFE gene mutations in North Indian adults. Indian Journal of Gastroenterology 2012; 31(1) doi: 10.1007/s12664-012-0170-8
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| 24 |
Mithun Sharma, Shasikala Mitnala, Ravi K. Vishnubhotla, Rathin Mukherjee, Duvvur N. Reddy, Padaki N. Rao. The Riddle of Nonalcoholic Fatty Liver Disease: Progression From Nonalcoholic Fatty Liver to Nonalcoholic Steatohepatitis. Journal of Clinical and Experimental Hepatology 2015; 5(2) doi: 10.1016/j.jceh.2015.02.002
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| 25 |
Zoon Tariq, Charlotte J. Green, Leanne Hodson. Are oxidative stress mechanisms the common denominator in the progression from hepatic steatosis towards non‐alcoholic steatohepatitis (NASH)?. Liver International 2014; 34(7) doi: 10.1111/liv.12523
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| 26 |
Pierre Brissot, Marie-Bérengère Troadec, Edouard Bardou-Jacquet, Caroline Le Lan, Anne-Marie Jouanolle, Yves Deugnier, Olivier Loréal. Current approach to hemochromatosis. Blood Reviews 2008; 22(4) doi: 10.1016/j.blre.2008.03.001
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| 27 |
Etheresia Pretorius, Janette Bester, Natasha Vermeulen, Boguslaw Lipinski, George S. Gericke, Douglas B. Kell, Thiruma V. Arumugam. Profound Morphological Changes in the Erythrocytes and Fibrin Networks of Patients with Hemochromatosis or with Hyperferritinemia, and Their Normalization by Iron Chelators and Other Agents. PLoS ONE 2014; 9(1) doi: 10.1371/journal.pone.0085271
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| 28 |
Danny Con, Amanda J. Nicoll. Hyperferritinaemia and iron overload in Asian patients: lessons from an Australian tertiary centre experience. Internal Medicine Journal 2021; 51(5) doi: 10.1111/imj.15316
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| 29 |
Mohd Talha Noor, Manish Tiwari, Ravindra Kumar. Non-HFE iron overload as a surrogate marker of disease severity in patients of liver cirrhosis. Indian Journal of Gastroenterology 2016; 35(1) doi: 10.1007/s12664-016-0623-6
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| 30 |
Shalu Jain, Sarita Agarwal, Parag Tamhankar, Prashant Verma, Gourdas Choudhuri. Lack of association of primary iron overload and common HFE gene mutations with liver cirrhosis in adult Indian population. Indian Journal of Gastroenterology 2011; 30(4) doi: 10.1007/s12664-011-0109-5
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| 31 |
V. M. Mitsura, T. L. Krasavtsev, E. V. Voropaev, O. Yu. Baranov, I. V. Paltsev, A. L. Kalinin. THE FREQUENCY OF HFE GENE MUTATIONS C282Y AND H63D REVEALING IN PATIENTS WITH CHRONIC HEPATITIS AND LIVER CIRRHOSIS OF DIFFERENT ETIOLOGY. Health and Ecology Issues 2008; (2) doi: 10.51523/2708-6011.2008-5-2-12
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