Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 30 Records) |
Query Trace: Iron Overload and HAMP[original query] |
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HAMP as a modifier gene that increases the phenotypic expression of the HFE pC282Y homozygous genotype. Blood 2004 Apr 103 (7): 2835-40. Jacolot Sandrine, Le Gac Gerald, Scotet Virginie, Quere Isabelle, Mura Catherine, Ferec Clau |
Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload. Human genetics 2004 Oct 115 (5): 409-17. Zaahl Monique G, Merryweather-Clarke Alison T, Kotze Maritha J, van der Merwe Schalk, Warnich Louise, Robson Kathryn J |
The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype. Human molecular genetics 2004 Sep 13 (17): 1913-8. Le Gac Gérald, Scotet Virginie, Ka Chandran, Gourlaouen Isabelle, Bryckaert Laurence, Jacolot Sandrine, Mura Catherine, Férec Clau |
H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload? European journal of haematology 2007 Jan 78 (1): 66-71. de Diego Carles, Opazo Sonsoles, Murga Maria J, Martínez-Castro Ped |
Hemochromatosis and severe iron overload associated with compound heterozygosity for TFR2 R455Q and two novel mutations TFR2 R396X and G792R. Acta haematologica 2006 1 115 (1-2): 102-5. Lee Pauline L, Barton James |
HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening. Genetic testing 2007 11 (3): 269-75. Barton James C, Acton Ronald T, Leiendecker-Foster Catherine, Lovato Laura, Adams Paul C, McLaren Gordon D, Eckfeldt John H, McLaren Christine E, Reboussin David M, Gordeuk Victor R, Speechley Mark R, Reiss Jacob A, Press Richard D, Dawkins Fitzroy W, |
Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes. Annals of hematology 2009 Mar 88 (3): 229-34. Mendes Ana Isabel, Ferro Ana, Martins Rute, Picanço Isabel, Gomes Susana, Cerqueira Rute, Correia Manuel, Nunes António Robalo, Esteves Jorge, Fleming Rita, Faustino Pau |
Down-regulation of hepcidin in porphyria cutanea tarda. Blood 2008 Dec 112 (12): 4723-8. Ajioka Richard S, Phillips John D, Weiss Robert B, Dunn Diane M, Smit Maria W, Proll Sean C, Katze Michael G, Kushner James |
Genetic study of the hepcidin gene (HAMP) promoter and functional analysis of the c.-582A > G variant. BMC genetics 2010 11 110. Parajes Silvia, González-Quintela Arturo, Campos Joaquín, Quinteiro Celsa, Domínguez Fernando, Loidi Lourd |
Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload. Genetic testing and molecular biomarkers 2010 Dec 14 (6): 803-6. de Lima Santos Paulo Caleb Júnior, Pereira Alexandre C, Cançado Rodolfo D, Schettert Isolmar T, Hirata Rosario D C, Hirata Mario H, Figueiredo Maria Stella, Chiattone Carlos S, Krieger Jose E, Guerra-Shinohara Elvira |
Cardiac iron overload in transfusion-dependent patients with myelodysplastic syndromes. British journal of haematology 2011 Jun . Roy NB, Myerson S, Schuh AH, Bignell P, Patel R, Wainscoat JS, McGowan S, Marchi E, Atoyebi W, Littlewood T, Chacko J, Vyas P, Killick SB |
Influence of iron regulating genes mutations on iron status in Egyptian patients with sickle cell disease. Annals of clinical and laboratory science 2014 44 (3): 304-9. Abdel Rahman Hala A, Abou-Elew Heba H, El-Shorbagy Reem M, Fawzy Rania, Youssry Ilh |
The hepcidin gene promoter nc.-1010C > T; -582A > G haplotype modulates serum ferritin in individuals carrying the common H63D mutation in HFE gene. Annals of hematology 2014 Dec 93 (12): 2063-6. Silva Bruno, Pita Lina, Gomes Susana, Gonçalves João, Faustino Pau |
The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Dec . Wallace Daniel F, Subramaniam V Nath |
The role of genetic factors in patients with hepatocellular carcinoma and iron overload - a prospective series of 234 patients. Liver international : official journal of the International Association for the Study of the Liver 2015 Oct . Funakoshi Natalie, Chaze Iphigénie, Alary Anne-Sophie, Tachon Gaëlle, Cunat Séverine, Giansily-Blaizot Muriel, Bismuth Michael, Larrey Dominique, Pageaux Georges-Philippe, Schved Jean-François, Donnadieu-Rigole Hélène, Blanc Pierre, Aguilar-Martinez Patric |
Rare HFE variants are the most frequent cause of hemochromatosis in non-c282y homozygous patients with hemochromatosis. American journal of hematology 2016 Aug . Hamdi-Rozé Houda, Beaumont-Epinette Marie-Pascale, Ben Ali Zeineb, Le Lan Caroline, Loustaud Ratti Véronique, Causse Xavier, Loreal Olivier, Deugnier Yves, Brissot Pierre, Jouanolle Anne-Marie, Bardou-Jacquet Edoua |
Interferon lambda polymorphisms associate with body iron indices and hepatic expression of interferon-responsive long non-coding RNA in chronic hepatitis C. Clinical and experimental medicine 2017 May 17 (2): 225-232. Wróblewska Anna, Bernat Agnieszka, Woziwodzka Anna, Markiewicz Joanna, Romanowski Tomasz, Bielawski Krzysztof P, Smiatacz Tomasz, Sikorska Katarzy |
Association of Single-Nucleotide Polymorphism in the Hepcidin Promoter Gene with Susceptibility to Extrapulmonary Tuberculosis. Genetic testing and molecular biomarkers 2017 May . Liang Li, Liu Huijuan, Yue Jun, Liu Li-Rong, Han Min, Luo Liu-Lin, Zhao Yan-Lin, Xiao Hepi |
Causes of iron overload in blood donors - a clinical study. Vox sanguinis 2017 12 113 (2): 110-119. Laursen A H, Bjerrum O W, Friis-Hansen L, Hansen T O, Marott J L, Magnussen |
Non-HFE mutations in haemochromatosis in China: combination of heterozygous mutations involving HJV signal peptide variants. Journal of medical genetics 2018 9 55 (10): 650-660. Lv Tingxia, Zhang Wei, Xu Anjian, Li Yanmeng, Zhou Donghu, Zhang Bei, Li Xiaojin, Zhao Xinyan, Wang Yu, Wang Xiaoming, Duan Weijia, Wang Qianyi, Xu Hexiang, Zheng JiShun, Zhao Rongrong, Zhu Longdong, Dong Yuwei, Lu Lungen, Chen Yongpeng, Long Jiang, Zheng Sujun, Wang Wei, You Hong, Jia Jidong, Ou Xiaojuan, Huang Ji |
Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease. Blood 2018 5 132 (1): 101-110. Sandhu Kam, Flintoff Kaledas, Chatfield Mark D, Dixon Jeannette L, Ramm Louise E, Ramm Grant A, Powell Lawrie W, Subramaniam V Nathan, Wallace Daniel |
Role of HAMP Genetic Variants on Pathophysiology of Iron Deficiency Anemia. Indian journal of clinical biochemistry : IJCB 2018 10 33 (4): 479-482. Pandey S, Pandey S K, Shah |
Hepcidin and HFE Polymorphisms and Ferritin Level in ?-Thalassemia Major. International journal of hematology-oncology and stem cell research 2019 6 13 (1): 42-48. Fekri Kiavash, Asle Rasouli Negar, Tavallai Zavareh Seyyed Abdolhossein, Jalil Milad, Moradi Fahimeh, Hosseinpour Maryam, Teimori Hosse |
Determination of mutations in iron regulating genes of beta thalassemia major patients of Khyber Pakhtunkhwa, Pakistan. Molecular genetics & genomic medicine 2020 6 8 (9): e1310. Shah Maryam, Danish Lubna, Khan Najeeb U, Zaman Fakhar, Ismail Muhammad, Hussain Mehfooz, Pervaiz Ruqiya, Iqbal Aq |
Hepcidin gene polymorphisms and iron overload in ?-thalassemia major patients refractory to iron chelating therapy. BMC medical genetics 2020 4 21 (1): 75. Zarghamian Parinaz, Azarkeivan Azita, Arabkhazaeli Ali, Mardani Ahmad, Shahabi Maj |
Hepcidin-regulating iron metabolism genes and pancreatic ductal adenocarcinoma: a pathway analysis of genome-wide association studies. The American journal of clinical nutrition 2021 7 114 (4): 1408-1417. Julián-Serrano Sachelly, Yuan Fangcheng, Wheeler William, Benyamin Beben, Machiela Mitchell J, Arslan Alan A, Beane-Freeman Laura E, Bracci Paige M, Duell Eric J, Du Mengmeng, Gallinger Steven, Giles Graham G, Goodman Phyllis J, Kooperberg Charles, Marchand Loic Le, Neale Rachel E, Shu Xiao-Ou, Van Den Eeden Stephen K, Visvanathan Kala, Zheng Wei, Albanes Demetrius, Andreotti Gabriella, Ardanaz Eva, Babic Ana, Berndt Sonja I, Brais Lauren K, Brennan Paul, Bueno-de-Mesquita Bas, Buring Julie E, Chanock Stephen J, Childs Erica J, Chung Charles C, Fabiánová Eleonora, Foretová Lenka, Fuchs Charles S, Gaziano J Michael, Gentiluomo Manuel, Giovannucci Edward L, Goggins Michael G, Hackert Thilo, Hartge Patricia, Hassan Manal M, Holcátová Ivana, Holly Elizabeth A, Hung Rayjean I, Janout Vladimir, Kurtz Robert C, Lee I-Min, Malats Núria, McKean David, Milne Roger L, Newton Christina C, Oberg Ann L, Perdomo Sandra, Peters Ulrike, Porta Miquel, Rothman Nathaniel, Schulze Matthias B, Sesso Howard D, Silverman Debra T, Thompson Ian M, Wactawski-Wende Jean, Weiderpass Elisabete, Wenstzensen Nicolas, White Emily, Wilkens Lynne R, Yu Herbert, Zeleniuch-Jacquotte Anne, Zhong Jun, Kraft Peter, Li Dounghui, Campbell Peter T, Petersen Gloria M, Wolpin Brian M, Risch Harvey A, Amundadottir Laufey T, Klein Alison P, Yu Kai, Stolzenberg-Solomon Rachael |
Identification of Novel Mutations by Targeted NGS Panel in Patients with Hyperferritinemia. Genes 2021 Nov 12 (11): . Ravasi Giulia, Pelucchi Sara, Bertola Francesca, Capelletti Martina Maria, Mariani Raffaella, Piperno Alber |
Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China. Orphanet journal of rare diseases 2021 09 16 (1): 398. Wu Liyan, Zhang Wei, Li Yanmeng, Zhou Donghu, Zhang Bei, Xu Anjian, Wu Zhen, Wu Lina, Li Shuxiang, Wang Xiaoming, Zhao Xinyan, Wang Qianyi, Li Min, Wang Yu, You Hong, Huang Jian, Ou Xiaojuan, Jia Jido |
Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis. Orphanet journal of rare diseases 2022 6 17 (1): 216. Zhang Wei, Li Yanmeng, Xu Anjian, Ouyang Qin, Wu Liyan, Zhou Donghu, Wu Lina, Zhang Bei, Zhao Xinyan, Wang Yu, Wang Xiaoming, Duan Weijia, Wang Qianyi, You Hong, Huang Jian, Ou Xiaojuan, Jia Jidong, |
Impact of HFE-2 and HAMP Gene Variations on Iron Overload in Pediatric Patients with Non-Transfusion Dependent Thalassemia: A Pilot Study. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2022 2 38 (1): 158-163. Bharadwaj Niteesh, Peyam Srinivasan, Bhatia Prateek, Bhatia Anmol, Das Reena, Singh Minu, Bansal Deepak, Trehan Amita, Jain Ric |
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- Page last updated:Apr 29, 2024
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