Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: Iron Overload and SLC40A1[original query] |
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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 |
SLC40A1 Q248H allele frequencies and Q248H-associated risk of non-HFE iron overload in persons of sub-Saharan African descent. Blood cells, molecules & diseases 0 39 (2): 206-11. Barton James C, Acton Ronald T, Lee Pauline L, West Car |
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, |
Does the SLC40A1 gene modify HFE-related haemochromatosis phenotypes? Annals of hematology 2009 Apr 88 (4): 341-5. Altès Albert, Bach Vanessa, Ruiz Angels, Esteve Anna, Remacha Angel F, Sardà M Pilar, Felez Jordi, Baiget Montserr |
Ferroportin disease: a systematic meta-analysis of clinical and molecular findings. Journal of hepatology 2010 Nov 53 (5): 941-9. Mayr Roman, Janecke Andreas R, Schranz Melanie, Griffiths William J H, Vogel Wolfgang, Pietrangelo Antonello, Zoller Hei |
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 |
Sex and acquired cofactors determine phenotypes of ferroportin disease. Gastroenterology 2011 1 140 (4): 1199-1207.e1-2. Le Lan Caroline, Mosser Annick, Ropert Martine, Detivaud Lénaïck, Loustaud-Ratti Véronique, Vital-Durand Denis, Roget Laurent, Bardou-Jacquet Edouard, Turlin Bruno, David Véronique, Loréal Olivier, Deugnier Yves, Brissot Pierre, Jouanolle Anne-Mar |
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.
Nature communications 2014 5 4926. Benyamin Beben, Esko Tonu, Ried Janina S, Radhakrishnan Aparna, Vermeulen Sita H, Traglia Michela, Gögele Martin, Anderson Denise, Broer Linda, Podmore Clara, Luan Jian'an, Kutalik Zoltan, Sanna Serena, van der Meer Peter, Tanaka Toshiko, Wang Fudi, Westra Harm-Jan, Franke Lude, Mihailov Evelin, Milani Lili, Hälldin Jonas, Häldin Jonas, Winkelmann Juliane, Meitinger Thomas, Thiery Joachim, Peters Annette, Waldenberger Melanie, Rendon Augusto, Jolley Jennifer, Sambrook Jennifer, Kiemeney Lambertus A, Sweep Fred C, Sala Cinzia F, Schwienbacher Christine, Pichler Irene, Hui Jennie, Demirkan Ayse, Isaacs Aaron, Amin Najaf, Steri Maristella, Waeber Gérard, Verweij Niek, Powell Joseph E, Nyholt Dale R, Heath Andrew C, Madden Pamela A F, Visscher Peter M, Wright Margaret J, Montgomery Grant W, Martin Nicholas G, Hernandez Dena, Bandinelli Stefania, van der Harst Pim, Uda Manuela, Vollenweider Peter, Scott Robert A, Langenberg Claudia, Wareham Nicholas J, , van Duijn Cornelia, Beilby John, Pramstaller Peter P, Hicks Andrew A, Ouwehand Willem H, Oexle Konrad, Gieger Christian, Metspalu Andres, Camaschella Clara, Toniolo Daniela, Swinkels Dorine W, Whitfield John |
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 |
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 |
[Analysis of HFE and Non-HFE Mutations in a Tibet Cohort with Iron Overload]. Zhongguo shi yan xue ye xue za zhi 2019 Apr 27 (2): 618-622. Sun Shu-Yao, Guo Yan-Hong, Sun Zeng-Mei, Wu Yun-Hong, Li Ming-X |
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 |
Assessment of iron overload in a cohort of Sri Lankan patients with transfusion dependent beta thalassaemia and its correlation with pathogenic variants in HBB, HFE, SLC40A1, and TFR2 genes. BMC pediatrics 2022 Jun 22 (1): 344. Dissanayake Ruwangi, Samarasinghe Nayana, Waidyanatha Samantha, Pathirana Sajeewani, Neththikumara Nilaksha, Dissanayake Vajira H W, Wetthasinghe Kalum, Gooneratne Lallindra, Wickramasinghe Pujit |
Associated Effect of SLC40A1 and TMPRSS6 Polymorphisms on Iron Overload. Metabolites 2022 10 12 (10): . Duca Lorena, Granata Francesca, Di Pierro Elena, Brancaleoni Valentina, Graziadei Giovanna, Nava Isabel |
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- Page last updated:May 13, 2024
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