Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 34 Records) |
| Query Trace: Iron Overload and TFR2[original query] |
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| Genotypic and phenotypic heterogeneity of African Americans with primary iron overload. Blood cells, molecules & diseases 0 31 (3): 310-9. Barton James C, Acton Ronald T, Rivers Charles A, Bertoli Luigi F, Gelbart Terri, West Carol, Beutler Erne |
| Analysis of HFE and TFR2 gene mutations in patients with acute leukemia. Leukemia research 2005 Jun 29 (6): 661-4. Veneri Dino, Franchini Massimo, Krampera Mauro, de Matteis Giovanna, Solero Pietro, Pizzolo Giovan |
| Investigation of genetic variants of genes of the hemochromatosis pathway and their role in breast cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2005 May 14 (5): 1102-7. Abraham Benny K, Justenhoven Christina, Pesch Beate, Harth Volker, Weirich Gregor, Baisch Christian, Rabstein Sylvia, Ko Yon-Dschun, Brüning Thomas, Fischer Hans-Peter, Haas Susanne, Brod Sandra, Oberkanins Christian, Hamann Ute, Brauch Hiltrud, |
| 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 |
| Hemochromatosis gene sequence deviations in German patients with porphyria cutanea tarda. Physiological research / Academia Scientiarum Bohemoslovaca 2006 55 Suppl 2 (): S75-83. Frank J, Poblete-Gutiérrez P, Weiskirchen R, Gressner O, Merk H F, Lammert |
| 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 |
| High prevalence of HFE gene mutations in patients with porphyria cutanea tarda in the Czech Republic. The British journal of dermatology 2008 Sep 159 (3): 585-90. Kratka K, Dostalikova-Cimburova M, Michalikova H, Stransky J, Vranova J, Horak |
| TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern Italy. Blood cells, molecules & diseases 2013 Sep . Radio FC, Majore S, Binni F, Valiante M, Ricerca BM, De Bernardo C, Morrone A, Grammatico P |
| Association between genetic variations in TFR2 gene and coronary heart disease in Chinese: a case-control study. Journal of cardiovascular medicine (Hagerstown, Md.) 2013 Jun . Shi Y, Lian Y, Zhou L, Huang L, Zhang X, Guo H, Wu T, Cheng L, He M |
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 |
| HJV and HFE Play Distinct Roles in Regulating Hepcidin. Antioxidants & redox signaling 2015 May 22 (15): 1325-36. Wu Qian, Wang Hao, An Peng, Tao Yunlong, Deng Jiali, Zhang Zhuzhen, Shen Yuanyuan, Chen Caiyong, Min Junxia, Wang Fu |
| 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 |
| Analysis of polymorphism and hepatic expression of duodenal cytochrome b in chronic hepatitis C. Journal of gastroenterology and hepatology 2017 Feb 32 (2): 482-486. Rudnicka Alina, Woziwodzka Anna, Wróblewska Anna, Rybicka Magda, Bielawski Krzysztof P, Sikorska Katarzyna, Bernat Agniesz |
| Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?
Human molecular genetics 2017 Mar . Raffield Laura M, Louie Tin, Sofer Tamar, Jain Deepti, Ipp Eli, Taylor Kent D, Papanicolaou George J, Avilés-Santa Larissa, Lange Leslie A, Laurie Cathy C, Conomos Matthew P, Thornton Timothy A, Ida Chen Yii-Der, Qi Qibin, Cotler Scott, Thyagarajan Bharat, Schneiderman Neil, Rotter Jerome I, Reiner Alex P, Lin Henry |
| 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 |
| [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 |
| Genetics of Iron Metabolism and Premenstrual Symptoms: A Mendelian Randomization Study. The Journal of nutrition 2021 3 151 (7): 1747-1754. Zeitoun Tara, Dehghan Noudeh Negar, Garcia-Bailo Bibiana, El-Sohemy Ahm |
| A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.
Communications biology 2021 Feb 4 (1): 156. Bell Steven, Rigas Andreas S, Magnusson Magnus K, Ferkingstad Egil, Allara Elias, Bjornsdottir Gyda, Ramond Anna, Sørensen Erik, Halldorsson Gisli H, Paul Dirk S, Burgdorf Kristoffer S, Eggertsson Hannes P, Howson Joanna M M, Thørner Lise W, Kristmundsdottir Snaedis, Astle William J, Erikstrup Christian, Sigurdsson Jon K, Vuckovic Dragana, Dinh Khoa M, Tragante Vinicius, Surendran Praveen, Pedersen Ole B, Vidarsson Brynjar, Jiang Tao, Paarup Helene M, Onundarson Pall T, Akbari Parsa, Nielsen Kaspar R, Lund Sigrun H, Juliusson Kristinn, Magnusson Magnus I, Frigge Michael L, Oddsson Asmundur, Olafsson Isleifur, Kaptoge Stephen, Hjalgrim Henrik, Runarsson Gudmundur, Wood Angela M, Jonsdottir Ingileif, Hansen Thomas F, Sigurdardottir Olof, Stefansson Hreinn, Rye David, , Peters James E, Westergaard David, Holm Hilma, Soranzo Nicole, Banasik Karina, Thorleifsson Gudmar, Ouwehand Willem H, Thorsteinsdottir Unnur, Roberts David J, Sulem Patrick, Butterworth Adam S, Gudbjartsson Daniel F, Danesh John, Brunak Søren, Di Angelantonio Emanuele, Ullum Henrik, Stefansson Ka |
| 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 |
| Evaluation of the Association of Transferrin Receptor Type 2 Gene Mutation (Y250X) with Iron Overload in Major ?- Thalassemia. Archives of Razi Institute 2022 3 76 (5): 1551-1554. Abdulmalek Jaafar J, Al-Rashedi N A |
| Genetic variants in promoter region of TFR2 is associated with the risk of non-alcoholic fatty liver disease in a Chinese Han population: a case-control study. Gastroenterology report 2022 11 10 goac060. Pan Xinting, Peng Hewei, Zhang Junchao, Wu Yunli, Hu Zhijian, Peng Xian |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 04, 2023
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