HuGE Literature Finder
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| HFE hemochromatosis in African Americans: Prevalence estimates of iron overload and iron overload-related disease. The American journal of the medical sciences 2022 Sep . Barton James C, Edwards Corwin Q, Acton Ronald |
| 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 |
| Hereditary Hemochromatosis Variant Associations with Incident Nonliver Malignancies: 11-Year Follow-up in UK Biobank. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2022 Jun . Atkins Janice L, Pilling Luke C, Torti Suzy V, Torti Frank M, Kuchel George A, Melzer Dav |
| HLA-A*03, the hemochromatosis ancestral haplotype, and phenotypes of referred hemochromatosis probands with HFE p.C282Y homozygosity. Hereditas 2022 Jun 159 (1): 25. Barton James C, Barton J Clayborn, Acton Ronald |
| Genetic modifiers of penetrance to liver endpoints in HFE hemochromatosis: Associations in a large community cohort. Hepatology (Baltimore, Md.) 2022 May . Pilling Luke C, Atkins Janice L, Melzer Dav |
| C282Y/H63D Compound Heterozygosity Is a Low Penetrance Genotype for Iron Overload-related Disease. Journal of the Canadian Association of Gastroenterology 2022 10 5 (5): 240-247. Hasan S M Mahmudul, Farrell James, Borgaonkar Ma |
| DNA methylation plays an important role in iron-overloaded Tibetans. Genes & genetic systems 2022 6 97 (2): 55-66. Zhao Qin, Ge Zhijing, Fu Suhong, Wan Sha, Shi Jing, Wu Yunhong, Zhang Yongq |
| Elevated transferrin saturation in individuals with alcohol use disorder: Association with HFE polymorphism and alcohol withdrawal severity. Addiction biology 2022 3 27 (2): e13144. Kroll Danielle S, McPherson Katherine L, Manza Peter, Schwandt Melanie L, Shen Pei-Hong, Goldman David, Diazgranados Nancy, Wang Gene-Jack, Wiers Corinde E, Volkow Nora |
| Frequency of Hereditary Hemochromatosis Gene (HFE) Variants in Sri Lankan Transfusion-Dependent Beta-Thalassemia Patients and Their Association With the Serum Ferritin Level. Frontiers in pediatrics 2022 7 10 890989. Padeniya Padmapani, Goonasekara Hemali, Abeysekera Gayan, Jayasekara Rohan, Dissanayake Vaji |
| 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 |
| Iron overload phenotypes and HFE genotypes in white hemochromatosis and iron overload screening study participants without HFE p.C282Y/p.C282Y. PloS one 2022 7 17 (7): e0271973. Barton James C, Barton J Clayborn, Acton Ronald |
| Quality of Life Scores Remained Different among the Genotypic Groups of Patients with Suspected Hemochromatosis, Even after Treatment Period. Genes 2022 1 13 (1): . Acevedo Luis Alfredo Utria, Alvarenga Aline Morgan, Fonseca Paula Fernanda Silva, da Silva Nathália Kozikas, Cançado Rodolfo Delfini, Naoum Flavio Augusto, Dinardo Carla Luana, Pereira Alexandre Costa, Brissot Pierre, Santos Paulo Caleb Junior Li |
| 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 |
| Evidence That HFE H63D Variant Is a Potential Disease Modifier in Cluster Headache. Journal of molecular neuroscience : MN 2021 Sep . Papasavva Maria, Vikelis Michail, Katsarou Martha-Spyridoula, Siokas Vasileios, Dermitzakis Emmanouil, Papademetriou Christoforos, Karakostis Konstantinos, Lazopoulos George, Dardiotis Efthimios, Drakoulis Nikola |
| Ceruloplasmin gene variants are associated with hyperferritinemia and increased liver iron in patients with NAFLD. Journal of hepatology 2021 Mar . Corradini Elena, Buzzetti Elena, Dongiovanni Paola, Scarlini Stefania, Caleffi Angela, Pelusi Serena, Bernardis Isabella, Ventura Paolo, Rametta Raffaela, Tenedini Elena, Tagliafico Enrico, Fracanzani Anna Ludovica, Fargion Silvia, Pietrangelo Antonello, Valenti Luca Vittor |
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 |
| Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort. Journal of Alzheimer's disease : JAD 2021 Jan . Atkins Janice L, Pilling Luke C, Heales Christine J, Savage Sharon, Kuo Chia-Ling, Kuchel George A, Steffens David C, Melzer Dav |
| Contributions of HFE polymorphisms to brain and blood iron load, and their links to cognitive and motor function in healthy adults. Neuropsychopharmacology reports 2021 7 41 (3): 393-404. Kalpouzos Grégoria, Mangialasche Francesca, Falahati Farshad, Laukka Erika J, Papenberg Gor |
| 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 |
| Factors associated with serum ferritin levels and iron excess: results from the EPIC-EurGast study. European journal of nutrition 2021 7 61 (1): 101-114. Iglesias-Vázquez Lucía, Arija Victoria, Aranda Núria, Aglago Elom K, Cross Amanda J, Schulze Matthias B, Quintana Pacheco Daniel, Kühn Tilman, Weiderpass Elisabete, Tumino Rosario, Redondo-Sánchez Daniel, de Magistris Maria Santucci, Palli Domenico, Ardanaz Eva, Laouali Nasser, Sonestedt Emily, Drake Isabel, Rizzolo Lucía, Santiuste Carmen, Sacerdote Carlotta, Quirós Ramón, Amiano Pilar, Agudo Antonio, Jakszyn Pau |
| 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 |
| 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 |
| Impact of HFE gene variants on iron overload, overall survival and leukemia-free survival in myelodysplastic syndromes. American journal of cancer research 2021 4 11 (3): 955-967. Schneeweiss-Gleixner Mathias, Greiner Georg, Herndlhofer Susanne, Schellnegger Julia, Krauth Maria-Theresa, Gleixner Karoline V, Wimazal Friedrich, Steinhauser Corinna, Kundi Michael, Thalhammer Renate, Schwarzinger Ilse, Hoermann Gregor, Esterbauer Harald, Födinger Manuela, Valent Peter, Sperr Wolfgang |
| MRI-Based Iron Phenotyping and Patient Selection for Next-Generation Sequencing of Non-Homeostatic Iron Regulator Hemochromatosis Genes. Hepatology (Baltimore, Md.) 2021 5 74 (5): 2424-2435. Viveiros André, Schaefer Benedikt, Panzer Marlene, Henninger Benjamin, Plaikner Michaela, Kremser Christian, Franke André, Franzenburg Sören, Hoeppner Marc P, Stauder Reinhard, Janecke Andreas, Tilg Herbert, Zoller Hei |
| Increased frequency of GNPAT p.D519G in compound HFE p.C282Y/p.H63D heterozygotes with elevated serum ferritin levels. Blood cells, molecules & diseases 2020 Jul 85 102463. Secondes Eriza S, Wallace Daniel F, Rishi Gautam, McLaren Gordon D, McLaren Christine E, Chen Wen-Pin, Ramm Louise E, Powell Lawrie W, Ramm Grant A, Barton James C, Subramaniam V Nath |
| 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 |
| Evaluation of a screening program for iron overload and HFE mutations in 50,493 blood donors. Annals of hematology 2020 8 99 (10): 2295-2301. Eckerström Carl, Frändberg Sofia, Lyxe Lena, Pardi Cecilia, Konar J |
| HFE-Related Hemochromatosis in a Chinese Patient: The First Reported Case. Frontiers in genetics 2020 3 11 77. Zhang Wei, Wang Xiaoming, Duan Weijia, Xu Anjian, Zhao Xinyan, Huang Jian, You Hong, Brissot Pierre, Ou Xiaojuan, Jia Jido |
| Investigation of correlation between H63D and C282Y mutations in HFE gene and serum Ferritin level in beta-thalassemia major patients. Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine 2019 May . Rahmani Romina, Naseri Parisa, Safaroghli-Azar Ava, Tarighi Shahriar, Hosseini Tahereh, Hojjati Mohammad Tah |
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- Page last updated:Mar 16, 2023
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