Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 332 Records) |
| Query Trace: Iron Overload and HFE[original query] |
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| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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, |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Platelet counts in HFE p.C282Y/p.C282Y and wt/wt post-screening clinical evaluation participants. Platelets 2023 6 34 (1): 2217933. James C Barton, J Clayborn Barton, Ronald T Act |
| Magnetic Resonance Liver Iron Concentration Can Guide Venesection Decision-Making in Hyperferritinemia. Digestive diseases and sciences 2023 3 . Bhuva Meha, Patterson Ilse, Godfrey Edmund M, Bowden David J, Griffiths William J |
| Frequency Evaluation of the Interleukin-6 -174G>C Polymorphism and Homeostatic Iron Regulator (HFE) Mutations as Disease Modifiers in Patients Affected by Systemic Lupus Erythematosus and Rheumatoid Arthritis. International journal of molecular sciences 2023 11 24 (22): . Mattia Carini, Micaela Fredi, Ilaria Cavazzana, Roberto Bresciani, Fabiana Ferrari, Eugenio Monti, Franco Franceschini, Giorgio Biasiot |
| Associations between metabolic hyperferritinaemia, fibrosis-promoting alleles and clinical outcomes in steatotic liver disease. Liver international : official journal of the International Association for the Study of the Liver 2023 11 . Deepika Suresh, Ashley Li, Matthew J Miller, Karn Wijarnpreecha, Vincent L Ch |
| Hemochromatosis Genetic Variants and Musculoskeletal Outcomes: 11.5-Year Follow-Up in the UK Biobank Cohort Study. JBMR plus 2023 10 7 (10): e10794. Lucy R Banfield, Karen M Knapp, Luke C Pilling, David Melzer, Janice L Atki |
| Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients. Biochemical genetics 2024 7 . Mona F Sokkar, Mona Hamdy, Mohamed B Taher, Heba El-Sayed, Eman Abdelmotaleb Bayomi, Khalda S Amr, Ghada Y El-Kam |
| Investigation of BMP6 mutations in Brazilian patients with iron overload. Hematology, transfusion and cell therapy 2024 5 . Ana Carolina Mourão Toreli, Isabella Toni, Dulcinéia Martins de Albuquerque, Carolina Lanaro, Jersey Heitor Maues, Kleber Yotsumoto Fertrin, Paula de Melo Campos, Fernando Ferreira Cos |
| MRI-derived brain iron, grey matter volume, and risk of dementia and Parkinson's disease: Observational and genetic analysis in the UK Biobank cohort. Neurobiology of disease 2024 5 197 106539. Francesco Casanova, Qu Tian, Daniel S Williamson, Yong Qian, David Zweibaum, Jun Ding, Janice L Atkins, David Melzer, Luigi Ferrucci, Luke C Pilli |
| Iron overload in hereditary spherocytosis: Are genetic factors the cause? British journal of haematology 2024 12 . Lucie Donaty, Muriel Giansily-Blaizot, Ivan Bertchansky, Séverine Cunat, Vincent Azoury, Perrine Mahe, Patricia Aguilar Martin |
| Re-evaluating the utility of iron indices in hereditary hemochromatosis genotyping: A retrospective study. Clinical biochemistry 2024 12 110860. Amy Lou, Manal O Elnenaei, Julie Zhu, Kevork Peltekian, Eric Liu, Jennifer A Jamieson, Hammam Said, Bassam A Nass |
- Page last reviewed:Feb 1, 2024
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