Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: Hemochromatosis and TF[original query] |
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Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.
![]() American journal of human genetics 2009 Jan 84 (1): 60-5. Benyamin Beben, McRae Allan F, Zhu Gu, Gordon Scott, Henders Anjali K, Palotie Aarno, Peltonen Leena, Martin Nicholas G, Montgomery Grant W, Whitfield John B, Visscher Peter |
Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Jun 153B (4): 955-9. Kauwe J S K, Bertelsen S, Mayo K, Cruchaga C, Abraham R, Hollingworth P, Harold D, Owen M J, Williams J, Lovestone S, Morris J C, Goate A M, |
Iron metabolism genes, low-level lead exposure, and QT interval. Environmental health perspectives 2009 Jan 117 (1): 80-5. Park Sung Kyun, Hu Howard, Wright Robert O, Schwartz Joel, Cheng Yawen, Sparrow David, Vokonas Pantel S, Weisskopf Marc |
Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project. Neurobiology of aging 2012 Jan 33 (1): 202.e1-13. Lehmann Donald J, Schuur Maaike, Warden Donald R, Hammond Naomi, Belbin Olivia, Kölsch Heike, Lehmann Michael G, Wilcock Gordon K, Brown Kristelle, Kehoe Patrick G, Morris Chris M, Barker Rachel, Coto Eliecer, Alvarez Victoria, Deloukas Panos, Mateo Ignacio, Gwilliam Rhian, Combarros Onofre, Arias-Vásquez Alejandro, Aulchenko Yurii S, Ikram M Arfan, Breteler Monique M, van Duijn Cornelia M, Oulhaj Abderrahim, Heun Reinhard, Cortina-Borja Mario, Morgan Kevin, Robson Kathryn, Smith A Dav |
HFE gene variants modify the association between maternal lead burden and infant birthweight: a prospective birth cohort study in Mexico City, Mexico. Environmental health : a global access science source 2010 9 (1): 43. Cantonwine David, Hu Howard, Téllez-Rojo Martha Maria, Sánchez Brisa N, Lamadrid-Figueroa Héctor, Ettinger Adrienne S, Mercado-García Adriana, Hernández-Avila Mauricio, Wright Robert |
HFE mutations and transferrin C1/C2 polymorphism among Croatian patients with schizophrenia and schizoaffective disorder. Molecular biology reports 2012 Mar 39 (3): 2253-8. Bureti?-Tomljanovi? Alena, Vranekovi? Jadranka, Rubeša Gordana, Jonovska Suzana, Tomljanovi? Draško, Sendula-Jengi? Vesna, Kapovi? Miljenko, Risti? Smilja |
Effects of hemochromatosis and transferrin gene mutations on iron dyshomeostasis, liver dysfunction and on the risk of Alzheimer's disease. Neurobiology of aging 2012 Aug 33 (8): 1633-41. Giambattistelli Federica, Bucossi Serena, Salustri Carlo, Panetta Valentina, Mariani Stefania, Siotto Mariacristina, Ventriglia Mariacarla, Vernieri Fabrizio, Dell'acqua Maria Luisa, Cassetta Emanuele, Rossini Paolo Maria, Squitti Rosan |
Genome-wide association study identifies genetic loci associated with iron deficiency.
![]() PloS one 2011 6 (3): e17390. McLaren Christine E, Garner Chad P, Constantine Clare C, McLachlan Stela, Vulpe Chris D, Snively Beverly M, Gordeuk Victor R, Nickerson Debbie A, Cook James D, Leiendecker-Foster Catherine, Beckman Kenneth B, Eckfeldt John H, Barcellos Lisa F, Murray Joseph A, Adams Paul C, Acton Ronald T, Killeen Anthony A, McLaren Gordon |
Associations of iron metabolism genes with blood manganese levels: a population-based study with validation data from animal models. Environmental health : a global access science source 2011 10 (1): 97. Claus Henn Birgit, Kim Jonghan, Wessling-Resnick Marianne, Téllez-Rojo Martha María, Jayawardene Innocent, Ettinger Adrienne S, Hernández-Avila Mauricio, Schwartz Joel, Christiani David C, Hu Howard, Wright Robert |
Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis. BMC medical genetics 2012 13 (1): 70. Gemmati Donato, Zeri Giulia, Orioli Elisa, De Gaetano Francesca E, Salvi Fabrizio, Bartolomei Ilaria, D'Alfonso Sandra, Dall'osso Claudia, Leone Maurizio A, Singh Ajay V, Asselta Rosanna, Zamboni Pao |
Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations. PloS one 2012 7 (6): e38339. McLaren Christine E, McLachlan Stela, Garner Chad P, Vulpe Chris D, Gordeuk Victor R, Eckfeldt John H, Adams Paul C, Acton Ronald T, Murray Joseph A, Leiendecker-Foster Catherine, Snively Beverly M, Barcellos Lisa F, Cook James D, McLaren Gordon |
Effects of hemochromatosis and transferrin gene mutations on peripheral iron dyshomeostasis in mild cognitive impairment and Alzheimer's and Parkinson's diseases. Frontiers in aging neuroscience 2013 5 37. Mariani S, Ventriglia M, Simonelli I, Spalletta G, Bucossi S, Siotto M, Assogna F, Melgari J M, Vernieri F, Squitti |
Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis. Human molecular genetics 2014 Jul 23 (14): 3883-90. Stickel Felix, Buch Stephan, Zoller Heinz, Hultcrantz Rolf, Gallati Sabina, Österreicher Christoph, Finkenstedt Armin, Stadlmayr Andreas, Aigner Elmar, Sahinbegovic Enijad, Sarrazin Christoph, Schafmayer Clemens, Braun Felix, Erhart Wiebke, Nothnagel Michael, Lerch Markus M, Mayerle Julia, Völzke Henry, Schaller André, Kratzer Wolfgang, Boehm Bernhard O, Sipos Bence, D'Amato Mauro, Torkvist Leif, Stal Per, Arlt Alexander, Franke Andre, Becker Thomas, Krawczak Michael, Zwerina Jochen, Berg Thomas, Hinrichsen Holger, Krones Elisabeth, Dejaco Christian, Strasser Michael, Datz Christian, Hampe Joch |
Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.
![]() Journal of hepatology 2015 Mar 62 (3): 664-72. de Tayrac Marie, Roth Marie-Paule, Jouanolle Anne-Marie, Coppin Hélène, le Gac Gérald, Piperno Alberto, Férec Claude, Pelucchi Sara, Scotet Virginie, Bardou-Jacquet Edouard, Ropert Martine, Bouvet Régis, Génin Emmanuelle, Mosser Jean, Deugnier Yv |
Maternal iron metabolism gene variants modify umbilical cord blood lead levels by gene-environment interaction: a birth cohort study. Environmental health : a global access science source 2014 13 77. Karwowski Mateusz P, Just Allan C, Bellinger David C, Jim Rebecca, Hatley Earl L, Ettinger Adrienne S, Hu Howard, Wright Robert |
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 |
Sudden sensorineural hearing loss and polymorphisms in iron homeostasis genes: new insights from a case-control study. BioMed research international 2015 2015 834736. Castiglione Alessandro, Ciorba Andrea, Aimoni Claudia, Orioli Elisa, Zeri Giulia, Vigliano Marco, Gemmati Dona |
Genome-wide association study of serum iron phenotypes in premenopausal women of European descent. Blood cells, molecules & diseases 2016 Mar 57 50-3. Koller Daniel L, Imel Erik A, Lai Dongbing, Padgett Leah R, Acton Dena, Gray Amie, Peacock Munro, Econs Michael J, Foroud Tatia |
MicroRNA Expression Analysis in Serum of Patients with Congenital Hemochromatosis and Age-Related Macular Degeneration (AMD). Medical science monitor : international medical journal of experimental and clinical research 2017 Aug 23 4050-4060. Szemraj Maciej, Oszajca Katarzyna, Szemraj Janusz, Jurowski Pio |
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 |
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases. PloS one 2018 13 (3): e0193867. Tisato Veronica, Zuliani Giovanni, Vigliano Marco, Longo Giovanna, Franchini Eugenia, Secchiero Paola, Zauli Giorgio, Paraboschi Elvezia Maria, Vikram Singh Ajay, Serino Maria Luisa, Ortolani Beatrice, Zurlo Amedeo, Bosi Cristina, Greco Antonio, Seripa Davide, Asselta Rosanna, Gemmati Dona |
Genetic factors influencing hemoglobin levels in 15,567 blood donors: results from the Danish Blood Donor Study. Transfusion 2019 01 59 (1): 226-231. Sørensen Erik, Rigas Andreas S, Didriksen Maria, Burgdorf Kristoffer S, Thørner Lise W, Pedersen Ole B, Hjalgrim Henrik, Petersen Mikkel S, Erikstrup Christian, Ullum Henr |
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