Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 31 Records) |
Query Trace: TFRC[original query] |
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HFE gene mutations in susceptibility to childhood leukemia: HuGE review. Genetics in medicine : official journal of the American College of Medical Genetics 2005 Mar 7 (3): 159-68. Dorak M Tevfik, Burnett Alan K, Worwood Ma |
[Correlation of TFRC polymorphism with the susceptibility and clinicopathologic phenotypes of IgA nephropathy]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2008 Aug 40 (4): 369-73. Feng Xian-zhu, Hou Ping, Zhu Li, Yu Lei, Zhang Ho |
Hereditary hemochromatosis gene (HFE) variants are associated with birth weight and childhood leukemia risk. Pediatric blood & cancer 2009 Dec 53 (7): 1242-8. Dorak M Tevfik, Mackay Rachel K, Relton Caroline L, Worwood Mark, Parker Louise, Hall Andrew |
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
Nature genetics 2009 Nov 41 (11): 1191-8. Ganesh Santhi K, Zakai Neil A, van Rooij Frank J A, Soranzo Nicole, Smith Albert V, Nalls Michael A, Chen Ming-Huei, Kottgen Anna, Glazer Nicole L, Dehghan Abbas, Kuhnel Brigitte, Aspelund Thor, Yang Qiong, Tanaka Toshiko, Jaffe Andrew, Bis Joshua C M, Verwoert Germaine C, Teumer Alexander, Fox Caroline S, Guralnik Jack M, Ehret Georg B, Rice Kenneth, Felix Janine F, Rendon Augusto, Eiriksdottir Gudny, Levy Daniel, Patel Kushang V, Boerwinkle Eric, Rotter Jerome I, Hofman Albert, Sambrook Jennifer G, Hernandez Dena G, Zheng Gang, Bandinelli Stefania, Singleton Andrew B, Coresh Josef, Lumley Thomas, Uitterlinden André G, Vangils Janine M, Launer Lenore J, Cupples L Adrienne, Oostra Ben A, Zwaginga Jaap-Jan, Ouwehand Willem H, Thein Swee-Lay, Meisinger Christa, Deloukas Panos, Nauck Matthias, Spector Tim D, Gieger Christian, Gudnason Vilmundur, van Duijn Cornelia M, Psaty Bruce M, Ferrucci Luigi, Chakravarti Aravinda, Greinacher Andreas, O'Donnell Christopher J, Witteman Jacqueline C M, Furth Susan, Cushman Mary, Harris Tamara B, Lin Jing-Pi |
Transferrin receptor-1 gene polymorphisms are associated with type 2 diabetes. European journal of clinical investigation 2010 Jul 40 (7): 600-7. Fernández-Real José Manuel, Mercader Josep Maria, Ortega Francisco José, Moreno-Navarrete Jose Maria, López-Romero Pedro, Ricart Wifre |
Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. The American journal of psychiatry 2011 Mar 168 (3): 302-16. Levinson Douglas F, Duan Jubao, Oh Sang, Wang Kai, Sanders Alan R, Shi Jianxin, Zhang Nancy, Mowry Bryan J, Olincy Ann, Amin Farooq, Cloninger C Robert, Silverman Jeremy M, Buccola Nancy G, Byerley William F, Black Donald W, Kendler Kenneth S, Freedman Robert, Dudbridge Frank, Pe'er Itsik, Hakonarson Hakon, Bergen Sarah E, Fanous Ayman H, Holmans Peter A, Gejman Pablo |
The functional significance of E277K and V295A HFE mutations. British journal of haematology 2012 Aug 158 (3): 399-408. Silva Bruno, Martins Rute, Proença Daniela, Fleming Rita, Faustino Pau |
MicroRNA target site polymorphisms in the VHL-HIF1a pathway predict renal cell carcinoma risk. Molecular carcinogenesis 2014 Jan 53 (1): 1-7. Wei Hua, Ke Hung-Lung, Lin Jie, Shete Sanjay, Wood Christopher G, Hildebrandt Michelle A |
Polymorphisms in iron homeostasis genes and urinary cadmium concentrations among nonsmoking women in Argentina and Bangladesh. Environmental health perspectives 2013 Apr 121 (4): 467-72. Rentschler Gerda, Kippler Maria, Axmon Anna, Raqib Rubhana, Ekström Eva-Charlotte, Skerfving Staffan, Vahter Marie, Broberg Kar |
Genetic and biochemical markers in patients with Alzheimer's disease support a concerted systemic iron homeostasis dysregulation. Neurobiology of aging 2014 Apr 35 (4): 777-85. Crespo Ângela C, Silva Bruno, Marques Liliana, Marcelino Erica, Maruta Carolina, Costa Sónia, Timóteo Angela, Vilares Arminda, Couto Frederico Simões, Faustino Paula, Correia Ana Paula, Verdelho Ana, Porto Graça, Guerreiro Manuela, Herrero Ana, Costa Cristina, de Mendonça Alexandre, Costa Luciana, Martins Madale |
Examination of HFE associations with childhood leukemia risk and extension to other iron regulatory genes. Leukemia research 2014 Sep 38 (9): 1055-60. Kennedy Amy E, Kamdar Kala Y, Lupo Philip J, Okcu M Fatih, Scheurer Michael E, Baum Marianna K, Dorak M Tevf |
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 |
Transferrin receptor levels and polymorphism of its gene in age-related macular degeneration. Acta biochimica Polonica 2015 62 (2): 177-84. Wysokinski Daniel, Danisz Katarzyna, Pawlowska Elzbieta, Dorecka Mariola, Romaniuk Dorota, Robaszkiewicz Jacek, Szaflik Marta, Szaflik Jerzy, Blasiak Janusz, Szaflik Jacek |
Expression of RNAs Coding for Metal Transporters in Blood of Patients with Huntington's Disease. Neurochemical research 2015 Oct . Szeliga Monika, Ró?ycka Aleksandra, J?drak Paulina, Bara?ska Sylwia, Janik Piotr, Jamrozik Zygmunt, Albrecht J |
Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.
PloS one 2016 11 (8): e0160335. Bacelis Jonas, Juodakis Julius, Sengpiel Verena, Zhang Ge, Myhre Ronny, Muglia Louis J, Nilsson Staffan, Jacobsson |
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 |
Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes. Scientific reports 2017 Jul 7 (1): 6037. Jäger Susanne, Wahl Simone, Kröger Janine, Sharma Sapna, Hoffmann Per, Floegel Anna, Pischon Tobias, Prehn Cornelia, Adamski Jerzy, Müller-Nurasyid Martina, Waldenberger Melanie, Strauch Konstantin, Peters Annette, Gieger Christian, Suhre Karsten, Grallert Harald, Boeing Heiner, Schulze Matthias B, Meidtner Kari |
Genetic Susceptibility to Postdiarrheal Hemolytic-Uremic Syndrome After Shiga Toxin-Producing Escherichia coli Infection: A Centers for Disease Control and Prevention FoodNet Study. The Journal of infectious diseases 2018 03 217 (6): 1000-1010. Kallianpur Asha R, Bradford Yuki, Mody Rajal K, Garman Katie N, Comstock Nicole, Lathrop Sarah L, Lyons Carol, Saupe Amy, Wymore Katie, Canter Jeffrey A, Olson Lana M, Palmer Amanda, Jones Timothy |
Detection of circulating tumour cell clusters in human glioblastoma. British journal of cancer 2018 8 119 (4): 487-491. Krol Ilona, Castro-Giner Francesc, Maurer Martina, Gkountela Sofia, Szczerba Barbara Maria, Scherrer Ramona, Coleman Niamh, Carreira Suzanne, Bachmann Felix, Anderson Stephanie, Engelhardt Marc, Lane Heidi, Evans Thomas Ronald Jeffry, Plummer Ruth, Kristeleit Rebecca, Lopez Juanita, Aceto Nico |
GWAS reveals loci associated with velopharyngeal dysfunction.
Scientific reports 2018 05 8 (1): 8470. Chernus Jonathan, Roosenboom Jasmien, Ford Matthew, Lee Myoung Keun, Emanuele Beth, Anderton Joel, Hecht Jacqueline T, Padilla Carmencita, Deleyiannis Frederic W B, Buxo Carmen J, Feingold Eleanor, Leslie Elizabeth J, Shaffer John R, Weinberg Seth M, Marazita Mary |
Association of SNPs in transferrin and transferrin receptor genes with blood iron levels in human. Legal medicine (Tokyo, Japan) 2018 Oct 36 17-20. Fujihara Junko, Yasuda Toshihiro, Kimura-Kataoka Kaori, Takeshita Har |
Iron-regulatory genes are associated with Neuroimaging measures in HIV infection. Brain imaging and behavior 2019 Jul . Fennema-Notestine Christine, Thornton-Wells Tricia A, Hulgan Todd, Letendre Scott, Ellis Ronald J, Franklin Donald R, Anderson Albert M, Heaton Robert K, Bloss Cinnamon S, Grant Igor, Kallianpur Asha R, |
Association of ACK1, TFRC polymorphism with diarrhoeagenic E. coli adhesion patterns and their jejunal expression profile in Indian Ghurrah pigs. 3 Biotech 2019 11 9 (11): 422. Rawat Chandrakanta, Sahoo Nihar Ranjan, Wagh Shivaji S, Kumar Pushpendra, Kumar Subodh, Sonwane Arvind, Qureshi Salauddin, Kumar Amit, Panigrahi Manj |
Transferrin receptor-involved HIF-1 signaling pathway in cervical cancer. Cancer gene therapy 2019 1 26 (11-12): 356-365. Xu Xiaofeng, Liu Tao, Wu Jun, Wang Yijin, Hong Ying, Zhou Huaij |
Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease. JAMA cardiology 2020 Oct . Morton Sarah U, Shimamura Akiko, Newburger Peter E, Opotowsky Alexander R, Quiat Daniel, Pereira Alexandre C, Jin Sheng Chih, Gurvitz Michelle, Brueckner Martina, Chung Wendy K, Shen Yufeng, Bernstein Daniel, Gelb Bruce D, Giardini Alessandro, Goldmuntz Elizabeth, Kim Richard W, Lifton Richard P, Porter George A, Srivastava Deepak, Tristani-Firouzi Martin, Newburger Jane W, Seidman J G, Seidman Christine |
The Associations of Dietary Iron Intake and the Transferrin Receptor (TFRC) rs9846149 Polymorphism with the Risk of Gastric Cancer: A Case-Control Study Conducted in Korea. Nutrients 2021 8 13 (8): . Tran Tao Thi, Gunathilake Madhawa, Lee Jeonghee, Choi Il Ju, Kim Young-Il, Kim Jeongse |
Contribution of miR-124 rs531564 polymorphism to the occurrence of congenital Zika syndrome. Epigenetics 2022 11 1-7. Gomes Julia A, Vieira Igor Araujo, Sgarioni Eduarda, Terças-Tretell Ana Cláudia P, da Silva Juliana H, Ribeiro Bethânia Fr, Galera Marcial F, de Oliveira Thalita M, Carvalho de Andrade Maria Denise F, Carvalho Isabella F, Schüler-Faccini Lavínia, Vianna Fernanda |
Transferrin receptor levels and its rare variant are associated with human obesity. Journal of diabetes 2023 8 . Jin Qiu, Zhiyin Zhang, Yepeng Hu, Yuhan Guo, Caizhi Liu, Yanru Chen, Dongmei Wang, Junlei Su, Sainan Wang, Mengshan Ni, Sainan Xu, Jian Yu, Tianhui Hu, Gaojie Song, Xinran Ma, Xuejiang Gu, Jiqiu Wang, Lingyan |
Identification of ferroptosis-related molecular subtypes and a methylation-related ferroptosis gene prognostic signature in cervical squamous cell carcinoma. Journal of cancer research and clinical oncology 2023 8 . Lijun Yu, Zhenwei Gao, Zeyu Li, Ping Liu, Ya Gao, Gang Lia |
Iron metabolism in autism spectrum disorder; inference through single nucleotide polymorphisms in key iron metabolism genes. Journal of the neurological sciences 2023 10 453 120817. Sabha Rabaya, Sameera Nairat, Khaldoun Bader, Mohammad M Herzallah, Hisham M Darwi |
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- Page last updated:Apr 16, 2024
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