Human Genome Epidemiology Literature Finder
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Records 1 - 23 (of 23 Records) |
| Query Trace: Disease and TMPRSS6[original query] |
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| Polymorphisms and mutations of human TMPRSS6 in iron deficiency anemia. Blood cells, molecules & diseases 2010 Jan 44 (1): 16-21. Beutler E, Van Geet C, te Loo D M W M, Gelbart T, Crain K, Truksa J, Lee P |
A genome-wide association study of red blood cell traits using the electronic medical record.
PloS one 2010 5 (9): 9. Kullo Iftikhar J, Ding Keyue, Jouni Hayan, Smith Carin Y, Chute Christopher |
| A novel SNaPshot assay to detect genetic mutations related to iron metabolism. Genetic testing and molecular biomarkers 2011 1 15 (3): 173-9. Bertoncini Stefania, Blanco-Rojo Ruth, Baeza Carlos, Arroyo-Pardo Eduardo, Vaquero María Pilar, López-Parra Ana Mar |
| The A736V TMPRSS6 polymorphism influences hepatic iron overload in nonalcoholic fatty liver disease. PloS one 2012 7 (11): e48804. Valenti Luca, Rametta Raffaela, Dongiovanni Paola, Motta Benedetta M, Canavesi Elena, Pelusi Serena, Pulixi Edoardo A, Fracanzani Anna L, Fargion Silv |
| 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 |
| 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 |
| About TMPRSS6 rs855791 polymorphism, iron metabolism and celiac disease. The American journal of gastroenterology 2015 Aug 110 (8): 1240. Zanella Isabella, Caimi Luigi, Biasiotto Giorg |
| Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes. Blood cells, molecules & diseases 2015 Jun 55 (1): 71-5. Radio Francesca Clementina, Majore Silvia, Aurizi Caterina, Sorge Fiammetta, Biolcati Gianfranco, Bernabini Sara, Giotti Irene, Torricelli Francesca, Giannarelli Diana, De Bernardo Carmelilia, Grammatico Pao |
| Does TMPRSS6 RS855791 polymorphism contribute to iron deficiency in treated celiac disease? The American journal of gastroenterology 2015 Jan 110 (1): 200-2. Elli Luca, Poggiali Erika, Tomba Carolina, Andreozzi Fabio, Nava Isabella, Bardella Maria Teresa, Campostrini Natascia, Girelli Domenico, Conte Dario, Cappellini Maria Domeni |
| The role of TMPRSS6 polymorphisms in iron deficiency anemia partially responsive to oral iron treatment. American journal of hematology 2015 Apr 90 (4): 306-9. Poggiali Erika, Andreozzi Fabio, Nava Isabella, Consonni Dario, Graziadei Giovanna, Cappellini Maria Domeni |
| Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals. American journal of human genetics 2016 Jun . Eicher John D, Chami Nathalie, Kacprowski Tim, Nomura Akihiro, Chen Ming-Huei, Yanek Lisa R, Tajuddin Salman M, Schick Ursula M, Slater Andrew J, Pankratz Nathan, Polfus Linda, Schurmann Claudia, Giri Ayush, Brody Jennifer A, Lange Leslie A, Manichaikul Ani, Hill W David, Pazoki Raha, Elliot Paul, Evangelou Evangelos, Tzoulaki Ioanna, Gao He, Vergnaud Anne-Claire, Mathias Rasika A, Becker Diane M, Becker Lewis C, Burt Amber, Crosslin David R, Lyytikäinen Leo-Pekka, Nikus Kjell, Hernesniemi Jussi, Kähönen Mika, Raitoharju Emma, Mononen Nina, Raitakari Olli T, Lehtimäki Terho, Cushman Mary, Zakai Neil A, Nickerson Deborah A, Raffield Laura M, Quarells Rakale, Willer Cristen J, Peloso Gina M, Abecasis Goncalo R, Liu Dajiang J, , Deloukas Panos, Samani Nilesh J, Schunkert Heribert, Erdmann Jeanette, , , Fornage Myriam, Richard Melissa, Tardif Jean-Claude, Rioux John D, Dube Marie-Pierre, de Denus Simon, Lu Yingchang, Bottinger Erwin P, Loos Ruth J F, Smith Albert Vernon, Harris Tamara B, Launer Lenore J, Gudnason Vilmundur, Velez Edwards Digna R, Torstenson Eric S, Liu Yongmei, Tracy Russell P, Rotter Jerome I, Rich Stephen S, Highland Heather M, Boerwinkle Eric, Li Jin, Lange Ethan, Wilson James G, Mihailov Evelin, Mägi Reedik, Hirschhorn Joel, Metspalu Andres, Esko Tõnu, Vacchi-Suzzi Caterina, Nalls Mike A, Zonderman Alan B, Evans Michele K, Engström Gunnar, Orho-Melander Marju, Melander Olle, O'Donoghue Michelle L, Waterworth Dawn M, Wallentin Lars, White Harvey D, Floyd James S, Bartz Traci M, Rice Kenneth M, Psaty Bruce M, Starr J M, Liewald David C M, Hayward Caroline, Deary Ian J, Greinacher Andreas, Völker Uwe, Thiele Thomas, Völzke Henry, van Rooij Frank J A, Uitterlinden André G, Franco Oscar H, Dehghan Abbas, Edwards Todd L, Ganesh Santhi K, Kathiresan Sekar, Faraday Nauder, Auer Paul L, Reiner Alex P, Lettre Guillaume, Johnson Andrew |
| The Effect of Iron Status on Risk of Coronary Artery Disease: A Mendelian Randomization Study-Brief Report. Arteriosclerosis, thrombosis, and vascular biology 2017 Jul . Gill Dipender, Del Greco M Fabiola, Walker Ann P, Srai Surjit K S, Laffan Michael A, Minelli Coset |
| The role of TMPRSS6 and HFE variants in iron deficiency anemia in celiac disease. American journal of hematology 2017 Dec . De Falco Luigia, Tortora Raffaella, Imperatore Nicola, Bruno Mariasole, Capasso Mario, Girelli Domenico, Castagna Annalisa, Caporaso Nicola, Iolascon Achille, Rispo Anton |
| Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal Disease. Disease markers 2019 2019 4864370. Dopsaj Violeta, Topi? Aleksandra, Savkovi? Miljan, Milinkovi? Neda, Novakovi? Ivana, ?uji? Danica, Simi?-Ogrizovi? San |
| TMPRSS6 rs855791 polymorphism and susceptibility to iron deficiency anaemia in non-dialysis chronic kidney disease patients in South Africa. International journal of molecular epidemiology and genetics 2019 10 (1): 1-9. Nalado Aishatu Muhammad, Dickens Caroline, Dix-Peek Therese, Mahlangu Johnny N, Olorunfemi Gbenga, Paget Graham, Duarte Raquel, Naicker Saralade |
| An investigation of the relationship between TMPRSS6 gene expression, genetic variants and clinical findings in breast cancer. Molecular biology reports 2020 May . Mete Meltem, Trabulus Didem Can, Talu Canan Kelten, Ozoran Emre, Mutlu Tuba, Tekin Bulent, Guven Mehm |
| TMPRSS6 rs855791 Polymorphism Status in Children with Celiac Disease and Anemia. Nutrients 2021 8 13 (8): . Urbaszek Klaudia, Drabi?ska Natalia, Szaflarska-Pop?awska Anna, Jarocka-Cyrta El?bie |
| HIF1A: A Putative Modifier of Hemochromatosis. International journal of molecular sciences 2021 1 22 (3): . Pelucchi Sara, Ravasi Giulia, Arosio Cristina, Mauri Mario, Piazza Rocco, Mariani Raffaella, Piperno Alber |
| Role of TMPRSS6 rs855791 (T > C) polymorphism in reproductive age women with iron deficiency anemia from Lahore, Pakistan. Saudi journal of biological sciences 2021 Jan 28 (1): 748-753. Lone Nasira Munawar, Shah Syed Hasnain Sajjad, Farooq Mariya, Arif Mizna, Younis Sidra, Riaz Sa |
| Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
American journal of human genetics 2021 4 108 (5): 874-893. Hu Yao, Stilp Adrienne M, McHugh Caitlin P, Rao Shuquan, Jain Deepti, Zheng Xiuwen, Lane John, Méric de Bellefon Sébastian, Raffield Laura M, Chen Ming-Huei, Yanek Lisa R, Wheeler Marsha, Yao Yao, Ren Chunyan, Broome Jai, Moon Jee-Young, de Vries Paul S, Hobbs Brian D, Sun Quan, Surendran Praveen, Brody Jennifer A, Blackwell Thomas W, Choquet Hélène, Ryan Kathleen, Duggirala Ravindranath, Heard-Costa Nancy, Wang Zhe, Chami Nathalie, Preuss Michael H, Min Nancy, Ekunwe Lynette, Lange Leslie A, Cushman Mary, Faraday Nauder, Curran Joanne E, Almasy Laura, Kundu Kousik, Smith Albert V, Gabriel Stacey, Rotter Jerome I, Fornage Myriam, Lloyd-Jones Donald M, Vasan Ramachandran S, Smith Nicholas L, North Kari E, Boerwinkle Eric, Becker Lewis C, Lewis Joshua P, Abecasis Goncalo R, Hou Lifang, O'Connell Jeffrey R, Morrison Alanna C, Beaty Terri H, Kaplan Robert, Correa Adolfo, Blangero John, Jorgenson Eric, Psaty Bruce M, Kooperberg Charles, Walton Russell T, Kleinstiver Benjamin P, Tang Hua, Loos Ruth J F, Soranzo Nicole, Butterworth Adam S, Nickerson Debbie, Rich Stephen S, Mitchell Braxton D, Johnson Andrew D, Auer Paul L, Li Yun, Mathias Rasika A, Lettre Guillaume, Pankratz Nathan, Laurie Cathy C, Laurie Cecelia A, Bauer Daniel E, Conomos Matthew P, Reiner Alexander P, |
| Polymorphisms Related to Iron Homeostasis Associate with Liver Disease in Chronic Hepatitis C. Viruses 2023 8 15 (8): . Anna Wróblewska, Anna Woziwodzka, Magda Rybicka, Krzysztof P Bielawski, Katarzyna Sikors |
| Genetic Variations of ferroportin-1(FPN1-8CG), TMPRSS6 (rs855791) and Hemojuvelin (I222N and G320V) Among a Cohort of Egyptian ?-Thalassemia Major Patients. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2023 4 39 (2): 258-265. El-Gharbawi Nesrine, Shaheen Iman, Hamdy Mona, Elgawhary Somaya, Samir Mohamed, Hanna Baher Matta, Ali Eman Yousief, Youssef Eman Ahm |
| The global prevalence and ethnic heterogeneity of iron-refractory iron deficiency anaemia. Orphanet journal of rare diseases 2023 1 18 (1): 2. Fan Shanghua, Zhao Ting, Sun L |
- Page last reviewed:Feb 1, 2024
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