Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 61 Records) |
Query Trace: HAMP[original query] |
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Non-HFE mutations in haemochromatosis in China: combination of heterozygous mutations involving HJV signal peptide variants. Journal of medical genetics 2018 9 55 (10): 650-660. Lv Tingxia, Zhang Wei, Xu Anjian, Li Yanmeng, Zhou Donghu, Zhang Bei, Li Xiaojin, Zhao Xinyan, Wang Yu, Wang Xiaoming, Duan Weijia, Wang Qianyi, Xu Hexiang, Zheng JiShun, Zhao Rongrong, Zhu Longdong, Dong Yuwei, Lu Lungen, Chen Yongpeng, Long Jiang, Zheng Sujun, Wang Wei, You Hong, Jia Jidong, Ou Xiaojuan, Huang Ji |
SLC40A1 and CP single nucleotide polymorphisms in porphyria cutanea tarda patients of mixed ancestry. Annals of human genetics 2018 May . Succi Isabella Brasil, Pôrto Luís Cristóvão, Silva Dayse, Nascimento Adriana, Neto Ronald Costa, Fonseca João Carl |
Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease. Blood 2018 5 132 (1): 101-110. Sandhu Kam, Flintoff Kaledas, Chatfield Mark D, Dixon Jeannette L, Ramm Louise E, Ramm Grant A, Powell Lawrie W, Subramaniam V Nathan, Wallace Daniel |
Nomograms incorporating genetic variants in BMP/Smad4/Hamp pathway to predict disease outcomes after definitive radiotherapy for non-small cell lung cancer. Cancer medicine 2018 May . Yang Ju, Xu Ting, Gomez Daniel R, Yuan Xianglin, Nguyen Quynh-Nhu, Jeter Melenda, Song Yipeng, Komaki Ritsuko, Hu Ye, Hahn Stephen M, Liao Zhongxi |
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 |
Role of HAMP Genetic Variants on Pathophysiology of Iron Deficiency Anemia. Indian journal of clinical biochemistry : IJCB 2018 10 33 (4): 479-482. Pandey S, Pandey S K, Shah |
Genetic Variability and Trajectories of DNA Methylation May Support a Role for HAMP in Patient Outcomes After Aneurysmal Subarachnoid Hemorrhage. Neurocritical care 2019 Jul . Heinsberg Lacey W, Arockiaraj Annie I, Crago Elizabeth A, Ren Dianxu, Shaffer John R, Sherwood Paula R, Sereika Susan M, Weeks Daniel E, Conley Yvette |
Hepcidin and HFE Polymorphisms and Ferritin Level in ?-Thalassemia Major. International journal of hematology-oncology and stem cell research 2019 6 13 (1): 42-48. Fekri Kiavash, Asle Rasouli Negar, Tavallai Zavareh Seyyed Abdolhossein, Jalil Milad, Moradi Fahimeh, Hosseinpour Maryam, Teimori Hosse |
Iron levels, genes involved in iron metabolism and antioxidative processes and lung cancer incidence. PloS one 2019 14 (1): e0208610. Sukiennicki Grzegorz Mariusz, Marciniak Wojciech, Muszy?ska Magdalena, Baszuk Piotr, Gupta Satish, Bia?kowska Katarzyna, Jaworska-Bieniek Katarzyna, Durda Katarzyna, Lener Marcin, Pietrzak Sandra, Gromowski Tomasz, Prajzendanc Karolina, ?ukomska Alicja, Waloszczyk Piotr, Wójcik Janusz Zenon, Scott Rodney, Lubi?ski Jan, Jakubowska An |
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 |
Hepcidin gene polymorphisms and iron overload in ?-thalassemia major patients refractory to iron chelating therapy. BMC medical genetics 2020 4 21 (1): 75. Zarghamian Parinaz, Azarkeivan Azita, Arabkhazaeli Ali, Mardani Ahmad, Shahabi Maj |
The Prevalence of Insomnia and the Link between Iron Metabolism Genes Polymorphisms, TF rs1049296 C>T, TF rs3811647 G>A, TFR rs7385804 A>C, HAMP rs10421768 A>G and Sleep Disorders in Polish Individuals with ASD. International journal of environmental research and public health 2020 Jan 17 (2): . Skonieczna-Zydecka Karolina, Jamiol-Milc Dominika, Borecki Krzysztof, Stachowska Ewa, Zabielska Paulina, Kaminska Magdalena, Karakiewicz Bea |
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 |
Frequency of the HAMP (c.-582 A>G) Polymorphism in Iron Deficiency in Saudi Arabia. Pakistan journal of biological sciences : PJBS 2021 Jan 24 (1): 146-150. Al-Amer Osama, Alsharif Khalaf |
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 |
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 |
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 |
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, |
Hepcidin (rs10421768), Transferrin (rs3811647, rs1049296) and Transferrin Receptor 2 (rs7385804) Gene Polymorphism Might Be Associated with the Origin of Multiple Sclerosis. International journal of environmental research and public health 2022 06 19 (11): . Stachowska Laura, Koziarska Dorota, Karakiewicz Beata, Kotwas Artur, Knyszy?ska Anna, Folwarski Marcin, Dec Karolina, Stachowska Ewa, Hawry?kowicz Viktoria, Kulaszy?ska Monika, So?ek-Pastuszka Joanna, Skonieczna-?ydecka Karoli |
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 |
Hepcidin is upregulated and is a potential therapeutic target associated with immunity in glioma. Frontiers in oncology 2022 10 12 963096. Dong Tianyu, Zhang Bo, Zhang Runjiao, Wang Chang, Liu Xiaopeng, Wang Fei, Hao Nana, Tan Ke, Chang Yan-Zho |
Myeloid cell iron uptake pathways and paramagnetic rim formation in multiple sclerosis. Acta neuropathologica 2023 9 . Annika Hofmann, Nik Krajnc, Assunta Dal-Bianco, Christian J Riedl, Tobias Zrzavy, Celia Lerma-Martin, Gregor Kasprian, Claudia E Weber, Francesco Pezzini, Fritz Leutmezer, Paulus Rommer, Gabriel Bsteh, Michael Platten, Achim Gass, Thomas Berger, Philipp Eisele, Roberta Magliozzi, Lucas Schirmer, Simon Hametn |
The landscape of tolerated genetic variation in humans and primates. Science (New York, N.Y.) 2023 6 380 (6648): eabn8153. Hong Gao, Tobias Hamp, Jeffrey Ede, Joshua G Schraiber, Jeremy McRae, Moriel Singer-Berk, Yanshen Yang, Anastasia S D Dietrich, Petko P Fiziev, Lukas F K Kuderna, Laksshman Sundaram, Yibing Wu, Aashish Adhikari, Yair Field, Chen Chen, Serafim Batzoglou, Francois Aguet, Gabrielle Lemire, Rebecca Reimers, Daniel Balick, Mareike C Janiak, Martin Kuhlwilm, Joseph D Orkin, Shivakumara Manu, Alejandro Valenzuela, Juraj Bergman, Marjolaine Rousselle, Felipe Ennes Silva, Lidia Agueda, Julie Blanc, Marta Gut, Dorien de Vries, Ian Goodhead, R Alan Harris, Muthuswamy Raveendran, Axel Jensen, Idriss S Chuma, Julie E Horvath, Christina Hvilsom, David Juan, Peter Frandsen, Fabiano R de Melo, Fabrício Bertuol, Hazel Byrne, Iracilda Sampaio, Izeni Farias, João Valsecchi do Amaral, Mariluce Messias, Maria N F da Silva, Mihir Trivedi, Rogerio Rossi, Tomas Hrbek, Nicole Andriaholinirina, Clément J Rabarivola, Alphonse Zaramody, Clifford J Jolly, Jane Phillips-Conroy, Gregory Wilkerson, Christian Abee, Joe H Simmons, Eduardo Fernandez-Duque, Sree Kanthaswamy, Fekadu Shiferaw, Dongdong Wu, Long Zhou, Yong Shao, Guojie Zhang, Julius D Keyyu, Sascha Knauf, Minh D Le, Esther Lizano, Stefan Merker, Arcadi Navarro, Thomas Bataillon, Tilo Nadler, Chiea Chuen Khor, Jessica Lee, Patrick Tan, Weng Khong Lim, Andrew C Kitchener, Dietmar Zinner, Ivo Gut, Amanda Melin, Katerina Guschanski, Mikkel Heide Schierup, Robin M D Beck, Govindhaswamy Umapathy, Christian Roos, Jean P Boubli, Monkol Lek, Shamil Sunyaev, Anne O'Donnell-Luria, Heidi L Rehm, Jinbo Xu, Jeffrey Rogers, Tomas Marques-Bonet, Kyle Kai-How Fa |
Rare penetrant mutations confer severe risk of common diseases. Science (New York, N.Y.) 2023 6 380 (6648): eabo1131. Petko P Fiziev, Jeremy McRae, Jacob C Ulirsch, Jacqueline S Dron, Tobias Hamp, Yanshen Yang, Pierrick Wainschtein, Zijian Ni, Joshua G Schraiber, Hong Gao, Dylan Cable, Yair Field, Francois Aguet, Marc Fasnacht, Ahmed Metwally, Jeffrey Rogers, Tomas Marques-Bonet, Heidi L Rehm, Anne O'Donnell-Luria, Amit V Khera, Kyle Kai-How Fa |
Rare penetrant mutations confer severe risk of common diseases. medRxiv : the preprint server for health sciences 2023 5 . Petko Fiziev, Jeremy McRae, Jacob C Ulirsch, Jacqueline S Dron, Tobias Hamp, Yanshen Yang, Pierrick Wainschtein, Zijian Ni, Joshua G Schraiber, Hong Gao, Dylan Cable, Yair Field, Francois Aguet, Marc Fasnacht, Ahmed Metwally, Jeffrey Rogers, Tomas Marques-Bonet, Heidi L Rehm, Anne O'Donnell-Luria, Amit V Khera, Kyle Kai-How Fa |
The landscape of tolerated genetic variation in humans and primates. bioRxiv : the preprint server for biology 2023 5 . Hong Gao, Tobias Hamp, Jeffrey Ede, Joshua G Schraiber, Jeremy McRae, Moriel Singer-Berk, Yanshen Yang, Anastasia Dietrich, Petko Fiziev, Lukas Kuderna, Laksshman Sundaram, Yibing Wu, Aashish Adhikari, Yair Field, Chen Chen, Serafim Batzoglou, Francois Aguet, Gabrielle Lemire, Rebecca Reimers, Daniel Balick, Mareike C Janiak, Martin Kuhlwilm, Joseph D Orkin, Shivakumara Manu, Alejandro Valenzuela, Juraj Bergman, Marjolaine Rouselle, Felipe Ennes Silva, Lidia Agueda, Julie Blanc, Marta Gut, Dorien de Vries, Ian Goodhead, R Alan Harris, Muthuswamy Raveendran, Axel Jensen, Idriss S Chuma, Julie Horvath, Christina Hvilsom, David Juan, Peter Frandsen, Fabiano R de Melo, Fabricio Bertuol, Hazel Byrne, Iracilda Sampaio, Izeni Farias, João Valsecchi do Amaral, Mariluce Messias, Maria N F da Silva, Mihir Trivedi, Rogerio Rossi, Tomas Hrbek, Nicole Andriaholinirina, Clément J Rabarivola, Alphonse Zaramody, Clifford J Jolly, Jane Phillips-Conroy, Gregory Wilkerson, Christian Abee, Joe H Simmons, Eduardo Fernandez-Duque, Ee Kanthaswamy, Fekadu Shiferaw, Dongdong Wu, Long Zhou, Yong Shao, Guojie Zhang, Julius D Keyyu, Sascha Knauf, Minh D Le, Esther Lizano, Stefan Merker, Arcadi Navarro, Thomas Batallion, Tilo Nadler, Chiea Chuen Khor, Jessica Lee, Patrick Tan, Weng Khong Lim, Andrew C Kitchener, Dietmar Zinner, Ivo Gut, Amanda Melin, Katerina Guschanski, Mikkel Heide Schierup, Robin M D Beck, Govindhaswamy Umapathy, Christian Roos, Jean P Boubli, Monkol Lek, Shamil Sunyaev, Anne O'Donnell, Heidi Rehm, Jinbo Xu, Jeffrey Rogers, Tomas Marques-Bonet, Kyle Kai-How Fa |
Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica) study group. British journal of haematology 2023 11 . Paola Corti, Giulia Maria Ferrari, Martha Caterina Faraguna, Giulia Capitoli, Filomena Longo, Elena Corradini, Tommaso Casini, Gianluca Boscarol, Valeria Maria Pinto, Roberta Ghilardi, Giovanna Russo, Raffaella Colombatti, Raffaella Mariani, Alberto Piper |
Increased IL-6 Levels and the Upregulation of Iron Regulatory Biomarkers Contribute to the Progression of Japanese Encephalitis Virus Infection's Pathogenesis. Neuromolecular medicine 2023 11 . Anjali Singh, Sneha Ghildiyal, Prabhaker Mishra, Gajendra Singh, Himanshu Dandu, Alok Kum |
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 |
Genetic Architecture of Pregnancy Loss: Co-inheritance of Risk Factors in Bosnian Women. Folia biologica 2024 1 69 (3): 75-80. Gra?yna Adler, Mateusz A Adler, Emir Mahmutbegov |
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- Page last updated:Apr 16, 2024
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