Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
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Query Trace: Blood Diseases |
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[Population characterization of mutations for sickle cell anemia and its treatment: One step towards personalized medicine for the disease]. Andes pediatrica : revista Chilena de pediatria 2024 4 95 (1): 41-52. Bernardita Cayupe, Rafael Bar |
Impact of MLL::AF9 Gene Rearrangement on Survival of Acute Myeloid Leukaemia Patients: An Insight into Pakistani Population. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2024 4 34 (4): 424-428. Muhammad Tariq, Sadaf Shahab, Javeria Rauf Saeed, Zeeshan Hussain, Uzma Zaidi, Tasneem Farzana, Sultan Ahm |
Two Novel Genetic Variants Involved in the Oxygen Sensing Pathway in JAK2-unmutated Erythrocytosis. Biochemical genetics 2024 4 . Qiang Ma, Ronghua Hu, Wuhan Hui, Hong Zhao, Dongmei Zou, Yan Liu, Wanling S |
[Analysis of clinical characteristics and molecular genetics in eighteen patients with 1q21.1 microdeletion syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 4 41 (4): 480-485. Xiaojin Luo, Hongyan Niu, Fei Zhou, Shuangwu Li, Zhenming Li, Yanyun G |
Blood Calcium, Genetic Risk, and Risk of Incident Kidney Stone: A Population-Based Cohort Study. Mayo Clinic proceedings 2024 4 . Xi Cao, Si Li, Yunlong Guan, Zhonghe Shao, Minghui Jiang, Miao Wang, Xingjie H |
Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis. Hemoglobin 2024 4 48 (2): 101-112. Aradhana Kumari, Ganesh Chauhan, Partha Kumar Chaudhuri, Sushma Kumari, Anupa Pras |
Estimating the serological underrecognition of patients with weak or partial RHD variants. Transfusion 2024 4 . Glenn Ramsey, Christina M Barrite |
The Association between Obstructive Sleep Apnea and Venous Thromboembolism: A Bidirectional Two-Sample Mendelian Randomization Study. Thrombosis and haemostasis 2024 4 . Zhihai Huang, Zhenzhen Zheng, Lingpin Pang, Kaili Fu, Junfen Cheng, Ming Zhong, Lingyue Song, Dingyu Guo, Qiaoyun Chen, Yanxi Li, Yongting Lv, Riken Chen, Xishi S |
Sex-specific impact on disease outcome and the mutational landscape in essential thrombocythemia: A retrospective cohort study. Chinese medical journal 2024 4 . Jia Chen, Huan Dong, Yang Li, Ting Sun, Rongfeng Fu, Xiaofan Liu, Feng Xue, Wei Liu, Yunfei Chen, Mankai Ju, Xinyue Dai, Ying Chi, Wentian Wang, Huiyuan Li, Renchi Yang, Lei Zha |
IL1B Polymorphism (rs1143634) and IL-1? Plasma Concentration as Predictors of Nutritional Disorders and Prognostic Factors in Multiple Myeloma Patients. Cancers 2024 4 16 (7): . Marcin Mazurek, Aneta Szudy-Szczyrek, Iwona Homa-Mlak, Marek Hus, Teresa Ma?ecka-Massalska, Rados?aw Ml |
Lessons from prospective longitudinal follow-up of a French APECED cohort. The Journal of clinical endocrinology and metabolism 2024 4 . Linda Humbert, Emmanuelle Proust-Lemoine, Sylvain Dubucquoi, Elisabeth Helen Kemp, Pascale Saugier-Veber, Nicole Fabien, Isabelle Raymond-Top, Catherine Cardot-Bauters, Jean-Claude Carel, Maryse Cartigny, Olivier Chabre, Philippe Chanson, Brigitte Delemer, Christine Do Cao, Laurence Guignat, Jean Emmanuel Kahn, Veronique Kerlan, Herve Lefebvre, Agnès Linglart, Roberto Mallone, Rachel Reynaud, Boualem Sendid, Pierre-François Souchon, Philippe Touraine, Jean-Louis Wémeau, Marie-Christine Vantygh |
Maternal and infant outcomes in women with sickle cell disease: a matched cohort study. Archives of disease in childhood. Fetal and neonatal edition 2024 4 . Oishi Sikdar, Hemant Ambulkar, Allan Jenkinson, Catherine Hedley, Jemma Johns, Ravindra Bhat, Theodore Dassios, Christopher Harris, Anne Greenou |
Interleukin-10 GCC/GCC haplotype is associated high risk of acute GVHD in patients undergoing allogeneic HSCT in the southern of Brazil. Transplant immunology 2024 1 102002. Mariela Granero Farias, Camila Andrade Dos Santos, Alessandra Aparecida Paz, Liane Esteves Dau |
QL1706 (anti-PD-1 IgG4/CTLA-4 antibody) plus chemotherapy with or without bevacizumab in advanced non-small cell lung cancer: a multi-cohort, phase II study. Signal transduction and targeted therapy 2024 1 9 (1): 23. Yan Huang, Yunpeng Yang, Yuanyuan Zhao, Hongyun Zhao, Ningning Zhou, Yaxiong Zhang, Likun Chen, Ting Zhou, Gang Chen, Ting Wu, Lu Lu, Shilin Xue, Xiaoyan Kang, Li Zhang, Wenfeng Fa |
PARP Inhibitors in Metastatic Prostate Cancer: A Comprehensive Systematic Review and Meta-analysis of Existing Evidence. Clinical genitourinary cancer 2024 1 . Francesco Ditonno, Alberto Bianchi, Sarah Malandra, Antonio Benito Porcaro, Emanuela Fantinel, Riccardo Negrelli, Matteo Ferro, Michele Milella, Matteo Brunelli, Riccardo Autorino, Maria Angela Cerruto, Alessandro Veccia, Alessandro Antonel |
Clinical and genetic risk factors associated with neonatal severe hyperbilirubinemia: a case-control study based on the China Neonatal Genomes Project. Frontiers in genetics 2024 1 14 1292921. Xiao Wang, Tiantian Xiao, Jin Wang, Bingbing Wu, Huijun Wang, Yulan Lu, Yaqiong Wang, Bin Chen, Liyuan Hu, Yun Cao, Rong Zhang, Guoqiang Cheng, Laishuan Wang, Zhihua Li, Xinran Dong, Lin Yang, Wenhao Zh |
A Post Hoc Analysis of Previously Untreated Patients With Severe Hemophilia A Who Developed Inhibitors in PUPs A-LONG. Blood advances 2024 1 . Manuel Carcao, Michele Schiavulli, Roshni Kulkarni, Pablo Rendo, Meredith C Foster, Elena Santagostino, Sandra Milena Casiano, Christoph Köni |
CETP gene polymorphisms and haplotypes are explanatory variables for HDL cholesterol level in sickle cell disease. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2024 1 57 e12879. N R C Cruz, T N S Valente, F O Ferreira, L R Macedo, A R Belisário, C M da Silva, N S Oliveira, A F F Gomides, C Velloso-Rodrigu |
Genomic classification and outcomes of young patients with polycythemia vera and essential thrombocythemia according to the presence of splanchnic vein thrombosis and its chronology. Annals of hematology 2024 1 . Marta Garrote, Mónica López-Guerra, Juan Carlos García-Pagán, Eduardo Arellano-Rodrigo, Francisca Ferrer-Marín, Juan Carlos Hernández-Boluda, Beatriz Bellosillo, Meritxell Nomdedeu, Virginia Hernández-Gea, Ana Triguero, Francesca Guijarro, José Álamo, Anna Baiges, Fanny Turon, Dolors Colomer, Francisco Cervantes, Alberto Alvarez-Larr |
A real-world study of PARP inhibitors in 75 patients with platinum-sensitive recurrent ovarian cancer from China. Frontiers in oncology 2024 1 13 1300199. Jinghong Chen, Mengpei Zhang, Kemin Li, Yuanqiong Duan, Xiaojuan Lin, Lan Zhong, Qintong Li, Rutie Y |
CALR mutation burden in essential thrombocythemia and disease outcome. Blood 2024 1 . Paola Guglielmelli, Natasha Szuber, Naseema Gangat, Giulio Capecchi, Chiara Maccari, Michaël Harnois, Omer Karrar, Maymona Abdelmagid, Manjola Balliu, Elena Nacca, Alessandro Atanasio, Ilaria Sestini, Audrey Desilets, Giuseppe Gaetano Loscocco, Giada Rotunno, Lambert Busque, Ayalew Tefferi, Alessandro Maria Vannucc |
Clinical and genomic predictors of adverse events in newly diagnosed glioblastoma. Clinical cancer research : an official journal of the American Association for Cancer Research 2024 1 . Mary Jane Lim-Fat, J Bryan Iorgulescu, Rifaquat Rahman, Varun Bhave, Alona Muzikansky, Eleanor Woodward, Sydney Whorral, Marie Allen, Mehdi Touat, Xiaomei Li, Gongwen Xu, Jay Patel, Elizabeth R Gerstner, Jayashree Kalpathy-Cramer, Gilbert Youssef, Ugonma Chukwueke, J Ricardo McFaline-Figueroa, Lakshmi Nayak, Eudocia Q Lee, David A Reardon, Rameen Beroukhim, Raymond Y Huang, Wenya Linda Bi, Keith L Ligon, Patrick Y W |
Genomic profiling of relapsed small cell lung cancer reveals potential pathways of therapeutic targets. Journal of thoracic disease 2024 1 15 (12): 6796-6805. Wen Ouyang, Jing Yu, Zihang Zeng, Jun Gong, Junhong Zhang, Conghua X |
Association of Normal and Mutated APOL1 G2 Rs60910145 alleles with SCD, Body Mass Index, and Renal Function Biomarkers and Indices. Current research in translational medicine 2024 1 72 (1): 103414. Abazar Mahmoud Ismail, Bakri Mohammed Nour, Adam Dawoud Abakar, Babiker Saad Almugadam, Hisham N Altayb, Rania TagEsir Ahmed, Mubarak Elsaeed Mustafa Elkarsa |
Idiopathic erythrocytosis: a germline disease? Clinical and experimental medicine 2024 1 24 (1): 11. E M Elli, M Mauri, D D'Aliberti, I Crespiatico, D Fontana, S Redaelli, S Pelucchi, S Spinelli, B Manghisi, F Cavalca, A Aroldi, A Ripamonti, S Ferrari, S Palamini, F Mottadelli, L Massimino, D Ramazzotti, G Cazzaniga, A Piperno, C Gambacorti-Passerini, R Piaz |
Catechol-O-methyltransferase gene (COMT) is associated with neurocognitive functioning in patients with sickle cell disease. Current research in translational medicine 2024 1 72 (2): 103433. Andrew M Heitzer, Sara R Rashkin, Ana Trpchevska, Jennifer N Longoria, Evadnie Rampersaud, Yunusa Olufadi, Winfred C Wang, Darcy Raches, Brian Potter, Martin H Steinberg, Allison A King, Guolian Kang, Clifford M Takemoto, Jane S Hanki |
One thousand patients with essential thrombocythemia: the Mayo Clinic experience. Blood cancer journal 2024 1 14 (1): 11. Naseema Gangat, Omer Karrar, Aref Al-Kali, Kebede H Begna, Michelle A Elliott, Alexandra P Wolanskyj-Spinner, Animesh Pardanani, Curtis A Hanson, Rhett P Ketterling, Ayalew Teffe |
One thousand patients with essential thrombocythemia: the Florence-CRIMM experience. Blood cancer journal 2024 1 14 (1): 10. Giuseppe G Loscocco, Francesca Gesullo, Giulio Capecchi, Alessandro Atanasio, Chiara Maccari, Francesco Mannelli, Alessandro M Vannucchi, Paola Guglielmel |
A survey of ficolin-3 activity in Systemic Lupus Erythematosus reveals a link to hematological disease manifestations and autoantibody profile. Journal of autoimmunity 2024 1 143 103166. Linnea Lindelöf, Solbritt Rantapää-Dahlqvist, Christian Lundtoft, Johanna K Sandling, Dag Leonard, Ahmed Sayadi, Lars Rönnblom, Helena Enocsson, Christopher Sjöwall, Andreas Jönsen, Anders A Bengtsson, Mun-Gwan Hong, Lina-Marcela Diaz-Gallo, Matteo Bianchi, Sergey V Kozyrev, Kerstin Lindblad-Toh, , , Kristina Nilsson Ekdahl, Bo Nilsson, Iva Gunnarsson, Elisabet Svenungsson, Oskar Erikss |
A novel nonsense mutation in the fumarate hydratase gene in a Chinese patient with recurrent leiomyomas. F&S reports 2024 1 4 (4): 410-415. Yiyin Ruan, Weiwei Feng, Chenmin Ya |
Blood donor biobank as a resource in personalised biomedical genetic research. European journal of human genetics : EJHG 2024 1 . Jonna Clancy, Jarmo Ritari, Eevaleena Vaittinen, Mikko Arvas, Silja Tammi, , Satu Koskela, Jukka Partan |
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- Page last updated:Apr 22, 2024
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