Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 564 Records) |
Query Trace: SCD[original query] |
---|
HLA-F and LILRB1 Genetic Polymorphisms Associated with Alloimmunisation in Sickle Cell Disease. International journal of molecular sciences 2023 9 24 (17): . Emmanuelle Bernit, Estelle Jean, Bastien Marlot, Laurine Laget, Caroline Izard, Isabelle Dettori, Sophie Beley, Isabelle Gautier, Imane Agouti, Coralie Frassati, Pascal Pedini, Christophe Picard, Julien Paganini, Jacques Chiaroni, Julie Di Cristofa |
Evaluation of a prophylactic transfusion program on obstetric outcomes in pregnant women with sickle cell disease: A single centre retrospective cohort study. European journal of obstetrics, gynecology, and reproductive biology 2023 9 290 103-108. O Sobczyk, E Gottardi, M Lefebvre, F Canouï-Poitrine, A Jebali, G De Luna, F Pirenne, D Redel, F Galacteros, E Boutin, P Bartolucci, B Haddad, A Habibi, E Lecarpenti |
Genetic variants and effect modifiers of QT interval prolongation in patients with sickle cell disease. Gene 2023 9 890 147824. Mengna Zhang, William B Hillegass, Xue Yu, Suvankar Majumdar, J Daryl Pollard, Erin Jackson, Jarrod Knudson, Douglas Wolfe, Gregory J Kato, Joseph F Maher, Hao M |
Left cardiac sympathetic denervation in children with Jervell Lange-Nielsen syndrome and drug refractory torsades - A case series. Pacing and clinical electrophysiology : PACE 2023 9 . Deepanjan Bhattacharya, Narayanan Namboodiri, Madhusoodanan Pillai Sreelekshmi, Mukund A Prabhu, Abhilash Sreevilasam Pushpangadhan, Sabarinath Menon, Baiju S Dharan, Ajitkumar Valaparamb |
The role of plasma neurofilament light chain and glial fibrillary acidic protein in subjective cognitive decline and mild cognitive impairment. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2023 9 . Salvatore Mazzeo, Assunta Ingannato, Giulia Giacomucci, Silvia Bagnoli, Arianna Cavaliere, Valentina Moschini, Juri Balestrini, Carmen Morinelli, Giulia Galdo, Filippo Emiliani, Diletta Piazzesi, Chiara Crucitti, Daniele Frigerio, Cristina Polito, Valentina Berti, Sonia Padiglioni, Sandro Sorbi, Benedetta Nacmias, Valentina Bes |
An alcohol dehydrogenase 7 gene polymorphism associates with both acute and chronic pain in sickle cell disease. Pharmacogenomics 2023 9 . Yavnika Kashyap, Ying He, Nilanjana Sadhu, Yingwei Yao, Diana J Wilkie, Robert E Molokie, Zaijie Jim Wa |
Neuropsychiatric symptoms in Alzheimer's continuum and their association with plasma biomarkers. Journal of affective disorders 2023 12 348 200-206. Lin Huang, Qi Huang, Fang Xie, Qihao G |
Non?synonymous polymorphisms in the HRC and ADRB1 genes may be associated with all?cause death in patients with non?ischemic heart failure. Experimental and therapeutic medicine 2023 12 27 (1): 48. Tanise Machado Telles, Bruna Miers May, Mauricio Pimentel, Bruna Letícia Da Silva Pereira, Michael Andrades, Luis Eduardo Rohde, Kátia Gonçalves Dos Sant |
Responses of ?-thalassemia and compound heterozygote of Sickle/?thalassemia of BCL11A Gene Polymorphism in Pakistani Patients. Pakistan journal of medical sciences 2023 11 39 (6): 1788-1792. Nayab Soomro, Mohsin Wahid, Mehreen Mehmood, Syed Hasan Dani |
HLA haplotype frequencies and diversity in patients with hemoglobinopathies. EJHaem 2023 11 4 (4): 963-969. Graziana M Scigliuolo, Wahid Boukouaci, Barbara Cappelli, Fernanda Volt, Monica M Rivera Franco, Nathalie Dhédin, Regis Peffault de Latour, Christine Devalck, Jean-Hugues Dalle, Martin Castelle, Olivier Hermine, Marie Ouachée Chardin, Xavier Poiré, Bénédicte Brichard, Catherine Paillard, Hanadi Rafii, Chantal Kenzey, Ching-Lien Wu, Jihène Bouassida, Marie Robin, Nicole Raus, Vanderson Rocha, Annalisa Ruggeri, Eliane Gluckman, Ryad Tamouza, |
Genetic QT Score and Sleep Apnea as Predictors of Sudden Cardiac Death in the UK Biobank. medRxiv : the preprint server for health sciences 2023 11 . Amit Arora, Wojciech Zareba, Raymond L Woosley, Yann C Klimentidis, Imran Y Patel, Stuart F Quan, Christopher Wendel, Fadi Shamoun, Stefano Guerra, Sairam Parthasarathy, Salma I Pat |
Silent Cerebral Infarcts in Iraqi Patients with Sickle Cell Disease. Hemoglobin 2023 11 1-4. Noor W Rashid, Nasir Al-Allawi, Hamdy I Tah |
Clinical and demographic factors modify the association between plasma phosphorylated tau-181 and cognition. medRxiv : the preprint server for health sciences 2023 11 . Corey J Bolton, Marilyn Steinbach, Omair A Khan, Dandan Liu, Julia O'Malley, Logan Dumitrescu, Amalia Peterson, Angela L Jefferson, Timothy J Hohman, Henrik Zetterberg, Katherine A Gifford, |
Machine learning-based classification of Alzheimer's disease and its at-risk states using personality traits, anxiety, and depression. International journal of geriatric psychiatry 2023 10 38 (10): e6007. Konrad F Waschkies, Joram Soch, Margarita Darna, Anni Richter, Slawek Altenstein, Aline Beyle, Frederic Brosseron, Friederike Buchholz, Michaela Butryn, Laura Dobisch, Michael Ewers, Klaus Fliessbach, Tatjana Gabelin, Wenzel Glanz, Doreen Goerss, Daria Gref, Daniel Janowitz, Ingo Kilimann, Andrea Lohse, Matthias H Munk, Boris-Stephan Rauchmann, Ayda Rostamzadeh, Nina Roy, Eike Jakob Spruth, Peter Dechent, Michael T Heneka, Stefan Hetzer, Alfredo Ramirez, Klaus Scheffler, Katharina Buerger, Christoph Laske, Robert Perneczky, Oliver Peters, Josef Priller, Anja Schneider, Annika Spottke, Stefan Teipel, Emrah Düzel, Frank Jessen, Jens Wiltfang, Björn H Schott, Jasmin M Kizilirm |
Improving sudden cardiac death risk stratification in hypertrophic cardiomyopathy using established clinical variables and genetic information. Clinical research in cardiology : official journal of the German Cardiac Society 2023 10 . Ali Amr, Jan Koelemen, Christoph Reich, Farbod Sedaghat-Hamedani, Elham Kayvanpour, Jan Haas, Karen Frese, David Lehmann, Hugo A Katus, Norbert Frey, Benjamin Med |
RAF1 mutation leading to hypertrophic cardiomyopathy in a Chinese family with a history of sudden cardiac death: A diagnostic insight into Noonan syndrome. Molecular genetics & genomic medicine 2023 10 e2290. Jingjing Zheng, Longyun Peng, Ruofei Cheng, Zhiyan Li, Jianjie Xie, Erwen Huang, Jianding Cheng, Qianhao Zh |
Sarcomeric gene variants among Indians with hypertrophic cardiomyopathy: A scoping review. The Indian journal of medical research 2023 10 158 (2): 119-135. Linda Koshy, Sanjay Ganapathi, Panniyammakal Jeemon, M Madhuma, Y Vysakh, L R Lakshmikanth, Sivadasanpillai Harikrishn |
THE ROLE OF LEFT VENTRICULAR HYPERTROPHY, RS1801253 AND RS1801252 ALLELIC POLYMORPHISMS OF ADRB1 IN ASSESSING THE RISK OF SUDDEN CARDIAC DEATH IN PATIENTS WITH ARTERIAL HYPERTENSION. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2023 10 76 (9): 2054-2060. Olexandr N Grytsay, Boris M Todurov, Yaroslav V Skybchyk, Dina V Shorikova, Eugene I Shorik |
Impact of Genetic Variations on Thromboembolic Risk in Saudis with Sickle Cell Disease. Genes 2023 10 14 (10): . Mohammad A Alshabeeb, Deemah Alwadaani, Farjah H Al Qahtani, Salah Abohelaika, Mohsen Alzahrani, Abdullah Al Zayed, Hussain H Al Saeed, Hala Al Ajmi, Barrak Alsomaie, Mamoon Rashid, Ann K Da |
Patients With Hypertrophic Cardiomyopathy and Normal Genetic Investigations Have Few Affected Relatives. Journal of the American College of Cardiology 2023 10 82 (18): 1751-1761. Søren K Nielsen, Frederikke G Hansen, Torsten B Rasmussen, Thomas Fischer, Jens F Lassen, Trine Madsen, Dorthe S Møller, Ib C Klausen, John B Brodersen, Morten S K Jensen, Jens Mogens |
Prevalence and Impact of HMOX1 Polymorphism (rs2071746: A?>?T) in Indian Sickle Cell Disease Patients. Journal of laboratory physicians 2023 10 15 (4): 583-589. Hareram Pandey, Kanwaljeet Singh, Ravi Ranjan, Jasmita Dass, Seema Tyagi, Tulika Seth, Renu Saxena, Manoranjan Mahapat |
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 |
Pathophysiology characterization of Alzheimer's disease in South China's aging population: for the Greater-Bay-Area Healthy Aging Brain Study (GHABS). Alzheimer's research & therapy 2024 4 16 (1): 84. Zhen Liu, Dai Shi, Yue Cai, Anqi Li, Guoyu Lan, Pan Sun, Lin Liu, Yalin Zhu, Jie Yang, Yajing Zhou, Lizhi Guo, Laihong Zhang, Shuqing Deng, Shuda Chen, Xianfeng Yu, Xuhui Chen, Ruiyue Zhao, Qingyong Wang, Pengcheng Ran, Linsen Xu, Liemin Zhou, Kun Sun, Xinlu Wang, Qiyu Peng, Ying Han, Tengfei G |
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 |
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 |
Characterization of cardiac involvement in patients with LMNA splice-site mutation-related dilated cardiomyopathy and sudden cardiac death. Frontiers in genetics 2024 1 14 1291411. Xuebin Ling, Yanjun Hou, Xingyu Jia, Youling Lan, Xiaoping Wu, Julan Wu, Wei Jie, Hui Liu, Shan Huang, Zhenling Wan, Tianfa Li, Junli Guo, Tiebiao Lia |
The influence of APOE status on rate of cognitive decline. GeroScience 2024 1 . Cassandra Morrison, Michael D Oliver, Virginia Berry, Farooq Kamal, Mahsa Dad |
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 |
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 |
Natural history and outcomes in paediatric RASopathy-associated hypertrophic cardiomyopathy. ESC heart failure 2024 1 . Olga Boleti, Gabrielle Norrish, Ella Field, Kathleen Dady, Kim Summers, Gauri Nepali, Vinay Bhole, Orhan Uzun, Amos Wong, Piers E F Daubeney, Graham Stuart, Precylia Fernandes, Karen McLeod, Maria Ilina, Muhammad Najih Liaqath Ali, Tara Bharucha, Grazia Delle Donne, Elspeth Brown, Katie Linter, Caroline B Jones, Jonathan Searle, William Regan, Sujeev Mathur, Nicola Boyd, Zdenka Reinhardt, Sophie Duignan, Terence Prendiville, Satish Adwani, Juan Pablo Kas |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: