Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 58 Records) |
Query Trace: Syndrome and SCD[original query] |
---|
Influence of functional polymorphism in MIF promoter on sudden cardiac death in Chinese populations. Forensic sciences research 2017 2 (3): 152-157. Yin Zhixia, Zhang Qing, Zhou Wei, Wang Shouyu, Wang Chaoqun, He Yan, Li Lijuan, Gao Yuzh |
Influence of genetic modifiers on sudden cardiac death cases. International journal of legal medicine 2017 12 132 (2): 379-385. Jenewein Tina, Neumann Thomas, Erkapic Damir, Kuniss Malte, Verhoff Marcel A, Thiel Gerhard, Kauferstein Sil |
Differences in prenatal aneuploidy screening among African-American women with hemoglobin S variants. Journal of perinatology : official journal of the California Perinatal Association 2018 7 38 (7): 797-803. Adams April D, Schaa Kendra, Overcash Rachael |
Genotype-phenotype relationship and risk stratification in loss-of-function SCN5A mutation carriers. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2018 5 23 (5): e12548. Robyns Tomas, Nuyens Dieter, Vandenberk Bert, Kuiperi Cuno, Corveleyn Anniek, Breckpot Jeroen, Garweg Christophe, Ector Joris, Willems R |
Role of copy number variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practice. European journal of human genetics : EJHG 2018 3 26 (7): 1014-1025. Mates Jesus, Mademont-Soler Irene, Del Olmo Bernat, Ferrer-Costa Carles, Coll Monica, Pérez-Serra Alexandra, Picó Ferran, Allegue Catarina, Fernandez-Falgueras Anna, Álvarez Patricia, Yotti Raquel, Espinosa Maria Angeles, Sarquella-Brugada Georgia, Cesar Sergi, Carro Ester, Brugada Josep, Arbelo Elena, Garcia-Pavia Pablo, Borregan Mar, Tizzano Eduardo, López-Granados Amador, Mazuelos Francisco, Díaz de Bustamante Aranzazu, Darnaude Maria Teresa, González-Hevia José Ignacio, Díaz-Flores Felícitas, Trujillo Francisco, Iglesias Anna, Fernandez-Aviles Francisco, Campuzano Oscar, Brugada Ram |
Lipid profiles in French West Indies sickle cell disease cohorts, and their general population. Lipids in health and disease 2018 3 17 (1): 38. Lalanne-Mistrih Marie-Laure, Connes Philippe, Lamarre Yann, Lemonne Nathalie, Hardy-Dessources Marie-Dominique, Tarer Vanessa, Etienne-Julan Maryse, Mougenel Dominique, Tressières Benoît, Romana Ma |
Atrial fibrillation is associated with sudden cardiac death: a systematic review and meta-analysis. Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing 2018 1 51 (2): 91-104. Rattanawong Pattara, Upala Sikarin, Riangwiwat Tanawan, Jaruvongvanich Veeravich, Sanguankeo Anawin, Vutthikraivit Wasawat, Chung Eugene |
Sudden cardiac death in families with premature cardiovascular disease. Heart (British Cardiac Society) 2019 8 106 (3): 228-232. Bruikman Caroline, de Ronde Maurice W J, Amin Ahmed, Levy Sonja, Lof Pien, de Ruijter Ursula, Hovingh Kees, Tan Hanno L, Pinto-Sietsma Sara-Jo |
A cellular model of Brugada syndrome with SCN10A variants using human-induced pluripotent stem cell-derived cardiomyocytes. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2019 5 21 (9): 1410-1421. El-Battrawy Ibrahim, Albers Sebastian, Cyganek Lukas, Zhao Zhihan, Lan Huan, Li Xin, Xu Qiang, Kleinsorge Mandy, Huang Mengying, Liao Zhenxing, Zhong Rujia, Rudic Boris, Müller Jonas, Dinkel Hendrik, Lang Siegfried, Diecke Sebastian, Zimmermann Wolfram-Hubertus, Utikal Jochen, Wieland Thomas, Borggrefe Martin, Zhou Xiaobo, Akin Ibrah |
Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry. QJM : monthly journal of the Association of Physicians 2019 1 112 (5): 343-350. Chen C-Y J, Juang J-M J, Lin L-Y, Liu Y-B, Ho L-T, Yu C-C, Huang H-C, Lin T-T, Liao M-C, Chen J-J, Hwang J-J, Chen W-J, Yeh S-F S, Yang D-H, Chiang F-T, Lin J-L, Lai L-P, Horie M, |
Association between MTHFR 677C>T polymorphism and vascular complications in sickle cell disease: A meta-analysis. Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine 2019 Jan . Lakkakula B V K |
Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana. PloS one 2020 9 15 (9): e0238691. Elenga Narcisse, Cuadro-Alvarez Emma, Martin Elise, Njuieyon Falucar, Defo Antoine, Maniassom Chimè |
Association of HIV infection with clinical and laboratory characteristics of sickle cell disease. BMC infectious diseases 2020 8 20 (1): 638. Belisário André Rolim, Blatyta Paula F, Vivanco Diana, Oliveira Claudia Di Lorenzo, Carneiro-Proietti Anna Bárbara, Sabino Ester Cerdeira, de Almeida-Neto Cesar, Loureiro Paula, Máximo Cláudia, de Oliveira Garcia Mateos Sheila, Flor-Park Miriam V, de Oliveira Werneck Rodrigues Daniela, Afonso Mota Rosimere, Gonçalez Thelma T, Hoffmann Thomas J, Kelly Shannon, Custer Brian, |
Sex differences in CSF biomarkers vary by Alzheimer disease stage and APOE ?4 genotype. Neurology 2020 Aug . Babapour Mofrad Rosha, Tijms Betty M, Scheltens Philip, Barkhof Frederik, van der Flier Wiesje M, Sikkes Sietske A M, Teunissen Charlotte |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death. EBioMedicine 2020 Jul 57 102843. Juang Jyh-Ming Jimmy, Binda Anna, Lee Shyh-Jye, Hwang Juey-Jen, Chen Wen-Jone, Liu Yen-Bin, Lin Lian-Yu, Yu Chih-Chieh, Ho Li-Ting, Huang Hui-Chun, Chen Ching-Yu Julius, Lu Tzu-Pin, Lai Liang-Chuan, Yeh Shih-Fan Sherri, Lai Ling-Ping, Chuang Eric Y, Rivolta Ilaria, Antzelevitch Charl |
Prognostic impact of misdiagnosis of cardiac channelopathies as epilepsy. PloS one 2020 4 15 (4): e0231442. Ramos-Maqueda Javier, Bermúdez-Jiménez Francisco, Ruiz Rosa Macías, Ramos Mercedes Cabrera, Lerma Manuel Molina, Millán Pablo Sánchez, López Miguel Álvarez, Sánchez Luis Tercedor, Jiménez-Jáimez Ju |
The Efficacy of Beta-Blockers in Patients With Long QT Syndrome 1-3 According to Individuals' Gender, Age, and QTc Intervals: A Network Meta-analysis. Frontiers in pharmacology 2020 12 11 579525. Han Lu, Liu Fuxiang, Li Qing, Qing Tao, Zhai Zhenyu, Xia Zirong, Li Juxia |
Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease. Frontiers in immunology 2020 10 11 2041. Tozatto-Maio Karina, Girot Robert, Ly Indou Deme, Silva Pinto Ana Cristina, Rocha Vanderson, Fernandes Francisco, Diagne Ibrahima, Benzerara Yahia, Dinardo Carla L, Soler Julia Pavan, Kashima Simone, Araujo Itauá Leston, Kenzey Chantal, Fonseca Guilherme H H, Rodrigues Evandra S, Volt Fernanda, Jarduli Luciana, Ruggeri Annalisa, Mariaselvam Christina, Gualandro Sandra F M, Rafii Hanadi, Cappelli Barbara, Nogueira Felipe Melo, Scigliuolo Graziana Maria, Guerino-Cunha Renato Luiz, Malmegrim Kelen Cristina Ribeiro, Simões Belinda P, Gluckman Eliane, Tamouza Ry |
Genetic Variants Associated With Unexplained Sudden Cardiac Death in Adult White and African American Individuals. JAMA cardiology 2021 Jun . Guo Liang, Torii Sho, Fernandez Raquel, Braumann Ryan E, Fuller Daniela T, Paek Ka-Hyun, Gadhoke Neel V, Maloney Kristin A, Harris Kathryn, Mayhew Christina M, Zarpak Roya, Stevens Laura M, Gaynor Brady J, Jinnouchi Hiroyuki, Sakamoto Atsushi, Sato Yu, Mori Hiroyoshi, Kutyna Matthew D, Lee Parker J, Weinstein Leah M, Collado-Rivera Carlos J, Ali Bakr B, Atmakuri Dheeraj R, Dhingra Roma, Finn Emma L B, Bell Mack W, Lynch Megan, Cornelissen Anne, Kuntz Salome H, Park Joo-Hyung, Kutys Robert, Park Ji-Eun, Wang Libin, Hong Susie N, Gupta Anuj, Hall Jennifer L, Kolodgie Frank D, Romero Maria E, Jeng Linda J B, Mitchell Braxton D, Surve Dipti, Fowler David R, Hong Charles C, Virmani Renu, Finn Aloke |
Novel SCN5A variants identified in a group of Iranian Brugada syndrome patients. Functional & integrative genomics 2021 2 21 (3-4): 331-340. Ghaffari Taraneh, Mirhosseini Motlagh Naser, Daraei Abdolreza, Tafrihi Majid, Saravi Mehrdad, Sabour Davo |
Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome. Frontiers in pharmacology 2022 9 13 984299. Zaklyazminskaya Elena, Shestak Anna, Podolyak Dmitry, Komoliatova Vera, Makarov Leonid, Novitskaya Anna, Revishvili Amir |
Genotype-Specific ECG-Based Risk Stratification Approaches in Patients With Long-QT Syndrome. Frontiers in cardiovascular medicine 2022 8 9 916036. Rieder Marina, Kreifels Paul, Stuplich Judith, Ziupa David, Servatius Helge, Nicolai Luisa, Castiglione Alessandro, Zweier Christiane, Asatryan Babken, Odening Katja |
A cortactin CTTN coding SNP contributes to lung vascular permeability and inflammatory disease severity in African descent subjects. Translational research : the journal of laboratory and clinical medicine 2022 2 244 56-74. Belvitch Patrick, Casanova Nancy, Sun Xiaoguang, Camp Sara M, Sammani Saad, Brown Mary E, Mascarhenas Joseph, Lynn Heather, Adyshev Djanybek, Siegler Jessica, Desai Ankit, Seyed-Saadat Laleh, Rizzo Alicia, Bime Christian, Shekhawat Gajendra S, Dravid Vinayak P, Reilly John P, Jones Tiffanie K, Feng Rui, Letsiou Eleftheria, Meyer Nuala J, Ellis Nathan, Garcia Joe G N, Dudek Steven |
Variation and impact of polygenic hematological traits in monogenic sickle cell disease. Haematologica 2022 Oct . Pincez Thomas, Lo Ken Sin, D'Orengiani Anne-Laure Pham Hung d'Alexandry, Garrett Melanie E, Brugnara Carlo, Ashley-Koch Allison E, Telen Marilyn J, Galacteros Frederic, Joly Philippe, Bartolucci Pablo, Lettre Guillau |
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 |
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 |
In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome. Molecular genetics & genomic medicine 2023 8 e2263. Hung Manh Pham, Duy Phuong Nguyen, Thanh Dat Ta, Thi Phuong Le, Phong Hai Phan, Hoai An Trinh, Tuan Viet Tran, Thi Lan Anh Luong, Ha Minh Nguyen, The-Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van-Khanh Tr |
Type of syncope and outcome in Brugada syndrome: A systematic review and meta-analysis. Journal of arrhythmia 2023 4 39 (2): 111-120. Rattanawong Pattara, Kewcharoen Jakrin, Yinadsawaphan Thanaboon, Fatunde Olubadewa A, Kanitsoraphan Chanavuth, Vutthikraivit Wasawat, Prasitlumkum Narut, Chung Eugene H, Shen Win-Kua |
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 |
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: