HuGE Literature Finder
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| Genetic characterization of juvenile sudden cardiac arrest and death in Tuscany: The ToRSADE registry. Frontiers in cardiovascular medicine 2023 1 9 1080608. Girolami Francesca, Spinelli Valentina, Maurizi Niccolò, Focardi Martina, Nesi Gabriella, Maio Vincenza, Grifoni Rossella, Albora Giuseppe, Bertaccini Bruno, Targetti Mattia, Coppini Raffaele, Favilli Silvia, Olivotto Iacopo, Cerbai Elisabet |
| Polymorphisms in gene UGT1A1 modify the association of prenatal exposure to polycyclic aromatic hydrocarbons with congenital heart diseases risk. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2023 3 36 (1): 2183743. Tao Jing, Li Nana, Liu Zhen, Deng Ying, Li Xiaohong, Luo Fangfang, Li Xiaoyan, Yu Ping, Zhu J |
| Rare copy number variation analysis identifies disease-related variants in atrioventricular septal defect patients. Frontiers in genetics 2023 2 14 1075349. Hu Huan, Geng Zilong, Zhang Shasha, Xu Yuejuan, Wang Qingjie, Chen Sun, Zhang Bing, Sun Kun, Lu Yan |
| The effect of maternal BMI, smoking and alcohol on congenital heart diseases: a Mendelian randomisation study. BMC medicine 2023 2 21 (1): 35. Taylor Kurt, Wootton Robyn E, Yang Qian, Oddie Sam, Wright John, Yang Tiffany C, Magnus Maria, Andreassen Ole A, Borges Maria Carolina, Caputo Massimo, Lawlor Deborah |
| Occurrence and morphology of ventricular arrhythmias in apparently normal hearts in relation to late gadolinium enhancement on cardiovascular magnetic resonance. The international journal of cardiovascular imaging 2022 Feb . Qian Wen, Liu Wang-Yan, Zhu Yin-Su, Gu Kai, Wang Jun, Zhou Xiao-Yue, Xu Yi, Zhu Xiao-M |
| The relationship between phosphodiesterase 4D gene polymorphism and coronary heart disease. Cellular and molecular biology (Noisy-le-Grand, France) 2022 Feb 67 (6): 26-32. Yan Laixing, Li Ketao, Zhang Weiwei, Shen Chengji, Ma Liping, Sun |
| Different outcomes of balloon atrial septostomy and the association of C677T polymorphism in MTHFR gene on TGA children. Cellular and molecular biology (Noisy-le-Grand, France) 2022 Jan 67 (4): 24-32. Salih Aso Faeq, NazdarAmin Banan |
| Cardiac Troponin I and Risk of Stroke: A Mendelian Randomization Study. International journal of general medicine 2022 15 1575-1582. Chen Heng, Sun Xingang, Zhuo Chengui, Zhao Jianqiang, Zu Aohan, Wang Qiqi, Zheng Liangro |
| Congenital Heart Diseases: Genetic Risk Variants and Their Methylation Status. Genes 2022 11 13 (11): . Calzada-Dávila Melissa, Calvo-Anguiano Geovana, Martínez-de-Villarreal Laura E, Lugo-Trampe José J, González-Peña Sandra M, Ancer-Rodríguez Patricia R, Hernández-Almaguer María D, Campos-Acevedo Luis |
| COVID-19 Course in Allergic Asthma Patients: A Spanish Cohort Analysis. Journal of asthma and allergy 2022 3 15 257-264. Habernau Mena Alicia, García-Moguel Ismael, Vazquez de la Torre Gaspar María, Mugica Victoria, Alvarado Izquierdo Maria Isabel, Jimenez Blanco Maria Aranzazu, Gandolfo-Cano Mar, Jiménez Lara Mar, Gonzalez Moreno Ana, Saura Foix Pilar, Navarro-Pulido Ana, Martin-Arriscado Arroba Cristina, Delgado Romero Julio, Dominguez-Ortega Javier, |
First report on genome wide association study in western Indian population reveals host genetic factors for COVID-19 severity and outcome.
Genomics 2022 6 114 (4): 110399. Pandit Ramesh, Singh Indra, Ansari Afzal, Raval Janvi, Patel Zarna, Dixit Raghav, Shah Pranay, Upadhyay Kamlesh, Chauhan Naresh, Desai Kairavi, Shah Meenakshi, Modi Bhavesh, Joshi Madhvi, Joshi Chaitan |
| Identification of a pleiotropic effect of ADIPOQ on cardiac dysfunction and Alzheimer's disease based on genetic evidence and health care records. Translational psychiatry 2022 9 12 (1): 389. Paik Hyojung, Lee Junehawk, Jeong Chan-Seok, Park Jun Sung, Lee Jeong Ho, Rappoport Nadav, Kim Younghoon, Sohn Hee-Young, Jo Chulman, Kim Jimin, Cho Seong Be |
| Investigation of Genetic Alterations in Congenital Heart Diseases in Prenatal Period. Global medical genetics 2022 2 9 (1): 29-33. Atli Emine Ikbal, Atli Engin, Yalcintepe Sinem, Demir Selma, Kalkan Rasime, Akurut Cisem, Ozen Yasemin, Gurkan Hak |
| miR194 hypomethylation regulates coronary artery disease pathogenesis. BMC medical genomics 2022 12 15 (1): 264. Duan Lian, Liu Yongmei, Li Jun, Zhang Yun, Liao Jiangquan, Dong Yan, Jie Wa |
| Modifiable potential risk factors in familial and sporadic frontotemporal dementia. Annals of clinical and translational neurology 2022 6 9 (8): 1195-1205. Soppela Helmi, Katisko Kasper, Gadola Yasmine, Krüger Johanna, Hartikainen Päivi, Alberici Antonella, Benussi Alberto, Koivisto Anne, Haapasalo Annakaisa, Remes Anne M, Borroni Barbara, Solje Ei |
| Octogenarians With Anaplastic Lymphoma Kinase-rearranged Non-small-cell Lung Cancer: A Case Series. Cancer diagnosis & prognosis 2022 11 2 (6): 711-715. Hattori Sou, Ojima Eiji, Okauchi Shinichiro, Sasatani Yuika, Shiozawa Toshihiro, Satoh Hiroaki, Hizawa Nobuyu |
| Risk genetic polymorphism and haplotype associated with papillary thyroid cancer and their relation to associated diseases in Slovak population. Bratislavske lekarske listy 2022 123 (7): 475-48. Duffek Marian, Skerenova Maria, Halasova Erika, Sarlinova Miroslava, Dzian Anton, Repiska Vanda, Dobrovodsky Andrej, Mistuna Dusan, Bernadic Michal, Matakova Tatia |
| Sex differences in the association between cardiovascular diseases and dementia subtypes: a prospective analysis of 464,616 UK Biobank participants. Biology of sex differences 2022 5 13 (1): 21. Dong Caiyun, Zhou Chunmiao, Fu Chunying, Hao Wenting, Ozaki Akihiko, Shrestha Nipun, Virani Salim S, Mishra Shiva Raj, Zhu Dongsh |
| SLC2A3 variants in familial and sporadic congenital heart diseases in a Chinese Yunnan population. Journal of clinical laboratory analysis 2022 4 36 (6): e24456. Ma Lijing, Xu Jiaxin, Tang Qisheng, Cao Yu, Kong Ruize, Li Kunlin, Liu Jie, Jiang Liho |
| Study the association of microRNA polymorphisms (miR-146a, miR-4513) with the risk of coronary heart diseases in Egyptian population. Journal of biochemical and molecular toxicology 2022 12 e23284. Ali Heba Mohamed, Ellakwa Doha El-Sayed, Elaraby Nesma Mohamed, Zaher Amr Mohamed, Amr Khalda Say |
| The effect of maternal polycyclic aromatic hydrocarbons exposure and methylation levels of congenital heart diseases-candidate genes on the risk of congenital heart diseases. Prenatal diagnosis 2022 5 42 (9): 1142-1154. Li Nana, Li Lu, Liu Zhen, Deng Ying, Wang Meixian, Zhao Jinju, Zeng Shengli, Kang Hong, Wang Yanping, Zhu Jun, Zhao Jianxin, Yu Pi |
| Mediation of the APOE associations with Alzheimer's and coronary heart diseases through body mass index and lipids. GeroScience 2021 Sep . Loika Yury, Feng Fan, Loiko Elena, Kulminski Alexander |
| The role of NKX2-5 gene polymorphisms in congenital heart disease (CHD): a systematic review and meta-analysis. The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology 2021 Aug 73 (1): 72. Ashiq Sana, Ashiq Kanwal, Sabar Muhammad Faro |
| Association and interaction effect of UCP2 gene polymorphisms and dietary factors with congenital heart diseases in Chinese Han population. Scientific reports 2021 Apr 11 (1): 8699. Zhang Senmao, Liu Xiaoying, Wang Tingting, Chen Lizhang, Yang Tubao, Huang Peng, Qin Jia |
| Clinical and genetic findings in patients with congenital cataract and heart diseases. Orphanet journal of rare diseases 2021 6 16 (1): 242. Li Xinru, Si Nuo, Song Zixun, Ren Yaqiong, Xiao W |
| Differential Methylation in the GSTT1 Regulatory Region in Sudden Unexplained Death and Sudden Unexpected Death in Epilepsy. International journal of molecular sciences 2021 4 22 (6): . Christiansen Steffan Noe, Jacobsen Stine Bøttcher, Andersen Jeppe Dyrberg, Kampmann Marie-Louise, Trudsø Linea Christine, Olsen Kristine Boisen, Tfelt-Hansen Jacob, Banner Jytte, Morling Nie |
| Exome Sequencing Highlights a Potential Role for Concealed Cardiomyopathies in Youthful Sudden Cardiac Death. Circulation. Genomic and precision medicine 2021 12 15 (1): e003497. Neves Raquel, Tester David J, Simpson Michael A, Behr Elijah R, Ackerman Michael J, Giudicessi John |
| Genetic evaluation of cardiomyopathies in Qatar identifies enrichment of pathogenic sarcomere gene variants and possible founder disease mutations in the Arabs. Molecular genetics & genomic medicine 2021 6 9 (7): e1709. Al-Shafai Kholoud N, Al-Hashemi Mohammed, Manickam Chidambaram, Musa Rania, Selvaraj Senthil, Syed Najeeb, Vempalli Fazulur, Ali Muneera, Yacoub Magdi, Estivill Xavi |
| Genotype-phenotype correlations in hypertrophic cardiomyopathy: a multicenter study in Portugal and Spain of the TPM1 p.Arg21Leu variant. Revista espanola de cardiologia (English ed.) 2021 3 75 (3): 242-250. Lamounier Junior Arsonval, Guitián González Alba, Rodríguez Vilela Alejandro, Repáraz Andrade Alfredo, Rubio Alcaide Álvaro, Berta Sousa Ana, Benito López Carmen, Alonso García Diego, Fernández Ferro Germán, Cruz Inês, Cárdenas Reyes Ivonne Johana, Salazar-Mendiguchía García Joel, Larrañaga-Moreira José María, Ochoa Juan Pablo, Palomino-Doza Julián, de la Higuera Romero Luis, Nicolás Cicerchia Marcos, Restrepo Córdoba María Alejandra, Peña-Peña María Luisa, Noël Brögger Maria, Loureiro Marilia, Mogollón Jiménez María Victoria, Bilbao Quesada Raquel, Franco Gutiérrez Raúl, García Hernández Soledad, Ripoll-Vera Tomás, Fernández Xusto, Azevedo Olga, García Pavía Pablo, Lopes Luis R, Ortiz Martín, Brito Dulce, Barriales-Villa Roberto, Monserrat Iglesias Loren |
| The Interaction Analysis of SNP Variants and DNA Methylation Identifies Novel Methylated Pathogenesis Genes in Congenital Heart Diseases. Frontiers in cell and developmental biology 2021 5 9 665514. Wang Jing, Ma Xiaoqin, Zhang Qi, Chen Yinghui, Wu Dan, Zhao Pengjun, Yu |
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- Page last updated:Mar 31, 2023
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