Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 197 Records) |
Query Trace: Heart diseases[original query] |
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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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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, |
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 |
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 |
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 |
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 |
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 |
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 |
ACE2 gene polymorphisms are associated with elevated pulmonary artery pressure in congenital heart diseases. Gene 2023 7 882 147642. Yang Zi-Yang, Xie Nanshan, Luo Dongling, Huang Tao, Huang Yigao, Yu Danqing, Zhang Caoj |
Case-control association study of congenital heart disease from a tertiary paediatric cardiac centre from North India. BMC pediatrics 2023 6 23 (1): 290. Prachi Kukshal, Radha O Joshi, Ajay Kumar, Shadab Ahamad, Prabhatha Rashmi Murthy, Yogesh Sathe, Krishna Manohar, Soma Guhathakurta, Subramanian Chellapp |
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 |
Associations between Selected ADRB1 and CYP2D6 Gene Polymorphisms in Children with Ventricular and Supraventricular Arrhythmias. Medicina (Kaunas, Lithuania) 2023 12 59 (12): . Ewa Moric-Janiszewska, S?awomir Smolik, Les?aw Szyd?owski, Ma?gorzata Kapr |
Identification of genetic loci jointly influencing COVID-19 and coronary heart diseases. Human genomics 2023 11 17 (1): 101. Siyue Wang, Hexiang Peng, Feng Chen, Chunfang Liu, Qiwen Zheng, Mengying Wang, Jiating Wang, Huan Yu, Enci Xue, Xi Chen, Xueheng Wang, Meng Fan, Xueying Qin, Yiqun Wu, Jin Li, Ying Ye, Dafang Chen, Yonghua Hu, Tao |
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 |
Genome-Wide Association Study of Accessory Atrioventricular Pathways. JAMA cardiology 2024 9 . Hildur M Aegisdottir, Laura Andreasen, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, Andrea B Jonsdottir, Lilja Stefansdottir, Gudmar Thorleifsson, Asgeir Sigurdsson, Gisli H Halldorsson, Julien Barc, Floriane Simonet, Vinicius Tragante, Asmundur Oddsson, Egil Ferkingstad, Jesper Hastrup Svendsen, Jonas Ghouse, Gustav Ahlberg, Christian Paludan-Müller, Katra Hadji-Turdeghal, Mariana Bustamante, Magnus O Ulfarsson, Anna Helgadottir, Solveig Gretarsdottir, Saedis Saevarsdottir, Ingileif Jonsdottir, Christian Erikstrup, Henrik Ullum, Erik Sørensen, Søren Brunak, Christian Jøns, Chaoqun Zheng, Connie R Bezzina, Kirk U Knowlton, Lincoln D Nadauld, Patrick Sulem, Sisse R Ostrowski, Ole B Pedersen, David O Arnar, Daniel F Gudbjartsson, Morten S Olesen, Henning Bundgaard, Hilma Holm, Kari Stefansson, |
Nanophotonic waveguide-based sensing of circulating cell-free mitochondrial DNA: implications for personalized medicine. Drug discovery today 2024 7 104086. Prasan Kaur, Nazim Nazeer, Vikas Gurjar, Rajnarayan Tiwari, Pradyumna Kumar Mish |
Results of comprehensive genetic testing in patients presenting to a multidisciplinary inherited heart disease clinic in India. Indian heart journal 2024 7 . Priya Chockalingam, Thenral S Geetha, Sandhya Nair, Nivedita Rajakumar, Deep Chandh Raja, Yash Lokhandwala, Vivek Chaturvedi, Raja J Selvaraj, Sakthivel Ramasamy, Sheetal Sharda, C Sundar, R Anantharam |
PYCARD gene polymorphisms and susceptibility to periodontal and coronary heart diseases. Journal of medicine and life 2024 5 17 (2): 195-200. Zina Ali Daily, Batool Hassan Al-Ghurabi, Ahmed Makki Al-Qarakh |
Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome. Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 2024 4 33 (2): 50-58. Yasuko Shoji, Ayaha Hata, Takatoshi Maeyama, Tamaki Wada, Yuiko Hasegawa, Eriko Nishi, Shinobu Ida, Yuri Etani, Tetsuya Niihori, Yoko Aoki, Nobuhiko Okamoto, Masanobu Kaw |
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