Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 8060 Records) |
Query Trace: High blood pressure or hypertension[original query] |
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Prognostic significance of SIRI in patients with late-stage lung adenocarcinoma receiving EGFR-TKI treatment. Current problems in cancer 2024 5 50 101099. Herong Wang, Wei |
Clinical and genetic factors involved in Porto-sinusoidal vascular disorder after oxaliplatin exposure. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2024 5 . A Puente, J I Fortea, C Del Pozo, M Serrano, M Alonso-Peña, A Giráldez, L Tellez, J Martinez, M Magaz, L Ibañez, J Garcia, E Llop, C Alvarez-Navascues, M Romero, E Rodriguez, M T Arias Loste, A Antón, V Echavarria, C López, A Albillos, V Hernández-Gea, J C Garcia-Pagán, R Bañares, J Crespo, |
No Association Between AGT Gene Polymorphisms with Hypertension in a South African Population. Diabetes, metabolic syndrome and obesity : targets and therapy 2024 5 17 1853-1865. Jyoti Rajan Sharma, Hannah Fokkens, Ria Laubscher, Teke Ruffin Apalata, Sibusiso Cyprian Nomatshila, Samuel Yao Alomatu, Hans Strijdom, Rabia Johns |
Chromosome-Y haplogroups in Asturias (Northern Spain) and their association with severe COVID-19. Molecular genetics and genomics : MGG 2024 5 299 (1): 49. Mar González-Fernández, Daniel Vázquez-Coto, Guillermo M Albaiceta, Laura Amado-Rodríguez, Marta G Clemente, Lucinda Velázquez-Cuervo, Claudia García-Lago, Juan Gómez, Eliecer Co |
Prognostic implications of left ventricular hypertrophy and mechanical function in Fabry disease: A longitudinal cohort study. Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography 2024 5 . Hao-Chih Chang, Ling Kuo, Shih-Hsien Sung, Dau-Ming Niu, Wen-Chung |
Causal relationship between hypertension and risk of constipation: A 2-way 2-sample Mendelian randomization study. Medicine 2024 5 103 (18): e38057. Rong Wang, Huiying Sun, Ting Yang, Junfeng |
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits. Nature genetics 2024 4 . Jacob M Keaton, Zoha Kamali, Tian Xie, Ahmad Vaez, Ariel Williams, Slavina B Goleva, Alireza Ani, Evangelos Evangelou, Jacklyn N Hellwege, Loic Yengo, William J Young, Matthew Traylor, Ayush Giri, Zhili Zheng, Jian Zeng, Daniel I Chasman, Andrew P Morris, Mark J Caulfield, Shih-Jen Hwang, Jaspal S Kooner, David Conen, John R Attia, Alanna C Morrison, Ruth J F Loos, Kati Kristiansson, Reinhold Schmidt, Andrew A Hicks, Peter P Pramstaller, Christopher P Nelson, Nilesh J Samani, Lorenz Risch, Ulf Gyllensten, Olle Melander, Harriette Riese, James F Wilson, Harry Campbell, Stephen S Rich, Bruce M Psaty, Yingchang Lu, Jerome I Rotter, Xiuqing Guo, Kenneth M Rice, Peter Vollenweider, Johan Sundström, Claudia Langenberg, Martin D Tobin, Vilmantas Giedraitis, Jian'an Luan, Jaakko Tuomilehto, Zoltan Kutalik, Samuli Ripatti, Veikko Salomaa, Giorgia Girotto, Stella Trompet, J Wouter Jukema, Pim van der Harst, Paul M Ridker, Franco Giulianini, Veronique Vitart, Anuj Goel, Hugh Watkins, Sarah E Harris, Ian J Deary, Peter J van der Most, Albertine J Oldehinkel, Bernard D Keavney, Caroline Hayward, Archie Campbell, Michael Boehnke, Laura J Scott, Thibaud Boutin, Chrysovalanto Mamasoula, Marjo-Riitta Järvelin, Annette Peters, Christian Gieger, Edward G Lakatta, Francesco Cucca, Jennie Hui, Paul Knekt, Stefan Enroth, Martin H De Borst, Ozren Polašek, Maria Pina Concas, Eulalia Catamo, Massimiliano Cocca, Ruifang Li-Gao, Edith Hofer, Helena Schmidt, Beatrice Spedicati, Melanie Waldenberger, David P Strachan, Maris Laan, Alexander Teumer, Marcus Dörr, Vilmundur Gudnason, James P Cook, Daniela Ruggiero, Ivana Kolcic, Eric Boerwinkle, Michela Traglia, Terho Lehtimäki, Olli T Raitakari, Andrew D Johnson, Christopher Newton-Cheh, Morris J Brown, Anna F Dominiczak, Peter J Sever, Neil Poulter, John C Chambers, Roberto Elosua, David Siscovick, Tõnu Esko, Andres Metspalu, Rona J Strawbridge, Markku Laakso, Anders Hamsten, Jouke-Jan Hottenga, Eco de Geus, Andrew D Morris, Colin N A Palmer, Ilja M Nolte, Yuri Milaneschi, Jonathan Marten, Alan Wright, Eleftheria Zeggini, Joanna M M Howson, Christopher J O'Donnell, Tim Spector, Mike A Nalls, Eleanor M Simonsick, Yongmei Liu, Cornelia M van Duijn, Adam S Butterworth, John N Danesh, Cristina Menni, Nicholas J Wareham, Kay-Tee Khaw, Yan V Sun, Peter W F Wilson, Kelly Cho, Peter M Visscher, Joshua C Denny, , , , , Daniel Levy, Todd L Edwards, Patricia B Munroe, Harold Snieder, Helen R Warr |
Hypothyroidism's effect on stroke limited to specific subtypes: A Mendelian randomization study. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2024 4 33 (7): 107737. Xinmin Deng, Wen Chang, Jingyi Zhu, Xiaofeng Lv, Rui Lai, Yu Cai, Shanshan Liu, Jingtao Lia |
Vitamin D receptor gene polymorphisms role in COVID-19 severity: Results of a Mexican patients' cohort. International journal of immunogenetics 2024 4 . Luis Antonio Ochoa-Ramírez, Alba Lissy Corona-Angulo, Efrén Rafael Ríos-Burgueño, Jorge Guillermo Sánchez-Zazueta, Denisse Stephania Becerra-Loaiza, Jesús Salvador Velarde-Fél |
[HLA alleles heterogeneity in a sample of colombian patients with a diagnosis of psoriatic arthritis]. Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993) 2024 4 71 (1): 83. María Alejandra Meneses-Toro, Ómar Javier Calixto, Paula Andrea Chacón-Jaramillo, Mónica Acevedo-Godoy, Luisa Constanza Robayo-Beltrán, Camilo Vera-Parra, Juan Manuel Bello-Gualtero, Wilson Bautista-Molano, Verónica Noguera-Castro, Consuelo Romero-Sánch |
Genetic polymorphisms and clinical parameters associated with renal toxicity in Thai hematologic malignancy patients receiving high dose methotrexate. Scientific reports 2024 4 14 (1): 9695. Palada Pitakkitnukun, Thanakit Pongpitakmetha, Thitima Benjachat Suttichet, Warumphon Sukkummee, Pajaree Chariyavilaskul, Chantana Polprase |
Associations of Matrix Metalloproteinase-8 Genotypes to Renal Cell Carcinoma in Taiwan. Anticancer research 2024 4 44 (5): 1931-1938. Cheng-Hsi Liao, Wei-Ching Chien, Shu-Yu Chang, Yu-Hsin Lin, Yun-Chi Wang, Wen-Chin Huang, Mei-Chin Mong, Ya-Chen Yang, Wen-Tzu Wu, Jaw-Chyun Chen, Chao-Hsiang Chang, Chia-Wen Tsai, DA-Tian Bau, Wen-Shin Cha |
Relevance of PNPLA3, TM6SF2, HSD17B13, and GCKR Variants to MASLD Severity in an Egyptian Population. Genes 2024 4 15 (4): . Nehal Elmansoury, Ahmed A Megahed, Ahmed Kamal, Nefertiti El-Nikhely, Marina Labane, Manal Abdelmageed, Ann K Daly, Ahmed Wah |
Impact of Thrombophilic Polymorphisms in Antenatal Women on Perinatal Health: A Single-Center Prospective Study. Journal of personalized medicine 2024 4 14 (4): . Vesna Sokol Karadjole, Antonio D'Amato, Milan Miloševi?, Mislav Herman, Mislav Mikuš, Antonio Simone Laganà, Vito Chiantera, Andrea Etrus |
Increased Complement Activation and Decreased ADAMTS13 Activity Are Associated with Genetic Susceptibility in Patients with Preeclampsia/HELLP Syndrome Compared to Healthy Pregnancies: An Observational Case-Controlled Study. Journal of personalized medicine 2024 4 14 (4): . Theodora-Maria Venou, Evangelia Vetsiou, Christos Varelas, Angelos Daniilidis, Kyriakos Psarras, Evaggelia-Evdoxia Koravou, Maria Koutra, Tasoula Touloumenidou, Vasilis Tsolakidis, Apostolia Papalexandri, Fani Minti, Evdokia Mandala, Konstantinos Dinas, Efthymia Vlachaki, Eleni Gavriila |
Effects of loneliness and isolation on cardiovascular diseases: a two sample Mendelian Randomization Study. Journal of geriatric cardiology : JGC 2024 4 21 (3): 340-348. Jia-Yin Cai, Xin Wang, Cong-Yi Zheng, Xue Cao, Zhen Hu, Run-Qing Gu, Yi-Xin Tian, Ye Tian, Lan Shao, Lin-Feng Zhang, Zeng-Wu Wa |
Genetic variability in stroke patients: CYP2C19 polymorphisms unraveled. BMC medical genomics 2024 4 17 (1): 109. Peiyi Peng, Yingxiu Xiao, Xuehong Peng, Jianqiang Chen, Nuan Ch |
Associations of the obesity gene FTO variant with complications and comorbidities in patients with type 1 diabetes. Diabetes research and clinical practice 2024 4 211 111683. Bartosz S?omi?ski, Maria Skrzypkowska, Ma?gorzata My?liwiec, Piotr Trzonkows |
Single cell transcriptomics of cerebrospinal fluid cells from patients with recent-onset narcolepsy. Journal of autoimmunity 2024 4 146 103234. Alina Huth, Ikram Ayoub, Lucie Barateau, Lisa Ann Gerdes, Dany Severac, Stefan Krebs, Helmut Blum, Hayrettin Tumani, Jürgen Haas, Brigitte Wildemann, Tania Kümpfel, Eduardo Beltrán, Roland S Liblau, Yves Dauvilliers, Klaus Dornma |
Genetic Polymorphisms of Endothelial Nitric Oxide Synthase Associated with Hypertension and Blood Homocysteine Levels. International journal of general medicine 2024 4 17 1509-1519. Charinya Chaichanabut, Piyamitr Sritara, Jintana Sirivaras |
Carpal Tunnel Syndrome and Transthyretin Amyloidosis in the All of Us Research Program. Mayo Clinic proceedings 2024 4 . Naman S Shetty, Akhil Pampana, Nirav Patel, Mathew S Maurer, Parag Goyal, Peng Li, Garima Arora, Pankaj Aro |
Tolerability of Antihypertensive Medications: The Influence of Age. High blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension 2024 4 . Giulia Rivasi, Antonio Coscarelli, Marco Capacci, Ludovica Ceolin, Giada Turrin, Virginia Tortù, Maria Flora D'Andria, Giuseppe Dario Testa, Andrea Ung |
Correlation Analysis of NAMPT rs61330082 Polymorphism in Type 2 Diabetes Mellitus Combined with Hypertension. Diabetes, metabolic syndrome and obesity : targets and therapy 2024 4 17 1809-1818. Chao Zuo, Yi Liu, Ziqiang Wang, Jing Cheng, Dongli Yang, Huasong Gong, Yu Wang, Yongchao Qi |
Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling. medRxiv : the preprint server for health sciences 2024 4 . Katherine A Kentistou, Brandon E M Lim, Lena R Kaisinger, Valgerdur Steinthorsdottir, Luke N Sharp, Kashyap A Patel, Vinicius Tragante, Gareth Hawkes, Eugene J Gardner, Thorhildur Olafsdottir, Andrew R Wood, Yajie Zhao, Gudmar Thorleifsson, Felix R Day, Susan E Ozanne, Andrew T Hattersley, Stephen O'Rahilly, Kari Stefansson, Ken K Ong, Robin N Beaumont, John R B Perry, Rachel M Freat |
Genetic variants of ANRIL and coronary artery disease: Insights from a Turkish study population. Gene 2024 4 917 148475. Aybike Sena Ozuynuk-Ertugrul, Cemre Buse Kirsan, Aycan Fahri Erkan, Berkay Ekici, Evrim Komurcu-Bayrak, Neslihan Cob |
Incidence and risk factors for non-cardiac syncope in a cohort of patients addressing an accredited Arterial Hypertension Center: the Innocent Study. Minerva medica 2024 4 . Filippo Numeroso, Luca Bottaro, Ali Younes, Andrea Ungar, Aderville Cabas |
Endothelin-converting Enzyme-1b Genetic Variants Increase the Risk of Coronary Artery Ectasia. Biochemical genetics 2024 4 . Gulcin Ozkara, Ezgi Irmak Aslan, Fidan Malikova, Cagatay Aydogan, Ozgur Selim Ser, Onur Kilicarslan, Sadiye Nur Dalgic, Ahmet Yildiz, Oguz Ozturk, Hulya Yilmaz-Aydog |
Polygenic risk score-based phenome-wide association for glaucoma and its impact on disease susceptibility in two large biobanks. Journal of translational medicine 2024 4 22 (1): 355. Jae-Seung Yun, Sang-Hyuk Jung, Su-Nam Lee, Seung Min Jung, , Hong-Hee Won, Dokyoon Kim, Jin A Ch |
Variations in the Cadherin 23 Gene Associated With Noise-Induced Hearing Loss. Journal of multidisciplinary healthcare 2024 4 17 1473-1482. Jie Jiao, Shanfa Yu, Guizhen Gu, Guoshun Chen, Huanling Zhang, Yuxin Zhe |
Association between sugar-sweetened beverages and pure fruit juice with risk of six cardiovascular diseases: a Mendelian randomization study. European journal of clinical nutrition 2024 4 . Hanzhang Xie, Yiyang Liu, Xiaohan Gu, Shuhan Liu, Yimeng Fang, Wenjie Zhong, Yinan Zhang, Shunyu Y |
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- Page last updated:May 13, 2024
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