Query Trace: Heart and Blood Vessel Diseases
Association of Angiotensin-Converting Enzyme Insertion/Deletion Polymorphism with the Risk of Atherosclerosis. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2019 Mar . Xia Man-Man, Wang Mingxu, Jiang Hong, Liu Yan, Ma Le, Lu Chao, Zhang W |
Association of PTPN22 1858C/T Polymorphism with Autoimmune Diseases: A Systematic Review and Bayesian Approach. Journal of clinical medicine 2019 Mar 8 (3): . Tizaoui Kalthoum, Kim Seon Hui, Jeong Gwang Hun, Kronbichler Andreas, Lee Kwang Seob, Lee Keum Hwa, Shin Jae |
Pathogenic RBM20-Variants Are Associated With a Severe Disease Expression in Male Patients With Dilated Cardiomyopathy. Circulation. Heart failure 2019 Mar 12 (3): e005700. Hey Thomas Morris, Rasmussen Torsten B, Madsen Trine, Aagaard Mads Malik, Harbo Maria, Mølgaard Henning, Møller Jacob E, Eiskjær Hans, Mogensen Je |
Association between polygenic risk for tobacco or alcohol consumption and liability to licit and illicit substance use in young Australian adults. Drug and alcohol dependence 2019 Feb 197 271-279. Chang Lun-Hsien, Couvy-Duchesne Baptiste, Liu Mengzhen, Medland Sarah E, Verhulst Brad, Benotsch Eric G, Hickie Ian B, Martin Nicholas G, Gillespie Nathan A, |
Smoking and Increased White and Red Blood Cells. Arteriosclerosis, thrombosis, and vascular biology 2019 Mar ATVBAHA118312338. Pedersen Kasper Mønsted, Çolak Yunus, Ellervik Christina, Hasselbalch Hans Carl, Bojesen Stig Egil, Nordestgaard Børge Grøn |
Effect of linoleic acid on ischemic heart disease and its risk factors: a Mendelian randomization study. BMC medicine 2019 Mar 17 (1): 61. Zhao Jie V, Schooling C Ma |
Association between CYP2C19*2/*3 Polymorphisms and Coronary Heart Disease. Current medical science 2019 Feb 39 (1): 44-51. Zhang Ying-Ying, Zhou Xin, Ji Wen-Jie, Liu Ting, Ma Jing, Zhang Ying, Li Yu-Mi |
Prenatal Tobacco Exposure Modulated the Association of Genetic variants with Diagnosed ADHD and its symptom domain in children: A Community Based Case-Control Study. Scientific reports 2019 Mar 9 (1): 4274. Wang Yanni, Hu Dan, Chen Wenjing, Xue Hongli, Du Yuk |
Association of Candidate Gene Polymorphisms With Chronic Kidney Disease: Results of a Case-Control Analysis in the Nefrona Cohort. Frontiers in genetics 2019 10 118. Valls Joan, Cambray Serafí, Pérez-Guallar Carles, Bozic Milica, Bermúdez-López Marcelino, Fernández Elvira, Betriu Àngels, Rodríguez Isabel, Valdivielso José |
Single nucleotide polymorphism rs3746444 in miR-499a affects susceptibility to non-small cell lung carcinoma by regulating the expression of CD200. International journal of molecular medicine 2019 Mar . Ge Nan, Mao Chunxia, Yang Qingbo, Han Bin, Wang Yongjie, Xu Linhao, Yang Xiuzhi, Jiao Wenjie, Li Chu |
Genome-Wide Copy Number Variation Association Study of Atrial Fibrillation Related Thromboembolic Stroke. Journal of clinical medicine 2019 Mar 8 (3): . Hsieh Chia-Shan, Huang Pang-Shuo, Chang Sheng-Nan, Wu Cho-Kai, Hwang Juey-Jen, Chuang Eric Y, Tsai Chia- |
Interaction between dietary patterns and Diabetes, metabolic syndrome and obesity : targets and therapy 2019 12 239-255. Cai Junxiu, Zhang Yan, Nuli Rebiya, Zhang Yangyi, Abudusemaiti Manfutong, Kadeer Aizhatiguli, Tian Xiaoli, Xiao H |
Shared genes between Alzheimer's disease and ischemic stroke. CNS neuroscience & therapeutics 2019 Mar . Wei Chang-Juan, Cui Pan, Li He, Lang Wen-Jing, Liu Gui-You, Ma Xiao-Fe |
Association study of the CTH 1364 G>T polymorphism with coronary artery disease in the Greek population. Drug metabolism and personalized therapy 2019 Mar . Giannakopoulou Efstathia, Konstantinou Fotios, Ragia Georgia, Gerontitis Zisis, Tavridou Anna, Papapetropoulos Andreas, Mikroulis Dimitrios, Manolopoulos Vangelis |
Genotypes of Common Polymorphisms in the PON1 Gene Associated With Paraoxonase Activity as Cardiovascular Risk Factor: A Cross-Sectional Study and Meta-Analysis of Studies Conducted in México. Archives of medical research 2019 Mar . Moreno-Godínez Ma Elena, Galarce-Sosa Claudia, Cahua-Pablo José Ángel, Rojas-García Aurora Elizabeth, Huerta-Beristain Gerardo, Alarcón-Romero Luz Del Carmen, Cruz Miguel, Valladares-Salgado Adán, Antonio-Véjar Verónica, Ramírez-Vargas Marco Antonio, Flores-Alfaro Eugen |
Investigation of novel variations of ORAI1 gene and their association with Kawasaki disease. Journal of human genetics 2019 Mar . Thiha Kyaw, Mashimo Yoichi, Suzuki Hiroyuki, Hamada Hiromichi, Hata Akira, Hara Toshiro, Tanaka Toshihiro, Ito Kaoru, Onouchi Yoshihiro, |
Strong association between the interleukin-8-251A/T polymorphism and coronary artery disease risk. Medicine 2019 Mar 98 (10): e14715. Wu Ying, Wang Wei, Li Xiao-Yan, Qian Ling-Ling, Dang Shi-Peng, Tang Xu, Chen Heng-Jian, Wang Ru-Xi |
Effects of X-chromosome Tenomodulin Genetic Variants on Obesity in a Children's Cohort and Implications of the Gene in Adipocyte Metabolism. Scientific reports 2019 Mar 9 (1): 3979. Ruiz-Ojeda Francisco Javier, Anguita-Ruiz Augusto, Rupérez Azahara I, Gomez-Llorente Carolina, Olza Josune, Vázquez-Cobela Rocío, Gil-Campos Mercedes, Bueno Gloria, Leis Rosaura, Cañete Ramón, Moreno Luis A, Gil Angel, Aguilera Concepcion Mar |
Genetic variant associated with stroke outcomes. Nature reviews. Neurology 2019 Mar . Kelsey Rebec |
Titin-truncating Variants Are Associated with Heart Failure Events in Patients with Left Ventricular Noncompaction Cardiomyopathy. Clinical cardiology 2019 Mar . Li Shijie, Zhang Ce, Liu Nana, Bai Hui, Hou Cuihong, Song Lei, Pu Jiel |
ALDH2 rs671 polymorphism and the risk of heart failure with preserved ejection fraction (HFpEF) in patients with cardiovascular diseases. Journal of human hypertension 2019 Mar . Xia Chun-Lei, Chu Peng, Liu Yi-Xian, Qu Xin-Liang, Gao Xiao-Fei, Wang Zhi-Mei, Dong Jing, Chen Shao-Liang, Zhang Jun-X |
Evaluation of the effects of ontogenetic or maturation functions and chronic heart failure on the model analysis for the dose-response relationship of warfarin in Japanese children. European journal of clinical pharmacology 2019 Mar . Tamura Rika, Watanabe Nao, Nakamura Saki, Yoshimura Naoki, Ozawa Sayaka, Hirono Keiichi, Ichida Fukiko, Taguchi Masa |
Serotonergic Regulation and Cognition after Stroke: The Role of Antidepressant Treatment and Genetic Variation. Cerebrovascular diseases (Basel, Switzerland) 2019 Mar 47 (1-2): 72-79. Damsbo Andreas Gammelgaard, Kraglund Kristian Lundsgaard, Buttenschøn Henriette Nørmølle, Johnsen Søren Paaske, Andersen Grethe, Mortensen Janne Kaergaa |
Associations of Genetic Variations in International journal of environmental research and public health 2019 Mar 16 (5): . Zhao Tian-Yu, Lei Song, Huang Liu, Wang Yi-Nan, Wang Xiao-Ni, Zhou Ping-Pu, Xu Xiao-Jun, Zhang Long, Xu Liang-Wen, Yang L |
The ABO locus is associated with increased platelet aggregation in patients with stable coronary artery disease. International journal of cardiology 2019 Feb . Christiansen Morten Krogh, Larsen Sanne Bøjet, Nyegaard Mette, Neergaard-Petersen Søs, Würtz Morten, Grove Erik Lerkevang, Hvas Anne-Mette, Jensen Henrik Kjærulf, Kristensen Steen Dal |
The relationship between plasma homocysteine levels and MTHFR gene variation, age, and sex in Northeast China. Nigerian journal of clinical practice 2019 Mar 22 (3): 380-385. Wang F, Sui X, Xu N, Yang J, Zhao H, Fei X, Zhang Z, Luo Z, Xin Y, Qin B, Zhao X, Cao S, Zhang Y, Yang |
Long-term coffee consumption, caffeine metabolism genetics, and risk of cardiovascular disease: a prospective analysis of up to 347,077 individuals and 8368 cases. The American journal of clinical nutrition 2019 Mar 109 (3): 509-516. Zhou Ang, Hyppönen Eli |
Variation in Complement Factor H Affects Complement Activation in Immunoglobulin A Vasculitis with Nephritis. Nephrology (Carlton, Vic.) 2019 Mar . Jia Meng, Zhu Li, Zhai Ya-Ling, Chen Pei, Xu Bo-Yang, Guo Wei-Yi, Shi Su-Fang, Liu Li-Jun, Lv Ji-Cheng, Zhang Ho |
Seize the Day for a Day With No Seizures: Modifiable Midlife Risk Factors Identified. Epilepsy currents 2019 Jan 19 (1): 27-28. Koubeissi Moham |
Ser96Ala genetic variant of the human histidine-rich calcium-binding protein is a genetic predictor of recurrence after catheter ablation in patients with paroxysmal atrial fibrillation. PloS one 2019 14 (3): e0213208. Amioka Michitaka, Nakano Yukiko, Ochi Hidenori, Onohara Yuko, Sairaku Akinori, Tokuyama Takehito, Motoda Chikaaki, Matsumura Hiroya, Tomomori Shunsuke, Hironobe Naoya, Okubo Yousaku, Okamura Sho, Chayama Kazuaki, Kihara Yasu |
LncRNA MALAT1 gene polymorphisms in coronary artery disease: a case-control study in a Chinese population. Bioscience reports 2019 Mar . Hu Weina, Ding Hanxi, Ouyang An, Zhang Xiaohong, Xu Qian, Han Yunan, Zhang Xueying, Jin Yuanz |
Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children. Molecular genetics & genomic medicine 2019 Mar e612. Behiry Eman G, Al-Azzouny Mahmoud A, Sabry Dina, Behairy Ola G, Salem Nessrine |
Association of the rs10830963 polymorphism in MTNR1B with fasting glucose, serum adipokine levels and components of metabolic syndrome in adult obese subjects. Nutricion hospitalaria 2019 Mar 36 (1): 60-65. de Luis Román Daniel Antonio, Primo David, Aller Rocio, Izaola Ola |
CT and clinical characteristics that predict risk of EGFR mutation in non-small cell lung cancer: a systematic review and meta-analysis. International journal of clinical oncology 2019 Mar . Zhang Hanfei, Cai Weiguo, Wang Yanfan, Liao Meiyan, Tian Sufa |
Circulating HO-1 levels are not associated with plasma sFLT-1 and GT Hypertension in pregnancy 2019 Mar 1-5. Sandrim Valeria, Coeli-Lacchini Fernanda Borchers, Tanus-Santos Jose Eduardo, Lacchini Riccardo, Cavalli Ricardo Carval |
Blood-brain barrier transcytosis genes, risk of dementia and stroke: a prospective cohort study of 74,754 individuals. European journal of epidemiology 2019 Mar . Juul Rasmussen Ida, Tybjærg-Hansen Anne, Rasmussen Katrine Laura, Nordestgaard Børge G, Frikke-Schmidt Ru |
Association between polymorphism in Cyclophilin A gene and its serum and placental expression in Han Chinese women with severe preeclampsia. Pregnancy hypertension 2019 Jan 15 84-92. Sun Wenjuan, Xu Yongping, Xin Qian, Zhang Yuan, Cui Baoxia, Hong Fanzh |
Interleukin-8 Gene -251 A/T (rs4073) Polymorphism and Coronary Artery Disease Risk: A Meta-Analysis. Medical science monitor : international medical journal of experimental and clinical research 2019 Mar 25 1645-1655. Zhang Shunrong, Gao Yue, Huang Jin |
Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population. Journal of clinical medicine 2019 Feb 8 (2): . Hong Eun Pyo, Kim Bong Jun, Cho Steve S, Yang Jin Seo, Choi Hyuk Jai, Kang Suk Hyung, Jeon Jin Pyeo |
Interaction of glutathione S-transferase polymorphisms and tobacco smoking during pregnancy in susceptibility to autism spectrum disorders. Scientific reports 2019 Mar 9 (1): 3206. Mandic-Maravic Vanja, Coric Vesna, Mitkovic-Voncina Marija, Djordjevic Miroslav, Savic-Radojevic Ana, Ercegovac Marko, Matic Marija, Simic Tatjana, Lecic-Tosevski Dusica, Toskovic Oliver, Pekmezovic Tatjana, Pljesa-Ercegovac Marija, Pejovic-Milovancevic Mili |
Mutational profile of Brazilian lung adenocarcinoma unveils association of EGFR mutations with high Asian ancestry and independent prognostic role of KRAS mutations. Scientific reports 2019 Mar 9 (1): 3209. Leal Letícia Ferro, de Paula Flávia Escremim, De Marchi Pedro, de Souza Viana Luciano, Pinto Gustavo Dix Junqueira, Carlos Carolina Dias, Berardinelli Gustavo Noriz, Miziara José Elias, da Silva Carlos Maciel, Silva Eduardo Caetano Albino, Pereira Rui, de Oliveira Marco Antonio, Scapulatempo-Neto Cristovam, Reis Rui Manu |
Promoter methylation and functional variants in arachidonate 5-lipoxygenase and forkhead box protein O1 genes associated with coronary artery disease. Journal of cellular biochemistry 2019 Mar . Heidari Laleh, Ghaderian Sayyed Mohammad Hossein, Vakili Hossein, Salmani Tayyeb A |
Association of age-related macular degeneration with complement activation products, smoking, and single nucleotide polymorphisms in South Carolinians of European and African descent. Molecular vision 2019 25 79-92. Rohrer Bärbel, Frazer-Abel Ashley, Leonard Anthony, Ratnapriya Rinki, Ward Tyson, Pietraszkiewicz Alexandra, O'Quinn Elizabeth, Adams Katherine, Swaroop Anand, Wolf Bethany Jaco |
Comprehensive analysis of age-related somatic mutation profiles in Chinese young lung adenocarcinoma patients. Cancer medicine 2019 Mar . Yang Bo, Li Jie, Li Fang, Zhou Hongxia, Shi Weiwei, Shi Huaiyin, Sun Shengjie, Sun Wending, Wang Jinliang, Ma Junxun, Yan Xiang, Hu Yi, Jiao Shuncha |
Genetic variability of inflammation and oxidative stress genes does not play a major role in the occurrence of adverse events of dopaminergic treatment in Parkinson's disease. Journal of neuroinflammation 2019 Feb 16 (1): 50. Redenšek Sara, Flisar Dušan, Kojovic Maja, Kramberger Milica Gregoric, Georgiev Dejan, Pirtošek Zvezdan, Trošt Maja, Dolžan Vi |
Effect of genetic polymorphism of brain-derived neurotrophic factor and serotonin transporter on smoking phenotypes: A pilot study of Japanese participants. Heliyon 2019 Feb 5 (2): e01234. Ohmoto Masanori, Takahashi Tats |
Evaluation of a weighted genetic risk score for the prediction of biomarkers of CYP2A6 activity. Addiction biology 2019 Feb . El-Boraie Ahmed, Taghavi Taraneh, Chenoweth Meghan J, Fukunaga Koya, Mushiroda Taisei, Kubo Michiaki, Lerman Caryn, Nollen Nicole L, Benowitz Neal L, Tyndale Rachel |
Increased burden of rare deleterious variants of the KCNQ1 gene in patients with large-vessel ischemic stroke. Molecular medicine reports 2019 Feb . Janicki Piotr K, Eyileten Ceren, Ruiz-Velasco Victor, Pordzik Justyna, Czlonkowska Anna, Kurkowska-Jastrzebska Iwona, Sugino Shigekazu, Imamura Kawasawa Yuka, Mirowska-Guzel Dagmara, Postula Mar |
Metabolomic Signature of Angiopoietin-Like Protein 3 Deficiency in Fasting and Postprandial State. Arteriosclerosis, thrombosis, and vascular biology 2019 Feb ATVBAHA118312021. Tikkanen Emmi, Minicocci Ilenia, Hällfors Jenni, Di Costanzo Alessia, D'Erasmo Laura, Poggiogalle Eleonora, Donini Lorenzo Maria, Würtz Peter, Jauhiainen Matti, Olkkonen Vesa M, Arca Marcel |
Circadian clock genes and circadian phenotypes in patients with myocardial infarction. Advances in medical sciences 2019 Feb 64 (2): 224-229. Škrlec Ivana, Milic Jakov, Heffer Marija, Wagner Jasenka, Peterlin Bor |
Influence of K656N Polymorphism of the Leptin Receptor Gene on Obesity-Related Traits in Nondiabetic Afro-Caribbean Individuals. Metabolic syndrome and related disorders 2019 Feb . Foucan Lydia, Bassien-Capsa Valérie, Rambhojan Christine, Lacorte Jean-Marc, Larifla Laure |
A Genetic Risk Score for Atrial Fibrillation Predicts the Response to Catheter Ablation. Korean circulation journal 2018 Dec . Choe Won Seok, Kang Jun Hyuk, Choi Eue Keun, Shin Seung Yong, Lubitz Steven A, Ellinor Patrick T, Oh Seil, Lim Hong E |
Association of mononucleotide polymorphisms of angiotensinogen gene at promoter region with antihypertensive response to angiotensin receptor blockers in hypertensive Chinese. Journal of the renin-angiotensin-aldosterone system : JRAAS 0 20 (1): 1470320319827205. Gong Hong-Tao, Mu Li-Ying, Zhang Tong, Xu Xiu-Ying, Du Feng- |
Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study. Neurology 2019 Feb 92 (9): e944-e950. Larsson Susanna C, Traylor Matthew, Burgess Stephen, Boncoraglio Giorgio B, Jern Christina, Michaëlsson Karl, Markus Hugh S, |
MAOA variants differ in oscillatory EEG & ECG activities in response to aggression-inducing stimuli. Scientific reports 2019 Feb 9 (1): 2680. Im Seung Yeong, Jeong Jinju, Jin Gwonhyu, Yeom Jiwoo, Jekal Janghwan, Lee Sang-Im, Cho Jung Ah, Lee Sukkyoo, Lee Youngmi, Kim Dae-Hwan, Bae Mijeong, Heo Jinhwa, Moon Cheil, Lee Chang-H |
Association of PTPN1 polymorphisms with breast cancer risk: A case-control study in Chinese females. Journal of cellular biochemistry 2019 Feb . Huang Shuya, Liu Liyuan, Xiang Yujuan, Wang Fei, Yu Lixiang, Zhou Fei, Cui Shude, Tian Fuguo, Fan Zhimin, Geng Cuizhi, Cao Xuchen, Yang Zhenlin, Wang Xiang, Liang Hong, Wang Shu, Jiang Hongchuan, Duan Xuening, Wang Haibo, Li Guolou, Wang Qitang, Zhang Jianguo, Jin Feng, Tang Jinhai, Li Liang, Zhu Shiguang, Zuo Wenshu, Ye Chunmiao, Zhou Wenzhong, Yin Gengshen, Ma Zhongbing, Yu Zhiga |
rs1234313 and rs45454293 are risk factors of cerebral arterial thrombosis, large artery atherosclerosis, and carotid plaque in the Han Chinese population: a case-control study. BMC neurology 2019 Feb 19 (1): 31. Jiang Yan, Liu Xiaomin, Du Yifeng, Zhou Shengni |
Lean mass, grip strength and risk of type 2 diabetes: a bi-directional Mendelian randomisation study. Diabetologia 2019 Feb . Yeung Chris Ho Ching, Au Yeung Shiu Lun, Fong Shirley Siu Ming, Schooling C Ma |
Associations of homocysteine status and homocysteine metabolism enzyme polymorphisms with hypertension and dyslipidemia in a Chinese hypertensive population. Clinical and experimental hypertension (New York, N.Y. : 1993) 2019 Feb 1-9. Yuan Xiaojie, Wang Tingcai, Gao Jie, Wang Yunchao, Chen Yajun, Kaliannan Kanakaraju, Li Xiaochun, Xiao Jing, Ma Tianyou, Zhang Lei, Shao Zhongj |
Relative effects of LDL-C on ischemic stroke and coronary disease: A Mendelian randomization study. Neurology 2019 Feb . Valdes-Marquez Elsa, Parish Sarah, Clarke Robert, Stari Traiani, Worrall Bradford B, , Hopewell Jemma |
TRIB1 and TRPS1 variants, G?×?G and G?×?E interactions on serum lipid levels, the risk of coronary heart disease and ischemic stroke. Scientific reports 2019 Feb 9 (1): 2376. Zhang Qing-Hui, Yin Rui-Xing, Chen Wu-Xian, Cao Xiao-Li, Wu Jin-Zh |
Association study between DNA methylation and genetic variation of Molecular biology research communications 2018 Dec 7 (4): 173-179. Ghaznavi Habib, Kiani Ali Asghar, Soltanpour Mohammad Soleim |
Associations between endothelial nitric oxide synthase gene polymorphisms and the risk of coronary artery disease: A systematic review and meta-analysis of 132 case-control studies. European journal of preventive cardiology 2019 Jan 26 (2): 160-170. Li Xiaoqing, Lin Yong, Zhang Ruiz |
High risk of heart failure associated with desmoglein-2 mutations compared to plakophilin-2 mutations in arrhythmogenic right ventricular cardiomyopathy/dysplasia. European journal of heart failure 2019 Feb . Hermida Alexis, Fressart Véronique, Hidden-Lucet Francoise, Donal Erwan, Probst Vincent, Deharo Jean-Claude, Chevalier Philippe, Klug Didier, Mansencal Nicolas, Delacretaz Etienne, Cosnay Pierre, Scanu Patrice, Extramiana Fabrice, Keller Dagmar I, Rouanet Stephanie, Charron Philippe, Gandjbakhch Estel |
The relationship between MMP9 and ADRA2A gene polymorphisms and mothers-newborns' nutritional status: an exploratory path model (STROBE compliant article). Pediatric research 2019 Feb . Marginean Cristina Oana, Marginean Claudiu, Banescu Claudia, Melit Lorena Elena, Tripon Florin, Iancu Mihae |
Association between RAGE variants and the susceptibility to atherosclerotic lesions in Chinese Han population. Experimental and therapeutic medicine 2019 Mar 17 (3): 2019-2030. Zhang Xiaolin, Cheng Minghui, Tong Fangnian, Su X |
Prognostic Risk Models for the Development of Cardiovascular Dysfunction in Adolescents with Essential Hypertension. Bulletin of experimental biology and medicine 2019 Feb . Kosovtseva A S, Bairova ? ?, Rychkova L V, Polyakov V M, Kolesnikova L |
Association of coronary artery disease with toll-like receptor 4 genetic variants: A meta-analysis. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2019 Feb . Sheng Jianlong, Xu Ji |
Homocysteine and Small Vessel Stroke: A Mendelian Randomization Analysis. Annals of neurology 2019 Feb . Larsson Susanna C, Traylor Matthew, Markus Hugh |
Genetic variants in nicotinic receptors and smoking cessation in Parkinson's disease. Parkinsonism & related disorders 2019 Feb . Chuang Yu-Hsuan, Paul Kimberly C, Sinsheimer Janet S, Bronstein Jeff M, Bordelon Yvette M, Ritz Bea |
PHACTR1 gene polymorphism with the risk of coronary artery disease in Chinese Han population. Postgraduate medical journal 2019 Feb . Chen Lishan, Qian Hang, Luo Zhihuan, Li Dongfeng, Xu Hao, Chen Jishun, He Peigen, Zhou Xintao, Zhang Tao, Chen Jun, Min Xinw |
Association between peroxisome proliferator-activated receptor gamma-2 gene Pro12Ala polymorphisms and risk of hypertension: an updated meta-analysis. Bioscience reports 2019 Feb . Zhang Miao, Zhang Jianping, Li Lifeng, Wang Qiang, Feng Lim |
Common Variations in Prothrombotic Genes and Susceptibility to Ischemic Stroke in Young Patients: A Case-Control Study in Southeast Iran. Medicina (Kaunas, Lithuania) 2019 Feb 55 (2): . Hashemi Seyed Mehdi, Ramroodi Nourollah, Amiri Fard Hamed, Talebian Sahar, Haghighi Rohani Maryam, Rezaei Mahnaz, Noora Mehrangiz, Salimi Saeed |
Effect of prothrombotic genotypes on the risk of venous thromboembolism in patients with and without ischemic stroke.The TromsØ Study. Journal of thrombosis and haemostasis : JTH 2019 Feb . Rinde Ludvig B, Morelli Vania M, Småbrekke Birgit, Mathiesen Ellisiv B, Løchen Maja-Lisa, Njølstad Inger, Wilsgaard Tom, Smith Erin, Rosendaal Frits R, Frazer Kelly A, Braekkan Sigrid K, Hansen John-Bjar |
The association between Neuropsychiatric disease and treatment 2019 15 339-347. Svob Strac Dubravka, Nedic Erjavec Gordana, Nikolac Perkovic Matea, Nenadic-Sviglin Korona, Konjevod Marcela, Grubor Mirko, Pivac Ne |
Role of 11ß HSD 1, rs12086634, and rs846910 single-nucleotide polymorphisms in metabolic-related skin diseases: a clinical, biochemical, and genetic study. Clinical, cosmetic and investigational dermatology 2019 12 91-102. Farag Azza Gaber Antar, Badr Eman Ae, Eltorgoman Abdel Monem A, Assar Mohamed Fa, Elshafey Eman N, Tayel Nermin Reda, Aboutaleb Hossam |
Personalized rosuvastatin therapy in problem patients with partial statin intolerance. Archives of medical sciences. Atherosclerotic diseases 2018 3 e83-e89. Shek Aleksandr B, Kurbanov Ravshanbek D, Alieva Rano B, Abdullaeva Guzal J, Nagay Aleksandr V, Abdullaev Alisher A, Hoshimov Shavkat U, Nizamov Ulugbek |
Association of ficolin-2 (FCN2) functional polymorphisms and protein levels with rheumatic fever and rheumatic heart disease: relationship with cardiac function. Archives of medical sciences. Atherosclerotic diseases 2018 3 e142-e155. Elshamaa Manal F, Hamza Hala, El Rahman Naglaa Abd, Emam Soha, Elghoroury Eman A, Farid Tarek M, Zaher Asmaa Zakareya, Ibrahim Mona H, Kamel Solaf, El-Aziz Doaa A |
Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy. ESC heart failure 2019 Feb . Jääskeläinen Pertti, Vangipurapu Jagadish, Raivo Joose, Kuulasmaa Teemu, Heliö Tiina, Aalto-Setälä Katriina, Kaartinen Maija, Ilveskoski Erkki, Vanninen Sari, Hämäläinen Liisa, Melin John, Kokkonen Jorma, Nieminen Markku S, , Laakso Markku, Kuusisto Johan |
Methionine Sulfoxide Reductase-B3 Risk Allele Implicated in Alzheimer's Disease Associates with Increased Odds for Brain Infarcts. Journal of Alzheimer's disease : JAD 2019 Feb . Conner Sarah C, Benayoun Laurent, Himali Jayandra J, Adams Stephanie L, Yang Qiong, DeCarli Charles, Blusztajn Jan K, Beiser Alexa, Seshadri Sudha, Delalle Iva |
Correlation between EGFR mutation status and F Thoracic cancer 2019 Feb . Zhu Lei, Yin Guotao, Chen Wei, Li Xiaofeng, Yu Xiaozhou, Zhu Xiang, Jiang Wei, Jia Chaoyang, Chen Peihe, Zhang Yufan, Lu Di, Yu Lijuan, Li Xubin, Xu Weng |
SLC22A3 is associated with lipoprotein (a) concentration and cardiovascular disease in familial hypercholesterolemia. Clinical biochemistry 2019 Feb . Paquette Martine, Bernard Sophie, Baass Alex |
No Causal Effect of Telomere Length on Ischemic Stroke and Its Subtypes: A Mendelian Randomization Study. Cells 2019 Feb 8 (2): . Cao Weijie, Li Xingang, Zhang Xiaoyu, Zhang Jie, Sun Qi, Xu Xizhu, Sun Ming, Tian Qiuyue, Li Qihuan, Wang Hao, Liu Jiaonan, Meng Xiaoni, Wu Lijuan, Song Manshu, Hou Haifeng, Wang Youxin, Wang W |
Gene-environment interactions related to blood pressure traits in two community-based Korean cohorts. Genetic epidemiology 2019 Feb . Lim Ji Eun, Kim Hye Ok, Rhee Sang Youl, Kim Mi Kyung, Kim Yeon-Jung, Oh Bermse |
Association of the coronary artery disease risk gene GUCY1A3 with ischaemic events after coronary intervention. Cardiovascular research 2019 Feb . Kessler Thorsten, Wolf Bernhard, Eriksson Niclas, Kofink Daniel, Mahmoodi Bakhtawar K, Rai Himanshu, Tragante Vinicius, Åkerblom Axel, Becker Richard C, Bernlochner Isabell, Bopp Roman, James Stefan, Katus Hugo A, Mayer Katharina, Munz Matthias, Nordio Francesco, O'Donoghue Michelle L, Sager Hendrik B, Sibbing Dirk, Solakov Linda, Storey Robert F, Wobst Jana, Asselbergs Folkert W, Byrne Robert A, Erdmann Jeanette, Koenig Wolfgang, Laugwitz Karl-Ludwig, Ten Berg Jurrien M, Wallentin Lars, Kastrati Adnan, Schunkert Heribe |
An African-specific haplotype in MRGPRX4 is associated with menthol cigarette smoking. PLoS genetics 2019 Feb 15 (2): e1007916. Kozlitina Julia, Risso Davide, Lansu Katherine, Olsen Reid Hans Johnson, Sainz Eduardo, Luiselli Donata, Barik Arnab, Frigerio-Domingues Carlos, Pagani Luca, Wooding Stephen, Kirchner Thomas, Niaura Ray, Roth Bryan, Drayna Denn |
Genetic Testing and Risk Scores: Impact on Familial Hypercholesterolemia. Frontiers in cardiovascular medicine 2019 6 5. Sarraju Ashish, Knowles Joshua |
Effects of angiotensin converting enzyme gene polymorphism on hypertension in Africa: A meta-analysis and systematic review. PloS one 2019 14 (2): e0211054. Mengesha Hayelom Gebrekirstos, Petrucka Pammla, Spence Cara, Tafesse Tadesse Beke |
The association between apelin polymorphisms and hypertension in China: A meta-analysis. Journal of the renin-angiotensin-aldosterone system : JRAAS 0 20 (1): 1470320319827204. Wang Tianyi, Liu Conghe, Jia Lili, Ding J |
The Oxford study of Calcium channel Antagonism, Cognition, Mood instability and Sleep (OxCaMS): study protocol for a randomised controlled, experimental medicine study. Trials 2019 Feb 20 (1): 120. Atkinson Lauren Z, Colbourne Lucy, Smith Alexander, Harmer Catherine H, Nobre Anna C, Rendell Jennifer, Jones Helen, Hinds Christopher, Mould Arne, Tunbridge Elizabeth M, Cipriani Andrea, Geddes John R, Saunders Kate E A, Harrison Paul |
Association of Genetic Polymorphisms in the Beta-1 Adrenergic Receptor with Recovery of Left Ventricular Ejection Fraction in Patients with Heart Failure. Journal of cardiovascular translational research 2019 Feb . Luzum Jasmine A, English Joseph D, Ahmad Umair S, Sun Jessie W, Canan Benjamin D, Sadee Wolfgang, Kitzmiller Joseph P, Binkley Philip |
Re-challenge of afatinib after 1st generation EGFR-TKI failure in patients with previously treated non-small cell lung cancer harboring EGFR mutation. Cancer chemotherapy and pharmacology 2019 Feb . Yamaguchi Ou, Kaira Kyoichi, Mouri Atsuto, Shiono Ayako, Hashimoto Kosuke, Miura Yu, Nishihara Fuyumi, Murayama Yoshitake, Kobayashi Kunihiko, Kagamu Hiros |
Analysis of the frequency of oncogenic driver mutations and correlation with clinicopathological characteristics in patients with lung adenocarcinoma from Northeastern Switzerland. Diagnostic pathology 2019 Feb 14 (1): 18. Grosse Alexandra, Grosse Claudia, Rechsteiner Markus, Soltermann Al |
Identification of Rare Copy Number Variants Associated With Pulmonary Atresia With Ventricular Septal Defect. Frontiers in genetics 2019 10 15. Xie Huilin, Hong Nanchao, Zhang Erge, Li Fen, Sun Kun, Yu |
Platelet mitochondrial cytochrome c oxidase subunit I variants with benzene poisoning. Journal of thoracic disease 2018 Dec 10 (12): 6811-6818. Wang Dianpeng, Yang Xiangli, Zhang Yanfang, Lin Dafeng, Li Paimao, Zhang Zhiming, Huang Xianqing, Gu Dayong, Loo Jacky Fong-Chu |
1-adrenoceptor polymorphisms and blood pressure: 49S variant increases plasma renin but not blood pressure in hypertensive patients. American journal of hypertension 2019 Feb . Sandilands Alastair J, O'Shaughnessy Kevin M, Yasmin |
Increased risk of post-stroke epilepsy in Chinese patients with a TRPM6 polymorphism. Neurological research 2019 Feb 1-6. Fu Chuan-Yi, Chen Shui-Jie, Cai Nan-Hua, Liu Zhao-Hui, Zhang Mao, Wang Peng-Cheng, Zhao Jian-No |
SERPINA1 Z allele is associated with cystic fibrosis liver disease. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Feb . Boëlle Pierre-Yves, Debray Dominique, Guillot Loic, Corvol Harriet, |
The Role of Polymorphism Gen Open access Macedonian journal of medical sciences 2019 Jan 7 (1): 29-32. Arina Cut Aria, Amir Darwin, Siregar Yahwardiah, Sembiring Rosita |
Association Between ABCB1 Polymorphisms and Outcomes of Clopidogrel Treatment in Patients With Minor Stroke or Transient Ischemic Attack: Secondary Analysis of a Randomized Clinical Trial. JAMA neurology 2019 Feb . Pan Yuesong, Chen Weiqi, Wang Yilong, Li Hao, Johnston S Claiborne, Simon Tabassome, Zhao Xingquan, Liu Liping, Wang David, Meng Xia, Wang Yongjun, |
Significance of bronchiolocentric fibrosis in patients with histopathologic usual interstitial pneumonia. Histopathology 2019 Feb . Tanizawa Kiminobu, Ley Brett, Vittinghoff Eric, Elicker Brett M, Henry Travis S, Wolters Paul J, Brownell Robert, Liu Shuo, Collard Harold R, Jones Kirk |
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