HLBS-PopOmics
Query Trace: HLBS
MBL2 gene polymorphism rs1800450 and rheumatic fever with and without rheumatic heart disease: an Egyptian pilot study. Pediatric rheumatology online journal 2018 Apr 16 (1): 24. Gomaa Maher Hassan, Ali Shawkey Sadik, Fattouh Aya Mohamed, Hamza Hala Salah, Badr Mohamed Moham |
Genome-wide and candidate gene approaches of clopidogrel efficacy using pharmacodynamic and clinical end points-Rationale and design of the International Clopidogrel Pharmacogenomics Consortium (ICPC). American heart journal 2018 Apr 198 152-159. Bergmeijer Thomas O, Reny Jean-Luc, Pakyz Ruth E, Gong Li, Lewis Joshua P, Kim Eun-Young, Aradi Daniel, Fernandez-Cadenas Israel, Horenstein Richard B, Lee Ming Ta Michael, Whaley Ryan M, Montaner Joan, Gensini Gian Franco, Cleator John H, Chang Kiyuk, Holmvang Lene, Hochholzer Willibald, Roden Dan M, Winter Stefan, Altman Russ B, Alexopoulos Dimitrios, Kim Ho-Sook, Déry Jean-Pierre, Gawaz Meinrad, Bliden Kevin, Valgimigli Marco, Marcucci Rossella, Campo Gianluca, Schaeffeler Elke, Dridi Nadia P, Wen Ming-Shien, Shin Jae Gook, Simon Tabassome, Fontana Pierre, Giusti Betti, Geisler Tobias, Kubo Michiaki, Trenk Dietmar, Siller-Matula Jolanta M, Ten Berg Jurriën M, Gurbel Paul A, Hulot Jean-Sebastien, Mitchell Braxton D, Schwab Matthias, Ritchie Marylyn DeRiggi, Klein Teri E, Shuldiner Alan R, |
Association Between Ethnicity and Postoperative Hyperglycemia in a Southeast Asian Population Undergoing Cardiac Surgery. Journal of cardiothoracic and vascular anesthesia 2018 Mar . Moorthy Vikaesh, Sim Ming Ann, Liu Weiling, Ti Lian Kah, Chew Sophia Tsong Hu |
Association of Fc?RI? polymorphisms with risk of asthma and allergic rhinitis: Evidence based on 29 case-control studies. Bioscience reports 2018 Apr . Guo Huanhuan, Peng Tao, Luo Ping, Li Huabin, Huang Shuo, Li Shuang, Zhao Weidong, Zhou Xuho |
Genetic susceptibility of five tagSNPs in the endothelin-1 (EDN1) gene to coronary artery disease in a Chinese Han population. Bioscience reports 2018 Apr . Liang Li-Li, Chen Lin, Zhou Meng-Yuan, Cai Meng-Yun, Cheng Jie, Chen Yi, You Si-Kun, Chen Lin-Bin, Tang Zi-Bin, Yang Xi-Li, Chen Can, Liu Xinguang, Xiong Xing-Do |
Association of the rs1870634 Variant in Long Intergenic Non-protein Coding RNA 841 with Coronary Artery Disease: A GWAS-Replication Study in an Iranian Population. Biochemical genetics 2018 Apr . Tarighi Shahriar, Alipoor Behnam, Zare Ali, Ghaedi Hamid, Shanaki Mehrnoo |
A Genome-Wide Association Study identifies new genes potentially associated with eyelid sagging. Experimental dermatology 2018 Apr . Laville Vincent, Le Clerc Sigrid, Ezzedine Khaled, Jdid Randa, Taing Lieng, Labib Toufik, Coulonges Cédric, Ulveling Damien, Galan Pilar, Guinot Christiane, Fezeu Leopold, Morizot Frédérique, Latreille Julie, Malvy Denis, Tschachler Erwin, Zagury Jean-Franço |
The correlation between growth hormone receptor (GHR) polymorphism and obstructive sleep apnea syndrome among the Han and Hani population in China. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2018 Apr . Ji Juanjuan, Yang Yunwei, Lin Yan, Li Xudong, Wu Xiaoguang, Yang Xi, Zhong Ling, Tang Ying, Huang Zhiyong, He Xiaogua |
Retraction: Is Endothelin Gene Polymorphism Associated with Postoperative Atrial Fibrillation in Patients Undergoing Coronary Artery Bypass Grafting? Annals of cardiac anaesthesia 0 21 (2): 222. Authors are not available |
Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations. PloS one 2018 13 (4): e0194842. Jmel Haifa, Romdhane Lilia, Ben Halima Yosra, Hechmi Meriem, Naouali Chokri, Dallali Hamza, Hamdi Yosr, Shan Jingxuan, Abid Abdelmajid, Jamoussi Henda, Trabelsi Sameh, Chouchane Lotfi, Luiselli Donata, Abdelhak Sonia, Kefi R |
[Association of OSMR gene polymorphisms with dilated cardiomyopathy in a Han Chinese population]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 Apr 35 (2): 210-214. Dai Xiaohui, Peng Ying, Zhou Bin, Li Chunmei, Song Huizi, Dou Qingyu, Xie Xiaochuan, Rao |
Combined effect of acid-sensing ion channel 3 and transient receptor potential vanilloid 1 gene polymorphisms on blood pressure variations in Taiwanese. Ci ji yi xue za zhi = Tzu-chi medical journal 0 30 (1): 29-36. Er Leay-Kiaw, Teng Ming-Sheng, Wu Semon, Hsu Lung-An, Tzeng I-Shiang, Cheng Ching-Feng, Chang Hsin-I, Chou Hsin-Hua, Ko Yu-L |
Association Between MicroRNAs Polymorphisms and Risk of Ischemic Stroke: A Meta-Analysis in Chinese Individuals. Frontiers in aging neuroscience 2018 10 82. Li Chen-Xi, Weng Hong, Zheng Jun, Feng Zhi-He, Ou Jian-Lin, Liao Wei-Ji |
Genetic polymorphisms of key enzymes in folate metabolism affect the efficacy of folate therapy in patients with hyperhomocysteinaemia. The British journal of nutrition 2018 Apr 119 (8): 887-895. Du Binghui, Tian Huizi, Tian Dandan, Zhang Chengda, Wang Wenhua, Wang Lianke, Ge Mengying, Hou Quanliang, Zhang Weido |
Resistin Is a Novel Marker for Postoperative Pain Intensity. Anesthesia and analgesia 2018 Apr . Hozumi Jun, Sumitani Masahiko, Nishizawa Daisuke, Nagashima Makoto, Ikeda Kazutaka, Abe Hiroaki, Kato Ryoji, Kusakabe Yoshiomi, Yamada Yoshitsugu, |
Deiodinases, Organic Anion Transporter Polypeptide Polymorphisms, and Thyroid Hormones in Patients with Myocardial Infarction. Genetic testing and molecular biomarkers 2018 Mar . Brozaitiene Julija, Skiriute Daina, Burkauskas Julius, Podlipskyte Aurelija, Jankauskiene Edita, Serretti Alessandro, Mickuviene Narse |
Association of Cardiomyopathy With MYBPC3 D389V and MYBPC3?25bpIntronic Deletion in South Asian Descendants. JAMA cardiology 2018 Apr . Viswanathan Shiv Kumar, Puckelwartz Megan J, Mehta Ashish, Ramachandra Chrishan J A, Jagadeesan Aravindakshan, Fritsche-Danielson Regina, Bhat Ratan V, Wong Philip, Kandoi Sangeetha, Schwanekamp Jennifer A, Kuffel Gina, Pesce Lorenzo L, Zilliox Michael J, Durai U Nalla B, Verma Rama Shanker, Molokie Robert E, Suresh Domodhar P, Khoury Philip R, Thomas Annie, Sanagala Thriveni, Tang Hak Chiaw, Becker Richard C, Knöll Ralph, Shim Winston, McNally Elizabeth M, Sadayappan Sakthiv |
Antenatal screening and diagnosis of tuberous sclerosis complex by fetal echocardiography and targeted genomic sequencing. Medicine 2018 Apr 97 (15): e0112. Gu Xiaoyan, Han Ling, Chen Jian, Wang Jianbin, Hao Xiaoyan, Zhang Ye, Zhang Jun, Ge Shuping, He Yih |
Polymorphism of CONNEXIN37 gene is a risk factor for ischemic stroke in Han Chinese population. Lipids in health and disease 2018 Apr 17 (1): 72. Li Hong, Yu Shasha, Wang Rui, Sun Zhaoqing, Zhou Xinghu, Zheng Liqiang, Yin Zhihua, Sun Yingxi |
Association of polymorphisms in MALAT1 with risk of coronary atherosclerotic heart disease in a Chinese population. Lipids in health and disease 2018 Apr 17 (1): 75. Wang Genan, Li Yaxiong, Peng Yong, Tang Jian, Li H |
Silencing mutations in JAG1 gene may play crucial roles in the pathogenesis of Tetralogy of Fallot. Cellular and molecular biology (Noisy-le-Grand, France) 2018 Mar 64 (4): 103-107. Safari-Arababadi Amin, Behjati-Ardakani Mostafa, Kalantar Seyed Mehdi, Jaafarinia Mojta |
Exome Sequencing in Children With Pulmonary Arterial Hypertension Demonstrates Differences Compared With Adults. Circulation. Genomic and precision medicine 2018 Apr 11 (4): e001887. Zhu Na, Gonzaga-Jauregui Claudia, Welch Carrie L, Ma Lijiang, Qi Hongjian, King Alejandra K, Krishnan Usha, Rosenzweig Erika B, Ivy D Dunbar, Austin Eric D, Hamid Rizwan, Nichols William C, Pauciulo Michael W, Lutz Katie A, Sawle Ashley, Reid Jeffrey G, Overton John D, Baras Aris, Dewey Frederick, Shen Yufeng, Chung Wendy |
New Common and Rare Variants Influencing Metabolic Syndrome and Its Individual Components in a Korean Population. Scientific reports 2018 Apr 8 (1): 5701. Lee Ho-Sun, Kim Yongkang, Park Taesu |
Contribution of adiponectin polymorphisms to the risk of coronary artery disease in a North-African Tunisian population. Journal of clinical laboratory analysis 2018 Apr e22446. Ghazouani Lakhdar, Elmufti Afoua, Baaziz Intissar, Chaabane Ibtissem, Ben Mansour He |
Mean platelet volume at baseline and immune thrombocytopenia relapse in Chinese newly-diagnosed patients: a retrospective cohort study. Hematology (Amsterdam, Netherlands) 2018 Apr 1-7. Chen Chi, Song Jun, Wang Qing, Wang Lin-Hui, Guo Peng-Xia |
Genetic polymorphisms are associated with exposure biomarkers for metals and persistent organic pollutants among Inuit from the Inuvialuit Settlement Region, Canada. The Science of the total environment 2018 Apr 634 569-578. Parajuli Rajendra Prasad, Goodrich Jaclyn M, Chan Laurie H M, Ayotte Pierre, Lemire Melanie, Hegele Robert A, Basu Nilad |
Interaction of iNOS Gene (C150T) Polymorphism and Endothelial Dysfunction in Pathophysiology of Metabolic Syndrome. The Tokai journal of experimental and clinical medicine 2018 Apr 43 (1): 24-29. Ahirwar Ashok Kumar, Jain Anju, Singh Archana, Bhardwaj Shilpa, Goswami Binita, Bhatnagar M K, Bhattacharjee Jayashr |
Cholinergic receptor nicotinic alpha 5 subunit polymorphisms are associated with smoking cessation success in women. BMC medical genetics 2018 Apr 19 (1): 55. Tomaz Paulo Roberto Xavier, Santos Juliana Rocha, Scholz Jaqueline, Abe Tânia Ogawa, Gaya Patrícia Viviane, Negrão André Brooking, Krieger José Eduardo, Pereira Alexandre Costa, Santos Paulo Caleb Júnior Li |
Genome-Wide Associations of Global Electrical Heterogeneity ECG Phenotype: The ARIC (Atherosclerosis Risk in Communities) Study and CHS (Cardiovascular Health Study). Journal of the American Heart Association 2018 Apr 7 (8): . Tereshchenko Larisa G, Sotoodehnia Nona, Sitlani Colleen M, Ashar Foram N, Kabir Muammar, Biggs Mary L, Morley Michael P, Waks Jonathan W, Soliman Elsayed Z, Buxton Alfred E, Biering-Sørensen Tor, Solomon Scott D, Post Wendy S, Cappola Thomas P, Siscovick David S, Arking Dan |
The Influence of CYP2C9 and VKORC1 Gene Polymorphisms on the Response to Warfarin in Egyptians. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2018 Apr 34 (2): 328-336. Bedewy Ahmed M L, Showeta Salah, Mostafa Mostafa Hasan, Kandil Lamia Sae |
Associations between thromboxane A synthase 1 gene polymorphisms and the risk of ischemic stroke in a Chinese Han population. Neural regeneration research 2018 Mar 13 (3): 463-469. Li Lei, He Zhi-Yi, Wang Yan-Zhe, Liu Xu, Yuan Li-Yi |
Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort. PloS one 2018 13 (4): e0194480. Chalazan Brandon, Mol Denise, Sridhar Arvind, Alzahrani Zain, Darbar Sara D, Ornelas-Loredo Aylin, Farooqui Abdullah, Argos Maria, Daviglus Martha L, Konda Sreenivas, Rehman Jalees, Darbar Dawo |
Genetic Risk Factors for Radiation Vasculopathy. Investigative ophthalmology & visual science 2018 Mar 59 (3): 1547-1553. Papakostas Thanos D, Morrison Margaux A, Lane Anne Marie, Awh Caroline, DeAngelis Margaret M, Gragoudas Evangelos S, Kim Ivana |
Role of genetic variations of chitinase 3 - like 1 in bronchial asthmatic patients. Clinical and molecular allergy : CMA 2018 16 9. Abe Kazuyuki, Nakamura Yutaka, Yamauchi Kohei, Maemondo Mako |
Sickle Cell Anemia Patients in Use of Hydroxyurea: Association between Polymorphisms in Genes Encoding Metabolizing Drug Enzymes and Laboratory Parameters. Disease markers 2018 2018 6105691. Yahouédéhou Sètondji Cocou Modeste Alexandre, Carvalho Magda Oliveira Seixas, Oliveira Rodrigo Mota, Santiago Rayra Pereira, da Guarda Caroline Conceição, Carvalho Suellen Pinheiro, Ferreira Júnia Raquel Dutra, Aleluia Milena Magalhães, Adorno Elisângela Vitória, Gonçalves Marilda de Sou |
Association of the melatonin circadian rhythms with clock 3111T/C gene polymorphism in Caucasian and Asian menopausal women with insomnia. Chronobiology international 2018 Apr 1-11. Semenova Natalya V, Madaeva Irina M, Bairova Tatiana A, Zhambalova Radzhana M, Sholokhov Leonid F, Kolesnikova Luybov |
The rs2609255 polymorphism in the FAM13A gene is reproducibly associated with silicosis susceptibility in a Chinese population. Gene 2018 Apr . Wang Wei, Yu Yuhui, Wu Shuangshuang, Sang Lingli, Wang Xiaohui, Qiu Anni, Yu Xiaoqiao, Li Jingzhi, Zhang Lu, Yi Min, Zheng Huiting, Gao Yuexia, Xiao Jing, Lu Yihua, Jiang Liying, Lian Yulong, Zhuang Xun, Tian Tian, Chu Minj |
Clinical Outcomes and Sustainability of Using CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention. Circulation. Genomic and precision medicine 2018 Apr 11 (4): e002069. Lee Craig R, Sriramoju Vindhya B, Cervantes Alexandra, Howell Lucius A, Varunok Nicholas, Madan Shivanshu, Hamrick Kasey, Polasek Melissa J, Lee John Andrew, Clarke Megan, Cicci Jonathan D, Weck Karen E, Stouffer George |
Correlation of rs1122608 SNP with acute myocardial infarction susceptibility and clinical characteristics in a Chinese Han population: A case-control study. Anatolian journal of cardiology 2018 Apr 19 (4): 249-258. Chen Quan Fang, Wang Wei, Huang Zhou, Huang Dong Ling, Li Tian, Wang Fan, Li J |
Single-agent panobinostat for relapsed/refractory diffuse large B-cell lymphoma: clinical outcome and correlation with genomic data. A phase 2 study of the Fondazione Italiana Linfomi. Leukemia & lymphoma 2018 Apr 1-7. Zaja Francesco, Salvi Flavia, Rossi Maura, Sabattini Elena, Evangelista Andrea, Ciccone Giovannino, Angelucci Emanuele, Gaidano Gianluca, Zanni Manuela, Ladetto Marco, Chiappella Annalisa, Vitolo Umberto, Zinzani Pier Luigi, Califano Catello, Tucci Alessandra, Patti Caterina, Pileri Stefano A, Lenti Valentina, Piccaluga Pier Paolo, Cavallo Federica, Volpetti Stefano, Perali Giulia, Assouline Sarit, Mann Koren Kathleen, Morin Ryan, Alcaide Miguel, Bushell Kevin, Fanin Renato, Levis Alessand |
FSHB -211 G>T is a major genetic modulator of reproductive physiology and health in childbearing age women. Human reproduction (Oxford, England) 2018 Mar . Rull Kristiina, Grigorova Marina, Ehrenberg Aivar, Vaas Pille, Sekavin Aire, Nõmmemees Diana, Adler Mart, Hanson Ele, Juhanson Peeter, Laan Mar |
CHRNA5 and CHRNA3 polymorphism and lung cancer susceptibility in Palestinian population. BMC research notes 2018 Apr 11 (1): 218. Ayesh Basim Mohammad, Al-Masri Rami, Abed Abdalla Ass |
Is the rs1801282 (G/C) Polymorphism of PPAR - Gamma Gene Associated with T2DM in Iraqi People? Open access Macedonian journal of medical sciences 2018 Mar 6 (3): 447-455. Al-Naemi Amjad Hazim, Ahmad Akram Jarje |
GATA1 Expression in BCR/ABL1-negative Myeloproliferative Neoplasms. Annals of laboratory medicine 2018 Jul 38 (4): 296-305. Yang Naery, Park Sholhui, Cho Min Sun, Lee Miae, Hong Ki Sook, Mun Yeung Chul, Seong Chu Myong, Huh Hee Jin, Huh Jungw |
The Serotonin Transporter Gene Polymorphisms and Risk of Ischemic Stroke. Cerebrovascular diseases (Basel, Switzerland) 2018 Apr 45 (3-4): 187-192. Mortensen Janne Kaergaard, Kraglund Kristian Lundsgaard, Johnsen Søren Paaske, Mors Ole, Andersen Grethe, Buttenschøn Henriette |
PPARgamma-2 and ADRB3 polymorphisms in connective tissue diseases and lipid disorders. Clinical interventions in aging 2018 13 463-472. Grygiel-Górniak Bogna, Zió?kowska-Suchanek Iwona, Kaczmarek El?bieta, Mosor Maria, Nowak Jerzy, Puszczewicz Mariu |
Genetic Survey of Adult-Onset Idiopathic Intracranial Hypertension. Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society 2018 Mar . Kuehn Markus H, Mishra Rajashree, Deonovic Benjamin E, Miller Kimberly N, McCormack Shana E, Liu Grant T, Kupersmith Mark J, Wall Michael, |
Relationship between vitamin D receptor gene polymorphism and susceptibility to chronic kidney disease and periodontal disease in community-dwelling elderly. Journal of clinical periodontology 2018 Apr . Yoshihara A, Kaneko N, Iwasaki M, Nohno K, Miyazaki |
CYP2E1 and GSTM1 gene polymorphisms, environmental factors, and the susceptibility to lung cancer. Journal of clinical laboratory analysis 2018 Mar e22403. He Qingfang, Wang Lixin, Zhang Jie, Lu Feng, Gong Weiwei, Pan Jin, Zhong Jieming, Hu Ruying, Yu M |
Upstream Stimulating Factor 1 (USF-1) Gene Polymorphisms and the Risk, Symptoms, and Outcome of Pediatric Ischemic Stroke. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2018 Mar . Balcerzyk Anna, Niemiec Pawe?, Iwanicki Tomasz, Nowak Tomasz, Kopyta Ilona, Emich-Widera Ewa, Pilarska Ewa, Pienczk-R?c?awowicz Karolina, Kaci?ski Marek, Wendorff Janusz, Górczy?ska-Kosiorz Sylwia, Grzeszczak W?adyslaw, ?ak Iwo |
Association of Matrix Metalloproteinase-7 Genotypes to the Risk of Oral Cancer in Taiwan. Anticancer research 2018 04 38 (4): 2087-2092. Shih Liang-Chun, Li Ching-Hao, Sun Kuo-Ting, Chen Liang-Yu, Hsu Che-Lun, Hung Yi-Wen, Wu Cheng-Nan, Hsia Te-Chun, Shen Te-Chun, Chang Wen-Shin, Shih Tzu-Ching, Tsai Chia-Wen, Bau DA-Ti |
The Association of Matrix Metalloproteinase-8 Promoter Genotypes in Breast Cancer. Anticancer research 2018 04 38 (4): 2181-2185. Hsiao Chieh-Lun, Liu Liang-Chih, Shih Tzu-Ching, Chuang Chin-Liang, Chen Guan-Liang, Wang Hwei-Chung, Pan Su-Yi, Shen Te-Chun, Tsai Chia-Wen, Chang Wen-Shin, Way Tzong-DER, Chung Jing-Gung, Bau DA-Ti |
Risk factors and methylenetetrahydrofolate reductase gene in congenital heart disease. Journal of thoracic disease 2018 Jan 10 (1): 441-447. Wang Lina, Yang Bo, Zhou Shiyuan, Gao Huafang, Wang Fengyu, Zhou Jiping, Wang Haili, Wang Yan |
The Variants in the 3' Untranslated Region of the Matrix Metalloproteinase 9 Gene as Modulators of Treatment Outcome in Children with Asthma. Lung 2018 Mar . Dragicevic Sandra, Kosnik Mitja, Divac Rankov Aleksandra, Rijavec Matija, Milosevic Katarina, Korosec Peter, Skerbinjek Kavalar Maja, Nikolic Aleksand |
Maternal consumption of coffee and tea during pregnancy and risk of childhood ALL: a pooled analysis from the childhood Leukemia International Consortium. Cancer causes & control : CCC 2018 Mar . Milne Elizabeth, Greenop Kathryn R, Petridou Eleni, Bailey Helen D, Orsi Laurent, Kang Alice Y, Baka Margarita, Bonaventure Audrey, Kourti Maria, Metayer Catherine, Clavel Jacqueli |
IL17A gene polymorphism rs4711998 and rs8193036 are not associated with post-bronchiolitis asthma in Finnish children. Acta paediatrica (Oslo, Norway : 1992) 2018 Mar . Nuolivirta Kirsi, Holster Annukka, Teräsjärvi Johanna, Lauhkonen Eero, Törmänen Sari, Helminen Merja, Koponen Petri, Korppi Matti, He Qiush |
Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function. Human immunology 2018 Mar . Coto Eliecer, Díaz-Corte Carmen, Tranche Salvador, Gómez Juan, Alonso Belén, Iglesias Sara, Reguero Julián R, López-Larrea Carlos, Coto-Segura Pab |
Association between 3'UTR polymorphisms in genes ACVR2A, AGTR1 and RGS2 and preeclampsia. General physiology and biophysics 2018 Mar 37 (2): 185-192. Mendelova Andrea, Holubekova Veronika, Grendar Marian, Zubor Pavol, Svecova Iveta, Loderer Dusan, Snahnicanova Zuzana, Biringer Kamil, Danko Jan, Lasabova Zo |
Analyses of genome wide association data, cytokines, and gene expression in African-Americans with benign ethnic neutropenia. PloS one 2018 13 (3): e0194400. Charles Bashira A, Hsieh Matthew M, Adeyemo Adebowale A, Shriner Daniel, Ramos Edward, Chin Kyung, Srivastava Kshitij, Zakai Neil A, Cushman Mary, McClure Leslie A, Howard Virginia, Flegel Willy A, Rotimi Charles N, Rodgers Griffin |
Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease. European heart journal 2018 Mar . Helgadottir Anna, Sulem Patrick, Thorgeirsson Gudmundur, Gretarsdottir Solveig, Thorleifsson Gudmar, Jensson Brynjar Ö, Arnadottir Gudny A, Olafsson Isleifur, Eyjolfsson Gudmundur I, Sigurdardottir Olof, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Ka |
Incidence of and Risk Factors Associated With Age-Related Macular Degeneration: Four-Year Follow-up From the ALIENOR Study. JAMA ophthalmology 2018 Mar . Saunier Valentine, Merle Bénédicte M J, Delyfer Marie-Noëlle, Cougnard-Grégoire Audrey, Rougier Marie-Bénédicte, Amouyel Philippe, Lambert Jean-Charles, Dartigues Jean-François, Korobelnik Jean-François, Delcourt Céci |
Erlotinib treatment after platinum-based therapy in elderly patients with non-small-cell lung cancer in routine clinical practice - results from the ElderTac study. BMC cancer 2018 Mar 18 (1): 333. Brueckl Wolfgang M, Achenbach H Jost, Ficker Joachim H, Schuette Wolfga |
Sequencing the exons of human glucocorticoid receptor (NR3C1) gene in Han Chinese with high-altitude pulmonary edema. Journal of physiological anthropology 2018 Mar 37 (1): 7. Du Hui, Zhao Jing, Su Zhanhai, Liu Yongnian, Yang Yingzho |
[Nrf2 and Keap1 Abnormalities in 104 Lung Adenocarcinoma Cases and Association with Clinicopathologic Features]. Zhongguo fei ai za zhi = Chinese journal of lung cancer 2018 Mar 21 (3): 241-250. Xiao Yu, Zhu Xiang, Gu Yangchun, Chen Sen, Liang Li, Cao Baosh |
A functional SNP upstream of the ADRB2 gene is associated with COPD. International journal of chronic obstructive pulmonary disease 2018 13 917-925. Li Jin-Xiu, Fu Wei-Ping, Zhang Jing, Zhang Xiao-Hua, Sun Chang, Dai Lu-Ming, Zhong Li, Yu Li, Zhang Ya-Pi |
Single nucleotide polymorphisms in asthma candidate genes TBXA2R , ADAM33 FCER1B and ORMDL3 in Pakistani asthmatics a case control study. Asthma research and practice 2018 4 4. Saba Nusrat, Yusuf Osman, Rehman Sadia, Munir Saeeda, Noor Amna, Saqlain Muhammad, Mansoor Atika, Raja Ghazala Kauk |
N-Acetyltransferase-2 (NAT2) phenotype is influenced by genotype-environment interaction in Ethiopians. European journal of clinical pharmacology 2018 Mar . Aklillu Eleni, Carrillo Juan Antonio, Makonnen Eyasu, Bertilsson Leif, Djordjevic Nata |
Spectrum of CFTR gene sequence variants in a northern Portugal population. Pulmonology 0 24 (1): 3-9. Grangeia A, Alves S, Gonçalves L, Gregório I, Santos A C, Barros H, Barros A, Carvalho F, Moura |
Common ?-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease. PLoS genetics 2018 Mar 14 (3): e1007293. Raffield Laura M, Ulirsch Jacob C, Naik Rakhi P, Lessard Samuel, Handsaker Robert E, Jain Deepti, Kang Hyun M, Pankratz Nathan, Auer Paul L, Bao Erik L, Smith Joshua D, Lange Leslie A, Lange Ethan M, Li Yun, Thornton Timothy A, Young Bessie A, Abecasis Goncalo R, Laurie Cathy C, Nickerson Deborah A, McCarroll Steven A, Correa Adolfo, Wilson James G, , Lettre Guillaume, Sankaran Vijay G, Reiner Alex |
Polymorphisms within RYR3 gene are Associated with Risk and Age at Onset of Hypertension, Diabetes and Alzheimer's Disease. American journal of hypertension 2018 Mar . Gong Shaoqing, Su Brenda Bin, Tovar Hugo, Mao ChunXiang, Gonzalez Valeria, Liu Ying, Lu Yongke, Wang Ke-Sheng, Xu Ch |
A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta. European heart journal 2018 Mar . Bjornsson Thorsteinn, Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Sulem Patrick, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Magnusdottir Audur, Danielsen Ragnar, Sigurdsson Emil L, Adalsteinsdottir Berglind, Gunnarsson Sverrir I, Jonsdottir Ingileif, Arnar David O, Helgason Hrodmar, Gudbjartsson Tomas, Gudbjartsson Daniel F, Thorsteinsdottir Unnur, Holm Hilma, Stefansson Ka |
Endoglin pathway genetic variation in preeclampsia: A validation study in Norwegian and Latina cohorts. Pregnancy hypertension 2017 Nov . Schmella Mandy J, Roberts James M, Conley Yvette P, Ren Dianxu, Storvold Gro L, Ingles Sue A, Wilson Melissa L, Staff Anne Catherine, Hubel Carl |
Association of Smoking and XPG, CYP1A1, OGG1, ERCC5, ERCC1, MMP2, and MMP9 Gene Polymorphisms with the early detection and occurrence of Laryngeal Squamous Carcinoma. Journal of Cancer 2018 9 (6): 968-977. Zhu Yi, Guo Luo, Wang ShengZi, Yu Qun, Lu JianXio |
Genetic variation of CXCR4 and risk of coronary artery disease: epidemiological study and functional validation of CRISPR/Cas9 system. Oncotarget 2018 Mar 9 (18): 14077-14083. Runmin Guo, Jiamei Jiang, Zhiliang Jing, Yonghua Chen, Zhizhou Shi, Guizhou Tao, Shuguang L |
Association analysis of SNPs present in plasma with adverse events and population pharmacokinetics in Chinese sunitinib treated patients with renal cell carcinoma. Oncotarget 2018 Mar 9 (18): 14109-14123. Zhang Yuanyuan, Mai Haixing, Guo Gang, Bi Guofang, Hao Guangtao, Li Yuanyuan, Wang Xiaofang, Cheng Longmei, Wang Jing, Dong Ruihua, Liu Zeyuan, Chen Lijun, Qu Hengy |
Metabolic and genetic markers' associations with elevated levels of alanine aminotransferase in adolescents. Journal of pediatric endocrinology & metabolism : JPEM 2018 Mar 31 (4): 407-414. Ramírez-López Guadalupe, Morán-Villota Segundo, Mendoza-Carrera Francisco, Portilla-de Buen Eliseo, Valles-Sánchez Victoria, Castro-Martínez Xochitl H, Sánchez-Corona José, Salmerón Jor |
Fish intake interacts with TM6SF2 gene variant to affect NAFLD risk: results of a case-control study. European journal of nutrition 2018 Mar . Kalafati I P, Dimitriou M, Borsa D, Vlachogiannakos J, Revenas K, Kokkinos A, Ladas S D, Dedoussis G |
Relation of locus 1p13 rs646776 polymorphism with the risk of preeclampsia. Hypertension in pregnancy 2018 Mar 1-6. Emam Rana H, Ghattas Maivel H, Mesbah Noha M, Abo-Elmatty Dina M, Mehanna Eman |
CD36 gene polymorphism and plasma sCD36 as the risk factor in higher cholesterolemia. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie 2018 Mar . Ra? M E, Safranow K, Garanty-Bogacka B, Dziedziejko V, Kurzawski G, Goschorska M, Kuligowska A, Pauli N, Chlubek |
Pharmacogenetics of vitamin K antagonists and bleeding risk prediction in atrial fibrillation. European journal of clinical investigation 2018 Mar e12929. Serna María José, Rivera-Caravaca José Miguel, Gonzalez-Conejero Rocío, Esteve-Pastor María Asunción, Valdés Mariano, Vicente Vicente, Lip Gregory Y H, Roldán Vanessa, Marín Francis |
NOTCH4 is a possible novel susceptibility gene for dilated cardiomyopathy in the Chinese population: A case-control study. Journal of clinical laboratory analysis 2018 Mar e22436. Shi Xiaoqing, Zhang Yang, Li Bingjie, Peng Mengle, Yuan Yingying, Wang Ximing, Li Xinqiang, Yu Dongze, Li Yongzhe, Qin Dongch |
Significant association between RGS14 rs12654812 and nephrolithiasis risk among Guangxi population in China. Journal of clinical laboratory analysis 2018 Mar e22435. Long Jun, Chen Yang, Lin Haisong, Liao Ming, Li Tianyu, Tong Lei, Wei Suchun, Xian Xiaoying, Zhu Jia, Chen Jianxin, Tian Jiarong, Wang Qiuyan, Mo Zengn |
Uromodulin rs4293393 T>C variation is associated with kidney disease in patients with type 2 diabetes. The Indian journal of medical research 2017 Nov 146 (Supplement): S15-S21. Kumar Vinod, Yadav Ashok Kumar, Kumar Vivek, Bhansali Anil, Jha Vivekana |
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CHL1 gene polymorphisms increase lung cancer susceptibility. Oncotarget 2018 Mar 9 (17): 13545-13550. Tian Wen, Li Xuelian, Ren Yangwu, Yin Zhihua, Quan Xiaowei, Zheng Chang, Zhou Baos |
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