Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 55 Records) |
| Query Trace: VCAM1[original query] |
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| Association of alpha-thalassemia, TNF-alpha (-308G>A) and VCAM-1 (c.1238G>C) gene polymorphisms with cerebrovascular disease in a newborn cohort of 411 children with sickle cell anemia. Blood cells, molecules & diseases 2015 Jan 54 (1): 44-50. Belisário André Rolim, Nogueira Frederico Lisboa, Rodrigues Rahyssa Sales, Toledo Nayara Evelin, Cattabriga Ana Luiza Moreira, Velloso-Rodrigues Cibele, Duarte Filipe Otávio Chaves, Silva Célia Maria, Viana Marcos Bora |
| Genetic variation and coronary atherosclerosis in patients with systemic lupus erythematosus. Lupus 2014 Aug 23 (9): 876-80. Chung C P, Solus J F, Oeser A, Li C, Raggi P, Smith J R, Stein C |
| Genetic polymorphisms modify bladder cancer recurrence and survival in a USA population-based prognostic study. BJU international 2015 Feb 115 (2): 238-47. Andrew Angeline S, Gui Jiang, Hu Ting, Wyszynski Asaf, Marsit Carmen J, Kelsey Karl T, Schned Alan R, Tanyos Sam A, Pendleton Eben M, Ekstrom Rebecca M, Li Zhongze, Zens Michael S, Borsuk Mark, Moore Jason H, Karagas Margaret |
| An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3. Arthritis research & therapy 2014 16 (5): 438. Zochling Jane, Newell Felicity, Charlesworth Jac C, Leo Paul, Stankovich Jim, Cortes Adrian, Zhou Yuan, Stevens Wendy, Sahhar Joanne, Roddy Janet, Nash Peter, Tymms Kathleen, Rischmueller Maureen, Lester Sue, Proudman Susanna, Brown Matthew |
| Can Genetic Analysis of Putative Blood Alzheimer's Disease Biomarkers Lead to Identification of Susceptibility Loci? PloS one 2015 10 (12): e0142360. Barber Robert C, Phillips Nicole R, Tilson Jeffrey L, Huebinger Ryan M, Shewale Shantanu J, Koenig Jessica L, Mitchel Jeffrey S, O'Bryant Sid E, Waring Stephen C, Diaz-Arrastia Ramon, Chasse Scott, Wilhelmsen Kirk C, |
| Genotype/allelic combinations as potential predictors of myocardial infarction. Molecular biology reports 2015 Dec . Nasibullin Timur R, Timasheva Yanina R, Sadikova Regina I, Tuktarova Ilsiyar A, Erdman Vera V, Nikolaeva Irina E, Sabo Jan, Kruzliak Peter, Mustafina Olga |
| Interaction between arsenic exposure from drinking water and genetic polymorphisms on cardiovascular disease in Bangladesh: a prospective case-cohort study. Environmental health perspectives 2015 May 123 (5): 451-7. Wu Fen, Jasmine Farzana, Kibriya Muhammad G, Liu Mengling, Cheng Xin, Parvez Faruque, Islam Tariqul, Ahmed Alauddin, Rakibuz-Zaman Muhammad, Jiang Jieying, Roy Shantanu, Paul-Brutus Rachelle, Slavkovich Vesna, Islam Tariqul, Levy Diane, VanderWeele Tyler J, Pierce Brandon L, Graziano Joseph H, Ahsan Habibul, Chen |
| Genetics in Sjögren Syndrome. Rheumatic diseases clinics of North America 2016 Aug 42 (3): 435-47. Reksten Tove Ragna, Lessard Christopher J, Sivils Kathy |
| Genetic Basis of Irritant Susceptibility in Health Care Workers. Journal of occupational and environmental medicine 2016 08 58 (8): 753-9. Yucesoy Berran, Talzhanov Yerkebulan, Barmada M Michael, Johnson Victor J, Kashon Michael L, Baron Elma, Wilson Nevin W, Frye Bonnie, Wang Wei, Fluharty Kara, Gharib Rola, Meade Jean, Germolec Dori, Luster Michael I, Nedorost Sus |
| Single nucleotide polymorphisms of the DGKB and VCAM1 genes are associated with granulocyte colony stimulating factor-mediated peripheral blood stem cell mobilization. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis 2016 Oct . Mishima Seiji, Matsuda Chikashi, Ishihara Tomoko, Nagase Mayumi, Taketani Takeshi, Nagai Atsus |
| Gene variants of adhesion molecules act as modifiers of disease severity in MS. Neurology(R) neuroimmunology & neuroinflammation 2017 Jul 4 (4): e350. Dardiotis Efthimios, Panayiotou Elena, Provatas Antonios, Christodoulou Kyproula, Hadjisavvas Andreas, Antoniades Athos, Lourbopoulos Athanasios, Pantzaris Marios, Grigoriadis Nikolaos, Hadjigeorgiou Georgios M, Kyriakides Theodor |
| Genetic determinants of essential hypertension in the population of Tatars from Russia. Journal of hypertension 2017 05 35 Suppl 1 S16-S23. Timasheva Yanina, Nasibullin Timur, Imaeva Elvira, Erdman Vera, Tuktarova Ilsiyar, Mustafina Ol |
| Elevated EBNA-1 IgG in MS is associated with genetic MS risk variants. Neurology(R) neuroimmunology & neuroinflammation 2017 Nov 4 (6): e406. Kreft Karim L, Van Nierop Gijsbert P, Scherbeijn Sandra M J, Janssen Malou, Verjans Georges M G M, Hintzen Rogier |
| Integrated Multiomics Approach to Identify Genetic Underpinnings of Heart Failure and Its Echocardiographic Precursors: Framingham Heart Study. Circulation. Genomic and precision medicine 2019 11 12 (12): e002489. Andersson Charlotte, Lin Honghuang, Liu Chunyu, Levy Daniel, Mitchell Gary F, Larson Martin G, Vasan Ramachandran |
| The Role of Inducible NOS2 Gene Polymorphism in the Development of Essential Arterial Hypertension. Bulletin of experimental biology and medicine 2019 11 168 (1): 79-83. Topchieva L V, Balan O V, Korneeva V A, Malysheva I |
| Gene variants of adhesion molecules predispose to MS: A case-control study. Neurology. Genetics 2019 Feb 5 (1): e304. Dardiotis Efthimios, Panayiotou Elena, Siokas Vasileios, Aloizou Athina-Maria, Christodoulou Kyproula, Hadjisavvas Andreas, Pantzaris Marios, Grigoriadis Nikolaos, Hadjigeorgiou Georgios M, Kyriakides Theodor |
| Biomarkers and genetic modulators of cerebral vasculopathy in sub-Saharan ancestry children with sickle cell anemia. Blood cells, molecules & diseases 2020 Jul 83 102436. Silva Marisa, Vargas Sofia, Coelho Andreia, Ferreira Emanuel, Mendonça Joana, Vieira Luís, Maia Raquel, Dias Alexandra, Ferreira Teresa, Morais Anabela, Soares Isabel Mota, Lavinha João, Silva Rita, Kjöllerström Paula, Faustino Pau |
| A Comparative Analysis of the Lipoprotein(a) and Low-Density Lipoprotein Proteomic Profiles Combining Mass Spectrometry and Mendelian Randomization. CJC open 2021 5 3 (4): 450-459. Bourgeois Raphaëlle, Girard Arnaud, Perrot Nicolas, Guertin Jakie, Mitchell Patricia L, Couture Christian, Gotti Clarisse, Bourassa Sylvie, Poggio Paolo, Mass Elvira, Capoulade Romain, Scipione Corey A, Després Audrey-Anne, Couture Patrick, Droit Arnaud, Pibarot Philippe, Boffa Michael B, Thériault Sébastien, Koschinsky Marlys L, Mathieu Patrick, Arsenault Benoit |
| The relationship of the carriership of allelic variations in rs2228145 (A > C) of the IL6R gene with the levels of VCAM1 and ICAM1 gene transcripts in patients with essential hypertension. Vavilovskii zhurnal genetiki i selektsii 2020 Feb 24 (1): 96-101. Topchieva L V, Korneva V A, Kurbatova I |
| Association of arsenic-induced cardiovascular disease susceptibility with genetic polymorphisms. Scientific reports 2021 Mar 11 (1): 6263. Al-Forkan Mohammad, Wali Fahmida Binta, Khaleda Laila, Alam Md Jibran, Chowdhury Rahee Hasan, Datta Amit, Rahman Md Zillur, Hosain Nazmul, Maruf Mohammad Fazle, Chowdhury Muhammad Abdul Quaium, Hasan N K M Mirazul, Shawon Injamamul Ismail, Raqib Rubha |
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.
Nature communications 2021 (1): 1258. Gharahkhani Puya, Jorgenson Eric, Hysi Pirro, Khawaja Anthony P, Pendergrass Sarah, Han Xikun, Ong Jue Sheng, Hewitt Alex W, Segrè Ayellet V, Rouhana John M, Hamel Andrew R, Igo Robert P, Choquet Helene, Qassim Ayub, Josyula Navya S, Cooke Bailey Jessica N, Bonnemaijer Pieter W M, Iglesias Adriana, Siggs Owen M, Young Terri L, Vitart Veronique, Thiadens Alberta A H J, Karjalainen Juha, Uebe Steffen, Melles Ronald B, Nair K Saidas, Luben Robert, Simcoe Mark, Amersinghe Nishani, Cree Angela J, Hohn Rene, Poplawski Alicia, Chen Li Jia, Rong Shi-Song, Aung Tin, Vithana Eranga Nishanthie, , , , , , , , Tamiya Gen, Shiga Yukihiro, Yamamoto Masayuki, Nakazawa Toru, Currant Hannah, Birney Ewan, Wang Xin, Auton Adam, Lupton Michelle K, Martin Nicholas G, Ashaye Adeyinka, Olawoye Olusola, Williams Susan E, Akafo Stephen, Ramsay Michele, Hashimoto Kazuki, Kamatani Yoichiro, Akiyama Masato, Momozawa Yukihide, Foster Paul J, Khaw Peng T, Morgan James E, Strouthidis Nicholas G, Kraft Peter, Kang Jae H, Pang Chi Pui, Pasutto Francesca, Mitchell Paul, Lotery Andrew J, Palotie Aarno, van Duijn Cornelia, Haines Jonathan L, Hammond Chris, Pasquale Louis R, Klaver Caroline C W, Hauser Michael, Khor Chiea Chuen, Mackey David A, Kubo Michiaki, Cheng Ching-Yu, Craig Jamie E, MacGregor Stuart, Wiggs Janey |
| Sex-specific association between inflammation and endothelial function relevant gene and vulnerable carotid plaque. Frontiers in physiology 2022 9 13 977578. Li Jie, Zhang Ping, Yi Xingyang, Luo Hua, Yu Ming, Chen Hong, Wang Ch |
| Genetic modulation of anemia severity, hemolysis level, and hospitalization rate in Angolan children with Sickle Cell Anemia. Molecular biology reports 2022 Sep . Germano Isabel, Santos Brígida, Delgadinho Mariana, Ginete Catarina, Lopes Pedro, Arez Ana Paula, Brito Miguel, Faustino Pau |
| Bioinformatics Analysis Revealing the Correlation between NF-?B Signaling Pathway and Immune Infiltration in Gastric Cancer. Computational and mathematical methods in medicine 2022 8 2022 5385456. Chen Qiuxiang, Du Xiaojing, Ruan Pengcheng, Ye Yumei, Zheng Jin, Hu Sunku |
| An immune-related gene prognostic risk index for pancreatic adenocarcinoma. Frontiers in immunology 2022 8 13 945878. Su Yang, Qi Ruoshan, Li Lanying, Wang Xu, Li Sijin, Zhao Xuan, Hou Rui, Ma Wen, Liu Dan, Zheng Junnian, Shi Mi |
| Multi-ancestry genome-wide association study of asthma exacerbations.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2022 06 33 (6): e13802. Herrera-Luis Esther, Ortega Victor E, Ampleford Elizabeth J, Sio Yang Yie, Granell Raquel, de Roos Emmely, Terzikhan Natalie, Vergara Ernesto Elorduy, Hernandez-Pacheco Natalia, Perez-Garcia Javier, Martin-Gonzalez Elena, Lorenzo-Diaz Fabian, Hashimoto Simone, Brinkman Paul, , Jorgensen Andrea L, Yan Qi, Forno Erick, Vijverberg Susanne J, Lethem Ryan, Espuela-Ortiz Antonio, Gorenjak Mario, Eng Celeste, González-Pérez Ruperto, Hernández-Pérez José M, Poza-Guedes Paloma, Sardón Olaia, Corcuera Paula, Hawkins Greg A, Marsico Annalisa, Bahmer Thomas, Rabe Klaus F, Hansen Gesine, Kopp Matthias Volkmar, Rios Raimon, Cruz Maria Jesus, González-Barcala Francisco-Javier, Olaguibel José María, Plaza Vicente, Quirce Santiago, Canino Glorisa, Cloutier Michelle, Del Pozo Victoria, Rodriguez-Santana Jose R, Korta-Murua Javier, Villar Jesús, Poto?nik Uroš, Figueiredo Camila, Kabesch Michael, Mukhopadhyay Somnath, Pirmohamed Munir, Hawcutt Daniel B, Melén Erik, Palmer Colin N, Turner Steve, Maitland-van der Zee Anke H, von Mutius Erika, Celedón Juan C, Brusselle Guy, Chew Fook Tim, Bleecker Eugene, Meyers Deborah, Burchard Esteban G, Pino-Yanes Mar |
| Protein Network Analysis of Whole Exome Sequencing of Severe Preeclampsia. Frontiers in genetics 2022 6 12 765985. Schuster Jessica, Tollefson George A, Zarate Valeria, Agudelo Anthony, Stabila Joan, Ragavendran Ashok, Padbury James, Uzun Alp |
| Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature 2022 10 611 (7934): 115-123. Mishra Aniket, Malik Rainer, Hachiya Tsuyoshi, Jürgenson Tuuli, Namba Shinichi, Posner Daniel C, Kamanu Frederick K, Koido Masaru, Le Grand Quentin, Shi Mingyang, He Yunye, Georgakis Marios K, Caro Ilana, Krebs Kristi, Liaw Yi-Ching, Vaura Felix C, Lin Kuang, Winsvold Bendik Slagsvold, Srinivasasainagendra Vinodh, Parodi Livia, Bae Hee-Joon, Chauhan Ganesh, Chong Michael R, Tomppo Liisa, Akinyemi Rufus, Roshchupkin Gennady V, Habib Naomi, Jee Yon Ho, Thomassen Jesper Qvist, Abedi Vida, Cárcel-Márquez Jara, Nygaard Marianne, Leonard Hampton L, Yang Chaojie, Yonova-Doing Ekaterina, Knol Maria J, Lewis Adam J, Judy Renae L, Ago Tetsuro, Amouyel Philippe, Armstrong Nicole D, Bakker Mark K, Bartz Traci M, Bennett David A, Bis Joshua C, Bordes Constance, Børte Sigrid, Cain Anael, Ridker Paul M, Cho Kelly, Chen Zhengming, Cruchaga Carlos, Cole John W, de Jager Phil L, de Cid Rafael, Endres Matthias, Ferreira Leslie E, Geerlings Mirjam I, Gasca Natalie C, Gudnason Vilmundur, Hata Jun, He Jing, Heath Alicia K, Ho Yuk-Lam, Havulinna Aki S, Hopewell Jemma C, Hyacinth Hyacinth I, Inouye Michael, Jacob Mina A, Jeon Christina E, Jern Christina, Kamouchi Masahiro, Keene Keith L, Kitazono Takanari, Kittner Steven J, Konuma Takahiro, Kumar Amit, Lacaze Paul, Launer Lenore J, Lee Keon-Joo, Lepik Kaido, Li Jiang, Li Liming, Manichaikul Ani, Markus Hugh S, Marston Nicholas A, Meitinger Thomas, Mitchell Braxton D, Montellano Felipe A, Morisaki Takayuki, Mosley Thomas H, Nalls Mike A, Nordestgaard Børge G, O'Donnell Martin J, Okada Yukinori, Onland-Moret N Charlotte, Ovbiagele Bruce, Peters Annette, Psaty Bruce M, Rich Stephen S, Rosand Jonathan, Sabatine Marc S, Sacco Ralph L, Saleheen Danish, Sandset Else Charlotte, Salomaa Veikko, Sargurupremraj Muralidharan, Sasaki Makoto, Satizabal Claudia L, Schmidt Carsten O, Shimizu Atsushi, Smith Nicholas L, Sloane Kelly L, Sutoh Yoichi, Sun Yan V, Tanno Kozo, Tiedt Steffen, Tatlisumak Turgut, Torres-Aguila Nuria P, Tiwari Hemant K, Trégouët David-Alexandre, Trompet Stella, Tuladhar Anil Man, Tybjærg-Hansen Anne, van Vugt Marion, Vibo Riina, Verma Shefali S, Wiggins Kerri L, Wennberg Patrik, Woo Daniel, Wilson Peter W F, Xu Huichun, Yang Qiong, Yoon Kyungheon, , , , , , , , , , , , , , , , Millwood Iona Y, Gieger Christian, Ninomiya Toshiharu, Grabe Hans J, Jukema J Wouter, Rissanen Ina L, Strbian Daniel, Kim Young Jin, Chen Pei-Hsin, Mayerhofer Ernst, Howson Joanna M M, Irvin Marguerite R, Adams Hieab, Wassertheil-Smoller Sylvia, Christensen Kaare, Ikram Mohammad A, Rundek Tatjana, Worrall Bradford B, Lathrop G Mark, Riaz Moeen, Simonsick Eleanor M, Kõrv Janika, França Paulo H C, Zand Ramin, Prasad Kameshwar, Frikke-Schmidt Ruth, de Leeuw Frank-Erik, Liman Thomas, Haeusler Karl Georg, Ruigrok Ynte M, Heuschmann Peter Ulrich, Longstreth W T, Jung Keum Ji, Bastarache Lisa, Paré Guillaume, Damrauer Scott M, Chasman Daniel I, Rotter Jerome I, Anderson Christopher D, Zwart John-Anker, Niiranen Teemu J, Fornage Myriam, Liaw Yung-Po, Seshadri Sudha, Fernández-Cadenas Israel, Walters Robin G, Ruff Christian T, Owolabi Mayowa O, Huffman Jennifer E, Milani Lili, Kamatani Yoichiro, Dichgans Martin, Debette Stephan |
| Gata2 Noncoding Genetic Variation as a Determinant of Hematopoietic Stem/Progenitor Cell Mobilization Efficiency. Blood advances 2023 10 . Alexandra A Soukup, Emery H Bresni |
| The influence of 4G/5G polymorphism in the plasminogen-activator-inhibitor-1 promoter on COVID-19 severity and endothelial dysfunction. Frontiers in immunology 2024 9 15 1445294. Tetiana Yatsenko, Ricardo Rios, Tatiane Nogueira, Yousef Salama, Satoshi Takahashi, Eisuke Adachi, Yoko Tabe, Nobutaka Hattori, Taro Osada, Toshio Naito, Kazuhisa Takahashi, Koichi Hattori, Beate Heiss |
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