Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: Inflammation and MAF[original query] |
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CRP polymorphisms and progression of chronic kidney disease in African Americans. Clinical journal of the American Society of Nephrology : CJASN 2010 Jan 5 (1): 24-33. Hung Adriana M, Crawford Dana C, Griffin Marie R, Brown-Gentry Kristin, Lipkowitz Michael S, Siew Edward D, Cavanaugh Kerri, Lewis Julia B, Ikizler T Alp, |
Genetic associations with C-reactive protein level and white blood cell count in the KARE study.
International journal of immunogenetics 2012 Jul . Kong M, Lee C |
Identifying and testing candidate genetic polymorphisms in the irritable bowel syndrome (IBS): association with TNFSF15 and TNFa. Gut 2013 Jul 62 (7): 985-94. Swan Caroline, Duroudier Nathalie P, Campbell Eugene, Zaitoun Abed, Hastings Margaret, Dukes George E, Cox Joanne, Kelly Fiona M, Wilde Jonathan, Lennon Mark G, Neal Keith R, Whorwell Peter J, Hall Ian P, Spiller Robin |
Inflammation and immune-related candidate gene associations with acute lung injury susceptibility and severity: a validation study. PloS one 2012 7 (12): 12. O'Mahony DS, Glavan BJ, Holden TD, Fong C, Black RA, Rona G, Tejera P, Christiani DC, Wurfel MM |
Phospholipase A2G1B polymorphisms and risk of colorectal neoplasia. International journal of molecular epidemiology and genetics 2013 4 (3): 140-9. Abbenhardt Clare, Poole Elizabeth M, Kulmacz Richard J, Xiao Liren, Curtin Karen, Galbraith Rachel L, Duggan David, Hsu Li, Makar Karen W, Caan Bette J, Koepl Lisel, Owen Robert W, Scherer Dominique, Carlson Christopher S, , Potter John D, Slattery Martha L, Ulrich Cornelia |
Impact of genetic polymorphisms on adenoma recurrence and toxicity in a COX2 inhibitor (celecoxib) trial: results from a pilot study. Pharmacogenetics and genomics 2013 Aug 23 (8): 428-37. Kraus Sarah, Hummler Simone, Toriola Adetunji T, Poole Elizabeth M, Scherer Dominique, Kotzmann Jana, Makar Karen W, Kazanov Dina, Galazan Lior, Naumov Inna, Coghill Anna E, Duggan David, Gigic Biljana, Arber Nadir, Ulrich Cornelia |
Exome sequencing of 75 individuals from multiply affected coeliac families and large scale resequencing follow up. PloS one 2015 10 (1): e0116845. Mistry Vanisha, Bockett Nicholas A, Levine Adam P, Mirza Muddassar M, Hunt Karen A, Ciclitira Paul J, Hummerich Holger, Neuhausen Susan L, Simpson Michael A, Plagnol Vincent, van Heel David |
Quantitative genetics of circulating Dickkopf-related protein 1 (DKK1) in community-based sample of UK twins. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2016 Jan . Prakash J, Williams F M K, Trofimov S, Surdulescu G, Spector T, Livshits |
Investigating the association of rs2910164 with cancer predisposition in an Irish cohort. Endocrine connections 2017 Nov 6 (8): 614-624. McVeigh T P, Mulligan R J, McVeigh U M, Owens P W, Miller N, Bell M, Sebag F, Guerin C, Quill D S, Weidhaas J B, Kerin M J, Lowery A |
Whole genome sequence analyses of brain imaging measures in the Framingham Study. Neurology 2017 12 90 (3): e188-e196. Sarnowski Chloé, Satizabal Claudia L, DeCarli Charles, Pitsillides Achilleas N, Cupples L Adrienne, Vasan Ramachandran S, Wilson James G, Bis Joshua C, Fornage Myriam, Beiser Alexa S, DeStefano Anita L, Dupuis Josée, Seshadri Sudha, , |
Association of TNF-? rs1799964 and IL-1? rs16944 polymorphisms with multiple system atrophy in Chinese Han population. The International journal of neuroscience 2017 Dec 1-16. Zhou Xin, Wang Chunrong, Chen Zhao, Peng Yun, Peng Huirong, Hou Xuan, Ye Wei, Qiu Rong, Xia Kun, Tang Beisha, Jiang Ho |
Next-generation DNA sequencing to identify novel genetic risk factors for cerebral vein thrombosis. Thrombosis research 2018 7 169 76-81. Gorski Marcin M, de Haan Hugoline G, Mancini Ilaria, Lotta Luca A, Bucciarelli Paolo, Passamonti Serena M, Cairo Andrea, Pappalardo Emanuela, van Hylckama Vlieg Astrid, Martinelli Ida, Rosendaal Frits R, Peyvandi Flo |
Utility of new red cell parameters for distinguishing functional iron deficiency from absolute iron deficiency in children with familial Mediterranean fever. International journal of laboratory hematology 2019 1 41 (2): 293-297. Gezgin Y?ld?r?m Deniz, Kaya Zühre, Bakkaloglu Sevcan |
High prevalence of rare FBLIM1 gene variants in an Italian cohort of patients with Chronic Non-bacterial Osteomyelitis (CNO). Pediatric rheumatology online journal 2020 Jul 18 (1): 55. d'Adamo Adamo Pio, Bianco Anna Monica, Ferrara Giovanna, La Bianca Martina, Insalaco Antonella, Tommasini Alberto, Pardeo Manuela, Cattalini Marco, La Torre Francesco, Finetti Martina, Alizzi Clotilde, Simonini Gabriele, Messia Virginia, Pastore Serena, Cimaz Rolando, Gattorno Marco, Taddio Andrea, |
Obesity status modifies the association between rs7556897T>C in the intergenic region SLC19A3-CCL20 and blood pressure in French children. Clinical chemistry and laboratory medicine 2020 4 58 (11): 1819-1827. El Shamieh Said, Stathopoulou Maria G, Bonnefond Amélie, Ndiaye Ndeye Coumba, Lecoeur Cécile, Meyre David, Dadé Sébastien, Chedid Pia, Salami Ali, Shahabi Payman, Dedoussis George V, Froguel Philippe, Visvikis-Siest Soph |
A rare missense variant in the milk fat globule-EGF factor 8 (MFGE8) increases T2DM susceptibility and cardiovascular disease risk with population-specific effects. Acta diabetologica 2020 Feb . Sapkota Bishwa R, Sanghera Dharambir |
Unveiling the genetic variation of severe continuous/mixed-type ossification of the posterior longitudinal ligament by whole-exome sequencing and bioinformatic analysis. The spine journal : official journal of the North American Spine Society 2021 7 21 (11): 1847-1856. Lee Chang-Hyun, Kim Ki Tae, Kim Chi Heon, Lee Eun Young, Lee Sang Gu, Seo Myung-Eui, Kim Ju Han, Chung Chun K |
Genetics of osteopontin in patients with chronic kidney disease: The German Chronic Kidney Disease study. PLoS genetics 2022 4 18 (4): e1010139. Cheng Yurong, Li Yong, Scherer Nora, Grundner-Culemann Franziska, Lehtimäki Terho, Mishra Binisha H, Raitakari Olli T, Nauck Matthias, Eckardt Kai-Uwe, Sekula Peggy, Schultheiss Ulla T, |
Exploring the Neandertal legacy of pancreatic ductal adenocarcinoma risk in Eurasians. Biological research 2023 8 56 (1): 46. Margherita Piccardi, Manuel Gentiluomo, Stefania Bertoncini, Raffaele Pezzilli, Bálint Er?ss, Stefania Bunduc, Faik G Uzunoglu, Renata Talar-Wojnarowska, Tomas Vanagas, Cosimo Sperti, Martin Oliverius, Mateus Nóbrega Aoki, Stefano Ermini, Tamás Hussein, Ugo Boggi, Krzysztof Jamroziak, Evaristo Maiello, Luca Morelli, Ludmila Vodickova, Gregorio Di Franco, Stefano Landi, Andrea Szentesi, Martin Lovecek, Marta Puzzono, Francesca Tavano, Hanneke W M van Laarhoven, Alessandro Zerbi, Beatrice Mohelnikova-Duchonova, Hannah Stocker, Eithne Costello, Gabriele Capurso, Laura Ginocchi, Rita T Lawlor, Giuseppe Vanella, Francesca Bazzocchi, Jakob R Izbicki, Anna Latiano, Bas Bueno-de-Mesquita, Ruggero Ponz de Leon Pisani, Ben Schöttker, Pavel Soucek, Péter Hegyi, Maria Gazouli, Thilo Hackert, Juozas Kupcinskas, Lina Poskiene, Matteo Tacelli, Susanne Roth, Silvia Carrara, Francesco Perri, Viktor Hlavac, George E Theodoropoulos, Olivier R Busch, Andrea Mambrini, Casper H J van Eijck, Paolo Arcidiacono, Aldo Scarpa, Claudio Pasquali, Daniela Basso, Maurizio Lucchesi, Anna Caterina Milanetto, John P Neoptolemos, Giulia Martina Cavestro, Dainius Janciauskas, Xuechen Chen, Roger Chammas, Mara Goetz, Hermann Brenner, Livia Archibugi, Michael Dannemann, Federico Canzian, Sergio Tofanelli, Daniele Cam |
Variants of NOD2 in Leishmania guyanensis-infected patients with cutaneous leishmaniasis and correlations with plasma circulating pro-inflammatory cytokines. PloS one 2023 2 18 (2): e0281814. Mesquita Tirza Gabrielle Ramos de, Junior José do Espírito Santo, Souza Josué Lacerda de, Silva Lener Santos da, Nascimento Tuanny Arruda do, Souza Mara Lúcia Gomes de, Guerra Marcus Vinitius de Farias, Ramasawmy Rajendrana |
Participation of Single-Nucleotide Variants in IFNAR1 and IFNAR2 in the Immune Response against SARS-CoV-2 Infection: A Systematic Review. Pathogens (Basel, Switzerland) 2023 11 12 (11): . María Fernanda López-Bielma, Ramcés Falfán-Valencia, Edgar Abarca-Rojano, Gloria Pérez-Rub |
Polycystic Ovarian Syndrome Physiologic Pathways Implicated Through Clustering of Genetic Loci. The Journal of clinical endocrinology and metabolism 2023 11 . Maria I Stamou, Kirk T Smith, Hyunkyung Kim, Ravikumar Balasubramanian, Kathryn J Gray, Miriam Udl |
Assessment of Stx-1A gene polymorphism (rs1569061) in relation to the development of multiple sclerosis in Egyptian patients. The Egyptian journal of immunology 2024 4 31 (2): 18-27. Christine A Habib, Aziza A El-Sebai, Mohamed M Fouad, Marwa A El-Mohamdy, Amani M Abdel Ghani, Somia A Bawa |
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- Page last updated:Apr 22, 2024
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