Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 39 Records) |
Query Trace: Sclerosis and GC[original query] |
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Association between -174 interleukin-6 gene polymorphism and biological response to rituximab in several systemic autoimmune diseases. DNA and cell biology 2012 Sep 31 (9): 1486-91. Robledo Gema, Dávila-Fajardo Cristina Lucía, Márquez Ana, Ortego-Centeno Norberto, Callejas Rubio José Luis, de Ramón Garrido Enrique, Sánchez-Román Julio, García-Hernández Francisco J, Ríos-Fernández Raquel, González-Escribano Maria Francisca, Camps García Maria Teresa, Castillo Palma Maria Jesús, Ayala Maria Del Mar, Martín Javi |
Association of common variants in KIF21B and ankylosing spondylitis in a Chinese Han population: a replication study. Immunogenetics 2013 Dec 65 (12): 835-9. Liu Yongchao, Zhang Hua, Li Jiangxia, Zhao Hailing, Xin Qian, Shan Shan, Dang Jie, Bian Xianli, Liu Qi |
Genetic and environmental determinants of 25-hydroxyvitamin D levels in multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England) 2014 Dec . Laursen Julie H, Søndergaard Helle Bach, Albrechtsen Anders, Frikke-Schmidt Ruth, Koch-Henriksen Nils, Soelberg Sørensen Per, Sellebjerg Finn, Oturai Annet |
HFE p.H63D polymorphism does not influence ALS phenotype and survival. Neurobiology of aging 2015 Oct 36 (10): 2906.e7-2906.e11. Chiò Adriano, Mora Gabriele, Sabatelli Mario, Caponnetto Claudia, Lunetta Christian, Traynor Bryan J, Johnson Janel O, Nalls Mike A, Calvo Andrea, Moglia Cristina, Borghero Giuseppe, Monsurrò Maria Rosaria, La Bella Vincenzo, Volanti Paolo, Simone Isabella, Salvi Fabrizio, Logullo Francesco O, Nilo Riva, Giannini Fabio, Mandrioli Jessica, Tanel Raffaella, Murru Maria Rita, Mandich Paola, Zollino Marcella, Conforti Francesca L, Penco Silvana, , , Brunetti Maura, Barberis Marco, Restagno Gabriel |
Association between age at onset of multiple sclerosis and vitamin D level-related factors. Neurology 2015 Oct . Laursen Julie Hejgaard, Søndergaard Helle Bach, Sørensen Per Soelberg, Sellebjerg Finn, Oturai Annette Ba |
Association between the three functional miR-146a single-nucleotide polymorphisms, rs2910164, rs57095329, and rs2431697, and autoimmune disease susceptibility: A meta-analysis. Autoimmunity 2016 Apr 1-8. Park Robin, Lee Won Jin, Ji Jong D |
Sequencing analysis of the human glucocorticoid receptor (NR3C1) gene in multiple sclerosis patients. Journal of the neurological sciences 2016 Apr 363 165-9. Kassi Eva, Semaniakou Anna, Sertedaki Amalia, Evangelopoulos Maria-Eleftheria, Kazazoglou Theodosia, Kominakis Antonios, Sfagos Constantinos, Charmandari Evangelia, Chrousos George P, Moutsatsou Paraske |
Glucocorticoid receptor haplotypes conferring increased sensitivity (BclI and N363S) are associated with faster progression of multiple sclerosis. Journal of neuroimmunology 2016 Oct 299 84-89. Melief Jeroen, Koper Jan W, Endert Erik, Møller Holger J, Hamann Jörg, Uitdehaag Bernard M, Huitinga In |
Vitamin D-binding protein gene polymorphisms are not associated with MS risk in an Italian cohort. Journal of neuroimmunology 2017 Apr 305 92-95. Agliardi Cristina, Guerini Franca Rosa, Zanzottera Milena, Bolognesi Elisabetta, Costa Andrea Saul, Clerici Mar |
Common genetic variation within miR-146a predicts disease onset and relapse in multiple sclerosis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2017 Nov . Zhou Yuan, Chen Ming, Simpson Steve, Lucas Robyn M, Charlesworth Jac C, Blackburn Nicholas, van der Mei Ingrid, Ponsonby Anne-Louise, , Taylor Bruce |
CYP27A1, CYP24A1, and RXR-? Polymorphisms, Vitamin D, and Multiple Sclerosis: a Pilot Study. Journal of molecular neuroscience : MN 2018 Sep 66 (1): 77-84. Agnello Luisa, Scazzone Concetta, Lo Sasso Bruna, Ragonese Paolo, Milano Salvatore, Salemi Giuseppe, Ciaccio Marcel |
STAT4 gene polymorphism in two major autoimmune diseases (multiple sclerosis and juvenile onset systemic lupus erythematosus) and its relation to disease severity. The Egyptian journal of neurology, psychiatry and neurosurgery 2018 54 (1): 16. Nageeb Rania S, Omran Alaa A, Nageeb Ghada S, Yousef Manal A, Mohammad Yassir A A, Fawzy Am |
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases. Amyotrophic lateral sclerosis & frontotemporal degeneration 2018 08 19 (5-6): 426-431. Corrado Lucia, Tiloca Cinzia, Locci Clarissa, Bagarotti Alessandra, Hamzeiy Hamid, Colombrita Claudia, De Marchi Fabiola, Barizzone Nadia, Cotella Diego, Ticozzi Nicola, Mazzini Letizia, Nazli Basak Ayse, Ratti Antonia, Silani Vincenzo, D'alfonso Sand |
The frequency of the C9orf72 expansion in a Brazilian population. Neurobiology of aging 2018 2 66 179.e1-179.e4. Cintra Vívian Pedigone, Bonadia Luciana Cardoso, Andrade Helen Maia T, de Albuquerque Milena, Eusébio Mayara Ferreira, de Oliveira Daniel Sabino, Claudino Rinaldo, Gonçalves Marcus Vinicius Magno, Teixeira Antônio Lúcio, de Godoy Rousseff Prado Laura, de Souza Leonardo Cruz, Dourado Mario Emilio Teixeira, Oliveira Acary Souza Bulle, Tumas Vitor, França Marcondes C, Marques Wils |
Novel SNARE Complex Polymorphisms Associated with Multiple Sclerosis: Signs of Synaptopathy in Multiple Sclerosis. Balkan medical journal 2019 05 36 (3): 174-178. Yal?n Osman Özgür, Gökdo?an Edgünlü Tuba, Karaka? Çelik Sevim, Emre Ufuk, Güne? Ta?k?n, Erdal Yüksel, Ero?lu Ünal Ays |
Exome sequencing of Saudi Arabian patients with ADPKD. Renal failure 2019 9 41 (1): 842-849. Al-Muhanna Fahad A, Al-Rubaish Abdullah M, Vatte Chittibabu, Mohiuddin Shamim Shaikh, Cyrus Cyril, Ahmad Arafat, Shakil Akhtar Mohammed, Albezra Mohammad Ahmad, Alali Rudaynah A, Almuhanna Afnan F, Huang Kai, Wang Lusheng, Al-Kuwaiti Feras, Elsalamouni Tamer S Ahmed, Al Hwiesh Abdullah, Huang Xiaoyan, Keating Brendan, Li Jiankang, Lanktree Matthew B, Al-Ali Amein |
Vitamin D genes influence MS relapses in children. Multiple sclerosis (Houndmills, Basingstoke, England) 2019 May 1352458519845842. Graves Jennifer S, Barcellos Lisa F, Krupp Lauren, Belman Anita, Shao Xiaorong, Quach Hong, Hart Janace, Chitnis Tanuja, Weinstock-Guttman Bianca, Aaen Gregory, Benson Leslie, Gorman Mark, Greenberg Benjamin, Lotze Timothy, Soe Mar, Ness Jayne, Rodriguez Moses, Rose John, Schreiner Teri, Tillema Jan-Mendelt, Waldman Amy, Casper T Charles, Waubant Emmanuel |
Polymorphisms in the CIITA -168A/G (rs3087456) and CIITA +1614G/C (rs4774) may influence severity in multiple sclerosis patients. Arquivos de neuro-psiquiatria 2019 Mar 77 (3): 166-173. Pereira Valéria Coelho Santa Rita, Fontes-Dantas Fabrícia Lima, Paradela Eduardo Ribeiro, Malfetano Fabíola Rachid, Scherpenhuijzen Simone de Souza Batista, Mansur Letícia Fêzer, Luiz Ronir Raggio, Oliveira André Peres De, Farinhas João Gabriel Dib, Maiolino Ângelo, Alves-Leon Soniza Viei |
Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing. Brain and behavior 2019 3 9 (4): e01272. Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor |
The association between repeat number in C9orf72 and phenotypic variability in Turkish patients with frontotemporal lobar degeneration. Neurobiology of aging 2019 1 76 216.e1-216.e7. Erzurumluoglu Ebru, Cilingir Oguz, Ozbabalik Adapinar Belgin Demet, Bilgic Basar, Kocagil Sinem, Ozen Hulya, Durak Aras Beyhan, Yenilmez Cinar, Artan Sevilh |
Identification of GGC repeat expansion in the NOTCH2NLC gene in amyotrophic lateral sclerosis. Neurology 2020 9 95 (24): e3394-e3405. Yuan Yanchun, Liu Zhen, Hou Xuan, Li Wanzhen, Ni Jie, Huang Ling, Hu Yiting, Liu Pan, Hou Xiaorong, Xue Jin, Sun Qiying, Tian Yun, Jiao Bin, Duan Ranhui, Jiang Hong, Shen Lu, Tang Beisha, Wang Junli |
No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers. Neurobiology of aging 2020 9 97 145.e1-145.e4. Koço?lu Cemile, Gossye Helena, Dillen Lubina, Van Mossevelde Sara, De Bleecker Jan L, Vandenberghe Rik, De Deyn Peter P, Sleegers Kristel, Cras Patrick, Engelborghs Sebastiaan, Van Broeckhoven Christine, van der Zee Julie, |
Glucocorticoid receptor mutations and clinical sensitivity to glucocorticoid in Chinese multiple sclerosis patients. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2020 Apr . Song Tian, Chang Haoxiao, Du Li, Yin Linlin, Shi Fudong, Zhang Xing |
Association of Vitamin D Metabolism Gene Polymorphisms with Autoimmunity: Evidence in Population Genetic Studies. International journal of molecular sciences 2020 Dec 21 (24): . Ruiz-Ballesteros Adolfo I, Meza-Meza Mónica R, Vizmanos-Lamotte Barbara, Parra-Rojas Isela, de la Cruz-Mosso Ulis |
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions.
Translational psychiatry 2021 9 11 (1): 451. Reus Lianne M, Jansen Iris E, Mol Merel O, van Ruissen Fred, van Rooij Jeroen, van Schoor Natasja M, Tesi Niccolò, Reinders Marcel J T, Huisman Martijn A, Holstege Henne, Visser Pieter Jelle, de Boer Sterre C M, Hulsman Marc, Ahmad Shahzad, Amin Najaf, Uitterlinden Andre G, Ikram Arfan, van Duijn Cornelia M, Seelaar Harro, Ramakers Inez H G B, Verhey Frans R J, van der Lugt Aad, Claassen Jurgen A H R, Jan Biessels Geert, De Deyn Peter Paul, Scheltens Philip, van der Flier Wiesje M, van Swieten John C, Pijnenburg Yolande A L, van der Lee Sven |
Association of NLRP3 rs35829419 and rs10754558 Polymorphisms With Risks of Autoimmune Diseases: A Systematic Review and Meta-Analysis. Frontiers in genetics 2021 12 690860. Wu Zubo, Wu Suyuan, Liang T |
Combined epigenetic/genetic study identified an ALS age of onset modifier. Acta neuropathologica communications 2021 4 9 (1): 75. Zhang Ming, Xi Zhengrui, Saez-Atienzar Sara, Chia Ruth, Moreno Danielle, Sato Christine, Montazer Haghighi Mahdi, Traynor Bryan J, Zinman Lorne, Rogaeva Ekateri |
Heritability Estimation of Multiple Sclerosis Related Plasma Protein Levels in Sardinian Families with Immunochip Genotyping Data. Life (Basel, Switzerland) 2022 7 12 (7): . Nova Andrea, Baldrighi Giulia Nicole, Fazia Teresa, Graziano Francesca, Saddi Valeria, Piras Marialuisa, Beecham Ashley, McCauley Jacob L, Bernardinelli Lui |
Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots.
Nature communications 2023 2 14 (1): 852. Albiñana Clara, Zhu Zhihong, Borbye-Lorenzen Nis, Boelt Sanne Grundvad, Cohen Arieh S, Skogstrand Kristin, Wray Naomi R, Revez Joana A, Privé Florian, Petersen Liselotte V, Bulik Cynthia M, Plana-Ripoll Oleguer, Musliner Katherine L, Agerbo Esben, Børglum Anders D, Hougaard David M, Nordentoft Merete, Werge Thomas, Mortensen Preben Bo, Vilhjálmsson Bjarni J, McGrath John |
Association between Gastric Cancer and 12 Autoimmune Diseases: A Mendelian Randomization Study. Genes 2023 10 14 (10): . Qi Wei, Ziyu Wang, Xuanyu Liu, Haibin Liang, Lei Ch |
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- Page last updated:Apr 16, 2024
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