HuGE Literature Finder
Records 1-30
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Meta-analysis of FOXP3 gene rs3761548 and rs2232365 polymorphism and multiple sclerosis susceptibility.
Medicine 2019 Sep 98 (38): e17224. Zhang Yijian, Zhang Junxin, Liu Hao, He Fan, Chen Angela, Yang Huilin, Pi B |
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Genetic polymorphisms and epigenetic regulation of survivin encoding gene, BIRC5, in multiple sclerosis patients.
BMC immunology 2019 Aug 20 (1): 30. Rahban Dariush, Mohammadi Forogh, Alidadi Mehdi, Ghantabpour Taha, Kheyli Pedram Abbasi Ghasem, Ahmadi Maj |
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Next-generation sequencing identifies contribution of both class I and II HLA genes on susceptibility of multiple sclerosis in Japanese.
Journal of neuroinflammation 2019 Aug 16 (1): 162. Ogawa Kotaro, Okuno Tatsusada, Hosomichi Kazuyoshi, Hosokawa Akiko, Hirata Jun, Suzuki Ken, Sakaue Saori, Kinoshita Makoto, Asano Yoshihiro, Miyamoto Katsuichi, Inoue Ituro, Kusunoki Susumu, Okada Yukinori, Mochizuki Hide |
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The rs3761548 FOXP3 variant is associated with multiple sclerosis and transforming growth factor ß1 levels in female patients.
Inflammation research : official journal of the European Histamine Research Society ... [et al.] 2019 Aug . Flauzino Tamires, Alfieri Daniela Frizon, de Carvalho Jennings Pereira Wildea Lice, Oliveira Sayonara Rangel, Kallaur Ana Paula, Lozovoy Marcell Alysson Batisti, Kaimen-Maciel Damacio Ramón, de Oliveira Karen Brajão, Simão Andrea Name Colado, Reiche Edna Maria Visso |
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Therapeutic efficacy of dimethyl fumarate in relapsing-remitting multiple sclerosis associates with ROS pathway in monocytes.
Nature communications 2019 Jul 10 (1): 3081. Carlström Karl E, Ewing Ewoud, Granqvist Mathias, Gyllenberg Alexandra, Aeinehband Shahin, Enoksson Sara Lind, Checa Antonio, Badam Tejaswi V S, Huang Jesse, Gomez-Cabrero David, Gustafsson Mika, Al Nimer Faiez, Wheelock Craig E, Kockum Ingrid, Olsson Tomas, Jagodic Maja, Piehl Fredr |
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Association of SHMT1, MAZ, ERG, and L3MBTL3 Gene Polymorphisms with Susceptibility to Multiple Sclerosis.
Biochemical genetics 2019 Jun 57 (3): 355-370. Nazari Mehrabani Seyede Zahra, Shushizadeh Mohammad Hossein, Abazari Mohammad Foad, Nouri Aleagha Maryam, Ardalan Abbas, Abdollahzadeh Rasoul, Azarnezhad Asa |
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Relationship between Multiple Sclerosis-Associated
Cells 2019 Jun 8 (6): . Buhelt Sophie, Søndergaard Helle Bach, Oturai Annette, Ullum Henrik, von Essen Marina Rode, Sellebjerg Fi |
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A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis.
Nature communications 2019 May 10 (1): 2236. Authors are not available |
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Association between polymorphisms of a folate - homocysteine - methionine - SAM metabolising enzyme gene and multiple sclerosis in a Polish population.
Neurologia i neurochirurgia polska 2019 May . Chorazy Monika, Wawrusiewicz-Kurylonek Natalia, Goscik Joanna, Posmyk Renata, Czarnowska Agata, Wiesik Marta, Kapica-Topczewska Katarzyna, Kretowski Adam Jacek, Kochanowicz Jan, Kulakowska Ali |
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HLA-alleles class I and II associated with genetic susceptibility to neuromyelitis optica in Brazilian patients.
Arquivos de neuro-psiquiatria 2019 May 77 (4): 239-247. Kay Cláudia Suemi Kamoi, Scola Rosana Herminia, Arndt Raquel Cristina, Lorenzoni Paulo José, Werneck Lineu Ces |
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Matrix metalloproteases 9 rs3918242 gene polymorphism and serum vit D in MS Egyptian patients.
Multiple sclerosis and related disorders 2019 May 32 103-106. Ibrahim Iman, Wassefy Mona El, Metwally Shereen Salah, Elmenshawi Ibrah |
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MAPK pathway and B cells overactivation in multiple sclerosis revealed by phosphoproteomics and genomic analysis.
Proceedings of the National Academy of Sciences of the United States of America 2019 Apr . Kotelnikova Ekaterina, Kiani Narsis A, Messinis Dimitris, Pertsovskaya Inna, Pliaka Vicky, Bernardo-Faura Marti, Rinas Melanie, Vila Gemma, Zubizarreta Irati, Pulido-Valdeolivas Irene, Sakellaropoulos Theodore, Faigle Wolfgang, Silberberg Gilad, Masso Mar, Stridh Pernilla, Behrens Janina, Olsson Tomas, Martin Roland, Paul Friedemann, Alexopoulos Leonidas G, Saez-Rodriguez Julio, Tegner Jesper, Villoslada Pab |
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Effect of age at puberty on risk of multiple sclerosis: A mendelian randomization study.
Neurology 2019 Mar . Harroud Adil, Morris John A, Forgetta Vincenzo, Mitchell Ruth, Smith George Davey, Sawcer Stephen J, Richards J Bre |
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IL-6, IL-12, and IL-23 STAT-Pathway Genetic Risk and Responsiveness of Lymphocytes in Patients with Multiple Sclerosis.
Cells 2019 Mar 8 (3): . von Essen Marina R, Søndergaard Helle B, Petersen Eva R S, Sellebjerg Fi |
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IL12B gene polymorphisms have sex-specific effects in relapsing-remitting multiple sclerosis.
Acta neurologica Belgica 2019 Mar 119 (1): 83-93. Miteva Lyuba, Trenova Anastasiya, Slavov Georgi, Stanilova Spas |
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MALAT1 Genomic Variants and Risk of Multiple Sclerosis.
Immunological investigations 2019 Mar 1-6. Eftekharian Mohammad Mahdi, Noroozi Rezvan, Komaki Alireza, Mazdeh Mehrdokht, Ghafouri-Fard Soudeh, Taheri Mohamm |
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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 |
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The association of rs703842 variants in CYP27B1 with multiple sclerosis susceptibility is influenced by the HLA-DRB1*15:01 allele in Slovaks.
Journal of neuroimmunology 2019 Mar 330 123-129. Cierny Daniel, Michalik Jozef, Dubovan Peter, Škerenová Mária, Javor Juraj, Kurca Egon, Dobrota Dušan, Lehotský J |
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A genetic variant associated with multiple sclerosis inversely affects the expression of CD58 and microRNA-548ac from the same gene.
PLoS genetics 2019 Feb 15 (2): e1007961. Hecker Michael, Boxberger Nina, Illner Nicole, Fitzner Brit, Schröder Ina, Winkelmann Alexander, Dudesek Ales, Meister Stefanie, Koczan Dirk, Lorenz Peter, Thiesen Hans-Jürgen, Zettl Uwe Kla |
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Familial multiple sclerosis in a Brazilian sample: Is HLA-DR15 involved in susceptibility to the disease?
Journal of neuroimmunology 2019 Feb 330 74-80. da Silva Bernardes Melina, Antão Paiva Carmen Lucia, Ribeiro Paradela Eduardo, Papais Alvarenga Marcos, Ferreira Pereira Fernanda, Vasconcelos Claudia Cristina, Papais Alvarenga Regina Mar |
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GAS5 genomic variants and risk of multiple sclerosis.
Neuroscience letters 2019 Feb 701 54-57. Mahdi Eftekharian Mohammad, Noroozi Rezvan, Komaki Alireza, Mazdeh Mehrdokht, Taheri Mohammad, Ghafouri-Fard Soud |
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Lipid-related genetic polymorphisms significantly modulate the association between lipids and disability progression in multiple sclerosis.
Journal of neurology, neurosurgery, and psychiatry 2019 Feb . Zhang Yan, Zhou Yuan, van der Mei Ingrid A F, Simpson Steve, Ponsonby Anne-Louise, Lucas Robyn M, Tettey Prudence, Charlesworth Jac, Kostner Karam, Taylor Bruce V, |
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Replication study of GWAS risk loci in Greek multiple sclerosis patients.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2019 Feb 40 (2): 253-260. Hadjigeorgiou Georgios M, Kountra Persia-Maria, Koutsis Georgios, Tsimourtou Vana, Siokas Vasileios, Dardioti Maria, Rikos Dimitrios, Marogianni Chrysoula, Aloizou Athina-Maria, Karadima Georgia, Ralli Styliani, Grigoriadis Nikolaos, Bogdanos Dimitrios, Panas Marios, Dardiotis Efthimi |
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The combined effect of IL-17F and CCL20 gene polymorphism in susceptibility to multiple sclerosis in Egypt.
Gene 2019 Feb 685 164-169. El Sharkawi Fathia Z, Ali Sahar A, Hegazy Mohamed I, Atya Hanaa |
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Admixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry.
PLoS genetics 2019 Jan 15 (1): e1007808. Chi Calvin, Shao Xiaorong, Rhead Brooke, Gonzales Edlin, Smith Jessica B, Xiang Anny H, Graves Jennifer, Waldman Amy, Lotze Timothy, Schreiner Teri, Weinstock-Guttman Bianca, Aaen Gregory, Tillema Jan-Mendelt, Ness Jayne, Candee Meghan, Krupp Lauren, Gorman Mark, Benson Leslie, Chitnis Tanuja, Mar Soe, Belman Anita, Casper Theron Charles, Rose John, Moodley Manikum, Rensel Mary, Rodriguez Moses, Greenberg Benjamin, Kahn Llana, Rubin Jennifer, Schaefer Catherine, Waubant Emmanuelle, Langer-Gould Annette, Barcellos Lisa |
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Association Between IL7R Promoter Polymorphisms and Multiple Sclerosis in Turkish Population.
Journal of molecular neuroscience : MN 2019 Jan 67 (1): 38-47. Simsek Hasan, Geckin Hikmet, Sensoz Nilay Padir, List Edward O, Arman Ahm |
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[Associations of single nucleotide polymorphisms of KIF1B gene with the severity of clinical manifestations of multiple sclerosis].
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2019 119 (10. Vyp. 2): 58-62. Arbusova E E, Selyanina N V, Karakulova Yu |
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Novel SNARE Complex Polymorphisms Associated with Multiple Sclerosis: Signs of Synaptopathy in Multiple Sclerosis
Balkan medical journal 2019 05 36 (3): 174-178. Yalin Osman Özgür, Gökdogan Edgünlü Tuba, Karakas Çelik Sevim, Emre Ufuk, Günes Taskin, Erdal Yüksel, Eroglu Ünal Ays |
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Relationship between genetic polymorphisms MTHFR (C677T, A1298C), MTR (A2756G) and MTRR (A66G) genes and multiple sclerosis: a case-control study.
Folia neuropathologica 2019 57 (1): 36-40. Cakina Suat, Ocak Ozgul, Ozkan Adile, Yucel Selma, Ozisik Karaman Handan Is |
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A genetic link between CXCR5 and IL2RA gene polymorphisms and susceptibility to multiple sclerosis.
Neurological research 2018 Dec 40 (12): 1040-1047. Xia Zong-Li, Qin Qing-Mei, Zhao Qing-Yi |
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Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk.
Cell 2018 Nov 175 (6): 1679-1687.e7. , |
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Genetic Variation in Intergenic and Exonic miRNA Sequence and Risk of Multiple Sclerosis in the Isfahan Patients.
Iranian journal of allergy, asthma, and immunology 2018 Oct 17 (5): 477-484. Golshani Zeynab, Hojati Zohreh, Sharifzadeh Ali, Shaygannejad Vahid, Jafarinia Mojta |
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Association of nod-like receptor protein-3 single nucleotide gene polymorphisms and expression with the susceptibility to relapsing-remitting multiple sclerosis.
International journal of immunogenetics 2018 Sep . Imani Danyal, Azimi Amirreza, Salehi Zahra, Rezaei Nima, Emamnejad Rahimeh, Sadr Maryam, Izad Mary |
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CYP27A1, CYP24A1, and RXR-a 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 |
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Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course.
Journal of neuroinflammation 2018 Sep 15 (1): 265. Gil-Varea Elia, Urcelay Elena, Vilariño-Güell Carles, Costa Carme, Midaglia Luciana, Matesanz Fuencisla, Rodríguez-Antigüedad Alfredo, Oksenberg Jorge, Espino-Paisan Laura, Dessa Sadovnick A, Saiz Albert, Villar Luisa M, García-Merino Juan Antonio, Ramió-Torrentà Lluís, Triviño Juan Carlos, Quintana Ester, Robles René, Sánchez-López Antonio, Arroyo Rafael, Alvarez-Cermeño Jose C, Vidal-Jordana Angela, Malhotra Sunny, Fissolo Nicolas, Montalban Xavier, Comabella Manu |
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Mitochondrial DNA G15927A and G15928A variations in patients with multiple sclerosis.
Multiple sclerosis and related disorders 2018 Sep 27 9-12. Andalib Sasan, Talebi Mahnaz, Sakhinia Ebrahim, Farhoudi Mehdi, Sadeghi-Bazargani Homayoun, Masoudian Nooshin, Michel Tanja M, Vafaee Manouchehr Seyedi, Gjedde Albe |
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Polymorphisms in the angiotensin I converting enzyme (ACE) gene are associated with multiple sclerosis risk and response to Interferon-? treatment.
International immunopharmacology 2018 Sep 64 275-279. Yaeghmaie Rana, Ghafouri-Fard Soudeh, Noroozi Rezvan, Tavakoli Fatemeh, Taheri Mohammad, Ayatollahi Seyed Abdulmaj |
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Absence of the tag polymorphism for the risk haplotype HLA-DR2 for multiple sclerosis in Wixárika subjects from Mexico.
Immunogenetics 2018 Aug 70 (8): 547-551. González-Enríquez G V, Torres-Mendoza B M, Márquez-Pedroza J, Macías-Islas M A, Ortiz G G, Cruz-Ramos J |
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Association of interleukin 6, interleukin 7 receptor alpha, and interleukin 12B gene polymorphisms with multiple sclerosis.
Acta neurologica Belgica 2018 Aug . Benešová Yvonne, Vašk? Anna, Bienertová-Vašk? Jul |
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Gender-Specific Association of Leptin and Adiponectin Genes With Multiple Sclerosis.
The American journal of the medical sciences 2018 Aug 356 (2): 159-167. Yousefian Marziyeh, Nemati Reza, Daryabor Gholamreza, Gholijani Naser, Nikseresht Alireza, Borhani-Haghighi Afshin, Kamali-Sarvestani Eskand |
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HLA-DRB1 polymorphism and susceptibility to multiple sclerosis in the Middle East North Africa region: A systematic review and meta-analysis.
Journal of neuroimmunology 2018 Aug 321 117-124. Mohajer Bahram, Abbasi Nooshin, Pishgar Farhad, Abdolalizadeh Amirhussein, Ebrahimi Hedyeh, Razaviyoun Taraneh, Mohebbi Farnam, Eskandarieh Sharareh, Sahraian Mohammad A |
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No C9orf72 repeat expansion in patients with primary progressive multiple sclerosis.
Multiple sclerosis and related disorders 2018 Aug 25 192-195. Tiloca Cinzia, Sorosina Melissa, Esposito Federica, Peroni Silvia, Colombrita Claudia, Ticozzi Nicola, Ratti Antonia, Boneschi Filippo Martinelli, Silani Vincen |
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Association between miRNA-146a and Polymorphisms of its Target Gene, IRAK1, Regarding Susceptibility to and Clinical Features of Systemic Lupus Erythematous and Multiple Sclerosis.
Laboratory medicine 2018 Jul . Labib Dalia A, Shaker Olfat G, El Refai Rasha M, Ghoniem Shada A, Elmazny Al |
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Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis.
Annals of neurology 2018 Jun . Jia Xiaoming, Madireddy Lohith, Caillier Stacy, Santaniello Adam, Esposito Federica, Comi Giancarlo, Stuve Olaf, Zhou Yuan, Taylor Bruce, Kilpatrick Trevor, Martinelli-Boneschi Filippo, Cree Bruce A C, Oksenberg Jorge R, Hauser Stephen L, Baranzini Sergio |
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HLA-G gene polymorphism and soluble HLA-G serum level in patients with multiple sclerosis.
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 2018 Jun 126 (6): 538-539. Jahanbani-Ardakani Hamidreza, Alsahebfosoul Fereshteh, Etemadifar Masoud, Salehi Rasoul, Eskandari Nahid, Abtahi Seyed-Hosse |
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A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica.
Nature communications 2018 May 9 (1): 1929. Estrada Karol, Whelan Christopher W, Zhao Fengmei, Bronson Paola, Handsaker Robert E, Sun Chao, Carulli John P, Harris Tim, Ransohoff Richard M, McCarroll Steven A, Day-Williams Aaron G, Greenberg Benjamin M, MacArthur Daniel |
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CCR5?32 - a piece of protection in the inflammatory puzzle of multiple sclerosis susceptibility.
Human immunology 2018 May . Troncoso Lian Lopes, Pontillo Alessandra, de Oliveira Enedina Maria Lobato, Finkelszteijn Alessandro, Schneider Silvete, Chies José Artur Bo |
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Suicidal ideation, anxiety, and depression in patients with multiple sclerosis.
Arquivos de neuro-psiquiatria 2018 May 76 (5): 296-301. Tauil Carlos Bernardo, Grippe Talyta Cortez, Dias Ronaldo Maciel, Dias-Carneiro Rafael Paternò Castello, Carneiro Narel Moita, Aguilar Ana Carolina Rodrigues, Silva Flávia Martins da, Bezerra Felipe, Almeida Leonardo Kenzo de, Massarente Vitoria Lana, Giovannelli Elaine de Carvalho, Tilbery Charles Peter, Brandão Carlos Otávio, Santos Leonilda Maria B, Santos-Neto Leopoldo D |
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Association Study of ANRIL Genetic Variants and Multiple Sclerosis.
Journal of molecular neuroscience : MN 2018 Apr . Rezazadeh Maryam, Gharesouran Jalal, Moradi Mohsen, Noroozi Rezvan, Omrani Mir Davood, Taheri Mohammad, Ghafouri-Fard Soud |
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Meta-analysis of the association of IL2RA polymorphisms rs2104286 and rs12722489 with multiple sclerosis risk.
Immunological investigations 2018 Apr 1-12. Wang Xiao-Xiong, Chen To |
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MIF functional polymorphisms (-794 CATT 5-8 and -173 G>C) are associated with MIF serum levels, severity and progression in male multiple sclerosis from western Mexican population.
Journal of neuroimmunology 2018 Apr . Castañeda-Moreno V A, De la Cruz-Mosso U, Torres-Carrillo N, Macías-Islas M A, Padilla-De la Torre O, Mireles-Ramírez M A, González-Pérez O, Ruiz-Sandoval J L, Huerta M, Trujillo X, Ortuño-Sahagún D, Jf Muñoz-Val |
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The HLA-DRB1 and HLA-DQB1 alleles are associated with multiple sclerosis disability progression in Slovak population.
Neurological research 2018 Apr 1-8. ?ierny Daniel, Lehotský Ján, Kantorová Ema, Sivák Štefan, Javor Juraj, Kur?a Egon, Dobrota Dušan, Michalik Joz |
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Autoimmune and immunogenetic profile of patients with optic neuritis in a population-based cohort.
Multiple sclerosis and related disorders 2018 Mar 21 97-102. Soelberg K, Nilsson A C, Nielsen C, Jarius S, Reindl M, Wildemann B, Lillevang S T, Asgari |
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Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials.
Multiple sclerosis (Houndmills, Basingstoke, England) 2018 Mar 1352458518763089. Buck Dorothea, Andlauer Till Fm, Igl Wilmar, Wicklein Eva-Maria, Mühlau Mark, Weber Frank, Köchert Karl, Pohl Christoph, Arnason Barry, Comi Giancarlo, Cook Stuart, Filippi Massimo, Hartung Hans-Peter, Jeffery Douglas, Kappos Ludwig, Barkhof Frederik, Edan Gilles, Freedman Mark S, Montalbán Xavier, Müller-Myhsok Bertram, Hemmer Bernhard, |
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HLA alleles modulate EBV viral load in multiple sclerosis.
Journal of translational medicine 2018 Mar 16 (1): 80. Agostini Simone, Mancuso Roberta, Guerini Franca R, D'Alfonso Sandra, Agliardi Cristina, Hernis Ambra, Zanzottera Milena, Barizzone Nadia, Leone Maurizio A, Caputo Domenico, Rovaris Marco, Clerici Mar |
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The Impact of Five VDR Polymorphisms on Multiple Sclerosis Risk and Progression: a Case-Control and Genotype-Phenotype Study.
Journal of molecular neuroscience : MN 2018 Mar . K?enek Pavel, Benešová Yvonne, Bienertová-Vašk? Julie, Vašk? An |
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The severity of ankylosing spondylitis and responses to anti-tumour necrosis factor biologics are not influenced by the tumour necrosis factor receptor polymorphism incriminated in multiple sclerosis.
Genes and immunity 2018 Mar . Watts Laura, Karaderi Tugce, Roberts Amity, Appleton Louise, Wordsworth Tom, Cohen Carla, Wordsworth Paul, Vecellio Matt |
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Variant of EOMES Associated with Increasing Risk in Chinese Patients with Relapsing-remitting Multiple Sclerosis.
Chinese medical journal 2018 Mar 131 (6): 643-647. Chen Sheng, Zhang Juan, Liu Qi-Bing, Zhuang Jing-Cong, Wu Lei, Xu Yong-Feng, Li Hong-Fu, Wu Zhi-Ying, Xiao Bao-G |
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Analysis of Vitamin D Receptor Polymorphisms in Patients with Familial Multiple Sclerosis.
Medical archives (Sarajevo, Bosnia and Herzegovina) 2018 Feb 72 (1): 58-61. Yucel Fatma Ebru, Kam?sl? Ozden, Acar Ceren, Sozen Mert, Tecellio?lu Mehmet, Ozcan Cem |
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Vitamin D-Binding Protein Polymorphisms, 25-Hydroxyvitamin D, Sunshine and Multiple Sclerosis.
Nutrients 2018 Feb 10 (2): . Langer-Gould Annette, Lucas Robyn M, Xiang Anny H, Wu Jun, Chen Lie H, Gonzales Edlin, Haraszti Samantha, Smith Jessica B, Quach Hong, Barcellos Lisa |
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Butyrylcholinesterase and Acetylcholinesterase polymorphisms in Multiple Sclerosis patients: implication in peripheral inflammation.
Scientific reports 2018 Jan 8 (1): 1319. Reale Marcella, Costantini Erica, Di Nicola Marta, D'Angelo Chiara, Franchi Sara, D'Aurora Marco, Di Bari Maria, Orlando Viviana, Galizia Sabrina, Ruggieri Serena, Stuppia Liborio, Gasperini Claudio, Tata Ada Maria, Gatta Valenti |
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Genetic basis for relapse rate in multiple sclerosis: Association with LRP2 genetic variation.
Multiple sclerosis (Houndmills, Basingstoke, England) 2018 Jan 1352458517749894. Hilven Kelly, Vandebergh Marijne, Smets Ide, Mallants Klara, Goris An, Dubois Bénédic |
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High resolution HLA analysis reveals independent class I haplotypes and amino-acid motifs protective for multiple sclerosis.
Genes and immunity 2018 Jan . Mack Steven J, Udell Julia, Cohen Franziska, Osoegawa Kazutoyo, Hawbecker Sharon K, Noonan David A, Ladner Martha B, Goodridge Damian, Trachtenberg Elizabeth A, Oksenberg Jorge R, Erlich Henry |
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Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells.
Brain : a journal of neurology 2018 Jan . Smets Ide, Fiddes Barnaby, Garcia-Perez Josselyn E, He Di, Mallants Klara, Liao Wenjia, Dooley James, Wang George, Humblet-Baron Stephanie, Dubois Bénédicte, Compston Alastair, Jones Joanne, Coles Alasdair, Liston Adrian, Ban Maria, Goris An, Sawcer Steph |
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Smoking affects the interferon beta treatment response in multiple sclerosis.
Neurology 2018 Jan . Petersen Eva R, Oturai Annette B, Koch-Henriksen Nils, Magyari Melinda, Sørensen Per S, Sellebjerg Finn, Søndergaard Helle |
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The association between vitamin D receptor polymorphisms and multiple sclerosis in a Turkish population.
Multiple sclerosis and related disorders 2018 Jan 20 78-81. Kamisli Ozden, Acar Ceren, Sozen Mert, Tecellioglu Mehmet, Yücel Fatma Ebru, Vaizoglu Dilara, Özcan Cem |
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The multiple sclerosis risk allele within the AHI1 gene is associated with relapses in children and adults.
Multiple sclerosis and related disorders 2018 Jan 19 161-165. Graves Jennifer S, Barcellos Lisa F, Simpson Steve, Belman Anita, Lin Rui, Taylor Bruce V, Ponsonby Anne-Louise, Dwyer Terence, Krupp Lauren, Waubant Emmanuelle, van der Mei Ingrid A |
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Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis.
PloS one 2018 13 (1): e0190601. Lavtar Polona, Rudolf Gorazd, Maver Aleš, Hodži? Alenka, Star?evi? ?izmarevi? Nada, Živkovi? Maja, Šega Jazbec Saša, Klemenc Ketiš Zalika, Kapovi? Miljenko, Din?i? Evica, Rai?evi? Ranko, Sep?i? Juraj, Lovre?i? Luca, Stankovi? Aleksandra, Risti? Smiljana, Peterlin Bor |
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Highly conserved extended haplotypes of the major histocompatibility complex and their relationship to multiple sclerosis susceptibility.
PloS one 2018 13 (2): e0190043. Goodin Douglas S, Khankhanian Pouya, Gourraud Pierre-Antoine, Vince Nicol |
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Iron-related gene variants and brain iron in multiple sclerosis and healthy individuals.
NeuroImage. Clinical 2018 17 530-540. Hagemeier Jesper, Ramanathan Murali, Schweser Ferdinand, Dwyer Michael G, Lin Fuchun, Bergsland Niels, Weinstock-Guttman Bianca, Zivadinov Robe |
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Polygenic analysis of inflammatory disease variants and effects on microglia in the aging brain.
Molecular neurodegeneration 2018 07 13 (1): 38. Felsky Daniel, Patrick Ellis, Schneider Julie A, Mostafavi Sara, Gaiteri Chris, Patsopoulos Nikolaos, Bennett David A, De Jager Philip |
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The genetic effect of the
Bioscience reports 2018 12 38 (6): . Jiang Chuan, Xie Chunli, Feng Jianli, Hao Maol |
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Association between VDR polymorphisms and multiple sclerosis: systematic review and updated meta-analysis of case-control studies.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2017 Nov . Zhang Yan-Jie, Zhang Li, Chen Shan-Yu, Yang Guo-Jun, Huang Xiao-Lei, Duan Yu, Yang Li-Juan, Ye Dong-Qing, Wang Ji |
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Can fibrinolytic system components explain cognitive impairment in multiple sclerosis?
Journal of the neurological sciences 2017 Nov 382 66-72. Pérez-Martín María Yaiza, González-Platas Montserrat, Jiménez-Sosa Alejandro, Plata-Bello Julio, Carrillo-Padilla Francisco Javier, Franco-Maside Andrés, Eguia-Del Río Pab |
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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 |
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Ecotropic Viral Integration Site 5 (EVI5) variants are associated with multiple sclerosis in Iranian population.
Multiple sclerosis and related disorders 2017 Nov 18 15-19. Mazdeh Mehrdokht, Ghafouri-Fard Soudeh, Noroozi Rezvan, Sayad Arezou, Khani Maryam, Taheri Mohammad, Davood Omrani M |
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Multiple sclerosis and HLA genotypes: A possible influence on brain atrophy.
Multiple sclerosis (Houndmills, Basingstoke, England) 2017 Nov 1352458517739989. Lorefice Lorena, Fenu Giuseppe, Sardu Claudia, Frau Jessica, Coghe Giancarlo, Costa Gianna, Schirru Lucia, Secci Maria Antonietta, Sechi Vincenzo, Barracciu Maria Antonietta, Marrosu Maria Giovanna, Cocco Eleono |
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NLRP3 polymorphisms and response to interferon-beta in multiple sclerosis patients.
Multiple sclerosis (Houndmills, Basingstoke, England) 2017 Nov 1352458517739137. Malhotra Sunny, Sorosina Melissa, Río Jordi, Peroni Silvia, Midaglia Luciana, Villar Luisa M, Álvarez-Cermeño José C, Schroeder Ina, Esposito Federica, Clarelli Ferdinando, Zettl Uwe K, Lechner-Scott Jeannette, Spataro Nino, Navarro Arcadi, Comi Giancarlo, Montalban Xavier, Martinelli-Boneschi Filippo, Comabella Manu |
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Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis: the impact of genome-wide association studies identified disease risk loci.
Pharmacogenomics 2017 Nov . Kulakova Olga, Bashinskaya Vitalina, Kiselev Ivan, Baulina Natalia, Tsareva Ekaterina, Nikolaev Ruslan, Kozin Maxim, Shchur Sergey, Favorov Alexander, Boyko Alexey, Favorova Ol |
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The +4259A>C polymorphism of TIM-3 but not -1637C>T polymorphism of TIM-1 is associated with Multiple sclerosis in Isfahan population.
Multiple sclerosis and related disorders 2017 Nov 18 152-156. Pouladian Masoumeh, Ganjalikhani-Hakemi Mazdak, Alsahebfosul Fereshteh, Homayouni Vida, Khosravi Sharifeh, Etemadifar Masoud, Mazrouei Fariba, Salehi Raso |
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Association of TNFSF4 Polymorphisms with Neuromyelitis Optica Spectrum Disorders in a Chinese Population.
Journal of molecular neuroscience : MN 2017 Oct . Lian Zhiyun, Liu Ju, Shi Ziyan, Chen Hongxi, Zhang Qin, Feng Huiru, Du Qin, Miao Xiaohui, Zhou Hong |
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Association of VDR gene polymorphisms with risk of Relapsing-remitting multiple sclerosis in an Iranian Kurdish population.
The International journal of neuroscience 2017 Oct 1-17. Abdollah Zadeh Rasoul, Moradi Pordanjani Parisa, Rahmani Farideh, Mashayekhi Fatemeh, Azarnezhad Asaad, Mansoori Yas |
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PER3 VNTR polymorphism in Multiple Sclerosis: A new insight to impact of sleep disturbances in MS.
Multiple sclerosis and related disorders 2017 Oct 17 84-86. Golalipour Masoud, Maleki Zahra, Farazmandfar Touraj, Shahbazi Maj |
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Combination of Myelin Basic Protein Gene Polymorphisms with HLA-DRB1*1501 in Iranian Patients with Multiple Sclerosis.
Iranian journal of immunology : IJI 2017 Sep 14 (3): 231-239. Nejati Parham, Attar Marzieh, Rahimian Maryam, Fathi Davood, Shahbazi Maj |
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TNFRSF1A and MEFV mutations in childhood onset multiple sclerosis.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2017 Sep . Blaschek Astrid, V Kries Rüdiger, Lohse Peter, Huss Kristina, Vill Katharina, Belohradsky Bernd H, Heinen Florian, Müller-Felber Wolfgang, Kümpfel Tan |
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Association between interleukin-32 polymorphism and multiple sclerosis.
Journal of the neurological sciences 2017 Aug 379 144-150. Morsaljahan Zaher, Rafiei Alireza, Valadan Reza, Abedini Mahmoud, Pakseresht Masoumeh, Khajavi Rezv |
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Association of CD58 gene polymorphisms with NMO spectrum disorders in a Han Chinese population.
Journal of neuroimmunology 2017 Aug 309 23-30. Liu Ju, Shi Ziyan, Lian Zhiyun, Chen Hongxi, Zhang Qin, Feng Huiru, Miao Xiaohui, Du Qin, Zhou Hong |
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Association of CYP2R1 rs10766197 with MS risk and disease progression.
Journal of neuroscience research 2017 Aug . Scazzone Concetta, Agnello Luisa, Ragonese Paolo, Lo Sasso Bruna, Bellia Chiara, Bivona Giulia, Schillaci Rosaria, Salemi Giuseppe, Ciaccio Marcel |
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Interleukin 7 Receptor Alpha Gene Variants Are Correlated with Gene Expression in Patients with Relapsing-remitting Multiple Sclerosis.
Iranian journal of allergy, asthma, and immunology 2017 Aug 16 (4): 338-346. Sayad Arezou, Omrani Mir Davood, Solgi Ghasem, Noroozi Rezvan, Arsang-Jang Shahram, Inoko Hidetoshi, Taheri Mohamm |
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis.
American journal of human genetics 2017 Aug 101 (2): 227-238. Manousaki Despoina, Dudding Tom, Haworth Simon, Hsu Yi-Hsiang, Liu Ching-Ti, Medina-Gómez Carolina, Voortman Trudy, van der Velde Nathalie, Melhus Håkan, Robinson-Cohen Cassianne, Cousminer Diana L, Nethander Maria, Vandenput Liesbeth, Noordam Raymond, Forgetta Vincenzo, Greenwood Celia M T, Biggs Mary L, Psaty Bruce M, Rotter Jerome I, Zemel Babette S, Mitchell Jonathan A, Taylor Bruce, Lorentzon Mattias, Karlsson Magnus, Jaddoe Vincent V W, Tiemeier Henning, Campos-Obando Natalia, Franco Oscar H, Utterlinden Andre G, Broer Linda, van Schoor Natasja M, Ham Annelies C, Ikram M Arfan, Karasik David, de Mutsert Renée, Rosendaal Frits R, den Heijer Martin, Wang Thomas J, Lind Lars, Orwoll Eric S, Mook-Kanamori Dennis O, Michaëlsson Karl, Kestenbaum Bryan, Ohlsson Claes, Mellström Dan, de Groot Lisette C P G M, Grant Struan F A, Kiel Douglas P, Zillikens M Carola, Rivadeneira Fernando, Sawcer Stephen, Timpson Nicholas J, Richards J Bre |
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No evidence of association between optic neuritis and secondary LHON mtDNA mutations in patients with multiple sclerosis.
Mitochondrion 2017 Aug . Andalib Sasan, Talebi Mahnaz, Sakhinia Ebrahim, Farhoudi Mehdi, Sadeghi-Bazargani Homayoun, Masoodian Nooshin, Vafaee Manouchehr Seyedi, Gjedde Albe |
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STAT4 Polymorphisms are Associated with Neuromyelitis Optica Spectrum Disorders.
Neuromolecular medicine 2017 Aug . Shi Ziyan, Zhang Qin, Chen Hongxi, Lian Zhiyun, Liu Ju, Feng Huiru, Miao Xiaohui, Du Qin, Zhou Hong |
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The vitamin D receptor gene FokI polymorphism and Multiple Sclerosis in a Northern Portuguese population.
Journal of neuroimmunology 2017 Aug 309 34-37. Bettencourt Andreia, Boleixa Daniela, Guimarães Ana Luísa, Leal Bárbara, Carvalho Cláudia, Brás Sandra, Samões Raquel, Santos Ernestina, Costa Paulo Pinho, Silva Berta, da Silva Ana Marti |
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Vitamin D receptor gene polymorphisms and the risk of multiple sclerosis: An updated meta-analysis.
Microbial pathogenesis 2017 Aug 110 594-602. Chen Xiao-Long, Zhang Ming-Liang, Zhu Lin, Peng Meng-Le, Liu Fang-Zhou, Zhang Guang-Xian, Wang Li-Mei, Zhao J |
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Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis.
Journal of neurology, neurosurgery, and psychiatry 2017 Jul . Zhou Yuan, Graves Jennifer S, Simpson Steve, Charlesworth Jac C, Mei Ingrid van der, Waubant Emmanuelle, Barcellos Lisa F, Belman Anita, Krupp Lauren, Lucas Robyn, Ponsonby Anne-Louise, Taylor Bruce V, |
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Combination of interleukin-10 gene promoter polymorphisms with HLA-DRB1*15 allele is associated with multiple sclerosis.
The Indian journal of medical research 2017 Jun 145 (6): 746-752. Shahbazi Majid, Abadi Javad Sadeghi Allah, Roshandel Danial, Koochaki Maryam, Amiri Hosein, Kohansal Rahim, Baghbanian Seied Mohammad, Zamani Mah |
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Indoleamine-2,3-dioxygenase(IDO)2 polymorphisms are not associated with multiple sclerosis in Italians.
Journal of the neurological sciences 2017 Jun 377 31-34. Agliardi Cristina, Guerini Franca Rosa, Zanzottera Milena, Rovaris Marco, Caputo Domenico, Clerici Mar |
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Multiple sclerosis risk pathways differ in Caucasian and Chinese populations.
Journal of neuroimmunology 2017 Jun 307 63-68. Liu Guiyou, Zhang Fang, Hu Yang, Jiang Yongshuai, Gong Zhongying, Liu Shoufeng, Chen Xiuju, Jiang Qinghua, Hao Junw |
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The interaction between smoking and HLA genes in multiple sclerosis: replication and refinement.
European journal of epidemiology 2017 Jun . Hedström Anna Karin, Katsoulis Michail, Hössjer Ola, Bomfim Izaura L, Oturai Annette, Sondergaard Helle Bach, Sellebjerg Finn, Ullum Henrik, Thørner Lise Wegner, Gustavsen Marte Wendel, Harbo Hanne F, Obradovic Dragana, Gianfrancesco Milena A, Barcellos Lisa F, Schaefer Catherine A, Hillert Jan, Kockum Ingrid, Olsson Tomas, Alfredsson La |
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Genetic modifiers of multiple sclerosis progression, severity and onset.
Clinical immunology (Orlando, Fla.) 2017 May 180 100-105. Sadovnick A Dessa, Traboulsee Anthony L, Zhao Yinshan, Bernales Cecily Q, Encarnacion Mary, Ross Jay P, Yee Irene M, Criscuoli Maria G, Vilariño-Güell Carl |
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