A High-Density Screen for Linkage in Multiple Sclerosis

Cited by (297)

Items 101–200 of 297

1. Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans
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2. X chromosome inactivation in females with multiple sclerosis
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3. The Role Of Glial–Neuronal Metabolic Cooperation in Modulating Progression of Multiple Sclerosis and Neuropathic Pain
   Rachel R. Robinson, Alina Kay Dietz, Asif Mirza Maroof, Reto Asmis, Thomas G. Forsthuber · 2019 · Immunotherapy
4. The T244I variant of the interleukin‐7 receptor‐alpha gene and multiple sclerosis
   Antonio Alcina, Marı́a Fedetz, Dorothy Ndagire, Óscar Fernández, Laura Leyva, M. Guerrero, Carmen Arnal, Concepción Delgado, Fuencisla Matesanz · 2008 · Tissue Antigens
5. Multiple Sclerosis Genetics 2010
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6. Towards a global view of multiple sclerosis genetics
   Benjamin M. Jacobs, Michelle Peter, Gavin Giovannoni, Alastair John Noyce, Huw R. Morris, Ruth Dobson · 2022 · Nature Reviews Neurology
7. HLA class II alleles in patients with multiple sclerosis in the Biscay province (Basque Country, Spain)
   Óscar Fernández, Alfredo Rodríguez Antigüedad, María Jesús Pinto-Medel, María M. Mendibe, Nestor Acosta, Begoña Oliver‐Martos, Miguel Guerrero, Marcos Papais-Alvarenga, Victoria Eugenia Fernández-Sánchez, Laura Leyva · 2009 · Journal of Neurology
8. The Norwegian Multiple Sclerosis National Competence Centre and National Multiple Sclerosis registry - a resource for clinical practice and research
   Kjell‐Morten Myhr, Nina Grytten, J. H. Aarseth, Harald Nyland · 2006 · Acta Neurologica Scandinavica
9. Three allele combinations associated with Multiple Sclerosis
   Olga O. Favorova, Alexander V. Favorov, Alexey N. Boiko, T. V. Andreewski, Marina A. Sudomoina, A. D. Alekseenkov, О. Г. Кулакова, Eugenyi I Gusev, Giovanni Parmigiani, Michael F. Ochs · 2006 · BMC Medical Genetics
10. Mining for single nucleotide polymorphisms in pig genome sequence data
    Hindrik H. D. Kerstens, Sonja Kollers, Arun Kommadath, Marisol del Rosario, Bert W. Dibbits, Sylvia M Kinders, Richard P. M. A. Crooijmans, Martien A. M. Groenen · 2009 · BMC Genomics
11. Characterization of Multiple Sclerosis candidate gene expression kinetics in rat experimental autoimmune encephalomyelitis
    Mélanie Thessén Hedreul, Alan Gillett, Tomas P Olsson, Maja Jagodic, Robert Adam Harris · 2009 · Journal of Neuroimmunology
12. Fine Mapping and Functional Analysis of the Multiple Sclerosis Risk Gene CD6
    Bhairavi Swaminathan, Angélica Cuapio, Iraide Alloza, Fuencisla Matesanz, Antonio Alcina, María García‐Barcina, Marı́a Fedetz, Óscar Fernández, Miguel Lucas, Teresa Órpez et al. · 2013 · PLoS ONE
13. CD24 Ala/Val polymorphism and multiple sclerosis
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14. NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk
    Jack Perry Antel, Maria Ban, Sergio E. Baranzini, Lisa F. Barcellos, Nadia Barizzone, Ashley Harris Beecham, Tone Berge, Luisa Bernardinelli, David Richmond Booth, Steffan D. Bos et al. · 2016 · Neuron
15. Multiple sclerosis susceptibility and the X chromosome
    BM Herrera, M. Zameel Cader, David A Dyment, Jordana T. Bell, Gabriele Carmine DeLuca, Cristen J. Willer, Matthew R. Lincoln, SV Ramagopalan, Melody Chao, S-M. Orton et al. · 2007 · Multiple Sclerosis Journal
16. A genome scan in a single pedigree with a high prevalence of multiple sclerosis
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17. Inflammation in white matter: Clinical and pathophysiological aspects
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18. CCL genes in multiple sclerosis and systemic lupus erythematosus
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19. Genetics of autoimmune neuroinflammation
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20. Fine-Mapping Chromosome 20 in 230 Systemic Lupus Erythematosus Sib Pair and Multiplex Families: Evidence for Genetic Epistasis with Chromosome 16q12
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21. Genetics of primary progressive multiple sclerosis
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22. The participation of minorities in published pediatric research.
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23. ITGA4 polymorphisms and susceptibility to multiple sclerosis
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24. Whole-Genome Amplification Enables Accurate Genotyping for Microarray-Based High-Density Single Nucleotide Polymorphism Array
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25. Progress in Multiple Sclerosis Genetics
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26. A new era in the genetic analysis of multiple sclerosis
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27. An integrated approach to design novel therapeutic interventions for demyelinating disorders
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28. The Impact of the Human Genome Project on Complex Disease
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29. A genetic basis for multiple sclerosis severity: Red herring or real?
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30. DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes
    Alexandre Xavier, Vicki E. Maltby, Ewoud Ewing, Maria Pia Campagna, Sean M. Burnard, Jesper N. Tegner, Mark Slee, Helmut Butzkueven, Ingrid Skelton Kockum, Lara Kular et al. · 2023 · International Journal of Molecular Sciences
31. Myelin oligodendrocyte glycoprotein peptide-induced experimental allergic encephalomyelitis and T cell responses are unaffected by immunoproteasome deficiency
    Ricardo F. Frausto, Stephen J. Crocker, Boreth Eam, Jason K. Whitmire, J. Lindsay Whitton · 2007 · Journal of Neuroimmunology
32. Monoclonal antibodies in the treatment of multiple sclerosis: emergence of B‐cell‐targeted therapies
    Ai‐Lan Nguyen, Melissa M. Gresle, Tessa Marshall, Helmut Butzkueven, Judith Field · 2017 · British Journal of Pharmacology
33. A linkage study in two families with multiple sclerosis and healthy members with oligoclonal CSF immunopathy
    Sara Haghighi, Oluf Andersen, Staffan Nilsson, Lennart Rydberg, J. Wahlström · 2006 · Multiple Sclerosis Journal
34. Multiple sclerosis: Motor dysfunction
    David S. Younger · 2023 · Handbook of clinical neurology
35. European multiple sclerosis risk variants in the south Asian population
    Lekha Pandit, Maria Ban, Ashley Harris Beecham, Jacob L. McCauley, Stephen J. Sawcer, Anitha D’Cunha, Chaithra Malli, Omar Malik · 2016 · Multiple Sclerosis Journal
36. Association analysis of the LAG3 and CD4 genes in multiple sclerosis in two independent populations
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37. Is multiple sclerosis progression associated with the HLA-DR15 haplotype?
    Klarissa Hanja Stürner, Inessa Siembab, Gerhard Schön, Jan‐Patrick Stellmann, Nika Heidari, Boris Fehse, Christoph Heesen, THOMAS H. EIERMANN, Roland Martinꝉ, Thomas M. Binder · 2019 · Multiple Sclerosis Journal - Experimental Translational and Clinical
38. Identity-by-descent mapping in a Scandinavian multiple sclerosis cohort
    Helga Westerlind, Kerstin Imrell, Ryan Ramanujam, Kjell‐Morten Myhr, Elisabeth Gulowsen Celius, Hanne Flinstad Harbo, Annette Bang Oturai, Anders Hamsten, Lars S. Alfredsson, Tomas P Olsson et al. · 2014 · European Journal of Human Genetics
39. Multiple sclerosis as a polygenic disease: An update
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40. Genome-wide homozygosity and multiple sclerosis in Orkney and Shetland Islanders
    Rebekah McWhirter, Ruth McQuillan, Elizabeth M Visser, Carl E Counsell, James F. Wilson · 2011 · European Journal of Human Genetics
41. Genome-Wide Association Study of the Four-Constitution Medicine
    Chang Shik Yin, Hi‐Joon Park, Joo‐Ho Chung, Hye‐Jung Lee, Byung-Cheol Lee · 2009 · The Journal of Alternative and Complementary Medicine
42. Modifiable Risk Factors for Multiple Sclerosis are Consistent Across Diverse Ethnic Backgrounds: A Nested Case-Control Study in a UK Population-Based Cohort
    Benjamin M. Jacobs, Pooja Tank, Jonathan Paul Bestwick, Alastair John Noyce, Charles R. Marshall, Rohini Mathur, Gavin Giovannoni, Ruth Dobson · 2022 · Journal of Neurology
43. The neuropeptide genes TAC1, TAC3, TAC4, VIP and PACAP(ADCYAP1), and susceptibility to multiple sclerosis
    Stephen Cunningham, Catherine O’Doherty, Chris C. Patterson, Gavin V McDonnell, Stanley A Hawkins, Maria Giovanna Marrosu, Koen Vandenbroeck · 2006 · Journal of Neuroimmunology
44. Early B-cell Factor gene association with multiple sclerosis in the Spanish population
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45. CRYAB promoter polymorphisms: Influence on multiple sclerosis susceptibility and clinical presentation
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46. Meta-analysis of genome-wide linkage studies for multiple sclerosis, using an extended GSMA method
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47. Association between Protective and Deleterious HLA Alleles with Multiple Sclerosis in Central East Sardinia
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48. HLA (A-B-C and -DRB1) alleles and brain MRI changes in multiple sclerosis: a longitudinal study
    Maria Liguori, Brian C. Healy, Bonnie I. Glanz, Samia Joseph Khoury, Nicola Moscufo, Howard L. Weiner, Philip L. De Jager, Charles R.G. Guttmann · 2010 · Genes and Immunity
49. Inflammation and susceptibility to neurodegeneration: The use of unbiased genetics to decipher critical regulatory pathways
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50. The Genetics of Multiple Sclerosis
    Jan A. Hillert · 2009 · Results and problems in cell differentiation
51. Increased Prevalence of Multiple Sclerosis Among COPD Patients and Their First-Degree Relatives: A Population-based Study
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52. TCR‐like antibodies distinguish conformational and functional differences in two‐ versus four‐domain auto reactive MHC class II–peptide complexes
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53. Genetic Correlations of Brain Lesion Distribution in Multiple Sclerosis: An Exploratory Study
    Madeleine H Sombekke, Machteld M. Vellinga, Bernard M.J. Uitdehaag, Frederik Barkhof, Chris H. Polman, D. Arteta, D. Tejedor, A. Martinez, J. Bart A. Crusius, Amado Salvador Peña et al. · 2011 · American Journal of Neuroradiology
54. HLA-association of serum levels of natural antibodies
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55. Follow-up investigation of 12 proposed linkage regions in multiple sclerosis
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56. Polygenic risk score prediction of multiple sclerosis in individuals of South Asian ancestry
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57. The SH2D2A gene and susceptibility to multiple sclerosis
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58. Combined-cross analysis of genome-wide linkage scans for experimental autoimmune encephalomyelitis in rat
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59. Risk in complex genetics: “All models are wrong but some are useful”
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60. Predicting Multiple Sclerosis: Challenges and Opportunities
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61. Human leucocyte antigen class II polymorphism in Irish patients with multiple sclerosis
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62. Overview of Linkage Analysis in Complex Traits
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63. An investigation of polymorphisms in the 17q11.2-12 CC chemokine gene cluster for association with multiple sclerosis in Australians
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64. Mapping candidate non-MHC susceptibility regions to multiple sclerosis
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65. Exome sequencing reveals novel rare variants in Iranian familial multiple sclerosis: The importance of POLD2 in the disease pathogenesis
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66. Prioritization of risk genes in multiple sclerosis by a refined Bayesian framework followed by tissue-specificity and cell type feature assessment
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67. A Genome‐Wide Linkage Screen in the Amish with Parkinson Disease Points to Chromosome 6
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68. CCSVI is associated with multiple sclerosis
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69. The genetic aspects of multiple sclerosis
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70. Techniques for Nucleic Acid Purification from Plant, Animal, and Microbial Samples
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71. Current issues in the basic mechanisms, pathophysiology, diagnosis and management of primary ciliary dyskinesia
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72. Recent advances in genetic analysis of multiple sclerosis: genetic associations and therapeutic implications
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73. Increase in Linkage Information by Stratification of Pedigree Data into Gold-Standard and Standard Diagnoses: Application to the NIMH Alzheimer Disease Genetics Initiative Dataset
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74. Multiple Sclerosis: Light at the end of the tunnel
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75. Laboratory Diagnosis of Intrathecal Synthesis of Immunoglobulins: A Review about the Contribution of OCBs and K-index
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76. Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis
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77. Profile of Differential Promoter Activity by Nucleotide Substitution at GWAS Signals For Multiple Sclerosis
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78. Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease
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79. Meta-Analysis of Differential Connectivity in Gene Co-Expression Networks in Multiple Sclerosis
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80. Exome-Sequence Analyses of Four Multi-Incident Multiple Sclerosis Families
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81. Genome-wide association study as a method to analyze the genome architecture in polygenic diseases, with the example of multiple sclerosis
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82. Multiple sclerosis: Postlinkage genetics
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83. No evidence for association of a European-specific chromosome 17 inversion with multiple sclerosis
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84. Know Thy Neighbor: A Survey of Diseases and Complex Syndromes that Map to Chromosomal Regions Encoding TRP Channels
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85. Burden of genetic risk variants in multiple sclerosis families in the Netherlands
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86. Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis
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87. Single-Nucleotide Polymorphism (SNP) Analysis to Associate Cancer Risk
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88. OCA-B promotes pathogenic maturation of stem-like CD4+ T cells and autoimmune demyelination
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89. Regulatory T Cells in MS
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90. ADAMS project: a genetic Association study in individuals from Diverse Ancestral backgrounds with Multiple Sclerosis based in the UK
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91. An investigation of polymorphisms in the 4q13.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in Australians
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92. An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients
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93. New Insights into Risk Genes and Their Candidates in Multiple Sclerosis
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94. Polymorphic markers of some genes associated with multiple sclerosis in the population of Kazakhstan
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95. Daclizumab, an IL-2 modulating antibody for treatment of multiple sclerosis
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96. Preliminary evidences of a NOS2A protective effect from Relapsing–Remitting Multiple Sclerosis
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97. The Genetics of Multiple Sclerosis
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98. In search of genes for stroke
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99. Coding region polymorphisms in T cell signal transduction genes. Prevalence and association to development of multiple sclerosis
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100. HLA class I & II alleles in multiple sclerosis patients from Puerto Rico.
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