scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1068965806 |
P356 | DOI | 10.2119/MOLMED.2015.00232 |
P932 | PMC publication ID | 4749491 |
P698 | PubMed publication ID | 26562150 |
P50 | author | Lennart Hammarström | Q5786999 |
Peter K. Gregersen | Q7175067 | ||
Piotr Szczudlik | Q56506957 | ||
Janine A Lamb | Q57008662 | ||
Anna Kostera-Pruszczyk | Q61638820 | ||
Hanne F Harbo | Q90089338 | ||
Benedicte A Lie | Q90324535 | ||
Michael F Seldin | Q107119154 | ||
Omar K Alkhairy | Q125218742 | ||
Ritva Pirskanen-Matell | Q125219775 | ||
P2093 | author name string | Annette T Lee | |
Fredrik Piehl | |||
Arthur Melms | |||
Angelina H Maniaol | |||
Nicholas Willcox | |||
Henri-Jean Garchon | |||
Jon Sussman | |||
J J G M Verschuuren | |||
David Mckee | |||
P2860 | cites work | A flexible and accurate genotype imputation method for the next generation of genome-wide association studies | Q21129496 |
Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations | Q24310432 | ||
A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function | Q24336057 | ||
Inference of population structure using multilocus genotype data | Q24548114 | ||
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis | Q24596087 | ||
RANK is essential for osteoclast and lymph node development | Q24598872 | ||
MicroRNA-27a Indirectly Regulates Estrogen Receptor {alpha} Expression and Hormone Responsiveness in MCF-7 Breast Cancer Cells | Q24607151 | ||
A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals | Q24644474 | ||
PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies | Q26734731 | ||
Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
Sexual dimorphism in autoimmunity | Q28080459 | ||
Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis | Q28141482 | ||
A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes | Q28248848 | ||
A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis | Q28267921 | ||
Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE. | Q28273794 | ||
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci | Q28293771 | ||
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype | Q28305142 | ||
RIN ZF, a novel zinc finger gene, encodes proteins that bind to the CACC element of the gastrin promoter | Q28567333 | ||
Novel associations for hypothyroidism include known autoimmune risk loci | Q28730714 | ||
Late-onset myasthenia gravis - CTLA4(low) genotype association and low-for-age thymic output of naïve T cells. | Q50800911 | ||
Estrogen receptor-alpha deficiency attenuates autoimmune disease in (NZB x NZW)F1 mice. | Q52584591 | ||
A susceptibility region for myasthenia gravis extending into the HLA-class I sector telomeric to HLA-C. | Q52916174 | ||
Haplotype-specific gene expression profiles in a telomeric major histocompatibility complex gene cluster and susceptibility to autoimmune diseases. | Q54581280 | ||
Clinical, pathological, HLA antigen and immunological evidence for disease heterogeneity in myasthenia gravis | Q72079873 | ||
Clinical characteristics and prognosis of myasthenia gravis in older people | Q73202560 | ||
SFEMG in ocular myasthenia gravis diagnosis | Q73955005 | ||
Linkage of HLA to myasthenia gravis and genetic heterogeneity depending on anti-titin antibodies | Q77162347 | ||
Clonal expansions of CD4+ B helper T cells in autoimmune myasthenia gravis | Q79833067 | ||
BAT1 promoter polymorphism is associated with rheumatoid arthritis susceptibility | Q80996106 | ||
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08 | Q28943379 | ||
Annotation of functional variation in personal genomes using RegulomeDB | Q29614867 | ||
LocusZoom: regional visualization of genome-wide association scan results | Q29614868 | ||
Imputing amino acid polymorphisms in human leukocyte antigens | Q30418816 | ||
HLA class I and genetic susceptibility to type 1 diabetes: results from the Type 1 Diabetes Genetics Consortium | Q30429923 | ||
A systematic review of population based epidemiological studies in Myasthenia Gravis. | Q33611231 | ||
Effect of mutations and variations of HLA-A2 on recognition of a virus peptide epitope by cytotoxic T lymphocytes | Q33681540 | ||
Electrophysiological and immunological study in myasthenia gravis: diagnostic sensitivity and correlation | Q34026174 | ||
Tyrosine phosphatase PTPN22: multifunctional regulator of immune signaling, development, and disease. | Q34039427 | ||
The association of PTPN22 R620W polymorphism is stronger with late-onset AChR-myasthenia gravis in Turkey. | Q34042062 | ||
Antibody to acetylcholine receptor in myasthenia gravis. Prevalence, clinical correlates, and diagnostic value | Q34068275 | ||
The incidence of myasthenia gravis: a systematic literature review | Q34096759 | ||
Insights into the classification of myasthenia gravis | Q34142620 | ||
Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis | Q34250412 | ||
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture | Q34268288 | ||
Late onset myasthenia gravis is associated with HLA DRB1*15:01 in the Norwegian population | Q34270872 | ||
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation | Q34350941 | ||
A general approach for haplotype phasing across the full spectrum of relatedness | Q34415720 | ||
minimac2: faster genotype imputation | Q34444539 | ||
Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America | Q34804773 | ||
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone | Q35552797 | ||
Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritis | Q35834701 | ||
Rank signaling links the development of invariant γδ T cell progenitors and Aire(+) medullary epithelium | Q36011240 | ||
Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans | Q36365695 | ||
DNase I sensitivity QTLs are a major determinant of human expression variation | Q36408973 | ||
A genome-wide association study of myasthenia gravis | Q36869250 | ||
Lifetime course of myasthenia gravis | Q37024294 | ||
Autoimmune myasthenia gravis: emerging clinical and biological heterogeneity | Q37315963 | ||
The X chromosome and the sex ratio of autoimmunity. | Q37966537 | ||
Genetic basis of myasthenia gravis - a comprehensive review | Q38173147 | ||
IL-10 gene expression is controlled by the transcription factors Sp1 and Sp3. | Q40872798 | ||
The role of Sp1 and NF-kappa B in regulating CD40 gene expression | Q42514630 | ||
Correlating extent of neuromuscular instability with acetylcholine receptor antibodies | Q46101147 | ||
Association of the PTPN22*R620W polymorphism with autoimmune myasthenia gravis. | Q46912103 | ||
Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia. | Q48292937 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P4510 | describes a project that uses | genome-wide association study | Q1098876 |
P407 | language of work or name | English | Q1860 |
P921 | main subject | myasthenia gravis | Q8285 |
genome-wide association study | Q1098876 | ||
P577 | publication date | 2015-10-10 | |
P1433 | published in | Molecular Medicine | Q6895961 |
P1476 | title | Genome-wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A, and Identification of ZBTB10 and Three Distinct HLA Associations |
Q26765172 | Clinical features, pathogenesis, and treatment of myasthenia gravis: a supplement to the Guidelines of the German Neurological Society |
Q37191879 | Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma |
Q47192132 | Immunopathogenesis in Myasthenia Gravis and Neuromyelitis Optica |
Q42696048 | Juvenile myasthenia gravis in Norway: HLA-DRB1*04:04 is positively associated with prepubertal onset. |
Q36715524 | Sonic Hedgehog regulates thymic epithelial cell differentiation |
Q33714351 | TNFAIP3 gene rs7749323 polymorphism is associated with late onset myasthenia gravis. |
Q46094020 | The immunogenetics of neurological disease. |
Search more.