Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 30 (of 31 Records) |
Query Trace: Inclusion Body Myositis[original query] |
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Apolipoprotein E and alpha-1-antichymotrypsin polymorphisms in sporadic inclusion body myositis. European neurology 2004 51 (4): 215-20. Gossrau G, Gestrich B, Koch R, Wunderlich C, Schröder J M, Schroeder S, Reichmann H, Lampe J |
Two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: critical evaluation of an association with HLA-DR3. Tissue antigens 2004 Nov 64 (5): 575-80. Price P, Santoso L, Mastaglia F, Garlepp M, Kok C C, Allcock R, Laing |
Immunogenetic risk and protective factors for the idiopathic inflammatory myopathies: distinct HLA-A, -B, -Cw, -DRB1 and -DQA1 allelic profiles and motifs define clinicopathologic groups in caucasians. Medicine 2005 Nov 84 (6): 338-49. O'Hanlon Terrance P, Carrick Danielle Mercatante, Arnett Frank C, Reveille John D, Carrington Mary, Gao Xiaojiang, Oddis Chester V, Morel Penelope A, Malley James D, Malley Karen, Dreyfuss Jonathan, Shamim Ejaz A, Rider Lisa G, Chanock Stephen J, Foster Charles B, Bunch Thomas, Plotz Paul H, Love Lori A, Miller Frederick |
Apolipoprotein epsilon alleles in sporadic inclusion body myositis: a reappraisal. Neuromuscular disorders : NMD 2008 Feb 18 (2): 150-2. Needham Merrilee, Hooper Amanda, James Ian, van Bockxmeer Frank, Corbett Alastair, Day Timothy, Garlepp Michael J, Mastaglia Frank |
Sporadic inclusion body myositis: phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian cases. Journal of neurology, neurosurgery, and psychiatry 2008 Sep 79 (9): 1056-60. Needham M, James I, Corbett A, Day T, Christiansen F, Phillips B, Mastaglia F |
Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype. Neuromuscular disorders : NMD 2009 Nov 19 (11): 763-5. Mastaglia Frank L, Needham Merrilee, Scott Adrian, James Ian, Zilko Paul, Day Timothy, Kiers Lynette, Corbett Alastair, Witt Campbell S, Allcock Richard, Laing Nigel, Garlepp Michael, Christiansen Frank |
TREX1 mutations are not associated with sporadic inclusion body myositis. European journal of neurology : the official journal of the European Federation of Neurological Societies 2010 Aug 17 (8): 1108-9. Cox F M, Boon E M J, van der Lans C A C, Bakker E, Verschuuren J J G M, Badrising U |
A three-way interplay of DR4, autoantibodies and synovitis in biopsy-proven idiopathic inflammatory myositis. Rheumatology international 2010 Dec . Limaye VS, Lester S, Bardy P, Thompson P, Cox S, Blumbergs P, Roberts-Thomson P |
Analysis of HLA-DRB3 alleles and supertypical genotypes in the MHC Class II region in sporadic inclusion body myositis. Journal of neuroimmunology 2013 Jan 254 (1-2): 174-7. Rojana-udomsart Arada, Mitrpant Chalermchai, James Ian, Witt Campbell, Needham Merrilee, Day Timothy, Kiers Lynette, Corbett Alastair, Martinez Patricia, Wilton Steve D, Mastaglia Frank |
The incidence and associations of malignancy in a large cohort of patients with biopsy-determined idiopathic inflammatory myositis. Rheumatology international 2012 Jul . Limaye V, Luke C, Tucker G, Hill C, Lester S, Blumbergs P, Roberts-Thomson P |
Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis. Journal of neuroimmunology 2012 Sep 250 (1-2): 66-70. Scott Adrian P, Laing Nigel G, Mastaglia Frank, Dalakas Marinos, Needham Merrilee, Allcock Richard J |
Frequency of autoantibodies and correlation with HLA-DRB1 genotype in sporadic inclusion body myositis (s-IBM): a population control study. Journal of neuroimmunology 2012 Aug 249 (1-2): 66-70. Rojana-Udomsart Arada, Bundell Christine, James Ian, Castley Alison, Martinez Patricia, Christiansen Frank, Hollingsworth Peter, Mastaglia Fra |
High-resolution HLA-DRB1 genotyping in an Australian inclusion body myositis (s-IBM) cohort: an analysis of disease-associated alleles and diplotypes. Journal of neuroimmunology 2012 Sep 250 (1-2): 77-82. Rojana-udomsart Arada, James Ian, Castley Alison, Needham Merrilee, Scott Adrian, Day Timothy, Kiers Lynette, Corbett Alastair, Sue Carolyn, Witt Campbell, Martinez Patricia, Christiansen Frank, Mastaglia Fra |
SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: a United States clinical testing lab experience. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2012 Feb 13 (2): 217-22. Brown Jeffrey A, Min Jionghong, Staropoli John F, Collin Elisa, Bi Stephen, Feng Xin, Barone Rosemary, Cao Yi, O'Malley Lei, Xin Winnie, Mullen Thomas E, Sims Katherine |
Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms. Neuromuscular disorders : NMD 2013 Dec 23 (12): 969-74. Mastaglia F L, Rojana-udomsart A, James I, Needham M, Day T J, Kiers L, Corbett J A, Saunders A M, Lutz M W, Roses A D, |
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups.
Annals of the rheumatic diseases 2015 Sep . Rothwell Simon, Cooper Robert G, Lundberg Ingrid E, Miller Frederick W, Gregersen Peter K, Bowes John, Vencovsky Jiri, Danko Katalin, Limaye Vidya, Selva-O'Callaghan Albert, Hanna Michael G, Machado Pedro M, Pachman Lauren M, Reed Ann M, Rider Lisa G, Cobb Joanna, Platt Hazel, Molberg Øyvind, Benveniste Olivier, Mathiesen Pernille, Radstake Timothy, Doria Andrea, De Bleecker Jan, De Paepe Boel, Maurer Britta, Ollier William E, Padyukov Leonid, O'Hanlon Terrance P, Lee Annette, Amos Christopher I, Gieger Christian, Meitinger Thomas, Winkelmann Juliane, Wedderburn Lucy R, Chinoy Hector, Lamb Janine A, |
Mitochondrial pathology in inclusion body myositis. Neuromuscular disorders : NMD 2015 Apr 25 (4): 281-8. Lindgren Ulrika, Roos Sara, Hedberg Oldfors Carola, Moslemi Ali-Reza, Lindberg Christopher, Oldfors Ande |
The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis. Neurobiology of aging 2015 Apr 36 (4): 1766.e1-3. Gang Qiang, Bettencourt Conceicao, Machado Pedro M, Fox Zoe, Brady Stefen, Healy Estelle, Parton Matt, Holton Janice L, Hilton-Jones David, Shieh Perry B, Zanoteli Edmar, De Paepe Boel, De Bleecker Jan, Shaibani Aziz, Ripolone Michela, Violano Raffaella, Moggio Maurizio, Barohn Richard J, Dimachkie Mazen M, Mora Marina, Mantegazza Renato, Zanotti Simona, Hanna Michael G, Houlden Henry, |
Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis. Neuromuscular disorders : NMD 2015 Apr 25 (4): 289-96. Weihl Conrad C, Baloh Robert H, Lee Youjin, Chou Tsui-Fen, Pittman Sara K, Lopate Glenn, Allred Peggy, Jockel-Balsarotti Jennifer, Pestronk Alan, Harms Matthew |
The PTPN22 gene is associated with idiopathic inflammatory myopathy. Muscle & nerve 2016 Jun . Maundrell Adam, Lester Sue, Rischmueller Maureen, Hill Catherine, Cleland Leslie G, Blumbergs Peter, Wiese Michael, Limaye Vid |
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis. Neurobiology of aging 2016 Nov 47 218.e1-218.e9. Gang Qiang, Bettencourt Conceição, Machado Pedro M, Brady Stefen, Holton Janice L, Pittman Alan M, Hughes Deborah, Healy Estelle, Parton Matthew, Hilton-Jones David, Shieh Perry B, Needham Merrilee, Liang Christina, Zanoteli Edmar, de Camargo Leonardo Valente, De Paepe Boel, De Bleecker Jan, Shaibani Aziz, Ripolone Michela, Violano Raffaella, Moggio Maurizio, Barohn Richard J, Dimachkie Mazen M, Mora Marina, Mantegazza Renato, Zanotti Simona, Singleton Andrew B, Hanna Michael G, Houlden Henry, |
Genetics in inclusion body myositis. Current opinion in rheumatology 2017 8 29 (6): 639-644. Rothwell Simon, Lilleker James B, Lamb Janine |
Association study reveals novel risk loci for sporadic inclusion body myositis. European journal of neurology 2017 Feb . Johari M, Arumilli M, Palmio J, Savarese M, Tasca G, Mirabella M, Sandholm N, Lohi H, Hackman P, Udd |
Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum. Arthritis & rheumatology (Hoboken, N.J.) 2017 Jan . Rothwell Simon, Cooper Robert G, Lundberg Ingrid E, Gregersen Peter K, Hanna Michael G, Machado Pedro M, Herbert Megan K, Pruijn Ger J M, Lilleker James B, Roberts Mark, Bowes John, Seldin Michael F, Vencovsky Jiri, Danko Katalin, Limaye Vidya, Selva-O'Callaghan Albert, Platt Hazel, Molberg Øyvind, Benveniste Olivier, Radstake Timothy R D J, Doria Andrea, De Bleecker Jan, De Paepe Boel, Gieger Christian, Meitinger Thomas, Winkelmann Juliane, Amos Christopher I, Ollier William E, Padyukov Leonid, Lee Annette T, Lamb Janine A, Chinoy Hector, |
HLA-DRB1 allele and autoantibody profiles in Japanese patients with inclusion body myositis. PloS one 2020 15 (8): e0237890. Oyama Munenori, Ohnuki Yuko, Inoue Michio, Uruha Akinori, Yamashita Satoshi, Yutani Sachiko, Tanboon Jantima, Nakahara Jin, Suzuki Shingo, Shiina Takashi, Nishino Ichizo, Suzuki Shigea |
Inclusion-body myositis and primary Sjögren syndrome: mechanisms for shared etiologies. Muscle & nerve 2020 2 61 (5): 570-574. Limaye Vidya S, Cash Kathy, Smith Caroline, Koszyca Barbara, Patel Sandy, Greenberg Steven A, Hissaria Prav |
Anti-mitochondrial autoantibodies are associated with cardiomyopathy, dysphagia, and features of more severe disease in adult-onset myositis. Clinical rheumatology 2021 4 40 (10): 4095-4100. Sabbagh Sara E, Pinal-Fernandez Iago, Casal-Dominguez Maria, Albayda Jemima, Paik Julie J, Miller Frederick W, Rider Lisa G, Mammen Andrew L, Christopher-Stine Lisa, |
47XXY and 47XXX in Scleroderma and Myositis. ACR open rheumatology 2022 3 4 (6): 528-533. Scofield R Hal, Lewis Valerie M, Cavitt Joshua, Kurien Biji T, Assassi Shervin, Martin Javier, Gorlova Olga, Gregersen Peter, Lee Annette, Rider Lisa G, O'Hanlon Terrance, Rothwell Simon, Lilleker James, , Kochi Yuta, Terao Chikacshi, Igoe Ann, Stevens Wendy, Sahhar Joanne, Roddy Janet, Rischmueller Maureen, Lester Sue, Proudman Susanna, Chen Sixia, Brown Matthew A, Mayes Maureen D, Lamb Janine A, Miller Frederick |
Genome-wide imputation identifies novel associations and localises signals in idiopathic inflammatory myopathies.
Arthritis & rheumatology (Hoboken, N.J.) 2022 12 . Rothwell Simon, Amos Christopher I, Miller Frederick W, Rider Lisa G, Lundberg Ingrid E, Gregersen Peter K, Vencovsky Jiri, McHugh Neil, Limaye Vidya, Selva-O'Callaghan Albert, Hanna Michael G, Machado Pedro M, Pachman Lauren M, Reed Ann M, Molberg Øyvind, Benveniste Olivier, Mathiesen Pernille, Radstake Timothy, Doria Andrea, De Bleecker Jan L, De Paepe Boel, Maurer Britta, Ollier William E, Padyukov Leonid, O'Hanlon Terrance P, Lee Annette, Wedderburn Lucy R, Chinoy Hector, Lamb Janine A, |
High-resolution HLA genotyping in inclusion body myositis refines 8.1 ancestral haplotype association to DRB1*03:01:01 and highlights pathogenic role of arginine-74 of DR?1 chain. Journal of autoimmunity 2023 12 142 103150. Nataliya Slater, Anuradha Sooda, Emily McLeish, Kelly Beer, Anna Brusch, Rakesh Shakya, Christine Bundell, Ian James, Abha Chopra, Frank L Mastaglia, Merrilee Needham, Jerome D Coude |
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- Page last updated:May 13, 2024
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