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Astrid Rasmussen
Astrid Rasmussen
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Year
2016 American College of Rheumatology/European League Against Rheumatism classification criteria for primary Sjögren's syndrome: a consensus and data‐driven methodology …
CH Shiboski, SC Shiboski, R Seror, LA Criswell, M Labetoulle, ...
Arthritis & rheumatology 69 (1), 35-45, 2017
23292017
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
T Matsuura, T Yamagata, DL Burgess, A Rasmussen, RP Grewal, ...
Nature genetics 26 (2), 191-194, 2000
6192000
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome
CJ Lessard, H Li, I Adrianto, JA Ice, A Rasmussen, KM Grundahl, JA Kelly, ...
Nature genetics 45 (11), 1284-1292, 2013
5532013
Mutations in EFHC1 cause juvenile myoclonic epilepsy
T Suzuki, AV Delgado-Escueta, K Aguan, ME Alonso, J Shi, Y Hara, ...
Nature genetics 36 (8), 842-849, 2004
4202004
and the International Sjögren's Syndrome Criteria Working Group. 2016 American College of Rheumatology/European League Against Rheumatism classification criteria for primary …
CH Shiboski
Rheumatol 69, 35, 2017
2522017
Comparison of the American-European Consensus Group Sjögren's syndrome classification criteria to newly proposed American College of Rheumatology criteria in a large, carefully …
A Rasmussen, JA Ice, H Li, K Grundahl, JA Kelly, L Radfar, DU Stone, ...
Annals of the rheumatic diseases 73 (1), 31-38, 2014
2322014
Influence of geolocation and ethnicity on the phenotypic expression of primary Sjögren's syndrome at diagnosis in 8310 patients: a cross-sectional study from the Big Data …
P Brito-Zerón, N Acar-Denizli, M Zeher, A Rasmussen, R Seror, ...
Annals of the rheumatic diseases 76 (6), 1042-1050, 2017
1842017
Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study
CJ Lessard, I Adrianto, JA Ice, GB Wiley, JA Kelly, SB Glenn, AJ Adler, ...
The American Journal of Human Genetics 90 (4), 648-660, 2012
1842012
Genome‐wide DNA methylation patterns in naive CD4+ T cells from patients with primary Sjögren's syndrome
N Altorok, P Coit, T Hughes, KA Koelsch, DU Stone, A Rasmussen, ...
Arthritis & rheumatology 66 (3), 731-739, 2014
1812014
Sjogren's syndrome: An update on disease pathogenesis, clinical manifestations and treatment
FB Vivino, VY Bunya, G Massaro-Giordano, CR Johr, SL Giattino, ...
Clinical immunology (Orlando, Fla.) 203, 81-121, 2019
1802019
How immunological profile drives clinical phenotype of primary Sjogren's syndrome at diagnosis: analysis of 10,500 patients (Sjogren Big Data Project)
P Brito-Zerón, N Acar-Denizli, WF Ng, M Zeher, A Rasmussen, T Mandl, ...
Clinical and experimental rheumatology 36 (3), S102-S112, 2018
1732018
Clinical and genetic analysis of 4 Mexican families with spinocerebellar ataxia type 10
A Rasmussen, T Matsuura, L Ruano, P Yescas, A Ochoa, T Ashizawa, ...
Annals of neurology 50 (2), 234-239, 2001
1652001
A missense variant in NCF1 is associated with susceptibility to multiple autoimmune diseases
J Zhao, J Ma, Y Deng, JA Kelly, K Kim, SY Bang, HS Lee, QZ Li, ...
Nature genetics 49 (3), 433-437, 2017
1542017
Genome‐wide association study in an Amerindian ancestry population reveals novel systemic lupus erythematosus risk loci and the role of European admixture
ME Alarcón‐Riquelme, JT Ziegler, J Molineros, TD Howard, ...
Arthritis & rheumatology 68 (4), 932-943, 2016
1482016
X chromosome dose and sex bias in autoimmune diseases: increased prevalence of 47, XXX in systemic lupus erythematosus and Sjögren's syndrome
K Liu, BT Kurien, SL Zimmerman, KM Kaufman, DH Taft, LC Kottyan, ...
Arthritis & Rheumatology 68 (5), 1290-1300, 2016
1472016
Huntington's disease–like 2 (HDL2) in North America and Japan
RL Margolis, SE Holmes, A Rosenblatt, L Gourley, E O'Hearn, CA Ross, ...
Annals of Neurology: Official Journal of the American Neurological …, 2004
1402004
Progressive GAA expansions in dorsal root ganglia of Friedreich's ataxia patients
I De Biase, A Rasmussen, D Endres, S Al‐Mahdawi, A Monticelli, ...
Annals of neurology 61 (1), 55-60, 2007
1372007
Huntington disease in children: genotype-phenotype correlation
A Rasmussen, R Macias, P Yescas, A Ochoa, G Davila, E Alonso
Neuropediatrics 31 (04), 190-194, 2000
1202000
Huntington’s disease–like 2 can present as chorea-acanthocytosis
RH Walker, A Rasmussen, D Rudnicki, SE Holmes, E Alonso, T Matsuura, ...
Neurology 61 (7), 1002-1004, 2003
1062003
Genotype–phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive …
S Ganesh, AV Delgado-Escueta, T Suzuki, S Francheschetti, C Riggio, ...
Human molecular genetics 11 (11), 1263-1271, 2002
1062002
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