Astrid Rasmussen to Phenotype
This is a "connection" page, showing publications Astrid Rasmussen has written about Phenotype.
Connection Strength
0.397
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Uptake of genetic testing and long-term tumor surveillance in von Hippel-Lindau disease. BMC Med Genet. 2010 Jan 12; 11:4.
Score: 0.070
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Clinical heterogeneity of recessive ataxia in the Mexican population. J Neurol Neurosurg Psychiatry. 2006 Dec; 77(12):1370-2.
Score: 0.056
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Childhood-onset of primary Sjögren's syndrome: phenotypic characterization at diagnosis of 158 children. Rheumatology (Oxford). 2021 10 02; 60(10):4558-4567.
Score: 0.039
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Defective Efferocytosis in a Murine Model of Sjögren's Syndrome Is Mediated by Dysfunctional Mer Tyrosine Kinase Receptor. Int J Mol Sci. 2021 Sep 08; 22(18).
Score: 0.039
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Systemic phenotype related to primary Sjögren's syndrome in 279 patients carrying isolated anti-La/SSB antibodies. Clin Exp Rheumatol. 2020 Jul-Aug; 38 Suppl 126(4):85-94.
Score: 0.037
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Epidemiological profile and north-south gradient driving baseline systemic involvement of primary Sjögren's syndrome. Rheumatology (Oxford). 2020 09 01; 59(9):2350-2359.
Score: 0.036
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How immunological profile drives clinical phenotype of primary Sjögren's syndrome at diagnosis: analysis of 10,500 patients (Sjögren Big Data Project). Clin Exp Rheumatol. 2018 May-Jun; 36 Suppl 112(3):102-112.
Score: 0.032
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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 Sjögren Project Consortium. Ann Rheum Dis. 2017 Jun; 76(6):1042-1050.
Score: 0.028
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Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosis. Am J Med Genet A. 2016 12; 170(12):3189-3196.
Score: 0.028
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Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures. Neurogenetics. 2014 Mar; 15(1):59-64.
Score: 0.023
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Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype. Hum Mol Genet. 2002 May 15; 11(11):1263-71.
Score: 0.010