Astrid Rasmussen to Pedigree
                            
                            
                                This is a "connection" page, showing publications Astrid Rasmussen has written about Pedigree.
                            
                            
                            
                                
                                    
                                            
    
        
        
        
            Connection Strength
            
                
            
            0.453
         
        
        
     
 
    
        
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            The lupus family registry and repository. Rheumatology (Oxford). 2011 Jan; 50(1):47-59.
            
            
                Score: 0.085
             
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            Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17. Ann Neurol. 2007 Jun; 61(6):607-10.
            
            
                Score: 0.068
             
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            Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population. Mov Disord. 2007 May 15; 22(7):1050-3.
            
            
                Score: 0.067
             
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            Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma. J Neurosurg. 2006 Mar; 104(3):389-94.
            
            
                Score: 0.062
             
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            Extensive cerebellar and thalamic degeneration in spinocerebellar ataxia type 10. Parkinsonism Relat Disord. 2019 09; 66:182-188.
            
            
                Score: 0.039
             
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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: 0.032
             
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            Clinical and molecular features of familial and sporadic cases of von Hippel-Lindau disease from Mexico. Clin Exp Ophthalmol. 2010 Apr; 38(3):277-83.
            
            
                Score: 0.021
             
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            Huntington's Disease-like 2 (HDL2) in North America and Japan. Ann Neurol. 2004 Nov; 56(5):670-4.
            
            
                Score: 0.014
             
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            Mutations in EFHC1 cause juvenile myoclonic epilepsy. Nat Genet. 2004 Aug; 36(8):842-9.
            
            
                Score: 0.014
             
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            Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10. Am J Hum Genet. 2004 Jun; 74(6):1216-24.
            
            
                Score: 0.014
             
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            Juvenile myoclonic epilepsy: linkage to chromosome 6p12 in Mexico families. Am J Med Genet. 2002 Dec 01; 113(3):268-74.
            
            
                Score: 0.012
             
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            Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5. Epilepsy Res. 2002 Aug; 50(3):265-75.
            
            
                Score: 0.012
             
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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: 0.012