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Connection

Sanjay Bidichandani to Female

This is a "connection" page, showing publications Sanjay Bidichandani has written about Female.
Connection Strength

0.298
  1. Methylated and unmethylated epialleles support variegated epigenetic silencing in Friedreich ataxia. Hum Mol Genet. 2021 02 04; 29(23):3818-3829.
    View in: PubMed
    Score: 0.058
  2. Epigenetic promoter silencing in Friedreich ataxia is dependent on repeat length. Ann Neurol. 2014 Oct; 76(4):522-8.
    View in: PubMed
    Score: 0.037
  3. Uptake of genetic testing and long-term tumor surveillance in von Hippel-Lindau disease. BMC Med Genet. 2010 Jan 12; 11:4.
    View in: PubMed
    Score: 0.027
  4. Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17. Ann Neurol. 2007 Jun; 61(6):607-10.
    View in: PubMed
    Score: 0.022
  5. Progressive GAA expansions in dorsal root ganglia of Friedreich's ataxia patients. Ann Neurol. 2007 Jan; 61(1):55-60.
    View in: PubMed
    Score: 0.022
  6. Clinical heterogeneity of recessive ataxia in the Mexican population. J Neurol Neurosurg Psychiatry. 2006 Dec; 77(12):1370-2.
    View in: PubMed
    Score: 0.022
  7. The GAA triplet-repeat is unstable in the context of the human FXN locus and displays age-dependent expansions in cerebellum and DRG in a transgenic mouse model. Hum Genet. 2007 Jan; 120(5):633-40.
    View in: PubMed
    Score: 0.021
  8. Friedreich ataxia in carriers of unstable borderline GAA triplet-repeat alleles. Ann Neurol. 2004 Dec; 56(6):898-901.
    View in: PubMed
    Score: 0.019
  9. What Mendel did not discover: exceptions in Mendelian genetics and their role in inherited human disease. J Okla State Med Assoc. 2004 Jan; 97(1):12-7.
    View in: PubMed
    Score: 0.018
  10. Very late-onset Friedreich ataxia despite large GAA triplet repeat expansions. Arch Neurol. 2000 Feb; 57(2):246-51.
    View in: PubMed
    Score: 0.013
  11. Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion. Am J Hum Genet. 1997 May; 60(5):1251-6.
    View in: PubMed
    Score: 0.011
  12. Acidic proline-rich protein Db and caries in young children. J Dent Res. 2007 Dec; 86(12):1176-80.
    View in: PubMed
    Score: 0.006
  13. Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population. Mov Disord. 2007 May 15; 22(7):1050-3.
    View in: PubMed
    Score: 0.006
  14. A mild case of Friedreich ataxia: lymphocyte and sural nerve analysis for GAA repeat length reveals somatic mosaicism. Muscle Nerve. 1998 Mar; 21(3):390-3.
    View in: PubMed
    Score: 0.003
  15. Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversions. Am J Hum Genet. 1997 May; 60(5):1184-93.
    View in: PubMed
    Score: 0.003
  16. Frataxin fracas. Nat Genet. 1997 Apr; 15(4):337-8.
    View in: PubMed
    Score: 0.003
  17. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science. 1996 Mar 08; 271(5254):1423-7.
    View in: PubMed
    Score: 0.003
  18. Circulating human factor IX produced in keratin-promoter transgenic mice: a feasibility study for gene therapy of haemophilia B. Hum Mol Genet. 1995 Jun; 4(6):993-9.
    View in: PubMed
    Score: 0.002
  19. Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition. Nucleic Acids Res. 1994 Nov 11; 22(22):4851-68.
    View in: PubMed
    Score: 0.002
  20. Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition. Nucleic Acids Res. 1994 Sep; 22(17):3511-33.
    View in: PubMed
    Score: 0.002
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.