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Sanjay I Bidichandani

TitleProf,David L Boren
InstitutionUniversity of Oklahoma Health Sciences Center
DepartmentDept of Pediatrics
AddressOUCPB 12106
1200 Childrens Ave
Oklahoma City OK 73104
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    R01NS072418     (BIDICHANDANI, SANJAY I)Sep 30, 2010 - Aug 31, 2017
    RNA-induced transcriptional gene silencing in Friedreich ataxia
    Role: Principal Investigator

    R01NS047596     (BIDICHANDANI, SANJAY I)Jan 1, 2004 - Dec 31, 2013
    Properties and determinants of GAA repeat instability
    Role: Principal Investigator

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Lam C, Gilliam KM, Rodden LN, Schadt KA, Lynch DR, Bidichandani S. FXN gene methylation determines carrier status in Friedreich ataxia. J Med Genet. 2023 Jan 12. PMID: 36635061.
      Citations:    Fields:    
    2. Rodden LN, Gilliam KM, Lam C, Rojsajjakul T, Mesaros C, Dionisi C, Pook M, Pandolfo M, Lynch DR, Blair IA, Bidichandani SI. DNA methylation in Friedreich ataxia silences expression of frataxin isoform E. Sci Rep. 2022 03 23; 12(1):5031. PMID: 35322126.
      Citations: 4     Fields:    Translation:HumansAnimalsCells
    3. Rodden LN, Gilliam KM, Lam C, Lynch DR, Bidichandani SI. Epigenetic Heterogeneity in Friedreich Ataxia Underlies Variable FXN Reactivation. Front Neurosci. 2021; 15:752921. PMID: 34899161.
      Citations: 3     
    4. Rodden LN, Chutake YK, Gilliam K, Lam C, Soragni E, Hauser L, Gilliam M, Wiley G, Anderson MP, Gottesfeld JM, Lynch DR, Bidichandani SI. Methylated and unmethylated epialleles support variegated epigenetic silencing in Friedreich ataxia. Hum Mol Genet. 2021 02 04; 29(23):3818-3829. PMID: 33432325.
      Citations: 18     Fields:    Translation:HumansCells
    5. Delatycki MB, Bidichandani SI. Friedreich ataxia- pathogenesis and implications for therapies. Neurobiol Dis. 2019 12; 132:104606. PMID: 31494282.
      Citations: 30     Fields:    Translation:HumansAnimals
    6. Chutake YK, Lam CC, Costello WN, Anderson MP, Bidichandani SI. Reversal of epigenetic promoter silencing in Friedreich ataxia by a class I histone deacetylase inhibitor. Nucleic Acids Res. 2016 06 20; 44(11):5095-104. PMID: 26896803.
      Citations: 10     Fields:    Translation:HumansCells
    7. Chutake YK, Costello WN, Lam CC, Parikh AC, Hughes TT, Michalopulos MG, Pook MA, Bidichandani SI. FXN Promoter Silencing in the Humanized Mouse Model of Friedreich Ataxia. PLoS One. 2015; 10(9):e0138437. PMID: 26393353.
      Citations: 10     Fields:    Translation:HumansAnimalsCells
    8. Chutake YK, Lam C, Costello WN, Anderson M, Bidichandani SI. Epigenetic promoter silencing in Friedreich ataxia is dependent on repeat length. Ann Neurol. 2014 Oct; 76(4):522-8. PMID: 25112975.
      Citations: 20     Fields:    Translation:HumansCells
    9. Chutake YK, Costello WN, Lam C, Bidichandani SI. Altered nucleosome positioning at the transcription start site and deficient transcriptional initiation in Friedreich ataxia. J Biol Chem. 2014 May 30; 289(22):15194-202. PMID: 24737321.
      Citations: 24     Fields:    Translation:HumansCells
    10. Chad DA, Bidichandani S, Bruijn L, Capra JD, Dickie B, Ferguson J, Figlewicz D, Forsythe M, Kaufmann P, Kirshner A, Monti W. Funding agencies and disease organizations: resources and recommendations to facilitate ALS clinical research. Amyotroph Lateral Scler Frontotemporal Degener. 2013 May; 14 Suppl 1:62-6. PMID: 23678881.
      Citations: 2     Fields:    Translation:Humans
    11. Bourn RL, De Biase I, Pinto RM, Sandi C, Al-Mahdawi S, Pook MA, Bidichandani SI. Pms2 suppresses large expansions of the (GAA·TTC)n sequence in neuronal tissues. PLoS One. 2012; 7(10):e47085. PMID: 23071719.
      Citations: 29     Fields:    Translation:HumansAnimalsCells
    12. Rindler PM, Bidichandani SI. Role of transcript and interplay between transcription and replication in triplet-repeat instability in mammalian cells. Nucleic Acids Res. 2011 Jan; 39(2):526-35. PMID: 20843782.
      Citations: 11     Fields:    Translation:AnimalsCells
    13. Rasmussen A, Alonso E, Ochoa A, De Biase I, Familiar I, Yescas P, Sosa AL, Rodríguez Y, Chávez M, López-López M, Bidichandani SI. Uptake of genetic testing and long-term tumor surveillance in von Hippel-Lindau disease. BMC Med Genet. 2010 Jan 12; 11:4. PMID: 20064270.
      Citations: 11     Fields:    Translation:HumansCells
    14. De Biase I, Chutake YK, Rindler PM, Bidichandani SI. Epigenetic silencing in Friedreich ataxia is associated with depletion of CTCF (CCCTC-binding factor) and antisense transcription. PLoS One. 2009 Nov 19; 4(11):e7914. PMID: 19956589.
      Citations: 68     Fields:    Translation:HumansCells
    15. Bourn RL, Rindler PM, Pollard LM, Bidichandani SI. E. coli mismatch repair acts downstream of replication fork stalling to stabilize the expanded (GAA.TTC)(n) sequence. Mutat Res. 2009 Feb 10; 661(1-2):71-7. PMID: 19046977.
      Citations: 2     Fields:    Translation:HumansCells
    16. Zakhary GM, Clark RM, Bidichandani SI, Owen WL, Slayton RL, Levine M. Acidic proline-rich protein Db and caries in young children. J Dent Res. 2007 Dec; 86(12):1176-80. PMID: 18037651.
      Citations: 14     Fields:    Translation:HumansCellsPHPublic Health
    17. Pollard LM, Bourn RL, Bidichandani SI. Repair of DNA double-strand breaks within the (GAA*TTC)n sequence results in frequent deletion of the triplet-repeat sequence. Nucleic Acids Res. 2008 Feb; 36(2):489-500. PMID: 18045804.
      Citations: 15     Fields:    Translation:HumansCells
    18. Pollard LM, Chutake YK, Rindler PM, Bidichandani SI. Deficiency of RecA-dependent RecFOR and RecBCD pathways causes increased instability of the (GAA*TTC)n sequence when GAA is the lagging strand template. Nucleic Acids Res. 2007; 35(20):6884-94. PMID: 17932052.
      Citations: 7     Fields:    Translation:HumansCells
    19. Rasmussen A, De Biase I, Fragoso-Benítez M, Macías-Flores MA, Yescas P, Ochoa A, Ashizawa T, Alonso ME, Bidichandani SI. Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17. Ann Neurol. 2007 Jun; 61(6):607-10. PMID: 17474109.
      Citations: 4     Fields:    Translation:HumansCells
    20. Alonso E, Martínez-Ruano L, De Biase I, Mader C, Ochoa A, Yescas P, Gutiérrez R, White M, Ruano L, Fragoso-Benítez M, Ashizawa T, Bidichandani SI, Rasmussen A. Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population. Mov Disord. 2007 May 15; 22(7):1050-3. PMID: 17427938.
      Citations: 20     Fields:    Translation:HumansCells
    21. De Biase I, Rasmussen A, Monticelli A, Al-Mahdawi S, Pook M, Cocozza S, Bidichandani SI. Somatic instability of the expanded GAA triplet-repeat sequence in Friedreich ataxia progresses throughout life. Genomics. 2007 Jul; 90(1):1-5. PMID: 17498922.
      Citations: 41     Fields:    Translation:HumansCells
    22. De Biase I, Rasmussen A, Endres D, Al-Mahdawi S, Monticelli A, Cocozza S, Pook M, Bidichandani SI. Progressive GAA expansions in dorsal root ganglia of Friedreich's ataxia patients. Ann Neurol. 2007 Jan; 61(1):55-60. PMID: 17262846.
      Citations: 57     Fields:    Translation:HumansCells
    23. Rasmussen A, Gómez M, Alonso E, Bidichandani SI. Clinical heterogeneity of recessive ataxia in the Mexican population. J Neurol Neurosurg Psychiatry. 2006 Dec; 77(12):1370-2. PMID: 17110750.
      Citations: 4     Fields:    Translation:Humans
    24. M Rindler P, Clark RM, Pollard LM, De Biase I, Bidichandani SI. Replication in mammalian cells recapitulates the locus-specific differences in somatic instability of genomic GAA triplet-repeats. Nucleic Acids Res. 2006; 34(21):6352-61. PMID: 17142224.
      Citations: 20     Fields:    Translation:HumansAnimalsCells
    25. Clark RM, De Biase I, Malykhina AP, Al-Mahdawi S, Pook M, Bidichandani SI. 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. PMID: 17024371.
      Citations: 34     Fields:    Translation:HumansAnimalsCells
    26. Clark RM, Bhaskar SS, Miyahara M, Dalgliesh GL, Bidichandani SI. Expansion of GAA trinucleotide repeats in mammals. Genomics. 2006 Jan; 87(1):57-67. PMID: 16316739.
      Citations: 22     Fields:    Translation:HumansAnimalsCells
    27. Sharma R, De Biase I, Gómez M, Delatycki MB, Ashizawa T, Bidichandani SI. Friedreich ataxia in carriers of unstable borderline GAA triplet-repeat alleles. Ann Neurol. 2004 Dec; 56(6):898-901. PMID: 15562408.
      Citations: 25     Fields:    Translation:HumansCells
    28. Pollard LM, Sharma R, Gómez M, Shah S, Delatycki MB, Pianese L, Monticelli A, Keats BJ, Bidichandani SI. Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxia. Nucleic Acids Res. 2004; 32(19):5962-71. PMID: 15534367.
      Citations: 29     Fields:    Translation:HumansCells
    29. Gómez M, Clark RM, Nath SK, Bhatti S, Sharma R, Alonso E, Rasmussen A, Bidichandani SI. Genetic admixture of European FRDA genes is the cause of Friedreich ataxia in the Mexican population. Genomics. 2004 Nov; 84(5):779-84. PMID: 15475256.
      Citations: 4     Fields:    Translation:HumansCells
    30. Clark RM, Dalgliesh GL, Endres D, Gomez M, Taylor J, Bidichandani SI. Expansion of GAA triplet repeats in the human genome: unique origin of the FRDA mutation at the center of an Alu. Genomics. 2004 Mar; 83(3):373-83. PMID: 14962663.
      Citations: 27     Fields:    Translation:HumansCells
    31. Potaman VN, Oussatcheva EA, Lyubchenko YL, Shlyakhtenko LS, Bidichandani SI, Ashizawa T, Sinden RR. Length-dependent structure formation in Friedreich ataxia (GAA)n*(TTC)n repeats at neutral pH. Nucleic Acids Res. 2004; 32(3):1224-31. PMID: 14978261.
      Citations: 44     Fields:    Translation:HumansCells
    32. Hern LM, Bidichandani SI. 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. PMID: 14998061.
      Citations:    Fields:    Translation:Humans
    33. Gomes-Pereira M, Bidichandani SI, Monckton DG. Analysis of unstable triplet repeats using small-pool polymerase chain reaction. Methods Mol Biol. 2004; 277:61-76. PMID: 15201449.
      Citations: 45     Fields:    Translation:Cells
    34. Sharma R, Bhatti S, Gomez M, Clark RM, Murray C, Ashizawa T, Bidichandani SI. The GAA triplet-repeat sequence in Friedreich ataxia shows a high level of somatic instability in vivo, with a significant predilection for large contractions. Hum Mol Genet. 2002 Sep 01; 11(18):2175-87. PMID: 12189170.
      Citations: 31     Fields:    Translation:HumansCells
    35. Hai M, Bidichandani SI, Patel PI. Identification of a positive regulatory element in the myelin-specific promoter of the PMP22 gene. J Neurosci Res. 2001 Sep 15; 65(6):508-19. PMID: 11550219.
      Citations: 10     Fields:    Translation:HumansCells
    36. Hai M, Bidichandani SI, Hogan ME, Patel PI. Competitive binding of triplex-forming oligonucleotides in the two alternate promoters of the PMP22 gene. Antisense Nucleic Acid Drug Dev. 2001 Aug; 11(4):233-46. PMID: 11572600.
      Citations: 4     Fields:    Translation:HumansAnimalsCells
    37. Désarnaud F, Bidichandani S, Patel PI, Baulieu EE, Schumacher M. Glucocorticosteroids stimulate the activity of the promoters of peripheral myelin protein-22 and protein zero genes in Schwann cells. Brain Res. 2000 May 19; 865(1):12-6. PMID: 10814728.
      Citations: 24     Fields:    Translation:AnimalsCells
    38. Bidichandani SI, Garcia CA, Patel PI, Dimachkie MM. Very late-onset Friedreich ataxia despite large GAA triplet repeat expansions. Arch Neurol. 2000 Feb; 57(2):246-51. PMID: 10681084.
      Citations: 7     Fields:    Translation:HumansCells
    39. Bidichandani SI, Purandare SM, Taylor EE, Gumin G, Machkhas H, Harati Y, Gibbs RA, Ashizawa T, Patel PI. Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequence. Hum Mol Genet. 1999 Dec; 8(13):2425-36. PMID: 10556290.
      Citations: 20     Fields:    Translation:HumansCells
    40. Machkhas H, Bidichandani SI, Patel PI, Harati Y. 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. PMID: 9486868.
      Citations: 4     Fields:    Translation:HumansCells
    41. Bidichandani SI, Ashizawa T, Patel PI. The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure. Am J Hum Genet. 1998 Jan; 62(1):111-21. PMID: 9443873.
      Citations: 130     Fields:    Translation:HumansCells
    42. Yang SP, Bidichandani SI, Figuera LE, Juyal RC, Saxon PJ, Baldini A, Patel PI. 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. PMID: 9150166.
      Citations: 9     Fields:    Translation:HumansCells
    43. Bidichandani SI, Ashizawa T, Patel PI. 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. PMID: 9150176.
      Citations: 37     Fields:    Translation:HumansCells
    44. Cossée M, Campuzano V, Koutnikova H, Fischbeck K, Mandel JL, Koenig M, Bidichandani SI, Patel PI, Moltè MD, Cañizares J, De Frutos R, Pianese L, Cavalcanti F, Monticelli A, Cocozza S, Montermini L, Pandolfo M. Frataxin fracas. Nat Genet. 1997 Apr; 15(4):337-8. PMID: 9090376.
      Citations: 15     Fields:    Translation:Humans
    45. Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science. 1996 Mar 08; 271(5254):1423-7. PMID: 8596916.
      Citations: 887     Fields:    Translation:HumansCells
    46. Alexander MY, Bidichandani SI, Cousins FM, Robinson CJ, Duffie E, Akhurst RJ. 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. PMID: 7544665.
      Citations: 4     Fields:    Translation:HumansAnimalsCells
    47. Bidichandani SI, Lanyon WG, Shiach CR, Lowe GD, Connor JM. Detection of mutations in ectopic factor VIII transcripts from nine haemophilia A patients and the correlation with phenotype. Hum Genet. 1995 May; 95(5):531-8. PMID: 7759074.
      Citations: 2     Fields:    Translation:HumansCells
    48. Tuddenham EG, Schwaab R, Seehafer J, Millar DS, Gitschier J, Higuchi M, Bidichandani S, Connor JM, Hoyer LW, Yoshioka A, et al. 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. PMID: 7984443.
      Citations: 13     Fields:    Translation:HumansCells
    49. Bidichandani SI, Lanyon WG, Connor JM. Characterisation of a 5-bp deletion in exon 4 of the factor VIII gene: concordance with slipped-mispairing at DNA replication. Hum Genet. 1994 Oct; 94(4):447-9. PMID: 7927348.
      Citations: 1     Fields:    Translation:HumansCells
    50. Tuddenham EG, Schwaab R, Seehafer J, Millar DS, Gitschier J, Higuchi M, Bidichandani S, Connor JM, Hoyer LW, Yoshioka A, et al. 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. PMID: 7937051.
      Citations: 8     Fields:    Translation:HumansCells
    51. Bidichandani SI, Shiach CR, Lanyon WG, Connor JM. A novel splice donor mutation affecting position +3 in intron 6 of the factor VIII gene. Hum Mol Genet. 1994 Apr; 3(4):651-3. PMID: 8069313.
      Citations: 4     Fields:    Translation:HumansCells
    52. Alexander MY, Bidichandani S, Robinson C, Trainer AH, Akhurst RJ. Physical methods of gene delivery using keratinocytes as a target for somatic cell gene therapy. Gene Ther. 1994; 1 Suppl 1:S57. PMID: 8542402.
      Citations:    Fields:    Translation:AnimalsCells
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