S. Jiralerspong

Most-cited papers

1. Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin.

   M. Babcock, D. D. de Silva, R. Oaks, S. Davis-Kaplan +4 more

   1997Science943 citations

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2. Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes.

   V. Campuzano, L. Montermini, Y. Lutz, L. Cova +12 more

   1997Human Molecular Genetics754 citations

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3. Using whole exome sequencing to identify inherited causes of autism

   Timothy W. Yu, Maria H. Chahrour, Michael E. Coulter, S. Jiralerspong +45 more

   2013Neuron452 citations Open access

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4. The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients.

   Zhao-Yang Zhao, Chang-Chi Lee, S. Jiralerspong, Ramesh C. Juyal +5 more

   1995Human Molecular Genetics118 citations

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5. Somatic mosaicism for Friedreich's ataxia GAA triplet repeat expansions in the central nervous system

   L. Montermini, S. Kish, S. Jiralerspong, J. Lamarche +1 more

   1997Neurology87 citations

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6. Manganese superoxide dismutase induction by iron is impaired in Friedreich ataxia cells

   S. Jiralerspong, B. Ge, T. Hudson, M. Pandolfo

   2001FEBS Letters82 citations

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7. Knock‐out of the cyaY gene in Escherichia coli does not affect cellular iron content and sensitivity to oxidants

   Dong-Sheng Li, K. Ohshima, S. Jiralerspong, M. Bojanowski +1 more

   1999FEBS Letters81 citations Open access

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8. Functional characterization of novel mutations in GNPAT and AGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3

   Brandon Itzkovitz, S. Jiralerspong, G. Nimmo, M. Loscalzo +5 more

   2012Human Mutation73 citations Open access

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9. Frataxin shows developmentally regulated tissue-specific expression in the mouse embryo.

   S. Jiralerspong, Yanling Liu, L. Montermini, Stefano Stifani +1 more

   1997Neurobiology of Disease73 citations Open access

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10. Recovery of PEX1-Gly843Asp peroxisome dysfunction by small-molecule compounds

    Rui Zhang, Li Chen, S. Jiralerspong, A. Snowden +2 more

    2010Proceedings of the National Academy of Sciences of the United States of America64 citations Open access

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11. A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population

    S. Lévesque, C. Morin, S. Guay, J. Villeneuve +8 more

    2012BMC Medical Genetics40 citations Open access

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12. Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome.

    S. Elsea, Ramesh C. Juyal, S. Jiralerspong, B. Finucane +5 more

    1995American Journal of Human Genetics40 citations

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13. The crystal structure and dimerization interface of GADD45γ

    J. Schrag, S. Jiralerspong, M. Banville, M. Jaramillo +1 more

    2008Proceedings of the National Academy of Sciences of the United States of America28 citations Open access

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14. Regulation of the Hypoxanthine Phosphoribosyltransferase Gene: In Vitro and In Vivo Approaches

    S. Jiralerspong, P. Patel

    1996Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine23 citations

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15. Crystal structure of Gadd45 gamma

    J. Schrag, S. Jiralerspong, M. Banville, M. Jaramillo +1 more

    20081 citations

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16. Analysis of two novel cDNAs from the Smith-Magenis syndrome region on chromosome 17

    Z.-Y. Zhao, C. C. Lee, S. Jiralerspong

    19940 citations

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