Jodi Morrison
University of Toronto
10 Papers
100 Citations
Jodi Morrison is an academic researcher from University of Toronto. The author has contributed to research in topics: Shwachman–Diamond syndrome & Gene. The author has an hindex of 8, co-authored 10 publications.
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Papers
Mutations in SBDS are associated with Shwachman–Diamond syndrome
Graeme R.B. Boocock,Jodi Morrison,Maja Popovic,Nicole Richards,Lynda Ellis,Peter R. Durie,Johanna M. Rommens +6 more
TL;DR: Identification of disease-associated mutations in an uncharacterized gene, SBDS, in the interval of 1.9 cM at 7q11 is reported, suggesting that SDS may be caused by a deficiency in an aspect of RNA metabolism essential for development of the exocrine pancreas, hematopoiesis and chrondrogenesis.
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Shwachman syndrome: phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar.
Hedy Ginzberg,Janey Shin,Lynda Ellis,Jodi Morrison,Wan Ip,Yigal Dror,Melvin H. Freedman,Leo A. Heitlinger,Mary Ann Belt,Mary Corey,Johanna M. Rommens,Peter R. Durie +11 more
TL;DR: Clinical features among patients with Shwachman syndrome varied between patients and with age, and similarities in phenotype between isolated cases and affected sibling sets support the hypothesis that Shwacman syndrome is a single disease entity.
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Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDS.
Outi Mäkitie,Lynda Ellis,Peter R. Durie,Jodi Morrison,Etienne Sochett,Johanna M. Rommens,William G. Cole +6 more
TL;DR: The results suggest that the characteristic skeletal changes are present in all patients with SDS and SBDS mutations, but their severity and localization varies with age, and no phenotype–genotype correlation was observed.
Serum pancreatic enzymes define the pancreatic phenotype in patients with Shwachman-Diamond syndrome.
Wan F. Ip,Annie Dupuis,Lynda Ellis,Satti Beharry,Jodi Morrison,Michael Stormon,Mary Corey,Johanna M. Rommens,Peter R. Durie +8 more
TL;DR: Serum pancreatic enzymes are useful for determining the pancreatic phenotype and confirming the diagnosis of Shwachman-Diamond syndrome.
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Segregation Analysis in Shwachman-Diamond Syndrome: Evidence for Recessive Inheritance
Hedy Ginzberg,J Shin,Lynda Ellis,Susan M. Goobie,Jodi Morrison,Mary Corey,Peter R. Durie,Johanna M. Rommens +7 more
TL;DR: Simulation and genetic analyses of Shwachman-Diamond syndrome should consider a recessive model of inheritance, and estimates of segregation proportion indicate that genetic heterogeneity cannot be excluded.
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