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Michael Geraghty

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TOP 3
Julie Rutberg; Martin S Green; Robert M Gow; Michael T Geraghty; Christina Honeywell; John Ewen; David H Birnie; Anthony Tang; Robert Lemery; Michael H Gollob
Molecular autopsy in the sudden cardiac death of a young woman: a first Canadian report.
Zuhair N Al-Hassnan; Simeon Boyd; V Praphanphoj; Ada Hamosh; Nancy Braverman; George H Thomas; Michael T Geraghty
The relationship of plasma glutamine to ammonium and of glycine to acid-base balance in propionic acidaemia.
Diana F Barron; Bernard A Cohen; Michael T Geraghty; Rick Violand; Peter C Rowe
Joint hypermobility is more common in children with chronic fatigue syndrome than in healthy controls.

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All Publications

2007: Julie Rutberg; Martin S Green; Robert M Gow; Michael T Geraghty; Christina Honeywell; John Ewen; David H Birnie; Anthony Tang; Robert Lemery; Michael H Gollob
Molecular autopsy in the sudden cardiac death of a young woman: a first Canadian report.
The Canadian journal of cardiology 2007;23(11):904-6.
2003: Zuhair N Al-Hassnan; Simeon Boyd; V Praphanphoj; Ada Hamosh; Nancy Braverman; George H Thomas; Michael T Geraghty
The relationship of plasma glutamine to ammonium and of glycine to acid-base balance in propionic acidaemia.
Journal of inherited metabolic disease 2003;26(1):89-91.
2002: Diana F Barron; Bernard A Cohen; Michael T Geraghty; Rick Violand; Peter C Rowe
Joint hypermobility is more common in children with chronic fatigue syndrome than in healthy controls.
The Journal of pediatrics 2002;141(3):421-5.
2002: Denise Li-Meng Goh; Ankita Patel; George H Thomas; Gajja S Salomons; D S M Schor; Cornelis Jakobs; Michael T Geraghty
Characterization of the human gene encoding alpha-aminoadipate aminotransferase (AADAT).
Molecular genetics and metabolism 2002;76(3):172-80.
2002: Reza Yaghmai; Amir H Kashani; Michael T Geraghty; Jay Okoh; Martin G Pomper; Albert Tangerman; Conrad Wagner; Sally P Stabler; Robert H Allen; S Harvey Mudd; Nancy Braverman
Progressive cerebral edema associated with high methionine levels and betaine therapy in a patient with cystathionine beta-synthase (CBS) deficiency.
American journal of medical genetics 2002;108(1):57-63.
2001: Julie E Hoover-Fong; Michael T Geraghty; Gerald V Raymond; George H Thomas
Gabapentin interference with urine histidine as measured by the Beckman amino acid analyser.
Journal of inherited metabolic disease 2001;24(3):415-6.
2001: Wendy R Kates; Courtney P Burnette; Ethylin Jabs; Julie Rutberg; Anne M Murphy; Grados Marco; Michael T Geraghty; Walter E Kaufmann; Godfrey D Pearlson
Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis.
Biological psychiatry 2001;49(8):677-84.
2001: V Praphanphoj; Katherine A Sacksteder; Stephen J Gould; George H Thomas; Michael T Geraghty
Identification of the alpha-aminoadipic semialdehyde dehydrogenase-phosphopantetheinyl transferase gene, the human ortholog of the yeast LYS5 gene.
Molecular genetics and metabolism 2001;72(4):336-42.
2000: Colyn B Cargile; Iain McIntosh; MV Clough; Julie Rutberg; Reza Yaghmai; Barbara K Goodman; Xiao-Ning Chen; Julie R Korenberg; George H Thomas; Michael T Geraghty
Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12).
American journal of medical genetics 2000;92(5):328-35.
2000: Katherine A Sacksteder; B J Biery; James C Morrell; Barbara K Goodman; Brian V Geisbrecht; R P Cox; Stephen J Gould; Michael T Geraghty
Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia.
American journal of human genetics 2000;66(6):1736-43.
2000: V Praphanphoj; Barbara K Goodman; George H Thomas; K M Niel; C Toomes; M J Dixon; Michael T Geraghty
Molecular cytogenetic evaluation in a patient with a translocation (3;21) associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES).
Genomics 2000;65(1):67-9.
2000: V Praphanphoj; Simeon Boyd; L J Waber; Saul W Brusilow; Michael T Geraghty
Three cases of intravenous sodium benzoate and sodium phenylacetate toxicity occurring in the treatment of acute hyperammonaemia.
Journal of inherited metabolic disease 2000;23(2):129-36.
1999: S Sigurdardottir; Barbara K Goodman; Julie Rutberg; George H Thomas; Ethylin Jabs; Michael T Geraghty
Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of "complete ring" syndrome.
American journal of medical genetics 1999;87(5):384-90.
1999: Peter C Rowe; Diana F Barron; Hugh Calkins; Irene H Maumenee; P Y Tong; Michael T Geraghty
Ehlers-Danlos syndrome.
The Journal of pediatrics 1999;135(4):513.
1999: Peter C Rowe; Diana F Barron; Hugh Calkins; Irene H Maumenee; P Y Tong; Michael T Geraghty
Orthostatic intolerance and chronic fatigue syndrome associated with Ehlers-Danlos syndrome.
The Journal of pediatrics 1999;135(4):494-9.
1999: Brian V Geisbrecht; K Schulz; K Nau; Michael T Geraghty; H Schulz; Ralf Erdmann; Stephen J Gould
Preliminary characterization of Yor180Cp: identification of a novel peroxisomal protein of saccharomyces cerevisiae involved in fatty acid metabolism.
Biochemical and biophysical research communications 1999;260(1):28-34.
1999: Jacob M Jones; K Nau; Michael T Geraghty; Ralf Erdmann; Stephen J Gould
Identification of peroxisomal acyl-CoA thioesterases in yeast and humans.
The Journal of biological chemistry 1999;274(14):9216-23.
1999: Michael T Geraghty; D Bassett; James C Morrell; Gregory J Gatto; Jianwu Bai; Brian V Geisbrecht; Philip Hieter; Stephen J Gould
Detecting patterns of protein distribution and gene expression in silico.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(6):2937-42.
1998: Brian V Geisbrecht; D Zhu; K Schulz; K Nau; James C Morrell; Michael T Geraghty; H Schulz; Ralf Erdmann; Stephen J Gould
Molecular characterization of Saccharomyces cerevisiae Delta3, Delta2-enoyl-CoA isomerase.
The Journal of biological chemistry 1998;273(50):33184-91.
1998: Barbara K Goodman; Lisa Shaffer; Julie Rutberg; M Leppert; KH Harum; S Gagos; J H Ray; M G Bialer; X Zhou; B A Pletcher; Stuart K Shapira; Michael T Geraghty
Inherited duplication Xq27-qter at Xp22.3 in severely affected males: molecular cytogenetic evaluation and clinical description in three unrelated families.
American journal of medical genetics 1998;80(4):377-84.
1998: Robert A Montgomery; Michael T Geraghty; E Bull; B D Gelb; M Johnson; Iain McIntosh; Clair A Francomano; Harry C Dietz
Multiple molecular mechanisms underlying subdiagnostic variants of Marfan syndrome.
American journal of human genetics 1998;63(6):1703-11.
1998: N Flanagan; Simeon Boyd; J Harper; L Kyne; M Earley; R Watson; Ethylin Jabs; Michael T Geraghty
Familial craniosynostosis, anal anomalies, and porokeratosis: CAP syndrome.
Journal of medical genetics 1998;35(9):763-6.
1998: Michael T Geraghty; D Vaughn; A J Nicholson; Wei-Wen Lin; Gerardo Jimenez-Sanchez; Cassandra Obie; M P Flynn; David Valle; HU CHIEN-AN
Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia.
Human molecular genetics 1998;7(9):1411-5.
1997: Sakkubai Naidu; Stephen R Dlouhy; Michael T Geraghty; ME Hodes
A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuria.
Journal of inherited metabolic disease 1997;20(6):811-6.
1997: E M Arch; Barbara K Goodman; R A Van Wesep; D Liaw; K Clarke; Ramon Parsons; Victor A McKusick; Michael T Geraghty
Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease.
American journal of medical genetics 1997;71(4):489-93.
1997: Raymond L Stallings; D Vaughn; K Hall; C Joyce; Fergus Ryan; David Barton; Michael T Geraghty
Mosaicism for trisomy 3q arising from an unbalanced, de novo t(3;15).
Journal of medical genetics 1997;34(6):512-4.
1994: M Marble; Michael T Geraghty; R de Franchis; J P Kraus; David Valle
Characterization of a cystathionine beta-synthase allele with three mutations in cis in a patient with B6 nonresponsive homocystinuria.
Human molecular genetics 1994;3(10):1883-6.
1993: Michael T Geraghty; William G Kearns; P L Pearson; David Valle
Isolation and characterization of an ornithine aminotransferase-related sequence (OATL3) mapping to 10q26.
Genomics 1993;17(2):510-3.
1993: Michael T Geraghty; L C Brody; L S Martin; M Marble; William G Kearns; P Pearson; Anthony P Monaco; H Lehrach; David Valle
The isolation of cDNAs from OATL1 at Xp 11.2 using a 480-kb YAC.
Genomics 1993;16(2):440-6.
1992: Michael T Geraghty; Elizabeth J. Perlman; L S Martin; Susan J Hayflick; James F Casella; D S Rosenblatt; David Valle
Cobalamin C defect associated with hemolytic-uremic syndrome.
The Journal of pediatrics 1992;120(6):934-7.