Associate Professor Bruce Bennetts

Associate Professor
Genetic Medicine, Children's Hospital, Westmead

Telephone +61 2 9845 3246
Fax +61 2 9891 3204

Map

Selected grants

2001

  • Detection of susceptibility genes for multiple sclerosis; Stewart G, Bennetts B, Heard R, Compston, A; National Health and Medical Research Council (NHMRC)/Project Grants.

Selected publications

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Journals

  • Biggin, A., Briody, J., Ormshaw, E., Wong, K., Bennetts, B., Munns, C. (2014). Fracture during Intravenous Bisphosphonate Treatment in a Child with Osteogenesis Imperfecta: An Argument for a More Frequent, Low-Dose Treatment Regimen. Hormone Research in Paediatrics, 81(3), 204-210. [More Information]
  • Christie, L., Wotton, T., Bennetts, B., Wiley, V., Wilcken, B., Rogers, C., Boyle, J., Turner, C., Hansen, J., Hunter, M., et al (2013). Maternal attitudes to newborn screening for fragile X syndrome. American Journal of Medical Genetics. Part A, 161A (2), 301-311. [More Information]
  • Shinar, Y., Obici, L., Aksentijevich, I., Bennetts, B., Austrup, F., Ceccherini, I., Costa, J., De Leener, A., Morris, M., et al (2012). Guidelines for the genetic diagnosis of hereditary recurrent fevers. Annals of the Rheumatic Diseases, 71(10), 1599-1605. [More Information]
  • Stark, Z., Storen, R., Bennetts, B., Savarirayan, R., Jamieson, R. (2011). Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring. European Journal of Human Genetics, 19(7), 753-756. [More Information]
  • Balasubramaniam, S., Rudduck, C., Bennetts, B., Peters, G., Wilcken, B., Ellaway, C. (2010). Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency. Molecular Genetics and Metabolism, 99(1), 34-41. [More Information]
  • White, R., Ho, G., Schmidt, S., Scheffer, I., Fischer, A., Yendle, S., Bienvenu, T., Nectoux, J., Ellaway, C., Darmanian, A., Cloosterman, D., Bennetts, B., Christodoulou, J., et al (2010). Cyclin-Dependent Kinase-Like 5 (CDKL5) Mutation Screening in Rett Syndrome and Related Disorders. Twin Research and Human Genetics, 13(2), 168-178. [More Information]
  • Hamvas, A., Nogee, L., Wegner, D., DePass, K., Christodoulou, J., Bennetts, B., McQuade, L., Gray, P., Deterding, R., Carroll, T. (2009). Inherited Surfactant Deficiency Caused by Uniparental Disomy of Rare Mutations in the Surfactant Protein-B and ATP Binding Cassette,Subfamily A, Member 3 Genes. The Journal of Pediatrics, 155(6), 854-859. [More Information]
  • Gallego, P., Craig, M., Duffin, A., Bennetts, B., Jenkins, A., Hofer, S., Lam, A., Donaghue, K. (2008). Association Between p.Leu54Met Polymorphism at the Paraoxonase-1 Gene and Plantar Fascia Thickness in Young Subjects With Type 1 Diabetes. Diabetes Care, 31(8), 1585-1589. [More Information]
  • Hardwick, S., Reuter, K., Williamson, S., Vasudevan, V., Donald, J., Slater, K., Bennetts, B., Bebbinton, A., Leonard, H., Williams, S., Christodoulou, J., et al (2007). Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband. European Journal of Human Genetics, 15(12), 1218-1229. [More Information]
  • Chiong, M., Bennetts, B., Strasser, S., Wilcken, B. (2007). Fatal late-onset ornithine transcarbamylase deficiency after coronary artery bypass surgery. Medical Journal of Australia, 186(8), 418-419. [More Information]
  • Peters, G., Bennetts, B., McGillivray, G., Wu, Z., Poon, C., Algar, E. (2007). The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: Two new reports. American Journal of Medical Genetics. Part A, 146, 137-48. [More Information]
  • Bugeja, M., Booth, D., Bennetts, B., Heard, R., Rubio, J., Stewart, G. (2006). An investigation of polymorphisms in the 17q11.2-12 CC chemokine gene cluster for association with multiple sclerosis in Australians. BMC Medical Genetics, 7, 64-64. [More Information]
  • Bugeja, M., Booth, D., Bennetts, B., Heard, R., Stewart, G. (2006). An investigation of polymorphisms in the 4q1 3.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in Australians. Multiple Sclerosis: clinical and laboratory research, 12(6), 710-722. [More Information]
  • Hofer, S., Bennetts, B., Chan, A., Holloway, B., Karschimkus, C., Jenkins, A., Silink, M., Donaghue, K. (2006). Association between PON 1 polymorphisms, PON activity and diabetes complications. Journal of Diabetes and Its Complications, 20(5), 322-328. [More Information]
  • Thamotharampillai, K., Chan, A., Bennetts, B., Craig, M., Cusumano, J., Silink, M., Oates, P., Donaghue, K. (2006). Decline in Neurophysiological Function After 7 Years in an Adolescent Diabetic Cohort and the Role of Aldose Reductase Gene Polymorphisms. Diabetes Care, 29(9), 2053-2057. [More Information]
  • Ades, L., Sullivan, K., Biggin, A., Haan, E., Brett, M., Holman, K., Dixon, J., Robertson, S., Holmes, A., Rogers, J., Bennetts, B. (2006). FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited. American Journal of Medical Genetics. Part A, 140(10), 1047-1058. [More Information]
  • Chiong, M., Marinaki, M., Duley, J., Bennetts, B., Ouvrier, R., Christodoulou, J. (2006). Lesch-Nyhan disease in a 20-year-old man incorrectly described as developing 'cerebral palsy' after general anaesthesia in infancy. Journal of Inherited Metabolic Disease (JIMD), 29(4), 594-DOI 10.1007/s10545-006-0281-4. [More Information]
  • Waddell, L., Wiley, V., Carpenter, K., Bennetts, B., Angel, L., Andresen, B., Wilcken, B. (2006). Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations. Molecular Genetics and Metabolism, 87(1), 32-39. [More Information]
  • Thamotharampillai, K., Craig, M., Chan, A., Bennetts, B., Silink, M., Cusumano, J., Donaghue, K. (2006). The role of aldose reductase gene (AKR1B1) polymorphisms in neurophysiological decline in adolescents with type 1 diabetes - a seven-year longitudinal study. Hormone Research, 65(Suppl. 4), 16-16.
  • Bugeja, M., Booth, D., Bennetts, B., Heard, R., Burgner, D., Stewart, G. (2005). An investigation of NOS2A promoter polymorphisms in Australian multiple sclerosis patients. European Journal of Human Genetics, 13(7), 815-822. [More Information]
  • Biggin, A., Henke, R., Bennetts, B., Thorburn, D., Christodoulou, J. (2005). Mutation screening of the mitochondrial genome using denaturing high-performance liquid chromatography. Molecular Genetics and Metabolism, 84(1), 61-74. [More Information]
  • Neas, K., Bennetts, B., Carpenter, K., White, R., Kirk, E., Wilson, M., Kelley, R., Baric, I., Christodoulou, J. (2005). OPA3 mutation screening in patients with unexplained 3-methylglutaconic aciduria. Journal of Inherited Metabolic Disease (JIMD), 28(4), 525-532. [More Information]
  • Donaghue, K., Margan, S., Chan, A., Holloway, B., Silink, M., Rangel, T., Bennetts, B. (2005). The association of aldose reductase gene (AKR1B1) polymorphisms with diabetic neuropathy in adolescents. Diabetic Medicine, 22(10), 1315-1320. [More Information]
  • Ginn, S., Smyth, C., Wong, M., Bennetts, B., Rowe, P., Alexander, I. (2004). A Novel Splice-Site Mutation In The Common Gamma Chain (Gammac) Gene Il2Rg Results In X-Linked Severe Combined Immunodeficiency With An Atypical Nk+ Phenotype. Human Mutation, 23(5), 522-523.
  • Bugeja, M., Booth, D., Bennetts, B., Guerin, J., Kaldor, J., Stewart, G. (2004). Analysis Of The Ccl3-L1 Gene For Association With Hiv-1 Susceptibility And Disease Progression. AIDS, 18(7), 1069-1071.
  • Teutsch, S., Booth, D., Bennetts, B., Heard, R., Stewart, G. (2004). Association Of Common T Cell Activation Gene Polymorphisms With Multiple Sclerosis In Australian Patients. Journal of Neuroimmunology, 148(2), 218-30. [More Information]
  • Biggin, A., Holman, K., Brett, M., Bennetts, B., Ades, L. (2004). Detection Of Thirty Novel FBN1 Mutations In Patients With Marfan Syndrome Or A Related Fibrillinopathy. Human Mutation, 23(1), 99-106.
  • Ades, L., Holman, K., Brett, M., Edwards, M., Bennetts, B. (2004). Ectopia Lentis Phenotypes And The Fbn1 Gene. American Journal of Medical Genetics. Part A, 126A (3), 284-289.
  • Weaving, L., Christodoulou, J., Williamson, S., Friend, K., McKenzie, O., Archer, H., Evans, J., Clarke, A., Pelka, G., Tam, P., Lahooti, H., Ellaway, C., Bennetts, B., Watson, C., et al (2004). Mutations Of Cdkl5 Cause A Severe Neurodevelopmental Disorder With Infantile Spasms And Mental Retardation. American Journal of Human Genetics, 75, 1079-1093.
  • Ban, M., Sawcer, S., Heard, R., Bennetts, B., Adams, S., Booth, D., Perich, V., Setakis, E., Compston, A., Stewart, G. (2003). A genome-wide screen for linkage disequilibrium in Australian HLA-DRB1*1501 positive multiple sclerosis patients. Journal of Neuroimmunology, 143(1-2), 60-64. [More Information]
  • Weaving, L., Williamson, S., Bennetts, B., Davis, M., Ellaway, C., Leonard, H., Thong, M., Delatycki, M., Thompson, E., Laing, N., Christodoulou, J. (2003). Effects of MECP2 mutation type, location and X-inactivation in modulating Rett Syndrome phenotype. American Journal of Medical Genetics. Part A, 118A, 103-114.
  • Urwin, R., Bennetts, B., Wilcken, B., Lampropoulos, B., Beumont, P., Russell, J., Tanner, S., Nunn, K. (2003). Gene-gene interaction between the monoamine oxidase A gene and solute carrier family 6 (neurotransmitter transporter, noradrenalin) member 2 gene in anorexia nervose (restrictive subtype). European Journal of Human Genetics, 11(12), 945-950.
  • Teutsch, S., Booth, D., Bennetts, B., Heard, R., Stewart, G. (2003). Identification of 11 novel and common single nucleotide polymorphisms in the interleukin-7 receptor-alpha gene and their associations with multiple sclerosis. European Journal of Human Genetics, 11(7), 509-515.
  • Wiley, V., Carpenter, K., Bennetts, B., Wilcken, B. (2003). Information overload - new technologies, can we store the data? Southeast Asian Journal of Tropical Medicine and Public Health, 34(S3), 59-62.
  • Urwin, R., Bennetts, B., Wilcken, B., Beumont, P., Russell, J., Nunn, K. (2003). Investigation of epistasis between the serotonin transporter and norepinephrine transproter genes in anorexia nervosa. Neuropsychopharmacology, 28(7), 1351-1355.
  • Christodoulou, J., Grimm, A., Maher, T., Bennetts, B. (2003). RettBASE: the IRSA MECP2 variation database-A new mutation database in evolution. Human Mutation, 21(5), 466-472.
  • Ban, M., Stewart, G., Bennetts, B., Heard, R., Simmons, R., Maranian, M., Compston, A., Sawcer, S. (2002). A genome screen for linkage in Australian sibling-pairs with multiple sclerosis. Genes and Immunity, 3(8), 464-469.
  • Milledge, J., Shaw, P., Mansour, A., Williamson, S., Bennetts, B., Roscioli, T., Curtin, J., Christodoulou, J. (2002). Allogeneic bone marrow transplantation: cure for familial Mediterranean fever. Blood, 100(3), 774-777.
  • Urwin, R., Bennetts, B., Wilcken, B., Lampropolous, B., Beumont, P., Clarke, S., Russell, J., Tanner, S., Nunn, K. (2002). Anorexia nervosa (restrictive subtype) is associated with a polymorphism in the novel noreprinephrine transporter gene promoter polymorphic region. Molecular Psychiatry, 7(6), 652-657.
  • Buhler, M., Craig, M., Donaghue, K., Badhwar, P., Willis, J., Manolios, N., Tait, B., Silink, M., Bennetts, B., Stewart, G. (2002). CCR5 Genotyping in an Australian and New Zealand type 1 Diabetes Cohort. Autoimmunity, 65(7), 457-461.
  • Kao, Y., Donaghue, K., Chan, A., Bennetts, B., Knight, J., Silink, M. (2002). Paraoxonase gene cluster is a genetic marker for early microvascular complications in Type 1 diabetes. Diabetic Medicine, 19(3), 212-215.
  • Bennetts, B., Donaghue, K., Silink, M., Kordonouri, O., James, R., Chan, A., Kao, Y., Danne, T. (2001). Modulation by blood glucose levels of activity and concentration of paraoxonase in young patients with Type 1 diabetes mellitus. Metabolism: clinical and experimental, 50, 657-660.
  • Hughes, J., Weston, S., Bennetts, B., Angulo,, R., Prasad, M., Jaworski, R., Jolles, S., Kossard, S., Fox, S., Benson, E. (2001). The application of a PCR technique for the detection of immunoglobulin heavy chain gene rearrangements in fresh or paraffin-embedded skin tissue. Pathology, 33, 222-225.
  • Huang, Q., Teutsch, S., Buhler, M., Bennetts, B., Heard, R., Manolios, N., Stewart, G. (2000). Evaluation of the Apo-1/Fas promoter Mva 1 polymorphism in multiple sclerosis. Multiple Sclerosis: clinical and laboratory research, 6(1), 14-18.

2014

  • Biggin, A., Briody, J., Ormshaw, E., Wong, K., Bennetts, B., Munns, C. (2014). Fracture during Intravenous Bisphosphonate Treatment in a Child with Osteogenesis Imperfecta: An Argument for a More Frequent, Low-Dose Treatment Regimen. Hormone Research in Paediatrics, 81(3), 204-210. [More Information]

2013

  • Christie, L., Wotton, T., Bennetts, B., Wiley, V., Wilcken, B., Rogers, C., Boyle, J., Turner, C., Hansen, J., Hunter, M., et al (2013). Maternal attitudes to newborn screening for fragile X syndrome. American Journal of Medical Genetics. Part A, 161A (2), 301-311. [More Information]

2012

  • Shinar, Y., Obici, L., Aksentijevich, I., Bennetts, B., Austrup, F., Ceccherini, I., Costa, J., De Leener, A., Morris, M., et al (2012). Guidelines for the genetic diagnosis of hereditary recurrent fevers. Annals of the Rheumatic Diseases, 71(10), 1599-1605. [More Information]

2011

  • Stark, Z., Storen, R., Bennetts, B., Savarirayan, R., Jamieson, R. (2011). Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring. European Journal of Human Genetics, 19(7), 753-756. [More Information]

2010

  • Balasubramaniam, S., Rudduck, C., Bennetts, B., Peters, G., Wilcken, B., Ellaway, C. (2010). Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency. Molecular Genetics and Metabolism, 99(1), 34-41. [More Information]
  • White, R., Ho, G., Schmidt, S., Scheffer, I., Fischer, A., Yendle, S., Bienvenu, T., Nectoux, J., Ellaway, C., Darmanian, A., Cloosterman, D., Bennetts, B., Christodoulou, J., et al (2010). Cyclin-Dependent Kinase-Like 5 (CDKL5) Mutation Screening in Rett Syndrome and Related Disorders. Twin Research and Human Genetics, 13(2), 168-178. [More Information]

2009

  • Hamvas, A., Nogee, L., Wegner, D., DePass, K., Christodoulou, J., Bennetts, B., McQuade, L., Gray, P., Deterding, R., Carroll, T. (2009). Inherited Surfactant Deficiency Caused by Uniparental Disomy of Rare Mutations in the Surfactant Protein-B and ATP Binding Cassette,Subfamily A, Member 3 Genes. The Journal of Pediatrics, 155(6), 854-859. [More Information]

2008

  • Gallego, P., Craig, M., Duffin, A., Bennetts, B., Jenkins, A., Hofer, S., Lam, A., Donaghue, K. (2008). Association Between p.Leu54Met Polymorphism at the Paraoxonase-1 Gene and Plantar Fascia Thickness in Young Subjects With Type 1 Diabetes. Diabetes Care, 31(8), 1585-1589. [More Information]

2007

  • Hardwick, S., Reuter, K., Williamson, S., Vasudevan, V., Donald, J., Slater, K., Bennetts, B., Bebbinton, A., Leonard, H., Williams, S., Christodoulou, J., et al (2007). Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband. European Journal of Human Genetics, 15(12), 1218-1229. [More Information]
  • Chiong, M., Bennetts, B., Strasser, S., Wilcken, B. (2007). Fatal late-onset ornithine transcarbamylase deficiency after coronary artery bypass surgery. Medical Journal of Australia, 186(8), 418-419. [More Information]
  • Peters, G., Bennetts, B., McGillivray, G., Wu, Z., Poon, C., Algar, E. (2007). The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: Two new reports. American Journal of Medical Genetics. Part A, 146, 137-48. [More Information]

2006

  • Bugeja, M., Booth, D., Bennetts, B., Heard, R., Rubio, J., Stewart, G. (2006). An investigation of polymorphisms in the 17q11.2-12 CC chemokine gene cluster for association with multiple sclerosis in Australians. BMC Medical Genetics, 7, 64-64. [More Information]
  • Bugeja, M., Booth, D., Bennetts, B., Heard, R., Stewart, G. (2006). An investigation of polymorphisms in the 4q1 3.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in Australians. Multiple Sclerosis: clinical and laboratory research, 12(6), 710-722. [More Information]
  • Hofer, S., Bennetts, B., Chan, A., Holloway, B., Karschimkus, C., Jenkins, A., Silink, M., Donaghue, K. (2006). Association between PON 1 polymorphisms, PON activity and diabetes complications. Journal of Diabetes and Its Complications, 20(5), 322-328. [More Information]
  • Thamotharampillai, K., Chan, A., Bennetts, B., Craig, M., Cusumano, J., Silink, M., Oates, P., Donaghue, K. (2006). Decline in Neurophysiological Function After 7 Years in an Adolescent Diabetic Cohort and the Role of Aldose Reductase Gene Polymorphisms. Diabetes Care, 29(9), 2053-2057. [More Information]
  • Ades, L., Sullivan, K., Biggin, A., Haan, E., Brett, M., Holman, K., Dixon, J., Robertson, S., Holmes, A., Rogers, J., Bennetts, B. (2006). FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited. American Journal of Medical Genetics. Part A, 140(10), 1047-1058. [More Information]
  • Chiong, M., Marinaki, M., Duley, J., Bennetts, B., Ouvrier, R., Christodoulou, J. (2006). Lesch-Nyhan disease in a 20-year-old man incorrectly described as developing 'cerebral palsy' after general anaesthesia in infancy. Journal of Inherited Metabolic Disease (JIMD), 29(4), 594-DOI 10.1007/s10545-006-0281-4. [More Information]
  • Waddell, L., Wiley, V., Carpenter, K., Bennetts, B., Angel, L., Andresen, B., Wilcken, B. (2006). Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations. Molecular Genetics and Metabolism, 87(1), 32-39. [More Information]
  • Thamotharampillai, K., Craig, M., Chan, A., Bennetts, B., Silink, M., Cusumano, J., Donaghue, K. (2006). The role of aldose reductase gene (AKR1B1) polymorphisms in neurophysiological decline in adolescents with type 1 diabetes - a seven-year longitudinal study. Hormone Research, 65(Suppl. 4), 16-16.

2005

  • Bugeja, M., Booth, D., Bennetts, B., Heard, R., Burgner, D., Stewart, G. (2005). An investigation of NOS2A promoter polymorphisms in Australian multiple sclerosis patients. European Journal of Human Genetics, 13(7), 815-822. [More Information]
  • Biggin, A., Henke, R., Bennetts, B., Thorburn, D., Christodoulou, J. (2005). Mutation screening of the mitochondrial genome using denaturing high-performance liquid chromatography. Molecular Genetics and Metabolism, 84(1), 61-74. [More Information]
  • Neas, K., Bennetts, B., Carpenter, K., White, R., Kirk, E., Wilson, M., Kelley, R., Baric, I., Christodoulou, J. (2005). OPA3 mutation screening in patients with unexplained 3-methylglutaconic aciduria. Journal of Inherited Metabolic Disease (JIMD), 28(4), 525-532. [More Information]
  • Donaghue, K., Margan, S., Chan, A., Holloway, B., Silink, M., Rangel, T., Bennetts, B. (2005). The association of aldose reductase gene (AKR1B1) polymorphisms with diabetic neuropathy in adolescents. Diabetic Medicine, 22(10), 1315-1320. [More Information]

2004

  • Ginn, S., Smyth, C., Wong, M., Bennetts, B., Rowe, P., Alexander, I. (2004). A Novel Splice-Site Mutation In The Common Gamma Chain (Gammac) Gene Il2Rg Results In X-Linked Severe Combined Immunodeficiency With An Atypical Nk+ Phenotype. Human Mutation, 23(5), 522-523.
  • Bugeja, M., Booth, D., Bennetts, B., Guerin, J., Kaldor, J., Stewart, G. (2004). Analysis Of The Ccl3-L1 Gene For Association With Hiv-1 Susceptibility And Disease Progression. AIDS, 18(7), 1069-1071.
  • Teutsch, S., Booth, D., Bennetts, B., Heard, R., Stewart, G. (2004). Association Of Common T Cell Activation Gene Polymorphisms With Multiple Sclerosis In Australian Patients. Journal of Neuroimmunology, 148(2), 218-30. [More Information]
  • Biggin, A., Holman, K., Brett, M., Bennetts, B., Ades, L. (2004). Detection Of Thirty Novel FBN1 Mutations In Patients With Marfan Syndrome Or A Related Fibrillinopathy. Human Mutation, 23(1), 99-106.
  • Ades, L., Holman, K., Brett, M., Edwards, M., Bennetts, B. (2004). Ectopia Lentis Phenotypes And The Fbn1 Gene. American Journal of Medical Genetics. Part A, 126A (3), 284-289.
  • Weaving, L., Christodoulou, J., Williamson, S., Friend, K., McKenzie, O., Archer, H., Evans, J., Clarke, A., Pelka, G., Tam, P., Lahooti, H., Ellaway, C., Bennetts, B., Watson, C., et al (2004). Mutations Of Cdkl5 Cause A Severe Neurodevelopmental Disorder With Infantile Spasms And Mental Retardation. American Journal of Human Genetics, 75, 1079-1093.

2003

  • Ban, M., Sawcer, S., Heard, R., Bennetts, B., Adams, S., Booth, D., Perich, V., Setakis, E., Compston, A., Stewart, G. (2003). A genome-wide screen for linkage disequilibrium in Australian HLA-DRB1*1501 positive multiple sclerosis patients. Journal of Neuroimmunology, 143(1-2), 60-64. [More Information]
  • Weaving, L., Williamson, S., Bennetts, B., Davis, M., Ellaway, C., Leonard, H., Thong, M., Delatycki, M., Thompson, E., Laing, N., Christodoulou, J. (2003). Effects of MECP2 mutation type, location and X-inactivation in modulating Rett Syndrome phenotype. American Journal of Medical Genetics. Part A, 118A, 103-114.
  • Urwin, R., Bennetts, B., Wilcken, B., Lampropoulos, B., Beumont, P., Russell, J., Tanner, S., Nunn, K. (2003). Gene-gene interaction between the monoamine oxidase A gene and solute carrier family 6 (neurotransmitter transporter, noradrenalin) member 2 gene in anorexia nervose (restrictive subtype). European Journal of Human Genetics, 11(12), 945-950.
  • Teutsch, S., Booth, D., Bennetts, B., Heard, R., Stewart, G. (2003). Identification of 11 novel and common single nucleotide polymorphisms in the interleukin-7 receptor-alpha gene and their associations with multiple sclerosis. European Journal of Human Genetics, 11(7), 509-515.
  • Wiley, V., Carpenter, K., Bennetts, B., Wilcken, B. (2003). Information overload - new technologies, can we store the data? Southeast Asian Journal of Tropical Medicine and Public Health, 34(S3), 59-62.
  • Urwin, R., Bennetts, B., Wilcken, B., Beumont, P., Russell, J., Nunn, K. (2003). Investigation of epistasis between the serotonin transporter and norepinephrine transproter genes in anorexia nervosa. Neuropsychopharmacology, 28(7), 1351-1355.
  • Christodoulou, J., Grimm, A., Maher, T., Bennetts, B. (2003). RettBASE: the IRSA MECP2 variation database-A new mutation database in evolution. Human Mutation, 21(5), 466-472.

2002

  • Ban, M., Stewart, G., Bennetts, B., Heard, R., Simmons, R., Maranian, M., Compston, A., Sawcer, S. (2002). A genome screen for linkage in Australian sibling-pairs with multiple sclerosis. Genes and Immunity, 3(8), 464-469.
  • Milledge, J., Shaw, P., Mansour, A., Williamson, S., Bennetts, B., Roscioli, T., Curtin, J., Christodoulou, J. (2002). Allogeneic bone marrow transplantation: cure for familial Mediterranean fever. Blood, 100(3), 774-777.
  • Urwin, R., Bennetts, B., Wilcken, B., Lampropolous, B., Beumont, P., Clarke, S., Russell, J., Tanner, S., Nunn, K. (2002). Anorexia nervosa (restrictive subtype) is associated with a polymorphism in the novel noreprinephrine transporter gene promoter polymorphic region. Molecular Psychiatry, 7(6), 652-657.
  • Buhler, M., Craig, M., Donaghue, K., Badhwar, P., Willis, J., Manolios, N., Tait, B., Silink, M., Bennetts, B., Stewart, G. (2002). CCR5 Genotyping in an Australian and New Zealand type 1 Diabetes Cohort. Autoimmunity, 65(7), 457-461.
  • Kao, Y., Donaghue, K., Chan, A., Bennetts, B., Knight, J., Silink, M. (2002). Paraoxonase gene cluster is a genetic marker for early microvascular complications in Type 1 diabetes. Diabetic Medicine, 19(3), 212-215.

2001

  • Bennetts, B., Donaghue, K., Silink, M., Kordonouri, O., James, R., Chan, A., Kao, Y., Danne, T. (2001). Modulation by blood glucose levels of activity and concentration of paraoxonase in young patients with Type 1 diabetes mellitus. Metabolism: clinical and experimental, 50, 657-660.
  • Hughes, J., Weston, S., Bennetts, B., Angulo,, R., Prasad, M., Jaworski, R., Jolles, S., Kossard, S., Fox, S., Benson, E. (2001). The application of a PCR technique for the detection of immunoglobulin heavy chain gene rearrangements in fresh or paraffin-embedded skin tissue. Pathology, 33, 222-225.

2000

  • Huang, Q., Teutsch, S., Buhler, M., Bennetts, B., Heard, R., Manolios, N., Stewart, G. (2000). Evaluation of the Apo-1/Fas promoter Mva 1 polymorphism in multiple sclerosis. Multiple Sclerosis: clinical and laboratory research, 6(1), 14-18.

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