Dr Hooshang Lahooti

Conjoint Lecturer
Medicine, Nepean Clinical School

Telephone +61 2 4734 1626
Fax +61 2 4734 2614

Map

Selected grants

2014

  • Thyretain TSI in Euthyroid Graves' Disease; Wall J, Lahooti H; Nepean Medical Research Foundation/Project Grant.

2013

  • Risk factors for ophthalmopathy determined using a human pregnancy model; Wall J, Lahooti H; Australian Women and Children's Research Foundation (OZWAC)/Medical Research Project Grant.

2009

  • Association of single Nucleotide Polymorphisms (SNP) of Calsequestrin Gene with Thyroid Associated Opthalmorpathy; Lahooti H; Nepean Medical Research Foundation/Project Grant.

Selected publications

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Journals

  • Ardley, M., McCorquodale, T., Lahooti, H., Champion, B., Wall, J. (2012). Eye findings and immunological markers in probands and their euthyroid relatives from a single family with multiple cases of thyroid autoimmunity. Thyroid Research, 5(1), 1-6. [More Information]
  • McCorquodale, T., Lahooti, H., Gopinath, B., Wall, J. (2012). Long-term follow-up of seven patients with ophthalmopathy not associated with thyroid autoimmunity: heterogeneity of autoimmune ophthalmopathy. Clinical Ophthalmology, 6, 1063-1071. [More Information]
  • Wall, J., Lahooti, H. (2011). Pathogenesis of thyroid eye disease - does autoimmunity against the TSH receptor explain all cases? Endokrynologia Polska, 62(SUPPL. 1), 1-7. [More Information]
  • de Haan, S., Lahooti, H., Morris, O., Wall, J. (2010). Epitopes, immunoglobulin classes and immunoglobulin G subclasses of calsequestrin antibodies in patients with thyroid eye disease. Autoimmunity, 43(8), 698-703. [More Information]
  • Tjiang, H., Lahooti, H., McCorquodale, T., Parmar, K., Wall, J. (2010). Eye and Eyelid Abnormalities Are Common in Patients with Hashimoto's Thyroiditis. Thyroid, 20(3), 287-290. [More Information]
  • Wall, J., Lahooti, H. (2010). Pathogenesis of thyroid eye disease - does autoimmunity against the TSH receptor explain all cases? Endokrynologia Polska, 61(2), 222-227. [More Information]
  • Lahooti, H., Parmar, K., Wall, J. (2010). Pathogenesis of thyroid-associated ophthalmopathy: does autoimmunity against calsequestrin and collagen XIII play a role? Clinical Ophthalmology, 4, 417-425. [More Information]
  • Wescombe, L., Lahooti, H., Gopinath, B., Wall, J. (2010). The cardiac calsequestrin gene (CASQ2) is up-regulated in the thyroid in patients with Graves' ophthalmopathy- support for a role of autoimmunity against calsequestrin as the triggering event. Clinical Endocrinology, 73(4), 522-528. [More Information]
  • Gopinath, B., Ma, G., Lahooti, H., Wall, J. (2008). A case of Hashimoto's thyroiditis presenting with chronic upper eyelid retraction and positive calsequestrin and collagen XIII antibodies. International Journal of Endocrinology and Metabolism, 6(1), 34-37.
  • Pelka, G., Watson, C., Radziewic, T., Hayward, M., Lahooti, H., Christodoulou, J., Tam, P. (2006). Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice. Brain, 129(Pt 4), 887-898. [More Information]
  • 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.

2012

  • Ardley, M., McCorquodale, T., Lahooti, H., Champion, B., Wall, J. (2012). Eye findings and immunological markers in probands and their euthyroid relatives from a single family with multiple cases of thyroid autoimmunity. Thyroid Research, 5(1), 1-6. [More Information]
  • McCorquodale, T., Lahooti, H., Gopinath, B., Wall, J. (2012). Long-term follow-up of seven patients with ophthalmopathy not associated with thyroid autoimmunity: heterogeneity of autoimmune ophthalmopathy. Clinical Ophthalmology, 6, 1063-1071. [More Information]

2011

  • Wall, J., Lahooti, H. (2011). Pathogenesis of thyroid eye disease - does autoimmunity against the TSH receptor explain all cases? Endokrynologia Polska, 62(SUPPL. 1), 1-7. [More Information]

2010

  • de Haan, S., Lahooti, H., Morris, O., Wall, J. (2010). Epitopes, immunoglobulin classes and immunoglobulin G subclasses of calsequestrin antibodies in patients with thyroid eye disease. Autoimmunity, 43(8), 698-703. [More Information]
  • Tjiang, H., Lahooti, H., McCorquodale, T., Parmar, K., Wall, J. (2010). Eye and Eyelid Abnormalities Are Common in Patients with Hashimoto's Thyroiditis. Thyroid, 20(3), 287-290. [More Information]
  • Wall, J., Lahooti, H. (2010). Pathogenesis of thyroid eye disease - does autoimmunity against the TSH receptor explain all cases? Endokrynologia Polska, 61(2), 222-227. [More Information]
  • Lahooti, H., Parmar, K., Wall, J. (2010). Pathogenesis of thyroid-associated ophthalmopathy: does autoimmunity against calsequestrin and collagen XIII play a role? Clinical Ophthalmology, 4, 417-425. [More Information]
  • Wescombe, L., Lahooti, H., Gopinath, B., Wall, J. (2010). The cardiac calsequestrin gene (CASQ2) is up-regulated in the thyroid in patients with Graves' ophthalmopathy- support for a role of autoimmunity against calsequestrin as the triggering event. Clinical Endocrinology, 73(4), 522-528. [More Information]

2008

  • Gopinath, B., Ma, G., Lahooti, H., Wall, J. (2008). A case of Hashimoto's thyroiditis presenting with chronic upper eyelid retraction and positive calsequestrin and collagen XIII antibodies. International Journal of Endocrinology and Metabolism, 6(1), 34-37.

2006

  • Pelka, G., Watson, C., Radziewic, T., Hayward, M., Lahooti, H., Christodoulou, J., Tam, P. (2006). Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice. Brain, 129(Pt 4), 887-898. [More Information]

2004

  • 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.

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