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Associate Professor Louise Conwell
Associate Professor

Louise Conwell

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Overview

Background

Louise Conwell, MBBS(HonsI) PGCert MEd (Dundee) FRACP PhD, is a Senior Staff Specialist (Eminent) in Paediatric Endocrinology and Diabetes at the Queensland Children’s Hospital, Children’s Health Queensland. Louise’s work as a Paediatric Endocrinologist involves working in a multi-disciplinary team to care for neonates, children and adolescents with a wide spectrum of endocrinologist disorders.

Louise commenced as Head of the Children's Health Queensland Clinical Unit, School of Clinical Medicine, University of Queensland in June 2018. She is also the Acting Head of the Mayne Academy of Paediatrics, Faculty of Medicine, University of Queensland.

Louise is a graduate of the University of Queensland and trained in paediatrics at the Mater Children’s Hospital, Brisbane. She then trained in paediatric endocrinology and diabetes at the Royal Children’s Hospital in Brisbane while completing a PhD at the University of Queensland. Louise undertook a post-specialty Clinical Fellowship at the Division of Endocrinology and Metabolism, The Hospital for Sick Children, Uinversity of Toronto, Ontario, Canada.

Louise has a particular interest in Congenital Hyperinsulinism and other beta-cell disorders including Type 1 and Monogenic Diabetes. Her other clinical interest areas include Disorders of Sexual Differentiation and endocrine oncology. Louise currently works in the endocrine oncology clinic connected with the After Cancer Therapy Service at the Queensland Children's Hospital, Brisbane.

Louise's PhD was in the field of insulin resistance and cardiovascular risk in obese children and adolescents. Louise remains active in clinical research with grant attainment, particularly in the field of beta-cell disorders.

Louise is a member of national and international professional bodies. She is the current President (past Secretary) of the Australasian Paediatric Endocrine Group, serving on Council since November 2017. She also has past or present committee memberships including the Scientific Organising Committee, Clinical Fellows School Committee, Diabetes Committee, the Disorders of Sexual Differentiation Committee, Registry Committee, Research Grant Committee, Thyroid Working Group and the Cancer Survivorship Working Group).

Louise also has engagement with stakeholder groups, particularly Congenital Hyperinsulinism International. She is co-chair of the Congenital Hyperinsulinism International Collaborative Research Network - Care Guidelines and Centres of Excellence.

Louise represents the Australasian Paediatric Endocrine Group on the International Consortium of Pediatric Endocrinology (ICPE) and is co-chair of ICPE's subcommittee, the Intersociety Clinical Guidelines Committee (ICGC).

Louise has an interest in Evidence-Based Medicine, with authorship in the Cochrane Database of Systematic Reviews. She is co-Chair of the International Clinical Guidelines Committee of the International Consortium of Paediatric Endocrinology.

A further interest area includes medical ecucation, completing a Postgraduate Certificate in Medical Education (University of Dundee, Scotland) in 2017. She has facilitated and contributed to a wide range of educational activities for a variety of student, professional and community stakeholder groups in a range of contexts. Louise is a supervisor of basic and advanced paediatric trainees of the Royal Australasian College of Physicians. Other roles include Supervisor, Reader and Examiner for Postgraduate Higher Degree Research students of the University of Queensland and other academic institutions in Australia.

Availability

Associate Professor Louise Conwell is:
Available for supervision

Qualifications

  • Bachelor of Medicine and Surgery and Medical Science, The University of Queensland
  • Doctor of Philosophy, The University of Queensland
  • Royal Australasian College of Physicians, Royal Australasian College of Physicians

Research interests

  • Congenital hyperinsulinism

  • Evidence Based Medicine

  • Obesity, Cardiovascular Risk and Insulin Resistance in Children and Adolescents

  • Type 1 Diabetes Mellitus

  • Other beta cells disorders - Monogenic Diabetes (MODY) and genetics

  • Disorders of Sexual Development

Works

Search Professor Louise Conwell’s works on UQ eSpace

161 works between 2003 and 2025

41 - 60 of 161 works

2019

Journal Article

Autonomous thyroid nodule: not just a disease of adulthood

Papadimos, Emily R., Perry, Emily, Goodwin, Bruce and Conwell, Louise S. (2019). Autonomous thyroid nodule: not just a disease of adulthood. Journal of Paediatrics and Child Health, 56 (7) jpc.14734, 1140-1143. doi: 10.1111/jpc.14734

Autonomous thyroid nodule: not just a disease of adulthood

2019

Conference Publication

Children's Health Queensland Interprofessional Review of Management Decisions in Differences of Sex Development

Conwell, Louise S. (2019). Children's Health Queensland Interprofessional Review of Management Decisions in Differences of Sex Development. Inaugural Children's Health Queensland Interprofessional Practice and Education Symposium, Brisbane, QLD, Australia, 26 June 2019.

Children's Health Queensland Interprofessional Review of Management Decisions in Differences of Sex Development

2019

Conference Publication

Hyperinsulinaemic Hypoglycaemia: A New Presentation of 16p11.2 Duplication Syndrome

Conwell, Louise and Flanagan, Sarah (2019). Hyperinsulinaemic Hypoglycaemia: A New Presentation of 16p11.2 Duplication Syndrome. 58th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Vienna, Austria, September 2019. Basel, Switzerland: Karger.

Hyperinsulinaemic Hypoglycaemia: A New Presentation of 16p11.2 Duplication Syndrome

2018

Journal Article

Predicted benign and synonymous variants in CYP11A1 causes primary adrenal insufficiency through missplicing

Maharaj, Avinaash, Buonocore, Federica, Meimaridou, Eirini, Ruiz-Babot, Gerard, Guasti, Leonardo, Peng, Hwei-Ming, Capper, Cameron P., Burgos-Tirado, Neikelyn, Prasad, Rathi, Hughes, Claire R., Maudhoo, Ashwini, Crowne, Elizabeth, Cheetham, Timothy D., Brain, Caroline E., Suntharalingham, Jenifer P., Striglioni, Niccolò, Yuksel, Bilgin, Gurbuz, Fatih, Gupta, Sangay, Lindsay, Robert, Couch, Robert, Spoudeas, Helen A., Guran, Tulay, Johnson, Stephanie, Fowler, Dallas J, Conwell, Louise S., McInerney-Leo, Aideen M., Drui, Delphine, Cariou, Bertrand ... Metherell, Louise A. (2018). Predicted benign and synonymous variants in CYP11A1 causes primary adrenal insufficiency through missplicing. Journal of the Endocrine Society, 3 (1), 201-221. doi: 10.1210/js.2018-00130

Predicted benign and synonymous variants in CYP11A1 causes primary adrenal insufficiency through missplicing

2018

Journal Article

Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY): a novel ABCC8 mutation in a previously screened family

Johnson, Stephanie R., Leo, Paul, Conwell, Louise S., Harris, Mark, Brown, Matthew A. and Duncan, Emma L. (2018). Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY): a novel ABCC8 mutation in a previously screened family. Journal of Diabetes, 10 (9), 764-767. doi: 10.1111/1753-0407.12778

Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY): a novel ABCC8 mutation in a previously screened family

2018

Journal Article

A novel INS mutation in a family with maturity-onset diabetes of the young: variable insulin secretion and putative mechanisms

Johnson, Stephanie R., Mcgown, Ivan, Oppermann, Udo, Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2018). A novel INS mutation in a family with maturity-onset diabetes of the young: variable insulin secretion and putative mechanisms. Pediatric Diabetes, 19 (5), 905-909. doi: 10.1111/pedi.12679

A novel INS mutation in a family with maturity-onset diabetes of the young: variable insulin secretion and putative mechanisms

2018

Conference Publication

Autonomous thyroid nodule – not just a disease of adulthood

Papadimos, E., Perry, E., Goodwin, B. and Conwell, L. S. (2018). Autonomous thyroid nodule – not just a disease of adulthood. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Newcastle, NSW Australia, July 2018.

Autonomous thyroid nodule – not just a disease of adulthood

2018

Conference Publication

Molecular and functional studies in a case of Familial Congenital Hyperinsulinism: co-inheritance of a dominant and recessive ABCC8 mutation

Conwell, Louise S., Shyng, Show-Ling, Kandasamy, Balamurugan, Wu, Yi and McGown, Ivan (2018). Molecular and functional studies in a case of Familial Congenital Hyperinsulinism: co-inheritance of a dominant and recessive ABCC8 mutation. Australian Functional Genomics Conference, Melbourne, Australia, September 2018.

Molecular and functional studies in a case of Familial Congenital Hyperinsulinism: co-inheritance of a dominant and recessive ABCC8 mutation

2018

Conference Publication

Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional finding of pancreatic mosaicism for trisomy 12

Conwell, Louise S., Harroway, James, Williams, Mark, Joy, Christopher, Scurry, Bonnie, Lee, Kevin, McBride, Craig, Choo, Kelvin, Huynh, Tony and Ng, Carolyn G. L. (2018). Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional finding of pancreatic mosaicism for trisomy 12. Australasian Paediatric Endocrine Group Annual Scientific Meetings, Newcastle, Australia, July 2018.

Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional finding of pancreatic mosaicism for trisomy 12

2017

Conference Publication

Co-inheritance of Dominant and Recessive ABCC8 Mutations in a Case of Familial Congenital Hyperinsulinism:- Molecular and Functional Studies

Conwell, Louise S. , Shyng, Show-Ling , Kandasamy, Balamurugan , Wu, Yi , McGown, Ivan , Choo, Kelvin and McBride, Craig (2017). Co-inheritance of Dominant and Recessive ABCC8 Mutations in a Case of Familial Congenital Hyperinsulinism:- Molecular and Functional Studies. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Hobart, Tasmania, Australia, 26-29 November 2017.

Co-inheritance of Dominant and Recessive ABCC8 Mutations in a Case of Familial Congenital Hyperinsulinism:- Molecular and Functional Studies

2017

Conference Publication

Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial congenital hyperinsulinism (CHI):- molecular and functional studies

Conwell, Louise S., Shyng, Show-Ling, Kandasamy, Balamurugan, Wu, Yi, Mcgown, Ivan, Choo, Kelvin L. and Mcbride, Craig A. (2017). Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial congenital hyperinsulinism (CHI):- molecular and functional studies. 10th International Meeting of Pediatric Endocrinology, Washington, DC, United States, 14 - 17 September 2017. Basel, Switzerland: S. Karger AG.

Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial congenital hyperinsulinism (CHI):- molecular and functional studies

2017

Conference Publication

Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial Congenital Hyperinsulinism (CHI):- molecular and functional studies

Conwell, Louise S., Shyng, Show-Ling , Kandasamy, Balamurugan , Wu, Yi , McGown, Ivan , Choo, Kelvin and McBride, Craig (2017). Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial Congenital Hyperinsulinism (CHI):- molecular and functional studies. 10th International Meeting of Pediatric Endocrinology, Washington, DC, United States, 14-17 September 2017.

Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial Congenital Hyperinsulinism (CHI):- molecular and functional studies

2017

Conference Publication

Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial congenital hyperinsulinism:- molecular and functional studies

Conwell, Louise S., Shyng, Show-Ling, Kandasamy, Balamurugan, Wu, Yi, McGown, Ivan, Choo, Kelvin and McBride, Craig (2017). Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial congenital hyperinsulinism:- molecular and functional studies. 3rd Annual Children's Health Queensland Research Symposium, Brisbane, Queensland, Australia, 1 November 2017.

Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial congenital hyperinsulinism:- molecular and functional studies

2017

Conference Publication

Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46,XX/46,XY):- postnatal clinical and gonadal phenotype

Conwell, Louise S. , Phillips, Gayle E., Nandini, Adayapalam , Borzi, Peter A. and Gabbett, Michael T. (2017). Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46,XX/46,XY):- postnatal clinical and gonadal phenotype. International Disorders of Sexual Development Conference, Copenhagan, Denmark, 29 June-1 July 2017. Copenhagen, Denmark: I-DSD.

Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46,XX/46,XY):- postnatal clinical and gonadal phenotype

2017

Conference Publication

Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46,XX/46,XY):- postnatal clinical and gonadal phenotype

Conwell, Louise S., Phillips, Gayle E. , Nandini, Adayapalam , Borzi, Peter A. and Gabbett, Michael T. (2017). Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46,XX/46,XY):- postnatal clinical and gonadal phenotype. 10th International Meeting of Pediatric Endocrinology, Washington, DC, United States, 14-17 September 2017.

Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46,XX/46,XY):- postnatal clinical and gonadal phenotype

2017

Conference Publication

Idiopathic ductopaenia in a paediatric patient: a case report and interesting clinical biochemistry

Ruddell, Richard G., Burgess, Christopher, Huynh, Tony, Conwell, Louise S., Balouch, Fariha, Burke, Matthew and Pretorius, Carel (2017). Idiopathic ductopaenia in a paediatric patient: a case report and interesting clinical biochemistry. Clinical Lipidology (3rd World Congress), Brisbane, QLD, Australia, unknown.

Idiopathic ductopaenia in a paediatric patient: a case report and interesting clinical biochemistry

2017

Conference Publication

Lessons Learnt from Two Cases of Congenital Hyperinsulinism from Remote Indigenous Australian Communities

Musthaffa, Yassmin M., Papadimos, Emily R. , Fairchild, Jan , Huynh, Tony and Conwell, Louise S. (2017). Lessons Learnt from Two Cases of Congenital Hyperinsulinism from Remote Indigenous Australian Communities. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Hobart , Tasmania, Australia, 26-29 November 2017.

Lessons Learnt from Two Cases of Congenital Hyperinsulinism from Remote Indigenous Australian Communities

2017

Conference Publication

46,XX Ovotesticular Disorder of Sex Developement (DSD):- duplication of the XX SR region upstream of the critical testicular gene SOX9

Conwell, Louise S., Stathis, Stephen, Franklin, Annie, Borzi, Peter A., Nandini, Adayapalam, Phillips, Gayle E., Ohnesorg, Thomas, Ayers, Katie L. and Sinclair, Andrew H. (2017). 46,XX Ovotesticular Disorder of Sex Developement (DSD):- duplication of the XX SR region upstream of the critical testicular gene SOX9. 3rd Annual Children's Health Queensland Research Symposium, Brisbane, Queensland, Australia, 1 November 2017.

46,XX Ovotesticular Disorder of Sex Developement (DSD):- duplication of the XX SR region upstream of the critical testicular gene SOX9

2017

Conference Publication

Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46, XX/46, XY): - postnatal clinical and gonadal phenotype

Conwell, Louise S., Phillips, Gayle E., Nandini, Adayapalam, Borzi, Peter A. and Gabbett, Michael T. (2017). Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46, XX/46, XY): - postnatal clinical and gonadal phenotype. 10th International Meeting of Pediatric Endocrinology, Washington, DC, United States, 14 - 17 September 2017. Basel, Switzerland: S. Karger AG. doi: 10.1159/000481424

Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46, XX/46, XY): - postnatal clinical and gonadal phenotype

2017

Conference Publication

Early complications of first presentation diabetic ketoacidosis are predicted by severity

Sharwood, Erin F. and Conwell, Louise S. (2017). Early complications of first presentation diabetic ketoacidosis are predicted by severity. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Hobart , Tasmania, Australia, 26-29 November 2017.

Early complications of first presentation diabetic ketoacidosis are predicted by severity

Supervision

Availability

Associate Professor Louise Conwell is:
Available for supervision

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Supervision history

Completed supervision

Media

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