Catherine S Choong - Concepedia

Author

Catherine S Choong

Also Known As

C. Choong, C. S. Choong, Catherine Choong, Catherine S Choong, Catherine S Y Choong, Catherine S. Choong, Catherine S. Y. Choong, Catherine S.Y. Choong, Catherine Seut Choong

Publications

673

Citations

H-Index

Concepts

All Affiliations

Princess Margaret Hospital for Children The University of Western Australia The Kids Research Institute Australia The University of Queensland Monash University

About

Catherine S Choong is an author at Princess Margaret Hospital for Children specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	287
2	Diabetes	3	3	80
3	Public Health	1	1	34
4	Biology	1	1	182
5	Endocrinology	1	1	29

Catherine S Choong

Publications

538

Citations

H-Index

Page 1

	Year	Citations
Germ-line and somatic DICER1 mutations in pineoblastoma Leanne de Kock, Nelly Sabbaghian, Harriet Druker, Acta Neuropathologica BiologySomatic VariantSomatic Cell GeneticsSomatic Dicer1 MutationsGenetics	2014	182
Congenital thyrotoxicosis in premature infants Christopher Smith, M. J. THOMSETT, Catherine S Choong, Clinical Endocrinology	2001	68
Parental pre‐pregnancy BMI is a dominant early‐life risk factor influencing BMI of offspring in adulthood. Shoshana Rath, Julie Marsh, John P. Newnham, Obesity Science & Practice	2016	41
Overexpression of Aromatase Associated With Loss of Heterozygosity of the<i>STK11</i>Gene Accounts for Prepubertal Gynecomastia in Boys with Peutz-Jeghers Syndrome Seungmin Ham, Sarah J. Meachem, Catherine S Choong, The Journal of Clinical Endocrinology & Metabolism	2013	37
Multinodular Goiter in Children: An Important Pointer to a Germline DICER1 Mutation Shoshana Rath, Anthony Bartley, Adrian Charles, The Journal of Clinical Endocrinology & Metabolism Important PointerGeneticsImmunodeficienciesGenetic EpidemiologyPathology	2014	34
Transient pseudohypoaldosteronism in infancy secondary to urinary tract infection Mary B. Abraham, Nicholas Larkins, Catherine S Choong, Journal of Paediatrics and Child Health	2017	33
Exploring the endocrine manifestations of DICER1 mutations Catherine S Choong, John R. Priest, William D. Foulkes Trends in Molecular Medicine Somatic VariantMendelian DisorderGenetic DisorderGeneticsEndocrinology	2012	29
The relationship between ACE genotype and risk of severe hypoglycaemia in a large population-based cohort of children and adolescents with type 1 diabetes Mahesh Bulsara, C. D’Arcy J. Holman, F. M. van Bockxmeer, Diabetologia Metabolic SyndromeType 1Diabetes EpidemiologyAce GenotypeDiabetes	2007	24
Angiotensinogen gene T235 variant: a marker for the development of persistent microalbuminuria in children and adolescents with type 1 diabetes mellitus Patricia Gallego, Neil Shephard, Max Bulsara, Journal of Diabetes and its Complications Type 1Persistent MicroalbuminuriaMedicineDiabetesGenetic Epidemiology	2008	22
NKX2-1 mutations in brain-lung-thyroid syndrome: a case series of four patients Vinutha B. Shetty, Cathy Kiraly‐Borri, Phillipa J. Lamont, Journal of Pediatric Endocrinology and Metabolism Mendelian DisorderGenetic DisorderGeneticsRespiratory DistressThyroid Disease	2013	20

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