Kate Gibson - Concepedia

Author

Kate Gibson

Also Known As

Gibson K, Hilary Longhurst, Jozef Gecz, K Gibson, K. Gibson, K. K. Gibson, Kate Gibson, Lauren Chong, Peter H. Dixon, S. White

Publications

2.5K

Citations

H-Index

Concepts

All Affiliations

Royal Children's Hospital Royal Brisbane and Women's Hospital Christchurch Hospital Victorian Clinical Genetics Services Sydney Children's Hospital

About

Kate Gibson is an author at Royal Children's Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	810
2	Engineering	3	3	127
3	Business	1	1	25
4	Health Sciences	1	1	25
5	Cell Biology	1	1	151

Kate Gibson

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5 Margaret J. McMillin, Anita E. Beck, Jessica X. Chong, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyPathology	2014	214
Complications of biliary T‐tubes after choledochotomy Vanessa Wills, Kate Gibson, Costa Karihaloo, ANZ Journal of Surgery	2002	159
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions Patricia Heyn, Clare V. Logan, Adeline Fluteau, Nature Genetics ChromatinGain-of-function Dnmt3a MutationsDevelopmental BiologyPolycomb-regulated RegionsGenetic Disorder	2018	151
Clinical and genetic aspects of KBG syndrome Karen Low, Tazeen Ashraf, Natalie Canham, American Journal of Medical Genetics Part A	2016	136
Mitochondrial Oxidative Phosphorylation Disorders Presenting in Neonates: Clinical Manifestations and Enzymatic and Molecular Diagnoses Kate Gibson, Jane Halliday, Denise M. Kirby, PEDIATRICS	2008	87
Prenatal diagnosis of mosaic trisomy 20 in New Zealand Paul A. James, Kate Gibson, Julie McGaughran Australian and New Zealand Journal of Obstetrics and Gynaecology	2002	79
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome Thomas Neumann, Judith Allanson, Ines Kavamura, European Journal of Human Genetics Cardio-facio-cutaneous SyndromeSurgical PathologyHistopathologyPathologyClinical Dermatology	2008	78
The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype Bregje W.M. van Bon, David A. Koolen, Louise Brueton, European Journal of Human Genetics Down SyndromeGenetic DisorderGeneticsPathologyMedicine	2009	77
Genetic abnormalities in a large cohort of Coffin–Siris syndrome patients Futoshi Sekiguchi, Yoshinori Tsurusaki, Nobuhiko Okamoto, Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic Epidemiology	2019	64
A loss-of-function <i>IFNAR1</i> allele in Polynesia underlies severe viral diseases in homozygotes Paul Bastard, Kuang‐Chih Hsiao, Qian Zhang, The Journal of Experimental Medicine	2022	64

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