Author

Anne M. Turner

Observed names: A. Turner, Anne M Turner, Anne Turner

Institution: Medical Research Institute of New Zealand

Observed institutions: Royal Children's Hospital, Women's and Children's Hospital, Canberra Hospital, Women's and Children's Health Network, Sydney Children's Hospital, Medical Research Institute of New Zealand, Act Health, ACT Government, The University of Adelaide

OpenAlex ID: A5106510344

Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa–Kuroki) syndrome

2004 · S.M. White, S.M. White, et al. · American Journal of Medical Genetics Part A · 103

Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype

2011 · Ingrid Scurr, Louise Wilson, et al. · American Journal of Medical Genetics Part A · 77

Deafness due to Pro250Arg mutation of FGFR3

1998 · Georgina E Hollway, Graeme K Suthers, et al. · The Lancet · 49

Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Cantú syndrome

1999 · Stephen P. Robertson, Edwin Kirk, et al. · American Journal of Medical Genetics · 35

Unintended Diagnosis of Von Hippel Lindau Syndrome Using Array Comparative Genomic Hybridization (CGH): Counseling Challenges Arising from Unexpected Information

2012 · Jennifer Hogan, A. Turner, et al. · Journal of Genetic Counseling · 10

Breast cancer risk is not increased in individuals with TWIST1 mutation confirmed Saethre–Chotzen syndrome: An Australian multicenter study

2009 · Paul A. James, Bronwyn Culling, et al. · Genes Chromosomes and Cancer · 3

Intermediate dose heparin thromboprophylaxis among critically ill patients with COVID-19: a randomized clinical trial

2026 · Charlotte A. Bradbury, Bryan J. McVerry, et al. · Journal of Thrombosis and Haemostasis · 2

Ivermectin for Critically and Noncritically Ill Hospitalized Patients With COVID-19: Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community-Acquired Pneumonia (REMAP-CAP)

2026 · Madiha Hashmi, Rashan Haniffa, et al. · Critical Care Medicine · 1

Mutations in the FGFR3 gene have been implicated in a various skeletal dysplasias in human beings.

1998 · Georgina E. Hollway, Graeme Suthers, et al.

Works count: 9

Citation count: 280

H-index: 5

I10-index: 5