Claudine M. Kraan

Murdoch Children's Research Institute

H指数:18

被引数:952

个人简介

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教育背景

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工作经历

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荣誉奖项

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Scoping review and recommendations for development and delivery of education resources for reproductive genetic carrier screening

生殖遗传携带者筛查教育资源开发与配送的综述与建议

European Journal of Human Genetics

IF4.6

2026-06-300

Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation

第五届FMR1前突变国际会议对脆性X前突变相关条件的见解和建议

CELLS

IF5.2

2023-09-2128

OAAI

Tassone, Flora; Protic, Dragana; Allen, Emily Graves; Archibald, Alison D.; Baud, Anna; Brown, Ted W.; Budimirovic, Dejan B.; Cohen, Jonathan; Dufour, Brett; Eiges, Rachel; Elvassore, Nicola; Gabis, Lidia V.; Grudzien, Samantha J.; Hall, Deborah A.; Hessl, David; Hogan, Abigail; Hunter, Jessica Ezzell; Jin, Peng; Jiraanont, Poonnada; Klusek, Jessica; Kooy, R. Frank; Kraan, Claudine M.; Laterza, Cecilia; Lee, Andrea; Lipworth, Karen; Losh, Molly; Loesch, Danuta; Lozano, Reymundo; Mailick, Marsha R.; Manolopoulos, Apostolos; Martinez-Cerdeno, Veronica; Mclennan, Yingratana; Miller, Robert M.; Montanaro, Federica Alice Maria; Mosconi, Matthew W.; Potter, Sarah Nelson; Raspa, Melissa; Rivera, Susan M.; Shelly, Katharine; Todd, Peter K.; Tutak, Katarzyna; Wang, Jun Yi; Wheeler, Anne; Winarni, Tri Indah; Zafarullah, Marwa; Hagerman, Randi J.; Kalyuzhny, Alexander E.

Men with FMR1 premutation alleles of less than 71 CGG repeats have low risk of being affected with fragile X-associated tremor/ataxia syndrome (FXTAS)

JOURNAL OF MEDICAL GENETICS

IF3.7

2021-07-284

PRE

FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome

SCIENTIFIC REPORTS

IF3.9

2020-07-1610

OAAI

Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome

与脆性X综合征的镶嵌相关的智力功能和行为特征