Claudine M Kraan (C M Kraan)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 6

Top Topics

Parkinson Disease

Dna Methylation

Top Venues

Developmental medicine and child neurology

American journal of medical genetics. Part A

Journal of intellectual disability research : JIDR

This page only lists publications with an associated author ORCID identifier.

Publications

Flora Tassone, Dragana D Protic, Emily Graves Allen, Alison Dalton Archibald, Anna Baud, Ted W Brown, Dejan B Budimirovic, Jonathan Cohen, Brett Dufour, Rachel Eiges, Nicola Elvassore, Lidia V Gabis, Samantha J Grudzien, Deborah A Hall, David R Hessl, Abigail Hogan, Jessica Ezzell Hunter, Peng Jin, Poonnada Jiraanont, Jessica Klusek, R Frank Kooy, Claudine M Kraan, Cecilia Laterza, Andrea Lee, Karen Lipworth, Molly Losh, Danuta Z Loesch, Reymundo Lozano, Marsha R Mailick, Apostolos Manolopoulos, Veronica Martinez-Cerdeno, Yingratana McLennan, Robert M Miller, Federica Alice Maria Montanaro, Matthew W Mosconi, Sarah Nelson Potter, Melissa Raspa, Susan M Rivera, Katharine Shelly, Peter K Todd, Katarzyna Tutak, Jun Yi Wang, Anne Wheeler, Tri Indah Winarni, Marwa Zafarullah, Randi J Hagerman
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation. Cells 12 (18) (2023)
Emma K Baker, Marta Arpone, Minh Q Bui, Claudine M Kraan, Ling Ling, David Francis, Matthew Frank Hunter, Carolyn Rogers, Michael J Field, Lorena Santa María, Víctor Faundes, Bianca Curotto, Paulina Morales, Cesar Trigo, Isabel Salas, Angelica M Alliende, David J Amor, David E Godler
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome. American journal of medical genetics. Part A (2022)
Claudine M Kraan, P Date, A Rattray, M Sangeux, Q M Bui, E K Baker, J Morison, D J Amor, D E Godler
Feasibility of wearable technology for 'real-world' gait analysis in children with Prader-Willi and Angelman syndromes. Journal of intellectual disability research : JIDR 66 (8-9) (2022)
Claudine M Kraan, Emma K Baker, Marta Arpone, Minh Q Bui, Ling Ling, Dinusha Gamage, Lesley Bretherton, Carolyn Rogers, Michael J Field, Tiffany L Wotton, David Francis, Matthew Frank Hunter, Jonathan Cohen, David J Amor, David E Godler
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome. International journal of molecular sciences 21 (20) (2020)
Claudine M Kraan, Kim M Cornish, Quang M Bui, Xin Li, Howard R Slater, David E Godler
β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies. PloS one 13 (2) (2018)
Claudine M Kraan, David E Godler, David J Amor
Epigenetics of fragile X syndrome and fragile X-related disorders. Developmental medicine and child neurology 61 (2) (2018)