Jaana Nopola‐Hemmi
Helsinki University Hospital(FI)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Reading and Literacy Development, Cognitive and developmental aspects of mathematical skills, Language Development and Disorders, Ubiquitin and proteasome pathways
Most-Cited Works
- → A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain(2003)377 cited
- → The Axon Guidance Receptor Gene ROBO1 Is a Candidate Gene for Developmental Dyslexia(2005)332 cited
- → A dominant gene for developmental dyslexia on chromosome 3(2001)168 cited
- → A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia(2007)121 cited
- → Two translocations of chromosome 15q associated with dyslexia(2000)106 cited
- → The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language(2012)76 cited
- → HumanROBO1Regulates Interaural Interaction in Auditory Pathways(2012)52 cited
- → Familial dyslexia: neurocognitive and genetic correlation in a large Finnish family(2002)34 cited