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You searched for: Author/Creator Hakobjan, Marina

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1. Contribution of common and rare genetic variants in CEP72 on vincristine‐induced peripheral neuropathy in brain tumour patients. Issue 7 (24th March 2022)

2. DNA methylation associated with persistent ADHD suggests TARBP1 as novel candidate. (15th February 2021)

3. Female‐specific association of NOS1 genotype with white matter microstructure in ADHD patients and controls. (7th June 2017)

4. MAOA‐VNTR genotype affects structural and functional connectivity in distributed brain networks. Issue 18 (23rd August 2019)

5. Variation in serotonin neurotransmission genes affects neural activation during response inhibition in adolescents and young adults with ADHD and healthy controls. (17th November 2015)