M. Hakobjan

发表

Common genetic variants influence human subcortical brain structures

Thomas E. Nichols, Robert W. Williams, Benjamin S. Aribisala, 2015, Nature.

MAOA‐VNTR genotype affects structural and functional connectivity in distributed brain networks

Lena S. Geiger, B. Franke, M. Rietschel, 2019, Human brain mapping.

Influence of DAT1 and COMT variants on neural activation during response inhibition in adolescents with attention-deficit/hyperactivity disorder and healthy controls

B. Franke, J. Buitelaar, C. Hartman, 2015, Psychological Medicine.

Variation in serotonin neurotransmission genes affects neural activation during response inhibition in adolescents and young adults with ADHD and healthy controls

B. Franke, J. Buitelaar, C. Hartman, 2015, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Female‐specific association of NOS1 genotype with white matter microstructure in ADHD patients and controls

B. Franke, J. Buitelaar, C. Hartman, 2017, Journal of child psychology and psychiatry, and allied disciplines.

Brunner Syndrome associated MAOA dysfunction in human induced dopaminergic neurons results in dysregulated NMDAR expression and increased network activity

B. Franke, D. Schubert, H. Brunner, 2019, bioRxiv.

Contribution of common and rare genetic variants in CEP72 on vincristine‐induced peripheral neuropathy in brain tumour patients

M. Coenen, M. Hakobjan, M. Massimino, 2022, British Journal of Clinical Pharmacology.

Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons

B. Franke, D. Schubert, M. Hakobjan, 2021, Neurobiology of Disease.

Brunner syndrome associated MAOA dysfunction in human dopaminergic neurons results in NMDAR hyperfunction and increased network activity

B. Franke, D. Schubert, H. Brunner, 2020, bioRxiv.

BDNF polymorphism associates with decline in set shifting in Parkinson's disease

B. Bloem, R. Kessels, B. P. Warrenburg, 2015, Neurobiology of Aging.

Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis

B. Franke, M. Hakobjan, P. Jongen, 2022, medRxiv.

Sequencing of the DKK1 gene in patients with anorectal malformations and hypospadias

H. Brunner, M. Hakobjan, N. Roeleveld, 2015, European Journal of Pediatrics.

Replication of a genetic variant in ACYP2 associated with cisplatin-induced hearing loss in patients with osteosarcoma

M. Coenen, H. Guchelaar, M. Hakobjan, 2016, Pharmacogenetics and genomics.

Genetic Variants as Predictive Markers for Ototoxicity and Nephrotoxicity in Patients with Locally Advanced Head and Neck Cancer Treated with Cisplatin-Containing Chemoradiotherapy (The PRONE Study)

M. Coenen, M. Hakobjan, J. Kaanders, 2019, Cancers.

DNA methylation associated with persistent ADHD suggests TARBP1 as novel candidate

B. Franke, J. Buitelaar, M. Hoogman, 2020, Neuropharmacology.

Response to IL‐17A inhibitors secukinumab and ixekizumab cannot be explained by genetic variation in the protein‐coding and untranslated regions of the IL‐17A gene: results from a multicentre study of four European psoriasis cohorts

M. Coenen, J. Lambert, M. Hakobjan, 2019, Journal of the European Academy of Dermatology and Venereology : JEADV.

Genetic Variation in Ataxia Gene ATXN7 Influences Cerebellar Grey Matter Volume in Healthy Adults

B. Franke, G. Fernández, M. Rijpkema, 2013, The Cerebellum.

Neural and genetic underpinnings of response inhibition in adolescents with attention-deficit/hyperactivity disorder

B. Franke, J. Buitelaar, C. Hartman, 2015 .

Genetic Variation in Ataxia Gene ATXN7 Influences Cerebellar Grey Matter Volume in Healthy Adults

B. Franke, G. Fernández, M. Rijpkema, 2012, The Cerebellum.

Variation in serotonin neurotransmission genes affects neural activation during response inhibition in adolescents and young adults with ADHD and healthy controls

B. Franke, J. Buitelaar, C. Hartman, 2015, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.