Salyakina, Daria

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Wang, K., Zhang, H., Ma, D., Bucan, M., Glessner, J. T., Abrahams, B. S., Salyakina, D., Imielinski, M., Bradfield, J. P., Sleiman, P. M. A., et al. (2009) · Nature

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 989

Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment

Binder, E. B., Salyakina, D., Lichtner, P., Wochnik, G. M., Ising, M., Pütz, B., Papiol, S., Seaman, S., Lucae, S., Kohli, M. A., et al. (2004) · Nature Genetics

Stress Responses and CortisolGenetic Associations and Epidemiology

Cited by 977

P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder

Lucae, S., Salyakina, D., Barden, N., Harvey, M., Gagné, B., Labbé, M., Binder, E. B., Uhr, M., Paez-Pereda, M., Sillaber, I., et al. (2006) · Human Molecular Genetics

Adenosine and Purinergic SignalingGenetic Associations and Epidemiology

Cited by 261

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

Hussman, J. P., Chung, R.-H., Griswold, A. J., Jaworski, J. M., Salyakina, D., Ma, D., Konidari, I., Whitehead, P. L., Vance, J. M., Martin, E. R., et al. (2011) · Molecular Autism

Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology

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The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression

Kohli, M. A., Lucae, S., Saemann, P. G., Schmidt, M. V., Demirkan, A., Hek, K., Czamara, D., Alexander, M., Salyakina, D., Ripke, S., et al. (2011) · Neuron

Genetic Associations and EpidemiologyNeurotransmitter Receptor Influence on Behavior

Cited by 228

A Genome‐wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1

Ma, D., Salyakina, D., Jaworski, J. M., Konidari, I., Whitehead, P. L., Andersen, A. N., Hoffman, J. D., Slifer, S. H., Hedges, D. J., Cukier, H. N., et al. (2009) · Annals of Human Genetics

Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology

Cited by 221

Syndromic Microphthalmia 9: Role of rapid genome sequencing and novel mutations in STRA6 gene

Saini, A., Almasarweh, S., Acosta, S., Jayakar, P., Janvier, M., Wong, T. C., Salyakina, D., & Sasaki, J. (2022) · Progress in Pediatric Cardiology

Ocular Disorders and TreatmentsGenomics and Rare Diseases

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