Fingerprint The Fingerprint is created by mining the titles and abstracts of the person's research outputs and projects/funding awards to create an index of weighted terms from discipline-specific thesauri.

  • 1 Similar Profiles
Autistic Disorder Medicine & Life Sciences
Oxytocin Medicine & Life Sciences
Human Pheromones Medicine & Life Sciences
Oxytocin Receptors Medicine & Life Sciences
Genes Medicine & Life Sciences
Vasopressins Medicine & Life Sciences
Serotonin Medicine & Life Sciences
N-Methyl-3,4-methylenedioxyamphetamine Medicine & Life Sciences

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Projects 2012 2019

community
Metabotropic Glutamate 5 Receptor
Autistic Disorder
Brain
Autistic Disorder
Research
Neurodevelopmental Disorders

Research Output 2000 2018

1 Citations

Chronic Intranasal Oxytocin has Dose-dependent Effects on Central Oxytocin and Vasopressin Systems in Prairie Voles (Microtus ochrogaster)

Guoynes, C. D., Simmons, T. C., Downing, G. M., Jacob, S., Solomon, M. & Bales, K. L. Jan 15 2018 In : Neuroscience. 369, p. 292-302 11 p.

Research output: Contribution to journalArticle

Arvicolinae
Oxytocin
Autistic Disorder
Vasopressins
Oxytocin Receptors

The journey to autism: Insights from neuroimaging studies of infants and toddlers

Wolff, J. J., Jacob, S. & Elison, J. T. May 1 2018 In : Development and psychopathology. 30, 2, p. 479-495 17 p.

Research output: Contribution to journalArticle

Autistic Disorder
Neuroimaging
Functional Neuroimaging
Phenotype
Research
1 Citations

Is there sexual dimorphism of hyperserotonemia in autism spectrum disorder?

Shuffrey, L. C., Guter, S. J., Delaney, S., Jacob, S., Anderson, G. M., Sutcliffe, J. S., Cook, E. H. & Veenstra-VanderWeele, J. Aug 1 2017 In : Autism Research. 10, 8, p. 1417-1423 7 p.

Research output: Contribution to journalArticle

Sex Characteristics
Serotonin
Genetic Linkage
Genetic Association Studies
Puberty
1 Citations

Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism

Chen, R., Davis, L. K., Guter, S., Wei, Q., Jacob, S., Potter, M. H., Cox, N. J., Cook, E. H., Sutcliffe, J. S. & Li, B. Mar 21 2017 In : Molecular Autism. 8, 1, 14

Research output: Contribution to journalArticle

Endophenotypes
Autistic Disorder
Serotonin
Genes
Gene Regulatory Networks
12 Citations

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Anney, R. J. L. , Ripke, S. , Anttila, V. , Grove, J. , Holmans, P. , Huang, H. , Klei, L. , Lee, P. H. , Medland, S. E. , Neale, B. , Robinson, E. , Weiss, L. A. , Zwaigenbaum, L. , Yu, T. W. , Wittemeyer, K. , Willsey, A. J. , Wijsman, E. M. , Werge, T. , Wassink, T. H. , Waltes, R. & 143 others Walsh, C. A., Wallace, S., Vorstman, J. A. S., Vieland, V. J., Vicente, A. M., Vanengeland, H., Tsang, K., Thompson, A. P., Szatmari, P., Svantesson, O., Steinberg, S., Stefansson, K., Stefansson, H., State, M. W., Soorya, L., Silagadze, T., Scherer, S. W., Schellenberg, G. D., Sandin, S., Sanders, S. J., Saemundsen, E., Rouleau, G. A., Rogé, B., Roeder, K., Roberts, W., Reichert, J., Reichenberg, A., Rehnström, K., Regan, R., Poustka, F., Poultney, C. S., Piven, J., Pinto, D., Pericak-Vance, M. A., Pejovic-Milovancevic, M., Pedersen, M. G., Pedersen, C. B., Paterson, A. D., Parr, J. R., Pagnamenta, A. T., Oliveira, G., Nurnberger, J. I., Nordentoft, M., Murtha, M. T., Mouga, S., Mortensen, P. B., Mors, O., Morrow, E. M., Moreno-De-Luca, D., Monaco, A. P., Minshew, N., Merikangas, A., McMahon, W. M., McGrew, S. G., Mattheisen, M., Martsenkovsky, I., Martin, D. M., Mane, S. M., Magnusson, P., Magalhaes, T., Maestrini, E., Lowe, J. K., Lord, C., Levitt, P., Martin, C. L., Ledbetter, D. H., Leboyer, M., Lecouteur, A. S., Ladd-Acosta, C., Kolevzon, A., Klauck, S. M., Jacob, S., Iliadou, B., Hultman, C. M., Hougaard, D. M., Hertz-Picciotto, I., Hendren, R., Hansen, C. S., Haines, J. L., Guter, S. J., Grice, D. E., Green, J. M., Green, A., Goldberg, A. P., Gillberg, C., Gilbert, J., Gallagher, L., Freitag, C. M., Fombonne, E., Folstein, S. E., Fernandez, B., Fallin, M. D., Ercan-Sencicek, A. G., Ennis, S., Duque, F., Duketis, E., Delorme, R., Derubeis, S., Dejonge, M. V., Dawson, G., Cuccaro, M. L., Correia, C. T., Conroy, J., Conceição, I. C., Chiocchetti, A. G., Celestino-Soper, P. B. S., Casey, J., Cantor, R. M., Café, C., Bybjerg-Grauholm, J., Brennan, S., Bourgeron, T., Bolton, P. F., Bölte, S., Bolshakova, N., Betancur, C., Bernier, R., Beaudet, A. L., Battaglia, A., Bal, V. H., Baird, G., Bailey, A. J., Bækvad-Hansen, M., Bader, J. S., Bacchelli, E., Anagnostou, E., Amaral, D., Almeida, J., Børglum, A. D., Buxbaum, J. D., Chakravarti, A., Cook, E. H., Coon, H., Geschwind, D. H., Gill, M., Hallmayer, J., Palotie, A., Santangelo, S., Sutcliffe, J. S., Arking, D. E., Devlin, B., Daly, M. J. & Hakonarson, H. May 22 2017 In : Molecular Autism. 8, 1, 21

Research output: Contribution to journalArticle

Genome-Wide Association Study
Meta-Analysis
Schizophrenia
Genome
Genomics