Heiman, Gary A.
Massachusetts General Hospital
6 papers on CoChatORCID 0000-0001-5859-0259
Most cited papers
- Verified
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders
Lee, P. H., Anttila, V., Won, H., Feng, Y.-C. A., Rosenthal, J., Zhu, Z., Tucker-Drob, E. M., Nivard, M. G., Grotzinger, A. D., Posthuma, D., et al. (2019) · Cell
Genetic Associations and EpidemiologySchizophrenia research and treatment
Cited by 1,381
- Verified
Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies
Yu, D., Sul, J. H., Tsetsos, F., Nawaz, M. S., Huang, A. Y., Zelaya, I., Illmann, C., Osiecki, L., Darrow, S. M., Hirschtritt, M. E., et al. (2019) · American Journal of Psychiatry
Obsessive-Compulsive Spectrum DisordersGenetic Associations and Epidemiology
Cited by 410
- Verified
Copy number variation in obsessive-compulsive disorder and tourette syndrome: A cross-disorder study
McGrath, L. M., Yu, D., Marshall, C., Davis, L. K., Thiruvahindrapuram, B., Li, B., Cappi, C., Gerber, G., Wolf, A., Schroeder, F. A., et al. (2014) · Journal of the American Academy of Child & Adolescent Psychiatry
Obsessive-Compulsive Spectrum DisordersGenomic variations and chromosomal abnormalities
Cited by 141
- Verified
No genetic linkage or association between a functional promoter polymorphism in the monoamine oxidase-A gene and panic disorder
Hamilton, S. P., Slager, S. L., Heiman, G. A., Haghighi, F., Klein, D. F., Hodge, S. E., Weissman, M. M., Fyer, A. J., & Knowles, J. A. (2000) · Molecular Psychiatry
Neurotransmitter Receptor Influence on BehaviorGenetic Associations and Epidemiology
Cited by 45
- Verified
Targeted re-sequencing approach of candidate genes implicates rare potentially functional variants in Tourette Syndrome etiology
Alexander, J., Potamianou, H., Xing, J., Deng, L., Karagiannidis, I., Tsetsos, F., Drineas, P., Tarnok, Z., Rizzo, R., Wolanczyk, T., et al. (2016) · Frontiers in Neuroscience
Obsessive-Compulsive Spectrum DisordersGenomics and Rare Diseases
Cited by 27
- Verified
De Novo Coding Variants Are Strongly Associated with Tourette Syndrome
Willsey, J., Fernandez, T., Yu, D., King, R., Dietrich, A., Xing, J., Sanders, S., Mandell, J., Neale, B., Coppola, G., et al. (2019) · European Neuropsychopharmacology
Obsessive-Compulsive Spectrum DisordersGenomics and Rare Diseases
Cited by 2
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