Gary Heiman

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1 Similar Profiles

3 Finished

1/7 Collaborative Genomic Studies of Tourette Disorder.
Heiman, G. (PI) & Tischfield, J. (CoPI)
National Institute of Mental Health
6/15/18 → 3/31/24
Project: Research project
1/8-Collaborative genomic studies of Tourette Disorder
Heiman, G. (PI) & Tischfield, J. (CoPI)
National Institute of Mental Health
9/15/11 → 6/30/15
Project: Research project
Shared Genetic Risk for Epilepsy and Depression
Heiman, G. G. A. (CoPI) & Heiman, G. (PI)
9/30/07 → 6/30/13
Project: Research project

84 Article
7 Letter
4 Review article
2 Chapter
More
- 2 Comment/debate

Mapping the genetic landscape across 14 psychiatric disorders
Nicotine Dependence GenOmics (iNDiGO) Consortium, Obsessive-Compulsive Disorder and Tourette Syndrome Working Group of the Psychiatric Genomics Consortium, Post-Traumatic Stress Disorder Working Group of the Psychiatric Genomics Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Substance Use Disorders Working Group of the Psychiatric Genomics Consortium, Anxiety Disorders Working Group of the Psychiatric Genomics Consortium, Attention-Deficit/Hyperactivity Disorder (ADHD) Working Group of the Psychiatric Genomics Consortium, Autism Spectrum Disorders Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Eating Disorders Working Group of the Psychiatric Genomics Consortium & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Jan 8 2026, In: Nature. 649, 8096, p. 406-415 10 p.
Research output: Contribution to journal › Article › peer-review

Open Access
55 Link opens in a new tab Scopus citations
A Celsr3 Mutation Linked to Tourette Disorder Disrupts Cortical Dendritic Patterning and Striatal Cholinergic Interneuron Excitability
Nasello, C., Yilmaz, G. D., Poppi, L. A., Kowalski, T. F., Ho-Nguyen, K. T., Wu, J., Matrongolo, M., Thackray, J. K., Shi, A., Carayannopoulos, N. L., Cheedalla, N., McGinnis, J., Chen, J., Khondker, A., Tissir, F., Heiman, G. A., Tischfield, J. A. & Tischfield, M. A., Nov 2025, In: International journal of molecular sciences. 26, 21, 10307.
Research output: Contribution to journal › Article › peer-review

Open Access
1 Link opens in a new tab Scopus citations
Evaluating pregnancy termination rates for fetal chromosome and single gene disorders
Herman, M. J., Rosenfeld, E. B., Kasatkin, N., Heiman, G. A., Khan, S. P. & Ashkinadze, E., Aug 2025, In: Journal of Genetic Counseling. 34, 4, e70099.
Research output: Contribution to journal › Article › peer-review

Open Access
1 Link opens in a new tab Scopus citations
Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders
Strom, N. I., Halvorsen, M. W., Grove, J., Ásbjörnsdóttir, B., Luðvígsson, P., Thorarensen, Ó., de Schipper, E., Bäckmann, J., Andrén, P., Tian, C., 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. & 114 others, Greenberg, E., Muller-Vahl, K. R., Stuhrmann, M., Dion, Y., Rouleau, G., Aschauer, H., Stamenkovic, M., Schlögelhofer, M., Sandor, P., Barr, C. L., Grados, M., Singer, H. S., Nöthen, M. M., Hebebrand, J., Hinney, A., King, R. A., Fernandez, T. V., Barta, C., Tarnok, Z., Nagy, P., Depienne, C., Worbe, Y., Hartmann, A., Budman, C. L., Rizzo, R., Lyon, G. J., McMahon, W. M., Batterson, J. R., Cath, D. C., Malaty, I. A., Okun, M. S., Berlin, C., Woods, D. W., Lee, P. C., Jankovic, J., Robertson, M. M., Gilbert, D. L., Brown, L. W., Coffey, B. J., Dietrich, A., Hoekstra, P. J., Kuperman, S., Zinner, S. H., Luðvigsson, P., Sæmundsen, E., Thorarensen, Ó., Atzmon, G., Barzilai, N., Wagner, M., Moessner, R., Ophoff, R., Pato, C. N., Pato, M. T., Knowles, J. A., Roffman, J. L., Smoller, J. W., Buckner, R. L., Willsey, J. A., Tischfield, J. A., Heiman, G. A., Stefansson, H., Stefansson, K., Posthuma, D., Cox, N. J., Pauls, D. L., Freimer, N. B., Neale, B. M., Davis, L. K., Paschou, P., Coppola, G., Mathews, C. A., Scharf, J. M., Agee, M., Auton, A., Bell, R. K., Bryc, K., Elson, S. L., Fontanillas, P., Furlotte, N. A., Hicks, B., Huber, K. E., Jewett, E. M., Jiang, Y., Kleinman, A., Lin, K. H., Litterman, N. K., McCreight, J. C., McIntyre, M. H., McManus, K. F., Mountain, J. L., Noblin, E. S., Northover, C. A. M., Pitts, S. J., Poznik, G. D., Sathirapongsasuti, J. F., Shelton, J. F., Shringarpure, S., Tung, J. Y., Vacic, V., Wang, X., Als, T. D., Nissen, J. B., Meier, S. M., Bybjerg-Grauholm, J., Hougaard, D. M., Werge, T., Børglum, A. D., Hinds, D. A., Rück, C., Mataix-Cols, D., Stefánsson, H., Stefansson, K., Crowley, J. J. & Mattheisen, M., Apr 1 2025, In: Biological Psychiatry. 97, 7, p. 743-752 10 p.
Research output: Contribution to journal › Article › peer-review

Open Access
6 Link opens in a new tab Scopus citations
Outcomes of pregnancies that screened positive for sex chromosome aneuploidy ascertained via cell-free DNA screening
FitzGerald, C., Khan, S. P., Shingala, P., Heiman, G. & Ashkinadze, E., Oct 2025, In: Journal of Genetic Counseling. 34, 5, e70107.
Research output: Contribution to journal › Article › peer-review

Open Access

Gary Heiman

Fingerprint

Collaborations and top research areas from the last five years

Dive into details

1/7 Collaborative Genomic Studies of Tourette Disorder.

1/8-Collaborative genomic studies of Tourette Disorder

Shared Genetic Risk for Epilepsy and Depression

Mapping the genetic landscape across 14 psychiatric disorders

A Celsr3 Mutation Linked to Tourette Disorder Disrupts Cortical Dendritic Patterning and Striatal Cholinergic Interneuron Excitability

Evaluating pregnancy termination rates for fetal chromosome and single gene disorders

Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders

Outcomes of pregnancies that screened positive for sex chromosome aneuploidy ascertained via cell-free DNA screening

Gary Heiman

Fingerprint

Collaborations and top research areas from the last five years

Projects

Research output