Gary Heiman

Research activity per year

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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
Rutgers, The State University
Project: Research
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
Rutgers, The State University
Project: Research
Shared Genetic Risk for Epilepsy and Depression
Heiman, G. G. A. (CoPI) & Heiman, G. (PI)
9/30/07 → 6/30/13
Rutgers, The State University
Project: Research

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

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
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
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.
Rutgers, The State University
Research output: Contribution to journal › Article › peer-review

Open Access
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.
Rutgers, The State University
Research output: Contribution to journal › Article › peer-review

Open Access
Uptake rates for non-invasive prenatal screening for single-gene disorders associated with advanced paternal age
Katz, K., Brandt, J. S., Heiman, G., Simone, L., Khan, S., Shingala, P. & Ashkinadze, E., Apr 2025, In: Journal of Genetic Counseling. 34, 2, e2025.
Rutgers, The State University
Research output: Contribution to journal › Article › peer-review

Open Access

Gary Heiman

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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

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

Uptake rates for non-invasive prenatal screening for single-gene disorders associated with advanced paternal age

Gary Heiman

Fingerprint

Collaborations and top research areas from the last five years

Projects

Research output