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Collaborations and top research areas from the last five years
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Investigation of Professional Coaching as an Intervention to Support the Success of URG Biomedical Ph.D. Students
Millonig, J. (PI), Blitz, C. (CoPI) & Runnels, L. L. W. (CoPI)
National Institute of General Medical Sciences
9/1/23 → 6/30/26
Project: Research project
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Role of CNNM2 in Neuronal Mg2+ Homeostasis, Function and Development
Runnels, L. L. W. (PI) & Millonig, J. (CoPI)
National Institute of Neurological Disorders and Stroke
2/1/25 → 1/31/26
Project: Research project
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IMSD at Rutgers - New Brunswick
Haimovich, B. (CoPI), Langer, J. (CoPI), Runnels, L. (CoPI), Runnels, L. L. W. (PI), Millonig, J. (CoPI) & Scott, T. T. E. (CoPI)
National Institute of General Medical Sciences
2/1/21 → 1/31/26
Project: Research project
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Interdisciplinary Job Opportunities for Biomedical Scientists - iJOBS
Yarmush, M. (PI) & Millonig, J. (CoPI)
9/18/14 → 3/31/21
Project: Research project
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A Mouse Knock-In Model for ENGRAILED 2 Autism Susceptibility
Millonig, J. (PI)
NATIONAL INSTITUTE OF MENTAL HEALTH
5/1/10 → 4/30/12
Project: Research project
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mTORC1 activity oscillates throughout the cell cycle, promoting mitotic entry and differentially influencing autophagy induction
Joshi, J. N., Lerner, A. D., Scallo, F., Grumet, A. N., Matteson, P., Millonig, J. H. & Valvezan, A. J., Aug 27 2024, In: Cell Reports. 43, 8, 114543.Research output: Contribution to journal › Article › peer-review
Open Access11 Link opens in a new tab Scopus citations -
Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex
Salamon, I., Park, Y., Miškić, T., Kopić, J., Matteson, P., Page, N. F., Roque, A., McAuliffe, G. W., Favate, J., Garcia-Forn, M., Shah, P., Judaš, M., Millonig, J. H., Kostović, I., De Rubeis, S., Hart, R. P., Krsnik, Ž. & Rasin, M. R., Dec 2023, In: Nature communications. 14, 1, 6025.Research output: Contribution to journal › Article › peer-review
Open Access21 Link opens in a new tab Scopus citations -
Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses
Connacher, R., Williams, M., Prem, S., Yeung, P. L., Matteson, P., Mehta, M., Markov, A., Peng, C., Zhou, X., McDermott, C. R., Pang, Z. P., Flax, J., Brzustowicz, L., Lu, C. W., Millonig, J. H. & DiCicco-Bloom, E., Jun 14 2022, In: Stem Cell Reports. 17, 6, p. 1380-1394 15 p.Research output: Contribution to journal › Article › peer-review
Open Access19 Link opens in a new tab Scopus citations -
Erratum: Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses (Stem Cell Reports (2022) 17(6) (1380–1394), (S2213671122002089), (10.1016/j.stemcr.2022.04.019))
Connacher, R., Williams, M., Prem, S., Yeung, P. L., Matteson, P., Mehta, M., Markov, A., Peng, C., Zhou, X., McDermott, C. R., Pang, Z. P., Flax, J., Brzustowicz, L., Lu, C. W., Millonig, J. H. & DiCicco-Bloom, E., Jul 12 2022, In: Stem Cell Reports. 17, 7, p. 1786 1 p.Research output: Contribution to journal › Comment/debate › peer-review
Open Access2 Link opens in a new tab Scopus citations -
Biallelic hypomorphic variants in ALDH1A2 cause a novel lethal human multiple congenital anomaly syndrome encompassing diaphragmatic, pulmonary, and cardiovascular defects
Beecroft, S. J., Ayala, M., McGillivray, G., Nanda, V., Agolini, E., Novelli, A., Digilio, M. C., Dotta, A., Carrozzo, R., Clayton, J., Gaffney, L., McLean, C. A., Ng, J., Laing, N. G., Matteson, P., Millonig, J. & Ravenscroft, G., May 2021, In: Human mutation. 42, 5, p. 506-519 14 p.Research output: Contribution to journal › Article › peer-review
Open Access18 Link opens in a new tab Scopus citations