Projects per year
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Dive into the research topics where Milen Velinov is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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Projects
- 4 Finished
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USING LONGITUDINAL DATA TO CHARACTERIZE THE NATURAL HISTORY OF FRAGILE X SYNDROME--COMPONENT A
Velinov, M. (PI)
National Center on Birth Defects and Developmental Disabilities
9/1/15 → 8/31/20
Project: Research project
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USING LONGITUDINAL DATA TO CHARACTERIZE THE NATURAL HISTORY OF FRAGILE X SYNDROME--COMPONENT A
Velinov, M. (PI)
National Center on Birth Defects and Developmental Disabilities
9/1/15 → 8/31/20
Project: Research project
-
USING LONGITUDINAL DATA TO CHARACTERIZE THE NATURAL HISTORY OF FRAGILE X SYNDROME--COMPONENT A
Velinov, M. (PI)
National Center on Birth Defects and Developmental Disabilities
9/1/15 → 8/31/20
Project: Research project
-
USING LONGITUDINAL DATA TO CHARACTERIZE THE NATURAL HISTORY OF FRAGILE X SYNDROME--COMPONENT A
Velinov, M. (PI)
National Center on Birth Defects and Developmental Disabilities
9/1/15 → 8/31/20
Project: Research project
-
Gene Therapy for Fragile X Syndrome, Challenges, and Promises
Velinov, M., Nov 2025, In: Journal of Gene Medicine. 27, 11, e70049.Research output: Contribution to journal › Review article › peer-review
Open Access -
Newborn Screening for Gaucher Disease: The New Jersey Experience
Menello, C., Pressley, S., Steffensen, M., Schmidt, S., Pedro, H., Jethva, R., Valdez-Gonzalez, K., Adams, D. J., Gupta, P., King, L. T., Velinov, M., Anderson, S., Bizargity, P., Pletcher, B., Tuite, A., Kresge, C., Day-Salvatore, D. L., Kuehl, R. & Ficicioglu, C., Jun 2025, In: International Journal of Neonatal Screening. 11, 2, 34.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Relationship Between Intellectual Disability and Behavioral Comorbidity in Children With Fragile X Syndrome
FORWARD Consortium, 2025, (Accepted/In press) In: Journal of Autism and Developmental Disorders.Research output: Contribution to journal › Article › peer-review
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Transgenerational Effects and Heritability of Folate Receptor Alpha Autoantibodies in Autism Spectrum Disorder
Frye, R. E., Cohen, I. L., Sequeira, J. M., Hill, Z., Espinoza, A., Brown, W. T., Mevs, C., Marchi, E., Flory, M., Jenkins, E. C., Velinov, M. T. & Quadros, E. V., Sep 2025, In: International journal of molecular sciences. 26, 17, 8293.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
A Second Case of Spondylocostal Dysplasia Including Urogenital Anomalies, Associated With Homozygous Variant c.699 G>C in Gene TBX6
Park, S. Y., Halari, A., Kotha, N., Chaudhry, S., Khan, M., Velinov, M. & Puvabanditsin, S., Jun 2024, Neonatal Intensive Care, 37, 3, p. 9-12 4 p.Research output: Contribution to specialist publication › Article