Milen Velinov

ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 7

Top Venues

Genes

Obesity (Silver Spring, Md.)

Clinical genetics

Prenatal diagnosis

Institute for Basic Research in Developmental Disabilities

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Institute for Basic Research in Developmental Disabilities Jul 01 1998

United States

Director of Genetic Services :: Human Genetics

Publications

Kathryn K Chadman, Tatyana Adayev, Aishwarya Udayan, Rida Ahmed, Chun-Ling Dai, Jeffrey H Goodman, Harry Meeker, Natalia Dolzhanskaya, Milen Velinov
Efficient Delivery of FMR1 across the Blood Brain Barrier Using AAVphp Construct in Adult FMR1 KO Mice Suggests the Feasibility of Gene Therapy for Fragile X Syndrome. Genes 14 (2) (2023)
Kathryn K Chadman, Tatyana Adayev, Aishwarya Udayan, Rida Ahmed, Chun-Ling Dai, Jeffrey H Goodman, Harry Meeker, Natalia Dolzhanskaya, Milen Velinov
Efficient Delivery of FMR1 across the Blood Brain Barrier Using AAVphp Construct in Adult FMR1 KO Mice Suggests the Feasibility of Gene Therapy for Fragile X Syndrome. Genes 14 (2) (2023)
Kathryn K Chadman, Tatyana Adayev, Aishwarya Udayan, Rida Ahmed, Chun-Ling Dai, Jeffrey H Goodman, Harry Meeker, Natalia Dolzhanskaya, Milen Velinov
Efficient Delivery of FMR1 across the Blood Brain Barrier Using AAVphp Construct in Adult FMR1 KO Mice Suggests the Feasibility of Gene Therapy for Fragile X Syndrome. Genes 14 (2) (2023)
Matthew S Alexander, Milen Velinov
DOCK3 -Associated Neurodevelopmental Disorder-Clinical Features and Molecular Basis. Genes 14 (10) (2023)
Tse-Hwei Choo, Qing Xu, Dejan Budimirovic, Reymundo Lozano, Amy N Esler, Richard E Frye, Howard Andrews, Milen Velinov
Height and BMI in fragile X syndrome: A longitudinal assessment. Obesity (Silver Spring, Md.) 30 (3) (2022)
Nima Naseri, Manu Sharma, Milen Velinov
Autosomal dominant neuronal ceroid lipofuscinosis: Clinical features and molecular basis. Clinical genetics 99 (1) (2020)
Chidinma Nwakalor, Sara Said-Delgado, Shifra Krinshpun, Milen Velinov
De novo HRAS gene mutation associated with Costello syndrome identified by non-invasive cell-free fetal DNA screening. Prenatal diagnosis 41 (1) (2020)

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Publication Activity (10 Years)

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Milen Velinov