Velinov M - Search Results

1

Height and BMI in fragile X syndrome: A longitudinal assessment.

Choo TH, Xu Q, Budimirovic D, Lozano R, Esler AN, Frye RE, Andrews H, Velinov M. Choo TH, et al. Among authors: velinov m. Obesity (Silver Spring). 2022 Mar;30(3):743-750. doi: 10.1002/oby.23368. Epub 2022 Feb 16. Obesity (Silver Spring). 2022. PMID: 35174658 Free PMC article.

2

Soy-Based Infant Formula is Associated with an Increased Prevalence of Comorbidities in Fragile X Syndrome.

Westmark CJ, Kniss C, Sampene E, Wang A, Milunovich A, Elver K, Hessl D, Talboy A, Picker J, Haas-Givler B, Esler A, Gropman AL, Uy R, Erickson C, Velinov M, Tartaglia N, Berry-Kravis EM. Westmark CJ, et al. Among authors: velinov m. Nutrients. 2020 Oct 14;12(10):3136. doi: 10.3390/nu12103136. Nutrients. 2020. PMID: 33066511 Free PMC article.

3

Seizures in Fragile X Syndrome: Associations and Longitudinal Analysis of a Large Clinic-Based Cohort.

Berry-Kravis E, Filipink RA, Frye RE, Golla S, Morris SM, Andrews H, Choo TH, Kaufmann WE; FORWARD Consortium. Berry-Kravis E, et al. Front Pediatr. 2021 Dec 30;9:736255. doi: 10.3389/fped.2021.736255. eCollection 2021. Front Pediatr. 2021. PMID: 35036394 Free PMC article.

4

The association between mosaicism type and cognitive and behavioral functioning among males with fragile X syndrome.

Meng L, Kaufmann WE, Frye RE, Ong K, Kaminski JW, Velinov M, Berry-Kravis E. Meng L, et al. Among authors: velinov m. Am J Med Genet A. 2022 Mar;188(3):858-866. doi: 10.1002/ajmg.a.62594. Epub 2021 Dec 8. Am J Med Genet A. 2022. PMID: 35148024 Free PMC article.

5

FMR1 and Autism, an Intriguing Connection Revisited.

Fyke W, Velinov M. Fyke W, et al. Among authors: velinov m. Genes (Basel). 2021 Aug 6;12(8):1218. doi: 10.3390/genes12081218. Genes (Basel). 2021. PMID: 34440392 Free PMC article. Review.

6

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.

Chadman KK, Adayev T, Udayan A, Ahmed R, Dai CL, Goodman JH, Meeker H, Dolzhanskaya N, Velinov M. Chadman KK, et al. Among authors: velinov m. Genes (Basel). 2023 Feb 16;14(2):505. doi: 10.3390/genes14020505. Genes (Basel). 2023. PMID: 36833432 Free PMC article.

7

Longitudinal telomere shortening and early Alzheimer's disease progression in adults with down syndrome.

Jenkins EC, Marchi EJ, Velinov MT, Ye L, Krinsky-McHale SJ, Zigman WB, Schupf N, Silverman WP. Jenkins EC, et al. Am J Med Genet B Neuropsychiatr Genet. 2017 Dec;174(8):772-778. doi: 10.1002/ajmg.b.32575. Epub 2017 Aug 30. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28856789

8

Reduced telomere length in older men with premutation alleles of the fragile X mental retardation 1 gene.

Jenkins EC, Tassone F, Ye L, Gu H, Xi M, Velinov M, Brown WT, Hagerman RJ, Hagerman PJ. Jenkins EC, et al. Among authors: velinov m. Am J Med Genet A. 2008 Jun 15;146A(12):1543-6. doi: 10.1002/ajmg.a.32342. Am J Med Genet A. 2008. PMID: 18478592 Free PMC article.

9

Variable clinical expression of mosaic trisomy 16 in the newborn infant.

Devi AS, Velinov M, Kamath MV, Eisenfeld L, Neu R, Ciarleglio L, Greenstein R, Benn P. Devi AS, et al. Among authors: velinov m. Am J Med Genet. 1993 Aug 15;47(2):294-8. doi: 10.1002/ajmg.1320470231. Am J Med Genet. 1993. PMID: 8213923 Review.

10

De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy.

de Lange IM, Helbig KL, Weckhuysen S, Møller RS, Velinov M, Dolzhanskaya N, Marsh E, Helbig I, Devinsky O, Tang S, Mefford HC, Myers CT, van Paesschen W, Striano P, van Gassen K, van Kempen M, de Kovel CG, Piard J, Minassian BA, Nezarati MM, Pessoa A, Jacquette A, Maher B, Balestrini S, Sisodiya S, Warde MT, De St Martin A, Chelly J; EuroEPINOMICS-RES MAE working group; van 't Slot R, Van Maldergem L, Brilstra EH, Koeleman BP. de Lange IM, et al. Among authors: velinov m. J Med Genet. 2016 Dec;53(12):850-858. doi: 10.1136/jmedgenet-2016-103909. Epub 2016 Jun 29. J Med Genet. 2016. PMID: 27358180 Free PMC article.

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