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Curtis Rogers

Explore the profile of Curtis Rogers including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 17
Citations 113
Followers 0
Related Specialties
Genetics
General Medicine
Neurology
Top 10 Co-Authors
Katy Phelan
Luigi Boccuto
Sara M Sarasua
Lavanya Jain
Kathleen Valentine
William E Bennett Jr
Valerie Biancalana
Sara Sarasua
Lauren Cascio
Diana Ivankovic
Published In
Genes (Basel)
Am J Med Genet A
Am J Hum Genet
Clin Genet
J S C Med Assoc
Affiliations
Soon will be listed here.
Recent Articles
1.
Bi-allelic MED16 variants cause a MEDopathy with intellectual disability, motor delay, and craniofacial, cardiac, and limb malformations
Guillouet C, Agostini V, Baujat G, Cocciadiferro D, Pippucci T, Lesieur-Sebellin M, et al.
Am J Hum Genet . 2025 Mar; PMID: 40081376
The Mediator complex regulates protein-coding gene transcription by coordinating the interaction of upstream enhancers with the basal transcription machinery at the promoter. Pathogenic variants in Mediator subunits typically lead to...
2.
Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions
Sagath L, Kiiski K, Naidu K, Patel K, Jonson P, Laarne M, et al.
medRxiv . 2025 Jan; PMID: 39802796
Introduction: Structural variants (SVs) of the nebulin gene (), including intragenic duplications, deletions, and copy number variation of the triplicate region, are an established cause of recessively inherited nemaline myopathies...
3.
The detection of a strong episignature for Chung-Jansen syndrome, partially overlapping with Börjeson-Forssman-Lehmann and White-Kernohan syndromes
Vos N, Haghshenas S, van der Laan L, Russel P, Rooney K, Levy M, et al.
Hum Genet . 2024 May; 143(6):761-773. PMID: 38787418
Chung-Jansen syndrome is a neurodevelopmental disorder characterized by intellectual disability, behavioral problems, obesity and dysmorphic features. It is caused by pathogenic variants in the PHIP gene that encodes for the...
4.
The vectoring competence of the mite for deformed wing virus of honey bees is dynamic and affects survival of the mite
Ryabov E, Posada-Florez F, Rogers C, Lamas Z, Evans J, Chen Y, et al.
Front Insect Sci . 2024 Mar; 2:931352. PMID: 38468796
The ectoparasitic mite, and the viruses it vectors, including types A and B of Deformed wing virus (DWV), pose a major threat to honey bees, . Analysis of 256 mites...
5.
Updated consensus guidelines on the management of Phelan-McDermid syndrome
Srivastava S, Sahin M, Buxbaum J, Berry-Kravis E, Soorya L, Thurm A, et al.
Am J Med Genet A . 2023 Jul; 191(8):2015-2044. PMID: 37392087
Phelan-McDermid syndrome (PMS) is a genetic condition caused by SHANK3 haploinsufficiency and characterized by a wide range of neurodevelopmental and systemic manifestations. The first practice parameters for assessment and monitoring...
6.
Lymphedema is associated with CELSR1 in Phelan-McDermid syndrome
Smith M, Sarasua S, Rogers C, Phelan K, Boccuto L
Clin Genet . 2023 May; 104(4):472-478. PMID: 37232218
Lymphedema is a troubling condition present in many disorders including the rare genetic disorder known as Phelan-McDermid syndrome (PMS). The neurobehavioral features of PMS, also known as 22q13.3 deletion syndrome,...
7.
Head Size in Phelan-McDermid Syndrome: A Literature Review and Pooled Analysis of 198 Patients Identifies Candidate Genes on 22q13
Sarasua S, DeLuca J, Rogers C, Phelan K, Rennert L, Powder K, et al.
Genes (Basel) . 2023 Mar; 14(3). PMID: 36980813
Phelan-McDermid syndrome (PMS) is a multisystem disorder that is associated with deletions of the 22q13 genomic region or pathogenic variants in the gene. Notable features include developmental issues, absent or...
8.
Stratification of a Phelan-McDermid Syndrome Population Based on Their Response to Human Growth Hormone and Insulin-like Growth Factor
Moffitt B, Sarasua S, Ivankovic D, Ward L, Valentine K, Bennett Jr W, et al.
Genes (Basel) . 2023 Feb; 14(2). PMID: 36833418
Phelan-McDermid syndrome (PMS), caused by pathogenic variants in the gene or 22q13 deletions, is characterized by intellectual disability, autistic features, developmental delays, and neonatal hypotonia. Insulin-like growth factor 1 (IGF-1)...
9.
Sleep and Phelan-McDermid Syndrome: Lessons from the International Registry and the scientific literature
Moffitt B, Sarasua S, Ward L, Ivankovic D, Valentine K, Rogers C, et al.
Mol Genet Genomic Med . 2022 Aug; 10(10):e2035. PMID: 35996993
Background: Sleep is essential to maintaining a healthy life. Sleep disturbances among individuals with neurodevelopmental disorders are not well studied, affecting their early detection and treatment. Sleep disturbances in individuals...
10.
RNA analysis of the GALNS transcript reveals novel pathogenic mechanisms associated with Morquio syndrome A
Sohn Y, Rogers C, Stallworth J, Cooley Coleman J, Buch L, Jozwiak E, et al.
Mol Genet Metab Rep . 2022 Jul; 31:100875. PMID: 35782621
Morquio syndrome A (Mucopolysaccharidosis IVA, MPS IVA) is an autosomal recessive lysosomal storage disorder caused by deficiency of -acetyl-galactosamine-6-sulfatase (GALNS) which catabolizes the glycosaminoglycans (GAG), keratan sulfate and chondroitin-6-sulfate. Homozygous...