Prof. Golder N. Wilson
TTUHSC, USA
Professor of Pediatrics
Email: [email protected]
Qualifications
Ph.D. University of Chicago, USA
M. D. University of Chicago
Publications (Selected)
-
Wilson, G. N., & Tonk, V. S. (2024). Clinical-Genomic Analysis of 1261 Patients with Ehlers–Danlos Syndrome Outlines an Articulo-Autonomic Gene Network (Entome). Current Issues in Molecular Biology, 46(3), 2620-2643.
-
Wilson, G. N., & Tonk, V. S. (2024). Clinical-DNA Correlates of Anxiety in Patients with Ehlers-Danlos Syndrome. Open Journal of Psychiatry, 14(4), 319-333.
-
Wilson, G. N. (2023). A clinical qualification protocol highlights overlapping genomic influences and neuro-autonomic mechanisms in Ehlers–Danlos and long COVID-19 syndromes. Current Issues in Molecular Biology, 45(7), 6003-6023.
-
Palmer, E. E., Pusch, M., Picollo, A., Forwood, C., Nguyen, M. H., Wilson, G. N., ... & Kalscheuer, V. M. (2023). Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition. Molecular psychiatry, 28(2), 668-697.
-
Muir, A. M., Gardner, J. F., van Jaarsveld, R. H., de Lange, I. M., van der Smagt, J. J., Wilson, G. N., ... & Mefford, H. C. (2021). Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia. Genetics in Medicine, 23(5), 881-887.
-
Mochel, F., Rastetter, A., Ceulemans, B., Platzer, K., Yang, S., Wilson, G. N., ... & Depienne, C. (2020). Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders. Brain, 143(12), 3564-3573.
-
Wilson, G. N., & Tonk, V. S. (2020). Mitochondrial dysfunction contributes to Ehlers-Danlos syndrome—A patient presentation. J Biol Lab Sci, 11, 190-202.
-
Wilson, G. N., Tonk, S. S., Tonk, V. S., & Lampe, R. (2020). Complement gene mutation and Ehlers-Danlos syndrome. Journal of Biosciences and Medicines, 8(06), 28.
-
Wilson, G. N. (2019). Genomic analysis of 727 patients with Ehlers-Danlos syndrome I: Clinical perspective relates 23 genes to a maternally influenced arthritis-adrenaline disorder. Journal of Biosciences and Medicines, 7(12), 181.
-
Wilson, G. N. (2019). Clinical analysis supports articulo-autonomic dysplasia as a unifying pathogenic mechanism in Ehlers-Danlos Syndrome and related conditions. Journal of Biosciences and Medicines, 7(06), 149.
-
Wilson, G. N. (2018). DNA needs a doctor: genomics review and commentary.
-
Tanaka, A. J., Cho, M. T., Willaert, R., Retterer, K., Zarate, Y. A., Wilson, G. N., ... & Chung, W. K. (2017). De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism. Molecular Case Studies, 3(6), a002097.
-
Lehalle, D., Mosca-Boidron, A. L., Begtrup, A., Boute-Benejean, O., Charles, P., Wilson, G. N., ... & Faivre, L. (2017). STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability. Journal of medical genetics, 54(7), 479-488.
-
Graham Jr, J. M., Zadeh, N., Kelley, M., Tan, E. S., Liew, W., Wilson, G. N., ... & Shalev, S. A. (2016). KCNK9 imprinting syndrome—further delineation of a possible treatable disorder. American Journal of Medical Genetics Part A, 170(10), 2632-2637.
Profile Details
WoS ResearcherID: IAO-6210-2023
https://www.healthgrades.com/physician/dr-golder-wilson-y9rx6
https://www.researchgate.net/profile/Golder-Wilson