Hope Northrup
Affiliations: | Epidemiology & Disease Control | The University of Texas School of Public Health |
Area:
Molecular Biology, Epidemiology, GeneticsGoogle:
"Hope Northrup"Children
Sign in to add trainee| Michelle R. O'Byrne | grad student | 2010 | The University of Texas School of Public Health |
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Publications
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| Zhang C, Jolly A, Shayota BJ, et al. (2022) Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability. Hgg Advances. 3: 100074 |
| Farach LS, Richard MA, Lupo PJ, et al. (2020) Epilepsy Risk Prediction Model for Patients With Tuberous Sclerosis Complex. Pediatric Neurology. 113: 46-50 |
| Hillman P, Baker C, Hebert L, et al. (2020) Identification of novel candidate risk genes for myelomeningocele within the glucose homeostasis/oxidative stress and folate/one-carbon metabolism networks. Molecular Genetics & Genomic Medicine. e1495 |
| Streff H, Posey JE, Mauer CB, et al. (2020) TSC1 Variant Associated With Mild or Absent Clinical Features of Tuberous Sclerosis Complex in a Three-Generation Family. Pediatric Neurology |
| Mowrey K, Koenig MK, Szabo CA, et al. (2020) Two different genetic etiologies for tuberous sclerosis complex (TSC) in a single family. Molecular Genetics & Genomic Medicine. e1296 |
| Scherrer B, Prohl AK, Taquet M, et al. (2019) The Connectivity Fingerprint of the Fusiform Gyrus Captures the Risk of Developing Autism in Infants with Tuberous Sclerosis Complex. Cerebral Cortex (New York, N.Y. : 1991) |
| Farach LS, Pearson DA, Woodhouse JP, et al. (2019) Tuberous Sclerosis Complex Genotypes and Developmental Phenotype. Pediatric Neurology |
| Hussain SA, Schmid E, Peters JM, et al. (2018) High vigabatrin dosage is associated with lower risk of infantile spasms relapse among children with tuberous sclerosis complex. Epilepsy Research. 148: 1-7 |
| Peron A, Au KS, Northrup H. (2018) Genetics, genomics, and genotype-phenotype correlations of TSC: Insights for clinical practice. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics |
| Findley TO, Tenpenny JC, O'Byrne MR, et al. (2017) Mutations in folate transporter genes and risk for human myelomeningocele. American Journal of Medical Genetics. Part A |