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Hope Northrup

University of Texas Health Science Center at Houston
University of Texas at Austin
Shriners Hospitals for Children

182

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7836

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Birth defect co-occurrence patterns in the Texas Birth Defects Registry

2021 Pediatric Research
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Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration.

2021 Scientific Reports
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Corrigendum to "Patterns of co-occurring birth defects among infants with hypospadiasˮ [J Pediatr Urol 17 (2021) 64.e1-64.e8].

2021 Journal of Pediatric Urology
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Tuber locations associated with infantile spasms map to a common brain network

2021 Annals of Neurology
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Epilepsy Is Heterogeneous in Early-Life Tuberous Sclerosis Complex.

2021 Pediatric Neurology
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The youngest pair of siblings with Mucopolysaccharidosis type IVA to receive enzyme replacement therapy to date: A case report.

2021 American Journal of Medical Genetics Part A
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TUBEROUS SCLEROSIS COMPLEX

2021
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Patterns of congenital anomalies among individuals with trisomy 13 in Texas.

2021 American Journal of Medical Genetics Part A
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Birth Defect Co-Occurrence Patterns Among Infants With Cleft Lip and/or Palate.

2021 The Cleft Palate-Craniofacial Journal
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Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations.

2021 Pediatric Neurology
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