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Paul Hillman
Paul Hillman
University of Texas Health Science Center at Houston
Gene
Biology
Genome
Genetics
Wnt signaling pathway
4
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7
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0
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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
Kit Sing Au
Luke Hebert
Paul Hillman
Craig Baker
Michael R. Brown
D.-K. Kim
Karen L. Soldano
Melanie E. Garrett
Allison E. Ashley-Koch
Sanghee Lee
J. Gleeson
James E. Hixson
Alanna C. Morrison
Hope Northrup
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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
Marta Frigeni
David Rodriguez-Buritica
Heather Saavedra
Kathryn Gunther
Paul Hillman
Duraisamy Balaguru
Hope Northrup
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Identification of novel candidate risk genes for myelomeningocele within the glucose homeostasis/oxidative stress and folate/one-carbon metabolism networks
2020
Molecular Genetics & Genomic Medicine
Paul Hillman
Craig Baker
Luke Hebert
Michael R. Brown
James E. Hixson
Allison E. Ashley-Koch
Alanna C. Morrison
Hope Northrup
Kit Sing Au
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Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients.
2020
PLOS ONE
Luke Hebert
Paul Hillman
Craig Baker
Michael R. Brown
Allison E. Ashley-Koch
James E. Hixson
Alanna C. Morrison
Hope Northrup
Kit Sing Au
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Citations (3)
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