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Author/Creator Timberlake, Andrew T

1. 125 De Novo Mutations in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus. Issue Volume 65:Issue CN(2018)Supplement 1 (16th August 2018)

Authors:
Furey, Charuta Gavankar; Jin, Sheng Chih; Timberlake, Andrew T; Choi, Jungmin; Zeng, Xue; Nelson-Williams, Carol; Mansuri, Mohammad; Lu, Qiongshi; Duran, Daniel; Panchagnula, Shreyas; Alloco, August; Karimy, Jason K; Gaillard, Jonathan; Khanna, Arjun; Butler, William; Smith, Edward R; Warf, Benja...
Journal:
Neurosurgery
Issue:
Volume 65:Issue CN(2018)Supplement 1
Page Start:
88
Record Type:
Journal Article
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2. Exome Sequencing Defines the Molecular Pathogenesis of Vein of Galen Malformation. (1st September 2019)

Authors:
Kundishora, Adam; Zeng, Xue; Duran, Daniel; Allocco, August A; Choi, Jungmin; Jin, Sheng Chih; Conine, Sierra B; Nelson-Williams, Carol; Gaillard, Jonathan; Furey, Charuta G; Timberlake, Andrew T; Mansuri, Mohammad; Sorscher, Michelle; Klein, Jennifer; Lu, Qiongshi; Montejo, Julio D; Vera, Albert...
Journal:
Neurosurgery
Issue:
Volume 66(2010)Supplement 1
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Record Type:
Journal Article
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3. Exome Sequencing Defines the Molecular Pathogenesis of Vein of Galen Malformation. (September 2019)

Authors:
Kundishora, Adam; Zeng, Xue; Duran, Daniel; Allocco, August A; Choi, Jungmin; Jin, Sheng Chih; Conine, Sierra B; Nelson‐Williams, Carol; Gaillard, Jonathan; Furey, Charuta G; Timberlake, Andrew T; Mansuri, Mohammad; Sorscher, Michelle; Klein, Jennifer; Lu, Qiongshi; Montejo, Julio D; Vera, Albert...
Journal:
Neurosurgery
Issue:
Volume 66(2019)Supplement
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Record Type:
Journal Article
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4. Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus. (16th November 2020)

Authors:
Panchagnula, Shreyas; Jin, Sheng C; Dong, Weilai; Kundishora, Adam; Moreno-De-Luca, Andres; Furey, Charuta G; Allocco, August A; Walker, Rebecca; Nelson-Williams, Carol; Smith, Hannah; Dunbar, Ashley; Conine, Sierra B; Lu, Qiongshi; Zen, Xue; Sierant, Michael; Knight, James; Sullivan, William; Ph...
Journal:
Neurosurgery
Issue:
Volume 67(2010)Supplement 1
Page Start:
Record Type:
Journal Article
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5. Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders. Issue 2 (12th January 2021)

Authors:
Calpena, Eduardo; Wurmser, Maud; McGowan, Simon J; Atique, Rodrigo; Bertola, Débora R; Cunningham, Michael L; Gustafson, Jonas A; Johnson, David; Morton, Jenny E V; Passos-Bueno, Maria Rita; Timberlake, Andrew T; Lifton, Richard P; Wall, Steven A; Twigg, Stephen R F; Maire, Pascal; Wilkie, Andrew...
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 2(2022)
Page Start:
165
Record Type:
Journal Article
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