Year |
Citation |
Score |
2020 |
Aldridge K, Cole KK, Moffitt Gunn AJ, Peck D, White DA, Christ SE. The effects of early-treated phenylketonuria on volumetric measures of the cerebellum. Molecular Genetics and Metabolism Reports. 25: 100647. PMID 32995290 DOI: 10.1016/J.Ymgmr.2020.100647 |
0.4 |
|
2017 |
Aldridge K, Collett BR, Wallace ER, Birgfeld C, Austin JR, Yeh R, Feil M, Kapp-Simon KA, Aylward EH, Cunningham ML, Speltz ML. Structural brain differences in school-age children with and without single-suture craniosynostosis. Journal of Neurosurgery. Pediatrics. 1-11. PMID 28156213 DOI: 10.3171/2016.9.Peds16107 |
0.436 |
|
2014 |
Motch Perrine SM, Cole TM, Martínez-Abadías N, Aldridge K, Jabs EW, Richtsmeier JT. Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice. Bmc Developmental Biology. 14: 8. PMID 24580805 DOI: 10.1186/1471-213X-14-8 |
0.618 |
|
2014 |
Chollet MB, Aldridge K, Pangborn N, Weinberg SM, Deleon VB. Landmarking the brain for geometric morphometric analysis: an error study. Plos One. 9: e86005. PMID 24489689 DOI: 10.1371/Journal.Pone.0086005 |
0.667 |
|
2014 |
Moffett EA, Aldridge K. Size of the anterior fontanelle: three-dimensional measurement of a key trait in human evolution. Anatomical Record (Hoboken, N.J. : 2007). 297: 234-9. PMID 24443185 DOI: 10.1002/Ar.22830 |
0.306 |
|
2013 |
Hill CA, MartÃnez-AbadÃas N, Motch SM, Austin JR, Wang Y, Jabs EW, Richtsmeier JT, Aldridge K. Postnatal brain and skull growth in an Apert syndrome mouse model. American Journal of Medical Genetics. Part A. 161: 745-57. PMID 23495236 DOI: 10.1002/Ajmg.A.35805 |
0.673 |
|
2013 |
Martínez-Abadías N, Motch SM, Pankratz TL, Wang Y, Aldridge K, Jabs EW, Richtsmeier JT. Tissue-specific responses to aberrant FGF signaling in complex head phenotypes. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 242: 80-94. PMID 23172727 DOI: 10.1002/Dvdy.23903 |
0.679 |
|
2013 |
Martínez-Abadías N, Motch SM, Pankratz TL, Wang Y, Aldridge K, Jabs EW, Richtsmeier JT. Tissue-specific responses to aberrant FGF signaling in complex head phenotypes: Complex Head Phenotypes inFgfr2cC342Y/+Mice Developmental Dynamics. 242. DOI: 10.1002/Dvdy.23940 |
0.559 |
|
2012 |
Bodner KE, Aldridge K, Moffitt AJ, Peck D, White DA, Christ SE. A volumetric study of basal ganglia structures in individuals with early-treated phenylketonuria. Molecular Genetics and Metabolism. 107: 302-7. PMID 23006929 DOI: 10.1016/J.Ymgme.2012.08.007 |
0.379 |
|
2012 |
Aldridge K, Wang L, Harms MP, Moffitt AJ, Cole KK, Csernansky JG, Selemon LD. A longitudinal analysis of regional brain volumes in macaques exposed to X-irradiation in early gestation. Plos One. 7: e43109. PMID 22905212 DOI: 10.1371/Journal.Pone.0043109 |
0.441 |
|
2011 |
Martínez-Abadías N, Heuzé Y, Wang Y, Jabs EW, Aldridge K, Richtsmeier JT. FGF/FGFR signaling coordinates skull development by modulating magnitude of morphological integration: evidence from Apert syndrome mouse models. Plos One. 6: e26425. PMID 22053191 DOI: 10.1371/Journal.Pone.0026425 |
0.647 |
|
2011 |
Aldridge K, George ID, Cole KK, Austin JR, Takahashi TN, Duan Y, Miles JH. Facial phenotypes in subgroups of prepubertal boys with autism spectrum disorders are correlated with clinical phenotypes. Molecular Autism. 2: 15. PMID 21999758 DOI: 10.1186/2040-2392-2-15 |
0.4 |
|
2011 |
Aldridge K. Patterns of differences in brain morphology in humans as compared to extant apes. Journal of Human Evolution. 60: 94-105. PMID 21056456 DOI: 10.1016/J.Jhevol.2010.09.007 |
0.452 |
|
2011 |
Hill CA, Vaddi S, Moffitt A, Kane AA, Marsh JL, Panchal J, Richtsmeier JT, Aldridge K. Intracranial volume and whole brain volume in infants with unicoronal craniosynostosis. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 48: 394-8. PMID 20815706 DOI: 10.1597/10-051 |
0.588 |
|
2010 |
MartÃnez-AbadÃas N, Percival C, Aldridge K, Hill CA, Ryan T, Sirivunnabood S, Wang Y, Jabs EW, Richtsmeier JT. Beyond the closed suture in apert syndrome mouse models: evidence of primary effects of FGFR2 signaling on facial shape at birth. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 239: 3058-71. PMID 20842696 DOI: 10.1002/Dvdy.22414 |
0.621 |
|
2010 |
Aldridge K, Hill CA, Austin JR, Percival C, Martinez-Abadias N, Neuberger T, Wang Y, Jabs EW, Richtsmeier JT. Brain phenotypes in two FGFR2 mouse models for Apert syndrome. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 239: 987-97. PMID 20077479 DOI: 10.1002/Dvdy.22218 |
0.683 |
|
2007 |
Aldridge K, Reeves RH, Olson LE, Richtsmeier JT. Differential effects of trisomy on brain shape and volume in related aneuploid mouse models. American Journal of Medical Genetics. Part A. 143: 1060-70. PMID 17431903 DOI: 10.1002/Ajmg.A.31721 |
0.615 |
|
2006 |
Richtsmeier JT, Aldridge K, DeLeon VB, Panchal J, Kane AA, Marsh JL, Yan P, Cole TM. Phenotypic integration of neurocranium and brain. Journal of Experimental Zoology. Part B, Molecular and Developmental Evolution. 306: 360-78. PMID 16526048 DOI: 10.1002/Jez.B.21092 |
0.718 |
|
2005 |
Aldridge K, Boyadjiev SA, Capone GT, DeLeon VB, Richtsmeier JT. Precision and error of three-dimensional phenotypic measures acquired from 3dMD photogrammetric images. American Journal of Medical Genetics. Part A. 138: 247-53. PMID 16158436 DOI: 10.1002/Ajmg.A.30959 |
0.657 |
|
2005 |
Aldridge K, Kane AA, Marsh JL, Panchal J, Boyadjiev SA, Yan P, Govier D, Ahmad W, Richtsmeier JT. Brain morphology in nonsyndromic unicoronal craniosynostosis. The Anatomical Record. Part a, Discoveries in Molecular, Cellular, and Evolutionary Biology. 285: 690-8. PMID 15977220 DOI: 10.1002/Ar.A.20201 |
0.648 |
|
2005 |
Aldridge K, Kane AA, Marsh JL, Yan P, Govier D, Richtsmeier JT. Relationship of brain and skull in pre- and postoperative sagittal synostosis. Journal of Anatomy. 206: 373-85. PMID 15817105 DOI: 10.1111/J.1469-7580.2005.00397.X |
0.638 |
|
2002 |
Aldridge K, Marsh JL, Govier D, Richtsmeier JT. Central nervous system phenotypes in craniosynostosis. Journal of Anatomy. 201: 31-9. PMID 12171474 DOI: 10.1046/J.1469-7580.2002.00074.X |
0.588 |
|
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