Albert M. Galaburda - Publications

Affiliations: 
Harvard Medical School, Boston, MA, United States 
Area:
Neuroscience

144 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Levman J, MacDonald P, Rowley S, Stewart N, Lim A, Ewenson B, Galaburda A, Takahashi E. Structural Magnetic Resonance Imaging Demonstrates Abnormal Regionally-Differential Cortical Thickness Variability in Autism: From Newborns to Adults. Frontiers in Human Neuroscience. 13: 75. PMID 30930758 DOI: 10.3389/Fnhum.2019.00075  0.366
2018 Levman J, Vasung L, MacDonald P, Rowley S, Stewart N, Lim A, Ewenson B, Galaburda A, Takahashi E. Regional Volumetric Abnormalities in Pediatric Autism Revealed by Structural Magnetic Resonance Imaging. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. PMID 30110650 DOI: 10.1016/J.Ijdevneu.2018.08.001  0.349
2017 Wilkinson M, Lim AR, Cohen AH, Galaburda AM, Takahashi E. Detection and Growth Pattern of Arcuate Fasciculus from Newborn to Adult. Frontiers in Neuroscience. 11: 389. PMID 28769741 DOI: 10.3389/Fnins.2017.00389  0.328
2015 Paldino MJ, Hedges K, Gaab N, Galaburda AM, Grant PE. Failure to Identify the Left Arcuate Fasciculus at Diffusion Tractography Is a Specific Marker of Language Dysfunction in Pediatric Patients with Polymicrogyria. Behavioural Neurology. 2015: 351391. PMID 26180373 DOI: 10.1155/2015/351391  0.545
2014 Truong DT, Che A, Rendall AR, Szalkowski CE, LoTurco JJ, Galaburda AM, Holly Fitch R. Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability. Genes, Brain, and Behavior. 13: 802-11. PMID 25130614 DOI: 10.1111/Gbb.12170  0.612
2014 Hoeft F, Dai L, Haas BW, Sheau K, Mimura M, Mills D, Galaburda A, Bellugi U, Korenberg JR, Reiss AL. Mapping genetically controlled neural circuits of social behavior and visuo-motor integration by a preliminary examination of atypical deletions with Williams syndrome. Plos One. 9: e104088. PMID 25105779 DOI: 10.1371/Journal.Pone.0104088  0.735
2014 Altarelli I, Leroy F, Monzalvo K, Fluss J, Billard C, Dehaene-Lambertz G, Galaburda AM, Ramus F. Planum temporale asymmetry in developmental dyslexia: Revisiting an old question. Human Brain Mapping. 35: 5717-35. PMID 25044828 DOI: 10.1002/Hbm.22579  0.652
2014 Song JW, Mitchell PD, Kolasinski J, Ellen Grant P, Galaburda AM, Takahashi E. Asymmetry of White Matter Pathways in Developing Human Brains. Cerebral Cortex (New York, N.Y. : 1991). PMID 24812082 DOI: 10.1093/Cercor/Bhu084  0.359
2014 Hoeft F, Dai L, Haas BW, Sheau K, Mimura M, Mills D, Galaburda A, Bellugi U, Korenberg JR, Reiss AL. Demographic information. Atypical deletion cases and their deviations from WS and TD groups. Plos One. DOI: 10.1371/Journal.Pone.0104088.T002  0.493
2014 Hoeft F, Dai L, Haas BW, Sheau K, Mimura M, Mills D, Galaburda A, Bellugi U, Korenberg JR, Reiss AL. Demographic information. WS and TD groups. Plos One. DOI: 10.1371/Journal.Pone.0104088.T001  0.479
2014 Hoeft F, Dai L, Haas BW, Sheau K, Mimura M, Mills D, Galaburda A, Bellugi U, Korenberg JR, Reiss AL. Schematic diagram of deleted genes in WS and in partial deletion participants (AWSdel). Plos One. DOI: 10.1371/Journal.Pone.0104088.G001  0.507
2013 Mills DL, Dai L, Fishman I, Yam A, Appelbaum LG, St George M, Galaburda A, Bellugi U, Korenberg JR. Genetic mapping of brain plasticity across development in Williams syndrome: ERP markers of face and language processing. Developmental Neuropsychology. 38: 613-42. PMID 24219698 DOI: 10.1080/87565641.2013.825617  0.686
2013 Platt MP, Adler WT, Mehlhorn AJ, Johnson GC, Wright KA, Choi RT, Tsang WH, Poon MW, Yeung SY, Waye MM, Galaburda AM, Rosen GD. Embryonic disruption of the candidate dyslexia susceptibility gene homolog Kiaa0319-like results in neuronal migration disorders. Neuroscience. 248: 585-93. PMID 23831424 DOI: 10.1016/J.Neuroscience.2013.06.056  0.799
2013 Adler WT, Platt MP, Mehlhorn AJ, Haight JL, Currier TA, Etchegaray MA, Galaburda AM, Rosen GD. Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes. Plos One. 8: e65179. PMID 23724130 DOI: 10.1371/Journal.Pone.0065179  0.779
2013 Im K, Pienaar R, Paldino MJ, Gaab N, Galaburda AM, Grant PE. Quantification and discrimination of abnormal sulcal patterns in polymicrogyria. Cerebral Cortex (New York, N.Y. : 1991). 23: 3007-15. PMID 22989584 DOI: 10.1093/Cercor/Bhs292  0.573
2012 Szalkowski CE, Fiondella CG, Galaburda AM, Rosen GD, Loturco JJ, Fitch RH. Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 30: 293-302. PMID 22326444 DOI: 10.1016/J.Ijdevneu.2012.01.009  0.791
2012 Takahashi E, Folkerth RD, Galaburda AM, Grant PE. Emerging cerebral connectivity in the human fetal brain: an MR tractography study. Cerebral Cortex (New York, N.Y. : 1991). 22: 455-64. PMID 21670100 DOI: 10.1093/Cercor/Bhr126  0.587
2011 Wang Y, Yin X, Rosen G, Gabel L, Guadiana SM, Sarkisian MR, Galaburda AM, Loturco JJ. Dcdc2 knockout mice display exacerbated developmental disruptions following knockdown of doublecortin. Neuroscience. 190: 398-408. PMID 21689730 DOI: 10.1016/J.Neuroscience.2011.06.010  0.725
2011 Currier TA, Etchegaray MA, Haight JL, Galaburda AM, Rosen GD. The effects of embryonic knockdown of the candidate dyslexia susceptibility gene homologue Dyx1c1 on the distribution of GABAergic neurons in the cerebral cortex. Neuroscience. 172: 535-46. PMID 21070838 DOI: 10.1016/J.Neuroscience.2010.11.002  0.809
2011 Takahashi E, Dai G, Rosen GD, Wang R, Ohki K, Folkerth RD, Galaburda AM, Wedeen VJ, Ellen Grant P. Developing neocortex organization and connectivity in cats revealed by direct correlation of diffusion tractography and histology. Cerebral Cortex (New York, N.Y. : 1991). 21: 200-11. PMID 20494968 DOI: 10.1093/Cercor/Bhq084  0.563
2010 Mimura M, Hoeft F, Kato M, Kobayashi N, Sheau K, Piggot J, Mills D, Galaburda A, Korenberg JR, Bellugi U, Reiss AL. A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome. Journal of Neurodevelopmental Disorders. 2: 93-98. PMID 21304831 DOI: 10.1007/S11689-009-9041-8  0.721
2010 Golarai G, Hong S, Haas BW, Galaburda AM, Mills DL, Bellugi U, Grill-Spector K, Reiss AL. The fusiform face area is enlarged in Williams syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 6700-12. PMID 20463232 DOI: 10.1523/Jneurosci.4268-09.2010  0.615
2010 Takahashi E, Dai G, Wang R, Ohki K, Rosen GD, Galaburda AM, Grant PE, Wedeen VJ. Development of cerebral fiber pathways in cats revealed by diffusion spectrum imaging. Neuroimage. 49: 1231-40. PMID 19747553 DOI: 10.1016/J.Neuroimage.2009.09.002  0.682
2010 Peschansky VJ, Burbridge TJ, Volz AJ, Fiondella C, Wissner-Gross Z, Galaburda AM, Lo Turco JJ, Rosen GD. The effect of variation in expression of the candidate dyslexia susceptibility gene homolog Kiaa0319 on neuronal migration and dendritic morphology in the rat. Cerebral Cortex (New York, N.Y. : 1991). 20: 884-97. PMID 19679544 DOI: 10.1093/Cercor/Bhp154  0.589
2010 Cohen JD, Mock JR, Nichols T, Zadina J, Corey DM, Lemen L, Bellugi U, Galaburda A, Reiss A, Foundas AL. Morphometry of human insular cortex and insular volume reduction in Williams syndrome. Journal of Psychiatric Research. 44: 81-9. PMID 19660766 DOI: 10.1016/J.Jpsychires.2009.07.001  0.669
2009 Collette JC, Chen XN, Mills DL, Galaburda AM, Reiss AL, Bellugi U, Korenberg JR. William's syndrome: gene expression is related to parental origin and regional coordinate control. Journal of Human Genetics. 54: 193-8. PMID 19282872 DOI: 10.1038/Jhg.2009.5  0.717
2009 Shi Y, Tu Z, Reiss AL, Dutton RA, Lee AD, Galaburda AM, Dinov I, Thompson PM, Toga AW. Joint sulcal detection on cortical surfaces with graphical models and boosted priors. Ieee Transactions On Medical Imaging. 28: 361-73. PMID 19244008 DOI: 10.1109/Tmi.2008.2004402  0.439
2008 Gothelf D, Searcy YM, Reilly J, Lai PT, Lanre-Amos T, Mills D, Korenberg JR, Galaburda A, Bellugi U, Reiss AL. Association between cerebral shape and social use of language in Williams syndrome. American Journal of Medical Genetics. Part A. 146: 2753-61. PMID 18924169 DOI: 10.1002/Ajmg.A.32507  0.747
2008 Higgins NC, Escabí MA, Rosen GD, Galaburda AM, Read HL. Spectral processing deficits in belt auditory cortex following early postnatal lesions of somatosensory cortex. Neuroscience. 153: 535-49. PMID 18384966 DOI: 10.1016/J.Neuroscience.2008.01.073  0.566
2008 Burbridge TJ, Wang Y, Volz AJ, Peschansky VJ, Lisann L, Galaburda AM, Lo Turco JJ, Rosen GD. Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat. Neuroscience. 152: 723-33. PMID 18313856 DOI: 10.1016/J.Neuroscience.2008.01.020  0.609
2008 Järvinen-Pasley A, Bellugi U, Reilly J, Mills DL, Galaburda A, Reiss AL, Korenberg JR. Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior. Development and Psychopathology. 20: 1-35. PMID 18211726 DOI: 10.1017/S0954579408000011  0.728
2007 Escabí MA, Higgins NC, Galaburda AM, Rosen GD, Read HL. Early cortical damage in rat somatosensory cortex alters acoustic feature representation in primary auditory cortex. Neuroscience. 150: 970-83. PMID 18022327 DOI: 10.1016/J.Neuroscience.2007.07.054  0.592
2007 Hoeft F, Barnea-Goraly N, Haas BW, Golarai G, Ng D, Mills D, Korenberg J, Bellugi U, Galaburda A, Reiss AL. More is not always better: increased fractional anisotropy of superior longitudinal fasciculus associated with poor visuospatial abilities in Williams syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 11960-5. PMID 17978036 DOI: 10.1523/Jneurosci.3591-07.2007  0.733
2007 Shi Y, Tu Z, Reiss AL, Dutton RA, Lee AD, Galaburda AM, Dinov I, Thompson PM, Toga AW. Joint sulci detection using graphical models and boosted priors. Information Processing in Medical Imaging : Proceedings of the ... Conference. 20: 98-109. PMID 17633692 DOI: 10.1007/978-3-540-73273-0_9  0.375
2007 Mobbs D, Eckert MA, Menon V, Mills D, Korenberg J, Galaburda AM, Rose FE, Bellugi U, Reiss AL. Reduced parietal and visual cortical activation during global processing in Williams syndrome. Developmental Medicine and Child Neurology. 49: 433-8. PMID 17518929 DOI: 10.1111/J.1469-8749.2007.00433.X  0.736
2007 Chiang MC, Reiss AL, Lee AD, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, Thompson PM. 3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry. Neuroimage. 36: 1096-109. PMID 17512756 DOI: 10.1016/J.Neuroimage.2007.04.024  0.742
2007 Tu Z, Zheng S, Yuille AL, Reiss AL, Dutton RA, Lee AD, Galaburda AM, Dinov I, Thompson PM, Toga AW. Automated extraction of the cortical sulci based on a supervised learning approach. Ieee Transactions On Medical Imaging. 26: 541-52. PMID 17427741 DOI: 10.1109/Tmi.2007.892506  0.495
2007 Rosen GD, Bai J, Wang Y, Fiondella CG, Threlkeld SW, LoTurco JJ, Galaburda AM. Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations. Cerebral Cortex (New York, N.Y. : 1991). 17: 2562-72. PMID 17218481 DOI: 10.1093/Cercor/Bhl162  0.733
2007 Mobbs D, Eckert MA, Mills D, Korenberg J, Bellugi U, Galaburda AM, Reiss AL. Frontostriatal dysfunction during response inhibition in Williams syndrome. Biological Psychiatry. 62: 256-61. PMID 16996488 DOI: 10.1016/J.Biopsych.2006.05.041  0.726
2007 Shi Y, Reiss AL, Lee AD, Dutton RA, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Dinov I, Thompson PM, Toga AW. Hamilton-jacobi skeletons on cortical surfaces with applications in characterizing the gyrification pattern in williams syndrome 2007 4th Ieee International Symposium On Biomedical Imaging: From Nano to Macro - Proceedings. 660-663. DOI: 10.1109/ISBI.2007.356938  0.682
2006 Zheng S, Tu Z, Yuille AL, Reiss AL, Dutton RA, Lee AD, Galaburda AM, Thompson PM, Dinov I, Toga AW. A learning based algorithm for automatic extraction of the cortical sulci. Medical Image Computing and Computer-Assisted Intervention : Miccai ... International Conference On Medical Image Computing and Computer-Assisted Intervention. 9: 695-703. PMID 17354951 DOI: 10.1007/11866565_85  0.369
2006 Galaburda AM, LoTurco J, Ramus F, Fitch RH, Rosen GD. From genes to behavior in developmental dyslexia. Nature Neuroscience. 9: 1213-7. PMID 17001339 DOI: 10.1038/Nn1772  0.801
2006 Wang Y, Paramasivam M, Thomas A, Bai J, Kaminen-Ahola N, Kere J, Voskuil J, Rosen GD, Galaburda AM, Loturco JJ. DYX1C1 functions in neuronal migration in developing neocortex. Neuroscience. 143: 515-22. PMID 16989952 DOI: 10.1016/J.Neuroscience.2006.08.022  0.717
2006 Gaser C, Luders E, Thompson PM, Lee AD, Dutton RA, Geaga JA, Hayashi KM, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, Reiss AL. Increased local gyrification mapped in Williams syndrome. Neuroimage. 33: 46-54. PMID 16901723 DOI: 10.1016/J.Neuroimage.2006.06.018  0.753
2006 Eckert MA, Galaburda AM, Karchemskiy A, Liang A, Thompson P, Dutton RA, Lee AD, Bellugi U, Korenberg JR, Mills D, Rose FE, Reiss AL. Anomalous sylvian fissure morphology in Williams syndrome. Neuroimage. 33: 39-45. PMID 16876437 DOI: 10.1016/J.Neuroimage.2006.05.062  0.739
2006 Eckert MA, Galaburda AM, Mills DL, Bellugi U, Korenberg JR, Reiss AL. The neurobiology of Williams syndrome: cascading influences of visual system impairment? Cellular and Molecular Life Sciences : Cmls. 63: 1867-75. PMID 16810457 DOI: 10.1007/S00018-005-5553-X  0.716
2006 Eckert MA, Tenforde A, Galaburda AM, Bellugi U, Korenberg JR, Mills D, Reiss AL. To modulate or not to modulate: differing results in uniquely shaped Williams syndrome brains. Neuroimage. 32: 1001-7. PMID 16806978 DOI: 10.1016/J.Neuroimage.2006.05.014  0.741
2006 Rosen GD, Mesples B, Hendriks M, Galaburda AM. Histometric changes and cell death in the thalamus after neonatal neocortical injury in the rat. Neuroscience. 141: 875-88. PMID 16725276 DOI: 10.1016/J.Neuroscience.2006.04.035  0.594
2006 Tosun D, Reiss AL, Lee AD, Dutton RA, Hayashi KM, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, Thompson PM. Use of 3-D cortical morphometry for mapping increased cortical gyrification and complexity in Williams syndrome 2006 3rd Ieee International Symposium On Biomedical Imaging: From Nano to Macro - Proceedings. 2006: 1172-1175.  0.69
2005 Thompson PM, Lee AD, Dutton RA, Geaga JA, Hayashi KM, Eckert MA, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, Reiss AL. Abnormal cortical complexity and thickness profiles mapped in Williams syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 4146-58. PMID 15843618 DOI: 10.1523/Jneurosci.0165-05.2005  0.753
2005 Holinger DP, Bellugi U, Mills DL, Korenberg JR, Reiss AL, Sherman GF, Galaburda AM. Relative sparing of primary auditory cortex in Williams Syndrome. Brain Research. 1037: 35-42. PMID 15777750 DOI: 10.1016/J.Brainres.2004.11.038  0.815
2005 Chang BS, Ly J, Appignani B, Bodell A, Apse KA, Ravenscroft RS, Sheen VL, Doherty MJ, Hackney DB, O'Connor M, Galaburda AM, Walsh CA. Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia. Neurology. 64: 799-803. PMID 15753412 DOI: 10.1212/01.Wnl.0000152874.57180.Af  0.337
2005 Eckert MA, Hu D, Eliez S, Bellugi U, Galaburda A, Korenberg J, Mills D, Reiss AL. Evidence for superior parietal impairment in Williams syndrome. Neurology. 64: 152-3. PMID 15642924 DOI: 10.1212/01.Wnl.0000148598.63153.8A  0.727
2004 Reiss AL, Eckert MA, Rose FE, Karchemskiy A, Kesler S, Chang M, Reynolds MF, Kwon H, Galaburda A. An experiment of nature: brain anatomy parallels cognition and behavior in Williams syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 5009-15. PMID 15163693 DOI: 10.1523/Jneurosci.5272-03.2004  0.542
2003 Galaburda AM, Holinger D, Mills D, Reiss A, Korenberg JR, Bellugi U. [Williams syndrome. A summary of cognitive, electrophysiological, anatomofunctional, microanatomical and genetic findings]. Revista De Neurologia. 36: S132-7. PMID 12599114  0.74
2003 Galaburda AM, Holinger D, Mills D, Reiss A, Korenberg JR, Bellugi U. El síndrome de Williams. Un resumen de hallazgos cognitivos, electrofisiológicos, anatomofuncionales, microanatómicos y genéticos Revista De NeurologíA. 36: 132. DOI: 10.33588/Rn.36S1.2003070  0.679
2002 Galaburda AM, Holinger DP, Bellugi U, Sherman GF. Williams syndrome: neuronal size and neuronal-packing density in primary visual cortex. Archives of Neurology. 59: 1461-7. PMID 12223034 DOI: 10.1001/Archneur.59.9.1461  0.775
2002 Schmitt JE, Watts K, Eliez S, Bellugi U, Galaburda AM, Reiss AL. Increased gyrification in Williams syndrome: evidence using 3D MRI methods. Developmental Medicine and Child Neurology. 44: 292-5. PMID 12033713 DOI: 10.1017/S0012162201002109  0.666
2001 Galaburda AM, Schmitt JE, Atlas SW, Eliez S, Bellugi U, Reiss AL. Dorsal forebrain anomaly in Williams syndrome. Archives of Neurology. 58: 1865-9. PMID 11708996 DOI: 10.1001/Archneur.58.11.1865  0.666
2001 Rosen GD, Windzio H, Galaburda AM. Unilateral induced neocortical malformation and the formation of ipsilateral and contralateral barrel fields. Neuroscience. 103: 931-9. PMID 11301202 DOI: 10.1016/S0306-4522(01)00044-6  0.589
2001 Galaburda AM, Rosen GD, Denenberg VH, Fitch RH, LoTurco JJ, Sherman GF. Models of temporal processing and language development Clinical Neuroscience Research. 1: 230-237. DOI: 10.1016/S1566-2772(01)00009-3  0.812
2000 Rosen GD, Galaburda AM. Single cause, polymorphic neuronal migration disorders: an animal model. Developmental Medicine and Child Neurology. 42: 652-62. PMID 11085292 DOI: 10.1017/S0012162200001213  0.601
2000 Jenner AR, Galaburda AM, Sherman GF. Connectivity of ectopic neurons in the molecular layer of the somatosensory cortex in autoimmune mice. Cerebral Cortex (New York, N.Y. : 1991). 10: 1005-13. PMID 11007551 DOI: 10.1093/Cercor/10.10.1005  0.709
2000 Galaburda AM, Bellugi U. V. Multi-level analysis of cortical neuroanatomy in Williams syndrome. Journal of Cognitive Neuroscience. 12: 74-88. PMID 10953235 DOI: 10.1162/089892900561995  0.646
2000 Gogal RM, Ahmed SA, Holladay SD, Walsh JE, Galaburda AM, Rosen GD. Induced minor malformations in the neocortex of normal mice do not alter immunological functions. Immunological Investigations. 29: 299-318. PMID 10933612 DOI: 10.3109/08820130009060869  0.555
2000 Pennington BF, Filipek PA, Lefly D, Chhabildas N, Kennedy DN, Simon JH, Filley CM, Galaburda A, DeFries JC. A twin MRI study of size variations in human brain. Journal of Cognitive Neuroscience. 12: 223-32. PMID 10769318 DOI: 10.1162/089892900561850  0.586
2000 Frenkel M, Sherman GF, Bashan KA, Galaburda AM, LoTurco JJ. Neocortical ectopias are associated with attenuated neurophysiological responses to rapidly changing auditory stimuli. Neuroreport. 11: 575-9. PMID 10718317 DOI: 10.1097/00001756-200002280-00029  0.766
2000 Rosen GD, Burstein D, Galaburda AM. Changes in efferent and afferent connectivity in rats with induced cerebrocortical microgyria. The Journal of Comparative Neurology. 418: 423-40. PMID 10713571 DOI: 10.1002/(Sici)1096-9861(20000320)418:4<423::Aid-Cne5>3.0.Co;2-5  0.605
1999 Pennington BF, Filipek PA, Lefly D, Churchwell J, Kennedy DN, Simon JH, Filley CM, Galaburda A, Alarcon M, DeFries JC. Brain morphometry in reading-disabled twins. Neurology. 53: 723-9. PMID 10489032 DOI: 10.1212/Wnl.53.4.723  0.586
1999 Jenner AR, Rosen GD, Galaburda AM. Neuronal asymmetries in primary visual cortex of dyslexic and nondyslexic brains. Annals of Neurology. 46: 189-96. PMID 10443884 DOI: 10.1002/1531-8249(199908)46:2<189::Aid-Ana8>3.0.Co;2-N  0.636
1999 Bellugi U, Lichtenberger L, Mills D, Galaburda A, Korenberg JR. Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome. Trends in Neurosciences. 22: 197-207. PMID 10322491 DOI: 10.1016/S0166-2236(99)01397-1  0.679
1999 Rosen GD, Herman AE, Galaburda AM. Sex differences in the effects of early neocortical injury on neuronal size distribution of the medial geniculate nucleus in the rat are mediated by perinatal gonadal steroids. Cerebral Cortex (New York, N.Y. : 1991). 9: 27-34. PMID 10022493 DOI: 10.1093/Cercor/9.1.27  0.579
1999 Sherman GF, Galaburda AM. Neuronal migration abnormalities in autoimmune mice: Implications for developmental dyslexia Developmental Neuropsychology. 16: 355-357. DOI: 10.1207/S15326942Dn1603_14  0.676
1998 Boehm GW, Sherman GF, Hoplight BJ, Hyde LA, Bradway DM, Galaburda AM, Ahmed SA, Denenberg VH. Learning in year-old female autoimmune BXSB mice. Physiology & Behavior. 64: 75-82. PMID 9661985 DOI: 10.1016/S0031-9384(98)00027-4  0.773
1997 Herman AE, Galaburda AM, Fitch RH, Carter AR, Rosen GD. Cerebral microgyria, thalamic cell size and auditory temporal processing in male and female rats. Cerebral Cortex (New York, N.Y. : 1991). 7: 453-64. PMID 9261574 DOI: 10.1093/Cercor/7.5.453  0.738
1997 Waters NS, Sherman GF, Galaburda AM, Denenberg VH. Effects of cortical ectopias on spatial delayed-matching-to-sample performance in BXSB mice. Behavioural Brain Research. 84: 23-9. PMID 9079769 DOI: 10.1016/S0166-4328(96)00130-1  0.766
1996 Boehm GW, Sherman GF, Rosen GD, Galaburda AM, Denenberg VH. Neocortical ectopias in BXSB mice: effects upon reference and working memory systems. Cerebral Cortex (New York, N.Y. : 1991). 6: 696-700. PMID 8921204 DOI: 10.1093/Cercor/6.5.696  0.775
1996 Rosen GD, Sherman GF, Galaburda AM. Birthdates of neurons in induced microgyria. Brain Research. 727: 71-8. PMID 8842384 DOI: 10.1016/0006-8993(96)00351-4  0.748
1996 Boehm GW, Sherman GF, Hoplight BJ, Hyde LA, Waters NS, Bradway DM, Galaburda AM, Denenberg VH. Learning and memory in the autoimmune BXSB mouse: effects of neocortical ectopias and environmental enrichment. Brain Research. 726: 11-22. PMID 8836540 DOI: 10.1016/0006-8993(96)00299-5  0.767
1996 Denenberg VH, Sherman G, Schrott LM, Waters NS, Boehm GW, Galaburda AM, Mobraaten LE. Effects of embryo transfer and cortical ectopias upon the behavior of BXSB-Yaa and BXSB-Yaa + mice. Brain Research. Developmental Brain Research. 93: 100-8. PMID 8804696 DOI: 10.1016/0165-3806(96)00010-7  0.774
1996 Galaburda AM, Rosen GD, Sherman GF. PLASTICITY ASSOCIATED WITH MINOR CORTICAL MALFORMATIONS Journal of Clinical Neurophysiology. 13: 444-445. DOI: 10.1097/00004691-199609000-00045  0.724
1995 Rosen GD, Sigel EA, Sherman GF, Galaburda AM. The neuroprotective effects of MK-801 on the induction of microgyria by freezing injury to the newborn rat neocortex. Neuroscience. 69: 107-14. PMID 8637609 DOI: 10.1016/0306-4522(95)00262-H  0.726
1995 Rosen GD, Waters NS, Galaburda AM, Denenberg VH. Behavioral consequences of neonatal injury of the neocortex. Brain Research. 681: 177-89. PMID 7552277 DOI: 10.1016/0006-8993(95)00312-E  0.748
1995 Galaburda AM, Wang PP, Rossen ML, Bellugi U. Cytoarchitectonic and immunohistochemical findings in Williams syndrome Genetic Counseling. 6: 142-144.  0.457
1994 Damasio H, Grabowski T, Frank R, Galaburda AM, Damasio AR. The return of Phineas Gage: clues about the brain from the skull of a famous patient. Science (New York, N.Y.). 264: 1102-5. PMID 8178168 DOI: 10.1126/Science.8178168  0.562
1994 Fitch RH, Tallal P, Brown CP, Galaburda AM, Rosen GD. Induced microgyria and auditory temporal processing in rats: a model for language impairment? Cerebral Cortex (New York, N.Y. : 1991). 4: 260-70. PMID 8075531 DOI: 10.1093/Cercor/4.3.260  0.72
1994 Galaburda AM, Menard MT, Rosen GD. Evidence for aberrant auditory anatomy in developmental dyslexia. Proceedings of the National Academy of Sciences of the United States of America. 91: 8010-3. PMID 8058748 DOI: 10.1073/Pnas.91.17.8010  0.619
1994 Galaburda AM, Wang PP, Bellugi U, Rossen M. Cytoarchitectonic anomalies in a genetically based disorder: Williams syndrome. Neuroreport. 5: 753-7. PMID 8018845 DOI: 10.1097/00001756-199403000-00004  0.615
1994 Rosen GD, Sherman GF, Galaburda AM. Radial glia in the neocortex of adult rats: effects of neonatal brain injury. Brain Research. Developmental Brain Research. 82: 127-35. PMID 7842500 DOI: 10.1016/0165-3806(94)90155-4  0.723
1993 Schachter SC, Galaburda AM, Ransil BJ. Associations of dyslexia with epilepsy, handedness, and gender. Annals of the New York Academy of Sciences. 682: 402-3. PMID 8323148 DOI: 10.1111/J.1749-6632.1993.Tb23006.X  0.33
1993 Rosen GD, Sherman GF, Galaburda AM. Neuronal subtypes and anatomic asymmetry: changes in neuronal number and cell-packing density. Neuroscience. 56: 833-9. PMID 8284037 DOI: 10.1016/0306-4522(93)90131-X  0.731
1993 Schrott LM, Waters NS, Boehm GW, Sherman GF, Morrison L, Rosen GD, Behan PO, Galaburda AM, Denenberg VH. Behavior, cortical ectopias, and autoimmunity in BXSB-Yaa and BXSB-Yaa+ mice. Brain, Behavior, and Immunity. 7: 205-23. PMID 8147964 DOI: 10.1006/Brbi.1993.1022  0.783
1992 Rademacher J, Galaburda AM, Kennedy DN, Filipek PA, Caviness VS. Human cerebral cortex: localization, parcellation, and morphometry with magnetic resonance imaging. Journal of Cognitive Neuroscience. 4: 352-74. PMID 23968129 DOI: 10.1162/Jocn.1992.4.4.352  0.383
1992 Schrott LM, Denenberg VH, Sherman GF, Waters NS, Rosen GD, Galaburda AM. Environmental enrichment, neocortical ectopias, and behavior in the autoimmune NZB mouse. Brain Research. Developmental Brain Research. 67: 85-93. PMID 1638744 DOI: 10.1016/0165-3806(92)90028-U  0.802
1992 Denenberg VH, Sherman GF, Morrison L, Schrott LM, Waters NS, Rosen GD, Behan PO, Galaburda AM. Behavior, ectopias and immunity in BD/DB reciprocal crosses. Brain Research. 571: 323-9. PMID 1611501 DOI: 10.1016/0006-8993(92)90671-U  0.795
1992 Denenberg VH, Sherman GF, Rosen GD, Morrison L, Behan PO, Galaburda AM. A behavior profile of the MRL/Mp lpr/lpr mouse and its association with hydrocephalus. Brain, Behavior, and Immunity. 6: 40-9. PMID 1571603 DOI: 10.1016/0889-1591(92)90058-V  0.796
1992 Rosen GD, Sherman GF, Galaburda AM. Biological substrates of anatomic asymmetry. Progress in Neurobiology. 39: 507-15. PMID 1529102 DOI: 10.1016/0301-0082(92)90004-X  0.755
1992 Sherman GF, Rosen GD, Stone LV, Press DM, Galaburda AM. The organization of radial glial fibers in spontaneous neocortical ectopias of newborn New Zealand black mice. Brain Research. Developmental Brain Research. 67: 279-83. PMID 1511521 DOI: 10.1016/0165-3806(92)90228-O  0.739
1992 Schrott LM, Denenberg VH, Sherman GF, Rosen GD, Galaburda AM. Lashley maze learning deficits in NZB mice. Physiology & Behavior. 52: 1085-9. PMID 1484864 DOI: 10.1016/0031-9384(92)90463-C  0.787
1992 Rosen GD, Press DM, Sherman GF, Galaburda AM. The development of induced cerebrocortical microgyria in the rat. Journal of Neuropathology and Experimental Neurology. 51: 601-11. PMID 1484290  0.732
1992 Rosen GD, Sherman GF, Richman JM, Stone LV, Galaburda AM. Induction of molecular layer ectopias by puncture wounds in newborn rats and mice. Brain Research. Developmental Brain Research. 67: 285-91. PMID 1380903 DOI: 10.1016/0165-3806(92)90229-P  0.73
1991 Humphreys P, Rosen GD, Press DM, Sherman GF, Galaburda AM. Freezing lesions of the developing rat brain: a model for cerebrocortical microgyria. Journal of Neuropathology and Experimental Neurology. 50: 145-60. PMID 2010774 DOI: 10.1097/00005072-199103000-00006  0.746
1991 Livingstone MS, Rosen GD, Drislane FW, Galaburda AM. Physiological and anatomical evidence for a magnocellular defect in developmental dyslexia. Proceedings of the National Academy of Sciences of the United States of America. 88: 7943-7. PMID 1896444 DOI: 10.1073/Pnas.88.18.7943  0.576
1991 Rosen GD, Sherman GF, Galaburda AM. Ontogenesis of neocortical asymmetry: a [3H]thymidine study. Neuroscience. 41: 779-90. PMID 1870712 DOI: 10.1016/0306-4522(91)90368-X  0.756
1991 Denenberg VH, Sherman GF, Schrott LM, Rosen GD, Galaburda AM. Spatial learning, discrimination learning, paw preference and neocortical ectopias in two autoimmune strains of mice. Brain Research. 562: 98-104. PMID 1799876 DOI: 10.1016/0006-8993(91)91192-4  0.794
1991 Denenberg VH, Mobraaten LE, Sherman GF, Morrison L, Schrott LM, Waters NS, Rosen GD, Behan PO, Galaburda AM. Effects of the autoimmune uterine/maternal environment upon cortical ectopias, behavior and autoimmunity. Brain Research. 563: 114-22. PMID 1786524 DOI: 10.1016/0006-8993(91)91522-3  0.794
1990 Rosen GD, Sherman GF, Emsbo K, Mehler C, Galaburda AM. The midsagittal area of the corpus callosum and total neocortical volume differ in three inbred strains of mice. Experimental Neurology. 107: 271-6. PMID 2307205 DOI: 10.1016/0014-4886(90)90145-I  0.723
1990 Humphreys P, Kaufmann WE, Galaburda AM. Developmental dyslexia in women: neuropathological findings in three patients. Annals of Neurology. 28: 727-38. PMID 2285260 DOI: 10.1002/Ana.410280602  0.54
1990 Sherman GF, Morrison L, Rosen GD, Behan PO, Galaburda AM. Brain abnormalities in immune defective mice. Brain Research. 532: 25-33. PMID 2282519 DOI: 10.1016/0006-8993(90)91737-2  0.754
1990 Sherman GF, Stone JS, Rosen GD, Galaburda AM. Neocortical VIP neurons are increased in the hemisphere containing focal cerebrocortical microdysgenesis in New Zealand Black mice. Brain Research. 532: 232-6. PMID 2282516 DOI: 10.1016/0006-8993(90)91764-8  0.768
1990 Galaburda AM, Rosen GD, Sherman GF. Individual variability in cortical organization: its relationship to brain laterality and implications to function. Neuropsychologia. 28: 529-46. PMID 2203994 DOI: 10.1016/0028-3932(90)90032-J  0.77
1990 Sherman GF, Stone JS, Press DM, Rosen GD, Galaburda AM. Abnormal architecture and connections disclosed by neurofilament staining in the cerebral cortex of autoimmune mice. Brain Research. 529: 202-7. PMID 2126480 DOI: 10.1016/0006-8993(90)90828-Y  0.766
1990 Habib M, Touze F, Galaburda AM. Chapter 4 Intrauterine Factors in Sinistrality: A Review Advances in Psychology. 67: 99-128. DOI: 10.1016/S0166-4115(08)61245-5  0.306
1989 Kaufmann WE, Galaburda AM. Cerebrocortical microdysgenesis in neurologically normal subjects: a histopathologic study. Neurology. 39: 238-44. PMID 2915796 DOI: 10.1212/Wnl.39.2.238  0.588
1989 Rosen GD, Galaburda AM, Sherman GF. Cerebrocortical microdysgenesis with anomalous callosal connections: a case study in the rat. The International Journal of Neuroscience. 47: 237-47. PMID 2807762 DOI: 10.3109/00207458908987438  0.755
1989 Rosen GD, Sherman GF, Mehler C, Emsbo K, Galaburda AM. The effect of developmental neuropathology on neocortical asymmetry in New Zealand black mice. The International Journal of Neuroscience. 45: 247-54. PMID 2744965 DOI: 10.3109/00207458908986237  0.763
1989 Rosen GD, Sherman GF, Galaburda AM. Interhemispheric connections differ between symmetrical and asymmetrical brain regions. Neuroscience. 33: 525-33. PMID 2636706 DOI: 10.1016/0306-4522(89)90404-1  0.743
1988 Sherman GF, Rosen GD, Galaburda AM. Neocortical anomalies in autoimmune mice: A model for the developmental neuropathology seen in the dyslexic brain Drug Development Research. 15: 307-314. DOI: 10.1002/Ddr.430150219  0.778
1987 Sherman GF, Galaburda AM, Behan PO, Rosen GD. Neuroanatomical anomalies in autoimmune mice. Acta Neuropathologica. 74: 239-42. PMID 3673516 DOI: 10.1007/Bf00688187  0.742
1987 Galaburda AM, Corsiglia J, Rosen GD, Sherman GF. Planum temporale asymmetry, reappraisal since Geschwind and Levitsky Neuropsychologia. 25: 853-868. DOI: 10.1016/0028-3932(87)90091-1  0.74
1986 Schachter SC, Galaburda AM. Development and biological associations of cerebral dominance: review and possible mechanisms. Journal of the American Academy of Child Psychiatry. 25: 741-50. PMID 3794116 DOI: 10.1016/S0002-7138(09)60191-6  0.309
1986 Galaburda AM, Aboitiz F, Rosen GD, Sherman GF. Histological asymmetry in the primary visual cortex of the rat: implications for mechanisms of cerebral asymmetry. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 22: 151-60. PMID 3709191 DOI: 10.1016/S0010-9452(86)80039-9  0.801
1986 Habib M, Galaburda AM. [Biological determinants of cerebral dominance]. Revue Neurologique. 142: 869-94. PMID 3551007  0.331
1986 Galaburda AM, Aboitiz F. [Biological foundations of dyslexia. A review]. Archivos De Biología Y Medicina Experimentales. 19: 57-65. PMID 3329488  0.594
1985 Galaburda AM, Sherman GF, Rosen GD, Aboitiz F, Geschwind N. Developmental dyslexia: four consecutive patients with cortical anomalies. Annals of Neurology. 18: 222-33. PMID 4037763 DOI: 10.1002/Ana.410180210  0.818
1985 Geschwind N, Galaburda AM. Cerebral lateralization. Biological mechanisms, associations, and pathology: I. A hypothesis and a program for research. Archives of Neurology. 42: 428-59. PMID 3994562 DOI: 10.1001/Archneur.1985.04060050026008  0.622
1985 Geschwind N, Galaburda AM. Cerebral lateralization. Biological mechanisms, associations, and pathology: II. A hypothesis and a program for research. Archives of Neurology. 42: 521-52. PMID 3890812 DOI: 10.1001/archneur.1985.04060060019009  0.485
1985 Damasio AR, Galaburda Am. Norman Geschwind. Archives of Neurology. 42: 500-4. PMID 3888155  0.364
1985 Geschwind N, Galaburda AM. Cerebral lateralization. Biological mechanisms, associations, and pathology: III. A hypothesis and a program for research. Archives of Neurology. 42: 634-54. PMID 3874617 DOI: 10.1001/archneur.1985.04060070024012  0.49
1985 Freeman RL, Galaburda AM, Cabal RD, Geschwind N. The neurology of depression. Cognitive and behavioral deficits with focal findings in depression and resolution after electroconvulsive therapy. Archives of Neurology. 42: 289-91. PMID 3872114 DOI: 10.1001/Archneur.1985.04060030111018  0.533
1985 Sherman GF, Galaburda AM, Geschwind N. Cortical anomalies in brains of New Zealand mice: a neuropathologic model of dyslexia? Proceedings of the National Academy of Sciences of the United States of America. 82: 8072-4. PMID 3865217 DOI: 10.1073/Pnas.82.23.8072  0.757
1984 Sherman GF, Galaburda AM. Neocortical asymmetry and open-field behavior in the rat. Experimental Neurology. 86: 473-82. PMID 6499988 DOI: 10.1016/0014-4886(84)90082-7  0.668
1984 Ross MH, Galaburda AM, Kemper TL. Down's syndrome: is there a decreased population of neurons? Neurology. 34: 909-16. PMID 6234479 DOI: 10.1212/Wnl.34.7.909  0.645
1983 Galaburda AM, Pandya DN. The intrinsic architectonic and connectional organization of the superior temporal region of the rhesus monkey. The Journal of Comparative Neurology. 221: 169-84. PMID 6655080 DOI: 10.1002/cne.902210206  0.425
1983 Schiff HB, Alexander MP, Naeser MA, Galaburda AM. Aphemia. Clinical-anatomic correlations. Archives of Neurology. 40: 720-7. PMID 6625983 DOI: 10.1001/Archneur.1983.04050110038005  0.303
1982 Sherman GF, Galaburda AM, Geschwind N. Neuroanatomical asymmetries in non-human species Trends in Neurosciences. 5: 429-431. DOI: 10.1016/0166-2236(82)90233-8  0.723
1981 Galaburda AM, Geschwind N. Anatomical asymmetries in the adult and developing brain and their implications for function. Advances in Pediatrics. 28: 271-92. PMID 7041560  0.53
1980 Galaburda AM, Geschwind N. The human language areas and cerebral asymmetries. Revue MéDicale De La Suisse Romande. 100: 119-28. PMID 6990448  0.517
1980 Galaburda A, Sanides F. Cytoarchitectonic organization of the human auditory cortex. The Journal of Comparative Neurology. 190: 597-610. PMID 6771305 DOI: 10.1002/Cne.901900312  0.75
1979 Galaburda AM, Kemper TL. Cytoarchitectonic abnormalities in developmental dyslexia: a case study. Annals of Neurology. 6: 94-100. PMID 496415 DOI: 10.1002/Ana.410060203  0.668
1978 Galaburda AM, Kemper TL. Auditory cytoarchitectonic abnormalities in a case of familial developmental dyslexia. Transactions of the American Neurological Association. 103: 262-5. PMID 757073  0.538
1978 Galaburda AM, Sanides F, Geschwind N. Human brain. Cytoarchitectonic left-right asymmetries in the temporal speech region. Archives of Neurology. 35: 812-7. PMID 718483 DOI: 10.1001/Archneur.1978.00500360036007  0.789
1978 Galaburda AM, LeMay M, Kemper TL, Geschwind N. Right-left asymmetrics in the brain. Science (New York, N.Y.). 199: 852-6. PMID 341314 DOI: 10.1126/Science.341314  0.737
1976 Galaburda AM, Waxman SG, Kemper TL, Jones HR. Progressive multifocal neurologic deficit with disseminated subpial demyelination. Journal of Neuropathology and Experimental Neurology. 35: 481-94. PMID 182927 DOI: 10.1097/00005072-197609000-00001  0.611
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