Agenesis of the corpus callosum: Genetic, developmental and functional aspects of connectivity

Diagnostic and Statistical Manual of Mental Disorders

Williams, J. B. W., & First, M. B. (2013) · Oxford University Press eBooks · doi:10.1093/acrefore/9780199975839.013.104 · Cited by 109,841 · see citing works

The Endophenotype Concept in Psychiatry: Etymology and Strategic Intentions

Gottesman, I. I., & Gould, T. D. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.4.636 · Cited by 5,615 · see citing works

Handbook of clinical neurology

(1986) · Journal of Neuroimmunology · doi:10.1016/0165-5728(86)90030-5 · Cited by 1,848 · see citing works

Looking into the functional architecture of the brain with diffusion MRI.

Le Bihan, D. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1119 · Cited by 1,571 · see citing works

Topography of the human corpus callosum revisited—Comprehensive fiber tractography using diffusion tensor magnetic resonance imaging

Hofer, S., & Frahm, J. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.05.044 · Cited by 1,197 · see citing works

Fiber Pathways of the Brain

Schmahmann, J. D., & Pandya, D. N. (2006) · doi:10.1093/acprof:oso/9780195104233.001.0001 · Cited by 1,157 · see citing works

Neuronal Subtype-Specific Genes that Control Corticospinal Motor Neuron Development In Vivo

Arlotta, P., Molyneaux, B. J., Chen, J., Inoue, J., Kominami, R., & Macklis, J. D. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.036 · Cited by 1,157 · see citing works

Time to give up on a single explanation for autism

Happé, F., Ronald, A., & Plomin, R. (2006) · Nature Neuroscience · doi:10.1038/nn1770 · Cited by 987 · see citing works

The musician's brain as a model of neuroplasticity

Münte, T. F., ALTENMÜLLER, E. O., & Jäncke, L. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn843 · Cited by 950 · see citing works

Increased corpus callosum size in musicians

Gottfried Schlaug, A., Jäncke, L., Huang, Y., Staiger, J. F., & Steinmetz, H. (1995) · Neuropsychologia · doi:10.1016/0028-3932(95)00045-5 · Cited by 818 · see citing works

Phenotype of mice lacking functional Deleted in colorectal cancer (Dec) gene

Fazeli, A., Dickinson, S., Hermiston, M. L., Tighe, R., Steen, R. G., Small, C. G., Stoeckli, E. T., Keino‐Masu, K., Masu, M., Rayburn, H., et al. (1997) · Nature · doi:10.1038/386796a0 · Cited by 778 · see citing works

Handbook of clinical neuropsychology

Filskov, S. B., & Boll, T. J. (1981) · Wiley eBooks · Cited by 777 · see citing works

Clinical Neuropsychology

Bond, T. C. (1980) · American Journal of Psychiatry · doi:10.1176/ajp.137.5.645-a · Cited by 767 · see citing works

Endocannabinoid-mediated rescue of striatal LTD and motor deficits in Parkinson's disease models

Kreitzer, A. C., & Malenka, R. C. (2007) · Nature · doi:10.1038/nature05506 · Cited by 735 · see citing works

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

Kitamura, K., Yanazawa, M., Sugiyama, N., Miura, H., Iizuka‐Kogo, A., Kusaka, M., Omichi, K., Suzuki, R., Fukui, Y., Kamiirisa, K., et al. (2002) · Nature Genetics · doi:10.1038/ng1009 · Cited by 708 · see citing works

Diffusion tensor imaging of cerebral white matter: a pictorial review of physics, fiber tract anatomy, and tumor imaging patterns.

Jellison, B. J., Field, A. S., Medow, J. E., Lazar, M., Salamat, M. S., & Alexander, A. L. (2004) · PubMed Central · Cited by 681 · see citing works

Structural Brain Imaging of Attention-Deficit/Hyperactivity Disorder

Seidman, L. J., Valera, E. M., & Makris, N. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.11.019 · Cited by 676 · see citing works

The Role of the Corpus Callosum in Interhemispheric Transfer of Information: Excitation or Inhibition?

Bloom, J. S., & Hynd, G. W. (2005) · Neuropsychology Review · doi:10.1007/s11065-005-6252-y · Cited by 591 · see citing works

Exuberance in the development of cortical networks

Innocenti, G. M., & Price, D. J. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1790 · Cited by 512 · see citing works

Forty-five years of split-brain research and still going strong

Gazzaniga, M. S. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1723 · Cited by 442 · see citing works

Lateralization of auditory language functions: A dynamic dual pathway model

Friederici, A. D., & Alter, K. (2003) · Brain and Language · doi:10.1016/s0093-934x(03)00351-1 · Cited by 412 · see citing works

Prefrontal white matter volume is disproportionately larger in humans than in other primates

Schoenemann, P. T., Sheehan, M. J., & Glotzer, L. D. (2005) · Nature Neuroscience · doi:10.1038/nn1394 · Cited by 405 · see citing works

Size, distribution, and number of fibres in the human Corpus Callosum

Tomasch, J. (1954) · The Anatomical Record · doi:10.1002/ar.1091190109 · Cited by 332 · see citing works

The Transcription Factor Gene Nfib Is Essential for both Lung Maturation and Brain Development

Steele-Perkins, G., Plachez, C., Butz, K. G., Yang, G., Bachurski, C. J., Kinsman, S. L., Litwack, E. D., Richards, L. J., & Gronostajski, R. M. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.2.685-698.2005 · Cited by 310 · see citing works

A Review of the Neuroanatomical Findings in Children with Fetal Alcohol Syndrome or Prenatal Exposure to Alcohol

Roebuck, T. M., Mattson, S. N., & Riley, E. P. (1998) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.1998.tb03658.x · Cited by 294 · see citing works

Abnormalities in Neuronal Process Extension, Hippocampal Development, and the Ventricular System of L1 Knockout Mice

Demyanenko, G. P., Tsai, A. Y., & Maness, P. F. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-12-04907.1999 · Cited by 286 · see citing works

Robo1 regulates the development of major axon tracts and interneuron migration in the forebrain

Andrews, W. D., Liapi, A., Plachez, C., Camurri, L., Zhang, J., Mori, S., Murakami, F., Parnavelas, J. G., Sundaresan, V., & Richards, L. J. (2006) · Development · doi:10.1242/dev.02379 · Cited by 271 · see citing works

Cortical Axon Guidance by the Glial Wedge during the Development of the Corpus Callosum

Shu, T., & Richards, L. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-08-02749.2001 · Cited by 265 · see citing works

Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15

Cassidy, S. B., Forsythe, M. E., Heeger, S., Nicholls, R. D., Schork, N. J., BENN, P. A., & Schwartz, S. (1997) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19970211)68:4 · Cited by 258 · see citing works

Loss of K‐Cl co‐transporter KCC3 causes deafness, neurodegeneration and reduced seizure threshold

Boettger, T., Rust, M. B., Maier, H., et al. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg519 · Cited by 248 · see citing works

Mechanisms regulating the development of the corpus callosum and its agenesis in mouse and human

Richards, L. J., Plachez, C., & Ren, T. (2004) · Clinical Genetics · doi:10.1111/j.1399-0004.2004.00354.x · Cited by 248 · see citing works

Mapping corpus callosum deficits in autism: An index of aberrant cortical connectivity

Vidal, C. N., Nicolson, R., DeVito, T. J., Hayashi, K. M., Geaga, J. A., Drost, D. J., Williamson, P. C., Rajakumar, N., Sui, Y., Dutton, R. A., et al. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.11.011 · Cited by 244 · see citing works

Corpus callosum size in autism

Hardan, A. Y., Minshew, N. J., & Keshavan, M. S. (2000) · Neurology · doi:10.1212/wnl.55.7.1033 · Cited by 243 · see citing works

Mowat-Wilson syndrome

Mowat, D. R., Wilson, M. J., & Goossens, M. (2003) · Journal of Medical Genetics · doi:10.1136/jmg.40.5.305 · Cited by 238 · see citing works

Hemispheric specialization for language.

Josse, G., & Tzourio-mazoyer, N. (2004) · Brain research. Brain research reviews · doi:10.1016/j.brainresrev.2003.10.001 · Cited by 220 · see citing works

Abnormal Development of Forebrain Midline Glia and Commissural Projections inNfiaKnock-Out Mice

Shu, T., Butz, K. G., Plachez, C., Gronostajski, R. M., & Richards, L. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00203.2003 · Cited by 213 · see citing works

Schizophrenia, neurodevelopment and corpus callosum

Innocenti, G. M., Ansermet, F., & Parnas, J. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001205 · Cited by 207 · see citing works

Postnatally Induced Formation of the Corpus Callosum in Acallosal Mice on Glia-Coated Cellulose Bridges

Silver, J., & Ogawa, M. Y. (1983) · Science · doi:10.1126/science.6844928 · Cited by 202 · see citing works

Anomalies of the Corpus Callosum: An MR Analysis of the Phenotypic Spectrum of Associated Malformations

Hetts, S. W., Sherr, E. H., Chao, S. D., Gobuty, S., & Barkovich, A. J. (2006) · American Journal of Roentgenology · doi:10.2214/ajr.05.0146 · Cited by 197 · see citing works

Some long-term motor effects of cerebral commissurotomy in man

Zaidel, D. W., & Sperry, R. W. (1977) · Neuropsychologia · doi:10.1016/0028-3932(77)90028-8 · Cited by 195 · see citing works

A house divided? Cognitive functioning with callosal agenesis

Chiarello, C. (1980) · Brain and Language · doi:10.1016/0093-934x(80)90116-9 · Cited by 193 · see citing works

The cognitive neuroscience of autism

Baron‐Cohen, S. (2004) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2003.018713 · Cited by 188 · see citing works

Frequency of Agenesis of the Corpus Callosum in the Developmentally Disabled Population as Determined by Computerized Tomography

Jeret, J. S., Serur, D. S., Wisniewski, K. E., et al. (2008) · Pediatric Neurosurgery · doi:10.1159/000120229 · Cited by 187 · see citing works

MEMORY IMPAIRMENT AFTER COMMISSUROTOMY IN MAN

Zaidel, D. W., & Sperry, R. W. (1974) · Brain · doi:10.1093/brain/97.1.263 · Cited by 183 · see citing works

X‐linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): Clinical, magnetic resonance imaging, and neuropathological findings

Bonneau, D., Toutain, A., Laquerrière, A., Marret, S., Saugier-Véber, P., Barthez, M., Radi, S., Biran, V., Rodriguez, D., & Gélot, A. (2002) · Annals of Neurology · doi:10.1002/ana.10119 · Cited by 176 · see citing works

Agenesis of the Corpus Callosum: Clinical and Genetic Study in 63 Young Patients

Bedeschi, M. F., Bonaglia, M. C., Grasso, R., Pellegri, A., Garghentino, R., Battaglia, M., Panarisi, A. M., Rocco, M. D., Balottin, U., Bresolin, N., et al. (2006) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2005.08.008 · Cited by 175 · see citing works

Communicative deficits in agenesis of the corpus callosum: Nonliteral language and affective prosody

Paul, L. K., Van Lancker-Sidtis, D., Schieffer, B., Dietrich, R., & Brown, W. S. (2003) · Brain and Language · doi:10.1016/s0093-934x(03)00062-2 · Cited by 171 · see citing works

Alexithymia in Twelve Commissurotomized Patients

Hoppe, K. D., & Bogen, J. E. (2010) · Psychotherapy and Psychosomatics · doi:10.1159/000287057 · Cited by 163 · see citing works

Midline radial glia translocation and corpus callosum formation require FGF signaling

Smith, K., Ohkubo, Y., Maragnoli, M., Rasin, M.-R., Schwartz, M. L., Šestan, N., & Vaccarino, F. (2006) · Nature Neuroscience · doi:10.1038/nn1705 · Cited by 161 · see citing works

Agenesis of the corpus callosum: A study of the frequency of associated malformations

Parrish, M. L., Roessmann, U., & Levinsohn, M. W. (1979) · Annals of Neurology · doi:10.1002/ana.410060408 · Cited by 161 · see citing works

A role for cingulate pioneering axons in the development of the corpus callosum

Rash, B. G., & Richards, L. J. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1170 · Cited by 160 · see citing works

Agenesis of corpus callosum: prenatal diagnosis and prognosis

Moutard, M., Kieffer, V., Feingold, J., Kieffer, F., Lewin, F., Adamsbaum, C., Gélot, A., Plana, J. C., Bogaert, P. V., André, M., et al. (2003) · Child s Nervous System · doi:10.1007/s00381-003-0781-6 · Cited by 159 · see citing works

Growth-Associated Protein-43 Is Required for Commissural Axon Guidance in the Developing Vertebrate Nervous System

Shen, Y., Mani, S., Donovan, S. L., Schwob, J. E., & Meiri, K. F. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00239.2002 · Cited by 155 · see citing works

Glia and Fetal Alcohol Syndrome

Guerri, C. (2001) · NeuroToxicology · doi:10.1016/s0161-813x(01)00037-7 · Cited by 152 · see citing works

Emotional Processing Deficits in Individuals With Unilateral Brain Damage

Borod, J. C., Bloom, R. L., Brickman, A. M., Nakhutina, L., & Curko, E. A. (2002) · Applied Neuropsychology · doi:10.1207/s15324826an0901_4 · Cited by 151 · see citing works

The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes

Sherr, E. H. (2003) · Current Opinion in Pediatrics · doi:10.1097/00008480-200312000-00004 · Cited by 151 · see citing works

Social and behavioral problems of children with agenesis of the corpus callosum

Badaruddin, D. H., Andrews, G. L., Bölte, S., Schilmoeller, K. J., Schilmoeller, G., Paul, L. K., & Brown, W. S. (2007) · Child Psychiatry and Human Development · doi:10.1007/s10578-007-0065-6 · Cited by 150 · see citing works

Commissure formation in the mammalian forebrain

Lindwall, C., Fothergill, T., & Richards, L. J. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.01.008 · Cited by 147 · see citing works

Imaging, anatomical, and molecular analysis of callosal formation in the developing human fetal brain

Ren, T., Anderson, A., Shen, W., Huang, H., Plachez, C., Zhang, J., Mori, S., Kinsman, S. L., & Richards, L. J. (2006) · The Anatomical Record Part A Discoveries in Molecular Cellular and Evolutionary Biology · doi:10.1002/ar.a.20282 · Cited by 144 · see citing works

Neuroplasticity in Human Callosal Dysgenesis: A Diffusion Tensor Imaging Study

Tovar-Moll, F. F., Moll, J., de Oliveira‐Souza, R., Bramati, I. E., Andreiuolo, P. Â., & Lent, R. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhj178 · Cited by 141 · see citing works

Clinical and Mutational Spectrum of Mowat–Wilson Syndrome

Zweier, C., Thiel, C. T., Dufke, A., et al. (2005) · European Journal of Medical Genetics · doi:10.1016/j.ejmg.2005.01.003 · Cited by 134 · see citing works

Bilateral field advantage and evoked potential interhemispheric transmission in commissurotomy and callosal agenesis

Brown, W. S., Jeeves, M. A., Dietrich, R. B., & Burnison, D. S. (1999) · Neuropsychologia · doi:10.1016/s0028-3932(99)00011-1 · Cited by 126 · see citing works

Autism

Barbaresi, W. J., Katusic, S. K., & Voigt, R. G. (2006) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.160.11.1167 · Cited by 125 · see citing works

Slit2 Guides Both Precrossing and Postcrossing Callosal Axons at the MidlineIn Vivo

Shu, T., Sundaresan, V., McCarthy, M. M., & Richards, L. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-22-08176.2003 · Cited by 123 · see citing works

Absence of disconnexion syndrome in callosal agenesis and early callosotomy: Brain reorganization or lack of structural specificity during ontogeny?

Lassonde, M. C., Sauerwein, H. C., Chicoine, A., & Geoffroy, G. (1991) · Neuropsychologia · doi:10.1016/0028-3932(91)90006-t · Cited by 120 · see citing works

Cognitive and psychosocial deficits in agenesis of the corpus callosum with normal intelligence

Brown, W. S., & Paul, L. K. (2000) · Cognitive Neuropsychiatry · doi:10.1080/135468000395781 · Cited by 117 · see citing works

Severe psychiatric disturbance and abnormalities of the corpus callosum: Review and case series

David, A. S., Wacharasindhu, A., & Lishman, W. A. (1993) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.56.1.85 · Cited by 115 · see citing works

Maturation of visual callosal connections in visually deprived kittens: a challenging critical period

Innocenti, G. M., Frost, D., & Illes, J. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-02-00255.1985 · Cited by 114 · see citing works

Reduced white matter connectivity in the corpus callosum of children with Tourette syndrome

Plessen, K. J., Grüner, R., Lundervold, A., Hirsch, J. G., Xu, D., Bansal, R., Hammar, Å., Lundervold, A. J., Wentzel‐Larsen, T., Lie, S. A., et al. (2006) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2006.01639.x · Cited by 112 · see citing works

Outcome in Prenatally Diagnosed Fetal Agenesis of the Corpus callosum

Goodyear, P. W. A., Bannister, C. M., Russell, S. S., & Rimmer, S. (2001) · Fetal Diagnosis and Therapy · doi:10.1159/000053898 · Cited by 112 · see citing works

Differential effects of ethanol antagonism and neuroprotection in peptide fragment NAPVSIPQ prevention of ethanol-induced developmental toxicity

Wilkemeyer, M. F., Chen, S.-Y., Menkari, C. E., Brenneman, D. E., Sulik, K. K., & Charness, M. E. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1331636100 · Cited by 112 · see citing works

Mechanisms of interhemispheric transfer and patterns of cognitive function in acallosal patients of normal intelligence

Fischer, M., Ryan, S. B., & Dobyns, W. B. (1992) · Archives of Neurology · doi:10.1001/archneur.1992.00530270085023 · Cited by 110 · see citing works

Alcohol Exposure Alters the Expression Pattern of Neural Cell Adhesion Molecules During Brain Development

Miñana, R., Climent, E., Barettino, D., Seguí-Simarro, J. M., Renau‐Piqueras, J., & Guerri, C. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0750954.x · Cited by 106 · see citing works

Absence makes the search grow longer.

Dobyns, W. B. (1996) · PubMed Central · Cited by 106 · see citing works

Ethanol exposure during embryogenesis decreases the radial glial progenitorpool and affects the generation of neurons and astrocytes

Rubert, G., Miñana, R., Pascual, M., & Guerri, C. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.20963 · Cited by 102 · see citing works

Interhemispheric collaboration in response to simultaneous bilateral input

Liederman, J., Merola, J. L., & Martinez, S. (1985) · Neuropsychologia · doi:10.1016/0028-3932(85)90068-5 · Cited by 100 · see citing works

Comprehension of humor in primary agenesis of the corpus callosum

Brown, W. S., Paul, L. K., Symington, M., & Dietrich, R. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2004.09.008 · Cited by 98 · cited 1× · see citing works

Role of thyroid hormones in the maturation of interhemispheric connections in rats

Berbel, P. J., Guadaño‐Ferraz, A., Jeréz, A. A., & Cerezo, J. R. (1994) · Behavioural Brain Research · doi:10.1016/0166-4328(94)90114-7 · Cited by 96 · see citing works

Bilateral visual field processing and evoked potential interhemispheric transmission time

Brown, W. S., & Jeeves, M. A. (1993) · Neuropsychologia · doi:10.1016/0028-3932(93)90097-j · Cited by 96 · see citing works

Hereditary motor and sensory neuropathy with agenesis of the corpus callosum

Dupré, N., Howard, H. C., Mathieu, J., et al. (2003) · Annals of Neurology · doi:10.1002/ana.77777 · Cited by 96 · see citing works

Development of midline glial populations at the corticoseptal boundary

Shu, T., Puché, A. C., & Richards, L. J. (2003) · Journal of Neurobiology · doi:10.1002/neu.10252 · Cited by 95 · see citing works

It's Early: Event-related Potential Evidence for Initial Interaction of Syntax and Prosody in Speech Comprehension

Eckstein, K., & Friederici, A. D. (2006) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2006.18.10.1696 · Cited by 95 · see citing works

The glial sling is a migratory population of developing neurons

Shu, T., Li, Y., Keller, A., & Richards, L. J. (2003) · Development · doi:10.1242/dev.00514 · Cited by 91 · see citing works

Brain development in mice lacking L1–L1 homophilic adhesion

Itoh, K., Cheng, L., Kamei, Y., et al. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200312107 · Cited by 90 · see citing works

Schizophrenia genetics: uncovering positional candidate genes

Karayiorgou, M., & Gogos, J. A. (2006) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201587 · Cited by 90 · see citing works

Development of midline cell types and commissural axon tracts requires Fgfr1 in the cerebrum

Tole, S., Gutin, G., Bhatnagar, L., Remedios, R., & Hébert, J. M. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.10.020 · Cited by 87 · see citing works

Late interaction of syntactic and prosodic processes in sentence comprehension as revealed by ERPs

Eckstein, K., & Friederici, A. D. (2005) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2005.05.003 · Cited by 87 · see citing works

Major brain lesions detected on sonographic screening of apparently normal term neonates

Yeh, T., Wang, L.-Y., & Huang, C. (2004) · Neuroradiology · doi:10.1007/s00234-003-1160-4 · Cited by 86 · see citing works

Deletion Polymorphism of Disc1 Is Common to All 129 Mouse Substrains: Implications for Gene-Targeting Studies of Brain Function

Clapcote, S. J., & Roder, J. (2006) · Genetics · doi:10.1534/genetics.106.060749 · Cited by 84 · see citing works

Architecture and Callosal Connections of Visual Areas 17, 18, 19 and 21 in the Ferret (Mustela putorius)

Innocenti, G. M. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.4.411 · Cited by 84 · see citing works

Social processing deficits in agenesis of the corpus callosum: narratives from the Thematic Apperception Test

Paul, L. K. (2003) · Archives of Clinical Neuropsychology · doi:10.1016/s0887-6177(03)00024-6 · Cited by 84 · see citing works

Clinical and Diagnostic Profile of Agenesis of the Corpus Callosum

Shevell, M. I. (2002) · Journal of Child Neurology · doi:10.1177/08830738020170122601 · Cited by 84 · see citing works

A Proposed Neurophysiological Basis of Alexithymia

Buchanan, D. C., Waterhouse, G. J., & West, S. C. (2010) · Psychotherapy and Psychosomatics · doi:10.1159/000287465 · Cited by 83 · see citing works

Some Limits to Interhemispheric Integration in Cases of Callosal Agenesis and Partial Commissurotomy

Jeeves, M. A. (1979) · doi:10.1007/978-1-349-03645-5_37 · Cited by 83 · see citing works

A Life-Span Perspective on Interaction Between the Cerebral Hemispheres

Banich, M. T., & Brown, W. S. (2000) · Developmental Neuropsychology · doi:10.1207/s15326942dn1801_1 · Cited by 81 · see citing works

Intra- and interhemispheric processing of visual information in callosal agenesis

Sauerwein, H. C., & Lassonde, M. C. (1983) · Neuropsychologia · doi:10.1016/0028-3932(83)90084-2 · Cited by 81 · see citing works

Callosal Agenesis: A Natural Split Brain?

Lassonde, M. C., & Jeeves, M. A. (2011) · Medical Entomology and Zoology · Cited by 78 · see citing works

Role of the corpus callosum in the development of a bimanual motor skill

Jeeves, M. A., Silver, P. H., & Milne, A. B. (1988) · Developmental Neuropsychology · doi:10.1080/87565648809540415 · Cited by 77 · see citing works

Hypoplasia of the Corpus Callosum: A Study of 445 Consecutive MRI Scans

Bodensteiner, J. B., Schaefer, G. B., Breeding, L. M., et al. (1994) · Journal of Child Neurology · doi:10.1177/088307389400900111 · Cited by 77 · see citing works

The large temporal horn: MR analysis in developmental brain anomalies versus hydrocephalus.

Baker, L. L., & Barkovich, A. J. (1992) · PubMed Central · Cited by 73 · see citing works

Idiom comprehension deficits in relation to corpus callosum agenesis and hypoplasia in children with spina bifida meningomyelocele

Huber-Okrainec, J., Blaser, S. E., & Dennis, M. (2005) · Brain and Language · doi:10.1016/j.bandl.2004.11.002 · Cited by 70 · see citing works

Neuroanatomical substrata of amusement and sadness: A PET activation study using film stimuli

Aalto, S., Näätänen, P., Wallius, E., Metsähonkala, L., Stenman, H., Niemi, P. M., & Karlsson, H. (2002) · Neuroreport · doi:10.1097/00001756-200201210-00018 · Cited by 68 · see citing works

Health‐related issues in individuals with agenesis of the corpus callosum

Doherty, D. R., Tu, S., Schilmoeller, K. J., & Schilmoeller, G. L. (2006) · Child Care Health and Development · doi:10.1111/j.1365-2214.2006.00602.x · Cited by 64 · see citing works

Reading in callosal agenesis*1

Temple, C. M. (1990) · Brain and Language · doi:10.1016/0093-934x(90)90013-7 · Cited by 64 · see citing works

Paralinguistic processing in children with callosal agenesis: Emergence of neurolinguistic deficits

Brown, W. S., Symingtion, M., VanLancker-Sidtis, D., Dietrich, R., & Paul, L. K. (2005) · Brain and Language · doi:10.1016/j.bandl.2004.09.003 · Cited by 61 · see citing works

Emotional arousal in agenesis of the corpus callosum

Paul, L. K., Lautzenhiser, A., Brown, W. S., Hart, A., Neumann, D., Spezio, M., & Adolphs, R. (2006) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2005.10.017 · Cited by 61 · see citing works

Trends in elective terminations of pregnancy between 1989 and 2000 in a French county (the Isère)

Guillem, P., Fabre, B., Cans, C., Robert‐Gnansia, E., & Jouk, P. (2003) · Prenatal Diagnosis · doi:10.1002/pd.711 · Cited by 61 · see citing works

Giant interhemispheric cysts associated with agenesis of the corpus callosum

Mori, K. (1992) · Journal of neurosurgery · doi:10.3171/jns.1992.76.2.0224 · Cited by 61 · see citing works

The influence of smoking on maternal serum AFP and free beta hCG levels and the impact on screening for Down syndrome

Spencer, K. (1998) · Prenatal Diagnosis · doi:10.1002/(sici)1097-0223(199803)18:3 · Cited by 58 · see citing works

Regulation of the L1 Cell Adhesion Molecule by Thyroid Hormone in the Developing Brain

Álvarez‐Dolado, M., Cuadrado, A., Navarro‐Yubero, C., Sonderegger, P., Furley, A. J., Bernal, J., & Múñoz, A. (2000) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2000.0879 · Cited by 58 · see citing works

Ten pen men: Rhyming skills in two children with callosal agenesis

Temple, C., Jeeves, M. A., & Vilarroya, Ó. (1989) · Brain and Language · doi:10.1016/0093-934x(89)90111-9 · Cited by 56 · see citing works

Prenatal formation of the normal mouse corpus callosum: A quantitative study with carbocyanine dyes

OZAKI, H. S., & Wahłsten, D. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903230107 · Cited by 56 · see citing works

Modulation of transcallosally mediated motor inhibition in children with attention deficit hyperactivity disorder (ADHD) by medication with methylphenidate (MPH)

Buchmann, J. A., Gierow, W., Weber, S., Hoeppner, J., Klauer, T., Wittstock, M., Benecke, R., Haessler, F., & Wolters, A. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.06.026 · Cited by 53 · see citing works

Alexithymia, Interhemispheric Transfer, and Right Hemispheric Specialization: A Critical Review

Tabibnia, G., & Zaidel, E. (2005) · Psychotherapy and Psychosomatics · doi:10.1159/000083166 · Cited by 52 · see citing works

Callosal Agenesis: A Natural Split Brain?

Hunter, A. G. W. (1995) · Europe PMC (PubMed Central) · Cited by 52 · see citing works

Neuronal network models of ADHD ? lateralization with respect to interhemispheric connectivity reconsidered

Roessner, V., Banaschewski, T., Uebel, H., Becker, A., & Rothenberger, A. (2004) · European Child & Adolescent Psychiatry · doi:10.1007/s00787-004-1007-5 · Cited by 51 · see citing works

Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies

Sherr, E. H., Owen, R., Albertson, D. G., et al. (2005) · Neurology · doi:10.1212/01.wnl.0000183066.09239.b6 · Cited by 51 · see citing works

Overall pattern of callosal connections in visual cortex of normal and enucleated cats

Olavarría, J. F., & Sluyters, R. C. V. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903630202 · Cited by 48 · see citing works

The corpus callosum and cerebral speech lateralization*1

Lassonde, M. C. (1990) · Brain and Language · doi:10.1016/0093-934x(90)90110-3 · Cited by 48 · see citing works

Ryk: A novel Wnt receptor regulating axon pathfinding

Keeble, T. R., & Cooper, H. (2006) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2006.07.005 · Cited by 47 · see citing works

The Autism Genome Project

Hu‐Lince, D., Craig, D. W., Huentelman, M. J., & Stephan, D. A. (2005) · American Journal of PharmacoGenomics · doi:10.2165/00129785-200505040-00004 · Cited by 47 · see citing works

Cognitive Functioning in Callosal Agenesis

Sauerwein, H. C., Nolin, P., & Lassonde, M. C. (1994) · Advances in behavioral biology · doi:10.1007/978-1-4613-0487-6_23 · Cited by 46 · see citing works

The relationships of agenesis of the corpus callosum to perception and learning

SOLURSH, L. P., MARGULIES, A. I., ASHEM, B., & STASIAK, E. A. (1965) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-196508000-00005 · Cited by 43 · see citing works

Sentence comprehension following agenesis of the corpus callosum

Sanders, R. J. (1989) · Brain and Language · doi:10.1016/0093-934x(89)90101-6 · Cited by 41 · see citing works

Localization of two new X‐linked quantitative trait loci controlling corpus callosum size in the mouse

Kusek, G. K., Wahłsten, D., Herron, B. J., Bolivar, V. J., & Flaherty, L. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00264.x · Cited by 39 · see citing works

Hemispheric equivalence and age-related differences in judgments of simultaneity to somatosensory stimuli

Brown, L. N., & Sainsbury, R. S. (2000) · Journal of Clinical and Experimental Neuropsychology · doi:10.1076/1380-3395(200010)22:5;1-9;ft587 · Cited by 35 · see citing works

Neurons in the corpus callosum of the cat during postnatal development

Riederer, B. M., Berbel, P. J., & Innocenti, G. M. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03305.x · Cited by 35 · see citing works

Distribution of transitory corpus callosum axons projecting to developing cat visual cortex revealed by DiI

Elberger, A. J. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903330303 · Cited by 33 · see citing works

Malformational complex in an infant with intrauterine influenza viral infection.

Conover, P. T., & Roessmann, U. (1990) · PubMed · Cited by 31 · see citing works

Interhemispheric Stroop effects in partial and complete agenesis of the corpus callosum

Brown, W. S., THRASHER, E. D., & Paul, L. K. (2001) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617701733048 · Cited by 31 · see citing works

Altered neuron–glia interactions in a low, chronic prenatal ethanol exposure

Evrard, S. G., Vega, M. D., Ramos, A. J., et al. (2003) · Developmental Brain Research · doi:10.1016/j.devbrainres.2003.09.004 · Cited by 31 · see citing works

Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder

Meyer, J., Johannssen, K., Freitag, C. M., Schraut, K., Teuber, I., Hahner, A., Mainhardt, C., Mößner, R., Volz, H., Wienker, T. F., et al. (2005) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145705005821 · Cited by 31 · see citing works

Phonemic Discrimination in Callosal Agenesis

Temple, C., & Ilsleya, J. (1993) · Cortex · doi:10.1016/s0010-9452(13)80187-6 · Cited by 29 · see citing works

Magnetic Resonance Imaging of Corpus Callosum Dysgenesis

Rauch, R. A., & Jinkins, J. R. (1994) · Advances in behavioral biology · doi:10.1007/978-1-4613-0487-6_11 · Cited by 28 · see citing works

A 23-year review of communication development in an individual with agenesis of the corpus callosum

Stickles, J. L., Schilmoeller, G. L., & Schilmoeller, K. J. (2002) · International Journal of Disability, Development and Education · doi:10.1080/1034912022000028349 · Cited by 27 · see citing works

Disturbances of spatial perception in a patient with agenesis of the corpus callosum

Meerwaldt, J. D. (1983) · Neuropsychologia · doi:10.1016/0028-3932(83)90083-0 · Cited by 23 · see citing works

Monozygotic twin cases of the agenesis of the corpus callosum with schizophrenic disorder

Motomura, N., Satani, S., & Inaba, M. (2002) · Psychiatry and Clinical Neurosciences · doi:10.1046/j.1440-1819.2002.00944.x · Cited by 22 · see citing works

A Case of Schizophrenia with Complete Agenesis of the Corpus Callosum

Chinnasamy, D., Rudd, R., & Velakoulis, D. (2006) · Australasian Psychiatry · doi:10.1080/j.1440-1665.2006.02299.x · Cited by 19 · see citing works

Is Disturbed Transfer of Learning in Callosal Agenesis due to a Disconnection Syndrome?

Imamura, T., Yamadori, A., Shiga, Y., Sahara, M., & Abiko, H. (1994) · Behavioural Neurology · doi:10.1155/1994/146072 · Cited by 18 · see citing works

Surrounded by Slit—How Forebrain Commissural Axons Can Be Led Astray

Richards, L. J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00566-4 · Cited by 18 · see citing works

Congenital CMV with callosal lipoma and agenesis

Mehta, N. M., & Hartnoll, G. (2001) · Pediatric Neurology · doi:10.1016/s0887-8994(00)00256-3 · Cited by 18 · see citing works

Is disturbed transfer of learning in callosal agenesis due to a disconnection syndrome?

Imamura, T., Yamadori, A., Shiga, Y., Sahara, M., & Abiko, H. (1994) · PubMed · doi:10.3233/ben-1994-7201 · Cited by 17 · see citing works

Complex sensory cross integration deficits in a case of corpus callosum agenesis with bilateral language representation: Positron-emission-tomography and neuropsychological findings

Kessler, J., Huber, M., Pawlik, G., et al. (1991) · International Journal of Neuroscience · doi:10.3109/00207459108985443 · Cited by 14 · see citing works

n‐2‐Hydroxyglutaric aciduria with absence of corpus callosum and neonatal intracranial haemorrhage

Wang, X., Jakobs, C., & Bawle, D. V. (2003) · Journal of Inherited Metabolic Disease · doi:10.1023/a:1024000202364 · Cited by 13 · see citing works

Linking acquired neurodevelopmental disorders to defects in cell adhesion

Greenberg, D. A. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1533226100 · Cited by 10 · see citing works

Dichotic listening, callosal agenesis and cerebral laterality

Lassonde, M. C. (1990) · Brain and Language · doi:10.1016/0093-934x(90)90154-9 · Cited by 8 · see citing works

Left hemianomia of musical symbols caused by callosal infarction

Satoh, M. (2006) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2005.068692 · Cited by 3 · see citing works

Language representation and sensory-motor mapping absent a corpus callosum

McAndrews, M. P., Lum, C., & Mikulis, D. J. (2001) · NeuroImage · doi:10.1016/s1053-8119(01)92158-5 · Cited by 1 · see citing works

Untitled work

(1997) · doi:10.1002/(sici)1098-1063(1997)7:1

Development, specification, and diversity of callosal projection neurons

Fame, R. M., MacDonald, J. L., & Macklis, J. D. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2010.10.002 · Cited by 381 · see citing works

The von Economo neurons in the frontoinsular and anterior cingulate cortex

Allman, J. M., Tetreault, N. A., Hakeem, A. Y., Manaye, K. F., Semendeferi, K., Erwin, J. M., Park, S., Goubert, V., & Hof, P. R. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.06011.x · Cited by 280 · see citing works

The anatomy of fronto-occipital connections from early blunt dissections to contemporary tractography

Forkel, S. J., Thiebaut de Schotten, M., Kawadler, J. M., Dell'Acqua, F., Danek, A., & Catani, M. (2014) · Cortex · doi:10.1016/j.cortex.2012.09.005 · Cited by 248 · see citing works

A Meta-Analysis of the Corpus Callosum in Autism

Frazier, T. W., & Hardan, A. Y. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.07.022 · Cited by 267 · see citing works

Molecular and behavioral aspects of the actions of alcohol on the adult and developing brain

Alfonso-Loeches, S., & Guerri, C. (2011) · Critical Reviews in Clinical Laboratory Sciences · doi:10.3109/10408363.2011.580567 · Cited by 254 · see citing works

Negative allosteric modulation of the mGluR5 receptor reduces repetitive behaviors and rescues social deficits in mouse models of autism

Silverman, J. L., Smith, D. G., Rizzo, S. J. S., Karras, M. N., Turner, S. M., Tolu, S. S., Bryce, D. K., Smith, D. L., Fonseca, K., Ring, R. H., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003501 · Cited by 251 · see citing works

Developmental neurotoxicity of inhaled ambient ultrafine particle air pollution: Parallels with neuropathological and behavioral features of autism and other neurodevelopmental disorders

Allen, J. L., Oberdorster, G., Morris-Schaffer, K., Wong, C., Klocke, C., Sobolewski, M., Conrad, K., Mayer-Proschel, M., & Cory-Slechta, D. A. (2017) · NeuroToxicology · doi:10.1016/j.neuro.2015.12.014 · Cited by 241 · see citing works

Three hypotheses for developmental defects that may underlie some forms of autism spectrum disorder

Rubenstein, J. L. (2010) · Current Opinion in Neurology · doi:10.1097/wco.0b013e328336eb13 · Cited by 230 · see citing works

The 16p11.2 Deletion Mouse Model of Autism Exhibits Altered Cortical Progenitor Proliferation and Brain Cytoarchitecture Linked to the ERK MAPK Pathway

Pucilowska, J., Vithayathil, J., Tavares, E. J., Kelly, C., Karlo, J. C., & Landreth, G. E. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4864-13.2015 · Cited by 207 · see citing works

Histopathologic characterization of the BTBR mouse model of autistic-like behavior reveals selective changes in neurodevelopmental proteins and adult hippocampal neurogenesis

Stephenson, D. T., O'Neill, S. M., Narayan, S., Tiwari, A., Arnold, E., Samaroo, H. D., Du, F., Ring, R. H., Campbell, B., Pletcher, M., et al. (2011) · Molecular Autism · doi:10.1186/2040-2392-2-7 · Cited by 180 · see citing works

Essential roles for the splicing regulator nSR100/SRRM4 during nervous system development

Quesnel-Vallières, M., Irimia, M., Cordes, S. P., & Blencowe, B. J. (2015) · Genes & Development · doi:10.1101/gad.256115.114 · Cited by 155 · see citing works

Neuroanatomical analysis of the BTBR mouse model of autism using magnetic resonance imaging and diffusion tensor imaging

Ellegood, J., Babineau, B. A., Henkelman, R. M., Lerch, J. P., & Crawley, J. N. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.12.029 · Cited by 135 · see citing works

Neuroimaging Evidence of Major Morpho-Anatomical and Functional Abnormalities in the BTBR T+TF/J Mouse Model of Autism

Dodero, L., Damiano, M., Galbusera, A., Bifone, A., Tsaftsaris, S. A., Scattoni, M. L., & Gozzi, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076655 · Cited by 116 · see citing works

Agenesis of the corpus callosum and autism: a comprehensive comparison

Paul, L. K., Corsello, C., Kennedy, D. P., & Adolphs, R. (2014) · Brain · doi:10.1093/brain/awu070 · Cited by 127 · see citing works

Postnatal lesion evidence against a primary role for the corpus callosum in mouse sociability

Yang, M., Clarke, A. M., & Crawley, J. N. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06714.x · Cited by 117 · see citing works

Contralateral targeting of the corpus callosum in normal and pathological brain function

Fenlon, L. R., & Richards, L. J. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.02.007 · Cited by 87 · see citing works

Unpacking the complexities of consciousness: Theories and reflections

Mudrik, L., Boly, M., Dehaene, S., Fleming, S. M., Lamme, V., Seth, A., & Melloni, L. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106053 · Cited by 81 · see citing works

Social narratives in agenesis of the corpus callosum: Linguistic analysis of the Thematic Apperception Test

Turk, A. A., Brown, W. S., Symington, M., & Paul, L. K. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.08.009 · Cited by 69 · see citing works

Low sociability is associated with reduced size of the corpus callosum in the BALB/cJ inbred mouse strain

Fairless, A. H., Dow, H. C., Toledo, M. M., Malkus, K. A., Edelmann, M., Li, H., Talbot, K., Arnold, S. E., Abel, T., & Brodkin, E. S. (2008) · Brain Research · doi:10.1016/j.brainres.2008.07.025 · Cited by 69 · see citing works

Selective reduction of Von Economo neuron number in agenesis of the corpus callosum

Kaufman, J. A., Paul, L. K., Manaye, K. F., Granstedt, A. E., Hof, P. R., Hakeem, A. Y., & Allman, J. M. (2008) · Acta Neuropathologica · doi:10.1007/s00401-008-0434-7 · Cited by 69 · see citing works

Quantitative trait loci for interhemispheric commissure development and social behaviors in the BTBR T+ tf/J mouse model of autism

Jones-Davis, D. M., Yang, M., Rider, E., Osbun, N. C., da Gente, G. J., Li, J., Katz, A. M., Weber, M. D., Sen, S., Crawley, J., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061829 · Cited by 61 · see citing works

Fetal functional imaging portrays heterogeneous development of emerging human brain networks

Jakab, A., Schwartz, E., Kasprian, G., Gruber, G. M., Prayer, D., Schöpf, V., & Langs, G. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00852 · Cited by 10 · see citing works

Agenesis of the corpus callosum: female monozygotic triplets

Ruge, J. R., & Newland, T. S. (1996) · Journal of neurosurgery · doi:10.3171/jns.1996.85.1.0152 · Cited by 5 · see citing works

Agenesis of corpus callosum prenatally diagnosed with fetal MRI: case report

Han, J. W., Oh, M., Kim, K. A., et al. (2005)

Beyond Isolated and Associated: A Novel Fetal MR Imaging–Based Scoring System Helps in the Prenatal Prognostication of Callosal Agenesis

Glatter, S., Kasprian, G. J., Bettelheim, D., et al. (2021) · American Journal of Neuroradiology · doi:10.3174/ajnr.a7064 · Cited by 12 · see citing works

[Agenesis of corpus callosum - a review].

Christova, R. (2010) · PubMed

Antenatal diagnosis of partial agenesis of the corpus callosum: A benign cause of ventriculomegaly

Lockwood, C. J., Ghidini, A., Aggarwal, R., et al. (1988) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(88)90518-2 · Cited by 27 · see citing works