Polina Bukshpun

发表

The Role of Corpus Callosum Development in Functional Connectivity and Cognitive Processing

Srikantan S. Nagarajan, Pratik Mukherjee, A. James Barkovich, 2012, PloS one.

White Matter Changes of Neurite Density and Fiber Orientation Dispersion during Human Brain Maturation

S. Nagarajan, P. Mukherjee, J. Berman, 2015, PloS one.

Sensorimotor Cortical Oscillations during Movement Preparation in 16p11.2 Deletion Carriers

W. Chung, S. Nagarajan, C. Dale, 2019, The Journal of Neuroscience.

Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplications

Pratik Mukherjee, Srikantan S Nagarajan, Jeffrey I Berman, 2016, Human brain mapping.

Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria

Joseph T. Glessner, S. Christian, J. Glessner, 2013, PLoS genetics.

Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication

Allison G. Dempsey, D. Ledbetter, A. Beaudet, 2016, Journal of Autism and Developmental Disorders.

Aberrant White Matter Microstructure in Children with 16p11.2 Deletions

Pratik Mukherjee, Srikantan S Nagarajan, Jeffrey I Berman, 2014, The Journal of Neuroscience.

Effects of eight neuropsychiatric copy number variants on human brain structure

Allison G. Dempsey, M. Owen, R. Buckner, 2021, Translational Psychiatry.

Brain MR Imaging Findings and Associated Outcomes in Carriers of the Reciprocal Copy Number Variation at 16p11.2.

R. Buckner, S. Nagarajan, P. Mukherjee, 2018, Radiology.

Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus Callosum.

L. Richards, J. Rubenstein, W. Reardon, 2016, Cell reports.

Autism Traits in Individuals with Agenesis of the Corpus Callosum

S. Baron-Cohen, S. Nagarajan, L. Hinkley, 2013, Journal of autism and developmental disorders.

Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption

William B Dobyns, Polina Bukshpun, Christopher Sullivan, 2013, American journal of medical genetics. Part A.

Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene

Wendy S. Schackwitz, L. Pennacchio, Jiang Li, 2011, American journal of medical genetics. Part A.

Dual-Mode Modulation of Smad Signaling by Smad-Interacting Protein Sip1 Is Required for Myelination in the Central Nervous System

Elliott H. Sherr, Polina Bukshpun, Qiaojun He, 2012, Neuron.

The structural connectome of the human brain in agenesis of the corpus callosum

Eric J. Friedman, Julia P. Owen, Pratik Mukherjee, 2013, NeuroImage.

The Contribution of the Corpus Callosum to Language Lateralization

Pratik Mukherjee, Srikantan S Nagarajan, A James Barkovich, 2016, The Journal of Neuroscience.

Test-Retest Reliability of Computational Network Measurements Derived from the Structural Connectome of the Human Brain

Timothy P. L. Roberts, Eric J. Friedman, Julia P. Owen, 2013, Brain Connect..

Resting-State Networks and the Functional Connectome of the Human Brain in Agenesis of the Corpus Callosum

Julia P. Owen, Srikantan S. Nagarajan, Pratik Mukherjee, 2013, Brain Connect..

Dual-Mode Modulation of Smad Signaling by Smad-Interacting Protein Sip1 Is Required for Myelination in the Central Nervous System

Qiaojun He, D. Huylebroeck, W. Shou, 2012, Neuron.

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

Allison G. Dempsey, S. Spence, D. Ledbetter, 2012, Journal of Medical Genetics.

Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus Callosum.

L. Richards, J. Rubenstein, W. Reardon, 2016, Cell Reports.