Kenneth Y. Kwan
Kenneth Y. Kwan
Michigan Neuroscience Inst. (MNI) & Dept. of Human Genetics, Univ. of Michigan
Verified email at - Homepage
Cited by
Cited by
Sequence variants in SLITRK1 are associated with Tourette's syndrome
JF Abelson, KY Kwan, BJ O'Roak, DY Baek, AA Stillman, TM Morgan, ...
Science 310 (5746), 317, 2005
Satb2 is a postmitotic determinant for upper-layer neuron specification in the neocortex
O Britanova, C de Juan Romero, A Cheung, KY Kwan, M Schwark, ...
Neuron 57 (3), 378-392, 2008
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
K Bilgüvar, AK Öztürk, A Louvi, KY Kwan, M Choi, B Tatlı, D Yalnızoğlu, ...
Nature 467 (7312), 207-210, 2010
Numb and Numbl are required for maintenance of cadherin-based adhesion and polarity of neural progenitors
MR Rašin, VR Gazula, JJ Breunig, KY Kwan, MB Johnson, S Liu-Chen, ...
Nature neuroscience 10 (7), 819-827, 2007
Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex
KY Kwan, N Šestan, ES Anton
Development 139 (9), 1535-1546, 2012
Zfp312 is required for subcortical axonal projections and dendritic morphology of deep-layer pyramidal neurons of the cerebral cortex
JG Chen, MR Rašin, KY Kwan, N Šestan
Proceedings of the National Academy of Sciences of the United States of …, 2005
SOX5 postmitotically regulates migration, postmigratory differentiation, and projections of subplate and deep-layer neocortical neurons
KY Kwan, M Lam, Ž Krsnik, YI Kawasawa, V Lefebvre, N Šestan
Proceedings of the National Academy of Sciences 105 (41), 16021, 2008
Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network
MJ McConnell, JV Moran, A Abyzov, S Akbarian, T Bae, I Cortes-Ciriano, ...
Science 356 (6336), eaal1641, 2017
TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract
W Han, KY Kwan, S Shim, M Lam, Y Shin, X Xu, Y Zhu, M Li, N Šestan
Proceedings of the National Academy of Sciences 108 (7), 3041, 2011
Cis-regulatory control of corticospinal system development and evolution
S Shim, KY Kwan, M Li, V Lefebvre, N Šestan
Nature 486 (7401), 74-79, 2012
Species-Dependent Posttranscriptional Regulation of NOS1 by FMRP in the Developing Cerebral Cortex
KY Kwan, M Lam, MB Johnson, U Dube, S Shim, MR Rašin, AMM Sousa, ...
Cell 149 (4), 899-911, 2012
Recessive LAMC3 mutations cause malformations of occipital cortical development
T Barak, KY Kwan, A Louvi, V Demirbilek, S Saygı, B Tüysüz, M Choi, ...
Nature genetics 43 (6), 590-594, 2011
Selective depletion of molecularly defined cortical interneurons in human holoprosencephaly with severe striatal hypoplasia
S Fertuzinhos, Ž Krsnik, YI Kawasawa, MR Rašin, KY Kwan, JG Chen, ...
Cerebral cortex 19 (9), 2196, 2009
Medicine: sequence variants in SLITRK1 are associated with Tourette's syndrome
JF Abelson, KY Kwan, BJ O'Roak, DY Baek, AA Stillman, TM Morgan, ...
Science 310 (5746), 317-320, 2005
A mouse model of X-linked intellectual disability associated with impaired removal of histone methylation
S Iwase, E Brookes, S Agarwal, AI Badeaux, H Ito, CN Vallianatos, ...
Cell reports 14 (5), 1000-1009, 2016
Brain transcriptome databases: a user's guide
JM Keil, A Qalieh, KY Kwan
Journal of Neuroscience 38 (10), 2399-2412, 2018
TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons
X Caubit, P Gubellini, J Andrieux, PL Roubertoux, M Metwaly, B Jacq, ...
Nature genetics 48 (11), 1359-1369, 2016
Axonal ribosomes and mRNAs associate with fragile X granules in adult rodent and human brains
MR Akins, HE Berk-Rauch, KY Kwan, ME Mitchell, KA Shepard, ...
Human molecular genetics 26 (1), 192-209, 2017
Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology
W Zhou, SB Emery, DA Flasch, Y Wang, KY Kwan, JM Kidd, JV Moran, ...
Nucleic acids research 48 (3), 1146-1163, 2020
Transcriptional dysregulation of neocortical circuit assembly in ASD
KY Kwan
International review of neurobiology 113, 167-205, 2013
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