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Kenneth Y. Kwan
Kenneth Y. Kwan
Michigan Neuroscience Inst. (MNI) & Dept. of Human Genetics, Univ. of Michigan
Verified email at umich.edu - Homepage
Title
Cited by
Cited by
Year
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
12272005
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
7002008
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
6162010
Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex
KY Kwan, N Šestan, ES Anton
Development 139 (9), 1535-1546, 2012
4192012
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
3692007
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
2922008
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
2832005
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
2432017
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
2142011
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
2052012
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
1512012
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
1232011
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
1222016
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
1152009
Brain transcriptome databases: a user's guide
JM Keil, A Qalieh, KY Kwan
Journal of Neuroscience 38 (10), 2399-2412, 2018
802018
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
762016
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
692020
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
672017
Transcriptional dysregulation of neocortical circuit assembly in ASD
KY Kwan
International review of neurobiology 113, 167-205, 2013
452013
Robust elimination of genome-damaged cells safeguards against brain somatic aneuploidy following Knl1 deletion
L Shi, A Qalieh, MM Lam, JM Keil, KY Kwan
Nature communications 10 (1), 2588, 2019
432019
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