Kenneth Y. Kwan, Ph.D. - Publications

Affiliations: 
Neuroscience University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Cortical development, neural circuit assembly, neurodevelopmental disorders
Website:
http://www.kwanlab.org

27 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
2022 Yang T, Veling MW, Zhao XF, Prin NP, Zhu L, Hergenreder T, Liu H, Liu L, Rane Z, Savelieff MG, Fuerst PG, Li Q, Kwan KY, Giger RJ, Wang Y, et al. Migrating pyramidal neurons require DSCAM to bypass the border of the developing cortical plate. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 35672151 DOI: 10.1523/JNEUROSCI.0997-21.2022  0.444
2021 Doyle DZ, Lam MM, Qalieh A, Qalieh Y, Sorel A, Funk OH, Kwan KY. Chromatin remodeler regulates subplate neuron identity and wiring of cortical connectivity. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34011608 DOI: 10.1073/pnas.2100686118  0.785
2020 Keil JM, Doyle DZ, Qalieh A, Lam MM, Funk OH, Qalieh Y, Shi L, Mohan N, Sorel A, Kwan KY. Symmetric neural progenitor divisions require chromatin-mediated homologous recombination DNA repair by Ino80. Nature Communications. 11: 3839. PMID 32737294 DOI: 10.1038/S41467-020-17551-4  0.716
2020 Bott CJ, McMahon LP, Keil JM, Yap CC, Kwan KY, Winckler B. Nestin selectively facilitates the phosphorylation of the Lissencephaly-linked protein doublecortin (DCX) by cdk5/p35 to regulate growth cone morphology and Sema3a sensitivity in developing neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 32273484 DOI: 10.1523/Jneurosci.2471-19.2020  0.653
2019 Shi L, Qalieh A, Lam MM, Keil JM, Kwan KY. Robust elimination of genome-damaged cells safeguards against brain somatic aneuploidy following Knl1 deletion. Nature Communications. 10: 2588. PMID 31197172 DOI: 10.1038/S41467-019-10411-W  0.59
2018 Keil JM, Qalieh A, Kwan KY. Brain transcriptome databases: a user's guide. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 29437890 DOI: 10.1523/JNEUROSCI.1930-17.2018  0.568
2017 Sun N, Nasello C, Deng L, Wang N, Zhang Y, Xu Z, Song Z, Kwan K, King RA, Pang ZP, Xing J, Heiman GA, Tischfield JA. The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family. Molecular Psychiatry. PMID 28894297 DOI: 10.1038/Mp.2017.179  0.367
2017 McConnell MJ, Moran JV, Abyzov A, Akbarian S, Bae T, Cortes-Ciriano I, Erwin JA, Fasching L, Flasch DA, Freed D, Ganz J, Jaffe AE, Kwan KY, Kwon M, Lodato MA, et al. Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network. Science (New York, N.Y.). 356. PMID 28450582 DOI: 10.1126/Science.Aal1641  0.741
2017 Akins MR, Berk-Rauch HE, Kwan KY, Mitchell ME, Shepard KA, Korsak LI, Stackpole EE, Warner-Schmidt JL, Sestan N, Cameron HA, Fallon JR. Axonal ribosomes and mRNAs associate with fragile X granules in adult rodent and human brains. Human Molecular Genetics. PMID 28082376 DOI: 10.1093/Hmg/Ddw381  0.723
2016 Caubit X, Gubellini P, Andrieux J, Roubertoux PL, Metwaly M, Jacq B, Fatmi A, Had-Aissouni L, Kwan KY, Salin P, Carlier M, Liedén A, Rudd E, Shinawi M, Vincent-Delorme C, et al. TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons. Nature Genetics. PMID 27668656 DOI: 10.1038/Ng.3681  0.769
2016 Iwase S, Brookes E, Agarwal S, Badeaux AI, Ito H, Vallianatos CN, Tomassy GS, Kasza T, Lin G, Thompson A, Gu L, Kwan KY, Chen C, Sartor MA, Egan B, et al. A Mouse Model of X-linked Intellectual Disability Associated with Impaired Removal of Histone Methylation. Cell Reports. PMID 26804915 DOI: 10.1016/J.Celrep.2015.12.091  0.402
2014 Colvin SM, Kwan KY. Dysregulated nitric oxide signaling as a candidate mechanism of fragile X syndrome and other neuropsychiatric disorders. Frontiers in Genetics. 5: 239. PMID 25101118 DOI: 10.3389/fgene.2014.00239  0.611
2014 Funk OH, Kwan KY. Nitric oxide signaling in the development and evolution of language and cognitive circuits. Neuroscience Research. 86: 77-87. PMID 24933499 DOI: 10.1016/j.neures.2014.06.001  0.768
2014 Robichaux MA, Chenaux G, Ho HY, Soskis MJ, Dravis C, Kwan KY, Šestan N, Greenberg ME, Henkemeyer M, Cowan CW. EphB receptor forward signaling regulates area-specific reciprocal thalamic and cortical axon pathfinding. Proceedings of the National Academy of Sciences of the United States of America. 111: 2188-93. PMID 24453220 DOI: 10.1073/Pnas.1324215111  0.739
2013 Kwan KY. Transcriptional dysregulation of neocortical circuit assembly in ASD. International Review of Neurobiology. 113: 167-205. PMID 24290386 DOI: 10.1016/B978-0-12-418700-9.00006-X  0.384
2012 Shim S, Kwan KY, Li M, Lefebvre V, Sestan N. Cis-regulatory control of corticospinal system development and evolution. Nature. 486: 74-9. PMID 22678282 DOI: 10.1038/nature11094  0.765
2012 Kwan KY, Lam MM, Johnson MB, Dube U, Shim S, RaÅ¡in MR, Sousa AM, Fertuzinhos S, Chen JG, Arellano JI, Chan DW, Pletikos M, Vasung L, Rowitch DH, Huang EJ, et al. Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortex. Cell. 149: 899-911. PMID 22579290 DOI: 10.1016/J.Cell.2012.02.060  0.744
2012 Kwan KY, Sestan N, Anton ES. Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex. Development (Cambridge, England). 139: 1535-46. PMID 22492350 DOI: 10.1242/dev.069963  0.784
2011 Barak T, Kwan KY, Louvi A, Demirbilek V, Sayg? S, Tüysüz B, Choi M, Boyac? H, Doerschner K, Zhu Y, Kaymakçalan H, Y?lmaz S, Bak?rc?o?lu M, Ca?layan AO, Oztürk AK, et al. Recessive LAMC3 mutations cause malformations of occipital cortical development. Nature Genetics. 43: 590-4. PMID 21572413 DOI: 10.1038/Ng.836  0.76
2011 Han W, Kwan KY, Shim S, Lam MM, Shin Y, Xu X, Zhu Y, Li M, Sestan N. TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract. Proceedings of the National Academy of Sciences of the United States of America. 108: 3041-6. PMID 21285371 DOI: 10.1073/Pnas.1016723108  0.778
2010 Bilgüvar K, Oztürk AK, Louvi A, Kwan KY, Choi M, Tatli B, Yalnizo?lu D, Tüysüz B, Ca?layan AO, Gökben S, Kaymakçalan H, Barak T, Bakircio?lu M, Yasuno K, Ho W, et al. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature. 467: 207-10. PMID 20729831 DOI: 10.1038/Nature09327  0.766
2009 Fertuzinhos S, Krsnik Z, Kawasawa YI, Rasin MR, Kwan KY, Chen JG, Judas M, Hayashi M, Sestan N. Selective depletion of molecularly defined cortical interneurons in human holoprosencephaly with severe striatal hypoplasia. Cerebral Cortex (New York, N.Y. : 1991). 19: 2196-207. PMID 19234067 DOI: 10.1093/Cercor/Bhp009  0.773
2008 Kwan KY, Lam MM, Krsnik Z, Kawasawa YI, Lefebvre V, Sestan N. SOX5 postmitotically regulates migration, postmigratory differentiation, and projections of subplate and deep-layer neocortical neurons. Proceedings of the National Academy of Sciences of the United States of America. 105: 16021-6. PMID 18840685 DOI: 10.1073/pnas.0806791105  0.77
2008 Britanova O, de Juan Romero C, Cheung A, Kwan KY, Schwark M, Gyorgy A, Vogel T, Akopov S, Mitkovski M, Agoston D, Sestan N, Molnár Z, Tarabykin V. Satb2 is a postmitotic determinant for upper-layer neuron specification in the neocortex. Neuron. 57: 378-92. PMID 18255031 DOI: 10.1016/J.Neuron.2007.12.028  0.772
2007 Rasin MR, Gazula VR, Breunig JJ, Kwan KY, Johnson MB, Liu-Chen S, Li HS, Jan LY, Jan YN, Rakic P, Sestan N. Numb and Numbl are required for maintenance of cadherin-based adhesion and polarity of neural progenitors. Nature Neuroscience. 10: 819-27. PMID 17589506 DOI: 10.1038/nn1924  0.77
2005 Chen JG, Rasin MR, Kwan KY, Sestan N. Zfp312 is required for subcortical axonal projections and dendritic morphology of deep-layer pyramidal neurons of the cerebral cortex. Proceedings of the National Academy of Sciences of the United States of America. 102: 17792-7. PMID 16314561 DOI: 10.1073/pnas.0509032102  0.815
2005 Abelson JF, Kwan KY, O'Roak BJ, Baek DY, Stillman AA, Morgan TM, Mathews CA, Pauls DL, Rasin MR, Gunel M, Davis NR, Ercan-Sencicek AG, Guez DH, Spertus JA, Leckman JF, et al. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science (New York, N.Y.). 310: 317-20. PMID 16224024 DOI: 10.1126/Science.1116502  0.765
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