| Year |
Citation |
Score |
| 2024 |
Molnár Z, Kwan KY. Development and Evolution of Thalamocortical Connectivity. Cold Spring Harbor Perspectives in Biology. 16. PMID 38167425 DOI: 10.1101/cshperspect.a041503 |
0.35 |
|
| 2023 |
Njoku IP, Kwan KY. Distinct microtubule networks mediate neuronal migration and polarization. Neuron. 111: 1168-1170. PMID 37080166 DOI: 10.1016/j.neuron.2023.03.026 |
0.354 |
|
| 2022 |
Funk OH, Qalieh Y, Doyle DZ, Lam MM, Kwan KY. Postmitotic accumulation of histone variant H3.3 in new cortical neurons establishes neuronal chromatin, transcriptome, and identity. Proceedings of the National Academy of Sciences of the United States of America. 119: e2116956119. PMID 35930666 DOI: 10.1073/pnas.2116956119 |
0.776 |
|
| 2022 |
Bae T, Fasching L, Wang Y, Shin JH, Suvakov M, Jang Y, Norton S, Dias C, Mariani J, Jourdon A, Wu F, Panda A, Pattni R, Chahine Y, Yeh R, ... ... Kwan KY, et al. Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutability. Science (New York, N.Y.). 377: 511-517. PMID 35901164 DOI: 10.1126/science.abm6222 |
0.733 |
|
| 2022 |
Doyle DZ, Kwan KY. Neurogenic-angiogenic synchrony via lactate. Nature Neuroscience. 25: 839-840. PMID 35788196 DOI: 10.1038/s41593-022-01111-8 |
0.661 |
|
| 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 |
0.442 |
|
| 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 |
0.792 |
|
| 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 |
0.729 |
|
| 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 |
0.572 |
|
| 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 |
0.369 |
|
| 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 |
0.786 |
|
| 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 |
0.765 |
|
| 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 |
0.799 |
|
| 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 |
0.414 |
|
| 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 |
0.607 |
|
| 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 |
0.779 |
|
| 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 |
0.776 |
|
| 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 |
0.375 |
|
| 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 |
0.8 |
|
| 2012 |
Kwan KY, Lam MM, Johnson MB, Dube U, Shim S, Rašin 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 |
0.759 |
|
| 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 |
0.817 |
|
| 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 |
0.794 |
|
| 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 |
0.785 |
|
| 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 |
0.799 |
|
| 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 |
0.785 |
|
| 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 |
0.805 |
|
| 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 |
0.808 |
|
| 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 |
0.772 |
|
| 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 |
0.816 |
|
| 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 |
0.769 |
|
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