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Seungshin Ha - Publications

Affiliations: 
Brigham and Women's Hospital and Seattle Children's Research Institute 
Area:
Development of the cerebral cortex
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8 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 Jamet S, Ha S, Ho TH, Houghtaling S, Timms A, Yu K, Paquette A, Maga AM, Greene NDE, Beier DR. The Arginine Methyltransferase Carm1 is Necessary for Heart Development. G3 (Bethesda, Md.). PMID 35736367 DOI: 10.1093/g3journal/jkac155  0.537
2020 Ha S, Tripathi PP, Daza RA, Hevner RF, Beier DR. Reelin Mediates Hippocampal Cajal-Retzius Cell Positioning and Infrapyramidal Blade Morphogenesis. Journal of Developmental Biology. 8. PMID 32962021 DOI: 10.3390/jdb8030020  0.634
2017 Ha S, Tripathi PP, Mihalas AB, Hevner RF, Beier DR. C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR, Causing Abnormal Development of the Cerebral Cortex and Hippocampus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 37: 960-971. PMID 28123028 DOI: 10.1523/Jneurosci.1826-16.2016  0.693
2016 Ha S, Tripathi PP, Mihalas AB, Hevner RF, Beier DR. C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR Causing Abnormal Development of the Cerebral Cortex and Hippocampus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 27986930 DOI: 10.1523/JNEUROSCI.1826-16.2016  0.685
2016 Ha S, Lindsay AM, Timms AE, Beier DR. Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice. G3 (Bethesda, Md.). PMID 27261005 DOI: 10.1534/G3.116.030791  0.632
2015 Ha S, Stottmann RW, Furley AJ, Beier DR. A forward genetic screen in mice identifies mutants with abnormal cortical patterning. Cerebral Cortex (New York, N.Y. : 1991). 25: 167-79. PMID 23968836 DOI: 10.1093/Cercor/Bht209  0.687
2012 Leshchiner I, Alexa K, Kelsey P, Adzhubei I, Austin-Tse CA, Cooney JD, Anderson H, King MJ, Stottmann RW, Garnaas MK, Ha S, Drummond IA, Paw BH, North TE, Beier DR, et al. Mutation mapping and identification by whole-genome sequencing. Genome Research. 22: 1541-8. PMID 22555591 DOI: 10.1101/Gr.135541.111  0.665
2008 Ha S, Redmond L. ERK mediates activity dependent neuronal complexity via sustained activity and CREB-mediated signaling. Developmental Neurobiology. 68: 1565-79. PMID 18837011 DOI: 10.1002/dneu.20682  0.622
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