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1
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
In: ISSN: 0002-9297 ; EISSN: 1537-6605 ; American Journal of Human Genetics ; https://hal-univ-rennes1.archives-ouvertes.fr/hal-03268683 ; American Journal of Human Genetics, Elsevier (Cell Press), 2021, 108 (2), pp.346-356. ⟨10.1016/j.ajhg.2021.01.007⟩ (2021)
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2
XTREME-R: Towards More Challenging and Nuanced Multilingual Evaluation ...
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3
ExplainaBoard: An Explainable Leaderboard for NLP ...
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4
SimCLS: A Simple Framework for Contrastive Learning of Abstractive Summarization ...
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5
SpanNER: Named Entity Re-/Recognition as Span Prediction ...
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6
CitationIE: Leveraging the Citation Graph for Scientific Information Extraction ...
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7
Target-Guided Structured Attention Network for Target-Dependent Sentiment Analysis
In: Transactions of the Association for Computational Linguistics, Vol 8, Pp 172-182 (2020) (2020)
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8
De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Callosum, Axon, Cardiac, Ocular, and Genital Defects
In: ISSN: 0002-9297 ; EISSN: 1537-6605 ; American Journal of Human Genetics ; https://hal.umontpellier.fr/hal-02556784 ; American Journal of Human Genetics, Elsevier (Cell Press), 2019, 105 (4), pp.854-868. ⟨10.1016/j.ajhg.2019.09.005⟩ (2019)
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9
Multi-Scale Self-Attention for Text Classification ...
Guo, Qipeng; Qiu, Xipeng; Liu, Pengfei. - : arXiv, 2019
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