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Qingbo Wang on Muck Rack

Qingbo Wang

As seen in: Nature, Wiley Online Library, Frontiers, MDPI, BMC Genomics, Royal Society of Chemistry, BioRxiv, Cell Press, Optica
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Articles

Scalable Aluminum-Doped Zinc Oxide Transparent Electrodes via Spatial ALD for High-Efficiency Perovskite Modules

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By Xuewei Jiang, Engineering Huazhong, Qingbo Wang
| Wiley Online Library Verified
1 Introduction Perovskite solar cells (PSCs) have gained significant attention for their exceptional power conversion efficiency (PCE) and simple fabrication process [1-3]. These advantages have enabled PSCs to progress rapidly, with single-junction PCE rising from an initial 3.8% to 27.3% in small-area PSCs (≤1 cm2) [4, 5]. However, scaling PSCs to large-area perovskite solar modules (PSMs) remains challenging, particularly in achieving scalable and efficient fabrication [6].
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Elucidating genetic backgrounds of myasthenia gravis in Japanese by genome-wide association studies and multi-omics analyses of thymoma

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By Hiroyuki Ueda, Tomoya Kubota, Risa Goto, Akari Suzuki, Takafumi Ojima, Kotaro Ogawa, Kyuto Sonehara, Shinichi Namba, Tatsuhiko Naito, Qingbo Wang, Shingo Konno, Makoto Samukawa, Naoki Kawaguchi, Takashi Kimura, Takamichi Sugimoto, Hiroyuki Murai, Kenichi Kaida, Daiki Tokuyasu, Manato Yasuda, Hiroyuki Akamine, Yosuke Onishi, Yosuke Ogawa, Yuya Shirai, Ryuya Edahiro, Kenichi Yamamoto, Hideki Nagata, Naoko Ose, Jun Takayama, Ken Suzuki, Shinichi Higashiue, Shuzo Kobayashi, Hiroki Yamaguchi, Yasushi Okazaki, Naoyuki Matsumoto, Kenta Motomura, Hidenobu Koga, BioBank Japan Project, Koichi Matsuda, Masayuki Yamamoto, Toshimasa Yamauchi, Takashi Kadowaki, Kazuhiko Yamamoto, Akiko Ohno, Tatsusada Okuno, Eiichi Morii, Hideki Mochizuki, Yuriko Nagane, Akiyuki Uzawa, Masayuki Masuda, Shigeaki Suzuki, Iichiro Shimomura, Yasushi Shintani, Kimiaki Utsugisawa, Masanori Takahashi, Yukinori Okada, Takemori Yamawaki, Naoya Minami
| Nature Verified
Abstract Myasthenia gravis (MG) is an autoimmune disorder characterized by impaired neuromuscular transmission and motor symptoms. Its genetic background remains unclear, particularly beyond specific subtypes reported in European populations. Here, we perform a genome-wide association study (GWAS) of 1,434 MG cases covering all disease subtypes and 42,913 controls of Japanese, which newly identify the TERT locus (odds ratio [OR] = 1.31, P = 1.7×10-10).
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Functional dissection of complex trait variants at single-nucleotide resolution - Nature

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By Layla Siraj, Rodrigo Castro, Hannah Dewey, Susan Kales, John C. Butts, Thanh Nguyen, Masahiro Kanai, Kousuke Mouri, Qingbo Wang, Petko Fiziev, Kristin Tsuo, Zachary R McCaw, Sager J. Gosai, Francois Aguet, Ran Ji Cui, Irfahan Kassam, Jeremy F McRae, Christopher M. Vockley, Caleb A Lareau, Sergey A. Abramov, Jeff Vierstra, Yukinori Okada, Alexander Gusev, Thouis R Jones, Eric S. Lander, Pardis Sabeti, Hilary Finucane, Steven Reilly, Jacob C. Ulirsch, Ryan Tewhey, Daniel Berenzy, Alexandr Boystov
| Nature Verified
Abstract Identifying the causal variants and mechanisms that drive complex traits and diseases remains a core problem in human genetics1,2,3,4,5. Most of these variants individually have weak effects6 and lie in non-coding gene-regulatory elements7,8,9,10, for which we lack a complete understanding of how single-nucleotide alterations modulate transcriptional processes to affect human phenotypes5,11,12,13,14,15.
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