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Articles by J. Suh
Four ppm measurement of the antihydrogen ground-state hyperfine splitting
Abstract The hydrogen atom is a touchstone for the foundations, evolution and frontiers of quantum theory1,2,3,4,5,6,7,8,9. Key spectral lines of this atom have been determined to remarkable precision10,11. Our research focuses on the study of antihydrogen, the antimatter counterpart of hydrogen. We test fundamental symmetries of nature (such as simultaneous charge conjugation, parity inversion, and time reversal or CPT symmetry) through precision comparisons of these atomic systems12.
Be+ assisted, simultaneous confinement of more than 15000 antihydrogen atoms - Nature Communications
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Abstract Antihydrogen, the bound state of a positron and an antiproton, is the only pure anti-atomic system ever studied. It is produced exclusively in the laboratory, as it has never been observed in nature. This unique system is of great interest for searching for tentative differences between matter and antimatter.
By C. Baker, N. Bhatt, G. Bonomi, A. Capra, I. Carli, C. L. Cesar, M. B. Charlton, A. Cridland Mathad, D. Duque Quiceno, J. Fajans, L. Golino, J. S. Hangst, D. Hodgkinson, S. A. Jones, S. Jonsell, N. M. Madsen, J. Nauta, A. Oliveira, J. Peszka, A. Powell, C. Rasmussen, F. Robicheaux, J. Schoonwater, J. D. Singh, G. R. Smith, S. Stracka, J. Suh, E. Thorpe-Woods, M. Urioni, T. Momose, T. Robertson-Brown, R. I. Thompson, P. Woosaree
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Nature
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Modification of The Paris System for urinary tract washing specimens using diagnostic cytological features
The Paris System (TPS), which was recently introduced, emphasised the key features of malignant urine cytology: a high nuclear to cytoplasmic ratio, nuclear hyperchromasia, irregular nuclear membranes and coarse chromatin. Although other diagnostic features have been described, the diagnostic significance of such features and their application to TPS have not been fully defined for urinary tract washing specimens.
Lung sarcomatoid carcinoma (LSC) harbors targetable genomic alterations and high mutational burden as observed by comprehensive genomic profiling (CGP)
Background: LSC is a rare, clinically aggressive, heterogeneous and poorly differentiated subtype of non-small cell lung cancer (NSCLC), which is typically difficult to diagnose and resistant to conventional therapies. We queried whether CGP could guide LSC patients to novel targeted therapies. Methods: Hybrid-capture based CGP was performed on 6,923 consecutive FFPE NSCLCs during the course of clinical care and 91 (1.3%) LSCs were identified.
Comprehensive genomic profiling of 8,654 breast carcinoma reveals therapeutically targetable molecular subtypes beyond those defined by hormone-receptor expression
Background: Breast carcinomas (BC) are commonly classified into 4 subtypes based on hormone receptor expression: basal, luminal A, luminal B, and HER2 overexpressed. Comprehensive genomic profiling (CGP) can reveal targetable genomic alterations (GA) and redefine BC classification into therapeutically relevant subtypes.
BRAF genomic alterations in breast cancer
Background: Targeting BRAF genomic alterations (GA) in non-melanoma cancer patients is well-established, but BRAF targeting for treating metastatic breast cancer (mBC) remains under investigation.
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