MicroRNA-301 Mediates Proliferation and Invasion in Human Breast Cancer von WEI SHI, GERSTER, Kate, MCCREADY, David, FYLES, Anthony, LIU, Fei-Fei, ALAJEZ, Nehad M, TSANG, Jasmine, WALDRON, Levi, PINTILIE, Melania, HUI, Angela B, SYKES, Jenna, P'NG, Christine, MILLER, Naomi

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Long-Range Indoor Navigation With PRM-RL von Francis, Anthony, Faust, Aleksandra, Chiang, Hao-Tien Lewis, Hsu, Jasmine, Kew, J. Chase, Fiser, Marek, Lee, Tsang-Wei Edward

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CTNNB1‐related neurodevelopmental disorder in a Chinese population: A case series von Ho, Stephanie, Tsang, Mandy Ho‐Yin, Fung, Jasmine Lee‐Fong, Huang, Haibo, Chow, Chun‐Bong, Cheng, Shirley Sze‐Wing, Luk, Ho‐Ming, Chung, Brian Hon‐Yin, Lo, Ivan Fai‐Man

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A three-year follow-up study evaluating clinical utility of exome sequencing and diagnostic potential of reanalysis von Fung, Jasmine L. F., Yu, Mullin H. C., Huang, Shushu, Chung, Claudia C. Y., Chan, Marcus C. Y., Pajusalu, Sander, Mak, Christopher C. Y., Hui, Vivian C. C., Tsang, Mandy H. Y., Yeung, Kit San, Lek, Monkol, Chung, Brian H. Y.

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Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES) von Leung, Gordon K C, Mak, Christopher C Y, Fung, Jasmine L F, Wong, Wilfred H S, Tsang, Mandy H Y, Yu, Mullin H C, Pei, Steven L C, Yeung, K S, Mok, Gary T K, Lee, C P, Hui, Amelia P W, Tang, Mary H Y, Chan, Kelvin Y K, Liu, Anthony P Y, Yang, Wanling, Sham, P C, Kan, Anita S Y, Chung, Brian H Y

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Diagnostic value of whole‐exome sequencing in Chinese pediatric‐onset neuromuscular patients von Tsang, Mandy H. Y., Chiu, Annie T. G., Kwong, Bernard M. H., Liang, Rui, Yu, Mullin H. C., Yeung, Kit‐San, Ho, Wetor H. L., Mak, Christopher C. Y., Leung, Gordon K. C., Pei, Steven L. C., Fung, Jasmine L. F., Wong, Virginia C. N., Muntoni, Francesco, Chung, Brian H. Y., Chan, Sophelia H. S.

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Effect of Cr doping in CeO2 nanostructures on photocatalysis and H2O2 assisted methylene blue dye degradation von Habib, Ishaq Y., Burhan, Jasmine, Jaladi, Fadhli, Lim, Chee Ming, Usman, A., Kumara, N.T.R.N., Tsang, Shik Chi Edman, Mahadi, Abdul Hanif

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Spectrum of Disease Severity and Phenotype in Choroideremia Carriers von Jauregui, Ruben, Park, Karen Sophia, Tanaka, Akemi J., Cho, Ahra, Paavo, Maarjaliis, Zernant, Jana, Francis, Jasmine H., Allikmets, Rando, Sparrow, Janet R., Tsang, Stephen H.

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A significant inflation in TGM6 genetic risk casts doubt in its causation in spinocerebellar ataxia type 35 von Fung, Jasmine L.F., Tsang, Mandy H.Y., Leung, Gordon K.C., Yeung, Kit San, Mak, Christopher C.Y., Fung, Cheuk Wing, Chan, Sophelia H.S., Yu, Mullin H.C., Chung, Brian H.Y.

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Rapid whole-exome sequencing facilitates precision medicine in paediatric rare disease patients and reduces healthcare costs von Chung, Claudia C.Y., Leung, Gordon K.C., Mak, Christopher C.Y., Fung, Jasmine L.F., Lee, Mianne, Pei, Steven L.C., Yu, Mullin H.C., Hui, Vivian C.C., Chan, Joshua C.K., Chau, Jeffrey F.T., Chan, Marcus C.Y., Tsang, Mandy H.Y., Wong, Wilfred H.S., Tung, Joanna Y.L., Lun, Kin Shing, Ng, Yiu Ki, Fung, Cheuk Wing, Wong, Mabel S.C., Wong, Rosanna M.S., Lau, Yu Lung, Chan, Godfrey C.F., Lee, So Lun, Yeung, Kit San, Chung, Brian H.Y.

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Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese population von Tsang, Mandy H Y, Kwong, Anna K Y, Chan, Kate L S, Fung, Jasmine L F, Yu, Mullin H C, Mak, Christopher C Y, Yeung, Kit-San, Rodenburg, Richard J T, Smeitink, Jan A M, Chan, Rachel, Tsoi, Thomas, Hui, Joannie, Wong, Shelia S N, Tai, Shuk-Mui, Chan, Victor C M, Ma, Che-Kwan, Fung, Sharon T H, Wu, Shun-Ping, Chak, W K, Chung, Brian H Y, Fung, Cheuk-Wing

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Actionable secondary findings in 1116 Hong Kong Chinese based on exome sequencing data von Yu, Mullin Ho Chung, Mak, Christopher Chun Yu, Fung, Jasmine Lee Fong, Lee, Mianne, Tsang, Mandy Ho Yin, Chau, Jeffrey Fong Ting, Chung, Patrick Ho-Yu, Yang, Wanling, Chan, Godfrey Chi Fung, Lee, So Lun, Lau, Yu Lung, Tam, Paul Kwong Hang, Tang, Clara Sze Man, Yeung, Kit San, Chung, Brian Hon Yin

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Clinical and molecular features of pleuropulmonary blastoma in children in Hong Kong: case reports von Anthony PY Liu, Fung, Marcus KL, Lee, Mianne, Fung, Jasmine LF, Tsang, Mandy HY, Luk, C W, Chung, Brian HY, Chan, Godfrey CF

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Exome sequencing in paediatric patients with movement disorders von Kwong, Anna Ka-Yee, Tsang, Mandy Ho-Yin, Fung, Jasmine Lee-Fong, Mak, Christopher Chun-Yu, Chan, Kate Lok-San, Rodenburg, Richard J T, Lek, Monkol, Huang, Shushu, Pajusalu, Sander, Yau, Man-Mut, Tsoi, Cheung, Fung, Sharon, Liu, Kam-Tim, Ma, Che-Kwan, Wong, Sheila, Yau, Eric Kin-Cheong, Tai, Shuk-Mui, Fung, Eva Lai-Wah, Wu, Nick Shun-Ping, Tsung, Li-Yan, Smeitink, Jan, Chung, Brian Hon-Yin, Fung, Cheuk-Wing

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Meta-Analysis of the Effectiveness of Heart Transplantation in Patients with a Failing Fontan von Tabarsi, Nazlee, MD, Guan, Meijiao, PhD, Simmonds, Jacob, MA, MB, Toma, Mustafa, MD, Kiess, Marla, MD, Tsang, Victor, MBBS, Ruygrok, Peter, MD, Konstantinov, Igor, MD PhD, Shi, William, MBBS, Grewal, Jasmine, MD

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The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes von Yeung, Kit San, Yu, Florrie N. Y., Fung, Cheuk Wing, Wong, Sheila, Lee, Hencher H. C., Fung, Sharon T. H., Fung, Genevieve P. G., Leung, Kwok Yin, Chung, Wai Hang, Lee, Yun Ting, Ng, Vivian K. S., Yu, Mullin H. C., Fung, Jasmine L. F., Tsang, Mandy H. Y., Chan, Kelvin Y. K., Chan, Sophelia H. S., Kan, Anita S. Y., Chung, Brian H. Y.

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Incidence and Outcomes of Acute Kidney Injury in Patients Admitted to Hospital With COVID-19: A Retrospective Cohort Study von Pitre, Tyler, Dong, Angela (Hong Tian), Jones, Aaron, Kapralik, Jessica, Cui, Sonya, Mah, Jasmine, Helmeczi, Wryan, Su, Johnny, Patel, Vivek, Zia, Zaka, Mallender, Michael, Tang, Xinxin, Webb, Cooper, Patro, Nivedh, Junek, Mats, Duong, MyLinh, Ho, Terence, Beauchamp, Marla K., Costa, Andrew P., Kruisselbrink, Rebecca, Tsang, Jennifer L.Y., Walsh, Michael

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Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population von Yu, Mullin Ho Chung, Chan, Marcus Chun Yin, Chung, Claudia Ching Yan, Li, Andrew Wang Tat, Yip, Chara Yin Wa, Mak, Christopher Chun Yu, Chau, Jeffrey Fong Ting, Lee, Mianne, Fung, Jasmine Lee Fong, Tsang, Mandy Ho Yin, Chan, Joshua Chun Ki, Wong, Wilfred Hing Sang, Yang, Jing, Chui, William Chun Ming, Chung, Patrick Ho Yu, Yang, Wanling, Lee, So Lun, Chan, Godfrey Chi Fung, Tam, Paul Kwong Hang, Lau, Yu Lung, Tang, Clara Sze Man, Yeung, Kit San, Chung, Brian Hon Yin

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Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease von Stranger, Barbara E, Brigham, Lori E, Hasz, Richard, Hunter, Marcus, Johns, Christopher, Johnson, Mark, Kopen, Gene, Leinweber, William F, Lonsdale, John T, McDonald, Alisa, Mestichelli, Bernadette, Myer, Kevin, Roe, Brian, Salvatore, Michael, Shad, Saboor, Thomas, Jeffrey A, Walters, Gary, Washington, Michael, Wheeler, Joseph, Bridge, Jason, Foster, Barbara A, Gillard, Bryan M, Karasik, Ellen, Kumar, Rachna, Miklos, Mark, Moser, Michael T, Jewell, Scott D, Montroy, Robert G, Rohrer, Daniel C, Valley, Dana R, Davis, David A, Mash, Deborah C, Gould, Sarah E, Guan, Ping, Koester, Susan, Little, A Roger, Martin, Casey, Moore, Helen M, Rao, Abhi, Struewing, Jeffery P, Volpi, Simona, Hansen, Kasper D, Hickey, Peter F, Rizzardi, Lindsay F, Hou, Lei, Liu, Yaping, Molinie, Benoit, Park, Yongjin, Rinaldi, Nicola, Wang, Li, Van Wittenberghe, Nicholas, Claussnitzer, Melina, Gelfand, Ellen T, Li, Qin, Linder, Sandra, Zhang, Rui, Smith, Kevin S, Tsang, Emily K, Chen, Lin S, Demanelis, Kathryn, Doherty, Jennifer A, Jasmine, Farzana, Kibriya, Muhammad G, Jiang, Lihua, Lin, Shin, Wang, Meng, Jian, Ruiqi, Li, Xiao, Chan, Joanne, Bates, Daniel, Diegel, Morgan, Halow, Jessica, Haugen, Eric, Johnson, Audra, Kaul, Rajinder, Lee, Kristen, Maurano, Matthew T, Nelson, Jemma, Neri, Fidencio J, Sandstrom, Richard, Fernando, Marian S, Linke, Caroline, Oliva, Meritxell, Skol, Andrew, Wu, Fan, Akey, Joshua M, Feinberg, Andrew P, Li, Jin Billy, Pierce, Brandon L, Stamatoyannopoulos, John A, Tang, Hua, Ardlie, Kristin G, Kellis, Manolis, Snyder, Michael P, Montgomery, Stephen B

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Association of CSF and Serum Neurofilament Light and Glial Fibrillary Acidic Protein, Injury Severity, and Outcome in Spinal Cord Injury von Stukas, Sophie, Cooper, Jennifer, Gill, Jasmine, Fallah, Nader, Skinnider, Michael A., Belanger, Lise, Ritchie, Leanna, Tsang, Angela, Dong, Kevin, Streijger, Femke, Street, John, Paquette, Scott, Ailon, Tamir, Dea, Nicolas, Charest-Morin, Raphaele, Fisher, Charles G., Bailey, Christopher S., Dhall, Sanjay, Mac-Thiong, Jean-Marc, Wilson, Jefferson R., Christie, Sean, Dvorak, Marcel F., Wellington, Cheryl L., Kwon, Brian K.

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