Solving Glycosylation Disorders: Fundamental Approaches Reveal Complicated Pathways
Freeze, Hudson H., Chong, Jessica X., Bamshad, Michael J., Ng, Bobby G.
Published in American journal of human genetics (06.02.2014)
Published in American journal of human genetics (06.02.2014)
Get full text
Journal Article
A New SITA Perimetric Threshold Testing Algorithm: Construction and a Multicenter Clinical Study
Heijl, Anders, Patella, Vincent Michael, Chong, Luke X., Iwase, Aiko, Leung, Christopher K., Tuulonen, Anja, Lee, Gary C., Callan, Thomas, Bengtsson, Boel
Published in American journal of ophthalmology (01.02.2019)
Published in American journal of ophthalmology (01.02.2019)
Get full text
Journal Article
Seed‐borne endophytic Bacillus velezensis LHSB1 mediate the biocontrol of peanut stem rot caused by Sclerotium rolfsii
Chen, L., Wu, Y.D., Chong, X.Y., Xin, Q.H., Wang, D.X., Bian, K.
Published in Journal of applied microbiology (01.03.2020)
Published in Journal of applied microbiology (01.03.2020)
Get full text
Journal Article
Mosaicism of the UDP-Galactose Transporter SLC35A2 Causes a Congenital Disorder of Glycosylation
Ng, Bobby G., Buckingham, Kati J., Raymond, Kimiyo, Kircher, Martin, Turner, Emily H., He, Miao, Smith, Joshua D., Eroshkin, Alexey, Szybowska, Marta, Losfeld, Marie E., Chong, Jessica X., Kozenko, Mariya, Li, Chumei, Patterson, Marc C., Gilbert, Rodney D., Nickerson, Deborah A., Shendure, Jay, Bamshad, Michael J., Freeze, Hudson H.
Published in American journal of human genetics (04.04.2013)
Published in American journal of human genetics (04.04.2013)
Get full text
Journal Article
Virtual simulated international placements as an innovation for internationalisation in undergraduate programs: a mixed methods study
Edgar, Amanda K, Armitage, James A, Arambewela-Colley, Nadeeka, Chong, Luke X, Narayanan, Anuradha
Published in BMC medical education (19.04.2023)
Published in BMC medical education (19.04.2023)
Get full text
Journal Article
Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results
Tabor, Holly K., Auer, Paul L., Jamal, Seema M., Chong, Jessica X., Yu, Joon-Ho, Gordon, Adam S., Graubert, Timothy A., O’Donnell, Christopher J., Rich, Stephen S., Nickerson, Deborah A., Bamshad, Michael J.
Published in American journal of human genetics (07.08.2014)
Published in American journal of human genetics (07.08.2014)
Get full text
Journal Article
Recessive Inactivating Mutations in TBCK, Encoding a Rab GTPase-Activating Protein, Cause Severe Infantile Syndromic Encephalopathy
Chong, Jessica X., Caputo, Viviana, Phelps, Ian G., Stella, Lorenzo, Worgan, Lisa, Dempsey, Jennifer C., Nguyen, Alina, Leuzzi, Vincenzo, Webster, Richard, Pizzuti, Antonio, Marvin, Colby T., Ishak, Gisele E., Ardern-Holmes, Simone, Richmond, Zara, Bamshad, Michael J., Ortiz-Gonzalez, Xilma R., Tartaglia, Marco, Chopra, Maya, Doherty, Dan
Published in American journal of human genetics (07.04.2016)
Published in American journal of human genetics (07.04.2016)
Get full text
Journal Article
Tectonics of the Solomon Sea Basin from Vertical Gravity Gradient and Seismic Data
GONG, Wei, XING, Junhui, MENG, Qingwei, XING, Lei, XU, Chong, ZHANG, Hao
Published in Acta geologica Sinica (Beijing) (01.04.2023)
Published in Acta geologica Sinica (Beijing) (01.04.2023)
Get full text
Journal Article
Pre-operative erector spinae plane block should be considered a viable option for laparoscopic colectomies
Wan, Fang-Ting, Chin, Shuen-Ern, Gwee, Ryan, Chong, Yvette, Au-Yong, Angie, Matthews, Abey, Zaw, Ma-Wai-Wai, Lie, Sui-An, Loh, Leonard, Koh, Daphne, Ladlad, Jasmine, Khoo, Nathanelle, Aw, Darius, Chong, Cheryl X. Z., Ho, Leonard M. L., Ng, Jia-Lin, Sivarajah, Sharmini S., Tan, Winson J., Foo, Fung-Joon, Koh, Frederick H.
Published in Surgical endoscopy (01.09.2023)
Published in Surgical endoscopy (01.09.2023)
Get full text
Journal Article
Congenital myasthenic syndrome secondary to pathogenic variants in the SLC5A7 gene: report of two cases
Muntadas, Javier A, Hyland, Martin R, Martínez, Maria Del Rosario Ortolá, Young, Jaime N, Chong, Jessica X, Bamshad, Michael J, Maselli, Ricardo A
Published in BMC medical genomics (12.08.2024)
Published in BMC medical genomics (12.08.2024)
Get full text
Journal Article
Recessive TRAPPC11 Mutations Cause a Disease Spectrum of Limb Girdle Muscular Dystrophy and Myopathy with Movement Disorder and Intellectual Disability
Bögershausen, Nina, Shahrzad, Nassim, Chong, Jessica X., von Kleist-Retzow, Jürgen-Christoph, Stanga, Daniela, Li, Yun, Bernier, Francois P., Loucks, Catrina M., Wirth, Radu, Puffenberger, Eric G., Hegele, Robert A., Schreml, Julia, Lapointe, Gabriel, Keupp, Katharina, Brett, Christopher L., Anderson, Rebecca, Hahn, Andreas, Innes, A. Micheil, Suchowersky, Oksana, Mets, Marilyn B., Nürnberg, Gudrun, McLeod, D. Ross, Thiele, Holger, Waggoner, Darrel, Altmüller, Janine, Boycott, Kym M., Schoser, Benedikt, Nürnberg, Peter, Ober, Carole, Heller, Raoul, Parboosingh, Jillian S., Wollnik, Bernd, Sacher, Michael, Lamont, Ryan E.
Published in American journal of human genetics (11.07.2013)
Published in American journal of human genetics (11.07.2013)
Get full text
Journal Article
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13
ALISKAN, Minal C, CHONG, Jessica X, MATERN, Dietrich, DAS, Soma, WAGGONER, Darrel, NICOLAE, Dan L, OBERL, Carole, URICCHIO, Lawrence, ANDERSON, Rebecca, PEIXIAN CHEN, SOUGNEZ, Carrie, GARIMELLA, Kiran, GABRIEL, Stacey B, DEPRISTO, Mark A, SHAKIR, Khalid
Published in Human molecular genetics (01.04.2011)
Published in Human molecular genetics (01.04.2011)
Get full text
Journal Article
Matchmaker Exchange
Sobreira, Nara L M, Arachchi, Harindra, Buske, Orion J, Chong, Jessica X, Hutton, Ben, Foreman, Julia, Schiettecatte, François, Groza, Tudor, Jacobsen, Julius O B, Haendel, Melissa A, Boycott, Kym M, Hamosh, Ada, Rehm, Heidi L
Published in Current protocols in human genetics (01.10.2017)
Published in Current protocols in human genetics (01.10.2017)
Get more information
Journal Article