المؤلفون: SG10K_Health Consortium, Chan, Sock Hoai, Bylstra, Yasmin, Teo, Jing Xian, Eriksson, Johan G.

المساهمون: Clinicum, Research Programs Unit, Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, HUS Helsinki and Uusimaa Hospital District

مصطلحات موضوعية: 3121 General medicine, internal medicine and other clinical medicine

وصف الملف: application/pdf

العلاقة: This study made use of data collected from the following participating cohorts in Singapore: (1) The Health for Life in Singapore (HELIOS) study at the Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, (2) The Growing Up in Singapore Towards Healthy Outcomes (GUSTO) study jointly hosted by the National University Hospital (NUH), KK Women’s and Children’s Hospital (KKH), the National University of Singapore (NUS) and the Singapore Institute for Clinical Sciences (SICS), Agency for Science Technology and Research (A*STAR), (3) The Singapore Epidemiology of Eye Diseases (SEED) cohort at Singapore Eye Research Institute (SERI), (4) The Multi-Ethnic Cohort (MEC), (5) The SingHealth Duke-NUS Institute of Precision Medicine (PRISM) cohort, (6) The Tan Tock Seng Hospital (TTSH) Personalised Medicine Normal Controls cohort.; SG10K_Health Consortium , Chan , S H , Bylstra , Y , Teo , J X & Eriksson , J G 2022 , ' Analysis of clinically relevant variants from ancestrally diverse Asian genomes ' , Nature Communications , vol. 13 , no. 1 , 6694 . https://doi.org/10.1038/s41467-022-34116-9Test; 85141355514; 072028e6-a6ca-4779-be34-f960f20f2db5; http://hdl.handle.net/10138/571308Test; 000879737500024

الإتاحة: http://hdl.handle.net/10138/571308Test

المؤلفون: Stolarova, Lenka, Kleiblova, Petra, Zemankova, Petra, Stastna, Barbora, Janatova, Marketa, Soukupova, Jana, Achatz, Maria Isabel, Ambrosone, Christine, Apostolou, Paraskevi, Arun, Banu K, Auer, Paul, Barnard, Mollie, Bertelsen, Birgitte, Blok, Marinus J, Boddicker, Nicholas, Brunet, Joan, Burnside, Elizabeth S, Calvello, Mariarosaria, Campbell, Ian, Chan, Sock Hoai, Chen, Fei, Chiang, Jian Bang, Coppa, Anna, Cortesi, Laura, Crujeiras-González, Ana, De Leeneer, Kim, De Putter, Robin, DePersia, Allison, Devereux, Lisa, Domchek, Susan, Efremidis, Anna, Engel, Christoph, Ernst, Corinna, Evans, D Gareth R, Feliubadaló, Lidia, Fostira, Florentia, Fuentes-Ríos, Olivia, Gómez-García, Encarna B, González, Sara, Haiman, Christopher, Hansen, Thomas van Overeem, Hauke, Jan, Hodge, James, Hu, Chunling, Huang, Hongyan, Ishak, Nur Diana Binte, Iwasaki, Yusuke, Konstantopoulou, Irene, Kraft, Peter, Lacey, James, Lázaro, Conxi, Li, Na, Lim, Weng Khong, Lindstrom, Sara, Lori, Adriana, Martinez, Elana, Martins, Alexandra, Matsuda, Koichi, Matullo, Giuseppe, McInerny, Simone, Michailidou, Kyriaki, Montagna, Marco, Monteiro, Alvaro N A, Mori, Luigi, Nathanson, Katherine, Neuhausen, Susan L, Nevanlinna, Heli, Olson, Janet E, Palmer, Julie, Pasini, Barbara, Patel, Alpa, Piane, Maria, Poppe, Bruce, Radice, Paolo, Renieri, Alessandra, Resta, Nicoletta, Richardson, Marcy E, Rosseel, Toon, Ruddy, Kathryn J, Santamariña, Marta, Dos Santos, Elizabeth Santana, Teras, Lauren, Toland, Amanda E, Trentham-Dietz, Amy, Vachon, Celine M, Volk, Alexander E, Weber-Lassalle, Nana, Weitzel, Jeffrey N, Wiesmuller, Lisa, Winham, Stacey, Yadav, Siddhartha, Yannoukakos, Drakoulis, Yao, Song, Zampiga, Valentina, Zethoven, Magnus, Zhang, Ze Wen, Zima, Tomas, Spurdle, Amanda B, Vega, Ana, Rossing, Maria, Del Valle, Jesús, De Nicolo, Arcangela, Hahnen, Eric, Claes, Kathleen B M, Ngeow, Joanne, Momozawa, Yukihide, James, Paul A, Couch, Fergus J, Macurek, Libor, Kleibl, Zdenek

المساهمون: Stolarova, Lenka, Kleiblova, Petra, Zemankova, Petra, Stastna, Barbora, Janatova, Marketa, Soukupova, Jana, Achatz, Maria Isabel, Ambrosone, Christine, Apostolou, Paraskevi, Arun, Banu K, Auer, Paul, Barnard, Mollie, Bertelsen, Birgitte, Blok, Marinus J, Boddicker, Nichola, Brunet, Joan, Burnside, Elizabeth S, Calvello, Mariarosaria, Campbell, Ian, Chan, Sock Hoai, Chen, Fei, Chiang, Jian Bang, Coppa, Anna, Cortesi, Laura, Crujeiras-González, Ana, De Leeneer, Kim, De Putter, Robin, Depersia, Allison, Devereux, Lisa, Domchek, Susan, Efremidis, Anna, Engel, Christoph, Ernst, Corinna, Evans, D Gareth R, Feliubadaló, Lidia, Fostira, Florentia, Fuentes-Ríos, Olivia, Gómez-García, Encarna B, González, Sara, Haiman, Christopher, Hansen, Thomas van Overeem, Hauke, Jan, Hodge, Jame, Hu, Chunling, Huang, Hongyan, Ishak, Nur Diana Binte, Iwasaki, Yusuke, Konstantopoulou, Irene, Kraft, Peter, Lacey, Jame, Lázaro, Conxi, Li, Na, Lim, Weng Khong, Lindstrom, Sara, Lori, Adriana, Martinez, Elana, Martins, Alexandra, Matsuda, Koichi, Matullo, Giuseppe, Mcinerny, Simone, Michailidou, Kyriaki, Montagna, Marco, Monteiro, Alvaro N A, Mori, Luigi, Nathanson, Katherine, Neuhausen, Susan L, Nevanlinna, Heli, Olson, Janet E, Palmer, Julie, Pasini, Barbara, Patel, Alpa, Piane, Maria, Poppe, Bruce, Radice, Paolo, Renieri, Alessandra, Resta, Nicoletta, Richardson, Marcy E, Rosseel, Toon, Ruddy, Kathryn J, Santamariña, Marta, Dos Santos, Elizabeth Santana, Teras, Lauren, Toland, Amanda E, Trentham-Dietz, Amy, Vachon, Celine M, Volk, Alexander E, Weber-Lassalle, Nana, Weitzel, Jeffrey N, Wiesmuller, Lisa, Winham, Stacey, Yadav, Siddhartha, Yannoukakos, Drakouli, Yao, Song, Zampiga, Valentina, Zethoven, Magnu, Zhang, Ze Wen, Zima, Toma, Spurdle, Amanda B, Vega, Ana, Rossing, Maria

مصطلحات موضوعية: chek2, breast cancer, germline missense variants

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37449874; info:eu-repo/semantics/altIdentifier/wos/WOS:001053492300001; volume:29; issue:16; firstpage:1; lastpage:14; numberofpages:14; journal:CLINICAL CANCER RESEARCH; https://hdl.handle.net/11573/1685106Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85168222787

الإتاحة: https://doi.org/10.1158/1078-0432.CCR-23-0212Test
https://hdl.handle.net/11573/1685106Test

المؤلفون: Zhang, Zewen, Nur Diana Binte Ishak, Que, Frances Victoria Fajardo, Chua, Zi Yang, Chan, Sock Hoai, Chiang, Jianbang, Ngeow, Joanne

المساهمون: Lee Kong Chian School of Medicine (LKCMedicine), National Cancer Centre, Singapore

مصطلحات موضوعية: Science::Medicine, Genetics, Vaccination

وصف الملف: application/pdf

العلاقة: Hereditary Cancer in Clinical Practice; Zhang, Z., Nur Diana Binte Ishak, Que, F. V. F., Chua, Z. Y., Chan, S. H., Chiang, J. & Ngeow, J. (2023). COVID-19 vaccination uptake and safety profile among germline BRCA1 and BRCA2 pathogenic variant carriers in Singapore. Hereditary Cancer in Clinical Practice, 21(1), 5-. https://dx.doi.org/10.1186/s13053-023-00248-2Test; https://hdl.handle.net/10356/169681Test; 2-s2.0-85153228270; 21

الإتاحة: https://doi.org/10.1186/s13053-023-00248-2Test
https://hdl.handle.net/10356/169681Test

المؤلفون: Chan, Jason Yongsheng, Loh, Jui Wan, Lim, Jing Quan, Liany, Herty, Lee, Elizabeth Chun Yong, Lee, Jing Yi, Kannan, Bavani, Lim, Boon Yee, Guo, Zexi, Lim, Kerry, Ha, Jeslin Chian Hung, Ng, Cedric Chuan-Young, Ko, Tun Kiat, Huang, Dachuan, Seow, Dominique Yuan Bin, Cheng, Chee Leong, Chan, Sock Hoai, Ngeow, Joanne, Teh, Bin Tean, Lim, Soon Thye, Ong, Choon Kiat

المصدر: Blood; May 2024, Vol. 143 Issue: 18 p1837-1844, 8p

المؤلفون: Kam, Michelle Li Wei, Chong, Siao Ting, Chan, Sock Hoai, Swigris, Jeffrey J., Chew, Ee Ling, Tan, Yi Hern, Ngeow, Joanne Yuen Yie, Low, Su Ying

المصدر: Respiratory Investigation; May 2024, Vol. 62 Issue: 3 p348-355, 8p

المؤلفون: Soon, Jonathan Jian Hao, Chan, Sock Hoai, Tan, Daniel Shao Weng, Ngeow, Joanne, Chiang, Jianbang

المساهمون: Lee Kong Chian School of Medicine (LKCMedicine), National Cancer Centre, Singapore, Duke-NUS Medical School, Institute of Molecular and Cellular Biology, A*STAR

مصطلحات موضوعية: Science::Medicine, Chronic Lung Disease, Lung Adenocarcinoma

وصف الملف: application/pdf

العلاقة: Cold Spring Harbor Molecular Case Studies; Soon, J. J. H., Chan, S. H., Tan, D. S. W., Ngeow, J. & Chiang, J. (2022). Case report: olaparib use in metastatic lung adenocarcinoma with BRCA2 pathogenic variant. Cold Spring Harbor Molecular Case Studies, 8(7), a006223-. https://dx.doi.org/10.1101/mcs.a006223Test; https://hdl.handle.net/10356/169833Test; 2-s2.0-85145050982; a006223

الإتاحة: https://doi.org/10.1101/mcs.a006223Test
https://hdl.handle.net/10356/169833Test

المؤلفون: Chan, Sock Hoai, Bylstra, Yasmin, Teo, Jing Xian, Kuan, Jyn Ling, Bertin, Nicolas, Gonzalez-Porta, Mar, Hebrard, Maxime, Tirado-Magallanes, Roberto, Tan, Joanna Hui Juan, Jeyakani, Justin, Li, Zhihui, Chai, Jin Fang, Chong, Yap Seng, Davila, Sonia, Goh, Liuh Ling, Lee, Eng Sing, Wong, Eleanor, Wong, Tien Yin, Prabhakar, Shyam, Liu, Jianjun, Cheng, Ching-Yu, Eisenhaber, Birgit, Karnani, Neerja, Leong, Khai Pang, Sim, Xueling, Yeo, Khung Keong, Chambers, John Campbell, Tai, E-Shyong, Tan, Patrick, Jamuar, Saumya S., Ngeow, Joanne, Lim, Weng Khong

المساهمون: Lee Kong Chian School of Medicine (LKCMedicine), National Cancer Centre Singapore, Duke-NUS Medical School, National Healthcare Group Polyclinics, Precision Health Research Singapore (PRECISE), Institute of Molecular and Cellular Biology, A*STAR

مصطلحات موضوعية: Science::Medicine, Epidemiology, Genetic Variation

وصف الملف: application/pdf

العلاقة: IAF-PP: H17/01/ a0/007; NMRC/STaR/0028/2017; IAF-PP: H18/01/a0/016; NMRC/TCR/004-NUS/2008; NMRC/TCR/ 012-NUHS/2014; IAF-PP: H17/01/a0/005; NMRC/CIRG/1417/2015; NMRC/CIRG/ 1488/2018; NMRC/OFLCG/004/2018; NMRC-0838/2004; BMRC (03/1/27/18/216, 05/1/21/19/425, 11/1/21/19/678); NMRC/CG/M006/2017_NHCS; NMRC/STaR/ 0011/2012; NMRC/STaR/0026/2015; 05/FY2020/EX/06-A41; NMRC/CG12AUG2017; CGAug16M012.G (MOH-000588); NMRC/CSA-INV/0017/2017; MOH000654; CSAINV21Jun-0003; NMRC/CSA-SI/0012/2017; Nature Communications; Chan, S. H., Bylstra, Y., Teo, J. X., Kuan, J. L., Bertin, N., Gonzalez-Porta, M., Hebrard, M., Tirado-Magallanes, R., Tan, J. H. J., Jeyakani, J., Li, Z., Chai, J. F., Chong, Y. S., Davila, S., Goh, L. L., Lee, E. S., Wong, E., Wong, T. Y., Prabhakar, S., .Lim, W. K. (2022). Analysis of clinically relevant variants from ancestrally diverse Asian genomes. Nature Communications, 13(1), 6694-. https://dx.doi.org/10.1038/s41467-022-34116-9Test; https://hdl.handle.net/10356/168639Test; 2-s2.0-85141355514; 13; 6694

الإتاحة: https://doi.org/10.1038/s41467-022-34116-9Test
https://hdl.handle.net/10356/168639Test

المؤلفون: Li, Longjie, Kolinjivadi, Arun Mouli, Ong, Kok Haur, Young, David M., Marini, Gabriel Pik Liang, Chan, Sock Hoai, Chong, Siao Ting, Chew, Ee Ling, Lu, Haoda, Gole, Laurent, Yu, Weimiao, Ngeow, Joanne

المساهمون: Lee Kong Chian School of Medicine (LKCMedicine)

مصطلحات موضوعية: Science::Medicine, Sofware, Replication

وصف الملف: application/pdf

العلاقة: NMRC/CSA-INV/0017/2017; MOH-000654; 2019-T1-001-018; Bioinformatics; Li, L., Kolinjivadi, A. M., Ong, K. H., Young, D. M., Marini, G. P. L., Chan, S. H., Chong, S. T., Chew, E. L., Lu, H., Gole, L., Yu, W. & Ngeow, J. (2022). Automatic DNA replication tract measurement to assess replication and repair dynamics at the single-molecule level. Bioinformatics, 38(18), 4395-4402. https://dx.doi.org/10.1093/bioinformatics/btac533Test; https://hdl.handle.net/10356/164980Test; 2-s2.0-85141891108; 18; 38; 4395; 4402

الإتاحة: https://doi.org/10.1093/bioinformatics/btac533Test
https://hdl.handle.net/10356/164980Test

المؤلفون: Bylstra, Yasmin, Lim, Weng Khong, Kam, Sylvia, Tham, Koei Wan, Wu, R. Ryanne, Teo, Jing Xian, Davila, Sonia, Kuan, Jyn Ling, Chan, Sock Hoai, Bertin, Nicolas, Yang, Cheng Xi, Rozen, Steve, Teh, Bin Tean, Yeo, Khung Keong, Cook, Stuart Alexander, Jamuar, Saumya Shekhar, Ginsburg, Geoffrey S., Orlando, Lori A., Tan, Patrick

المساهمون: DUKE-NUS MEDICAL SCHOOL, DEAN'S OFFICE (DUKE-NUS MEDICAL SCHOOL), DEPT OF MEDICINE, CANCER SCIENCE INSTITUTE OF SINGAPORE, PHYSIOLOGY

المصدر: Scopus OA2021

مصطلحات موضوعية: Cancer, Clinically actionable variants, Family history, Population genomics screening

العلاقة: Bylstra, Yasmin, Lim, Weng Khong, Kam, Sylvia, Tham, Koei Wan, Wu, R. Ryanne, Teo, Jing Xian, Davila, Sonia, Kuan, Jyn Ling, Chan, Sock Hoai, Bertin, Nicolas, Yang, Cheng Xi, Rozen, Steve, Teh, Bin Tean, Yeo, Khung Keong, Cook, Stuart Alexander, Jamuar, Saumya Shekhar, Ginsburg, Geoffrey S., Orlando, Lori A., Tan, Patrick (2021-01-07). Family history assessment significantly enhances delivery of precision medicine in the genomics era. Genome Medicine 13 (1) : 3. ScholarBank@NUS Repository. https://doi.org/10.1186/s13073-020-00819-1Test; https://scholarbank.nus.edu.sg/handle/10635/233608Test

الإتاحة: https://doi.org/10.1186/s13073-020-00819-1Test
https://scholarbank.nus.edu.sg/handle/10635/233608Test

المؤلفون: Chan, Sock Hoai, Chiang, Jianbang, Ngeow, Joanne

المساهمون: National Medical Research Council

المصدر: Hereditary Cancer in Clinical Practice ; volume 19, issue 1 ; ISSN 1897-4287

مصطلحات موضوعية: Genetics (clinical), Oncology

الإتاحة: https://doi.org/10.1186/s13053-021-00178-xTest