Zejuan Li lab Publications


Cell-free DNA 5-hydroxymethylcytosine is highly sensitive for MRD assessment in acute myeloid leukemia
Shao, J, Shah, S, Ganguly, S, Zu, Y, He, C & Li, Z 2023, , Clinical Epigenetics, vol. 15, no. 1, 134. https://doi.org/10.1186/s13148-023-01547-0

TET2-mediated mRNA demethylation regulates leukemia stem cell homing and self-renewal
Li, Y, Xue, M, Deng, X, Dong, L, Nguyen, LXT, Ren, L, Han, L, Li, C, Xue, J, Zhao, Z, Li, W, Qing, Y, Shen, C, Tan, B, Chen, Z, Leung, K, Wang, K, Swaminathan, S, Li, L, Wunderlich, M, Mulloy, JC, Li, X, Chen, H, Zhang, B, Horne, D, Rosen, ST, Marcucci, G, Xu, M, Li, Z, Wei, M, Tian, J, Shen, B, Su, R & Chen, J 2023, , Cell Stem Cell, vol. 30, no. 8, pp. 1072-1090.e10. https://doi.org/10.1016/j.stem.2023.07.001

Classification of Acute Myeloid Leukemia by Cell-Free DNA 5-Hydroxymethylcytosine
Shao, J, Shah, S, Ganguly, S, Zu, Y, He, C & Li, Z 2023, , Genes, vol. 14, no. 6, 1180. https://doi.org/10.3390/genes14061180

Cell-free DNA 5-hydroxymethylcytosine as a marker for common cancer detection
Shao, J, Bernicker, EH, He, C & Li, Z 2022, , Clinical and Translational Discovery, vol. 2, no. 4, e136. https://doi.org/10.1002/ctd2.136

Cell-free DNA 5-hydroxymethylcytosine as a marker for common cancer detection
Shao, J, Bernicker, EH, He, C & Li, Z 2022, , Clinical and Translational Discovery, vol. 2, no. 4, e136. https://doi.org/10.1002/ctd2.136

Revision of RUNX1 variant curation rules
the Myeloid Malignancy Variant Curation Expert Panel 2022, , Blood Advances, vol. 6, no. 16, pp. 4726-4730. https://doi.org/10.1182/bloodadvances.2022008017

Exome sequencing identifies PD-L2 as a potential predisposition gene for lymphoma
Shao, J, Gao, L, Leung, ML, Gallinger, B, Inglese, C, Meyn, MS, Del Gaudio, D, Das, S & Li, Z 2022, , Hematological Oncology, vol. 40, no. 3, pp. 475-478. https://doi.org/10.1002/hon.3033

Cell-free DNA 5-hydroxymethylcytosine is an emerging marker of acute myeloid leukemia
Shao, J, Wang, S, West-Szymanski, D, Karpus, J, Shah, S, Ganguly, S, Smith, J, Zu, Y, He, C & Li, Z 2022, , Scientific Reports, vol. 12, no. 1, 12410, pp. 12410. https://doi.org/10.1038/s41598-022-16685-3

Prognostic value of KIT and other clonal genetic mutations in core-binding factor acute myeloid leukemia
Wu, TM, Xue, SL, Li, Z, Yu, JQ, Wang, J, Wang, BR, Wan, CL, Shen, XD, Qiu, QC, Bao, XB & Wu, DP 2021, , Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, vol. 42, no. 8, pp. 646-653. https://doi.org/10.3760/cma.j.issn.0253-2727.2021.08.006

Prognostic value of KIT and other clonal genetic mutations in core-binding factor acute myeloid leukemia
Wu, TM, Xue, SL, Li, Z, Yu, JQ, Wang, J, Wang, BR, Wan, CL, Shen, XD, Qiu, QC, Bao, XB & Wu, DP 2021, , Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, vol. 42, no. 8, pp. 646-653. https://doi.org/10.3760/cma.j.issn.0253-2727.2021.08.006

R-2-hydroxyglutarate attenuates aerobic glycolysis in leukemia by targeting the FTO/m6A/PFKP/LDHB axis
Qing, Y, Dong, L, Gao, L, Li, C, Li, Y, Han, L, Prince, E, Tan, B, Deng, X, Wetzel, C, Shen, C, Gao, M, Chen, Z, Li, W, Zhang, B, Braas, D, ten Hoeve, J, Sanchez, GJ, Chen, H, Chan, LN, Chen, CW, Ann, D, Jiang, L, Müschen, M, Marcucci, G, Plas, DR, Li, Z, Su, R & Chen, J 2021, , Molecular Cell, vol. 81, no. 5, pp. 922-939.e9. https://doi.org/10.1016/j.molcel.2020.12.026

Identifying possible germline variants from tumor-only sequencing of hematological malignancies
Shao, J, Subedi, S, Pepper, K, Badgett, S, Christensen, PA, Hendrickson, HL, Thomas, JS, Olsen, RJ & Li, Z 2021, , Leukemia and Lymphoma, vol. 62, no. 2, pp. 482-485. https://doi.org/10.1080/10428194.2020.1832665

Germline variants drive myelodysplastic syndrome in young adults
Feurstein, S, Churpek, JE, Walsh, T, Keel, S, Hakkarainen, M, Schroeder, T, Germing, U, Geyh, S, Heuser, M, Thol, F, Pohlkamp, C, Haferlach, T, Gao, J, Owen, C, Goehring, G, Schlegelberger, B, Verma, D, Krause, DS, Gao, G, Cronin, T, Gulsuner, S, Lee, M, Pritchard, CC, Subramanian, HP, del Gaudio, D, Li, Z, Das, S, Kilpivaara, O, Wartiovaara-Kautto, U, Wang, ES, Griffiths, EA, Döhner, K, Döhner, H, King, MC & Godley, LA 2021, , Leukemia, vol. 35, no. 8, pp. 2439-2444. https://doi.org/10.1038/s41375-021-01137-0

Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentations
Feurstein, S, Adegunsoye, A, Mojsilovic, D, Vij, R, West DePersia, AH, Rajagopal, PS, Osman, A, Collins, RH, Kim, RH, Gore, SD, Greenberg, P, Godley, LA, Li, Z, Del Gaudio, D, Subramanian, HP, Das, S, Walsh, T, Gulsuner, S, Segal, JP, Husain, AN, Gurbuxani, S, King, MC, Strek, ME & Churpek, JE 2020, , Blood Advances, vol. 4, no. 19, pp. 4883-4886. https://doi.org/10.1182/BLOODADVANCES.2020001721

Targeting FTO Suppresses Cancer Stem Cell Maintenance and Immune Evasion
Su, R, Dong, L, Li, Y, Gao, M, Han, L, Wunderlich, M, Deng, X, Li, H, Huang, Y, Gao, L, Li, C, Zhao, Z, Robinson, S, Tan, B, Qing, Y, Qin, X, Prince, E, Xie, J, Qin, H, Li, W, Shen, C, Sun, J, Kulkarni, P, Weng, H, Huang, H, Chen, Z, Zhang, B, Wu, X, Olsen, MJ, Müschen, M, Marcucci, G, Salgia, R, Li, L, Fathi, AT, Li, Z, Mulloy, JC, Wei, M, Horne, D & Chen, J 2020, , Cancer Cell, vol. 38, no. 1, pp. 79-96.e11. https://doi.org/10.1016/j.ccell.2020.04.017

Development and validation of Houston Methodist Variant Viewer version 3: Updates to our application for interpretation of next-generation sequencing data
Christensen, PA, Subedi, S, Pepper, K, Hendrickson, HL, Li, Z, Thomas, JS, Wesley Long, S & Olsen, RJ 2020, , JAMIA Open, vol. 3, no. 2, pp. 299-305. https://doi.org/10.1093/jamiaopen/ooaa004

ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants
Luo, X, Feurstein, S, Mohan, S, Porter, CC, Jackson, SA, Keel, S, Chicka, M, Brown, AL, Kesserwan, C, Agarwal, A, Luo, M, Li, Z, Ross, JE, Baliakas, P, Pineda-Alvarez, D, DiNardo, CD, Bertuch, AA, Mehta, N, Vulliamy, T, Wang, Y, Nichols, KE, Malcovati, L, Walsh, MF, Rawlings, LH, McWeeney, SK, Soulier, J, Raimbault, A, Routbort, MJ, Zhang, L, Ryan, G, Speck, NA, Plon, SE, Wu, D & Godley, LA 2019, , Blood Advances, vol. 3, no. 20, pp. 2962-2979. https://doi.org/10.1182/bloodadvances.2019000644

Somatic mutation panels: Time to clear their names
Trottier, AM, Cavalcante de Andrade Silva, M, Li, Z & Godley, LA 2019, , Cancer Genetics, vol. 235-236, pp. 84-92. https://doi.org/10.1016/j.cancergen.2019.04.065

Targeted exome analysis identifies the genetic basis of disease in over 50% of patients with a wide range of ataxia-related phenotypes
Sun, M, Johnson, AK, Nelakuditi, V, Guidugli, L, Fischer, D, Arndt, K, Ma, L, Sandford, E, Shakkottai, V, Boycott, K, Chardon, JW, Li, Z, del Gaudio, D, Burmeister, M, Gomez, CM, Waggoner, DJ & Das, S 2019, , Genetics in Medicine, vol. 21, no. 1, pp. 195-206. https://doi.org/10.1038/s41436-018-0007-7

Frequency of germline mutations in cancer susceptibility genes in malignant mesothelioma
Panou, V, Gadiraju, M, Wolin, A, Weipert, CM, Skarda, E, Husain, AN, Patel, JD, Rose, B, Zhang, SR, Weatherly, M, Nelakuditi, V, Johnson, AK, Helgeson, M, Fischer, D, Desai, A, Sulai, N, Ritterhouse, L, Røe, OD, Turaga, KK, Huo, D, Segal, J, Kadri, S, Li, Z, Kindler, HL & Churpek, JE 2018, , Journal of Clinical Oncology, vol. 36, no. 28, pp. 2863-2871. https://doi.org/10.1200/JCO.2018.78.5204