Year |
Citation |
Score |
2020 |
Abel MK, Brabham CE, Guo R, Fahrner-Scott K, Wong J, Alvarado M, Ewing C, Esserman LJ, Mukhtar RA. Breast conservation therapy versus mastectomy in the surgical management of invasive lobular carcinoma measuring 4 cm or greater. American Journal of Surgery. PMID 32622509 DOI: 10.1016/J.Amjsurg.2020.05.038 |
0.305 |
|
2020 |
Rosenberger LH, Thomas SM, Nimbkar SN, Hieken TJ, Ludwig KK, Jacobs LK, Miller ME, Gallagher KK, Wong J, Neuman HB, Tseng J, Hassinger TE, Jakub JW. Germline Genetic Mutations in a Multi-center Contemporary Cohort of 550 Phyllodes Tumors: An Opportunity for Expanded Multi-gene Panel Testing. Annals of Surgical Oncology. PMID 32504368 DOI: 10.1245/S10434-020-08480-Z |
0.313 |
|
2020 |
Zambetti NA, Firestone AJ, Remsberg JR, Huang BJ, Wong JC, Long AM, Predovic M, Suciu RM, Inguva A, Kogan SC, Haigis KM, Cravatt BF, Shannon K. Genetic disruption of N-RasG12D palmitoylation perturbs hematopoiesis and prevents myeloid transformation in mice. Blood. PMID 32219446 DOI: 10.1182/Blood.2019003530 |
0.348 |
|
2020 |
Zambetti NA, Firestone AJ, Wong JC, Long AM, Inguva A, Remsberg JR, Suciu RM, Cravatt BF, Haigis KM, Shannon K. Abstract A25: In vivo evidence validating the palmitoylation/depalmitoylation cycle as a therapeutic target in NRAS mutant hematologic cancers Molecular Cancer Research. 18. DOI: 10.1158/1557-3125.Ras18-A25 |
0.346 |
|
2020 |
Wei JM, Kim P, Ewing C, Wong J, Esserman LJ, Alvarado MD, Olusanya AO, Stewart S, Tydon A, Daroui P, Kuo JV, Park HL, Lane KT, Jeong E, Brown K, et al. Abstract OT3-09-01: Use of Oncotype DX DCIS for disease management in a prospective DCIS registry Cancer Research. 80. DOI: 10.1158/1538-7445.Sabcs19-Ot3-09-01 |
0.32 |
|
2019 |
Huang BJ, Wandler AM, Meyer LK, Dail M, Daemen A, Sampath D, Li Q, Wang X, Wong JC, Nakitandwe J, Downing JR, Zhang J, Taylor BS, Shannon K. Convergent genetic aberrations in murine and human T lineage acute lymphoblastic leukemias. Plos Genetics. 15: e1008168. PMID 31199785 DOI: 10.1371/Journal.Pgen.1008168 |
0.399 |
|
2018 |
Wong JC, Bryant V, Lamprecht T, Ma J, Walsh M, Schwartz J, Del Pilar Alzamora M, Mullighan CG, Loh ML, Ribeiro R, Downing JR, Carroll WL, Davis J, Gold S, Rogers PC, et al. Germline SAMD9 and SAMD9L mutations are associated with extensive genetic evolution and diverse hematologic outcomes. Jci Insight. 3. PMID 30046003 DOI: 10.1172/Jci.Insight.121086 |
0.34 |
|
2018 |
Varghese F, Wong J. Breast Cancer in the Elderly. The Surgical Clinics of North America. 98: 819-833. PMID 30005776 DOI: 10.1016/J.Suc.2018.04.002 |
0.319 |
|
2018 |
Bryant V, Wong J, Schwartz J, Lamprecht T, Ma J, Mullighan C, Loh M, Shannon K, Klco J. Abstract 2063: SAMD9/SAMD9L mutations in familial monosomy 7 Cancer Research. 78: 2063-2063. DOI: 10.1158/1538-7445.Am2018-2063 |
0.329 |
|
2016 |
Campbell MJ, Baehner F, O'Meara T, Ojukwu E, Han B, Mukhtar R, Tandon V, Endicott M, Zhu Z, Wong J, Krings G, Au A, Gray JW, Esserman L. Characterizing the immune microenvironment in high-risk ductal carcinoma in situ of the breast. Breast Cancer Research and Treatment. PMID 27785654 DOI: 10.1007/S10549-016-4036-0 |
0.31 |
|
2016 |
Wandler AM, Huang B, Scacchetti A, Craig J, Yan H, Monsalve G, Li Q, Dail M, Wong JC, Nakitandwe J, Weinberg O, Hasserjian RP, Kogan SC, Sampath D, Downing JR, et al. Resistant T-Cell Acute Lymphoblastic Leukemias That Emerge after In Vivo Treatment with Dexamethasone Frequently Down-Regulate Glucocorticoid Receptor Protein Expression Blood. 128: 753-753. DOI: 10.1182/Blood.V128.22.753.753 |
0.315 |
|
2015 |
Price ER, Wong J, Mukhtar R, Hylton N, Esserman LJ. How to use magnetic resonance imaging following neoadjuvant chemotherapy in locally advanced breast cancer. World Journal of Clinical Cases. 3: 607-13. PMID 26244152 DOI: 10.12998/Wjcc.V3.I7.607 |
0.3 |
|
2015 |
Wong JC, Weinfurtner KM, Alzamora MD, Kogan SC, Burgess MR, Zhang Y, Nakitandwe J, Ma J, Cheng J, Chen SC, Ho TT, Flach J, Reynaud D, Passegué E, Downing JR, et al. Functional evidence implicating chromosome 7q22 haploinsufficiency in myelodysplastic syndrome pathogenesis. Elife. 4. PMID 26193121 DOI: 10.7554/Elife.07839 |
0.367 |
|
2014 |
Wong JC, Weinfurtner K, Alzamora P, Kogan SC, Burgess MR, Zhang Y, Nakitandwe J, Ma J, Cheng J, Chen S, Flach J, Reynaud D, Passegue E, Downing JR, Shannon K. Aberrant Hematopoietic Stem Cell Function in Mice Haploinsufficient for a 2 Mb Deletion of Chromosome 5A3 Syntenic to a Region of Human 7q22 Frequently Deleted in Myelodysplastic Syndromes Blood. 124: 3247-3247. DOI: 10.1182/Blood.V124.21.3247.3247 |
0.388 |
|
2011 |
Wong JC, Weinfurtner K, Zhang Y, Alzamora P, Hwang E, Kogan SC, Shannon KM. Heterozygous Germ Line Deletion of a 2Mb Interval in Mice That Models Loss of 7q22 in Human Myeloid Malignancies Results in Defective Hematopoietic Stem Cell Function Reminiscent of Premature Aging Blood. 118: 2340-2340. DOI: 10.1182/Blood.V118.21.2340.2340 |
0.321 |
|
2009 |
Zhang Y, Wong J, Klinger M, Tran MT, Shannon KM, Killeen N. MLL5 contributes to hematopoietic stem cell fitness and homeostasis. Blood. 113: 1455-63. PMID 18818388 DOI: 10.1182/Blood-2008-05-159905 |
0.406 |
|
2008 |
Wong JC, Le Beau MM, Shannon K. Tumor suppressor gene inactivation in myeloid malignancies. Best Practice & Research. Clinical Haematology. 21: 601-14. PMID 19041599 DOI: 10.1016/J.Beha.2008.09.001 |
0.383 |
|
2007 |
Wong JC, Zhang Y, Tran MT, Lieuw KH, Wolff L, Killeen N, Shannon K. Use of Chromosome Engineering To Model a Leukemia-Associated 7q22 Deletion in the Mouse. Blood. 110: 2654-2654. DOI: 10.1182/Blood.V110.11.2654.2654 |
0.403 |
|
2003 |
Wong JC, Gokgoz N, Alon N, Andrulis IL, Buchwald M. Cloning and mutation analysis of ZFP276 as a candidate tumor suppressor in breast cancer. Journal of Human Genetics. 48: 668-71. PMID 14605947 DOI: 10.1007/S10038-003-0088-1 |
0.535 |
|
2003 |
Wong JC, Alon N, Mckerlie C, Huang JR, Meyn MS, Buchwald M. Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia. Human Molecular Genetics. 12: 2063-76. PMID 12913077 DOI: 10.1093/Hmg/Ddg219 |
0.55 |
|
2002 |
Wong JC, Buchwald M. Disease model: Fanconi anemia. Trends in Molecular Medicine. 8: 139-42. PMID 11879775 DOI: 10.1016/S1471-4914(01)02262-6 |
0.537 |
|
2000 |
Wong JC, Alon N, Norga K, Kruyt FA, Youssoufian H, Buchwald M. Cloning and analysis of the mouse Fanconi anemia group A cDNA and an overlapping penta zinc finger cDNA. Genomics. 67: 273-83. PMID 10936049 DOI: 10.1006/Geno.2000.6252 |
0.522 |
|
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