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Jenise C. Wong, MD PhD
Jenise C. Wong, MD PhD
Verified email at ucsf.edu
Title
Cited by
Cited by
Year
The Wilms tumor suppressor WT1 encodes a transcriptional activator of amphiregulin
SB Lee, K Huang, R Palmer, VB Truong, D Herzlinger, KA Kolquist, ...
Cell 98 (5), 663-673, 1999
3641999
Real-Time Continuous Glucose Monitoring Among Participants in the T1D Exchange Clinic Registry
JC Wong, NC Foster, DM Maahs, D Raghinaru, RM Bergenstal, ...
Diabetes care 37 (10), 2702-2709, 2014
3412014
Severe hypoglycemia and diabetic ketoacidosis among youth with type 1 diabetes in the T1D Exchange clinic registry
E Cengiz, D Xing, JC Wong, JI Wolfsdorf, MW Haymond, A Rewers, ...
Pediatric diabetes 14 (6), 447-454, 2013
2872013
A contrast between children and adolescents with excellent and poor control: the T1D Exchange clinic registry experience
MS Campbell, DA Schatz, V Chen, JC Wong, A Steck, WV Tamborlane, ...
Pediatric diabetes 15 (2), 110-117, 2014
1352014
Inhibition of cellular proliferation by the Wilms tumor suppressor WT1 requires association with the inducible chaperone Hsp70
S Maheswaran, C Englert, G Zheng, SB Lee, J Wong, DP Harkin, J Bean, ...
Genes & development 12 (8), 1108-1120, 1998
1221998
Induction of BAIAP3 by the EWS-WT1 chimeric fusion implicates regulated exocytosis in tumorigenesis
RE Palmer, SB Lee, JC Wong, PA Reynolds, H Zhang, V Truong, ...
Cancer cell 2 (6), 497-505, 2002
972002
PedsQL 3.2 diabetes module for children, adolescents, and young adults: reliability and validity in type 1 diabetes
JW Varni, AM Delamater, KK Hood, JK Raymond, NT Chang, KA Driscoll, ...
Diabetes care 41 (10), 2064-2071, 2018
922018
Prevalence of cardiovascular risk factors in youth with type 1 diabetes and elevated body mass index
MJ Redondo, NC Foster, IM Libman, SN Mehta, JM Hathway, KE Bethin, ...
Acta diabetologica 53, 271-277, 2016
862016
A low, adaptive dose of gamma-rays reduced the number and altered the spectrum of S1− mutants in human-hamster hybrid A L cells
AM Ueno, DB Vannais, DL Gustafson, JC Wong, CA Waldren
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 358 (2 …, 1996
781996
Self-Monitoring of Blood Glucose
SK Garg, IB Hirsch, K Ngaosuwan, S Osataphan, MC Carolan-OIah, ...
Diabetes Technology & Therapeutics 19 (S1), S-3-S-10, 2017
74*2017
Diabetes Technology and the Human Factor
A Liberman, B Buckingham, KD Barnard, MV Venkat, K Close, ...
Diabetes technology & therapeutics 18 (S1), S-101-S-111, 2016
722016
Inequities in diabetic ketoacidosis among patients with type 1 diabetes and COVID-19: data from 52 US clinical centers
O Ebekozien, S Agarwal, N Noor, A Albanese-O’Neill, JC Wong, ...
The Journal of Clinical Endocrinology & Metabolism 106 (4), 1755-1762, 2021
692021
Evaluation of Pump Discontinuation and Associated Factors in the T1D Exchange Clinic Registry
JC Wong, C Boyle, LA DiMeglio, LD Mastrandrea, KL Abel, E Cengiz, ...
Journal of diabetes science and technology 11 (2), 224-232, 2017
672017
A minority of patients with type 1 diabetes routinely downloads and retrospectively reviews device data
JC Wong, AB Neinstein, M Spindler, S Adi
Diabetes technology & therapeutics 17 (8), 555-562, 2015
642015
A case study in open source innovation: developing the Tidepool Platform for interoperability in type 1 diabetes management
A Neinstein, J Wong, H Look, B Arbiter, K Quirk, S McCanne, Y Sun, ...
Journal of the American Medical Informatics Association 23 (2), 324-332, 2016
612016
Insulin pump use and glycemic control in adolescents with type 1 diabetes: predictors of change in method of insulin delivery across two years
JC Wong, LM Dolan, TT Yang, KK Hood
Pediatric diabetes 16 (8), 592-599, 2015
592015
Primary γ-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile
CG Bönnemann, J Wong, KJ Jones, HGW Lidov, CA Feener, F Shapiro, ...
Neuromuscular Disorders 12 (3), 273-280, 2002
582002
Induction of the interleukin-2/15 receptor beta-chain by the EWS-WT1 translocation product.
JC Wong, SB Lee, MD Bell, PA Reynolds, E Fiore, I Stamenkovic, ...
Oncogene 21 (13), 2009-2019, 2002
522002
LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3
CG Bönnemann, J Wong, CB Hamida, MB Hamida, F Hentati, LM Kunkel
Neuromuscular Disorders 8 (3-4), 193-197, 1998
481998
LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3
CG Bönnemann, J Wong, CB Hamida, MB Hamida, F Hentati, LM Kunkel
Neuromuscular Disorders 8 (3-4), 193-197, 1998
451998
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