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Wendy K Chung - Publications

Affiliations: 
Pediatrics Columbia University, New York, NY 
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27 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Zhu N, LeDuc CA, Fennoy I, Laferrère B, Doege CA, Shen Y, Chung WK, Leibel RL. Rare predicted loss of function alleles in Bassoon (BSN) are associated with obesity. Npj Genomic Medicine. 8: 33. PMID 37865656 DOI: 10.1038/s41525-023-00376-7  0.592
2023 Zhu N, LeDuc CA, Fennoy I, Laferr Re B, Doege CA, Shen Y, Chung WK, Leibel RL. Predicted loss of function alleles in Bassoon (BSN) are associated with obesity. Medrxiv : the Preprint Server For Health Sciences. PMID 36865254 DOI: 10.1101/2023.02.19.23285978  0.589
2022 González BJ, Zhao H, Niu J, Williams DJ, Lee J, Goulbourne CN, Xing Y, Wang Y, Oberholzer J, Blumenkrantz MH, Chen X, LeDuc CA, Chung WK, Colecraft HM, Gromada J, et al. Reduced calcium levels and accumulation of abnormal insulin granules in stem cell models of HNF1A deficiency. Communications Biology. 5: 779. PMID 35918471 DOI: 10.1038/s42003-022-03696-z  0.674
2021 De Rosa MC, Glover HJ, Stratigopoulos G, LeDuc CA, Su Q, Shen Y, Sleeman MW, Chung WK, Leibel RL, Altarejos JY, Doege CA. Gene expression atlas of energy balance brain regions. Jci Insight. PMID 34283813 DOI: 10.1172/jci.insight.149137  0.578
2021 Breidbart E, Deng L, Lanzano P, Fan X, Guo J, Leibel RL, LeDuc CA, Chung WK. Frequency and characterization of mutations in genes in a large cohort of patients referred to MODY registry. Journal of Pediatric Endocrinology & Metabolism : Jpem. 34: 633-638. PMID 33852230 DOI: 10.1515/jpem-2020-0501  0.535
2020 Lugo-Candelas C, Pang Y, Lee S, Cha J, Hong S, Ranzenhofer L, Korn R, Davis H, McInerny H, Schebendach J, Chung WK, Leibel RL, Walsh BT, Posner J, Rosenbaum M, et al. Differences in brain structure and function in children with the obesity-risk allele. Obesity Science & Practice. 6: 409-424. PMID 32874676 DOI: 10.1002/Osp4.417  0.567
2019 Ranzenhofer LM, Mayer LES, Davis HA, Mielke-Maday HK, McInerney H, Korn R, Gupta N, Brown AJ, Schebendach J, Tanofsky-Kraff M, Thaker V, Chung WK, Leibel RL, Walsh BT, Rosenbaum M. The FTO Gene and Measured Food Intake in 5- to 10-Year-Old Children Without Obesity. Obesity (Silver Spring, Md.). 27: 1023-1029. PMID 31119882 DOI: 10.1002/Oby.22464  0.577
2018 Melhorn SJ, Askren MK, Chung WK, Kratz M, Bosch TA, Tyagi V, Webb MF, De Leon MRB, Grabowski TJ, Leibel RL, Schur EA. FTO genotype impacts food intake and corticolimbic activation. The American Journal of Clinical Nutrition. 107: 145-154. PMID 29529147 DOI: 10.1093/Ajcn/Nqx029  0.54
2017 Mosialou I, Shikhel S, Liu JM, Maurizi A, Luo N, He Z, Huang Y, Zong H, Friedman RA, Barasch J, Lanzano P, Deng L, Leibel RL, Rubin M, Nickolas T, ... Chung W, et al. Corrigendum: MC4R-dependent suppression of appetite by bone-derived lipocalin 2. Nature. 546: 440. PMID 28617454 DOI: 10.1038/Nature22808  0.454
2017 Mosialou I, Shikhel S, Liu JM, Maurizi A, Luo N, He Z, Huang Y, Zong H, Friedman RA, Barasch J, Lanzano P, Deng L, Leibel RL, Rubin M, Nicholas T, ... Chung W, et al. MC4R-dependent suppression of appetite by bone-derived lipocalin 2. Nature. PMID 28273060 DOI: 10.1038/Nature21697  0.523
2017 Hua H, Shang L, Martinez H, Freeby M, Gallagher MP, Ludwig T, Deng L, Greenberg E, LeDuc C, Chung WK, Goland R, Leibel RL, Egli D. iPSC-derived β cells model diabetes due to glucokinase deficiency. The Journal of Clinical Investigation. PMID 28094769 DOI: 10.1172/JCI92775  0.64
2014 Stratigopoulos G, Martin Carli JF, O'Day DR, Wang L, Leduc CA, Lanzano P, Chung WK, Rosenbaum M, Egli D, Doherty DA, Leibel RL. Hypomorphism for RPGRIP1L, a ciliary gene vicinal to the FTO locus, causes increased adiposity in mice. Cell Metabolism. 19: 767-79. PMID 24807221 DOI: 10.1016/J.Cmet.2014.04.009  0.695
2014 Shang L, Hua H, Foo K, Martinez H, Watanabe K, Zimmer M, Kahler DJ, Freeby M, Chung W, LeDuc C, Goland R, Leibel RL, Egli D. β-cell dysfunction due to increased ER stress in a stem cell model of Wolfram syndrome. Diabetes. 63: 923-33. PMID 24227685 DOI: 10.2337/Db13-0717  0.666
2014 Gill R, Cheung YH, Shen Y, Lanzano P, Mirza NM, Ten S, MacLaren NK, Motaghedi R, Han JC, Yanovski JA, Leibel RL, Chung WK. Whole-Exome sequencing identifies novel LEPR mutations in individuals with severe early onset obesity Obesity. 22: 576-584. PMID 23616257 DOI: 10.1002/Oby.20492  0.582
2013 Hua H, Shang L, Martinez H, Freeby M, Gallagher MP, Ludwig T, Deng L, Greenberg E, Leduc C, Chung WK, Goland R, Leibel RL, Egli D. iPSC-derived β cells model diabetes due to glucokinase deficiency. The Journal of Clinical Investigation. 123: 3146-53. PMID 23778137 DOI: 10.1172/Jci67638  0.67
2011 Tiwari HK, Patki A, Lieberman J, Stroup TS, Allison DB, Leibel RL, Chung WK. Association of Allelic Variation in Genes Mediating Aspects of Energy Homeostasis with Weight Gain during Administration of Antipsychotic Drugs (CATIE Study). Frontiers in Genetics. 2: 56. PMID 22039372 DOI: 10.3389/Fgene.2011.00056  0.53
2011 Stratigopoulos G, LeDuc CA, Cremona ML, Chung WK, Leibel RL. Cut-like homeobox 1 (CUX1) regulates expression of the fat mass and obesity-associated and retinitis pigmentosa GTPase regulator-interacting protein-1-like (RPGRIP1L) genes and coordinates leptin receptor signaling. The Journal of Biological Chemistry. 286: 2155-70. PMID 21037323 DOI: 10.1074/jbc.M110.188482  0.554
2009 Chung WK, Shin M, Jaramillo TC, Leibel RL, LeDuc CA, Fischer SG, Tzilianos E, Gheith AA, Lewis AS, Chetkovich DM. Absence epilepsy in apathetic, a spontaneous mutant mouse lacking the h channel subunit, HCN2. Neurobiology of Disease. 33: 499-508. PMID 19150498 DOI: 10.1016/j.nbd.2008.12.004  0.483
2009 Chung WK, Patki A, Matsuoka N, Boyer BB, Liu N, Musani SK, Goropashnaya AV, Tan PL, Katsanis N, Johnson SB, Gregersen PK, Allison DB, Leibel RL, Tiwari HK. Analysis of 30 genes (355 SNPS) related to energy homeostasis for association with adiposity in European-American and Yup'ik Eskimo populations. Human Heredity. 67: 193-205. PMID 19077438 DOI: 10.1159/000181158  0.565
2009 Stratigopoulos G, LeDuc CA, Matsuoka N, Gutman R, Rausch R, Robertson SA, Myers MG, Chung WK, Chua SC, Leibel RL. Functional consequences of the human leptin receptor (LEPR) Q223R transversion. Obesity (Silver Spring, Md.). 17: 126-35. PMID 18997673 DOI: 10.1038/oby.2008.489  0.563
2008 Chung WK, Leibel RL. Considerations regarding the genetics of obesity Obesity. 16. PMID 19037210 DOI: 10.1038/oby.2008.514  0.592
2008 Dokmanovic-Chouinard M, Chung WK, Chevre JC, Watson E, Yonan J, Wiegand B, Bromberg Y, Wakae N, Wright CV, Overton J, Ghosh S, Sathe GM, Ammala CE, Brown KK, Ito R, et al. Positional cloning of "Lisch-Like", a candidate modifier of susceptibility to type 2 diabetes in mice. Plos Genetics. 4: e1000137. PMID 18654634 DOI: 10.1371/Journal.Pgen.1000137  0.555
2008 Stratigopoulos G, Padilla SL, LeDuc CA, Watson E, Hattersley AT, McCarthy MI, Zeltser LM, Chung WK, Leibel RL. Regulation of Fto/Ftm gene expression in mice and humans. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 294: R1185-96. PMID 18256137 DOI: 10.1152/Ajpregu.00839.2007  0.599
2006 Chung WK, Leibel RL. The links between obesity, leptin, and prostate cancer Cancer Journal. 12: 178-181. PMID 16803674 DOI: 10.1097/00130404-200605000-00004  0.513
2006 Phan LK, Chung WK, Leibel RL. The mahoganoid mutation (Mgrn1md) improves insulin sensitivity in mice with mutations in the melanocortin signaling pathway independently of effects on adiposity. American Journal of Physiology. Endocrinology and Metabolism. 291: E611-20. PMID 16638826 DOI: 10.1152/ajpendo.00034.2006  0.587
2005 Chung WK, Leibel RL. Molecular physiology of syndromic obesities in humans Trends in Endocrinology and Metabolism. 16: 267-272. PMID 16005242 DOI: 10.1016/j.tem.2005.06.009  0.559
2003 Phan LK, Lin F, LeDuc CA, Chung WK, Leibel RL. The mouse mahoganoid coat color mutation disrupts a novel C3HC4 RING domain protein. The Journal of Clinical Investigation. 110: 1449-59. PMID 12438443 DOI: 10.1172/JCI16131  0.56
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