Gong JY - Search Results

1

Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis.

Luan W, Hao CZ, Li JQ, Wei Q, Gong JY, Qiu YL, Lu Y, Shen CH, Xia Q, Xie XB, Zhang MH, Abuduxikuer K, Li ZD, Wang L, Xing QH, Knisely AS, Wang JS. Luan W, et al. Among authors: gong jy. J Med Genet. 2021 Aug;58(8):514-525. doi: 10.1136/jmedgenet-2019-106706. Epub 2020 Jul 31. J Med Genet. 2021. PMID: 32737136

2

Citrin deficiency presenting as acute liver failure in an eight-month-old infant.

Zhang MH, Gong JY, Wang JS. Zhang MH, et al. Among authors: gong jy. World J Gastroenterol. 2015 Jun 21;21(23):7331-4. doi: 10.3748/wjg.v21.i23.7331. World J Gastroenterol. 2015. PMID: 26109823 Free PMC article.

3

Hypothyroidism Associated with ATP8B1 Deficiency.

Li L, Deheragoda M, Lu Y, Gong J, Wang J. Li L, et al. J Pediatr. 2015 Dec;167(6):1334-9.e1. doi: 10.1016/j.jpeds.2015.08.037. Epub 2015 Sep 15. J Pediatr. 2015. PMID: 26382629

4

The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency.

Wang NL, Li LT, Wu BB, Gong JY, Abuduxikuer K, Li G, Wang JS. Wang NL, et al. Among authors: gong jy. PLoS One. 2016 Apr 6;11(4):e0153114. doi: 10.1371/journal.pone.0153114. eCollection 2016. PLoS One. 2016. PMID: 27050426 Free PMC article.

5

Fibrinogen storage disease in a Chinese boy with de novo fibrinogen Aguadilla mutation: Incomplete response to carbamazepine and ursodeoxycholic acid.

Zhang MH, Knisely AS, Wang NL, Gong JY, Wang JS. Zhang MH, et al. Among authors: gong jy. BMC Gastroenterol. 2016 Aug 12;16(1):92. doi: 10.1186/s12876-016-0507-3. BMC Gastroenterol. 2016. PMID: 27520927 Free PMC article.

6

A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions.

Wang NL, Lu YL, Zhang P, Zhang MH, Gong JY, Lu Y, Xie XB, Qiu YL, Yan YY, Wu BB, Wang JS. Wang NL, et al. Among authors: gong jy. PLoS One. 2016 Oct 5;11(10):e0164058. doi: 10.1371/journal.pone.0164058. eCollection 2016. PLoS One. 2016. PMID: 27706244 Free PMC article.

7

Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ-glutamyltransferase cholestasis.

Qiu YL, Gong JY, Feng JY, Wang RX, Han J, Liu T, Lu Y, Li LT, Zhang MH, Sheps JA, Wang NL, Yan YY, Li JQ, Chen L, Borchers CH, Sipos B, Knisely AS, Ling V, Xing QH, Wang JS. Qiu YL, et al. Among authors: gong jy. Hepatology. 2017 May;65(5):1655-1669. doi: 10.1002/hep.29020. Epub 2017 Mar 23. Hepatology. 2017. PMID: 28027573 Free PMC article.

8

Novel NBAS mutations and fever-related recurrent acute liver failure in Chinese children: a retrospective study.

Li JQ, Qiu YL, Gong JY, Dou LM, Lu Y, Knisely AS, Zhang MH, Luan WS, Wang JS. Li JQ, et al. Among authors: gong jy. BMC Gastroenterol. 2017 Jun 19;17(1):77. doi: 10.1186/s12876-017-0636-3. BMC Gastroenterol. 2017. PMID: 28629372 Free PMC article.

9

Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis: Genetics, Immunostaining, Mass Spectrometry.

Gong JY, Setchell KDR, Zhao J, Zhang W, Wolfe B, Lu Y, Lackner K, Knisely AS, Wang NL, Hao CZ, Zhang MH, Wang JS. Gong JY, et al. J Pediatr Gastroenterol Nutr. 2017 Nov;65(5):561-568. doi: 10.1097/MPG.0000000000001730. J Pediatr Gastroenterol Nutr. 2017. PMID: 28937538

10

Comprehensive bile acid profiling in hereditary intrahepatic cholestasis: Genetic and clinical correlations.

Liu T, Wang RX, Han J, Hao CZ, Qiu YL, Yan YY, Li LT, Wang NL, Gong JY, Lu Y, Zhang MH, Xie XB, Yang JC, You YJ, Li JQ, Knisely AS, Borchers CH, Ling V, Wang JS. Liu T, et al. Among authors: gong jy. Liver Int. 2018 Sep;38(9):1676-1685. doi: 10.1111/liv.13714. Epub 2018 Mar 12. Liver Int. 2018. PMID: 29412511

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