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2022
Chen, Jing, de la Roche, Luz Angela, Kahlert, Ulf D., Isachenko, Vladimir, Huang, Hui, Hennefruend, Joerg, Yan, Xiaohong, Chen, Qionghua, Shi, Wenjie and Li, Youzhu (2022). Artificial Ovary for Young Female Breast Cancer Patients. Front. Med., 9. LAUSANNE: FRONTIERS MEDIA SA. ISSN 2296-858X
2021
Li, Jianhua, Chen, Jing, Sun, Tiecheng, Zhang, Shuiwen, Jiao, Tingting, Chian, Ri-Cheng, Li, Youzhu and Xu, Ye 
ORCID: 0000-0003-4649-3624
(2021).
Chromosome aneuploidy analysis in embryos derived from in vivo and in vitro matured human oocytes.
J. Transl. Med., 19 (1).
LONDON:
BMC.
ISSN 1479-5876
Liang, Lei, Mei, Libin, Shi, Yingying, Huang, Lingling, Su, Zhiying, Zeng, Yu, Gao, Haijie, He, Xuemei, Huang, Hui, Huang, Yanru, Li, Ping and Chen, Jing (2021). Turner syndrome with Xp deletions and rare endometrial abnormalities A case report. Medicine (Baltimore), 100 (46). PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS. ISSN 1536-5964
Sha, Yanwei, Liu, Wensheng, Li, Lin, Serafimovski, Mario, Isachenko, Vladimir, Li, Youzhu, Chen, Jing, Zhao, Bangrong, Wang, Yifeng and Wei, Xiaoli (2021). Pathogenic Variants in ACTRT1 Cause Acephalic Spermatozoa Syndrome. Front. Cell. Dev. Biol., 9. LAUSANNE: FRONTIERS MEDIA SA. ISSN 2296-634X
Wei, Xiaoli, Liu, Wensheng, Zhu, Xingshen, Li, Youzhu, Zhang, Xiaoya, Chen, Jing, Isachenko, Vladimir, Sha, Yanwei and Lu, Zhongxian (2021). Biallelic mutations in KATNAL2 cause male infertility due to oligo-astheno-teratozoospermia. Clin. Genet., 100 (4). S. 376 - 386. HOBOKEN: WILEY. ISSN 1399-0004
2018
van der Ven, Amelie T., Kobbe, Birgit, Kohl, Stefan, Shril, Shirlee, Pogoda, Hans-Martin, Imhof, Thomas, Ityel, Hadas, Vivante, Asaf, Chen, Jing, Hwang, Daw-Yang, Connaughton, Dervla M., Mann, Nina, Widmeier, Eugen ORCID: 0000-0002-7773-5190, Taglienti, Mary, Schmidt, Johanna Magdalena, Nakayama, Makiko, Senguttuvan, Prabha, Kumar, Selvin, Tasic, Velibor ORCID: 0000-0002-3377-1245, Kehinde, Elijah O., Mane, Shrikant M., Lifton, Richard P., Soliman, Neveen ORCID: 0000-0002-8942-1973, Lu, Weining ORCID: 0000-0002-6570-3044, Bauer, Stuart B., Hammerschmidt, Matthias, Wagener, Raimund and Hildebrandt, Friedhelm
(2018).
A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral refluxy.
PLoS One, 13 (1).
SAN FRANCISCO:
PUBLIC LIBRARY SCIENCE.
ISSN 1932-6203
2017
Chen, Jing ORCID: 0000-0003-0538-689X, Liao, Hai-Jun, Xie, Hai-Dong, Han, Xing-Jie, Huang, Rui-Zhen, Cheng, Song, Wei, Zhong-Chao, Xie, Zhi-Yuan and Xiang, Tao ORCID: 0000-0001-5998-7338
(2017).
Phase Transition of the q-State Clock Model: Duality and Tensor Renormalization.
Chin. Phys. Lett., 34 (5).
BRISTOL:
IOP PUBLISHING LTD.
ISSN 1741-3540
Vivante, Asaf, Hwang, Daw-Yang, Kohl, Stefan, Chen, Jing, Shril, Shirlee, Schulz, Julian, van der Ven, Annelle, Daouk, Ghaleb, Soliman, Neveen A., Kumar, Aravind Selvin, Senguttuvan, Prabha, Kehinde, Elijah O., Tasic, Velibor ORCID: 0000-0002-3377-1245 and Hildebrandt, Friedhelm
(2017).
Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract.
J. Am. Soc. Nephrol., 28 (1).
S. 69 - 76.
WASHINGTON:
AMER SOC NEPHROLOGY.
ISSN 1533-3450
2016
Kohl, Stefan, Chen, Jing, Vivante, Asaf, Hwang, Daw-Yang, Shril, Shirlee, Dworschak, Gabriel C., Van der Ven, Amelie, Sanna-Cherchi, Simone, Bauer, Stuart B., Lee, Richard S., Soliman, Neveen A., Kehinde, Elijah O., Reutter, Heiko M., Tasic, Velibor ORCID: 0000-0002-3377-1245 and Hildebrandt, Friedhelm
(2016).
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract.
Nephrol. Dial. Transplant., 31 (8).
S. 1280 - 1284.
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2385