Ye Cao (Y Cao)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 13

Top Topics

Dna Methylation

Polycystic Kidney Disease

Top Venues

Prenatal diagnosis

American journal of medical genetics. Part A

Human reproduction (Oxford, England)

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Wing Ting Tse, Ye Cao, Pensi Ping Hei Lam, Kwok Ming Law, Kwong-Wai Choy, Yuen Ha Ting
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene. Prenatal diagnosis (2023)
Wing Ting Tse, Ye Cao, Pensi Ping Hei Lam, Kwok Ming Law, Kwong-Wai Choy, Yuen Ha Ting
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene. Prenatal diagnosis 44 (2) (2023)
Ying Li, Matthew Hoi Kin Chau, Ying Xin Zhang, Yilin Zhao, Shuwen Xue, Tin-Chiu Li, Ye Cao, Zirui Dong, Kwong-Wai Choy, Jacqueline Pui Wah Chung
A pilot investigation of low-pass genome sequencing identifying site-specific variation in chromosomal mosaicisms by a multiple site sampling approach in first-trimester miscarriages. Human reproduction (Oxford, England) (2023)
Wing Ting Tse, Ye Cao, Pensi Ping Hei Lam, Kwok Ming Law, Kwong-Wai Choy, Yuen Ha Ting
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene. Prenatal diagnosis 44 (2) (2023)
Wing Ting Tse, Ye Cao, Pensi Ping Hei Lam, Kwok Ming Law, Kwong-Wai Choy, Yuen Ha Ting
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene. Prenatal diagnosis 44 (2) (2023)
Wing Ting Tse, Ye Cao, Pensi Ping Hei Lam, Kwok Ming Law, Kwong-Wai Choy, Yuen Ha Ting
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene. Prenatal diagnosis 44 (2) (2023)
Yu Zheng, Lo Wong, Angel Hoi Wan Kwan, Zirui Dong, Ka Yin Kwok, Kwong-Wai Choy, Hongzheng Dai, Ye Cao
Prenatal diagnosis of polycystic kidney caused by biallelic hypomorphic variants in the PKD1 gene. Prenatal diagnosis (2023)
Josephine Shuk Ching Chong, Ye Cao, Eva L W Fung, Soledad Kleppe, Karen W Gripp, Jozef Hertecant, Ayman W. El-Hattab, Jehan Suleiman, Gary Clark, Gretchen von Allmen, Olga Rodziyevska, Richard Alan Lewis, Jill Anne Rosenfeld, Jie Dong, null null, Xia Wang, Marcus J Miller, Weimin Bi, Pengfei Liu, Fernando Scaglia
Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy. American journal of medical genetics. Part A 191 (3) (2022)
Josephine Shuk Ching Chong, Ye Cao, Eva L W Fung, Soledad Kleppe, Karen W Gripp, Jozef Hertecant, Ayman W. El-Hattab, Jehan Suleiman, Gary Clark, Gretchen von Allmen, Olga Rodziyevska, Richard Alan Lewis, Jill Anne Rosenfeld, Jie Dong, null null, Xia Wang, Marcus J Miller, Weimin Bi, Pengfei Liu, Fernando Scaglia
Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy. American journal of medical genetics. Part A (2022)
Josephine Shuk Ching Chong, Ye Cao, Eva L W Fung, Soledad Kleppe, Karen W Gripp, Jozef Hertecant, Ayman W. El-Hattab, Jehan Suleiman, Gary Clark, Gretchen von Allmen, Olga Rodziyevska, Richard Alan Lewis, Jill Anne Rosenfeld, Jie Dong, null null, Xia Wang, Marcus J Miller, Weimin Bi, Pengfei Liu, Fernando Scaglia
Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy. American journal of medical genetics. Part A 191 (3) (2022)
Josephine Shuk Ching Chong, Ye Cao, Eva L W Fung, Soledad Kleppe, Karen W Gripp, Jozef Hertecant, Ayman W. El-Hattab, Jehan Suleiman, Gary Clark, Gretchen von Allmen, Olga Rodziyevska, Richard Alan Lewis, Jill Anne Rosenfeld, Jie Dong, null null, Xia Wang, Marcus J Miller, Weimin Bi, Pengfei Liu, Fernando Scaglia
Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy. American journal of medical genetics. Part A 191 (3) (2022)
Ye Cao, Matthew Hoi Kin Chau, Y Zheng, Y Zhao, Angel Hoi Wan Kwan, Shuk Yi Annie Hui, Y H Lam, T Y T Tan, Ada W T Tse, Lo Wong, Tak Yeung Leung, Z Dong, Kwong-Wai Choy
Exploring the diagnostic utility of genome sequencing for fetal congenital heart defects. Prenatal diagnosis 42 (7) (2022)
Ye Cao, Melanie Manning, Kathleen Pope, Weimin He, Francesco Vetrini, Carly Siskind, Jill Anne Rosenfeld, Yaping Yang, Rui Xiao
Genotype-phenotype study and expansion of ARL6IP1-related complicated hereditary spastic paraplegia. Clinical genetics 99 (3) (2020)