Ping Li

发表

HOMA-IR for predicting clinical pregnancy rate during IVF.

Yuhua Shi, Haixia Song, Zhenqing Yu, 2021, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Genetic factors contributing to human primary ciliary dyskinesia and male infertility

Ping Li, Zhiyong Ji, L. Ding, 2016, Asian journal of andrology.

Mutations in FIGLA Associated With Premature Ovarian Insufficiency in a Chinese Population

Yanru Huang, Yuhua Shi, Xuemei He, 2021, Frontiers in Medicine.

Incidence and Clinical Manifestations of Primary Ciliary Dyskinesia/ Kartagener's Syndrome

Ping Li, L. Ding, Yan-Wei Sha, 2022 .

Digital PCR Detection of mtDNA/gDNA Ratio in Embryo Culture Medium for Prediction of Embryo Development Potential

Ping Li, H. Ji, Xianjing Huang, 2021, Pharmacogenomics and personalized medicine.

Sperm-egg fusion disorder in a Chinese male patient was associated with a rare ADAM20 variant

Ping Li, H. Ji, Zhiyong Ji, 2017, Oncotarget.

A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy

Yanru Huang, Ping Li, Xiaomin Ma, 2021, Frontiers in Genetics.

ANGPTL4 Expression in Ovarian Granulosa Cells Is Associated With Polycystic Ovary Syndrome

Yuhua Shi, Ping Li, T. Song, 2022, Frontiers in Endocrinology.

Predictive value of serum human chorionic gonadotropin concentrations for pregnancy outcomes of in vitro fertilization in women of different ages

Ping Li, H. Ji, Long Wang, 2021 .

A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF).

Ping Li, Li-bin Mei, Yan-Wei Sha, 2017, Gene.

A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.

C. Yin, Shaobin Lin, Ping Li, 2018, Gene.

Two cases of complex balanced autosomal translocations associated with severe oligozoospermia.

Ping Li, Zhiyong Ji, Li-bin Mei, 2018, Gene.

A successful pregnancy by intracytoplasmic sperm injection using ejaculate sperm from an infertile man with 46, XX/46, XY true hermaphrodite

Shaobin Lin, Ping Li, Zhiyong Ji, 2016, Asian journal of andrology.

Comprehensive Genome Profiling of Single Sperm Cells by Multiple Annealing and Looping‐Based Amplification Cycles and Next‐Generation Sequencing from Carriers of Robertsonian Translocation

Shaobin Lin, Ping Li, Zhiyong Ji, 2017, Annals of human genetics.

Non-chimerism and chimerism pseudo dicentric Y chromosome: two case reports about azoospermia and cytogenetic/molecular genetic analysis in the Chinese population

E. Werner, Ping Li, Yan-Wei Sha, 2013, Journal of Assisted Reproduction and Genetics.

Two novel biallelic mutations in PSMC3IP in a patient affected by premature ovarian insufficiency.

Yanru Huang, Xuemei He, Ping Li, 2021, Molecular medicine reports.

DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population.

Shenmin Yang, Xiaoyu Yang, Ping Li, 2017, Fertility and sterility.

TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family.

C. Yin, Xiong Wang, Chengrong Wang, 2018, Gene.

Predictive value of serum HCG concentrations for outcomes of vitrified-warmed blastocyst transfers in women of different ages.

Ping Li, H. Ji, Long Wang, 2021, Reproductive biomedicine online.

A Case of Bilateral Testicular Tumors Subsequently Diagnosed as Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Xuemei He, Ping Li, L. Ding, 2015, International journal of fertility & sterility.

First successful pregnancy outcome after intracytoplasmic sperm injection with short-tailed sperm from an infertile Han Chinese man

Ping Li, L. Ding, Yan-Wei Sha, 2016, Asian journal of andrology.

Gaq-PKD/PKCμ regulates the IkB transcription to limit the NF-kB mediated inflammatory response essential for early pregnancy

Guixiu Shi, Dunjin Chen, Gaizhen Li, 2022, bioRxiv.

Identification of a novel mutation in FGFR1 gene in patients with Kallmann syndrome by high throughput sequencing

Shaobin Lin, Ping Li, Xianjing Huang, 2018, Systems Biology in Reproductive Medicine.

Globozoospermic infertility associated with balanced DPY19L2 translocation/gene deletion at the chromosomal breakpoint

Ping Li, Zhiyong Ji, Li-bin Mei, 2017, Asian journal of andrology.

High-Throughput Sequencing Profiles About lncRNAs and mRNAs of Ovarian Granulosa Cells in Polycystic Ovary Syndrome

Yuhua Shi, Ping Li, Yuehong Bian, 2021, Frontiers in Medicine.

Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian China.

Shaobin Lin, Yulin Zhou, Ping Li, 2018, Gene.

Biallelic mutations in PMFBP1 cause acephalic spermatozoa

Xiong Wang, S. Kong, Jing Chen, 2018, Clinical genetics.

Turner syndrome with Xp deletions and rare endometrial abnormalities

Jing Chen, Yanru Huang, Xuemei He, 2021, Medicine.

Whole-exome sequencing identified a homozygous BRDT mutation in a patient with acephalic spermatozoa

Binbin Wang, Jing Wang, Kehkooi Kee, 2017, Oncotarget.

Two novel biallelic mutations in PSMC3IP in a Chinese patient affected by primary ovarian insufficiency: case report and review of the literature

Yanru Huang, Xuemei He, Ping Li, 2020 .

Patients with multiple morphological abnormalities of the sperm flagella harbouring CFAP44 or CFAP43 mutations have a good pregnancy outcome following intracytoplasmic sperm injection

Xiong Wang, H. Bao, Ping Li, 2018, Andrologia.

DNAH6 is a novel candidate gene associated with sperm head anomaly

X. Xu, C. Yin, C. Wang, 2018, Andrologia.

Gαq-PKD/PKCμ signal regulating the nuclear export of HDAC5 to induce the IκB expression and limit the NF-κB-mediated inflammatory response essential for early pregnancy

Guixiu Shi, Gaizhen Li, Haibin Wang, 2023, eLife.

A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review

Xiaoyu Yang, Shaobin Lin, Ping Li, 2018, BMC Medical Genetics.

Exome sequencing identifies compound heterozygous KCTD7 mutations in a girl with progressivemyoclonus epilepsy.

Yanru Huang, J. Chen, Shaobin Lin, 2019, Clinica chimica acta; international journal of clinical chemistry.

A familial study of twins with severe asthenozoospermia identified a homozygous SPAG17 mutation by whole‐exome sequencing

X. Xu, Ping Li, H. Ji, 2018, Clinical genetics.