Weiwei Li

Zhongshan East Road 305
Nanjing, 210002, China

Last Updated: 09/26/2026

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Found 15 publications

Ionizing radiation-induced disruption of Rela-Bclaf1-spliceosome regulatory axis in primary spermatocytes causing spermatogenesis dysfunction.

Ionizing radiation-induced disruption of Rela-Bclaf1-spliceosome regulatory axis in primary spermatocytes causing spermatogenesis dysfunction.

Journal: Cell communication and signaling : CCS

Published: November 29, 2024

Screening the pathogenic causes of congenital cataract via whole exome sequencing technology in three families: Molecular genetics of congenital cataract.

Screening the pathogenic causes of congenital cataract via whole exome sequencing technology in three families: Molecular genetics of congenital cataract.

Journal: Molecular medicine reports

Published: January 16, 2023

Finding new cancer epigenetic and genetic biomarkers from cell-free DNA by combining SALP-seq and machine learning.

Finding new cancer epigenetic and genetic biomarkers from cell-free DNA by combining SALP-seq and machine learning.

Journal: Computational and structural biotechnology journal

Published: March 24, 2020

What do we learn from dystrophic epidermolysis bullosa, nails only? Idiopathic nail dystrophy may harbor a COL7A1 mutation as the underlying cause.

What do we learn from dystrophic epidermolysis bullosa, nails only? Idiopathic nail dystrophy may harbor a COL7A1 mutation as the underlying cause.

Journal: The Journal of dermatology

Published: December 18, 2019

Identification of a novel DDB2 mutation in a Chinese Han family with Xeroderma pigmentosum group E:a case report and literature review.

Identification of a novel DDB2 mutation in a Chinese Han family with Xeroderma pigmentosum group E:a case report and literature review.

Journal: BMC medical genetics

Published: November 29, 2019

Decoding genetic and epigenetic information embedded in cell free DNA with adapted SALP-seq.

Decoding genetic and epigenetic information embedded in cell free DNA with adapted SALP-seq.

Journal: International journal of cancer

Published: July 11, 2018

Detection of target DNA with a novel Cas9/sgRNAs-associated reverse PCR (CARP) technique.

Detection of target DNA with a novel Cas9/sgRNAs-associated reverse PCR (CARP) technique.

Journal: Analytical and bioanalytical chemistry

Published: November 08, 2017

A novel mutation of MIP in a Chinese family with congenital nuclear cataract identified by whole-exome sequencing.

A novel mutation of MIP in a Chinese family with congenital nuclear cataract identified by whole-exome sequencing.

Journal: Ophthalmic genetics

Published: August 25, 2017

Polymorphisms of protamine genes contribute to male infertility susceptibility in the Chinese Han population.

Polymorphisms of protamine genes contribute to male infertility susceptibility in the Chinese Han population.

Journal: Oncotarget

Published: March 21, 2017

The susceptibility of FSHB -211G > T and FSHR G-29A, 919A > G, 2039A > G polymorphisms to men infertility: an association study and meta-analysis.

The susceptibility of FSHB -211G > T and FSHR G-29A, 919A > G, 2039A > G polymorphisms to men infertility: an association study and meta-analysis.

Journal: BMC medical genetics

Published: December 15, 2016

Application of next‑generation sequencing for molecular diagnosis in a large family with osteogenesis imperfecta type I.

Application of next‑generation sequencing for molecular diagnosis in a large family with osteogenesis imperfecta type I.

Journal: Molecular medicine reports

Published: September 19, 2016

Prenatal diagnosis and genetic counseling in a fetus associated with risk of Angelman syndrome with a small supernumerary marker chromosome derived from chromosome 22.

Prenatal diagnosis and genetic counseling in a fetus associated with risk of Angelman syndrome with a small supernumerary marker chromosome derived from chromosome 22.

Journal: Molecular cytogenetics

Published: November 10, 2015

Showing 1-12 of 15

Last Updated: 09/26/2026