Ren-juan Y. Shen

Beijing Key Laboratory For Ophthalmic Cell And Gene Therapy
Beijing, 100730, China

Last Updated: 09/26/2026

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Found 25 publications

Cis-regulatory evolution reveals sensory trade-offs as a genetic basis for temporal niche evolution in tapirs.

Cis-regulatory evolution reveals sensory trade-offs as a genetic basis for temporal niche evolution in tapirs.

Journal: Science advances

Published: March 04, 2026

Establishment of a human induced pluripotent stem cell line (BTHBIOi005-A) from a retinitis pigmentosa patient with a MERTK gene mutation.

Establishment of a human induced pluripotent stem cell line (BTHBIOi005-A) from a retinitis pigmentosa patient with a MERTK gene mutation.

Journal: Stem cell research

Published: January 04, 2026

Practice Patterns and Challenges in Managing Inherited Retinal Diseases Across Asia-Pacific: A Survey from the APIED Network.

Practice Patterns and Challenges in Managing Inherited Retinal Diseases Across Asia-Pacific: A Survey from the APIED Network.

Journal: Asia-Pacific journal of ophthalmology (Philadelphia, Pa.)

Published: April 18, 2024

MFRP, PRSS56, and MYRF account for 60.5% of a Chinese cohort with nanophthalmos.

MFRP, PRSS56, and MYRF account for 60.5% of a Chinese cohort with nanophthalmos.

Journal: Clinical & experimental ophthalmology

Published: March 04, 2024

Distinct methylomic signatures of high-altitude acclimatization and adaptation in the Tibetan Plateau.

Distinct methylomic signatures of high-altitude acclimatization and adaptation in the Tibetan Plateau.

Journal: Cell discovery

Published: December 01, 2023

Rationale and protocol paper for the Asia Pacific Network for inherited eye diseases.

Rationale and protocol paper for the Asia Pacific Network for inherited eye diseases.

Journal: Asia-Pacific journal of ophthalmology (Philadelphia, Pa.)

Published: September 29, 2023

Genetic control of DNA methylation is largely shared across European and East Asian populations.

Genetic control of DNA methylation is largely shared across European and East Asian populations.

Journal: Nature communications

Published: May 29, 2023

Exome sequencing in retinal dystrophy patients reveals a novel candidate gene ER membrane protein complex subunit 3.

Exome sequencing in retinal dystrophy patients reveals a novel candidate gene ER membrane protein complex subunit 3.

Journal: Heliyon

Published: May 05, 2023

Development of parenting behavior scale for caregivers of children aged 2 to 6 years and analysis for its reliability and validity

Development of parenting behavior scale for caregivers of children aged 2 to 6 years and analysis for its reliability and validity

Journal: Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]

Published: January 19, 2023

Global spectrum of USH2A mutation in inherited retinal dystrophies: Prompt message for development of base editing therapy.

Global spectrum of USH2A mutation in inherited retinal dystrophies: Prompt message for development of base editing therapy.

Journal: Frontiers in aging neuroscience

Published: May 19, 2022

Second hit impels oncogenesis of retinoblastoma in patient-induced pluripotent stem cell-derived retinal organoids: direct evidence for Knudson's theory.

Second hit impels oncogenesis of retinoblastoma in patient-induced pluripotent stem cell-derived retinal organoids: direct evidence for Knudson's theory.

Journal: PNAS nexus

Published: May 03, 2022

Mutation of SLC7A14 causes auditory neuropathy and retinitis pigmentosa mediated by lysosomal dysfunction.

Mutation of SLC7A14 causes auditory neuropathy and retinitis pigmentosa mediated by lysosomal dysfunction.

Journal: Science advances

Published: April 08, 2022

Showing 1-12 of 25

Last Updated: 09/26/2026