List of works - Zi-Bing Jin

'RetinoGenetics': a comprehensive mutation database for genes related to inherited retinal degeneration

scientific article

A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal Degeneration

scientific article

A new subset of small stem cells in bovine bone marrow stromal cell populations

scientific article published on 15 April 2019

A novel Bruch's membrane-mimetic electrospun substrate scaffold for human retinal pigment epithelium cells.

scientific article published on 15 September 2014

A novel truncating Rs1 mutation associated with X-linked juvenile retinoschisis

scientific article published on 01 January 2007

A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family

scientific article

ATP1A3 mutation as a candidate cause of autosomal dominant cone-rod dystrophy

scientific article published on 21 May 2020

Allelic copy number variation in FSCN2 detected using allele-specific genotyping and multiplex real-time PCRs.

scientific article published on 30 April 2008

An overview of myopia genetics

scientific article published on 28 August 2019

Association of CD59 and CFH polymorphisms with acute anterior uveitis in Chinese population.

scientific article published on 15 July 2016

CFHR2-rs2986127 as a genetic protective marker for acute anterior uveitis in Chinese patients.

scientific article published on 16 June 2016

CFI-rs7356506 is a genetic protective factor for acute anterior uveitis in Chinese patients.

scientific article published on 29 July 2014

COCO enhances the efficiency of photoreceptor precursor differentiation in early human embryonic stem cell-derived retinal organoids

scientific article published on 24 August 2020

Circular RNAs in human and vertebrate neural retinas

scientific article published on 02 April 2019

Clinical and genetic analyses reveal novel pathogenic ABCA4 mutations in Stargardt disease families.

scientific article published on 14 October 2016

Comparison of non-canonical PAMs for CRISPR/Cas9-mediated DNA cleavage in human cells

scientific article

Comprehensive molecular diagnosis of Bardet-Biedl syndrome by high-throughput targeted exome sequencing.

scientific article

Consanguinity-based analysis of exome sequencing yields likely genetic causes in patients with inherited retinal dystrophy

scientific article published on 15 June 2021

Correction: A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal Degeneration

scientific article

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

scientific article published on 20 September 2017

Detection of localized retinal malfunction in retinal degeneration model using a multielectrode array system.

scientific article published in July 2009

Electrical stimulation ameliorates light-induced photoreceptor degeneration in vitro via suppressing the proinflammatory effect of microglia and enhancing the neurotrophic potential of Müller cells

scientific article published on 10 September 2012

Embryonic stem-cell-derived retinal pigment epithelial cells for macular degeneration

scientific article published in The Lancet

Emerging roles of noncoding RNAs in retinal diseases: A review

scientific article published on 09 June 2020

Expanding the Phenotypic and Genotypic Landscape of Nonsyndromic High Myopia: A Cross-Sectional Study in 731 Chinese Patients

scientific article published on 01 September 2019

Functional characterization of CEP250 variant identified in nonsyndromic retinitis pigmentosa

scientific article published on 18 April 2019

Gene Correction Reverses Ciliopathy and Photoreceptor Loss in iPSC-Derived Retinal Organoids from Retinitis Pigmentosa Patients.

scientific article published on 28 February 2018

Genetic signatures of high-altitude adaptation in Tibetans

scientific article

Genome-Wide Detection of Copy Number Variations in Unsolved Inherited Retinal Disease.

scientific article published in January 2017

Genotype-Phenotype Analysis and Mutation Spectrum in a Cohort of Chinese Patients With Congenital Nystagmus

scientific article published on 19 February 2021

Genotype-phenotype correlation and mutation spectrum in a large cohort of patients with inherited retinal dystrophy revealed by next-generation sequencing.

scientific article

Geographic Difference Shaped Human Ocular Surface Metagenome of Young Han Chinese From Beijing, Wenzhou, and Guangzhou Cities

scientific article published on 01 February 2020

Human embryonic stem cell-derived organoid retinoblastoma reveals a cancerous origin

scientific article published on 14 December 2020

Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophy

scientific article published on 4 January 2017

Identification of a novel GJA8 (Cx50) point mutation causes human dominant congenital cataracts.

scientific article published on 18 February 2014

Identification of a novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa.

scientific article published in October 2007

Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.

scientific article published on 20 November 2017

Identification of false-negative mutations missed by next-generation sequencing in retinitis pigmentosa patients: a complementary approach to clinical genetic diagnostic testing.

scientific article published on 8 January 2015

Identification of novel mutations by targeted exome sequencing and the genotype-phenotype assessment of patients with achromatopsia.

scientific article

Identification of three novel mutations in the FRMD7 gene for X-linked idiopathic congenital nystagmus

scientific article published on 17 January 2014

Identifying pathogenic genetic background of simplex or multiplex retinitis pigmentosa patients: a large scale mutation screening study.

scientific article

Loss of miR-182 affects B-cell extrafollicular antibody response

scientific article published on 5 February 2016

Lysosomal storage disease in the brain: mutations of the β-mannosidase gene identified in autosomal dominant nystagmus

scientific article

Macular hole formation in patients with retinitis pigmentosa and prognosis of pars plana vitrectomy

scientific article published in April 2008

Modeling human retinoblastoma using embryonic stem cell-derived retinal organoids

scientific article published on 07 April 2021

Modeling retinal degeneration using patient-specific induced pluripotent stem cells

scientific article

Modeling retinitis pigmentosa through patient-derived retinal organoids

scientific article published on 08 April 2021

Molecular diagnosis of putative Stargardt disease by capture next generation sequencing

scientific article (publication date: 2014)

Molecular genetic analysis and phenotypic characteristics of a consanguineous family with glycogen storage disease type Ia.

scientific article published on 9 August 2016

Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmus

scientific article published on April 2016

Molecular screening of the LPCAT1 gene in patients with retinitis pigmentosa without defined mutations in known retinitis pigmentosa genes.

scientific article published on 10 August 2015

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

scientific article published on 08 April 2022

Mutation spectrum and genotype-phenotype correlation of inherited retinal dystrophy in Taiwan

scientific article published on 24 December 2019

Mutational screening of AGRN, SLC39A5, SCO2, P4HA2, BSG, ZNF644, and CPSF1 in a Chinese cohort of 103 patients with nonsyndromic high myopia

scientific article published on 07 December 2021

Mutational screening of SLC39A5, LEPREL1 and LRPAP1 in a cohort of 187 high myopia patients.

scientific article

Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.

scientific article published on May 2017

Nonhuman Primate Model of Oculocutaneous Albinism with TYR and OCA2 Mutations

scientific article published on 11 March 2020

Novel CHM mutations identified in Chinese families with Choroideremia

scientific article published on 14 October 2016

Novel RPGR-ORF15 mutations in X-linked retinitis pigmentosa patients.

scientific article published on 12 June 2011

R102W mutation in the RS1 gene responsible for retinoschisis and recurrent glaucoma.

scientific article published on 18 February 2014

Relationship Between Cone Loss and Microvasculature Change in Retinitis Pigmentosa

scientific article published on 01 November 2019

Response to Heller and Bolz

scientific article

SLC7A14 linked to autosomal recessive retinitis pigmentosa.

scientific article published on 27 March 2014

Slc7a14 Is Indispensable in Zebrafish Retinas

scientific article published on 12 December 2019

Somatic and gonadal mosaicism in X-linked retinitis pigmentosa

scientific article published on 01 November 2007

Stemming retinal regeneration with pluripotent stem cells

scientific article published on 09 November 2018

Targeted exome sequencing identified novel USH2A mutations in Usher syndrome families.

scientific article

Targeted exome sequencing identified two novel truncation mutations in GPR98 causing Usher syndrome

scientific article published on 12 November 2015

Targeting NLRP3 and staphylococcal pore-forming toxin receptors in human-induced pluripotent stem cell-derived macrophages

scientific article published on 12 June 2020

Targeting neuronal and glial cell types with synthetic promoter AAVs in mice, non-human primates and humans

scientific article published on 08 July 2019

The Association between Maternal Reproductive Age and Progression of Refractive Error in Urban Students in Beijing

scientific article published on 30 September 2015

The Circular RNome of Developmental Retina in Mice

scientific article published on 26 November 2019

Toll-Like Receptor 3 Activation Initiates Photoreceptor Cell Death In Vivo and In Vitro.

scientific article published on February 2017

Towards stem cell-based neuronal regeneration for glaucoma

scientific article published on 29 June 2020

Trio-based exome sequencing arrests de novo mutations in early-onset high myopia

scientific article

USH2A variants in Chinese patients with Usher syndrome type II and non-syndromic retinitis pigmentosa

scientific article published on 16 July 2020

Unique presentation of congenital cataract concurrent with microcornea, microphthalmia plus posterior capsule defect in monozygotic twins caused by a novel GJA8 mutation

scientific article published on 29 November 2018

Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations.

scientific article published on 22 August 2017

Use of lectins to enrich mouse ES-derived retinal progenitor cells for the purpose of transplantation therapy.

scientific article published on 9 October 2009

VEGF-mediated proliferation of human adipose tissue-derived stem cells.

scientific article

Versatile Genome Engineering Techniques Advance Human Ocular Disease Researches in Zebrafish

scientific article published on 12 July 2018

Whole exome sequencing reveals genetic predisposition in a large family with retinitis pigmentosa

scientific article

Whole-Exome Sequencing in a Cohort of High Myopia Patients in Northwest China

scientific article published on 18 June 2021

Whole-exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndrome

scientific article published on 22 April 2019

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese.

scientific article published on 17 November 2017

miR-182 Regulates Metabolic Homeostasis by Modulating Glucose Utilization in Muscle

scientific article published on 5 July 2016

miR-183/96 plays a pivotal regulatory role in mouse photoreceptor maturation and maintenance.

scientific article

List of works by Zi-Bing Jin

'RetinoGenetics': a comprehensive mutation database for genes related to inherited retinal degeneration

A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal Degeneration

A new subset of small stem cells in bovine bone marrow stromal cell populations

A novel Bruch's membrane-mimetic electrospun substrate scaffold for human retinal pigment epithelium cells.

A novel truncating Rs1 mutation associated with X-linked juvenile retinoschisis

A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family

ATP1A3 mutation as a candidate cause of autosomal dominant cone-rod dystrophy

Allelic copy number variation in FSCN2 detected using allele-specific genotyping and multiplex real-time PCRs.

An overview of myopia genetics

Association of CD59 and CFH polymorphisms with acute anterior uveitis in Chinese population.

CFHR2-rs2986127 as a genetic protective marker for acute anterior uveitis in Chinese patients.

CFI-rs7356506 is a genetic protective factor for acute anterior uveitis in Chinese patients.

COCO enhances the efficiency of photoreceptor precursor differentiation in early human embryonic stem cell-derived retinal organoids

Circular RNAs in human and vertebrate neural retinas

Clinical and genetic analyses reveal novel pathogenic ABCA4 mutations in Stargardt disease families.

Comparison of non-canonical PAMs for CRISPR/Cas9-mediated DNA cleavage in human cells

Comprehensive molecular diagnosis of Bardet-Biedl syndrome by high-throughput targeted exome sequencing.

Consanguinity-based analysis of exome sequencing yields likely genetic causes in patients with inherited retinal dystrophy

Correction: A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal Degeneration

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

Detection of localized retinal malfunction in retinal degeneration model using a multielectrode array system.

Electrical stimulation ameliorates light-induced photoreceptor degeneration in vitro via suppressing the proinflammatory effect of microglia and enhancing the neurotrophic potential of Müller cells

Embryonic stem-cell-derived retinal pigment epithelial cells for macular degeneration

Emerging roles of noncoding RNAs in retinal diseases: A review

Expanding the Phenotypic and Genotypic Landscape of Nonsyndromic High Myopia: A Cross-Sectional Study in 731 Chinese Patients

Functional characterization of CEP250 variant identified in nonsyndromic retinitis pigmentosa

Gene Correction Reverses Ciliopathy and Photoreceptor Loss in iPSC-Derived Retinal Organoids from Retinitis Pigmentosa Patients.

Genetic signatures of high-altitude adaptation in Tibetans

Genome-Wide Detection of Copy Number Variations in Unsolved Inherited Retinal Disease.

Genotype-Phenotype Analysis and Mutation Spectrum in a Cohort of Chinese Patients With Congenital Nystagmus

Genotype-phenotype correlation and mutation spectrum in a large cohort of patients with inherited retinal dystrophy revealed by next-generation sequencing.

Geographic Difference Shaped Human Ocular Surface Metagenome of Young Han Chinese From Beijing, Wenzhou, and Guangzhou Cities

Human embryonic stem cell-derived organoid retinoblastoma reveals a cancerous origin

Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophy

Identification of a novel GJA8 (Cx50) point mutation causes human dominant congenital cataracts.

Identification of a novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa.

Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.

Identification of false-negative mutations missed by next-generation sequencing in retinitis pigmentosa patients: a complementary approach to clinical genetic diagnostic testing.

Identification of novel mutations by targeted exome sequencing and the genotype-phenotype assessment of patients with achromatopsia.

Identification of three novel mutations in the FRMD7 gene for X-linked idiopathic congenital nystagmus

Identifying pathogenic genetic background of simplex or multiplex retinitis pigmentosa patients: a large scale mutation screening study.

Loss of miR-182 affects B-cell extrafollicular antibody response

Lysosomal storage disease in the brain: mutations of the β-mannosidase gene identified in autosomal dominant nystagmus

Macular hole formation in patients with retinitis pigmentosa and prognosis of pars plana vitrectomy

Modeling human retinoblastoma using embryonic stem cell-derived retinal organoids

Modeling retinal degeneration using patient-specific induced pluripotent stem cells

Modeling retinitis pigmentosa through patient-derived retinal organoids

Molecular diagnosis of putative Stargardt disease by capture next generation sequencing

Molecular genetic analysis and phenotypic characteristics of a consanguineous family with glycogen storage disease type Ia.

Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmus

Molecular screening of the LPCAT1 gene in patients with retinitis pigmentosa without defined mutations in known retinitis pigmentosa genes.

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

Mutation spectrum and genotype-phenotype correlation of inherited retinal dystrophy in Taiwan

Mutational screening of <i>AGRN</i>, <i>SLC39A5</i>, <i>SCO2</i>, <i>P4HA2, BSG</i>, <i>ZNF644</i>, and <i>CPSF1</i> in a Chinese cohort of 103 patients with nonsyndromic high myopia

Mutational screening of SLC39A5, LEPREL1 and LRPAP1 in a cohort of 187 high myopia patients.

Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.

Nonhuman Primate Model of Oculocutaneous Albinism with TYR and OCA2 Mutations

Novel CHM mutations identified in Chinese families with Choroideremia

Novel RPGR-ORF15 mutations in X-linked retinitis pigmentosa patients.

R102W mutation in the RS1 gene responsible for retinoschisis and recurrent glaucoma.

Relationship Between Cone Loss and Microvasculature Change in Retinitis Pigmentosa

Response to Heller and Bolz

SLC7A14 linked to autosomal recessive retinitis pigmentosa.

Slc7a14 Is Indispensable in Zebrafish Retinas

Somatic and gonadal mosaicism in X-linked retinitis pigmentosa

Stemming retinal regeneration with pluripotent stem cells

Targeted exome sequencing identified novel USH2A mutations in Usher syndrome families.

Targeted exome sequencing identified two novel truncation mutations in GPR98 causing Usher syndrome

Targeting NLRP3 and staphylococcal pore-forming toxin receptors in human-induced pluripotent stem cell-derived macrophages

Targeting neuronal and glial cell types with synthetic promoter AAVs in mice, non-human primates and humans

The Association between Maternal Reproductive Age and Progression of Refractive Error in Urban Students in Beijing

The Circular RNome of Developmental Retina in Mice

Toll-Like Receptor 3 Activation Initiates Photoreceptor Cell Death In Vivo and In Vitro.

Towards stem cell-based neuronal regeneration for glaucoma

Trio-based exome sequencing arrests de novo mutations in early-onset high myopia

USH2A variants in Chinese patients with Usher syndrome type II and non-syndromic retinitis pigmentosa

Unique presentation of congenital cataract concurrent with microcornea, microphthalmia plus posterior capsule defect in monozygotic twins caused by a novel GJA8 mutation

Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations.

Use of lectins to enrich mouse ES-derived retinal progenitor cells for the purpose of transplantation therapy.