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Single-cell evaluation reveals shifts in the tumor-immune niches that shape and maintain aggressive lesions in the breast

Nature communications, 2021-08, Vol.12 (1), p.5024-5024, Article 5024

2021

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Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patients

Investigative ophthalmology & visual science, 2015-02, Vol.56 (3), p.1937-1946

2015

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Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa

American journal of human genetics, 2016-12, Vol.99 (6), p.1305-1315

2016

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Folic acid exerts antidepressant effects by upregulating brain-derived neurotrophic factor and glutamate receptor 1 expression in brain

Neuroreport, 2017-11, Vol.28 (16), p.1078-1084

2017

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SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data

BMC bioinformatics, 2017-03, Vol.18 (1), p.147-147, Article 147

2017

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REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking

Human molecular genetics, 2017-07, Vol.26 (14), p.2667-2677

2017

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Mutations in human IFT140 cause non-syndromic retinal degeneration

Human genetics, 2015-10, Vol.134 (10), p.1069-1078

2015

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Comparison and quantitative verification of mapping algorithms for whole-genome bisulfite sequencing

Nucleic acids research, 2014-04, Vol.42 (6), p.e43-e43

2014

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Spatially resolved transcriptomics of high-grade serous ovarian carcinoma

iScience, 2022-03, Vol.25 (3), p.103923-103923, Article 103923

2022

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A new switching control for T‐S fuzzy systems with mixed time delays

International journal of robust and nonlinear control, 2023-11, Vol.33 (16), p.9843-9861

2023

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GRIPT: a novel case-control analysis method for Mendelian disease gene discovery

Genome Biology, 2018-11, Vol.19 (1), p.203-20, Article 203

2018

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The phenotypic variability of HK1-associated retinal dystrophy

Scientific reports, 2017-08, Vol.7 (1), p.7051-7051, Article 7051

2017

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A Novel Dominant Mutation in SAG, the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States

Investigative ophthalmology & visual science, 2017-05, Vol.58 (5), p.2774-2784

2017

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Prognostic role of systemic inflammatory response in renal cell carcinoma: a systematic review and meta-analysis

Journal of cancer research and clinical oncology, 2011-05, Vol.137 (5), p.887-896

2011

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Investigating the disease association of USH2A p.C759F variant by leveraging large retinitis pigmentosa cohort data

Ophthalmic genetics, 2018-03, Vol.39 (2), p.291-292

2018

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Stabilisation of T-S fuzzy systems with mixed time delays

International journal of systems science, 2020-07, Vol.51 (10), p.1814-1824

2020

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Membership-difference-dependent switching control for time-delay T–S fuzzy systems

Journal of the Franklin Institute, 2024-03, Vol.361 (4), p.106635, Article 106635

2024

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Observer-Based Switching Control for T–S Fuzzy Systems with Mixed Time Delays

International journal of fuzzy systems, 2023-06, Vol.25 (4), p.1480-1494

2023

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Distributed hunting problem of multi-quadrotor systems via bearing constraint method subject to time delays

Journal of the Franklin Institute, 2020-08, Vol.357 (12), p.7537-7555

2020

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Abstract 2822: Single-cell evaluation to identify tumor-stroma niches driving the transition from in situ to invasive breast cancer

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.2822-2822

2020

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Next-generation sequencing-based molecular diagnosis of 35 Hispanic retinitis pigmentosa probands

Scientific reports, 2016-09, Vol.6 (1), p.32792-32792, Article 32792

2016

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PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHY

Retina (Philadelphia, Pa.), 2019-10, Vol.39 (10), p.2040-2052

2019

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Structure-function analysis reveals a novel mechanism for regulation of histone demethylase LSD2/AOF1/KDM1b

Cell research, 2013-02, Vol.23 (2), p.225-241

2013

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CEP78 is mutated in a distinct type of Usher syndrome

Journal of medical genetics, 2017-03, Vol.54 (3), p.190-195

2017

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Single-cell evaluation reveals shifts in the tumor-immune niches that shape and maintain aggressive lesions in the breast

Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patients

Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa

Folic acid exerts antidepressant effects by upregulating brain-derived neurotrophic factor and glutamate receptor 1 expression in brain

SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data

REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking

Mutations in human IFT140 cause non-syndromic retinal degeneration

Mouse‐INtraDuctal (MIND): an in vivo model for studying the underlying mechanisms of DCIS malignancy

Comparison and quantitative verification of mapping algorithms for whole-genome bisulfite sequencing

Spatially resolved transcriptomics of high-grade serous ovarian carcinoma

A new switching control for T‐S fuzzy systems with mixed time delays

GRIPT: a novel case-control analysis method for Mendelian disease gene discovery

The phenotypic variability of HK1-associated retinal dystrophy

A Novel Dominant Mutation in SAG, the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States

Prognostic role of systemic inflammatory response in renal cell carcinoma: a systematic review and meta-analysis

Investigating the disease association of USH2A p.C759F variant by leveraging large retinitis pigmentosa cohort data

Stabilisation of T-S fuzzy systems with mixed time delays

Membership-difference-dependent switching control for time-delay T–S fuzzy systems

Observer-Based Switching Control for T–S Fuzzy Systems with Mixed Time Delays

Distributed hunting problem of multi-quadrotor systems via bearing constraint method subject to time delays

Abstract 2822: Single-cell evaluation to identify tumor-stroma niches driving the transition from in situ to invasive breast cancer

Next-generation sequencing-based molecular diagnosis of 35 Hispanic retinitis pigmentosa probands

PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHY

Structure-function analysis reveals a novel mechanism for regulation of histone demethylase LSD2/AOF1/KDM1b

CEP78 is mutated in a distinct type of Usher syndrome

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