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Abusive supervision: exploring the relationship with narcissism, self-promotion and unpredictability

The Journal of management development, 2021-04, Vol.40 (3), p.209-223

2021

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Deep learning segmentation of hyperautofluorescent fleck lesions in Stargardt disease

Scientific reports, 2020-10, Vol.10 (1), p.16491-16491, Article 16491

2020

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Characterising splicing defects of ABCA4 variants within exons 13–50 in patient-derived fibroblasts

Experimental eye research, 2022-12, Vol.225, p.109276-109276, Article 109276

2022

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Analysis of Coffee for the Presence of Acrylamide by LC-MS/MS

Journal of agricultural and food chemistry, 2004-04, Vol.52 (7), p.1996-2002

2004

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Secondary education in England: 1870 - 1902; public activity and private enterprise

Roach, John

1991

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Evaluation and single laboratory validation of an on-line turbulent flow extraction tandem mass spectrometry method for melamine in infant formula

Journal of Chromatography A, 2011-07, Vol.1218 (28), p.4284-4290

2011

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Microperimetry and Adaptive Optics Imaging Reveal Localized Functional and Structural Changes in Asymptomatic RPGR Mutation Carriers

Investigative ophthalmology & visual science, 2023-01, Vol.64 (1), p.3-3

2023

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Rugged LC-MS/MS Survey Analysis for Acrylamide in Foods

Journal of agricultural and food chemistry, 2003-12, Vol.51 (26), p.7547-7554

2003

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Development of High-Throughput Clinical Testing of RPGR ORF15 Using a Large Inherited Retinal Dystrophy Cohort

Investigative ophthalmology & visual science, 2018-09, Vol.59 (11), p.4434-4440

2018

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CLASSIFYING ABCA4 MUTATION SEVERITY USING AGE-DEPENDENT ULTRA-WIDEFIELD FUNDUS AUTOFLUORESCENCE-DERIVED TOTAL LESION SIZE

Retina (Philadelphia, Pa.), 2021-12, Vol.41 (12), p.2578-2588

2021

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Enhanced Visualization of Subtle Outer Retinal Pathology by En Face Optical Coherence Tomography and Correlation with Multi-Modal Imaging

PloS one, 2016-12, Vol.11 (12), p.e0168275

2016

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A novel phenotype in a family with autosomal dominant retinal dystrophy due to c.1430A > G in retinoid isomerohydrolase (RPE65) and c.37C > T in bestrophin 1 (BEST1)

Documenta ophthalmologica, 2021-08, Vol.143 (1), p.61-73

2021

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SIBLING CONCORDANCE IN SYMPTOM ONSET AND ATROPHY GROWTH RATES IN STARGARDT DISEASE USING ULTRA-WIDEFIELD FUNDUS AUTOFLUORESCENCE

Retina (Philadelphia, Pa.), 2022-08, Vol.42 (8), p.1545-1559

2022

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Longitudinal Analysis of Functional and Structural Outcome Measures in PRPH2-Associated Retinal Dystrophy

Ophthalmology retina, 2023-01, Vol.7 (1), p.81-91

2023

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Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1

Stem cell research, 2021-07, Vol.54, p.102403-102403, Article 102403

2021

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Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4

Stem cell research, 2020-10, Vol.48, p.101947-101947, Article 101947

2020

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Maternal uniparental isodisomy of chromosome 6 unmasks a novel variant in TULP1 in a patient with early onset retinal dystrophy

Molecular vision, 2018-07, Vol.24, p.478-484

2018

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Genotype-Specific Lesion Growth Rates in Stargardt Disease

Genes, 2021-12, Vol.12 (12), p.1981

2021

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Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200

Stem cell research, 2021-03, Vol.51, p.102154-102154, Article 102154

2021

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Generation of three induced pluripotent stem cell lines from an isolated inherited retinal dystrophy patient with RCBTB1 frameshifting mutations

Stem cell research, 2019-10, Vol.40, p.101549-101549, Article 101549

2019

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Denitrification mitigates N flux through the stream-floodplain complex of a desert city

Ecological applications, 2011-10, Vol.21 (7), p.2618-2636

2011

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Determination of Bisphenol A in U.S. Infant Formulas: Updated Methods and Concentrations

Journal of agricultural and food chemistry, 2010-02, Vol.58 (4), p.2307-2313

2010

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Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461–10T>C;5603A>T];[6077T>C] mutations in the ABCA4 gene

Stem cell research, 2021-07, Vol.54, p.102439-102439, Article 102439

2021

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Clinical Evidence for the Importance of the Wild-Type PRPF31 Allele in the Phenotypic Expression of RP11

Genes, 2021-06, Vol.12 (6), p.915

2021

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Is computer-assisted learning the key to widespread high-dosage tutoring?

Monthly labor review, 2024-07, p.1

Roach, John C

2024

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Abusive supervision: exploring the relationship with narcissism, self-promotion and unpredictability

Deep learning segmentation of hyperautofluorescent fleck lesions in Stargardt disease

Characterising splicing defects of ABCA4 variants within exons 13–50 in patient-derived fibroblasts

Analysis of Coffee for the Presence of Acrylamide by LC-MS/MS

Secondary education in England: 1870 - 1902; public activity and private enterprise

Evaluation and single laboratory validation of an on-line turbulent flow extraction tandem mass spectrometry method for melamine in infant formula

Microperimetry and Adaptive Optics Imaging Reveal Localized Functional and Structural Changes in Asymptomatic RPGR Mutation Carriers

Rugged LC-MS/MS Survey Analysis for Acrylamide in Foods

Development of High-Throughput Clinical Testing of RPGR ORF15 Using a Large Inherited Retinal Dystrophy Cohort

CLASSIFYING ABCA4 MUTATION SEVERITY USING AGE-DEPENDENT ULTRA-WIDEFIELD FUNDUS AUTOFLUORESCENCE-DERIVED TOTAL LESION SIZE

Enhanced Visualization of Subtle Outer Retinal Pathology by En Face Optical Coherence Tomography and Correlation with Multi-Modal Imaging

A novel phenotype in a family with autosomal dominant retinal dystrophy due to c.1430A > G in retinoid isomerohydrolase (RPE65) and c.37C > T in bestrophin 1 (BEST1)

SIBLING CONCORDANCE IN SYMPTOM ONSET AND ATROPHY GROWTH RATES IN STARGARDT DISEASE USING ULTRA-WIDEFIELD FUNDUS AUTOFLUORESCENCE

Longitudinal Analysis of Functional and Structural Outcome Measures in PRPH2-Associated Retinal Dystrophy

Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1

Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4

Maternal uniparental isodisomy of chromosome 6 unmasks a novel variant in TULP1 in a patient with early onset retinal dystrophy

Genotype-Specific Lesion Growth Rates in Stargardt Disease

Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200

Generation of three induced pluripotent stem cell lines from an isolated inherited retinal dystrophy patient with RCBTB1 frameshifting mutations

Denitrification mitigates N flux through the stream-floodplain complex of a desert city

Determination of Bisphenol A in U.S. Infant Formulas: Updated Methods and Concentrations

Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461–10T>C;5603A>T];[6077T>C] mutations in the ABCA4 gene

Clinical Evidence for the Importance of the Wild-Type PRPF31 Allele in the Phenotypic Expression of RP11

Is computer-assisted learning the key to widespread high-dosage tutoring?

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