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Statistical Meta-Analysis of Risk Factors for Endometrial Cancer and Development of a Risk Prediction Model Using an Artificial Neural Network Algorithm

Cancers, 2021-07, Vol.13 (15), p.3689

2021

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What works for wellbeing? A systematic review of wellbeing outcomes for music and singing in adults

Perspectives in Public Health, 2018-01, Vol.138 (1), p.39-46

2018

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

Nature genetics, 2000-01, Vol.24 (1), p.79-83

2000

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Machine Learning with Applications in Breast Cancer Diagnosis and Prognosis

Designs, 2018-06, Vol.2 (2), p.13

2018

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Analysis of Friedreich's ataxia patient clinical data reveals importance of accurate GAA repeat determination in disease prognosis and gender differences in cardiac measures

Informatics in medicine unlocked, 2019, Vol.17, p.100266, Article 100266

2019

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Multi-membership gene regulation in pathway based microarray analysis

Algorithms for molecular biology, 2011-09, Vol.6 (1), p.22-22, Article 22

2011

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Epigenetic Inactivation Implies Independent Functions for Insulin-like Growth Factor Binding Protein (IGFBP)-Related Protein 1 and the Related IGFBPL1 in Inhibiting Breast Cancer Phenotypes

Clinical cancer research, 2007-07, Vol.13 (14), p.4061-4068

2007

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A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

Nature genetics, 1999-04, Vol.21 (4), p.355-356

1999

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Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

Nature genetics, 1999-10, Vol.23 (2), p.217-221

1999

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Diagnostic Accuracy of Liquid Biomarkers for the Non-Invasive Diagnosis of Endometrial Cancer: A Systematic Review and Meta-Analysis

Cancers, 2022-09, Vol.14 (19), p.4666

2022

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Comparative (Computational) Analysis of the DNA Methylation Status of Trinucleotide Repeat Expansion Diseases

Journal of Nucleic Acids, 2013, Vol.2013 (2013), p.65-73

2013

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Wavelet Coherence Analysis of Change Blindness

Mehran University research journal of engineering and technology, 2013-01, Vol.32 (1), p.103-110

2013

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Sport and dance interventions for healthy young people (15–24 years) to promote subjective well-being: a systematic review

BMJ open, 2018-07, Vol.8 (7), p.e020959-e020959

2018

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A Collaborative-Filtering-Based Data Collection Strategy for Friedreich’s Ataxia

Cognitive computation, 2020, Vol.12 (1), p.249-260

2020

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HIV- 1 lentivirus tethering to the genome is associated with transcription factor binding sites found in genes that favour virus survival

Gene therapy, 2022-12, Vol.29 (12), p.720-729

2022

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Orexin receptors exert a neuroprotective effect in Alzheimer’s disease (AD) via heterodimerization with GPR103

Scientific reports, 2015-07, Vol.5 (1), p.12584-12584, Article 12584

2015

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Identification of differentially expressed immune receptor genes in osteosarcoma

Bone Reports, 2022-05, Vol.16, p.101489, Article 101489

2022

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Genome wide classification and characterisation of CpG sites in cancer and normal cells

Computers in biology and medicine, 2016-01, Vol.68, p.57-66

2016

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Computer Simulations Improve University Instructional Laboratories

Cell biology education, 2004, Vol.3 (4), p.263-269

2004

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A Novel Locus for Leber Congenital Amaurosis (LCA4) with Anterior Keratoconus Mapping to Chromosome 17p13

Investigative ophthalmology & visual science, 2000-03, Vol.41 (3), p.629-633

2000

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GCAP1(Y99C) Mutant Is Constitutively Active in Autosomal Dominant Cone Dystrophy

Molecular cell, 1998-07, Vol.2 (1), p.129-133

1998

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A mixed methods investigation of alcohol use in sheltered accommodation

Payne, Annette

2018

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Spectrum of Mutations in USH2A in British Patients with Usher Syndrome Type II

Experimental eye research, 2001-05, Vol.72 (5), p.503-509

2001

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Rifampin Reduces Oral Morphine Absorption: A Case of Transdermal Buprenorphine Selection Based on Morphine Pharmacokinetics

Journal of pain & palliative care pharmacotherapy, 2012-12, Vol.26 (4), p.362-367

2012

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Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies

Journal of medical genetics, 1999-09, Vol.36 (9), p.691-693

1999

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Statistical Meta-Analysis of Risk Factors for Endometrial Cancer and Development of a Risk Prediction Model Using an Artificial Neural Network Algorithm

What works for wellbeing? A systematic review of wellbeing outcomes for music and singing in adults

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

Machine Learning with Applications in Breast Cancer Diagnosis and Prognosis

Analysis of Friedreich's ataxia patient clinical data reveals importance of accurate GAA repeat determination in disease prognosis and gender differences in cardiac measures

Multi-membership gene regulation in pathway based microarray analysis

Epigenetic Inactivation Implies Independent Functions for Insulin-like Growth Factor Binding Protein (IGFBP)-Related Protein 1 and the Related IGFBPL1 in Inhibiting Breast Cancer Phenotypes

A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

Diagnostic Accuracy of Liquid Biomarkers for the Non-Invasive Diagnosis of Endometrial Cancer: A Systematic Review and Meta-Analysis

Comparative (Computational) Analysis of the DNA Methylation Status of Trinucleotide Repeat Expansion Diseases

Wavelet Coherence Analysis of Change Blindness

Sport and dance interventions for healthy young people (15–24 years) to promote subjective well-being: a systematic review

A Collaborative-Filtering-Based Data Collection Strategy for Friedreich’s Ataxia

HIV- 1 lentivirus tethering to the genome is associated with transcription factor binding sites found in genes that favour virus survival

Orexin receptors exert a neuroprotective effect in Alzheimer’s disease (AD) via heterodimerization with GPR103

Identification of differentially expressed immune receptor genes in osteosarcoma

Genome wide classification and characterisation of CpG sites in cancer and normal cells

Computer Simulations Improve University Instructional Laboratories

A Novel Locus for Leber Congenital Amaurosis (LCA4) with Anterior Keratoconus Mapping to Chromosome 17p13

GCAP1(Y99C) Mutant Is Constitutively Active in Autosomal Dominant Cone Dystrophy

A mixed methods investigation of alcohol use in sheltered accommodation

Spectrum of Mutations in USH2A in British Patients with Usher Syndrome Type II

Rifampin Reduces Oral Morphine Absorption: A Case of Transdermal Buprenorphine Selection Based on Morphine Pharmacokinetics

Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies

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