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Publications by Graham Holder
Whole-Exome Sequencing in the Investigation of Retinal Dystrophy
The Lancet
Medicine
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Whole Exome Sequencing in Monogenic Dyslipidemias
Journal of Atherosclerosis and Thrombosis
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Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
Proceedings of the National Academy of Sciences of the United States of America
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Clinical Application of Whole-Exome Sequencing
JAMA Neurology
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High Diagnostic Yield of Whole Exome Sequencing in Participants With Retinal Dystrophies in a Clinical Ophthalmology Setting
American Journal of Ophthalmology
Ophthalmology
Whole Exome Sequencing in Systemic Juvenile Idiopathic Arthritis
Pediatric Rheumatology
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Allergy
Perinatology
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Application of Whole Exome Sequencing in the Diagnosis of Hereditary Neurological Diseases
Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova
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A Stroke Gene Panel for Whole-Exome Sequencing
European Journal of Human Genetics
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Parental Perceptions of Prenatal Whole Exome Sequencing (PPPWES) Study
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Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and Limitations
PLoS ONE
Multidisciplinary