John Taylor - Concepedia

Author

John Taylor

Also Known As

Dyer, Brainerd, Hanadi Kazkaz, J M Taylor, J. M. Taylor, J. Taylor, JOHN M. TAYLOR, Jenny C Taylor, John M Taylor, John M. Taylor, John Taylor

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

University of Oxford Centre for Human Genetics Oxford University Hospitals NHS Trust National Institute for Health Research Churchill Hospital

About

John Taylor is an author at University of Oxford specializing in molecular diagnostics, medicine, and sequencing.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	537
2	Engineering	2	2	59
3	Humanities	1	1	31
4	Law	1	1	31
5	Natural Sciences	1	1	27

John Taylor

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders Jenny C. Taylor, Hilary C. Martin, Stefano Lise, Nature Genetics SequencingPsychiatryClinical GenomeGeneticsMedicine	2015	378
The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United Kingdom Katharina Schwarze, James Buchanan, Jilles M. Fermont, Genetics in Medicine	2019	225
Diagnostic value of exome and whole genome sequencing in craniosynostosis Kerry A. Miller, Stephen R.F. Twigg, Simon J. McGowan, Journal of Medical Genetics	2016	120
On computer-assisted analysis of biological sequences: proline punctuation, consensus sequences, and apolipoprotein repeats. Mark S. Boguski, Mark Freeman, Nabil A. Elshourbagy, Journal of Lipid Research	1990	98
A Recurrent Mosaic Mutation in SMO , Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones Syndrome Stephen R.F. Twigg, Robert B. Hufnagel, Kerry A. Miller, The American Journal of Human Genetics	2016	91
“Not pathogenic until proven otherwise”: perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project Elizabeth Ormondroyd, Michael P. Mackley, Edward Blair, Genetics in Medicine Genetic TestingSequencingMedicineGenomes ProjectGenetic Epidemiology	2017	67
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases Alistair T. Pagnamenta, Edoardo Giacopuzzi, John Taylor, Genome Medicine	2023	63
Delineation of dominant and recessive forms of <i>LZTR1</i>‐associated Noonan syndrome Alistair T. Pagnamenta, Pamela J. Kaisaki, Fenella Bennett, Clinical Genetics Heart DefectsDevelopmental BiologyAutoimmune DiseaseMendelian DisorderGenetic Disorder	2019	60
Bayesian Inference Associates Rare <i>KDR</i> Variants With Specific Phenotypes in Pulmonary Arterial Hypertension Emilia M. Swietlik, Daniel Greene, Na Zhu, Circulation Genomic and Precision Medicine	2020	44
Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series John Taylor, Jude Craft, E Blair, Genome Medicine	2019	39

Page 1