Peter Farndon - Concepedia

Author

Peter Farndon

Also Known As

P A Farndon, P Farndon, P Farndon~, P. A. FARNDON, P. A. Farndon, P. FARNDON, P. Farndon, P.A. Farndon, Peter A Farndon, Peter A. Farndon

Publications

4.7K

Citations

H-Index

103

Concepts

All Affiliations

Birmingham Women's Hospital University of Birmingham St. Mary's Hospital Birmingham Children's Hospital University College London

About

Peter Farndon is an author at Birmingham Women's Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	28	3.4K
2	Public Health	9	9	355
3	Education	2	2	78
4	Natural Sciences	1	1	12
5	Nursing	1	1	26

Peter Farndon

Publications

3.9K

Citations

H-Index

Page 1

	Year	Citations
Complications of the naevoid basal cell carcinoma syndrome: results of a population based study. D. Gareth Evans, E J Ladusans, S. Rimmer, Journal of Medical Genetics OphthalmologyMany Potential ComplicationsEar MoldingNaevoid Basal CellGynecology	1993	594
A Novel X-Linked Disorder of Immune Deficiency and Hypohidrotic Ectodermal Dysplasia Is Allelic to Incontinentia Pigmenti and Due to Mutations in IKK-gamma (NEMO) Jonathan Zonana, Melissa E. Elder, Lynda C. Schneider, The American Journal of Human Genetics Novel X-linked DisorderUrologyImmune DeficiencyAutoimmune DiseaseGenetic Disorder	2000	521
The fetal valproate syndrome John H. DiLiberti, Peter Farndon, Nicholas R. Dennis, American Journal of Medical Genetics Developmental ToxicologyFetal MedicinePediatricsGynecologyMaternal Health	1984	397
Location of gene for Gorlin syndrome Peter Farndon, Richard G. Del Mastro, M W Kilpatrick, The Lancet Mendelian DisorderGenetic DisorderGeneticsGorlin SyndromeGenetic Epidemiology	1992	396
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene Maria Bitner‐Glindzicz, Keith Lindley, Paul Rutland, Nature Genetics Infantile HyperinsulinismMendelian DisorderGenetic DisorderGeneticsClinical Genetics	2000	324
Mutations in BMP4 Cause Eye, Brain, and Digit Developmental Anomalies: Overlap between the BMP4 and Hedgehog Signaling Pathways Preeti Bakrania, Maria Efthymiou, Johannes Klein, The American Journal of Human Genetics Knockout MouseDevelopmental BiologyHedgehog Signaling PathwaysGenetic DisorderDevelopmental Genetics	2008	249
A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene Antti M. Salo, Helen Cox, Peter Farndon, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsConnective Tissue DisorderLysyl Hydroxylase 3	2008	130
A trisomic germ cell line and precocious chromatid segregation leads to recurrent trisomy 21 conception J. Cozzi, C. M. Conn, Joyce Harper, Human Genetics ChromatinDevelopmental BiologyFertilityGerm CellCytogenetics	1999	117
Epidermal mosaicism and Blaschko's lines. Celia Moss, S. Larkins, Michael W. Stacey, Journal of Medical Genetics	1993	98
REPORT on the Third International Workshop on Chromosome 9 Sue Povey, John A.L. Armour, Peter Farndon, Annals of Human Genetics ChromatinGeneticsChromosome BiologyChromosomal RearrangementGenomics	1994	81

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