Lampros A. Mavrogiannis

Author

Also Known As

L A Mavrogiannis, L Mavrogiannis, L. A. Mavrogiannis, L. Mavrogiannis, Lampros A Mavrogiannis, Lampros A. Mavrogiannis, Lampros Mavrogiannis, Mavrogiannis, Lampros A., S. Tennant

Publications

685

Citations

H-Index

Concepts

All Affiliations

University of Oxford John Radcliffe Hospital

About

Lampros A. Mavrogiannis is an author at University of Oxford specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	292
2	Molecular Genetics	2	2	93
3	Biology	1	1	83
4	Neurology	1	1	50
5	Pathology	1	1	50

Lampros A. Mavrogiannis

Publications

649

Citations

H-Index

Page 1

	Year	Citations
The Yeast Fre1p/Fre2p Cupric Reductases Facilitate Copper Uptake and Are Regulated by the Copper-modulated Mac1p Activator Elena Georgatsou, Lampros A. Mavrogiannis, George S. Fragiadakis, Journal of Biological Chemistry	1997	287
Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects Lampros A. Mavrogiannis, Ileana Antonopoulou, A Baxová, Nature Genetics Developmental BiologyBone Morphogenic ProteinCraniofacial DisorderGeneticsSkull Ossification Defects	2001	149
Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype Lampros A. Mavrogiannis, Indira B. Taylor, Sally Davies, European Journal of Human Genetics BiologyHomeobox Genes Alx4Allelic VariantDevelopmental AnomalyDevelopmental Biology	2005	83
<i>Alx4</i> and <i>Msx2</i> play phenotypically similar and additive roles in skull vault differentiation Ileana Antonopoulou, Lampros A. Mavrogiannis, Andrew O.M. Wilkie, Journal of Anatomy	2004	57
Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2 Sixto García‐Miñaúr, Lampros A. Mavrogiannis, Sahan V. Rannan‐Eliya, European Journal of Human Genetics Cleidocranial DysplasiaDevelopmental AnomalyParietal ForaminaGenetic DisorderPathology	2003	50
Quantitation of X-Y homologous genes in patients with schizophrenia by multiplex polymerase chain reaction Norman Ross, Lampros A. Mavrogiannis, Carole A. Sargent, Psychiatric Genetics	2003	13
Novel human pathological mutations Lampros A. Mavrogiannis, Carol Chu, Ruth Charlton Human Genetics Somatic VariantMendelian DisorderGenetic DisorderMedicineGenetics	2009	10

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