Gudrun E. Moore - Concepedia

Author

Gudrun E. Moore

University College London ORCID

Also Known As

A.J. Copp, G E Moore, G Moore, G. E. MOORE, G. E. Moore, G. MOORE, G. Moore, G.E. Moore, GUDRUN E. MOORE, GUDRUN MOORE

236

Publications

9.5K

Citations

H-Index

148

Concepts

All Affiliations

University College London Queen Charlotte's and Chelsea Hospital Imperial College London Great Ormond Street Hospital University of London

About

Gudrun E. Moore is an author at University College London specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	62	4.4K
2	Natural Sciences	13	13	986
3	Public Health	11	12	729
4	Health Sciences	3	3	158
5	Engineering	2	2	40

Gudrun E. Moore

109

Publications

7.3K

Citations

H-Index

Page 1

	Year	Citations
Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS Veronica A. Kinsler, Anna Thomas, Miho Ishida, Journal of Investigative Dermatology	2013	343
The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta M. Noguer-Dance, Sayeda Abu‐Amero, Mohamed Al-Khtib, Human Molecular Genetics Epigenetic ChangeGeneticsDna MethylationEpigeneticsEmbryology	2010	323
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia Claire Braybrook, Kit Doudney, Ana Carolina B. Marçano, Nature Genetics Developmental BiologyGeneticsX-linked Cleft PalateTranscription FactorsMedicine	2001	263
Functional Variants of the Central Bile Acid Sensor FXR Identified in Intrahepatic Cholestasis of Pregnancy Saskia W. C. van Mil, Alexandra Milona, Peter Dixon, Gastroenterology HepatologyBiliary TractLiver PhysiologyGastroenterologyPathology	2007	258
Limited evolutionary conservation of imprinting in the human placenta David Monk, Philippe Arnaúd, Sophia Apostolidou, Proceedings of the National Academy of Sciences FertilityEpigenetic ChangeGeneticsEpigeneticsEmbryology	2006	254
Epigenotype–phenotype correlations in Silver–Russell syndrome Emma Wakeling, S. A. Amero, Mariëlle Alders, Journal of Medical Genetics	2010	218
Human Chromosome 7: DNA Sequence and Biology Stephen W. Scherer, Joseph Cheung, Jeffrey R. MacDonald, Science DnaCytogeneticsGeneticsMolecular BiologyHigher Order Description	2003	214
Contribution of variant alleles of <i>ABCB11</i> to susceptibility to intrahepatic cholestasis of pregnancy Peter Dixon, Saskia W. C. van Mil, Jenny Chambers, Gut	2008	214
Routine addition of human insulin-like growth factor-I ligand could benefit clinical in-vitro fertilization culture Antony D. Lighten, Gudrun E. Moore, Robert Winston, Human Reproduction Routine AdditionFertilityHuman GrowthGynecologyHuman Preimplantation Development	1998	173
Expression of cyclooxygenase types 1 and 2 in human fetal membranes at term Donna M. Slater, Louise C. Berger, Robert Newton, American Journal of Obstetrics and Gynecology BiosynthesisDevelopmental BiologyBiochemistryPlacental DevelopmentFetal Medicine	1995	164

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