Caroline Mackie Ogilvie

Author

Guy's and St Thomas' NHS Foundation Trust ORCID

Also Known As

C M Ogilvie, C Mackie Ogilvie, C Ogilvie, C. M Ogilvie, C. M. Ogilvie, C. Mackie Ogilvie, C. Ogilvie, C.Mackie Ogilvie, CAROLINE OGILVIE, Caroline F. Wright

214

Publications

8.6K

Citations

H-Index

170

Concepts

All Affiliations

Guy's and St Thomas' NHS Foundation Trust Guy's Hospital King's College London St Thomas' Hospital University College London

About

Caroline Mackie Ogilvie is an author at Guy's and St Thomas' NHS Foundation Trust specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	31	55	3.3K
2	Public Health	18	23	1.7K
3	Education	4	4	149
4	Natural Sciences	3	3	86
5	Engineering	2	2	106

Caroline Mackie Ogilvie

Publications

5.5K

Citations

H-Index

Page 1

	Year	Citations
Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis Paul N. Scriven, Alan H. Handyside, Caroline Mackie Ogilvie Prenatal Diagnosis Genetic TestingCytogeneticsGeneticsGynecologyPreimplantation Genetic Testing	1998	258
Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder Andrea K. Vaags, Anath C. Lionel, Daisuke Sato, The American Journal of Human Genetics Rare DeletionsSyndromic AutismGeneticsPsychiatric GeneticsAutism	2011	213
Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis Kathy Mann, Susan P. Fox, Stephen Abbs, The Lancet Newborn ScreeningPrenatal Genetic TestingPrenatal Genetic ScreeningDiagnosisGynecology	2001	209
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags, Human Molecular Genetics Astn2/trim32 LocusBrain DevelopmentAutism Spectrum DisordersGeneticsMolecular Biology	2013	172
Male-Biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders Maria Tropeano, Joo Wook Ahn, Richard Dobson, PLoS ONE	2013	156
Proof of principle and first cases using preimplantation genetic haplotyping – a paradigm shift for embryo diagnosis Pamela Renwick, Jane Trussler, Elham Ostad-Saffari, Reproductive BioMedicine Online First CasesDevelopmental BiologyGeneticsPreimplantation Genetic TestingAneuploidy	2006	152
Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis Celia Donaghue, Kathy Mann, Zoe Docherty, Prenatal Diagnosis	2005	149
Strategies for the rapid prenatal diagnosis of chromosome aneuploidy Kathy Mann, Celia Donaghue, Susan P. Fox, European Journal of Human Genetics ChromatinCytogeneticsPrenatal Genetic TestingGeneticsRapid Prenatal Diagnosis	2004	140
Meiotic outcomes in reciprocal translocation carriers ascertained in 3-day human embryos Caroline Mackie Ogilvie, Paul N. Scriven European Journal of Human Genetics 3-Day Human EmbryosDevelopmental BiologyFertilityCell DivisionOogenesis	2002	140
Assisted reproductive technologies to prevent human mitochondrial disease transmission Andy Greenfield, Peter Braude, Frances Flinter, Nature Biotechnology InfertilityMitochondrial TransplantationFertilityMitochondrial FunctionMitochondrial Therapy	2017	110

Page 1