Maggie Meeks - Concepedia

Author

Maggie Meeks

Also Known As

M Meeks, M. Meeks, Maggie G. Meeks, Maggie Meeks, Margaret G. Meeks, Margaret Meeks, Meeks, M, Meeks, Maggie, Molly N. Meeks

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

University College London The Royal Free Hospital University Hospital of Geneva University of Geneva Hospital Clínico Universitario de Valencia

About

Maggie Meeks is an author at University College London specializing in pathology, medicine, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	853
2	Pathology	5	5	853
3	Molecular Genetics	3	3	288
4	Clinical Genetics	2	2	700
5	Genetic Epidemiology	1	1	68

Maggie Meeks

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry Heike Olbrich, Karsten Häffner, Andreas Kispert, Nature Genetics Genome InstabilityMendelian DisorderGenetic DisorderGeneticsPathology	2002	550
Mutations in the <i>DNAH11</i> (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia Lucia Bartoloni, Jean‐Louis Blouin, Yanzhen Pan, Proceedings of the National Academy of Sciences	2002	359
Primary ciliary dyskinesia: age at diagnosis and symptom history ME Coren, Maggie Meeks, Ian Morrison, Acta Paediatrica	2002	226
Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity J-L Blouin, Maggie Meeks, Uppala Radhakrishna, European Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyComplex Disease	2000	150
Axonemal Beta Heavy Chain Dynein DNAH9: cDNA Sequence, Genomic Structure, and Investigation of Its Role in Primary Ciliary Dyskinesia Lucia Bartoloni, Jean‐Louis Blouin, Amit K. Maiti, Genomics GeneticsPathologyDegenerative DiseaseMolecular GeneticsGenomic Structure	2001	70
A locus for primary ciliary dyskinesia maps to chromosome 19q Maggie Meeks Journal of Medical Genetics Pcd LocusMendelian DisorderGenetic DisorderMedicineGenetics	2000	68
No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with Primary Ciliary Dyskinesia (PCD) Amit K. Maiti, Lucia Bartoloni, Hannah M. Mitchison, Cytogenetic and Genome Research	2000	37
Primary ciliary dyskinesia Maggie Meeks Current Paediatrics Neurological DisorderHistopathologyDiagnosisPathologyCiliary Body	1998	15
Macronutrient Composition of Donated Human Milk in a New Zealand Population Rachael Lamb, Jillian J. Haszard, Helen Little, Journal of Human Lactation	2020	15

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