Noreen L. Rudd - Concepedia

Author

Noreen L. Rudd

Alberta Children's Hospital

Also Known As

N L Rudd, N RUDD, N Rudd, N. L. Rudd, N. Rudd, N.L. Rudd, NOREEN L. RUDD, Noreen L. Rudd, Noreen Rudd

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Alberta Children's Hospital Hospital for Sick Children University of Calgary University of Toronto Toronto General Hospital

About

Noreen L. Rudd is an author at Alberta Children's Hospital specializing in medicine, genetics, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	23	1.1K
2	Public Health	7	7	519
3	Anatomy	2	2	76
4	Health Sciences	1	1	45
5	Biology	1	1	11

Noreen L. Rudd

Publications

Citations

H-Index

Page 1

	Year	Citations
Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high. Y. Tatuch, John Christodoulou, Annette Feigenbaum, PubMed	1992	484
The chromosome constitution of 1000 human spermatozoa Renée H. Martin, Wayne Balkan, K. Burns, Human Genetics SpermatogenesisInfertilityFertilityCytogeneticsChromosome Constitution	1983	203
Craniosynostosis. I. Sagittal synostosis; Its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s) Alasdair G. W. Hunter, Noreen L. Rudd Teratology	1976	202
PREGNANCY COMPLICATIONS IN TYPE IV EHLERS-DANLOS SYNDROME Noreen L. Rudd The Lancet FertilityReproductive HealthGynecologyMaternal HealthObstetrics	1983	147
Craniosynostosis. II. Coronal synostosis: Its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly Alasdair G. W. Hunter, Noreen L. Rudd Teratology	1977	108
Prenatal Diagnosis of G<sub>M1</sub>-Gangliosidosis J. A. Lowden, Ernest Cutz, P.E. Conen, New England Journal of Medicine Fetal MedicineDiagnosisPathologyGynecologyAffected Fetus	1973	102
Kinetochore immunofluorescence in micronuclei: A rapid method for the in situ detection of aneuploidy and chromosome breakage in human fibroblasts Ursula Hennig, Noreen L. Rudd, David I. Hoar Mutation Research/Environmental Mutagenesis and Related Subjects ChromatinCell DivisionCytogeneticsMedicineGenetics	1988	90
A dominantly inherited cytogenetic anomaly: A possible cell division mutant Noreen L. Rudd, Iluko E. Teshima, Renée H. Martin, Human Genetics Genome InstabilityDevelopmental BiologyCell DivisionCytogeneticsCytogenetic Anomaly	1983	51
Prenatal Diagnosis of Hypophosphatasia Noreen L. Rudd, M. Miskin, David I. Hoar, New England Journal of Medicine Fetal HeadInherited Metabolic DiseasePhysiologyPediatricsDiagnosis	1976	48
Maxillonasal Dysplasia (Binderʼs Syndrome) Ian R. Munro, W. J. Sinclair, Noreen L. Rudd, Plastic & Reconstructive Surgery DiagnosisPathologyOral MedicineLe FortSurgery	1979	45

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