Michael A. Walter - Concepedia

Author

Michael A. Walter

Also Known As

Alexander Tokarewicz, Fahed Elian, M A Walter, M Walter, M. A. H. B. Walter, M. A. Walter, M. Walter, M.A. Walter, MA Walter, MICHAEL A. WALTER

311

Publications

7.6K

Citations

H-Index

172

Concepts

All Affiliations

University of Alberta Hospital for Sick Children Medical Genetics Center University of Toronto SickKids Foundation

About

Michael A. Walter is an author at University of Alberta specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	10	11	820
2	Health Sciences	5	5	204
3	Education	3	3	36
4	Business	1	1	12
5	Language Studies	1	1	12

Michael A. Walter

Publications

6.4K

Citations

H-Index

Page 1

	Year	Citations
Circular transcripts of the testis-determining gene Sry in adult mouse testis Blanche Capel, Amanda Swain, Silvia K. Nicolis, Cell BiologySpermatogenesisDevelopmental BiologyAdult Mouse TestisNatural Sciences	1993	1.1K
The Forkhead/Winged Helix Gene Mf1 Is Disrupted in the Pleiotropic Mouse Mutation congenital hydrocephalus Tsutomu Kume, Ke-Yu Deng, Virginia P. Winfrey, Cell Knockout MouseDevelopmental BiologyGenetic DisorderDevelopmental GeneticsGenetics	1998	389
A method for constructing radiation hybrid maps of whole genomes Michael A. Walter, Dominique J. Spillett, Philip Thomas, Nature Genetics ChromatinEngineeringHybridizationGeneticsComputational Genomics	1994	369
Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly Alan J. Mears, Tim Jordan, Farideh Mirzayans, The American Journal of Human Genetics Somatic VariantMendelian DisorderGenetic DisorderGeneticsAxenfeld-rieger Anomaly	1998	326
FOXC1 Is a Potential Prognostic Biomarker with Functional Significance in Basal-like Breast Cancer Partha Ray, Jinhua Wang, Ying Qu, Cancer Research Breast OncologyEngineeringPathologyCancer BiologyTumor Biology	2010	233
Roles for the Winged Helix Transcription Factors MF1 and MFH1 in Cardiovascular Development Revealed by Nonallelic Noncomplementation of Null Alleles Glenn E. Winnier, Tsutomu Kume, Ke‐Yu Deng, Developmental Biology Transcriptional RegulationDevelopmental BiologyGeneticsTranscription RegulationGenomic Mechanism	1999	171
Genotype-Phenotype Correlations in Axenfeld-Rieger Malformation and Glaucoma Patients with<i>FOXC1</i>and<i>PITX2</i>Mutations M. Hermina Strungaru, Irina Dinu, Michael A. Walter Investigative Ophthalmology & Visual Science	2006	168
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies M. Ye, Karyn M. Berry-Wynne, Mika Asai-Coakwell, Human Molecular Genetics	2009	160
Mutation of the PAX6 gene in patients with autosomal dominant keratitis. Farideh Mirzayans, W G Pearce, Ian M. MacDonald, PubMed	1995	147
Mutation in the RIEG1 Gene in Patients with Iridogoniodysgenesis Syndrome Stephen C. Kulak, K. Kozlowski, Elena V. Semina, Human Molecular Genetics	1998	123

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