Grody, Wayne W.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

Richards, S., Aziz, N., Bale, S., Bick, D., Das, S., Gastier-Foster, J., Grody, W. W., Hegde, M., Lyon, E., Spector, E., et al. (2015) · Genetics in Medicine

Genomics and Rare DiseasesPrenatal Screening and Diagnostics

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ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007

Richards, C. S., Bale, S., Bellissimo, D. B., Das, S., Grody, W. W., Hegde, M. R., Lyon, E., & Ward, B. E. (2008) · Genetics in Medicine

Genomics and Rare DiseasesClinical Laboratory Practices and Quality Control

Cited by 832

Laboratory standards and guidelines for population-based cystic fibrosis carrier screening

Grody, W. W., Cutting, G. R., Klinger, K. W., Richards, C. S., Watson, M. S., & Desnick, R. J. (2001) · Genetics in Medicine

Cystic Fibrosis Research AdvancesGenomics and Rare Diseases

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DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies

Ji, J., Lee, H., Argiropoulos, B., Dorrani, N., Mann, J., Martinez-Agosto, J. A., Gomez-Ospina, N., Gallant, N., Bernstein, J. A., Hudgins, L., et al. (2015) · European Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 145

Cloning and Characterization of Human Agmatinase

Iyer, R. K., Kim, H. K., Tsoa, R. W., Grody, W. W., & Cederbaum, S. D. (2002) · Molecular Genetics and Metabolism

Polyamine Metabolism and ApplicationsAmino Acid Enzymes and Metabolism

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