Wayne W. Grody
Affiliations: | University of California, Los Angeles, Los Angeles, CA |
Area:
Molecular Biology, Microbiology Biology, GeneticsGoogle:
"Wayne Grody"Children
Sign in to add trainee| Joshua L. Deignan | grad student | 2007 | UCLA |
| Shannon M. Mumenthaler | grad student | 2008 | UCLA |
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Publications
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| Deignan JL, Gregg AR, Grody WW, et al. (2023) Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100867 |
| Deignan JL, Astbury C, Cutting GR, et al. (2020) CFTR variant testing: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Yazdani S, Badjatiya A, Dorrani N, et al. (2020) Genetic characterization and long-term management of severely affected siblings with intellectual developmental disorder with cardiac arrhythmia syndrome. Molecular Genetics and Metabolism Reports. 23: 100582 |
| Delatycki MB, Alkuraya F, Archibald A, et al. (2019) International perspectives on the implementation of reproductive carrier screening. Prenatal Diagnosis |
| Eno CC, Barton SK, Dorrani N, et al. (2019) Confidential genetic testing and electronic health records: A survey of current practices among Huntington disease testing centers. Molecular Genetics & Genomic Medicine. e1026 |
| Ngo KJ, Rexach JE, Lee H, et al. (2019) A Diagnostic Ceiling for Exome Sequencing in Cerebellar Ataxia and Related Neurological Disorders. Human Mutation |
| Grody WW. (2019) The transformation of medical genetics by clinical genomics: hubris meets humility. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Datkhaeva I, Arboleda VA, Senaratne TN, et al. (2018) Identification of novel PIEZO1 variants using prenatal exome sequencing and correlation to ultrasound and autopsy findings of recurrent hydrops fetalis. American Journal of Medical Genetics. Part A |
| Mullegama SV, Klein SD, Nguyen DC, et al. (2017) Is it time to retire fragile X testing as a first-tier test for developmental delay, intellectual disability, and autism spectrum disorder? Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Mullegama SV, Jensik P, Li C, et al. (2017) Coupling clinical exome sequencing with functional characterization studies to diagnose a patient with familial Mediterranean fever and MED13L haploinsufficiency syndromes. Clinical Case Reports. 5: 833-840 |