Wayne W. Grody

University of California, Los Angeles — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

56h-index46.8kcitations326works3.42yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Genomics and Rare Diseases(51), Cystic Fibrosis Research Advances(39), Amino Acid Enzymes and Metabolism(28), Genomic variations and chromosomal abnormalities(26), BRCA gene mutations in cancer(23)

Publications325 total

The GigaAssay: A combined high throughput and highly accurate platform for variant classification
New Biotechnology·2025Open Access
High-throughput characterization of 5886 HER2 variants identifies 112 new in cellulo gain-of-function mutations
Genomics·2025Open Access
New Gain-of-Function Mutations Prioritize Mechanisms of HER2 Activation
2025· 1 citedOpen Access
Whole-Exome Sequencing Identifies Novel GATA5/6 Variants in Right-Sided Congenital Heart Defects
International Journal of Molecular Sciences·2025· 2 citedOpen Access
The Gigaassay: A Combined High Throughput and Highly Accurate Platform for Variant Classification
SSRN Electronic Journal·2025Open Access
Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participants
Genetics in Medicine·2024· 19 citedOpen Access
High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects
International Journal of Molecular Sciences·2024· 5 citedOpen Access
P672: Commercial cystic fibrosis carrier screening tests and coverage of the ACMG 100 recommended variants
Genetics in Medicine Open·2024Open Access
A Primer on Gene Editing: What Does It Mean for Pathologists?
Archives of Pathology & Laboratory Medicine·2023· 2 citedOpen Access
Large-Scale Whole Genome Sequence Analysis of >22,000 Subjects Provides no Evidence of FMR1 Premutation Allele Involvement in Autism Spectrum Disorder
Genes·2023· 5 citedOpen Access
The Gregor Mendel Bicentennial Tribute—Enduring Mementos of the Founder of Genetics
JAMA·2023· 1 cited
Synonymous Variants of Uncertain Silence
International Journal of Molecular Sciences·2023· 3 citedOpen Access
Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine·2023· 30 citedOpen Access
S2464 Misnomer Leading to Delayed Diagnosis of an Autoinflammatory Syndrome in a Latino Male
The American Journal of Gastroenterology·2022
Stewardship of Patient Genomic Data: A Policy Statement of the American College of Medical Genetics and Genomics (ACMG)
Obstetrical & Gynecological Survey·2022
Sa1051: UTILIZATION OF A MULTIDISCIPLINARY TELEHEALTH MODEL TO IMPROVE ACCESS TO CARE AND MAINTAIN AN ACADEMIC TEACHING PARADIGM FOR A UNIQUE PATIENT POPULATION DURING THE COVID-19 PANDEMIC
Gastroenterology·2022Open Access
Stewardship of patient genomic data: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine·2021· 7 cited
Response to Biesecker et al.
The American Journal of Human Genetics·2021· 5 citedOpen Access
Recessive ciliopathy mutations in primary endocardial fibroelastosis: a rare neonatal cardiomyopathy in a case of Alstrom syndrome
Journal of Molecular Medicine·2021· 7 citedOpen Access
Central 22q11.2 deletion (<scp>LCR22 B‐D</scp>) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of <scp><i>CRKL</i></scp> haploinsufficiency in the pathogenesis of 22q11.2 deletion syndrome
American Journal of Medical Genetics Part A·2021· 6 cited
page 1 of 17Next →

Frequent Co-authors

Stanley F. Nelson(8), Stephen D. Cederbaum(8), Hane Lee(7), Joshua L. Deignan(7), Éric Vilain(7), Rita M. Kern(7), Ramaswamy K. Iyer(6), Madhuri Hegde(4), Michael S. Watson(4), Naghmeh Dorrani(4), Samuel P. Strom(4), Fabiola Quintero‐Rivera(4), Garry R. Cutting(4), Hong Yu(4), Sue Richards(3), Nazneen Aziz(3), Sherri J. Bale(3), Soma Das(3), Karl V. Voelkerding(3), Heidi L. Rehm(3)