Wayne W. Grody
Impact in
- Genetics top 0.05%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
- Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 64
- Genomics and Rare Diseases 39
- Genomic variations and chromosomal abnormalities 18
- BRCA gene mutations in cancer 17
- Biochemistry 23
- Amino Acid Enzymes and Metabolism 23
- Co-authors
- Heidi L. Rehm (5 shared papers)Madhuri Hegde (6 shared papers)Sherri J. Bale (5 shared papers)Soma Das (4 shared papers)Elaine Lyon (4 shared papers)Nazneen Aziz (4 shared papers)Karl V. Voelkerding (4 shared papers)Sue M. Richards (4 shared papers)
- Journals
- Genetics in Medicine (36 papers)Journal of Molecular Diagnostics (9 papers)Molecular Genetics and Metabolism (8 papers)Archives of Pathology & Laboratory Medicine (7 papers)Diagnostic Molecular Pathology (7 papers)
- Partner nations
- United StatesUnited KingdomPoland
In The Last Decade
Wayne W. Grody
219 papers receiving 35.9k citations
Wayne W. Grody's Hit Papers
Peers
Comparison fields: 5 of 173
- Genetics 13.0k
- Cancer Research 3.0k
- Clinical Biochemistry 1.4k
- Genetics 1.8k
- Molecular Biology 11.5k
Countries citing papers authored by Wayne W. Grody
This map shows the geographic impact of Wayne W. Grody's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Wayne W. Grody with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wayne W. Grody more than expected).
Fields of papers citing papers by Wayne W. Grody
This network shows the impact of papers produced by Wayne W. Grody. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Wayne W. Grody. The network helps show where Wayne W. Grody may publish in the future.
Co-authors
The 25 scholars most cited alongside Wayne W. Grody, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 235 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 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 Hit paper breakdown → | 2015 | 23722 |
| 2 | ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing Hit paper breakdown → | 2013 | 2018 |
| 3 | Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders Hit paper breakdown → | 2014 | 780 |
| 4 | DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study Hit paper breakdown → | 2011 | 725 |
| 5 | ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007 Hit paper breakdown → | 2008 | 689 |
| 6 | DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study Hit paper breakdown → | 2012 | 422 |
| 7 | 2001 | 378 | |
| 8 | 2004 | 371 | |
| 9 | 1982 | 300 | |
| 10 | 2014 | 299 | |
| 11 | 2017 | 281 | |
| 12 | 2004 | 215 | |
| 13 | 2013 | 198 | |
| 14 | 2014 | 196 | |
| 15 | 2014 | 186 | |
| 16 | 1996 | 173 | |
| 17 | 1990 | 168 | |
| 18 | 2008 | 159 | |
| 19 | 2002 | 156 | |
| 20 | 2001 | 142 |
About Wayne W. Grody
Wayne W. Grody is a scholar working on Genetics, Genetics, Biochemistry, Hematology and Pulmonary and Respiratory Medicine, having authored 235 papers that have together received 36.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (39 papers), Cystic Fibrosis Research Advances (32 papers), Amino Acid Enzymes and Metabolism (23 papers), Genomic variations and chromosomal abnormalities (18 papers), BRCA gene mutations in cancer (17 papers), Metabolism and Genetic Disorders (15 papers), Genetic factors in colorectal cancer (15 papers) and Prenatal Screening and Diagnostics (13 papers). The work is most often cited by research in Genetics (13.0k citations), Cancer Research (3.0k citations), Clinical Biochemistry (1.4k citations), Genetics (1.8k citations) and Molecular Biology (11.5k citations). Wayne W. Grody has collaborated with scholars based in United States, United Kingdom and Poland. Frequent co-authors include Heidi L. Rehm, Madhuri Hegde, Sherri J. Bale, Soma Das, Elaine Lyon, Nazneen Aziz, Karl V. Voelkerding, Sue M. Richards, Elaine Spector and David P Bick. Their work appears in journals such as Genetics in Medicine, Journal of Molecular Diagnostics, Molecular Genetics and Metabolism, Archives of Pathology & Laboratory Medicine and Diagnostic Molecular Pathology.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.