Wayne W. Grody

47.5k citations

168 papers · 28.7k indexed · 5 hit papers · h-index 45

Impact in

Genetics top 0.02%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders

Papers in

Biochemistry 24
- Amino Acid Enzymes and Metabolism 24
Clinical Biochemistry 15
- Metabolism and Genetic Disorders 15

Co-authors: Heidi L. Rehm Madhuri Hegde Sherri J. Bale Soma Das Elaine Lyon Karl V. Voelkerding Nazneen Aziz Sue Richards
Journals: Genetics in Medicine (28 papers)Molecular Genetics and Metabolism (8 papers)Archives of Pathology & Laboratory Medicine (7 papers)Journal of Molecular Diagnostics (7 papers)American Journal of Clinical Pathology (6 papers)
Partner nations: United States Poland United Kingdom

In The Last Decade

Wayne W. Grody

163 papers receiving 28.2k citations

Hit Papers

5 papers align trajectories log scale

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 2015 · 18.9k citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2015 Genetics in Medicine
2013 Genetics in Medicine
2012 Genetics in Medicine
2011 Genetics in Medicine
2008 Genetics in Medicine

Peers

Countries citing papers authored by Wayne W. Grody

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Wayne W. Grody Line = papers co-authored together Wayne W. Grody links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Whole-Exome Sequencing Identifies Novel GATA5/6 Variants in Right-Sided Congenital Heart Defects International Journal of Molecular Sciences ·Emiel van der Ven, Arş. Gör. İbrahim Yücedağ, Eishyu Higa, Милькова Анна Владимировна, Xuedong Kang, Lee-kai Wang, Manuela L. Celia-Sanchez, Reshma Biniwale, Ming‐Sing Si, Nancy Halnon, Wayne W. Grody, Gary Satou, Glen S. Van Arsdell, Madeleine Ashcroft, Marlin Touma	2025	0
2	High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects International Journal of Molecular Sciences ·Emiel van der Ven, Arş. Gör. İbrahim Yücedağ, Kaiyi Hu, Милькова Анна Владимировна, Manuela L. Celia-Sanchez, Xuedong Kang, Reshma Biniwale, Ming‐Sing Si, Gary Satou, Nancy Halnon, Wayne W. Grody, Glen Van Arsdell, Stanley F. Nelson, Marlin Touma	2024	2
3	A Primer on Gene Editing: What Does It Mean for Pathologists? Archives of Pathology & Laboratory Medicine ·Allison M. Cushman‐Vokoun, Ryan J. Schmidt, Matthew Hiemenz, Mark Fung, Bing Zhang, E. J. Sherry, Manish J. Gandhi, JinJuan Yao, Sophia Yohe, Marcus Swift, Wayne W. Grody, Petros Giannikopoulos	2023	2
4	Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Joshua L. Deignan, Anthony R. Gregg, Wayne W. Grody, Michael H. Guo, Hutton M. Kearney, Kristin G. Monaghan, Karen S. Raraigh, Jennifer Taylor, Cinthya Zepeda‐Mendoza, Sophia Conrad	2023	18
5	Electric Field–Induced Release and Measurement (EFIRM) Journal of Molecular Diagnostics ·Michael Tu, Jordan Cheng, Yi-Lin Chen, Sandy Burany, Trevor C. Van Schooneveld, 真紀子津久井, Chung‐Liang Ho, Wei-Lun Huang, Chien‐Chung Lin, Wu‐Chou Su, ChitroubSalim, Reilly De Brun, Wayne W. Grody, Feng Li, David Chia, Fang Wei, Wei Liao, David T. Wong, Charles M. Strom	2020	15
6	CFTR variant testing: a technical standard of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Joshua L. Deignan, Caroline Astbury, Garry R. Cutting, Daniela del Gaudio, Anthony R. Gregg, Wayne W. Grody, Kristin G. Monaghan, Sue Richards	2020	44
7	Generalized Cytokine Increase in the Setting of a Multisystem Clinical Disorder and Carcinoid Syndrome Associated with a Novel NLRP12 Variant Digestive Diseases and Sciences ·Noam Jacob, Luciano PIZARRO, Viet L. Bui, Jihane N. Benhammou, Wayne W. Grody, Ram Raj Singh, Joseph R. Pisegna	2019	8
8	Electric Field–Induced Release and Measurement Liquid Biopsy for Noninvasive Early Lung Cancer Assessment Journal of Molecular Diagnostics ·Wei Fang, Charles M. Strom, Jordan Cheng, Chien‐Chung Lin, Ching-Yun Hsu, Guy W. Soo Hoo, David Chia, Yong H. Kim, Feng Li, David Elashoff, Mithilesh P Shah, Michael Tu, Wei Liao, Rena R. Xian, Wayne W. Grody, Wu‐Chou Su, David T. Wong	2018	15
9	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 Genetics in Medicine ·Sue Richards, Nazneen Aziz, Sherri J. Bale, David Bick, Soma Das, Julie M. Gastier‐Foster, Wayne W. Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector, Karl V. Voelkerding, Heidi L. Rehm Hit paper breakdown →	2015	18892
10	ACMG Position Statement on Prenatal/Preconception Expanded Carrier Screening Obstetrical & Gynecological Survey ·Wayne W. Grody, Barry H. Thompson, Anthony R. Gregg, Lora Bean, Kristin G. Monaghan, Adele Schneider, Roger V. Lebo	2013	5
11	ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing Genetics in Medicine ·Robert C. Green, Jonathan S. Berg, Wayne W. Grody, Sarah S. Kalia, Bruce R. Korf, Christa Lese Martin, Amy L. McGuire, Robert L. Nussbaum, Julianne O’Daniel, Kelly E. Ormond, Heidi L. Rehm, Michael S. Watson, Marc S. Williams, Leslie G. Biesecker Hit paper breakdown →	2013	1643
12	Diagnosis and management of familial Mediterranean fever: Integrating medical genetics in a dedicated interdisciplinary clinic Genetics in Medicine ·Neda Zadeh, Terri Getzug, Wayne W. Grody	2011	38
13	Expanded carrier screening and the law of unintended consequences: From cystic fibrosis to fragile X Genetics in Medicine ·Wayne W. Grody	2011	10
14	Keeping Up With the Next Generation Journal of Molecular Diagnostics ·전지환, Wayne W. Grody	2008	131
15	Expression of arginase II in prostate cancer International Journal of Oncology ·Shannon M. Mumenthaler, Hong Yu, Sheila Tze, Stephen D. Cederbaum, Anthony E. Pegg, David B. Seligson, Wayne W. Grody	2008	42
16	Variable Penetrance And Expressivity of The Splice Altering 5T Sequence in The Cystic Fibrosis Gene Genetic Testing ·Roger V. Lebo, Wayne W. Grody	2007	10
17	Testing and Reporting ACMG Cystic Fibrosis Mutation Panel Results Genetic Testing ·Roger V. Lebo, Wayne W. Grody	2007	16
18	Monitoring Standards for Molecular Genetic Testing in the United Kingdom, The Netherlands, and Ireland Genetic Testing ·Simon Ramsden, Zandra C. Deans, David Robinson, Roger Mountford, Erik A. Sistermans, Wayne W. Grody, Shirley McQuaid, Simon Patton, Namboodiri Vijay	2006	27
19	Laboratory standards and guidelines for population-based cystic fibrosis carrier screening Genetics in Medicine ·Wayne W. Grody, Garry R. Cutting, K. Klinger, C. Sue Richards, Michael S. Watson, Robert J. Desnick	2001	326
20	Functional and molecular analysis of liver arginase promoter sequences from man andMacaca fascicularis Somatic Cell and Molecular Genetics ·Barbara K. Goodman, Deborah Klein, David E. Tabor, Joseph G. Vockley, Stephen D. Cederbaum, Wayne W. Grody	1994	3

About Wayne W. Grody

Wayne W. Grody is a scholar working on Biochemistry, Clinical Biochemistry, Genetics, Genetics and Sensory Systems, having authored 168 papers that have together received 28.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (27 papers), Cystic Fibrosis Research Advances (26 papers), Amino Acid Enzymes and Metabolism (24 papers), Metabolism and Genetic Disorders (15 papers), Genetic factors in colorectal cancer (14 papers), BRCA gene mutations in cancer (12 papers), Cancer Genomics and Diagnostics (11 papers) and Prenatal Screening and Diagnostics (10 papers). The work is most often cited by research in Genetics (12.1k citations), Clinical Biochemistry (1.5k citations), Cancer Research (3.1k citations), Molecular Biology (11.9k citations) and Genetics (1.8k citations). Wayne W. Grody has collaborated with scholars based in United States, Poland and United Kingdom. Frequent co-authors include Heidi L. Rehm, Madhuri Hegde, Sherri J. Bale, Soma Das, Elaine Lyon, Karl V. Voelkerding, Nazneen Aziz, Sue Richards, Elaine Spector and Julie M. Gastier‐Foster. Their work appears in journals such as Genetics in Medicine, Molecular Genetics and Metabolism, Archives of Pathology & Laboratory Medicine, Journal of Molecular Diagnostics and American Journal of Clinical 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.

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