Lawrence R. Shapiro
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders 18
- Genomic variations and chromosomal abnormalities 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetic Syndromes and Imprinting 4
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- Prenatal Screening and Diagnostics 11
- Molecular Biology top 10%
- Congenital heart defects research 6
- Urology top 5%
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- Congenital Anomalies and Fetal Surgery 10
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- Autism Spectrum Disorder Research 4
- Co-authors
- Peter A. DuncanWeisong ShanKazuyoshi TamuraWayne A. HendricksonRobert M. KleinPatrick L. WilmotPaul K. WoolfSapna Sharma
- Partner nations
- United StatesCanadaDenmark
In The Last Decade
Lawrence R. Shapiro
66 papers receiving 2.2k citations
Hit Papers
Peers
Comparison fields: 5 of 116
- Cardiology and Cardiovascular Medicine 510
- Genetics 577
- Pediatrics, Perinatology and Child Health 396
- Molecular Biology 1.1k
- Urology 98
Countries citing papers authored by Lawrence R. Shapiro
This map shows the geographic impact of Lawrence R. Shapiro'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 Lawrence R. Shapiro with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lawrence R. Shapiro more than expected).
Fields of papers citing papers by Lawrence R. Shapiro
This network shows the impact of papers produced by Lawrence R. Shapiro. 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 Lawrence R. Shapiro. The network helps show where Lawrence R. Shapiro may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Lawrence R. Shapiro, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2024 | 21 | |
| 3 | 2016 | 37 | |
| 4 | 2008 | 49 | |
| 5 | 2000 | 68 | |
| 6 | Mutations in Sarcomere Protein Genes as a Cause of Dilated Cardiomyopathybreakdown → | 2000 | 527 |
| 7 | 1998 | 283 | |
| 8 | 1997 | 12 | |
| 9 | 1993 | 15 | |
| 10 | 1992 | 105 | |
| 11 | 1991 | 24 | |
| 12 | 1991 | 26 | |
| 13 | 1991 | 35 | |
| 14 | 1990 | 12 | |
| 15 | 1989 | 21 | |
| 16 | 1988 | 13 | |
| 17 | 1988 | 1 | |
| 18 | 1972 | 6 | |
| 19 | 1970 | 3 | |
| 20 | 1966 | 2 |
About Lawrence R. Shapiro
Lawrence R. Shapiro is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 69 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (18 papers), Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (11 papers), Congenital Anomalies and Fetal Surgery (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Congenital heart defects research (6 papers), Genetic Syndromes and Imprinting (4 papers) and Autism Spectrum Disorder Research (4 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (510 citations), Genetics (577 citations) and Pediatrics, Perinatology and Child Health (396 citations). Lawrence R. Shapiro has collaborated with scholars based in United States, Canada and Denmark. Frequent co-authors include Peter A. Duncan, Weisong Shan, Kazuyoshi Tamura, Wayne A. Hendrickson, Robert M. Klein, Patrick L. Wilmot, Paul K. Woolf, Sapna Sharma, Mary P. Mullen and J G Seidman. Their work appears in journals such as Nature, New England Journal of Medicine and Neuron.
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.