Laura E. Schultz‐Rogers
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 19
- Genetics and Neurodevelopmental Disorders 10
- Genomics and Rare Diseases 8
- Dermatological and Skeletal Disorders 1
- Genomic variations and chromosomal abnormalities 1
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- Neurogenesis and neuroplasticity mechanisms 2
- Co-authors
- Eric W. Klee (8 shared papers)Brendan C. Lanpher (2 shared papers)Wesley A. Wierson (3 shared papers)Kristin M. Zimmerman Savill (1 shared paper)Demetrios T. Braddock (1 shared paper)Tanya L. Schwab (3 shared papers)Anupam Kotwal (1 shared paper)Rajiv Kumar (1 shared paper)
- Journals
- The American Journal of Human Genetics (3 papers)Nature Communications (2 papers)Genetics in Medicine (2 papers)Molecular Genetics and Metabolism (1 paper)Clinical Epigenetics (1 paper)
- Partner nations
- United StatesNetherlandsCanada
In The Last Decade
Laura E. Schultz‐Rogers
26 papers receiving 705 citations
Peers
Comparison fields: 5 of 70
- Genetics 318
- Developmental Neuroscience 21
- Cellular and Molecular Neuroscience 78
- Psychiatry and Mental health 81
- Nephrology 30
Countries citing papers authored by Laura E. Schultz‐Rogers
This map shows the geographic impact of Laura E. Schultz‐Rogers'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 Laura E. Schultz‐Rogers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laura E. Schultz‐Rogers more than expected).
Fields of papers citing papers by Laura E. Schultz‐Rogers
This network shows the impact of papers produced by Laura E. Schultz‐Rogers. 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 Laura E. Schultz‐Rogers. The network helps show where Laura E. Schultz‐Rogers may publish in the future.
Co-authors
The 25 scholars most cited alongside Laura E. Schultz‐Rogers, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 198 | |
| 2 | 2021 | 71 | |
| 3 | 2021 | 61 | |
| 4 | 2021 | 50 | |
| 5 | 2020 | 44 | |
| 6 | 2019 | 40 | |
| 7 | 2020 | 30 | |
| 8 | 2021 | 28 | |
| 9 | 2023 | 25 | |
| 10 | 2019 | 21 | |
| 11 | 2021 | 21 | |
| 12 | 2020 | 20 | |
| 13 | 2020 | 18 | |
| 14 | 2022 | 17 | |
| 15 | 2022 | 16 | |
| 16 | 2020 | 15 | |
| 17 | 2022 | 9 | |
| 18 | 2020 | 8 | |
| 19 | 2024 | 8 | |
| 20 | 2020 | 3 |
About Laura E. Schultz‐Rogers
Laura E. Schultz‐Rogers is a scholar working on Genetics, Developmental Neuroscience, Molecular Biology, Psychiatry and Mental health and Gastroenterology, having authored 26 papers that have together received 712 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Genomics and Rare Diseases (8 papers), Epigenetics and DNA Methylation (3 papers), Epilepsy research and treatment (2 papers), Neurogenesis and neuroplasticity mechanisms (2 papers), Developmental Biology and Gene Regulation (2 papers), Dermatological and Skeletal Disorders (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Genetics (318 citations), Developmental Neuroscience (21 citations), Cellular and Molecular Neuroscience (78 citations), Psychiatry and Mental health (81 citations) and Nephrology (30 citations). Laura E. Schultz‐Rogers has collaborated with scholars based in United States, Netherlands and Canada. Frequent co-authors include Eric W. Klee, Brendan C. Lanpher, Wesley A. Wierson, Kristin M. Zimmerman Savill, Demetrios T. Braddock, Tanya L. Schwab, Anupam Kotwal, Rajiv Kumar, Filippo Pinto e Vairo and Ravinder Jit Singh. Their work appears in journals such as The American Journal of Human Genetics, Nature Communications, Genetics in Medicine, Molecular Genetics and Metabolism and Clinical Epigenetics.
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.