Laurel K. Willig
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Pharmacology top 5%
- Pharmacogenetics and Drug Metabolism
Papers in
- Genetics 8
- Genomics and Rare Diseases 6
- Co-authors
- Stephen F. Kingsmore (7 shared papers)Laurie D. Smith (5 shared papers)Joshua E. Petrikin (1 shared paper)Josh E Petrikin (5 shared papers)Emily Farrow (7 shared papers)Julie A. Cakici (4 shared papers)Neil Miller (4 shared papers)Suzanne Herd (3 shared papers)
- Journals
- npj Genomic Medicine (3 papers)Genome Medicine (2 papers)Pediatric Research (1 paper)Neurogenetics (1 paper)Clinical Immunology (1 paper)
- Partner nations
- United States
In The Last Decade
Laurel K. Willig
13 papers receiving 715 citations
Peers
Comparison fields: 5 of 79
- Genetics 449
- Pharmacology 74
- Clinical Biochemistry 46
- Pediatrics, Perinatology and Child Health 101
- Cancer Research 75
Countries citing papers authored by Laurel K. Willig
This map shows the geographic impact of Laurel K. Willig'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 Laurel K. Willig with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laurel K. Willig more than expected).
Fields of papers citing papers by Laurel K. Willig
This network shows the impact of papers produced by Laurel K. Willig. 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 Laurel K. Willig. The network helps show where Laurel K. Willig may publish in the future.
Co-authors
The 25 scholars most cited alongside Laurel K. Willig, 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 | 2015 | 179 | |
| 2 | 2018 | 142 | |
| 3 | 2015 | 124 | |
| 4 | 2016 | 90 | |
| 5 | 2015 | 73 | |
| 6 | 2015 | 25 | |
| 7 | 2018 | 25 | |
| 8 | 2016 | 20 | |
| 9 | 2023 | 19 | |
| 10 | 2021 | 13 | |
| 11 | 2020 | 10 | |
| 12 | 2018 | 6 | |
| 13 | 2018 | 5 | |
| 14 | 2025 | 0 | |
| 15 | 2023 | 0 |
About Laurel K. Willig
Laurel K. Willig is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Cancer Research and Surgery, having authored 15 papers that have together received 731 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Cancer Genomics and Diagnostics (3 papers), Neonatal Respiratory Health Research (3 papers), Metabolism and Genetic Disorders (2 papers), Biomedical Research and Pathophysiology (1 paper), Polyomavirus and related diseases (1 paper), Renal Transplantation Outcomes and Treatments (1 paper) and Drug Transport and Resistance Mechanisms (1 paper). The work is most often cited by research in Genetics (449 citations), Pharmacology (74 citations), Clinical Biochemistry (46 citations), Pediatrics, Perinatology and Child Health (101 citations) and Cancer Research (75 citations). Laurel K. Willig has collaborated with scholars based in United States. Frequent co-authors include Stephen F. Kingsmore, Laurie D. Smith, Joshua E. Petrikin, Josh E Petrikin, Emily Farrow, Julie A. Cakici, Neil Miller, Suzanne Herd, Carol Saunders and Isabelle Thiffault. Their work appears in journals such as npj Genomic Medicine, Genome Medicine, Pediatric Research, Neurogenetics and Clinical Immunology.
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.