Laurie Demmer
- Genetics top 5%
- Genomics and Rare Diseases 6
- BRCA gene mutations in cancer 6
-
- Protein Tyrosine Phosphatases 5
- Biochemistry top 10%
-
- Prenatal Screening and Diagnostics 5
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders 3
-
- Folate and B Vitamins Research 4
-
- Biomedical Research and Pathophysiology 3
-
- Galectins and Cancer Biology 3
- Co-authors
- Jeffrey I. GordonDavid A. SweetserJennifer MalinowskiM S LevinAldons J. LusisTimothy W. YuLauren MassinghamDanny E. Miller
- Journals
- Proceedings of the National Academy of Sciences (2 papers)Journal of Biological Chemistry (1 paper)The Journal of Immunology (1 paper)
- Partner nations
- United StatesGermanyCanada
In The Last Decade
Laurie Demmer
33 papers receiving 1.2k citations
Hit Papers
Peers
Comparison fields: 5 of 84
- Genetics 534
- Molecular Biology 634
- Biochemistry 54
- Pediatrics, Perinatology and Child Health 167
- Clinical Biochemistry 54
Countries citing papers authored by Laurie Demmer
This map shows the geographic impact of Laurie Demmer'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 Laurie Demmer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laurie Demmer more than expected).
Fields of papers citing papers by Laurie Demmer
This network shows the impact of papers produced by Laurie Demmer. 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 Laurie Demmer. The network helps show where Laurie Demmer may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Laurie Demmer, 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 | 2023 | 4 | |
| 2 | Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)breakdown → | 2021 | 288 |
| 3 | 2019 | 0 | |
| 4 | 2016 | 4 | |
| 5 | 2014 | 10 | |
| 6 | 2013 | 6 | |
| 7 | 2013 | 17 | |
| 8 | 2012 | 3 | |
| 9 | 2012 | 22 | |
| 10 | 2010 | 7 | |
| 11 | 2010 | 45 | |
| 12 | 2009 | 43 | |
| 13 | 2009 | 42 | |
| 14 | 2008 | 0 | |
| 15 | 2007 | 4 | |
| 16 | 2006 | 32 | |
| 17 | 2004 | 10 | |
| 18 | 2001 | 3 | |
| 19 | 1999 | 55 | |
| 20 | 1992 | 18 |
About Laurie Demmer
Laurie Demmer is a scholar working on Genetics, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 35 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), BRCA gene mutations in cancer (6 papers), Protein Tyrosine Phosphatases (5 papers), Prenatal Screening and Diagnostics (5 papers), Folate and B Vitamins Research (4 papers), Metabolism and Genetic Disorders (3 papers), Biomedical Research and Pathophysiology (3 papers) and Galectins and Cancer Biology (3 papers). The work is most often cited by research in Genetics (534 citations), Molecular Biology (634 citations) and Biochemistry (54 citations). Laurie Demmer has collaborated with scholars based in United States, Germany and Canada. Frequent co-authors include Jeffrey I. Gordon, David A. Sweetser, Jennifer Malinowski, M S Levin, Aldons J. Lusis, Timothy W. Yu, Lauren Massingham, Danny E. Miller, Sawona Biswas and Kandamurugu Manickam. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of 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.