Carll Ladd
Impact in
- Genetics top 10%
- Forensic and Genetic Research
- Genetic diversity and population structure
- Race, Genetics, and Society
- Obstetrics and Gynecology top 10%
- Uterine Myomas and Treatments
Papers in
- Genetics 11
- Forensic and Genetic Research 8
- Genetic diversity and population structure 5
- Advances in Cucurbitaceae Research 1
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- Molecular Biology Techniques and Applications 6
- Co-authors
- Henry Lee (6 shared papers)Heather Miller Coyle (3 shared papers)Timothy M. Palmbach (3 shared papers)Ann Marie Gross (3 shared papers)Bradley J. Quade (1 shared paper)Bruce Budowle (3 shared papers)Roberta Vanni (1 shared paper)David M. Neskey (1 shared paper)
- Journals
- American Journal of Forensic Medicine & Pathology (3 papers)Forensic Science International (3 papers)Journal of Forensic Sciences (2 papers)In Silico Biology (1 paper)Biochemical Genetics (1 paper)
- Partner nations
- United StatesCanadaSouth Africa
In The Last Decade
Carll Ladd
14 papers receiving 451 citations
Peers
Comparison fields: 5 of 75
- Genetics 295
- Obstetrics and Gynecology 39
- Molecular Biology 253
- Reproductive Medicine 23
- Ecology 68
Countries citing papers authored by Carll Ladd
This map shows the geographic impact of Carll Ladd'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 Carll Ladd with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carll Ladd more than expected).
Fields of papers citing papers by Carll Ladd
This network shows the impact of papers produced by Carll Ladd. 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 Carll Ladd. The network helps show where Carll Ladd may publish in the future.
Co-authors
The 25 scholars most cited alongside Carll Ladd, 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 | 2004 | 78 | |
| 2 | Fusion transcripts involving HMGA2 are not a common molecular mechanism in uterine leiomyomata with rearrangements in 12q15. | 2003 | 77 |
| 3 | Preservation and collection of biological evidence. | 2001 | 56 |
| 4 | 2005 | 55 | |
| 5 | An overview of DNA methods for the identification and individualization of marijuana. | 2003 | 45 |
| 6 | 2005 | 42 | |
| 7 | Interpretation of complex forensic DNA mixtures. | 2001 | 34 |
| 8 | 2003 | 27 | |
| 9 | 1998 | 27 | |
| 10 | 1994 | 20 | |
| 11 | 2002 | 9 | |
| 12 | 2006 | 8 | |
| 13 | 2004 | 3 | |
| 14 | 1987 | 1 |
About Carll Ladd
Carll Ladd is a scholar working on Genetics, Molecular Biology, Plant Science, Surgery and Pharmacology, having authored 14 papers that have together received 482 indexed citations. Recurring topics across this work include Forensic and Genetic Research (8 papers), Molecular Biology Techniques and Applications (6 papers), Genetic diversity and population structure (5 papers), Gynecological conditions and treatments (1 paper), Advances in Cucurbitaceae Research (1 paper), Uterine Myomas and Treatments (1 paper), Chromosomal and Genetic Variations (1 paper) and Blood groups and transfusion (1 paper). The work is most often cited by research in Genetics (295 citations), Obstetrics and Gynecology (39 citations), Molecular Biology (253 citations), Reproductive Medicine (23 citations) and Ecology (68 citations). Carll Ladd has collaborated with scholars based in United States, Canada and South Africa. Frequent co-authors include Henry Lee, Heather Miller Coyle, Timothy M. Palmbach, Ann Marie Gross, Bradley J. Quade, Bruce Budowle, Roberta Vanni, David M. Neskey, Xavier G. Aranda and Benjamin E. Krenke. Their work appears in journals such as American Journal of Forensic Medicine & Pathology, Forensic Science International, Journal of Forensic Sciences, In Silico Biology and Biochemical Genetics.
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.