Deborah E. McFadden
Impact in
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- Prenatal Screening and Diagnostics
- Birth, Development, and Health
- Obstetrics and Gynecology top 1%
- Pregnancy and preeclampsia studies
Papers in
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- Prenatal Screening and Diagnostics 23
- Genetics 24
- Genetic Syndromes and Imprinting 16
- Genomic variations and chromosomal abnormalities 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Co-authors
- Wendy P. Robinson (27 shared papers)Jerian F. Lim (1 shared paper)Stevan R. Knezevich (1 shared paper)Poul H. Sorensen (1 shared paper)Maria S. Peñaherrera (10 shared papers)Sylvie Langlois (8 shared papers)Peter von Dadelszen (6 shared papers)Ryan K. C. Yuen (5 shared papers)
- Journals
- The Journal of Urology (4 papers)Pediatric and Developmental Pathology (4 papers)Journal of Medical Genetics (3 papers)Prenatal Diagnosis (3 papers)Epigenetics & Chromatin (3 papers)
- Partner nations
- CanadaUnited StatesGermany
In The Last Decade
Deborah E. McFadden
78 papers receiving 4.0k citations
Deborah E. McFadden's Hit Papers
Peers
Comparison fields: 5 of 112
- Pediatrics, Perinatology and Child Health 1.5k
- Obstetrics and Gynecology 488
- Genetics 997
- Public Health, Environmental and Occupational Health 712
- Rheumatology 369
Countries citing papers authored by Deborah E. McFadden
This map shows the geographic impact of Deborah E. McFadden'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 Deborah E. McFadden with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Deborah E. McFadden more than expected).
Fields of papers citing papers by Deborah E. McFadden
This network shows the impact of papers produced by Deborah E. McFadden. 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 Deborah E. McFadden. The network helps show where Deborah E. McFadden may publish in the future.
Co-authors
The 25 scholars most cited alongside Deborah E. McFadden, 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 79 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma Hit paper breakdown → | 1998 | 637 |
| 2 | 1993 | 319 | |
| 3 | 2008 | 285 | |
| 4 | 2010 | 178 | |
| 5 | 2013 | 174 | |
| 6 | 2009 | 155 | |
| 7 | 1993 | 130 | |
| 8 | 1991 | 117 | |
| 9 | 2011 | 110 | |
| 10 | 2013 | 102 | |
| 11 | 1997 | 101 | |
| 12 | 2016 | 97 | |
| 13 | 2005 | 95 | |
| 14 | 2001 | 93 | |
| 15 | 2000 | 79 | |
| 16 | 1986 | 74 | |
| 17 | 2013 | 66 | |
| 18 | 2011 | 65 | |
| 19 | 2012 | 62 | |
| 20 | 2006 | 62 |
About Deborah E. McFadden
Deborah E. McFadden is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Public Health, Environmental and Occupational Health and Surgery, having authored 79 papers that have together received 4.4k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (23 papers), Genetic Syndromes and Imprinting (16 papers), Gestational Trophoblastic Disease Studies (11 papers), Pregnancy and preeclampsia studies (7 papers), Epigenetics and DNA Methylation (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Chromatin Remodeling and Cancer (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1.5k citations), Obstetrics and Gynecology (488 citations), Genetics (997 citations), Public Health, Environmental and Occupational Health (712 citations) and Rheumatology (369 citations). Deborah E. McFadden has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Wendy P. Robinson, Jerian F. Lim, Stevan R. Knezevich, Poul H. Sorensen, Maria S. Peñaherrera, Sylvie Langlois, Peter von Dadelszen, Ryan K. C. Yuen, Jan M. Friedman and Dagmar K. Kalousek. Their work appears in journals such as The Journal of Urology, Pediatric and Developmental Pathology, Journal of Medical Genetics, Prenatal Diagnosis and Epigenetics & Chromatin.
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.