Nancy C. Rose
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
-
- Prenatal Screening and Diagnostics 21
- Fetal and Pediatric Neurological Disorders 7
- Genetics 15
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- Mary E. Norton (2 shared papers)Peter Benn (2 shared papers)Priya Prasad (1 shared paper)Natalia T. Leach (1 shared paper)Kristin G. Monaghan (1 shared paper)Adele Schneider (1 shared paper)Anthony R. Gregg (1 shared paper)Ronald J. Wapner (1 shared paper)
- Journals
- Genetics in Medicine (9 papers)American Journal of Obstetrics and Gynecology (6 papers)Prenatal Diagnosis (4 papers)Obstetrics and Gynecology (4 papers)American Journal of Perinatology (3 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Nancy C. Rose
48 papers receiving 1.1k citations
Nancy C. Rose's Hit Papers
Peers
Comparison fields: 5 of 101
- Pediatrics, Perinatology and Child Health 623
- Genetics 400
- Obstetrics and Gynecology 68
- Pulmonary and Respiratory Medicine 211
- Critical Care and Intensive Care Medicine 31
Countries citing papers authored by Nancy C. Rose
This map shows the geographic impact of Nancy C. Rose'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 Nancy C. Rose with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nancy C. Rose more than expected).
Fields of papers citing papers by Nancy C. Rose
This network shows the impact of papers produced by Nancy C. Rose. 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 Nancy C. Rose. The network helps show where Nancy C. Rose may publish in the future.
Co-authors
The 25 scholars most cited alongside Nancy C. Rose, 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 247 | |
| 2 | The use of fetal exome sequencing in prenatal diagnosis: a points to consider document of the American College of Medical Genetics and Genomics (ACMG) Hit paper breakdown → | 2020 | 157 |
| 3 | 2013 | 76 | |
| 4 | 2022 | 46 | |
| 5 | 2017 | 41 | |
| 6 | 2014 | 41 | |
| 7 | 2016 | 38 | |
| 8 | 2023 | 37 | |
| 9 | 2015 | 31 | |
| 10 | 2017 | 29 | |
| 11 | 2021 | 29 | |
| 12 | 2018 | 29 | |
| 13 | 2016 | 28 | |
| 14 | 2018 | 23 | |
| 15 | 2008 | 23 | |
| 16 | 1994 | 19 | |
| 17 | 1985 | 14 | |
| 18 | 2023 | 13 | |
| 19 | 2010 | 13 | |
| 20 | The single ventricle heart in the fetus: accuracy of prenatal diagnosis and outcome. | 1997 | 13 |
About Nancy C. Rose
Nancy C. Rose is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Surgery, Infectious Diseases and Pulmonary and Respiratory Medicine, having authored 51 papers that have together received 1.1k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (21 papers), Genomics and Rare Diseases (8 papers), Fetal and Pediatric Neurological Disorders (7 papers), Parvovirus B19 Infection Studies (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Metabolism and Genetic Disorders (5 papers), Congenital Anomalies and Fetal Surgery (5 papers) and Cystic Fibrosis Research Advances (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (623 citations), Genetics (400 citations), Obstetrics and Gynecology (68 citations), Pulmonary and Respiratory Medicine (211 citations) and Critical Care and Intensive Care Medicine (31 citations). Nancy C. Rose has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Mary E. Norton, Peter Benn, Priya Prasad, Natalia T. Leach, Kristin G. Monaghan, Adele Schneider, Anthony R. Gregg, Ronald J. Wapner, Gerald L. Feldman and Katie Stoll. Their work appears in journals such as Genetics in Medicine, American Journal of Obstetrics and Gynecology, Prenatal Diagnosis, Obstetrics and Gynecology and American Journal of Perinatology.
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.