Jacquelyn R. Roberson
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Prenatal Screening and Diagnostics 8
- Fetal and Pediatric Neurological Disorders 2
- Genetics 12
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Co-authors
- Daniel L. Van Dyke (12 shared papers)Lester Weiss (10 shared papers)Anne E. Wiktor (3 shared papers)V. Ramesh Babu (5 shared papers)Charles E. Jackson (2 shared papers)Peter Ainsworth (1 shared paper)Gary B. Talpos (1 shared paper)Isabelle Schuffenecker (2 shared papers)
- Journals
- Prenatal Diagnosis (4 papers)Genetics in Medicine (2 papers)Pediatric Research (2 papers)The Journal of Pediatrics (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United StatesCanadaAustralia
In The Last Decade
Jacquelyn R. Roberson
23 papers receiving 387 citations
Peers
Comparison fields: 5 of 44
- Genetics 245
- Developmental Biology 16
- Endocrinology, Diabetes and Metabolism 83
- Pediatrics, Perinatology and Child Health 80
- Genetics 26
Countries citing papers authored by Jacquelyn R. Roberson
This map shows the geographic impact of Jacquelyn R. Roberson'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 Jacquelyn R. Roberson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jacquelyn R. Roberson more than expected).
Fields of papers citing papers by Jacquelyn R. Roberson
This network shows the impact of papers produced by Jacquelyn R. Roberson. 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 Jacquelyn R. Roberson. The network helps show where Jacquelyn R. Roberson may publish in the future.
Co-authors
The 25 scholars most cited alongside Jacquelyn R. Roberson, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 95 | |
| 2 | 1992 | 81 | |
| 3 | 1991 | 41 | |
| 4 | 2006 | 36 | |
| 5 | 1990 | 33 | |
| 6 | 1991 | 20 | |
| 7 | A practical metaphase marker of the inactive X chromosome. | 1986 | 19 |
| 8 | 2001 | 18 | |
| 9 | 1998 | 13 | |
| 10 | 1989 | 11 | |
| 11 | 2012 | 10 | |
| 12 | 2006 | 7 | |
| 13 | 1985 | 6 | |
| 14 | 1993 | 6 | |
| 15 | 2005 | 6 | |
| 16 | 1989 | 5 | |
| 17 | 2021 | 5 | |
| 18 | 2007 | 4 | |
| 19 | 1984 | 2 | |
| 20 | Breast cancer metastatic to the foot with massive bone loss. | 1990 | 2 |
About Jacquelyn R. Roberson
Jacquelyn R. Roberson is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Developmental Biology, Infectious Diseases and Molecular Biology, having authored 23 papers that have together received 423 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Parvovirus B19 Infection Studies (3 papers), Fetal and Pediatric Neurological Disorders (2 papers), Thyroid Cancer Diagnosis and Treatment (2 papers) and Congenital limb and hand anomalies (2 papers). The work is most often cited by research in Genetics (245 citations), Developmental Biology (16 citations), Endocrinology, Diabetes and Metabolism (83 citations), Pediatrics, Perinatology and Child Health (80 citations) and Genetics (26 citations). Jacquelyn R. Roberson has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Daniel L. Van Dyke, Lester Weiss, Anne E. Wiktor, V. Ramesh Babu, Charles E. Jackson, Peter Ainsworth, Gary B. Talpos, Isabelle Schuffenecker, Gerald L. Feldman and Andrew Saxe. Their work appears in journals such as Prenatal Diagnosis, Genetics in Medicine, Pediatric Research, The Journal of Pediatrics and Journal of Medical 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.