Vikram Jaswaney
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Reproductive Medicine top 10%
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 5
- Genetic Syndromes and Imprinting 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
-
- Congenital heart defects research 2
- Co-authors
- Stuart Schwartz (6 shared papers)Rachel D. Burnside (4 shared papers)Inder Gadi (4 shared papers)Peter Papenhausen (3 shared papers)Hiba Risheg (3 shared papers)James Tepperberg (3 shared papers)Romela Pasion (3 shared papers)Janice Smith (3 shared papers)
- Journals
- Human Genetics (2 papers)Fetal Diagnosis and Therapy (1 paper)Fertility and Sterility (1 paper)The Journal of Clinical Endocrinology & Metabolism (1 paper)Journal of Reproductive Immunology (1 paper)
- Partner nations
- United States
In The Last Decade
Vikram Jaswaney
12 papers receiving 446 citations
Peers
Comparison fields: 5 of 45
- Genetics 377
- Reproductive Medicine 48
- Pediatrics, Perinatology and Child Health 105
- Molecular Biology 198
- Developmental Biology 5
Countries citing papers authored by Vikram Jaswaney
This map shows the geographic impact of Vikram Jaswaney'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 Vikram Jaswaney with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vikram Jaswaney more than expected).
Fields of papers citing papers by Vikram Jaswaney
This network shows the impact of papers produced by Vikram Jaswaney. 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 Vikram Jaswaney. The network helps show where Vikram Jaswaney may publish in the future.
Co-authors
The 25 scholars most cited alongside Vikram Jaswaney, 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 | 2011 | 183 | |
| 2 | 2011 | 116 | |
| 3 | 1993 | 79 | |
| 4 | 1997 | 42 | |
| 5 | 2013 | 30 | |
| 6 | 1988 | 12 | |
| 7 | 1993 | 5 | |
| 8 | Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay Rachel D. BurnsideRomela PasionFady M. MikhailAndrew J. CarrollNathaniel H. Robin • Erin L. YoungsInder K. GadiElizabeth KeitgesVikram L. JaswaneyPeter R. Papenhausen • Venkateswara R. PotluriHiba RishegBrooke RushJanice L. SmithStuart Schwartz • | 2011 | 3 |
| 9 | 1987 | 2 | |
| 10 | 1987 | 2 | |
| 11 | 1997 | 2 | |
| 12 | 2009 | 1 |
About Vikram Jaswaney
Vikram Jaswaney is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Immunology and Surgery, having authored 12 papers that have together received 477 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Genetic Syndromes and Imprinting (2 papers), Chromosomal and Genetic Variations (2 papers), T-cell and B-cell Immunology (2 papers), Congenital heart defects research (2 papers), Monoclonal and Polyclonal Antibodies Research (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Genetics (377 citations), Reproductive Medicine (48 citations), Pediatrics, Perinatology and Child Health (105 citations), Molecular Biology (198 citations) and Developmental Biology (5 citations). Vikram Jaswaney has collaborated with scholars based in United States. Frequent co-authors include Stuart Schwartz, Rachel D. Burnside, Inder Gadi, Peter Papenhausen, Hiba Risheg, James Tepperberg, Romela Pasion, Janice Smith, Elisabeth A. Keitges and John Pappas. Their work appears in journals such as Human Genetics, Fetal Diagnosis and Therapy, Fertility and Sterility, The Journal of Clinical Endocrinology & Metabolism and Journal of Reproductive 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.