Solveig Pflueger
Impact in
- Obstetrics and Gynecology top 10%
- Pregnancy and preeclampsia studies
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 8
- Genetic Syndromes and Imprinting 3
- Genomic variations and chromosomal abnormalities 2
- Genetics and Neurodevelopmental Disorders 1
-
- Prenatal Screening and Diagnostics 6
- Co-authors
- Shuk‐Mei Ho (1 shared paper)Irwin Leav (1 shared paper)Kin‐Mang Lau (1 shared paper)Jason Y. Adams (1 shared paper)M. Judith Radin (1 shared paper)Alan Leviton (3 shared papers)Harvey J. Kliman (3 shared papers)Theonia K. Boyd (3 shared papers)
- Journals
- Archives of Pathology & Laboratory Medicine (2 papers)Pediatric and Developmental Pathology (2 papers)Clinical Genetics (1 paper)The Prostate (1 paper)Diagnostic Molecular Pathology (1 paper)
- Partner nations
- United States
In The Last Decade
Solveig Pflueger
15 papers receiving 499 citations
Peers
Comparison fields: 5 of 74
- Obstetrics and Gynecology 68
- Pediatrics, Perinatology and Child Health 135
- Genetics 163
- Urology 24
- Small Animals 25
Countries citing papers authored by Solveig Pflueger
This map shows the geographic impact of Solveig Pflueger'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 Solveig Pflueger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Solveig Pflueger more than expected).
Fields of papers citing papers by Solveig Pflueger
This network shows the impact of papers produced by Solveig Pflueger. 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 Solveig Pflueger. The network helps show where Solveig Pflueger may publish in the future.
Co-authors
The 25 scholars most cited alongside Solveig Pflueger, 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 | 1996 | 81 | |
| 2 | 2002 | 76 | |
| 3 | 2008 | 74 | |
| 4 | 2008 | 71 | |
| 5 | 2007 | 60 | |
| 6 | 1984 | 26 | |
| 7 | 2000 | 25 | |
| 8 | 2009 | 24 | |
| 9 | 2000 | 21 | |
| 10 | 2002 | 16 | |
| 11 | 2007 | 16 | |
| 12 | 2013 | 14 | |
| 13 | 1998 | 12 | |
| 14 | 1992 | 2 | |
| 15 | 1997 | 1 | |
| 16 | 2006 | 0 |
About Solveig Pflueger
Solveig Pflueger is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Surgery, Molecular Biology and Urology, having authored 16 papers that have together received 519 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (3 papers), Urological Disorders and Treatments (2 papers), Pregnancy and preeclampsia studies (2 papers), Congenital Anomalies and Fetal Surgery (2 papers), Congenital Diaphragmatic Hernia Studies (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Obstetrics and Gynecology (68 citations), Pediatrics, Perinatology and Child Health (135 citations), Genetics (163 citations), Urology (24 citations) and Small Animals (25 citations). Solveig Pflueger has collaborated with scholars based in United States. Frequent co-authors include Shuk‐Mei Ho, Irwin Leav, Kin‐Mang Lau, Jason Y. Adams, M. Judith Radin, Alan Leviton, Harvey J. Kliman, Theonia K. Boyd, Jonathan L. Hecht and Kenneth A Eaton. Their work appears in journals such as Archives of Pathology & Laboratory Medicine, Pediatric and Developmental Pathology, Clinical Genetics, The Prostate and Diagnostic Molecular Pathology.
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.