E.W. Lovrien
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Connective tissue disorders research
- Hematology top 5%
- Hemophilia Treatment and Research
Papers in
-
- Cancer-related gene regulation 4
- Connexins and lens biology 3
- Genetics 20
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 3
- Co-authors
- Frederick Hecht (10 shared papers)R.E. Magenis (14 shared papers)R. Ellen Magenis (5 shared papers)Irene H. Maumenee (5 shared papers)Richard G. Weleber (3 shared papers)M. Litt (3 shared papers)Jeremy Nathans (1 shared paper)Brian N. Bachynski (1 shared paper)
- Journals
- Human Genetics (4 papers)Proceedings of the National Academy of Sciences (3 papers)Science (3 papers)The Journal of Pediatrics (2 papers)Annals of Human Genetics (2 papers)
- Partner nations
- United StatesGermanyNorway
In The Last Decade
E.W. Lovrien
47 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 100
- Genetics 525
- Hematology 158
- Ophthalmology 95
- Genetics 115
- Molecular Biology 720
Countries citing papers authored by E.W. Lovrien
This map shows the geographic impact of E.W. Lovrien'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 E.W. Lovrien with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E.W. Lovrien more than expected).
Fields of papers citing papers by E.W. Lovrien
This network shows the impact of papers produced by E.W. Lovrien. 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 E.W. Lovrien. The network helps show where E.W. Lovrien may publish in the future.
Co-authors
The 25 scholars most cited alongside E.W. Lovrien, 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 58 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1989 | 236 | |
| 2 | 1983 | 129 | |
| 3 | 1970 | 99 | |
| 4 | Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families. | 1990 | 71 |
| 5 | 1977 | 64 | |
| 6 | 1973 | 63 | |
| 7 | 1993 | 58 | |
| 8 | 1982 | 55 | |
| 9 | 1996 | 48 | |
| 10 | Linkage analysis in dominant optic atrophy. | 1983 | 48 |
| 11 | 1968 | 42 | |
| 12 | 1985 | 39 | |
| 13 | 1990 | 39 | |
| 14 | Human chromosome variation: the discriminatory power of Q-band heteromorphism (variant) analysis in distinguishing between individuals, with specific application to cases of questionable paternity. | 1986 | 37 |
| 15 | 1973 | 37 | |
| 16 | 1991 | 34 | |
| 17 | 1975 | 34 | |
| 18 | 1976 | 29 | |
| 19 | Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I. | 1973 | 29 |
| 20 | 1972 | 28 |
About E.W. Lovrien
E.W. Lovrien is a scholar working on Molecular Biology, Genetics, Hematology, Surgery and Plant Science, having authored 58 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Hemophilia Treatment and Research (7 papers), Chromosomal and Genetic Variations (6 papers), Cancer-related gene regulation (4 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers), Connexins and lens biology (3 papers), Prenatal Screening and Diagnostics (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (525 citations), Hematology (158 citations), Ophthalmology (95 citations), Genetics (115 citations) and Molecular Biology (720 citations). E.W. Lovrien has collaborated with scholars based in United States, Germany and Norway. Frequent co-authors include Frederick Hecht, R.E. Magenis, R. Ellen Magenis, Irene H. Maumenee, Richard G. Weleber, M. Litt, Jeremy Nathans, Brian N. Bachynski, J. Fielding Hejtmancik and Gerald A. Fishman. Their work appears in journals such as Human Genetics, Proceedings of the National Academy of Sciences, Science, The Journal of Pediatrics and Annals of Human 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.