E.W. Lovrien
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Hematology top 5%
- Hemophilia Treatment and Research
Papers in ⓘ
- Hematology 10
- Hemophilia Treatment and Research 7
- Blood Coagulation and Thrombosis Mechanisms 4
- Co-authors
- Frederick Hecht (10 shared papers)R.E. Magenis (14 shared papers)Irene H. Maumenee (5 shared papers)R. Ellen Magenis (5 shared papers)Richard G. Weleber (3 shared papers)M. Litt (3 shared papers)John Chamberlin (5 shared papers)R. Bigley (4 shared papers)
- Journals
- Cytogenetic and Genome Research (13 papers)Human Genetics (4 papers)Science (3 papers)Proceedings of the National Academy of Sciences (3 papers)The Journal of Pediatrics (2 papers)
- Partner nations
- United StatesGermanyNorway
In The Last Decade
E.W. Lovrien
57 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 104
- Genetics 585
- Hematology 179
- Ophthalmology 127
- Molecular Biology 805
- Genetics 124
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 | 232 | |
| 2 | 1983 | 129 | |
| 3 | 1970 | 99 | |
| 4 | Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families. | 1990 | 71 |
| 5 | 1977 | 65 | |
| 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 | 1990 | 39 | |
| 13 | 1985 | 39 | |
| 14 | 1973 | 37 | |
| 15 | 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 |
| 16 | 1975 | 34 | |
| 17 | 1991 | 33 | |
| 18 | Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I. | 1973 | 29 |
| 19 | 1976 | 29 | |
| 20 | 1972 | 28 |
About E.W. Lovrien
E.W. Lovrien is a scholar working on Developmental Biology, Hematology, Genetics, Genetics and Biotechnology, having authored 58 papers that have together received 1.6k 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), Enzyme Production and Characterization (3 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Genetics (585 citations), Hematology (179 citations), Ophthalmology (127 citations), Molecular Biology (805 citations) and Genetics (124 citations). E.W. Lovrien has collaborated with scholars based in United States, Germany and Norway. Frequent co-authors include Frederick Hecht, R.E. Magenis, Irene H. Maumenee, R. Ellen Magenis, Richard G. Weleber, M. Litt, John Chamberlin, R. Bigley, Jeremy Nathans and J. Fielding Hejtmancik. Their work appears in journals such as Cytogenetic and Genome Research, Human Genetics, Science, Proceedings of the National Academy of Sciences and The Journal of Pediatrics.
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.