E.W. Lovrien

2.2k total citations
58 papers, 1.6k citations indexed

About

E.W. Lovrien is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, E.W. Lovrien has authored 58 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 20 papers in Genetics and 10 papers in Hematology. Recurrent topics in E.W. Lovrien's work include Genomic variations and chromosomal abnormalities (11 papers), Hemophilia Treatment and Research (7 papers) and Chromosomal and Genetic Variations (6 papers). E.W. Lovrien is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Hemophilia Treatment and Research (7 papers) and Chromosomal and Genetic Variations (6 papers). E.W. Lovrien collaborates with scholars based in United States, Germany and Norway. E.W. Lovrien's co-authors include Frederick Hecht, R.E. Magenis, R. Ellen Magenis, Irene H. Maumenee, Richard G. Weleber, M. Litt, John Chamberlin, R. Bigley, Brian N. Bachynski and J. Fielding Hejtmancik and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

E.W. Lovrien

57 papers receiving 1.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
E.W. Lovrien United States	23	805	585	179	179	173	58	1.6k
Nancy E. Simpson Canada	24	810 1.0×	591 1.0×	226 1.3×	78 0.4×	141 0.8×	83	2.0k
Tatsuro Ikeuchi Japan	28	1.4k 1.7×	869 1.5×	451 2.5×	105 0.6×	370 2.1×	106	2.6k
FS Collins United States	25	1.1k 1.3×	349 0.6×	157 0.9×	405 2.3×	98 0.6×	50	2.2k
Emilie H. Mules United States	19	825 1.0×	239 0.4×	105 0.6×	135 0.8×	155 0.9×	29	1.6k
Noriko Hosoya Japan	22	1.2k 1.5×	435 0.7×	353 2.0×	255 1.4×	81 0.5×	53	2.2k
Jeffery L. Cole United States	17	989 1.2×	506 0.9×	99 0.6×	139 0.8×	208 1.2×	19	3.4k
Mohnish Suri United Kingdom	24	1.2k 1.5×	736 1.3×	224 1.3×	75 0.4×	61 0.4×	82	2.2k
Güven Lüleci Türkiye	21	750 0.9×	808 1.4×	177 1.0×	112 0.6×	78 0.5×	110	1.7k
J. de Grouchy France	35	1.6k 2.0×	2.0k 3.4×	167 0.9×	176 1.0×	661 3.8×	135	3.4k
J.M.N. Hoovers Netherlands	24	1.3k 1.6×	1.0k 1.8×	183 1.0×	38 0.2×	342 2.0×	59	2.1k

Countries citing papers authored by E.W. Lovrien

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of E.W. Lovrien

This figure shows the co-authorship network connecting the top 25 collaborators of E.W. Lovrien. A scholar is included among the top collaborators of E.W. Lovrien based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with E.W. Lovrien. E.W. Lovrien is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Kramer, P. L., et al.. (1996). A Second Gene for Cerulean Cataracts Maps to the β Crystallin Region on Chromosome 22. Genomics. 35(3). 539–542. 48 indexed citations

Ragni, MV, Ronald Jaffe, CW McMillan, et al.. (1993). Acquired immunodeficiency syndrome-associated non-Hodgkin's lymphomas and other malignancies in patients with hemophilia. Blood. 81(7). 1889–1897. 58 indexed citations

Beals, Rodney K. & E.W. Lovrien. (1992). Diffuse Capillary Hemangiomas Associated with Skeletal Hypotrophy. Journal of Pediatric Orthopaedics. 12(3). 401–402. 4 indexed citations

Chen, Shi-Han, Min Zhang, E.W. Lovrien, C. Ronald Scott, & Arthur R. Thompson. (1991). CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series. Human Genetics. 87(2). 177–182. 33 indexed citations

Lovrien, E.W., et al.. (1990). Microphthalmos in the presumed homozygous offspring of a first cousin marriage and linkage analysis of a locus in a family with autosomal dominant cerulean congenital cataracts. American Journal of Medical Genetics. 37(1). 54–59. 14 indexed citations

Coleman, R. D., et al.. (1990). Oral motor dysfunction in individuals at risk of huntington disease. American Journal of Medical Genetics. 37(1). 36–39. 8 indexed citations

Godfrey, Maurice, Victor Menashe, Richard G. Weleber, et al.. (1990). Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families.. PubMed. 46(4). 652–60. 71 indexed citations

Bale, Sherri J., Mark H. Greene, & E.W. Lovrien. (1986). Hereditary melanoma, the dysplastic nevus syndrome, and transferrin. Cancer Genetics and Cytogenetics. 23(3). 279–280. 3 indexed citations

Chamberlin, John, et al.. (1979). The 8p- syndrome. Human Genetics. 47(2). 135–140. 19 indexed citations

10.

Lovrien, E.W., et al.. (1978). Linkage study of antithrombin III. Cytogenetic and Genome Research. 22(1-6). 319–323. 12 indexed citations

11.

Magenis, R.E., et al.. (1978). Exclusion of glutathione reductase from 8pter→8p22 and localization to 8p21. Cytogenetic and Genome Research. 22(1-6). 446–448. 7 indexed citations

12.

Magenis, R.E., et al.. (1978). Linkage relationships of HLA and a familial chromosome 6 inversion (pter→p23::q23→p23::q23→qter): lack of dose effect in duplication-deficient offspring. Cytogenetic and Genome Research. 22(1-6). 418–420. 5 indexed citations

13.

Magenis, R.E., et al.. (1977). Parental origin of the extra chromosome in Down's syndrome. Human Genetics. 37(1). 7–16. 65 indexed citations

14.

King, Charles R., E.W. Lovrien, & Jacob A. Reiss. (1977). Central nervous system arteriovenous malformations in multiple generations of a family with hereditary hemorrhagic telangiectasia. Clinical Genetics. 12(6). 372–381. 25 indexed citations

15.

McCaw, B. Kaiser, et al.. (1976). Ovarian teratomas: cytologic data. Cytogenetic and Genome Research. 16(1-5). 391–395. 7 indexed citations

16.

Conneally, P.M., E.W. Lovrien, R.E. Magenis, et al.. (1976). The linkage and mapping relationships of 1qh. Cytogenetic and Genome Research. 16(1-5). 347–350. 4 indexed citations

17.

Meyers, Deborah A., P.M. Conneally, E.W. Lovrien, et al.. (1976). Linkage group I: the simultaneous estimation of recombination and interference. Cytogenetic and Genome Research. 16(1-5). 335–339. 13 indexed citations

18.

Magenis, R.E., et al.. (1975). Exclusion gene mapping utilizing patients with chromosome imbalance: The HL-A system as a prototype. PubMed. 27(2). 91–109. 20 indexed citations

19.

Merritt, A.D., E.W. Lovrien, Marian L. Rivas, & P. M. Conneally. (1973). Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I.. PubMed. 25(5). 523–38. 29 indexed citations

20.

Hecht, Frederick, et al.. (1968). Nonrandomness of Translocations in Man: Preferential Entry of Chromosomes into 13-15/21 Translocations. Science. 161(3839). 371–372. 42 indexed citations

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.

Explore authors with similar magnitude of impact