B.L. Rosi

4.1k total citations · 1 hit paper
8 papers, 3.2k citations indexed

About

B.L. Rosi is a scholar working on Physiology, Molecular Biology and Pharmacology. According to data from OpenAlex, B.L. Rosi has authored 8 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Physiology, 6 papers in Molecular Biology and 3 papers in Pharmacology. Recurrent topics in B.L. Rosi's work include Alzheimer's disease research and treatments (7 papers), Dementia and Cognitive Impairment Research (3 papers) and Cholinesterase and Neurodegenerative Diseases (3 papers). B.L. Rosi is often cited by papers focused on Alzheimer's disease research and treatments (7 papers), Dementia and Cognitive Impairment Research (3 papers) and Cholinesterase and Neurodegenerative Diseases (3 papers). B.L. Rosi collaborates with scholars based in United States and United Kingdom. B.L. Rosi's co-authors include Allen D. Roses, Ann M. Saunders, James F. Gusella, Jeffery M. Vance, Barbara J. Crain, Dmitry Goldgaber, Warren J. Strittmatter, D. E. Schmechel, Peter St George‐Hyslop and Sun Hyung Joo and has published in prestigious journals such as Neurology, Annals of Neurology and Annals of the New York Academy of Sciences.

In The Last Decade

B.L. Rosi

7 papers receiving 3.1k citations

Hit Papers

Association of apolipoprotein E allele ϵ4 with late‐onset... 1993 2026 2004 2015 1993 1000 2.0k 3.0k

Peers

B.L. Rosi
Zsuzsanna Nagy United Kingdom
Corinne Lendon United Kingdom
Richard Crook United States
A D Roses United States
Sun Hyung Joo South Korea
P. A. Locke United States
Zsuzsanna Nagy United Kingdom
B.L. Rosi
Citations per year, relative to B.L. Rosi B.L. Rosi (= 1×) peers Zsuzsanna Nagy

Countries citing papers authored by B.L. Rosi

Since Specialization
Citations

This map shows the geographic impact of B.L. Rosi'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 B.L. Rosi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B.L. Rosi more than expected).

Fields of papers citing papers by B.L. Rosi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by B.L. Rosi. 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 B.L. Rosi. The network helps show where B.L. Rosi may publish in the future.

Co-authorship network of co-authors of B.L. Rosi

This figure shows the co-authorship network connecting the top 25 collaborators of B.L. Rosi. A scholar is included among the top collaborators of B.L. Rosi 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 B.L. Rosi. B.L. Rosi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

8 of 8 papers shown
1.
Scott, William K., Larry H. Yamaoka, P. A. Locke, et al.. (1997). No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease. Genetic Epidemiology. 14(3). 307–315. 28 indexed citations
2.
Stajich, Jeffrey M., James M. Gilchrist, Felicia Lennon, et al.. (1997). Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation. Neuromuscular Disorders. 7. S75–S81. 6 indexed citations
3.
Scott, William K., Larry H. Yamaoka, P. A. Locke, et al.. (1997). No association or linkage between an intronic polymorphism of presenilin‐1 and sporadic or late‐onset familial Alzheimer disease. Genetic Epidemiology. 14(3). 307–315.
4.
Xia, Yu, B.L. Rosi, Larry H. Yamaoka, et al.. (1996). Genetic studies in Alzheimer's disease with an NACP/α‐synuclein polymorphism. Annals of Neurology. 40(2). 207–215. 91 indexed citations
5.
Haines, Jonathan L., Ann M. Saunders, Joellen M. Schildkraut, et al.. (1996). No Association between α1‐Antichymotrypsin and Familial Alzheimer's Diseasesa. Annals of the New York Academy of Sciences. 802(1). 35–41. 10 indexed citations
6.
Haines, Jonathan L., Ann M. Saunders, J.M. Schildkraut, et al.. (1996). No Genetic Effect of α1-Antichymotrypsin in Alzheimer Disease. Genomics. 33(1). 53–56. 77 indexed citations
7.
Saunders, Ann M., P. C. Gaskell, Gary W. Small, et al.. (1996). No association between very low density lipoprotein receptor (VLDL-R) and Alzheimer disease in American Caucasians. Neuroscience Letters. 209(2). 105–108. 25 indexed citations
8.
Saunders, Ann M., Warren J. Strittmatter, D. E. Schmechel, et al.. (1993). Association of apolipoprotein E allele ϵ4 with late‐onset familial and sporadic Alzheimer's disease. Neurology. 43(8). 1467–1467. 3008 indexed citations breakdown →

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.

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