Upload Records Snowball Search Search OpenAlex
About the database ScholarIQanswers from OpenAlex & ORCID
Pauline L. Lee
ResearcherPublications, citations & collaboration network
Pauline L. Lee is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 39 works, 2,090 citations, an h-index of 18 and an i10-index of 26.
39
Works
2,090
Citations
18
h-index
26
i10-index
IDs:OpenAlex
How has Pauline L. Lee's publication output changed over time?
ScholarIQpublication output · 1989–2017
Output grew0% over the shown period — from 1 works in 1989 to 1 in 2017.
1
1
1
2
1
2
1
1
1
198919901998200120032004200620092017
What are the most-cited papers on Pauline L. Lee?
ScholarIQmost cited works
Purification and Complementary DNA Cloning of a Receptor for Basic Fibroblast Growth Factor
Pauline L. Lee, Daniel E. Johnson, Lawrence S. Cousens, Victor A. Fried, Lewis T. Williams
Science. 1989659 Citations
The Human Nramp2 Gene: Characterization of the Gene Structure, Alternative Splicing, Promoter Region and Polymorphisms
Pauline L. Lee, Terri Gelbart, Carol West, Carol Halloran, Ernest Beutler
S183588319. 1998315 Citations
Regulation of Hepcidin and Iron-Overload Disease
Pauline L. Lee, Ernest Beutler
S188288600. 2009175 Citations
Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin
Pauline L. Lee, Ernest Beutler, Sreenivas V. Rao, James C. Barton
Blood. 2004136 CitationsOPEN ACCESS
Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans
Ernest Beutler, James C. Barton, Vincent J. Felitti, Terri Gelbart, Carol West, Pauline L. Lee, Jill Waalen, Chris D. Vulpe
S183588319. 2003129 Citations
Related on ScholarIQ
Scripps Research Institute
Institution
Purification and Complementary DNA Cloning of a Receptor for Basic Fibroblast Growth Factor
Paper
The Human Nramp2 Gene: Characterization of the Gene Structure, Alternative Splicing, Promoter Region and Polymorphisms
Paper
Regulation of Hepcidin and Iron-Overload Disease
Paper
Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin
Paper
Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans
Paper