Joni B. Drost

551 total citations
12 papers, 413 citations indexed

About

Joni B. Drost is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Joni B. Drost has authored 12 papers receiving a total of 413 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Hematology and 3 papers in Genetics. Recurrent topics in Joni B. Drost's work include Hemophilia Treatment and Research (8 papers), Cancer-related gene regulation (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Joni B. Drost is often cited by papers focused on Hemophilia Treatment and Research (8 papers), Cancer-related gene regulation (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Joni B. Drost collaborates with scholars based in United States, Mexico and Colombia. Joni B. Drost's co-authors include W. Robert Lee, Steve S. Sommer, Carol K. Kasper, Erik C. Thorland, William A. Scaringe, Indira Warrier, Jeanne M. Lusher, Judith A. Westman, Xuemin Li and Marion A. Koerper and has published in prestigious journals such as Human Mutation, Environmental and Molecular Mutagenesis and Haemophilia.

In The Last Decade

Joni B. Drost

12 papers receiving 404 citations

Peers

Joni B. Drost
Pauline Parry United States
Michael J. Macera United States
S. Kohno Japan
Jamie Love United Kingdom
Antonella Palena Italy
Anna Jauch Germany
Héra Der‐Sarkissian France
H. Anne F. Booth United Kingdom
Lindsay J. Frehlick Canada
Pauline Parry United States
Joni B. Drost
Citations per year, relative to Joni B. Drost Joni B. Drost (= 1×) peers Pauline Parry

Countries citing papers authored by Joni B. Drost

Since Specialization
Citations

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

Fields of papers citing papers by Joni B. Drost

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joni B. Drost

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

All Works

12 of 12 papers shown
1.
Feng, Jinong, Joni B. Drost, William A. Scaringe, Qiang Liu, & Steve S. Sommer. (2001). Mutations in the factor IX gene (F9) during the past 150 years have relative rates similar to ancient mutations. Human Mutation. 19(1). 49–57. 4 indexed citations
2.
Drost, Joni B., William A. Scaringe, Ana Rebeca Jaloma‐Cruz, et al.. (2000). Novel hotspot detector software reveals a non-CpG hotspot of germline mutation in the factor IX gene (F9) in Latin Americans. Human Mutation. 16(3). 203–210. 7 indexed citations
3.
Jaloma‐Cruz, Ana Rebeca, William A. Scaringe, Joni B. Drost, et al.. (2000). Nine independentF9 mutations in the Mexican hemophilia B population: Nonrandom recurrences of point mutation events in the human germline. Human Mutation. 15(1). 116–117. 11 indexed citations
4.
Li, Xuemin, Joni B. Drost, Stacy Roberts, Carol K. Kasper, & Steve S. Sommer. (2000). Factor IX mutations in South Africans and African Americans are compatible with primarily endogenous influences upon recent germline mutations. Human Mutation. 16(4). 371–371. 13 indexed citations
5.
Li, Xuemin, Joni B. Drost, Erik C. Thorland, et al.. (2000). The human factor IX gene as germline mutagen test: Samples from mainland China have the putatively endogenous pattern of mutation. Human Mutation. 16(1). 31–36. 15 indexed citations
6.
Liu, Jingzhong, Xuemin Li, Joni B. Drost, et al.. (2000). The human factor IX gene as germline mutagen test: Samples from mainland China have the putatively endogenous pattern of mutation. Human Mutation. 16(1). 31–31. 3 indexed citations
7.
8.
Ketterling, Rhett P., Joni B. Drost, William A. Scaringe, et al.. (1999). Reported in vivo splice-site mutations in the factor IX gene: Severity of splicing defects and a hypothesis for predicting deleterious splice donor mutations. Human Mutation. 13(3). 221–231. 41 indexed citations
9.
Thorland, Erik C., Joni B. Drost, Jeanne M. Lusher, et al.. (1999). Anaphylactic response to factor IX replacement therapy in haemophilia B patients: complete gene deletions confer the highest risk. Haemophilia. 5(2). 101–105. 66 indexed citations
10.
Drost, Joni B. & W. Robert Lee. (1998). The developmental basis for germline mosaicism in mouse and Drosophila melanogaster. PubMed. 102-103(1-6). 421–443. 24 indexed citations
11.
Drost, Joni B. & W. Robert Lee. (1998). The developmental basis for germline mosaicism in mouse and Drosophila melanogaster. Genetica. 102-103(0). 421–443. 19 indexed citations
12.
Drost, Joni B. & W. Robert Lee. (1995). Biological basis of germline mutation: Comparisons of spontaneous germline mutation rates among drosophila, mouse, and human. Environmental and Molecular Mutagenesis. 25(S2). 48–64. 209 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

Breakdown of academic impact, for papers by Pauline Parry Breakdown of academic impact, for papers by Michael J. Macera Breakdown of academic impact, for papers by S. Kohno Breakdown of academic impact, for papers by Jamie Love Breakdown of academic impact, for papers by Antonella Palena Breakdown of academic impact, for papers by Anna Jauch Breakdown of academic impact, for papers by Héra Der‐Sarkissian Breakdown of academic impact, for papers by H. Anne F. Booth Breakdown of academic impact, for papers by Lindsay J. Frehlick
Rankless by CCL
2026