Ferdouse Begum

2.1k total citations
13 papers, 231 citations indexed

About

Ferdouse Begum is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ferdouse Begum has authored 13 papers receiving a total of 231 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ferdouse Begum's work include Genomic variations and chromosomal abnormalities (7 papers), Genetic Associations and Epidemiology (5 papers) and RNA modifications and cancer (4 papers). Ferdouse Begum is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genetic Associations and Epidemiology (5 papers) and RNA modifications and cancer (4 papers). Ferdouse Begum collaborates with scholars based in United States, Canada and Germany. Ferdouse Begum's co-authors include Eleanor Feingold, Debashis Ghosh, George C. Tseng, Stephanie L. Sherman, Vivian G. Cheung, Emily G. Allen, Reshmi Chowdhury, Lora Jh Bean, Stuart W. Tinker and Mary L. Marazita and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Ferdouse Begum

11 papers receiving 226 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ferdouse Begum United States 7 147 103 55 28 23 13 231
Anne-Marie Van Der Kevie-Kersemaekers Netherlands 7 124 0.8× 92 0.9× 61 1.1× 35 1.3× 15 0.7× 13 212
Carla S. D’Angelo Brazil 10 229 1.6× 156 1.5× 42 0.8× 27 1.0× 6 0.3× 15 302
Francisco Álvarez‐Nava Venezuela 9 181 1.2× 145 1.4× 39 0.7× 42 1.5× 17 0.7× 25 254
Shawn Fayer United States 7 166 1.1× 95 0.9× 47 0.9× 9 0.3× 30 1.3× 13 241
Géraldine Joly‐Hélas France 5 104 0.7× 81 0.8× 30 0.5× 26 0.9× 26 1.1× 10 162
Bikem Soygur United States 8 45 0.3× 109 1.1× 52 0.9× 31 1.1× 65 2.8× 18 237
Alexandra Spadola United States 2 180 1.2× 290 2.8× 77 1.4× 10 0.4× 17 0.7× 3 348
Meral Yirmibeş Karaoğuz Türkiye 10 94 0.6× 35 0.3× 60 1.1× 32 1.1× 11 0.5× 36 218
Hatip Aydın Türkiye 6 50 0.3× 79 0.8× 18 0.3× 8 0.3× 29 1.3× 13 164
M. Barr United States 6 144 1.0× 199 1.9× 93 1.7× 24 0.9× 12 0.5× 6 346

Countries citing papers authored by Ferdouse Begum

Since Specialization
Citations

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

Fields of papers citing papers by Ferdouse Begum

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ferdouse Begum. 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 Ferdouse Begum. The network helps show where Ferdouse Begum may publish in the future.

Co-authorship network of co-authors of Ferdouse Begum

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

All Works

13 of 13 papers shown
1.
Truta, Brindusa, Ferdouse Begum, Lisa W. Datta, et al.. (2022). Inflammatory Bowel Diseases Before and After 1990. SHILAP Revista de lepidopterología. 2(1). 22–32.
2.
Bureau, Alexandre, Ferdouse Begum, Margaret A. Taub, et al.. (2018). Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants. Genetic Epidemiology. 43(1). 37–49. 4 indexed citations
3.
Holzinger, Emily, Qing Li, Margaret M. Parker, et al.. (2017). Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families. Molecular Genetics & Genomic Medicine. 5(5). 570–579. 10 indexed citations
4.
Begum, Ferdouse, Ingo Ruczinski, John E. Hokanson, et al.. (2016). Hemizygous Deletion on Chromosome 3p26.1 Is Associated with Heavy Smoking among African American Subjects in the COPDGene Study. PLoS ONE. 11(10). e0164134–e0164134. 4 indexed citations
5.
Xiao, Yanzi, Margaret A. Taub, Ingo Ruczinski, et al.. (2016). Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios. Genetic Epidemiology. 41(3). 244–250. 23 indexed citations
6.
Begum, Ferdouse, Reshmi Chowdhury, Vivian G. Cheung, Stephanie L. Sherman, & Eleanor Feingold. (2016). Genome-Wide Association Study of Meiotic Recombination Phenotypes. G3 Genes Genomes Genetics. 6(12). 3995–4007. 6 indexed citations
7.
Begum, Ferdouse, Ingo Ruczinski, Edwin K. Silverman, et al.. (2015). Identifying a Deletion Affecting Total Lung Capacity Among Subjects in the COPDGene Study Cohort. Genetic Epidemiology. 40(1). 81–88. 4 indexed citations
8.
Begum, Ferdouse, et al.. (2015). Regionally Smoothed Meta-Analysis Methods for GWAS Datasets. Genetic Epidemiology. 40(2). 154–160. 3 indexed citations
9.
Oliver, Tiffany, Candace D. Middlebrooks, Stuart W. Tinker, et al.. (2014). An Examination of the Relationship between Hotspots and Recombination Associated with Chromosome 21 Nondisjunction. PLoS ONE. 9(6). e99560–e99560. 14 indexed citations
10.
Middlebrooks, Candace D., Nandita Mukhopadhyay, Stuart W. Tinker, et al.. (2013). Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21. Human Molecular Genetics. 23(2). 408–417. 17 indexed citations
11.
Begum, Ferdouse, Debashis Ghosh, George C. Tseng, & Eleanor Feingold. (2012). Comprehensive literature review and statistical considerations for GWAS meta-analysis. Nucleic Acids Research. 40(9). 3777–3784. 111 indexed citations
12.
Oliver, Tiffany, Stuart W. Tinker, Emily G. Allen, et al.. (2011). Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21. Human Genetics. 131(7). 1039–1046. 35 indexed citations
13.
Longman, Cheryl, et al.. (2003). The Southwest of Scotland Structural Chromosomal Abnormalities Database: an assessment of its contribution to genetic counselling in affected families.. PubMed. 14(2). 187–94.

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 Anne-Marie Van Der Kevie-Kersemaekers Breakdown of academic impact, for papers by Carla S. D’Angelo Breakdown of academic impact, for papers by Francisco Álvarez‐Nava Breakdown of academic impact, for papers by Shawn Fayer Breakdown of academic impact, for papers by Géraldine Joly‐Hélas Breakdown of academic impact, for papers by Bikem Soygur Breakdown of academic impact, for papers by Alexandra Spadola Breakdown of academic impact, for papers by Meral Yirmibeş Karaoğuz Breakdown of academic impact, for papers by Hatip Aydın Breakdown of academic impact, for papers by M. Barr
Rankless by CCL
2026