Erika A. Bosman

531 total citations
8 papers, 421 citations indexed

About

Erika A. Bosman is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Erika A. Bosman has authored 8 papers receiving a total of 421 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Erika A. Bosman's work include Congenital Ear and Nasal Anomalies (4 papers), TGF-β signaling in diseases (3 papers) and Congenital heart defects research (3 papers). Erika A. Bosman is often cited by papers focused on Congenital Ear and Nasal Anomalies (4 papers), TGF-β signaling in diseases (3 papers) and Congenital heart defects research (3 papers). Erika A. Bosman collaborates with scholars based in United Kingdom, Belgium and Netherlands. Erika A. Bosman's co-authors include Karen P. Steel, Ross Kettleborough, Andrew C. Penn, Derek L. Stemple, John C. Ambrose, Jorieke E. H. Bergman, Francesca Vitelli, Angela N. Barrett, Katrina Prescott and Karen McCue and has published in prestigious journals such as Journal of Clinical Investigation, Development and Human Molecular Genetics.

In The Last Decade

Erika A. Bosman

8 papers receiving 413 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Erika A. Bosman United Kingdom	7	254	186	148	85	79	8	421
Toru Udaka Japan	9	138 0.5×	167 0.9×	152 1.0×	107 1.3×	84 1.1×	14	338
Fatemehsadat Esteghamat Iran	13	191 0.8×	124 0.7×	38 0.3×	23 0.3×	72 0.9×	17	412
Karen McCue United Kingdom	7	262 1.0×	73 0.4×	79 0.5×	42 0.5×	45 0.6×	11	352
Hilda Tateossian United Kingdom	11	227 0.9×	67 0.4×	48 0.3×	38 0.4×	100 1.3×	17	515
Josephine Wincent Sweden	12	243 1.0×	86 0.5×	75 0.5×	51 0.6×	214 2.7×	19	467
Sophie Audollent France	7	178 0.7×	73 0.4×	104 0.7×	121 1.4×	109 1.4×	9	346
Alison J. May United States	9	145 0.6×	62 0.3×	65 0.4×	67 0.8×	25 0.3×	14	395
Beate Mitulla Germany	10	187 0.7×	102 0.5×	37 0.3×	160 1.9×	262 3.3×	13	477
Karen J. Harrison Canada	10	248 1.0×	23 0.1×	77 0.5×	43 0.5×	252 3.2×	17	461
Daniel Amram France	6	340 1.3×	28 0.2×	29 0.2×	22 0.3×	26 0.3×	9	421

Countries citing papers authored by Erika A. Bosman

Since Specialization

Citations

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

Fields of papers citing papers by Erika A. Bosman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erika A. Bosman. 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 Erika A. Bosman. The network helps show where Erika A. Bosman may publish in the future.

Co-authorship network of co-authors of Erika A. Bosman

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

All Works

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8 of 8 papers shown

Bosman, Erika A., Jeanne Estabel, Ozama Ismail, et al.. (2012). Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1. Mammalian Genome. 24(1-2). 44–53. 3 indexed citations

Bosman, Erika A., Elizabeth Quint, Helmut Fuchs, Martin Hrabě de Angelis, & Karen P. Steel. (2009). Catweasel mice: A novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome. Developmental Biology. 328(2). 285–296. 29 indexed citations

Bergman, Jorieke E. H., et al.. (2009). Study of smell and reproductive organs in a mouse model for CHARGE syndrome. European Journal of Human Genetics. 18(2). 171–177. 40 indexed citations

McCue, Karen, Catherine Roberts, Vanessa Kyriakopoulou, et al.. (2009). Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. Journal of Clinical Investigation. 119(11). 3301–10. 111 indexed citations

Bosman, Erika A., Kirstie A. Lawson, Joke Debruyn, et al.. (2006). Smad5 determines murine amnion fate through the control of bone morphogenetic protein expression and signalling levels. Development. 133(17). 3399–3409. 22 indexed citations

Bosman, Erika A., Andrew C. Penn, John C. Ambrose, et al.. (2005). Multiple mutations in mouse Chd7 provide models for CHARGE syndrome. Human Molecular Genetics. 14(22). 3463–3476. 179 indexed citations

Zwijsen, An, Leo A. van Grunsven, Erika A. Bosman, et al.. (2001). Transforming growth factor β signalling in vitro and in vivo: activin ligand–receptor interaction, Smad5 in vasculogenesis, and repression of target genes by the δEF1/ZEB-related SIP1 in the vertebrate embryo. Molecular and Cellular Endocrinology. 180(1-2). 13–24. 18 indexed citations

Zwijsen, An, Marga A. van Rooijen, Marie‐José Goumans, et al.. (2000). Expression of the inhibitory Smad7 in early mouse development and upregulation during embryonic vasculogenesis. Developmental Dynamics. 218(4). 663–670. 19 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.

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