Beatrice Sellinger

1.0k total citations
17 papers, 743 citations indexed

About

Beatrice Sellinger is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Beatrice Sellinger has authored 17 papers receiving a total of 743 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Beatrice Sellinger's work include Congenital heart defects research (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Sarcoma Diagnosis and Treatment (4 papers). Beatrice Sellinger is often cited by papers focused on Congenital heart defects research (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Sarcoma Diagnosis and Treatment (4 papers). Beatrice Sellinger collaborates with scholars based in United States and Canada. Beatrice Sellinger's co-authors include Marcia L. Budarf, Beverly S. Emanuel, Deborah A. Driscoll, Donna M. McDonald‐McGinn, Elaine H. Zackai, Heather E. McDermid, C.A. Griffin, B S Emanuel, S Gottlieb and Frederic G. Barr and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Investigative Dermatology and Genomics.

In The Last Decade

Beatrice Sellinger

17 papers receiving 725 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Beatrice Sellinger United States	11	567	293	228	204	99	17	743
R Wadey United Kingdom	9	943 1.7×	417 1.4×	281 1.2×	273 1.3×	163 1.6×	14	1.1k
Tonghuan Hu United States	7	828 1.5×	217 0.7×	114 0.5×	239 1.2×	84 0.8×	8	904
Raimund Fahsold Germany	14	344 0.6×	159 0.5×	130 0.6×	90 0.4×	29 0.3×	27	777
Duane Superneau United States	13	259 0.5×	202 0.7×	64 0.3×	297 1.5×	67 0.7×	22	868
Maia V. Ouspenskaia United States	14	622 1.1×	267 0.9×	63 0.3×	126 0.6×	56 0.6×	16	876
Smita M. Purandare United States	11	323 0.6×	160 0.5×	114 0.5×	59 0.3×	47 0.5×	15	598
Donna C. Rich United States	7	260 0.5×	176 0.6×	88 0.4×	89 0.4×	29 0.3×	8	580
Georg Klaus Hinkel Germany	17	498 0.9×	528 1.8×	82 0.4×	36 0.2×	90 0.9×	41	933
Bryan K. Hall United States	10	303 0.5×	245 0.8×	112 0.5×	93 0.5×	28 0.3×	13	591
Cecilia Surace Italy	12	328 0.6×	201 0.7×	58 0.3×	40 0.2×	52 0.5×	33	595

Countries citing papers authored by Beatrice Sellinger

Since Specialization

Citations

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

Fields of papers citing papers by Beatrice Sellinger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beatrice Sellinger

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

All Works

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17 of 17 papers shown

Shaikh, Tamim H., et al.. (1999). Characterization of CDC45L: a gene in the 22q11.2 deletion region expressed during murine and human development. Mammalian Genome. 10(3). 322–326. 14 indexed citations

Bashir, Muhammad M., William R. Abrams, Thomas J. Tucker, et al.. (1998). Molecular Cloning and Characterization of the Bovine and Human Tuftelin Genes. Connective Tissue Research. 39(1-3). 13–24. 10 indexed citations

Budarf, Marcia L., et al.. (1997). Localization of the Human Gene for Macrophage Migration Inhibitory Factor (MIF) to Chromosome 22q11.2. Genomics. 39(2). 235–236. 37 indexed citations

Gottlieb, S, et al.. (1997). The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development.. PubMed. 60(5). 1194–201. 52 indexed citations

Schnur, Rhonda E., et al.. (1996). Type I Oculocutaneous Albinism Associated with a Full-Length Deletion of the Tyrosinase Gene. Journal of Investigative Dermatology. 106(5). 1137–1140. 19 indexed citations

Robin, Nathaniel H., Beatrice Sellinger, Donna M. McDonald‐McGinn, et al.. (1995). Classical Noonan syndrome is not associated with deletions of 22q11. American Journal of Medical Genetics. 56(1). 94–96. 7 indexed citations

Budarf, Marcia L., et al.. (1994). Narrowing the DiGeorge Region (DGCR) using DGS-VCFS associated translocation breakpoints. The American Journal of Human Genetics. 55. 8 indexed citations

Mears, Alan J., Alessandra M.V. Duncan, Marcia L. Budarf, et al.. (1994). Molecular characterization of the marker chromosome associated with cat eye syndrome.. PubMed. 55(1). 134–42. 70 indexed citations

Driscoll, Deborah A., Beatrice Sellinger, Marcia L. Budarf, et al.. (1993). Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.. Journal of Medical Genetics. 30(10). 813–817. 361 indexed citations

10.

Bs, Emanuel, Deborah A. Driscoll, Elizabeth Goldmuntz, et al.. (1993). Molecular and phenotypic analysis of the chromosome 22 microdeletion syndromes.. PubMed. 384. 207–24. 10 indexed citations

11.

Stambolian, Dwight, et al.. (1992). Cytogenetic and molecular investigation of a balanced Xq13q translocation in a patient with retinoblastoma. American Journal of Medical Genetics. 42(6). 771–776. 4 indexed citations

12.

Barr, Frederic G., Beatrice Sellinger, & Beverly S. Emanuel. (1991). Localization of the rhabdomyosarcoma t(2;13) breakpoint on a physical map of chromosome 13. Genomics. 11(4). 941–947. 14 indexed citations

13.

Budarf, Marcia L., Heather E. McDermid, Beatrice Sellinger, & Beverly S. Emanuel. (1991). Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22. Genomics. 10(4). 996–1002. 31 indexed citations

14.

Barr, Frederic G., Jaclyn A. Biegel, Beatrice Sellinger, Richard B. Womer, & Beverly S. Emanuel. (1991). Molecular and cytogenetic analysis of chromosomal arms 2q and 13q in alveolar rhabdomyosarcoma. Genes Chromosomes and Cancer. 3(2). 153–161. 25 indexed citations

15.

Budarf, Marcia L., Beatrice Sellinger, C.A. Griffin, & Beverly S. Emanuel. (1989). Comparative mapping of the constitutional and tumor-associated 11;22 translocations.. PubMed. 45(1). 128–39. 49 indexed citations

16.

Budarf, Marcia L., Beatrice Sellinger, C. A. Griffin, & B S Emanuel. (1987). Molecular mapping of the constitutional and tumor associated 11 22 translocation. 114. 4 indexed citations

17.

Emanuel, Beverly S., Beatrice Sellinger, Lorraine J. Gudas, & Jeanne C. Myers. (1986). Localization of the human procollagen alpha 1(IV) gene to chromosome 13q34 by in situ hybridization.. PubMed. 38(1). 38–44. 28 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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