Rhonda Spiro

459 total citations
8 papers, 286 citations indexed

About

Rhonda Spiro is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Rhonda Spiro has authored 8 papers receiving a total of 286 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 4 papers in Molecular Biology. Recurrent topics in Rhonda Spiro's work include Prenatal Screening and Diagnostics (5 papers), Genetic Syndromes and Imprinting (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Rhonda Spiro is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genetic Syndromes and Imprinting (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Rhonda Spiro collaborates with scholars based in United States and Spain. Rhonda Spiro's co-authors include Susan L. Christian, Beryl R. Benacerraf, David H. Ledbetter, Robert L. Rosenfield, Gordana Raca, Kristin M. May, Margaret P Adam, Alastair J. Martin, Peter R. Huttenlocher and Debra Rita and has published in prestigious journals such as Scientific Reports, The Journal of Pediatrics and Journal of Medical Genetics.

In The Last Decade

Rhonda Spiro

8 papers receiving 267 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rhonda Spiro United States	8	249	120	120	41	38	8	286
Erika Carter United States	10	268 1.1×	118 1.0×	82 0.7×	26 0.6×	54 1.4×	15	338
Annice Hill United States	7	212 0.9×	108 0.9×	69 0.6×	16 0.4×	49 1.3×	10	253
Alaa K. Kamel Egypt	9	180 0.7×	138 1.1×	61 0.5×	21 0.5×	25 0.7×	34	227
Aziza Lebbar France	9	274 1.1×	167 1.4×	99 0.8×	25 0.6×	57 1.5×	22	321
L.E. Bernard Canada	7	294 1.2×	150 1.3×	289 2.4×	25 0.6×	18 0.5×	10	376
Amelia Villa Spain	9	176 0.7×	83 0.7×	75 0.6×	33 0.8×	50 1.3×	12	241
Olga Žilina Estonia	12	242 1.0×	132 1.1×	92 0.8×	11 0.3×	54 1.4×	23	314
A. Kleczkowska Belgium	11	282 1.1×	114 0.9×	109 0.9×	23 0.6×	89 2.3×	33	329
Carla S. D’Angelo Brazil	10	229 0.9×	156 1.3×	42 0.3×	30 0.7×	27 0.7×	15	302
Isidora López‐Pajares Spain	10	187 0.8×	113 0.9×	60 0.5×	19 0.5×	55 1.4×	11	242

Countries citing papers authored by Rhonda Spiro

Since Specialization

Citations

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

Fields of papers citing papers by Rhonda Spiro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rhonda Spiro

This figure shows the co-authorship network connecting the top 25 collaborators of Rhonda Spiro. A scholar is included among the top collaborators of Rhonda Spiro 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 Rhonda Spiro. Rhonda Spiro 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

1.

Durán, Iván, S. Paige Taylor, Wenjuan Zhang, et al.. (2016). Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome. Scientific Reports. 6(1). 34232–34232. 28 indexed citations

2.

Raca, Gordana, et al.. (2008). Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9p. Genetics in Medicine. 10(8). 599–611. 51 indexed citations

3.

Benacerraf, Beryl R., et al.. (2000). Using three‐dimensional ultrasound to detect craniosynostosis in a fetus with Pfeiffer syndrome. Ultrasound in Obstetrics and Gynecology. 16(4). 391–394. 41 indexed citations

4.

Spiro, Rhonda, Susan L. Christian, David H. Ledbetter, et al.. (1999). Intrauterine Growth Retardation Associated with Maternal Uniparental Disomy for Chromosome 6 Unmasked by Congenital Adrenal Hyperplasia. Pediatric Research. 46(5). 510–510. 31 indexed citations

5.

Christian, Susan L., Barry H. Rich, Rohitkumar Vasa, et al.. (1999). Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal diabetes mellitus. The Journal of Pediatrics. 134(1). 42–46. 35 indexed citations

6.

Precht, Kathrin S., Christa M. Lese, Rhonda Spiro, et al.. (1998). Two 22q telomere deletions serendipitously detected by FISH.. Journal of Medical Genetics. 35(11). 939–942. 55 indexed citations

7.

Spiro, Rhonda, et al.. (1996). TRISOMY 12/MONOSOMY X/NORMAL FEMALE MOSAICISM: PRENATAL DETECTION AND CONFIRMATION IN A LIVEBORN. Prenatal Diagnosis. 16(8). 734–740. 9 indexed citations

8.

Booth, Carol, et al.. (1995). Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism. Prenatal Diagnosis. 15(9). 843–848. 36 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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