Beth A. Torchia

656 total citations
11 papers, 369 citations indexed

About

Beth A. Torchia is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science. According to data from OpenAlex, Beth A. Torchia has authored 11 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 5 papers in Plant Science. Recurrent topics in Beth A. Torchia's work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (5 papers). Beth A. Torchia is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (5 papers). Beth A. Torchia collaborates with scholars based in United States and Canada. Beth A. Torchia's co-authors include Lisa G. Shaffer, Blake C. Ballif, Bassem A. Bejjani, Aaron Theisen, Arthur S. Aylsworth, Jill A. Rosenfeld, Justine Coppinger, Sarah Alliman, Cynthia M. Powell and Ann Lucas and has published in prestigious journals such as PLoS ONE, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Beth A. Torchia

11 papers receiving 328 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Beth A. Torchia United States 7 281 177 139 71 35 11 369
Barbara Delle Chiaie Belgium 7 251 0.9× 136 0.8× 195 1.4× 38 0.5× 30 0.9× 10 423
Drew Duckett United Kingdom 9 249 0.9× 128 0.7× 142 1.0× 63 0.9× 36 1.0× 23 353
Maria Paola Recalcati Italy 11 240 0.9× 89 0.5× 191 1.4× 46 0.6× 25 0.7× 21 378
Morag N. Collinson United Kingdom 14 381 1.4× 123 0.7× 210 1.5× 97 1.4× 25 0.7× 21 473
María Ángeles Mori Spain 10 205 0.7× 136 0.8× 109 0.8× 19 0.3× 46 1.3× 17 280
C. Le Caignec France 7 181 0.6× 136 0.8× 89 0.6× 32 0.5× 28 0.8× 7 242
Fernando Santos Spain 9 228 0.8× 84 0.5× 193 1.4× 21 0.3× 23 0.7× 13 325
N. Morichon-Delvallez France 12 320 1.1× 143 0.8× 173 1.2× 74 1.0× 66 1.9× 26 418
Helena G. Ilyina Switzerland 8 411 1.5× 254 1.4× 289 2.1× 18 0.3× 33 0.9× 10 484
Nicole Chia Australia 7 202 0.7× 93 0.5× 122 0.9× 78 1.1× 137 3.9× 11 373

Countries citing papers authored by Beth A. Torchia

Since Specialization
Citations

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

Fields of papers citing papers by Beth A. Torchia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beth A. Torchia

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

All Works

11 of 11 papers shown
1.
2.
Rosenfeld, Jill A., Justine Coppinger, Blake C. Ballif, et al.. (2011). Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes. European Journal of Human Genetics. 19(5). 547–554. 15 indexed citations
3.
Haeri, Sina, Patricia Devers, Kathleen Kaiser‐Rogers, et al.. (2010). Deletion of Hepatocyte Nuclear Factor-1-Beta in an Infant with Prune Belly Syndrome. American Journal of Perinatology. 27(7). 559–563. 40 indexed citations
4.
5.
Rosenfeld, Jill A., Blake C. Ballif, Ann Lucas, et al.. (2009). Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome. PLoS ONE. 4(8). e6568–e6568. 93 indexed citations
6.
Theisen, Aaron, Jill A. Rosenfeld, Sandra A. Farrell, et al.. (2009). aCGH detects partial tetrasomy of 12p in blood from Pallister–Killian syndrome cases without invasive skin biopsy. American Journal of Medical Genetics Part A. 149A(5). 914–918. 41 indexed citations
7.
Tsuchiya, Karen D., Lisa G. Shaffer, Swaroop Aradhya, et al.. (2009). Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories. Genetics in Medicine. 11(12). 866–873. 40 indexed citations
8.
Shaffer, Lisa G., Blake C. Ballif, Aaron Theisen, et al.. (2008). In the middle of it all: a centered approach to chromosome analysis. Expert Opinion on Medical Diagnostics. 2(2). 221–229. 2 indexed citations
9.
Tsuchiya, Karen D., Kent E. Opheim, Mark Hannibal, et al.. (2008). Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization. Molecular Cytogenetics. 1(1). 7–7. 28 indexed citations
10.
Shaffer, Lisa G., Justine Coppinger, Sarah Alliman, et al.. (2008). Comparison of microarray‐based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens. Prenatal Diagnosis. 28(9). 789–795. 102 indexed citations
11.
Shaffer, Lisa G., Justine Coppinger, Sarah Alliman, et al.. (2008). Comparison of Microarray-Based Detection Rates for Cytogenetic Abnormalities in Prenatal and Neonatal Specimens. Obstetrical & Gynecological Survey. 63(11). 696–697. 2 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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