Sarah T. South

8.0k total citations · 2 hit papers
82 papers, 4.3k citations indexed

About

Sarah T. South is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Sarah T. South has authored 82 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Genetics, 31 papers in Pediatrics, Perinatology and Child Health and 29 papers in Molecular Biology. Recurrent topics in Sarah T. South's work include Genomic variations and chromosomal abnormalities (47 papers), Prenatal Screening and Diagnostics (30 papers) and Chromosomal and Genetic Variations (14 papers). Sarah T. South is often cited by papers focused on Genomic variations and chromosomal abnormalities (47 papers), Prenatal Screening and Diagnostics (30 papers) and Chromosomal and Genetic Variations (14 papers). Sarah T. South collaborates with scholars based in United States, Italy and United Kingdom. Sarah T. South's co-authors include Hutton M. Kearney, Stephen J. Gould, Erik C. Thorland, Kerry K. Brown, Fabiola Quintero‐Rivera, John C. Carey, Erica Andersen, Athena M. Cherry, Ankita Patel and Allen N. Lamb and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Sarah T. South

79 papers receiving 4.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)

2019 879 citations Erin Rooney Riggs, Erica Andersen et al. Genetics in Medicine profile →
American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants

2011 643 citations Hutton M. Kearney, Erik C. Thorland et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sarah T. South United States	28	2.4k	2.0k	1.2k	331	322	82	4.3k
Erik C. Thorland United States	28	2.1k 0.9×	1.8k 0.9×	843 0.7×	284 0.9×	360 1.1×	61	4.2k
Lidia Larizza Italy	43	2.3k 1.0×	3.7k 1.9×	780 0.7×	407 1.2×	573 1.8×	271	6.3k
Hutton M. Kearney United States	21	2.2k 0.9×	1.1k 0.6×	1.0k 0.9×	196 0.6×	350 1.1×	40	3.2k
Björn Menten Belgium	36	1.7k 0.7×	2.5k 1.2×	851 0.7×	505 1.5×	912 2.8×	131	4.3k
Hülya Kayserili Türkiye	35	1.7k 0.7×	2.8k 1.4×	473 0.4×	164 0.5×	229 0.7×	152	4.4k
Elisabeth Blennow Sweden	34	1.5k 0.6×	1.6k 0.8×	678 0.6×	704 2.1×	124 0.4×	87	3.0k
Koh-ichiro Yoshiura Japan	31	1.2k 0.5×	1.8k 0.9×	331 0.3×	135 0.4×	469 1.5×	159	3.4k
Judith A. Goodship United Kingdom	39	1.9k 0.8×	2.9k 1.4×	550 0.5×	119 0.4×	239 0.7×	64	6.0k
Ying Qi China	23	1.8k 0.7×	1.9k 0.9×	399 0.3×	591 1.8×	658 2.0×	97	3.6k
Cédric Le Caignec France	29	1.5k 0.6×	1.7k 0.9×	770 0.7×	298 0.9×	256 0.8×	76	3.1k

Countries citing papers authored by Sarah T. South

Since Specialization

Citations

This map shows the geographic impact of Sarah T. South'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 Sarah T. South with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah T. South more than expected).

Fields of papers citing papers by Sarah T. South

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah T. South. 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 Sarah T. South. The network helps show where Sarah T. South may publish in the future.

Co-authorship network of co-authors of Sarah T. South

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

All Works

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20 of 20 papers shown

Riggs, Erin Rooney, Erica Andersen, Athena M. Cherry, et al.. (2019). Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen). Genetics in Medicine. 22(2). 245–257. 879 indexed citations breakdown →

Vanzo, Rena, Karen S. Ho, Aparna Prasad, et al.. (2018). Clinical significance of copy number variants involving KANK1 in patients with neurodevelopmental disorders. European Journal of Medical Genetics. 62(1). 15–20. 13 indexed citations

Lu, James T., Matthew J. Ferber, Jill Hagenkord, et al.. (2018). Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing. Journal of Molecular Diagnostics. 21(1). 3–12. 18 indexed citations

Cherry, Athena M., Yassmine Akkari, Hutton M. Kearney, et al.. (2017). Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 19(8). 845–850. 29 indexed citations

Hensel, Charles H., Rena Vanzo, Megan Martin, et al.. (2017). Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions. PLoS Currents. 9. 7 indexed citations

Andersen, Erica, Christian N. Paxton, Dennis P. O’Malley, et al.. (2017). Genomic analysis of follicular dendritic cell sarcoma by molecular inversion probe array reveals tumor suppressor-driven biology. Modern Pathology. 30(9). 1321–1334. 22 indexed citations

Paxton, Christian N., Dennis P. O’Malley, Andrew M. Bellizzi, et al.. (2017). Genetic evaluation of juvenile xanthogranuloma: genomic abnormalities are uncommon in solitary lesions, advanced cases may show more complexity. Modern Pathology. 30(9). 1234–1240. 21 indexed citations

Ho, Karen S., Sarah T. South, Charles H. Hensel, et al.. (2016). Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf–Hirschhorn syndrome. Journal of Medical Genetics. 53(4). 256–263. 29 indexed citations

Fisch, Gene S., et al.. (2016). Deletion 2q37 syndrome: Cognitive‐behavioral trajectories and autistic features related to breakpoint and deletion size. American Journal of Medical Genetics Part A. 170(9). 2282–2291. 7 indexed citations

10.

Braddock, Stephen R., et al.. (2016). Braddock–Carey syndrome: A 21q22 contiguous gene syndrome encompassing RUNX1. American Journal of Medical Genetics Part A. 170(10). 2580–2586. 22 indexed citations

11.

Cohen, Adam L., Mariko Sato, Kenneth Aldape, et al.. (2015). DNA copy number analysis of Grade II–III and Grade IV gliomas reveals differences in molecular ontogeny including chromothripsis associated with IDH mutation status. Acta Neuropathologica Communications. 3(1). 34–34. 63 indexed citations

12.

South, Sarah T., Charles Lee, Allen N. Lamb, Anne W. Higgins, & Hutton M. Kearney. (2013). ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013. Genetics in Medicine. 15(11). 901–909. 232 indexed citations

13.

Kearney, Hutton M., Sarah T. South, Daynna J. Wolff, et al.. (2011). American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities. Genetics in Medicine. 13(7). 676–679. 73 indexed citations

14.

South, Sarah T., et al.. (2010). Large Clinically Consequential Imbalances Detected at the Breakpoints of Apparently Balanced and Inherited Chromosome Rearrangements. Journal of Molecular Diagnostics. 12(5). 725–729. 5 indexed citations

15.

Battaglia, Agatino, Sarah T. South, & John C. Carey. (2010). Clinical utility gene card for: Wolf–Hirschhorn (4p-) syndrome. European Journal of Human Genetics. 19(4). 492–492. 7 indexed citations

16.

Curry, Cynthia J., Rong Mao, Emily Aston, et al.. (2008). Homozygous deletions of a copy number change detected by array CGH: A new cause for mental retardation?. American Journal of Medical Genetics Part A. 146A(15). 1903–1910. 10 indexed citations

17.

South, Sarah T., Heidi Whitby, Teresa M. Maxwell, et al.. (2008). Co‐occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: Modification of the Wolf–Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith–Wiedemann or Russell–Silver phenotype. American Journal of Medical Genetics Part A. 146A(20). 2691–2697. 40 indexed citations

18.

Bleyl, Steven B., Janice L. B. Byrne, Sarah T. South, et al.. (2007). Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes. American Journal of Medical Genetics Part A. 143A(23). 2785–2795. 13 indexed citations

19.

Blakemore, Karin J., Gail Stetten, Karin D. Berg, et al.. (2004). In utero hematopoietic stem cell transplantation with haploidentical donor adult bone marrow in a canine model. American Journal of Obstetrics and Gynecology. 190(4). 960–971. 27 indexed citations

20.

South, Sarah T., Katherine A. Sacksteder, Xiaoling Li, Yifei Liu, & Stephen J. Gould. (2000). Inhibitors of Copi and Copii Do Not Block PEX3-Mediated Peroxisome Synthesis. The Journal of Cell Biology. 149(7). 1345–1360. 125 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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