Robert A. Saul

2.8k total citations
43 papers, 1.5k citations indexed

About

Robert A. Saul is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Robert A. Saul has authored 43 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 12 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Robert A. Saul's work include Genetics and Neurodevelopmental Disorders (8 papers), Congenital heart defects research (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Robert A. Saul is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Congenital heart defects research (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Robert A. Saul collaborates with scholars based in United States, Canada and Australia. Robert A. Saul's co-authors include Beth A. Tarini, Marilyn C. Jones, Emily Chen, Debra Freedenberg, Joan M. Stoler, John B. Moeschler, Rizwan Hamid, Michael Shevell, Joseph H. Hersh and Jack Tarleton and has published in prestigious journals such as PEDIATRICS, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

Robert A. Saul

43 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert A. Saul United States 19 845 562 316 198 120 43 1.5k
Henry G. Dunn Canada 26 522 0.6× 459 0.8× 185 0.6× 237 1.2× 161 1.3× 65 1.5k
Paulo Alberto Otto Brazil 25 825 1.0× 885 1.6× 111 0.4× 183 0.9× 51 0.4× 130 1.9k
Julie S. Cohen United States 22 578 0.7× 617 1.1× 76 0.2× 146 0.7× 121 1.0× 44 1.4k
Manuela Volta Italy 13 523 0.6× 1.5k 2.6× 59 0.2× 256 1.3× 117 1.0× 16 1.9k
Siddharth Srivastava United States 21 1000 1.2× 700 1.2× 392 1.2× 100 0.5× 42 0.3× 80 1.7k
Beverly J. White United States 26 935 1.1× 660 1.2× 132 0.4× 294 1.5× 25 0.2× 61 1.9k
Jennifer L. Ingram United States 17 523 0.6× 395 0.7× 642 2.0× 183 0.9× 27 0.2× 41 1.7k
P D’Eufemia Italy 19 371 0.4× 286 0.5× 318 1.0× 55 0.3× 28 0.2× 55 1.2k
Michael Freilinger Austria 19 206 0.2× 447 0.8× 106 0.3× 220 1.1× 59 0.5× 42 1.2k
Kim L. McBride United States 30 807 1.0× 1.3k 2.4× 298 0.9× 209 1.1× 27 0.2× 108 2.7k

Countries citing papers authored by Robert A. Saul

Since Specialization
Citations

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

Fields of papers citing papers by Robert A. Saul

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert A. Saul

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

All Works

20 of 20 papers shown
1.
Saul, Robert A., et al.. (2017). Survey of family history taking and genetic testing in pediatric practice. Journal of Community Genetics. 8(2). 109–115. 20 indexed citations
2.
Saul, Robert A., et al.. (2016). Beyond the Genetic Diagnosis: Providing Parents What They Want to Know. Pediatrics in Review. 37(7). 269–278. 8 indexed citations
3.
Bupp, Caleb, Laurie Demmer, & Robert A. Saul. (2014). Surveying the current landscape of clinical genetics residency training. Genetics in Medicine. 17(5). 386–390. 10 indexed citations
4.
Moeschler, John B., Michael Shevell, Robert A. Saul, et al.. (2014). Comprehensive Evaluation of the Child With Intellectual Disability or Global Developmental Delays. PEDIATRICS. 134(3). e903–e918. 352 indexed citations
5.
Tinkle, Brad T., Howard M. Saal, Robert A. Saul, et al.. (2013). Health Supervision for Children With Marfan Syndrome. PEDIATRICS. 132(4). e1059–e1072. 34 indexed citations
6.
Boccuto, Luigi, Kazuhiro Aoki, Heather Flanagan‐Steet, et al.. (2013). A mutation in a ganglioside biosynthetic enzyme, ST3GAL5, results in salt & pepper syndrome, a neurocutaneous disorder with altered glycolipid and glycoprotein glycosylation. Human Molecular Genetics. 23(2). 418–433. 131 indexed citations
7.
Hersh, Joseph H. & Robert A. Saul. (2011). Health Supervision for Children With Fragile X Syndrome. PEDIATRICS. 127(5). 994–1006. 75 indexed citations
8.
Ladd, Sydney, et al.. (2007). Dedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilities. Genomics. 91(2). 195–202. 72 indexed citations
9.
Saul, Robert A., Virginia K. Proud, Harold A. Taylor, Jules G. Leroy, & Jürgen W. Spranger. (2005). Prenatal mucolipidosis type II (I‐cell disease) can present as Pacman dysplasia. American Journal of Medical Genetics Part A. 135A(3). 328–332. 15 indexed citations
10.
Vervoort, Virginie, et al.. (2004). POMGnT1 gene alterations in a family with neurological abnormalities. Annals of Neurology. 56(1). 143–148. 23 indexed citations
11.
Saul, Robert A., et al.. (2003). Is Jaffe–Campanacci syndrome just a manifestation of neurofibromatosis type 1?. American Journal of Medical Genetics Part A. 123A(1). 60–63. 18 indexed citations
12.
Phelan, Mary C., R. Curtis Rogers, Robert A. Saul, et al.. (2001). 22q13 deletion syndrome. American Journal of Medical Genetics. 101(2). 91–99. 206 indexed citations
13.
Desnick, Robert J., et al.. (2000). Summary of the association of professors of human and medical genetics fourth annual workshop. American Journal of Medical Genetics. 90(2). 169–172. 1 indexed citations
14.
Phelan, Mary C., et al.. (1995). Prenatal diagnosis of mosaic 4p – in a fetus with trisomy 21. Prenatal Diagnosis. 15(3). 274–277. 3 indexed citations
15.
Tarleton, Jack & Robert A. Saul. (1993). Molecular genetic advances in fragile Xsyndrome. The Journal of Pediatrics. 122(2). 169–185. 38 indexed citations
16.
Phelan, Mary C., Gordon R. Thomas, Robert A. Saul, et al.. (1992). Cytogenetic, biochemical, and molecular analyses of a 22q13 deletion. American Journal of Medical Genetics. 43(5). 872–876. 42 indexed citations
17.
Schwartz, Charles E., Angela Brown, Vazken M. Der Kaloustian, James McGill, & Robert A. Saul. (1991). DNA Fingerprinting: The Utilization of Minisatellite Probes to Detect a Somatic Mutation in the Proteus Syndrome. Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions. 58. 95–105. 16 indexed citations
18.
Saul, Robert A. & William G. Wilson. (1990). A “new” skeletal dysplasia in two unrelated boys. American Journal of Medical Genetics. 35(3). 388–393. 14 indexed citations
19.
Schwartz, Charles E., Mary C. Phelan, Gordon H. Wilkes, et al.. (1988). Fragile X syndrome: Incidence, clinical and cytogenetic findings in the black and white populations of South Carolina. American Journal of Medical Genetics. 30(1-2). 641–654. 17 indexed citations
20.
Hartman, Paul A., et al.. (1967). Lactobacilli in Ensiled High-Moisture Corn1. Applied Microbiology. 15(1). 49–54. 3 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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