E. Robert Wassman

951 total citations
23 papers, 603 citations indexed

About

E. Robert Wassman is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, E. Robert Wassman has authored 23 papers receiving a total of 603 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in E. Robert Wassman's work include Genomic variations and chromosomal abnormalities (12 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Prenatal Screening and Diagnostics (7 papers). E. Robert Wassman is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Prenatal Screening and Diagnostics (7 papers). E. Robert Wassman collaborates with scholars based in United States, Canada and Italy. E. Robert Wassman's co-authors include JoAnn C. Kelly, Lee Venolia, P. H. Yen, T. Mohandas, Stanley M. Gartler, Larry J. Shapiro, Rena Vanzo, Charles H. Hensel, Megan Martin and Leonard O. Langer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

E. Robert Wassman

23 papers receiving 571 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Robert Wassman United States 13 375 223 136 95 83 23 603
Giorgio Filippi Italy 14 281 0.7× 304 1.4× 80 0.6× 61 0.6× 54 0.7× 27 581
Natalia T. Leach United States 9 264 0.7× 199 0.9× 245 1.8× 113 1.2× 44 0.5× 17 587
Mette Viuff Denmark 16 592 1.6× 428 1.9× 114 0.8× 45 0.5× 44 0.5× 26 814
Lutgarde Govaerts Netherlands 16 441 1.2× 191 0.9× 459 3.4× 35 0.4× 84 1.0× 32 723
G. Fekete Hungary 12 173 0.5× 281 1.3× 75 0.6× 48 0.5× 39 0.5× 32 490
Alba Pilotta Italy 15 268 0.7× 229 1.0× 86 0.6× 28 0.3× 63 0.8× 26 586
Frédérique Tihy Canada 11 215 0.6× 120 0.5× 146 1.1× 25 0.3× 30 0.4× 18 384
Simona Cavani Italy 16 393 1.0× 313 1.4× 160 1.2× 23 0.2× 38 0.5× 31 692
Anna Cereda Italy 17 372 1.0× 478 2.1× 195 1.4× 44 0.5× 123 1.5× 41 836
Marie‐Pierre Cordier France 11 189 0.5× 168 0.8× 119 0.9× 24 0.3× 82 1.0× 34 438

Countries citing papers authored by E. Robert Wassman

Since Specialization
Citations

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

Fields of papers citing papers by E. Robert Wassman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Robert Wassman

This figure shows the co-authorship network connecting the top 25 collaborators of E. Robert Wassman. A scholar is included among the top collaborators of E. Robert Wassman 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 E. Robert Wassman. E. Robert Wassman 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.
Vanzo, Rena, Aparna Prasad, Charles H. Hensel, et al.. (2020). The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism. Journal of Personalized Medicine. 11(1). 21–21. 3 indexed citations
2.
Wassman, E. Robert, Karen J. Ho, Kyle Davis, et al.. (2019). Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders. Neurology Genetics. 5(6). e378–e378. 2 indexed citations
3.
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
4.
Prasad, Aparna, Rena Vanzo, Patricia Mowery‐Rushton, et al.. (2018). Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis. BMC Medical Genetics. 19(1). 46–46. 19 indexed citations
5.
Ho, Karen S., Lenora M. Olson, Xiaoming Sheng, et al.. (2018). A survey of antiepileptic drug responses identifies drugs with potential efficacy for seizure control in Wolf–Hirschhorn syndrome. Epilepsy & Behavior. 81. 55–61. 10 indexed citations
6.
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
7.
Vivian, Jay L., R. Tanner Hagelstrom, Waheeda A. Hossain, et al.. (2017). A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson Syndrome. Molecular Syndromology. 8(4). 211–218. 15 indexed citations
8.
Ho, Karen S., E. Robert Wassman, Charles H. Hensel, et al.. (2016). Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders. International Journal of Molecular Sciences. 17(12). 2070–2070. 50 indexed citations
9.
Peabody, John, Megan Martin, Lisa DeMaria, et al.. (2016). Clinical Utility of a Comprehensive, Whole Genome CMA Testing Platform in Pediatrics: A Prospective Randomized Controlled Trial of Simulated Patients in Physician Practices. PLoS ONE. 11(12). e0169064–e0169064. 5 indexed citations
10.
Ho, Karen S. & E. Robert Wassman. (2016). A case for cannabidiol in Wolf–Hirschhorn syndrome seizure management. American Journal of Medical Genetics Part A. 173(2). 324–326. 2 indexed citations
11.
Sanden, Mats, et al.. (2015). Clinicians’ Real World Perceptions of Pre-Nephrectomy Diagnostic Biopsy Performance as a Driver of Reduction in Unnecessary Surgeries in Renal Tumors. SHILAP Revista de lepidopterología. 2(1). 1–14. 4 indexed citations
12.
Schrijver, Iris, Sudha Ramalingam, S. Ramalingam, et al.. (2005). Diagnostic Testing by CFTR Gene Mutation Analysis in a Large Group of Hispanics. Journal of Molecular Diagnostics. 7(2). 289–299. 34 indexed citations
13.
Wassman, E. Robert, et al.. (1990). Second trimester maternal serum pregnancy specific beta‐1 glycoprotein (SP‐1) levels in normal and down syndrome pregnancies. American Journal of Medical Genetics. 37(1). 114–118. 16 indexed citations
14.
Kelly, JoAnn C., et al.. (1989). Amniotic fluid acetylcholinesterase ratios in prenatal diagnosis of fetal abnormalities. American Journal of Obstetrics and Gynecology. 161(3). 703–705. 5 indexed citations
15.
Grundy, Howard, et al.. (1989). Prenatal detection of cyclopia associated with interstitial deletion of 2p. American Journal of Medical Genetics. 34(2). 268–270. 13 indexed citations
16.
Wassman, E. Robert, et al.. (1989). Prenatal screening for Down syndrome with maternal serum human chorionic gonadotropin levels. American Journal of Obstetrics and Gynecology. 161(5). 1168–1173. 48 indexed citations
17.
Benson, Kaaron, et al.. (1986). Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46, XX, del(2) (q31q33). American Journal of Medical Genetics. 25(3). 405–411. 30 indexed citations
18.
Jenkins, Edmund C., W. Ted Brown, Miriam G. Wilson, et al.. (1986). The prenatal detection of the fragile X chromosome: Review of recent experience. American Journal of Medical Genetics. 23(1-2). 297–311. 28 indexed citations
19.
Pauli, Richard M., Charles I. Scott, E. Robert Wassman, et al.. (1984). Apnea and sudden unexpected death in infants with achondroplasia. The Journal of Pediatrics. 104(3). 342–348. 147 indexed citations
20.
Venolia, Lee, Stanley M. Gartler, E. Robert Wassman, et al.. (1982). Transformation with DNA from 5-azacytidine-reactivated X chromosomes.. Proceedings of the National Academy of Sciences. 79(7). 2352–2354. 126 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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