Robert Wallerstein
Impact in
- Developmental Biology top 5%
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 32
- Genomic variations and chromosomal abnormalities 17
- Genetic Syndromes and Imprinting 8
- Neurogenetic and Muscular Disorders Research 4
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- Congenital heart defects research 5
- Glycosylation and Glycoproteins Research 4
- Co-authors
- John Sum (3 shared papers)Adolfo Correa (1 shared paper)John L. Kitzmiller (1 shared paper)Ellen Moran (2 shared papers)Hana Aviv (3 shared papers)Lynne T. Smith (1 shared paper)Fatima Rouan (1 shared paper)Tod A. Brown (1 shared paper)
- Journals
- Clinical Genetics (4 papers)Journal of Medical Genetics (2 papers)The Cleft Palate-Craniofacial Journal (2 papers)Prenatal Diagnosis (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Robert Wallerstein
62 papers receiving 916 citations
Peers
Comparison fields: 5 of 80
- Developmental Biology 46
- Genetics 402
- Pediatrics, Perinatology and Child Health 187
- Immunology and Allergy 48
- Urology 40
Countries citing papers authored by Robert Wallerstein
This map shows the geographic impact of Robert Wallerstein'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 Wallerstein with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Wallerstein more than expected).
Fields of papers citing papers by Robert Wallerstein
This network shows the impact of papers produced by Robert Wallerstein. 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 Wallerstein. The network helps show where Robert Wallerstein may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert Wallerstein, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 66 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 151 | |
| 2 | 1998 | 96 | |
| 3 | 2010 | 60 | |
| 4 | 1997 | 48 | |
| 5 | 2008 | 48 | |
| 6 | 1997 | 43 | |
| 7 | 2013 | 38 | |
| 8 | 2005 | 37 | |
| 9 | 2002 | 34 | |
| 10 | 2000 | 32 | |
| 11 | 2008 | 32 | |
| 12 | 2015 | 27 | |
| 13 | 2016 | 24 | |
| 14 | 1997 | 24 | |
| 15 | 2017 | 23 | |
| 16 | 2006 | 22 | |
| 17 | 2009 | 21 | |
| 18 | 2006 | 20 | |
| 19 | 2000 | 19 | |
| 20 | 2000 | 16 |
About Robert Wallerstein
Robert Wallerstein is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 66 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (13 papers), Genetic Syndromes and Imprinting (8 papers), Congenital heart defects research (5 papers), Congenital limb and hand anomalies (5 papers), Glycosylation and Glycoproteins Research (4 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Congenital Anomalies and Fetal Surgery (4 papers). The work is most often cited by research in Developmental Biology (46 citations), Genetics (402 citations), Pediatrics, Perinatology and Child Health (187 citations), Immunology and Allergy (48 citations) and Urology (40 citations). Robert Wallerstein has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include John Sum, Adolfo Correa, John L. Kitzmiller, Ellen Moran, Hana Aviv, Lynne T. Smith, Fatima Rouan, Tod A. Brown, Jouni Uitto and Maria C. Garzón. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, The Cleft Palate-Craniofacial Journal, Prenatal Diagnosis and The American Journal of Human Genetics.
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.