Rena E. Falk
Impact in
- Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Cleft Lip and Palate Research
Papers in
- Genetics 17
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 4
- Connective tissue disorders research 4
- Neurogenetic and Muscular Disorders Research 3
- Co-authors
- Kari Casas (2 shared papers)Nathan Fischel‐Ghodsian (2 shared papers)Nicola Ragge (2 shared papers)Ralph Nelson (1 shared paper)Toni R. Prezant (1 shared paper)Kathleen S. Arnos (1 shared paper)L Makowka (1 shared paper)Bryce Taylor (1 shared paper)
- Journals
- Fertility and Sterility (4 papers)Prenatal Diagnosis (2 papers)Journal of Child Neurology (2 papers)Eye (2 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (2 papers)
- Partner nations
- United StatesAustraliaBelgium
In The Last Decade
Rena E. Falk
39 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 81
- Sensory Systems 78
- Genetics 413
- Clinical Biochemistry 75
- Hepatology 55
- Pediatrics, Perinatology and Child Health 127
Countries citing papers authored by Rena E. Falk
This map shows the geographic impact of Rena E. Falk'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 Rena E. Falk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rena E. Falk more than expected).
Fields of papers citing papers by Rena E. Falk
This network shows the impact of papers produced by Rena E. Falk. 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 Rena E. Falk. The network helps show where Rena E. Falk may publish in the future.
Co-authors
The 25 scholars most cited alongside Rena E. Falk, 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 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 123 | |
| 2 | 1976 | 85 | |
| 3 | 2007 | 77 | |
| 4 | Examination of patient selection and outcome for hepatic resection for metastatic disease. | 1987 | 73 |
| 5 | 1990 | 72 | |
| 6 | 2004 | 71 | |
| 7 | 2001 | 62 | |
| 8 | 1993 | 40 | |
| 9 | 1997 | 36 | |
| 10 | 1998 | 33 | |
| 11 | 1998 | 30 | |
| 12 | 2009 | 28 | |
| 13 | 2010 | 24 | |
| 14 | 2013 | 23 | |
| 15 | 2012 | 21 | |
| 16 | 1995 | 21 | |
| 17 | 1988 | 21 | |
| 18 | 2005 | 20 | |
| 19 | Role of amniocentesis in ultrasound-detected fetal malformations. | 1986 | 19 |
| 20 | 1992 | 16 |
About Rena E. Falk
Rena E. Falk is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Developmental Biology, having authored 39 papers that have together received 1.0k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (8 papers), Congenital limb and hand anomalies (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Connective tissue disorders research (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Chromosomal and Genetic Variations (3 papers) and Neurofibromatosis and Schwannoma Cases (2 papers). The work is most often cited by research in Sensory Systems (78 citations), Genetics (413 citations), Clinical Biochemistry (75 citations), Hepatology (55 citations) and Pediatrics, Perinatology and Child Health (127 citations). Rena E. Falk has collaborated with scholars based in United States, Australia and Belgium. Frequent co-authors include Kari Casas, Nathan Fischel‐Ghodsian, Nicola Ragge, Ralph Nelson, Toni R. Prezant, Kathleen S. Arnos, L Makowka, Bryce Taylor, B Langer and Stephen D. Cederbaum. Their work appears in journals such as Fertility and Sterility, Prenatal Diagnosis, Journal of Child Neurology, Eye and American Journal of Medical Genetics Part C Seminars in Medical 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.