Bernice E. Morrow
Impact in
- Genetics top 0.2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 0.5%
- Congenital heart defects research
- Genomics and Chromatin Dynamics
Papers in
-
- Congenital heart defects research 91
- Genomics and Chromatin Dynamics 10
- Genetics 50
- Genomic variations and chromosomal abnormalities 29
- Co-authors
- Rosalie Goldberg (11 shared papers)Robert J. Shprintzen (12 shared papers)David R. Soll (9 shared papers)Jonathan R. Warner (10 shared papers)Raju Kucherlapati (11 shared papers)Peter Scambler (8 shared papers)Raj K. Pandita (10 shared papers)Jun Liao (8 shared papers)
- Journals
- The American Journal of Human Genetics (11 papers)Human Molecular Genetics (11 papers)Molecular and Cellular Biology (7 papers)PLoS ONE (6 papers)Developmental Biology (5 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Bernice E. Morrow
146 papers receiving 8.8k citations
Bernice E. Morrow's Hit Papers
Peers
Comparison fields: 5 of 141
- Genetics 3.1k
- Molecular Biology 6.3k
- Sensory Systems 351
- Epidemiology 1.7k
- Developmental Neuroscience 143
Countries citing papers authored by Bernice E. Morrow
This map shows the geographic impact of Bernice E. Morrow'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 Bernice E. Morrow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernice E. Morrow more than expected).
Fields of papers citing papers by Bernice E. Morrow
This network shows the impact of papers produced by Bernice E. Morrow. 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 Bernice E. Morrow. The network helps show where Bernice E. Morrow may publish in the future.
Co-authors
The 25 scholars most cited alongside Bernice E. Morrow, 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 150 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 22q11.2 deletion syndrome Hit paper breakdown → | 2015 | 859 |
| 2 | 1995 | 497 | |
| 3 | 1996 | 487 | |
| 4 | 1994 | 335 | |
| 5 | 1996 | 306 | |
| 6 | 1997 | 284 | |
| 7 | 1996 | 257 | |
| 8 | 1999 | 252 | |
| 9 | 2002 | 208 | |
| 10 | Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome. | 1995 | 188 |
| 11 | 2005 | 187 | |
| 12 | 1991 | 179 | |
| 13 | 2001 | 154 | |
| 14 | 2010 | 147 | |
| 15 | 2004 | 146 | |
| 16 | 1992 | 140 | |
| 17 | 2006 | 134 | |
| 18 | 1993 | 129 | |
| 19 | 2006 | 121 | |
| 20 | 1990 | 117 |
About Bernice E. Morrow
Bernice E. Morrow is a scholar working on Molecular Biology, Genetics, Epidemiology, Pulmonary and Respiratory Medicine and Plant Science, having authored 150 papers that have together received 9.1k indexed citations. Recurring topics across this work include Congenital heart defects research (91 papers), Genomic variations and chromosomal abnormalities (29 papers), Congenital Heart Disease Studies (29 papers), Chromosomal and Genetic Variations (14 papers), Coronary Artery Anomalies (12 papers), Hearing, Cochlea, Tinnitus, Genetics (11 papers), Genomics and Chromatin Dynamics (10 papers) and Tissue Engineering and Regenerative Medicine (9 papers). The work is most often cited by research in Genetics (3.1k citations), Molecular Biology (6.3k citations), Sensory Systems (351 citations), Epidemiology (1.7k citations) and Developmental Neuroscience (143 citations). Bernice E. Morrow has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Rosalie Goldberg, Robert J. Shprintzen, David R. Soll, Jonathan R. Warner, Raju Kucherlapati, Peter Scambler, Raj K. Pandita, Jun Liao, Donna M. McDonald‐McGinn and Lisa Edelmann. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics, Molecular and Cellular Biology, PLoS ONE and Developmental Biology.
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.