Nancy E. Maestri
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
- Biochemistry top 2%
- Amino Acid Enzymes and Metabolism
Papers in
-
- Metabolism and Genetic Disorders 8
- Genetics 16
- Cleft Lip and Palate Research 6
- Genetic Associations and Epidemiology 4
- Craniofacial Disorders and Treatments 4
- Co-authors
- Saul W. Brusilow (8 shared papers)David B. Clissold (3 shared papers)Terri H. Beaty (10 shared papers)Diego F. Wyszynski (6 shared papers)Susan Spear Bassett (1 shared paper)Luigi De Luca (3 shared papers)Dennis Bartholomew (1 shared paper)Elizabeth R. Hauser (1 shared paper)
- Journals
- Genetic Epidemiology (6 papers)The Journal of Pediatrics (4 papers)Environmental Health Perspectives (2 papers)Human Heredity (2 papers)Human Genetics (2 papers)
- Partner nations
- United StatesMexicoGermany
In The Last Decade
Nancy E. Maestri
39 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 106
- Clinical Biochemistry 693
- Biochemistry 214
- Genetics 744
- Molecular Biology 841
- Pediatrics, Perinatology and Child Health 213
Countries citing papers authored by Nancy E. Maestri
This map shows the geographic impact of Nancy E. Maestri'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 Nancy E. Maestri with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nancy E. Maestri more than expected).
Fields of papers citing papers by Nancy E. Maestri
This network shows the impact of papers produced by Nancy E. Maestri. 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 Nancy E. Maestri. The network helps show where Nancy E. Maestri may publish in the future.
Co-authors
The 25 scholars most cited alongside Nancy E. Maestri, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 296 | |
| 2 | 1996 | 227 | |
| 3 | Analysis of phenotypic features and FGFR2 mutations in Apert syndrome. | 1995 | 209 |
| 4 | 1996 | 165 | |
| 5 | 1997 | 131 | |
| 6 | 1991 | 121 | |
| 7 | 1999 | 109 | |
| 8 | 1997 | 97 | |
| 9 | 1998 | 88 | |
| 10 | 1985 | 83 | |
| 11 | 1972 | 74 | |
| 12 | 1997 | 65 | |
| 13 | 1973 | 63 | |
| 14 | 1992 | 58 | |
| 15 | 1992 | 56 | |
| 16 | 1996 | 50 | |
| 17 | 1995 | 36 | |
| 18 | 1988 | 28 | |
| 19 | 1997 | 23 | |
| 20 | 1989 | 15 |
About Nancy E. Maestri
Nancy E. Maestri is a scholar working on Clinical Biochemistry, Genetics, Molecular Biology, Cancer Research and Pulmonary and Respiratory Medicine, having authored 40 papers that have together received 2.1k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (8 papers), Cleft Lip and Palate Research (6 papers), Genetic Associations and Epidemiology (4 papers), Craniofacial Disorders and Treatments (4 papers), Biochemical and Molecular Research (3 papers), Cancer, Hypoxia, and Metabolism (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Tracheal and airway disorders (2 papers). The work is most often cited by research in Clinical Biochemistry (693 citations), Biochemistry (214 citations), Genetics (744 citations), Molecular Biology (841 citations) and Pediatrics, Perinatology and Child Health (213 citations). Nancy E. Maestri has collaborated with scholars based in United States, Mexico and Germany. Frequent co-authors include Saul W. Brusilow, David B. Clissold, Terri H. Beaty, Diego F. Wyszynski, Susan Spear Bassett, Luigi De Luca, Dennis Bartholomew, Elizabeth R. Hauser, Iain B. McIntosh and Julie S. Fryburg. Their work appears in journals such as Genetic Epidemiology, The Journal of Pediatrics, Environmental Health Perspectives, Human Heredity and 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.