Nancy B. Spinner
Impact in
Papers in
- Co-authors
- David A. Piccoli (44 shared papers)Ian D. Krantz (51 shared papers)Anna Genin (14 shared papers)Leslie G. Biesecker (2 shared papers)Elizabeth B. Rand (10 shared papers)Elaine H. Zackai (41 shared papers)Binita M. Kamath (22 shared papers)Karan M. Emerick (4 shared papers)
- Journals
- Human Mutation (10 papers)Genetics in Medicine (8 papers)The American Journal of Human Genetics (7 papers)Journal of Pediatric Gastroenterology and Nutrition (7 papers)Human Genetics (4 papers)
- Partner nations
- United StatesCanadaItaly
In The Last Decade
Nancy B. Spinner
192 papers receiving 11.7k citations
Nancy B. Spinner's Hit Papers
Peers
Comparison fields: 5 of 137
- Genetics 4.1k
- Surgery 4.3k
- Hepatology 760
- Pulmonary and Respiratory Medicine 2.2k
- Pediatrics, Perinatology and Child Health 1.3k
Countries citing papers authored by Nancy B. Spinner
This map shows the geographic impact of Nancy B. Spinner'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 B. Spinner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nancy B. Spinner more than expected).
Fields of papers citing papers by Nancy B. Spinner
This network shows the impact of papers produced by Nancy B. Spinner. 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 B. Spinner. The network helps show where Nancy B. Spinner may publish in the future.
Co-authors
The 25 scholars most cited alongside Nancy B. Spinner, 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 197 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1 Hit paper breakdown → | 1997 | 1025 |
| 2 | Mutations in the human Jagged1 gene are responsible for Alagille syndrome Hit paper breakdown → | 1997 | 902 |
| 3 | NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway Hit paper breakdown → | 2006 | 575 |
| 4 | Features of Alagille Syndrome in 92 Patients: Frequency and Relation to Prognosis Hit paper breakdown → | 1999 | 488 |
| 5 | A genomic view of mosaicism and human disease Hit paper breakdown → | 2013 | 455 |
| 6 | Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents Hit paper breakdown → | 2015 | 394 |
| 7 | 2010 | 350 | |
| 8 | 1992 | 320 | |
| 9 | 1998 | 319 | |
| 10 | 2004 | 268 | |
| 11 | 2012 | 265 | |
| 12 | 2002 | 229 | |
| 13 | 2000 | 186 | |
| 14 | 2009 | 185 | |
| 15 | 1998 | 184 | |
| 16 | 2011 | 172 | |
| 17 | 1999 | 155 | |
| 18 | 1997 | 137 | |
| 19 | 2001 | 136 | |
| 20 | 1999 | 123 |
About Nancy B. Spinner
Nancy B. Spinner is a scholar working on Genetics, Surgery, Molecular Biology, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health, having authored 197 papers that have together received 12.5k indexed citations. Recurring topics across this work include Pediatric Hepatobiliary Diseases and Treatments (73 papers), Genomic variations and chromosomal abnormalities (60 papers), Gallbladder and Bile Duct Disorders (39 papers), Congenital Anomalies and Fetal Surgery (25 papers), Chromosomal and Genetic Variations (22 papers), Prenatal Screening and Diagnostics (21 papers), Cholangiocarcinoma and Gallbladder Cancer Studies (19 papers) and Genomics and Rare Diseases (19 papers). The work is most often cited by research in Genetics (4.1k citations), Surgery (4.3k citations), Hepatology (760 citations), Pulmonary and Respiratory Medicine (2.2k citations) and Pediatrics, Perinatology and Child Health (1.3k citations). Nancy B. Spinner has collaborated with scholars based in United States, Canada and Italy. Frequent co-authors include David A. Piccoli, Ian D. Krantz, Anna Genin, Leslie G. Biesecker, Elizabeth B. Rand, Elaine H. Zackai, Binita M. Kamath, Karan M. Emerick, Laura K. Conlin and Kathleen M. Loomes. Their work appears in journals such as Human Mutation, Genetics in Medicine, The American Journal of Human Genetics, Journal of Pediatric Gastroenterology and Nutrition 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.