Nathaniel H. Robin
Impact in
- Genetics top 0.5%
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders
- Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
- Genetics 85
- Craniofacial Disorders and Treatments 28
- Genomic variations and chromosomal abnormalities 25
- Cleft Lip and Palate Research 24
- BRCA gene mutations in cancer 11
- Co-authors
- Maximilian MuenkeRobert J. ShprintzenAnne L. MatthewsAndreas HehrMaryAnn O’RiordanRobin M. WinterElaine H. ZackaiH. Wolfgang Losken
- Journals
- Genetics in Medicine (14 papers)Current Opinion in Pediatrics (9 papers)Human Genetics (6 papers)The Journal of Pediatrics (5 papers)Human Molecular Genetics (4 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Nathaniel H. Robin
143 papers receiving 4.0k citations
Peers
Comparison fields: 5 of 141
- Genetics 2.4k
- Sensory Systems 351
- Developmental Biology 127
- Pediatrics, Perinatology and Child Health 672
- Otorhinolaryngology 146
Countries citing papers authored by Nathaniel H. Robin
This map shows the geographic impact of Nathaniel H. Robin'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 Nathaniel H. Robin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nathaniel H. Robin more than expected).
Fields of papers citing papers by Nathaniel H. Robin
This network shows the impact of papers produced by Nathaniel H. Robin. 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 Nathaniel H. Robin. The network helps show where Nathaniel H. Robin may publish in the future.
Co-authors
The 25 scholars most cited alongside Nathaniel H. Robin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 0 | |
| 2 | 2024 | 1 | |
| 3 | 2024 | 1 | |
| 4 | 2021 | 10 | |
| 5 | 2021 | 8 | |
| 6 | 2017 | 2 | |
| 7 | 2013 | 3 | |
| 8 | 2013 | 7 | |
| 9 | 2013 | 34 | |
| 10 | 2008 | 3 | |
| 11 | 2008 | 1 | |
| 12 | 2007 | 40 | |
| 13 | 2005 | 5 | |
| 14 | Advances in the genetics of pediatric heart disease | 2002 | 1 |
| 15 | 2002 | 11 | |
| 16 | 1998 | 94 | |
| 17 | 1998 | 8 | |
| 18 | 1996 | 9 | |
| 19 | 1994 | 466 | |
| 20 | 1993 | 34 |
About Nathaniel H. Robin
Nathaniel H. Robin is a scholar working on Genetics, Developmental Biology, Sensory Systems, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 151 papers that have together received 4.2k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (28 papers), Genomic variations and chromosomal abnormalities (25 papers), Congenital heart defects research (24 papers), Cleft Lip and Palate Research (24 papers), Prenatal Screening and Diagnostics (16 papers), Hearing, Cochlea, Tinnitus, Genetics (13 papers), Congenital Anomalies and Fetal Surgery (13 papers) and BRCA gene mutations in cancer (11 papers). The work is most often cited by research in Genetics (2.4k citations), Sensory Systems (351 citations), Developmental Biology (127 citations), Pediatrics, Perinatology and Child Health (672 citations) and Otorhinolaryngology (146 citations). Nathaniel H. Robin has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Maximilian Muenke, Robert J. Shprintzen, Anne L. Matthews, Andreas Hehr, MaryAnn O’Riordan, Robin M. Winter, Elaine H. Zackai, H. Wolfgang Losken, Albert Schinzel and Paul Rutland. Their work appears in journals such as Genetics in Medicine, Current Opinion in Pediatrics, Human Genetics, The Journal of Pediatrics and Human Molecular 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.