N. Philip
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Congenital Ear and Nasal Anomalies
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
- Genetics 43
- Genomic variations and chromosomal abnormalities 13
- Connective tissue disorders research 9
- Genetics and Neurodevelopmental Disorders 8
- Genetic Syndromes and Imprinting 6
- Craniofacial Disorders and Treatments 6
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- Congenital heart defects research 11
- Co-authors
- J. F. Mattéi (11 shared papers)Marie‐Geneviève Mattéi (14 shared papers)E. Passage (2 shared papers)Jean‐Paul Moisan (1 shared paper)Jean‐Louis Mandel (1 shared paper)Sabine Sigaudy (18 shared papers)Ségolène Aymé (11 shared papers)D. Gambarelli (7 shared papers)
In The Last Decade
N. Philip
75 papers receiving 1.9k citations
Peers
Comparison fields: 5 of 101
- Genetics 829
- Genetics 275
- Pediatrics, Perinatology and Child Health 331
- Developmental Biology 36
- Pharmacy 60
Countries citing papers authored by N. Philip
This map shows the geographic impact of N. Philip'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 N. Philip with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N. Philip more than expected).
Fields of papers citing papers by N. Philip
This network shows the impact of papers produced by N. Philip. 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 N. Philip. The network helps show where N. Philip may publish in the future.
Co-authors
The 25 scholars most cited alongside N. Philip, 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 82 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1985 | 302 | |
| 2 | 1998 | 180 | |
| 3 | 2003 | 92 | |
| 4 | 1994 | 88 | |
| 5 | 2008 | 85 | |
| 6 | 1992 | 85 | |
| 7 | 1989 | 53 | |
| 8 | 2007 | 51 | |
| 9 | 1991 | 41 | |
| 10 | 2006 | 37 | |
| 11 | 1997 | 35 | |
| 12 | 1994 | 34 | |
| 13 | 1996 | 32 | |
| 14 | 2009 | 32 | |
| 15 | 2010 | 32 | |
| 16 | 1987 | 32 | |
| 17 | 2003 | 31 | |
| 18 | 2006 | 31 | |
| 19 | 1995 | 29 | |
| 20 | 1998 | 29 |
About N. Philip
N. Philip is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 82 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Congenital heart defects research (11 papers), Prenatal Screening and Diagnostics (11 papers), Connective tissue disorders research (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genetic Syndromes and Imprinting (6 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Craniofacial Disorders and Treatments (6 papers). The work is most often cited by research in Genetics (829 citations), Genetics (275 citations), Pediatrics, Perinatology and Child Health (331 citations), Developmental Biology (36 citations) and Pharmacy (60 citations). N. Philip has collaborated with scholars based in France, Belgium and India. Frequent co-authors include J. F. Mattéi, Marie‐Geneviève Mattéi, E. Passage, Jean‐Paul Moisan, Jean‐Louis Mandel, Sabine Sigaudy, Ségolène Aymé, D. Gambarelli, A. Moncla and A. Potier. Their work appears in journals such as European Journal of Pediatrics, Human Genetics, Journal of Medical Genetics, Clinical Genetics and Prenatal Diagnosis.
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.