Albert David
Impact in
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
- Molecular Biology top 5%
- Congenital heart defects research
- Sexual Differentiation and Disorders
- RNA and protein synthesis mechanisms
Papers in
-
- Congenital heart defects research 6
- RNA modifications and cancer 6
- Epigenetics and DNA Methylation 5
- Genetics 41
- Genomic variations and chromosomal abnormalities 10
- Connective tissue disorders research 9
- Genetics and Neurodevelopmental Disorders 7
- Co-authors
- Cédric Le Caignec (31 shared papers)Bertrand Isidor (29 shared papers)Olivier Pichon (12 shared papers)Patrick Calvas (2 shared papers)Martine Raynaud (3 shared papers)Alain Verloès (13 shared papers)Marie Gomot (2 shared papers)Jamel Chelly (2 shared papers)
- Journals
- Human Mutation (8 papers)European Journal of Medical Genetics (7 papers)The American Journal of Human Genetics (4 papers)European Journal of Human Genetics (3 papers)American Journal of Medical Genetics Part A (23 papers)
- Partner nations
- FranceBelgiumUnited Kingdom
In The Last Decade
Albert David
92 papers receiving 3.3k citations
Albert David's Hit Papers
Peers
Comparison fields: 5 of 145
- Genetics 1.5k
- Molecular Biology 1.7k
- Sensory Systems 97
- Cognitive Neuroscience 358
- Cell Biology 274
Countries citing papers authored by Albert David
This map shows the geographic impact of Albert David'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 Albert David with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Albert David more than expected).
Fields of papers citing papers by Albert David
This network shows the impact of papers produced by Albert David. 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 Albert David. The network helps show where Albert David may publish in the future.
Co-authors
The 25 scholars most cited alongside Albert David, 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 93 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family Hit paper breakdown → | 2004 | 608 |
| 2 | 2013 | 246 | |
| 3 | 2010 | 177 | |
| 4 | 2011 | 159 | |
| 5 | 2002 | 141 | |
| 6 | 2009 | 101 | |
| 7 | Les nouvelles fondations des sciences de gestion | 2000 | 77 |
| 8 | 1998 | 72 | |
| 9 | 2003 | 64 | |
| 10 | 2014 | 63 | |
| 11 | 2002 | 59 | |
| 12 | 2006 | 57 | |
| 13 | 2006 | 57 | |
| 14 | 2009 | 56 | |
| 15 | 2011 | 53 | |
| 16 | 2010 | 50 | |
| 17 | 2001 | 49 | |
| 18 | 1994 | 47 | |
| 19 | 2009 | 43 | |
| 20 | 2011 | 42 |
About Albert David
Albert David is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Cell Biology, having authored 93 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Connective tissue disorders research (9 papers), Genetics and Neurodevelopmental Disorders (7 papers), Congenital heart defects research (6 papers), RNA modifications and cancer (6 papers), Prenatal Screening and Diagnostics (6 papers), Skin and Cellular Biology Research (6 papers) and Epigenetics and DNA Methylation (5 papers). The work is most often cited by research in Genetics (1.5k citations), Molecular Biology (1.7k citations), Sensory Systems (97 citations), Cognitive Neuroscience (358 citations) and Cell Biology (274 citations). Albert David has collaborated with scholars based in France, Belgium and United Kingdom. Frequent co-authors include Cédric Le Caignec, Bertrand Isidor, Olivier Pichon, Patrick Calvas, Martine Raynaud, Alain Verloès, Marie Gomot, Jamel Chelly, Sébastien Jacquemont and Sylvain Briault. Their work appears in journals such as Human Mutation, European Journal of Medical Genetics, The American Journal of Human Genetics, European Journal of Human Genetics and American Journal of Medical Genetics Part A.
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.