Blanca Gener
Impact in
-
- Neuroscience of respiration and sleep
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 17
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 4
- Connective tissue disorders research 3
- Genetic Syndromes and Imprinting 3
- Genetic and Kidney Cyst Diseases 3
- Co-authors
- Heather Etchevers (1 shared paper)Pierre F. Ray (1 shared paper)Arnold Münnich (1 shared paper)Michel Simonneau (1 shared paper)Ha Trang (1 shared paper)Michel Vekemans (1 shared paper)Delphine Trochet (1 shared paper)Tania Attié‐Bitach (1 shared paper)
- Journals
- The American Journal of Human Genetics (3 papers)Pediatric Neurology (2 papers)Genes (1 paper)Clinical and Translational Medicine (1 paper)Prenatal Diagnosis (1 paper)
- Partner nations
- SpainUnited KingdomFrance
In The Last Decade
Blanca Gener
31 papers receiving 1.5k citations
Blanca Gener's Hit Papers
Peers
Comparison fields: 5 of 88
- Endocrine and Autonomic Systems 425
- Genetics 434
- Pediatrics, Perinatology and Child Health 226
- Developmental Biology 23
- Urology 58
Countries citing papers authored by Blanca Gener
This map shows the geographic impact of Blanca Gener'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 Blanca Gener with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Blanca Gener more than expected).
Fields of papers citing papers by Blanca Gener
This network shows the impact of papers produced by Blanca Gener. 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 Blanca Gener. The network helps show where Blanca Gener may publish in the future.
Co-authors
The 25 scholars most cited alongside Blanca Gener, 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome Hit paper breakdown → | 2003 | 624 |
| 2 | 2004 | 208 | |
| 3 | 2015 | 91 | |
| 4 | 2013 | 89 | |
| 5 | 2009 | 87 | |
| 6 | 2005 | 79 | |
| 7 | 2010 | 73 | |
| 8 | 2021 | 32 | |
| 9 | 2013 | 31 | |
| 10 | 2008 | 27 | |
| 11 | 2013 | 26 | |
| 12 | 2018 | 21 | |
| 13 | 2009 | 19 | |
| 14 | 2010 | 18 | |
| 15 | 2003 | 18 | |
| 16 | 2020 | 18 | |
| 17 | 2016 | 14 | |
| 18 | 2004 | 13 | |
| 19 | 2013 | 13 | |
| 20 | 2007 | 12 |
About Blanca Gener
Blanca Gener is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Cognitive Neuroscience, having authored 31 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Connective tissue disorders research (3 papers), Autism Spectrum Disorder Research (3 papers), Genetic Syndromes and Imprinting (3 papers), Genetic and Kidney Cyst Diseases (3 papers), Prenatal Screening and Diagnostics (3 papers) and Bone and Dental Protein Studies (2 papers). The work is most often cited by research in Endocrine and Autonomic Systems (425 citations), Genetics (434 citations), Pediatrics, Perinatology and Child Health (226 citations), Developmental Biology (23 citations) and Urology (58 citations). Blanca Gener has collaborated with scholars based in Spain, United Kingdom and France. Frequent co-authors include Heather Etchevers, Pierre F. Ray, Arnold Münnich, Michel Simonneau, Ha Trang, Michel Vekemans, Delphine Trochet, Tania Attié‐Bitach, Jeanne Amiel and Stanislas Lyonnet. Their work appears in journals such as The American Journal of Human Genetics, Pediatric Neurology, Genes, Clinical and Translational Medicine 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.