Blanca Gener
Impact in
-
- Neuroscience of respiration and sleep
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 18
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 5
- Connective tissue disorders research 3
- Genetic and Kidney Cyst Diseases 3
- Genetic Syndromes and Imprinting 3
- Co-authors
- Ha Trang (1 shared paper)Heather Etchevers (1 shared paper)Michel Simonneau (1 shared paper)Delphine Trochet (1 shared paper)Claude Gaultier (1 shared paper)Arnold Münnich (1 shared paper)Béatrice Laudier (1 shared paper)Tania Attié‐Bitach (1 shared paper)
- Journals
- Pediatric Neurology (2 papers)Nature Genetics (1 paper)Orphanet Journal of Rare Diseases (1 paper)Human Molecular Genetics (1 paper)Frontiers in Cell and Developmental Biology (1 paper)
- Partner nations
- SpainUnited KingdomFrance
In The Last Decade
Blanca Gener
31 papers receiving 1.4k citations
Blanca Gener's Hit Papers
Peers
Comparison fields: 5 of 92
- Endocrine and Autonomic Systems 434
- Genetics 480
- Pediatrics, Perinatology and Child Health 307
- Developmental Biology 28
- Pulmonary and Respiratory Medicine 326
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 | 619 |
| 2 | 2004 | 207 | |
| 3 | 2013 | 89 | |
| 4 | 2015 | 89 | |
| 5 | 2009 | 86 | |
| 6 | 2005 | 79 | |
| 7 | 2021 | 31 | |
| 8 | 2013 | 31 | |
| 9 | 2008 | 27 | |
| 10 | 2013 | 26 | |
| 11 | 2018 | 21 | |
| 12 | 2009 | 19 | |
| 13 | 2020 | 18 | |
| 14 | 2003 | 18 | |
| 15 | 2010 | 18 | |
| 16 | 2004 | 14 | |
| 17 | 2016 | 14 | |
| 18 | 2013 | 13 | |
| 19 | 2007 | 12 | |
| 20 | 2019 | 10 |
About Blanca Gener
Blanca Gener is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Epidemiology, having authored 31 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers), Prenatal Screening and Diagnostics (4 papers), Connective tissue disorders research (3 papers), Genetic and Kidney Cyst Diseases (3 papers), Autism Spectrum Disorder Research (3 papers), Genetic Syndromes and Imprinting (3 papers) and Bone and Dental Protein Studies (3 papers). The work is most often cited by research in Endocrine and Autonomic Systems (434 citations), Genetics (480 citations), Pediatrics, Perinatology and Child Health (307 citations), Developmental Biology (28 citations) and Pulmonary and Respiratory Medicine (326 citations). Blanca Gener has collaborated with scholars based in Spain, United Kingdom and France. Frequent co-authors include Ha Trang, Heather Etchevers, Michel Simonneau, Delphine Trochet, Claude Gaultier, Arnold Münnich, Béatrice Laudier, Tania Attié‐Bitach, Michel Vekemans and Jeanne Amiel. Their work appears in journals such as Pediatric Neurology, Nature Genetics, Orphanet Journal of Rare Diseases, Human Molecular Genetics and Frontiers in Cell and Developmental Biology.
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.