Blanca Gener

6.4k total citations · 1 hit paper
31 papers, 1.5k citations indexed

About

Blanca Gener is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Blanca Gener has authored 31 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 14 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Blanca Gener's work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Prenatal Screening and Diagnostics (4 papers). Blanca Gener is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Prenatal Screening and Diagnostics (4 papers). Blanca Gener collaborates with scholars based in Spain, United Kingdom and France. Blanca Gener's co-authors include Claude Gaultier, Béatrice Laudier, Delphine Trochet, Heather Etchevers, Loïc de Pontual, Tania Attié‐Bitach, Stanislas Lyonnet, Arnold Münnich, Pierre F. Ray and Michel Simonneau and has published in prestigious journals such as Nature Genetics, PEDIATRICS and The American Journal of Human Genetics.

In The Last Decade

Blanca Gener

31 papers receiving 1.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

2003 619 citations Jeanne Amiel, Béatrice Laudier et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Blanca Gener Spain	15	491	480	434	326	319	31	1.5k
Tuija Löppönen Finland	14	458 0.9×	368 0.8×	204 0.5×	143 0.4×	208 0.7×	22	1.1k
Graziella Pinto France	26	1.0k 2.0×	717 1.5×	136 0.3×	126 0.4×	324 1.0×	65	2.1k
Piero Pirazzoli Italy	25	686 1.4×	430 0.9×	117 0.3×	63 0.2×	245 0.8×	64	1.7k
Thomas Moshang United States	33	622 1.3×	396 0.8×	76 0.2×	318 1.0×	474 1.5×	83	2.9k
Arpad von Moers Germany	22	1.1k 2.3×	533 1.1×	168 0.4×	159 0.5×	292 0.9×	58	2.3k
Laurie E. Cohen United States	31	739 1.5×	629 1.3×	83 0.2×	105 0.3×	360 1.1×	78	2.9k
Margaret G. Norman Canada	22	370 0.8×	146 0.3×	99 0.2×	192 0.6×	216 0.7×	48	1.4k
Charlotte Höybye Sweden	30	560 1.1×	1.2k 2.5×	92 0.2×	90 0.3×	661 2.1×	112	2.8k
Melanie Manning United States	19	338 0.7×	504 1.1×	147 0.3×	74 0.2×	64 0.2×	30	2.4k
Josette Mancini France	19	484 1.0×	454 0.9×	137 0.3×	54 0.2×	98 0.3×	29	1.2k

Countries citing papers authored by Blanca Gener

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Blanca Gener

This figure shows the co-authorship network connecting the top 25 collaborators of Blanca Gener. A scholar is included among the top collaborators of Blanca Gener based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Blanca Gener. Blanca Gener is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Infante, Arantza, Iratxe Macías, Dalia Medhat, et al.. (2024). Galunisertib downregulates mutant type I collagen expression and promotes MSCs osteogenesis in pediatric osteogenesis imperfecta. Biomedicine & Pharmacotherapy. 175. 116725–116725. 6 indexed citations

Mori, Roberta De, Silvia Giliani, Lucio Giordano, et al.. (2024). Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitro. Cell and Tissue Research. 396(2). 255–267. 4 indexed citations

Infante, Arantza, Blanca Gener, Miguél Vázquez, et al.. (2021). Reiterative infusions of MSCs improve pediatric osteogenesis imperfecta eliciting a pro‐osteogenic paracrine response: TERCELOI clinical trial. Clinical and Translational Medicine. 11(1). e265–e265. 31 indexed citations

Hoz, Ana B. de la, Olatz Villate, Isabel Llano‐Rivas, et al.. (2020). Targeted Next-Generation Sequencing in Patients with Suggestive X-Linked Intellectual Disability. Genes. 11(1). 51–51. 18 indexed citations

Infante, Arantza, et al.. (2019). Suitability and limitations of mesenchymal stem cells to elucidate human bone illness. World Journal of Stem Cells. 11(9). 578–593. 10 indexed citations

Morin, Matías, Patrícia Locosque Ramos, Marta Galdós, et al.. (2018). Parental Mosaicism in PAX6 Causes Intra-Familial Variability: Implications for Genetic Counseling of Congenital Aniridia and Microphthalmia. Frontiers in Genetics. 9. 479–479. 21 indexed citations

Pangrazio, Alessandra, Manuela Oppo, Maria Consuelo Valentini, et al.. (2013). Exome sequencing identifies CTSK mutations in patients originally diagnosed as intermediate osteopetrosis. Bone. 59. 122–126. 26 indexed citations

Pereda, Arrate, Intza Garin, María García‐Barcina, et al.. (2013). Brachydactyly E: isolated or as a feature of a syndrome. Orphanet Journal of Rare Diseases. 8(1). 141–141. 31 indexed citations

McInerney‐Leo, Aideen, Miriam Schmidts, Claudio R. Cortés, et al.. (2013). Short-Rib Polydactyly and Jeune Syndromes Are Caused by Mutations in WDR60. The American Journal of Human Genetics. 93(3). 515–523. 89 indexed citations

10.

Martínez-Bouzas, Cristina, Ainhoa García-Ribes, Encarna Guillén‐Navarro, et al.. (2013). MECP2 Gene Study in a Large Cohort. Journal of Molecular Diagnostics. 15(5). 723–729. 4 indexed citations

11.

Cuscó, Ivon, Blanca Gener, Mireia Vilardell, et al.. (2009). Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder. Human Molecular Genetics. 18(10). 1795–1804. 86 indexed citations

12.

Wieczorek, Dagmar, Blanca Gener, Saskia Seland, et al.. (2009). Microcephaly, microtia, preauricular tags, choanal atresia and developmental delay in three unrelated patients: A mandibulofacial dysostosis distinct from Treacher Collins syndrome. American Journal of Medical Genetics Part A. 149A(5). 837–843. 19 indexed citations

13.

Cuscó, Ivon, Miguel Del Campo, Mireia Vilardell, et al.. (2008). Array-CGH in patients with Kabuki-like phenotype: Identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration. BMC Medical Genetics. 9(1). 27–27. 27 indexed citations

14.

Garne, Ester, Maria Loane, Vera Nelen, et al.. (2007). Survival and Health in Liveborn Infants with Transposition of Great Arteries?A Population-based Study. Congenital Heart Disease. 2(3). 165–169. 8 indexed citations

15.

Villa, Olaya, Miguel Del Campo, Marta Salido, et al.. (2007). Small supernumerary marker chromosome causing partial trisomy 6p in a child with craniosynostosis. American Journal of Medical Genetics Part A. 143A(10). 1108–1113. 12 indexed citations

16.

Garne, Ester, Maria Loane, Helen Dolk, et al.. (2004). Prenatal diagnosis of severe structural congenital malformations in Europe. Ultrasound in Obstetrics and Gynecology. 25(1). 6–11. 207 indexed citations

17.

Garne, Ester, Maria Loane, Catherine De Vigan, et al.. (2004). Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe. Prenatal Diagnosis. 24(11). 908–912. 14 indexed citations

18.

Amiel, Jeanne, Béatrice Laudier, Tania Attié‐Bitach, et al.. (2003). Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nature Genetics. 33(4). 459–461. 619 indexed citations breakdown →

19.

Gener, Blanca, et al.. (2003). Episodic spontaneous hypothermia: a periodic childhood syndrome. Pediatric Neurology. 28(4). 304–306. 18 indexed citations

20.

Prats, J M, et al.. (2001). Multilocular hydrocephalus: ultrasound studies of origin and development. Pediatric Neurology. 24(2). 149–151. 1 indexed citations

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.

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