Ivon Cuscó

2.9k citations

42 papers · 1.5k indexed · 1 hit paper · h-index 23

Molecular Biology top 10%
Genetics top 1%
Genetics top 5%
Surgery top 10%
Cognitive Neuroscience top 10%

Co-authors: Eduardo F. Tizzano Luis A. Pérez‐Jurado Montserrat Baiget M. J. Barceló Raquel Flores Pablo Fuentes‐Prior Laura Alías Sara Bernal
Topics: Neurogenetic and Muscular Disorders Research (17 papers)RNA modifications and cancer (12 papers)Genetics and Neurodevelopmental Disorders (11 papers)
Cited by: Genetics Molecular Biology
Journals: PLoS ONE Neurology Annals of Neurology
Partner nations: Spain United States Palestinian Territory

In The Last Decade

Ivon Cuscó

41 papers receiving 1.5k 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.

Correlation between SMA type and SMN2 copy number revisited: An analysis of 625 unrelated Spanish patients and a compilation of 2834 reported cases

2018 298 citations Maite Calucho, Sara Bernal et al. Neuromuscular Disorders profile →

Peers

Countries citing papers authored by Ivon Cuscó

Since Specialization

Citations

This map shows the geographic impact of Ivon Cuscó'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 Ivon Cuscó with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ivon Cuscó more than expected).

Fields of papers citing papers by Ivon Cuscó

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ivon Cuscó. 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 Ivon Cuscó. The network helps show where Ivon Cuscó may publish in the future.

Co-authorship network of co-authors of Ivon Cuscó

This figure shows the co-authorship network connecting the top 25 collaborators of Ivon Cuscó. A scholar is included among the top collaborators of Ivon Cuscó 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 Ivon Cuscó. Ivon Cuscó 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

#	Work	Indexed citations
1	Experience using singleton exome sequencing of probands as an approach to preconception carrier screening in consanguineous couples 2022 ·Journal of Medical Genetics ·Anna Abulí,(unknown),Marta Codina‐Solà,Irene Valenzuela,(unknown),(unknown),Anna M. Cueto‐González,Paula Fernández‐Álvarez,Elena García‐Arumí,Ivon Cuscó,Eduardo F. Tizzano	1
2	A Novel Intragenic Duplication in the HDAC8 Gene Underlying a Case of Cornelia de Lange Syndrome 2022 ·Genes ·(unknown),Irene Valenzuela,Ana Latorre,(unknown),(unknown),María Arnedo,Beatriz Puisac,(unknown),Alberto Plaja,(unknown),Ivon Cuscó,(unknown),Feliciano J. Ramos,Eduardo F. Tizzano,Paulino Gómez‐Puertas,Juan Pié	1
3	Beyond copy number: A new, rapid, and versatile method for sequencing the entire SMN2 gene in SMA patients 2021 ·Human Mutation ·Laura Campello Blasco,Ida Paramonov,(unknown),Sara Bernal,Laura Alías,Pablo Fuentes‐Prior,Ivon Cuscó,Eduardo F. Tizzano	29
4	Generation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering Williams-Beuren syndrome (7q11.23 deletion) 2020 ·Stem Cell Research ·Bernd Kuebler,Begoña Arán,Raquel Flores,Luis A. Pérez‐Jurado,Anna Veiga,Roser Corominas,Ivon Cuscó	2
5	Derivation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering 7q11.23 microduplication syndrome 2020 ·Stem Cell Research ·Bernd Kuebler,Begoña Arán,Raquel Flores,Luis A. Pérez‐Jurado,Anna Veiga,Ivon Cuscó,Roser Corominas	0
6	Genetic factors contributing to autism spectrum disorder in Williams-Beuren syndrome 2019 ·Journal of Medical Genetics ·Marta Codina‐Solà,(unknown),(unknown),Raquel Flores,(unknown),Ivon Cuscó,Luis A. Pérez‐Jurado	11
7	Correlation between SMA type and SMN2 copy number revisited: An analysis of 625 unrelated Spanish patients and a compilation of 2834 reported casesbreakdown → 2018 ·Neuromuscular Disorders ·Maite Calucho,Sara Bernal,Laura Alías,Francesca March,Adoración Venceslá,Francisco Javier Álvarez Rodríguez,Elena Aller,Raquel M. Fernández,Salud Borrego,José M. Millán,Concepción Hernández-Chico,Ivon Cuscó,Pablo Fuentes‐Prior,Eduardo F. Tizzano	298
8	Provision of Genetic Services for Autism and its Impact on Spanish Families 2017 ·Journal of Autism and Developmental Disorders ·Marta Codina‐Solà,Luis A. Pérez‐Jurado,Ivon Cuscó,Clara Serra‐Juhé	15
9	DNA methylation abnormalities in congenital heart disease 2015 ·Epigenetics ·Clara Serra‐Juhé,Ivon Cuscó,(unknown),Raquel Flores,Núria Torán,Luis A. Pérez‐Jurado	94
10	Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiency 2014 ·EMBO Molecular Medicine ·Jesús Argente,Raquel Flores,(unknown),Bhupendra Verma,Gabriel Ángel Martos‐Moreno,Ivon Cuscó,Ali Oghabian,Julie A. Chowen,Mikko J. Frilander,Luis A. Pérez‐Jurado	74
11	Contribution of Rare Copy Number Variants to Isolated Human Malformations 2012 ·PLoS ONE ·Clara Serra‐Juhé,Benjamín Rodríguez‐Santiago,Ivon Cuscó,Teresa Vendrell,Núria Camats,Núria Torán,Luis A. Pérez‐Jurado	18
12	Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC 2012 ·The World Journal of Biological Psychiatry ·Claudio Toma,Amaia Hervás,(unknown),Marta Morgade Salgado,(unknown),Elisabet Vilella,(unknown),(unknown),Ivon Cuscó,(unknown),Luis A. Pérez‐Jurado,(unknown),Yolanda de Diego‐Otero,(unknown),Josep Antoni Ramos‐Quiroga,Marta Ribasès,Mónica Bayés,Bru Cormand	35
13	Analysis of two language-related genes in autism 2012 ·Psychiatric Genetics ·Claudio Toma,Amaia Hervás,Bàrbara Torrico,(unknown),Marta Morgade Salgado,(unknown),Elisabet Vilella,Rafael Martínez‐Leal,(unknown),Ivon Cuscó,Miguel Del Campo,Luis A. Pérez‐Jurado,(unknown),Yolanda de Diego‐Otero,Lucía Pérez-Costillas,Josep Antoni Ramos‐Quiroga,Marta Ribasès,Mónica Bayés,Bru Cormand	48
14	Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion 2008 ·Genome Research ·Ivon Cuscó,Roser Corominas,Mónica Bayés,Raquel Flores,(unknown),Victoria Campuzano,Luis A. Pérez‐Jurado	56
15	Array-CGH in patients with Kabuki-like phenotype: Identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration 2008 ·BMC Medical Genetics ·Ivon Cuscó,Miguel Del Campo,Mireia Vilardell,Eva González‐Roca,Blanca Gener,Enrique Galán,(unknown),Luis A. Pérez‐Jurado	27
16	Implication of Fetal SMN2 Expression in Type I SMA Pathogenesis: Protection or Pathological Gain of Function? 2005 ·Journal of Neuropathology & Experimental Neurology ·Carolina Soler‐Botija,Ivon Cuscó,(unknown),Eva López,Montserrat Baiget,Eduardo F. Tizzano	41
17	Choline acetyltransferase expression does not identify early pathogenic events in fetal SMA spinal cord 2005 ·Neuromuscular Disorders ·Carolina Soler‐Botija,Ivon Cuscó,Eva López,(unknown),Ignasi Gich,Montserrat Baiget,Isidró Ferrer,Eduardo F. Tizzano	8
18	SMN2 copy number predicts acute or chronic spinal muscular atrophy but does not account for intrafamilial variability in siblings 2005 ·Journal of Neurology ·Ivon Cuscó,M. J. Barceló,Ricard Rojas‐García,Isabel Illa,Josep Gámez,Carlos Cervera,Adolf Pou,Guillermo Izquierdo,Montserrat Baiget,Eduardo F. Tizzano	86
19	A genetic and phenotypic analysis in Spanish spinal muscular atrophy patients with c.399_402del AGAG, the most frequently found subtle mutation in the SMN1 gene 2003 ·Human Mutation ·Ivon Cuscó,Eva López,Carolina Soler‐Botija,M. J. Barceló,Montserrat Baiget,Eduardo F. Tizzano	38
20	Should gamete donors be tested for spinal muscular atrophy? 2002 ·Fertility and Sterility ·Eduardo F. Tizzano,Ivon Cuscó,M. J. Barceló,(unknown),Montserrat Baiget	11

About Ivon Cuscó

Ivon Cuscó is a scholar working on Genetics, Developmental Neuroscience and Space and Planetary Science, having authored 42 papers that have together received 1.5k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (17 papers), RNA modifications and cancer (12 papers) and Genetics and Neurodevelopmental Disorders (11 papers). The work is most often cited by research in Genetics (721 citations), Genetics (460 citations) and Molecular Biology (989 citations). Ivon Cuscó has collaborated with scholars based in Spain, United States and Palestinian Territory. Frequent co-authors include Eduardo F. Tizzano, Luis A. Pérez‐Jurado, Montserrat Baiget, M. J. Barceló, Raquel Flores, Pablo Fuentes‐Prior, Laura Alías, Sara Bernal, Maite Calucho and Concepción Hernández-Chico. Their work appears in journals such as PLoS ONE, Neurology and Annals of Neurology.

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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