Vanesa López‐González

1.8k citations

24 papers · 532 indexed · h-index 15

Genetics top 10%
Molecular Biology
Rheumatology top 10%
Pulmonary and Respiratory Medicine
Pediatrics, Perinatology and Child Health

Co-authors: Encarna Guillén‐Navarro María Juliana Ballesta‐Martínez Pablo Lapunzina Sixto García‐Miñáur Víctor L. Ruiz‐Pérez Víctor Martínez‐Glez Eulalia Valencia Fransiska Malfait
Topics: Genomic variations and chromosomal abnormalities (5 papers)Reproductive Health and Technologies (4 papers)Connective tissue disorders research (4 papers)
Cited by: Genetics Rheumatology Molecular Biology
Journals: SHILAP Revista de lepidopterologíaGene Genomics
Partner nations: Spain Germany United States

In The Last Decade

Vanesa López‐González

24 papers receiving 498 citations

Peers

Countries citing papers authored by Vanesa López‐González

Since Specialization

Citations

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

Fields of papers citing papers by Vanesa López‐González

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vanesa López‐González. 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 Vanesa López‐González. The network helps show where Vanesa López‐González may publish in the future.

Co-authorship network of co-authors of Vanesa López‐González

This figure shows the co-authorship network connecting the top 25 collaborators of Vanesa López‐González. A scholar is included among the top collaborators of Vanesa López‐González 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 Vanesa López‐González. Vanesa López‐González 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	Validation of clinical exome sequencing in the diagnostic procedure of patients with intellectual disability in clinical practice 2023 ·Orphanet Journal of Rare Diseases ·María Juliana Ballesta‐Martínez,Virginia Pérez‐Fernández,Vanesa López‐González,(unknown),(unknown),(unknown),María Barreda‐Sánchez,(unknown),Encarna Guillén‐Navarro	6
2	Extremely variable expressivity in Smith-Lemli-Opitz syndrome: Review of 4 cases 2022 ·SHILAP Revista de lepidopterología ·(unknown),(unknown),Vanesa López‐González,María Juliana Ballesta‐Martínez,Encarna Guillén‐Navarro	1
3	Health impact of acute intermittent porphyria in latent and non-recurrent attacks patients 2021 ·Orphanet Journal of Rare Diseases ·(unknown),María Barreda‐Sánchez,(unknown),María Juliana Ballesta‐Martínez,Vanesa López‐González,(unknown),(unknown),M. Elena Pérez-Tomás,(unknown),(unknown),(unknown),(unknown),Encarna Guillén‐Navarro	26
4	Riesgo de malformaciones mayores y menores en niños concebidos por técnicas de reproducción asistida (FIV/ICSI): estudio prospectivo de cohorte controlado 2021 ·Anales de Pediatría ·(unknown),Vanesa López‐González,María Juliana Ballesta‐Martínez,(unknown),(unknown),(unknown),Virginia Pérez‐Fernández,Encarna Guillén‐Navarro	1
5	Assessment of psychomotor development of Spanish children up to 3 years of age conceived by assisted reproductive techniques: Prospective matched cohort study 2020 ·SHILAP Revista de lepidopterología ·(unknown),Vanesa López‐González,María Juliana Ballesta‐Martínez,(unknown),Rosario Domingo‐Jiménez,(unknown),Encarna Guillén‐Navarro	2
6	Expanding the phenotype of CRYAA nucleotide variants to a complex presentation of anterior segment dysgenesis 2020 ·Orphanet Journal of Rare Diseases ·Andrey V. Marakhonov,A. A. Voskresenskaya,(unknown),Fedor A. Konovalov,Tatyana A. Vasilyeva,Fiona Blanco‐Kelly,N. A. Pozdeyevа,(unknown),Vanesa López‐González,Encarna Guillén‐Navarro,Carmen Ayuso,Р. А. Зинченко,Marta Cortón	10
7	High penetrance of acute intermittent porphyria in a Spanish founder mutation population and CYP2D6 genotype as a susceptibility factor 2019 ·Orphanet Journal of Rare Diseases ·María Barreda‐Sánchez,(unknown),(unknown),(unknown),María Juliana Ballesta‐Martínez,Vanesa López‐González,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Encarna Guillén‐Navarro	19
8	EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population 2019 ·Orphanet Journal of Rare Diseases ·(unknown),María Juliana Ballesta‐Martínez,Vanesa López‐González,(unknown),(unknown),María Barreda‐Sánchez,(unknown),(unknown),(unknown),Paloma Sánchez‐Pedreño,(unknown),(unknown),Encarna Guillén‐Navarro	23
9	Evaluación del desarrollo psicomotor hasta los 3 años de edad de niños españoles concebidos por técnicas de reproducción asistida (FIV/ICSI): estudio prospectivo de cohorte controlado 2019 ·Anales de Pediatría ·(unknown),Vanesa López‐González,María Juliana Ballesta‐Martínez,(unknown),(unknown),Virginia Pérez‐Fernández,Encarna Guillén‐Navarro	6
10	Two novel POC1A mutations in the primordial dwarfism, SOFT syndrome: Clinical homogeneity but also unreported malformations 2015 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Luis Salamanca,(unknown),Vanesa López‐González,Lucia Sentchordi,Ángela del Pozo,Fernando Santos‐Simarro,Ángel Campos‐Barros,Pablo Lapunzina,Encarna Guillén‐Navarro,I. González Casado,Sixto García‐Miñáur,Karen E. Heath	15
11	Clinical comparison of 10q26 overlapping deletions: Delineating the critical region for urogenital anomalies 2015 ·American Journal of Medical Genetics Part A ·(unknown),Vanesa López‐González,(unknown),María Juliana Ballesta‐Martínez,(unknown),Encarna Guillén‐Navarro,(unknown)	30
12	Expanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants 2014 ·European Journal of Human Genetics ·Beatriz Paumard‐Hernández,(unknown),Eva Barroso,(unknown),(unknown),Sara Benito‐Sanz,(unknown),Fernando Santos,(unknown),A. Romance,(unknown),Vanesa López‐González,Ángel Campos‐Barros,Jaime Cruz‐Rojo,Encarna Guillén‐Navarro,Jaime Sánchez del Pozo,Pablo Lapunzina,Sixto García‐Miñáur,Karen E. Heath	41
13	Two mutations in IFITM5 causing distinct forms of osteogenesis imperfecta 2014 ·American Journal of Medical Genetics Part A ·Encarna Guillén‐Navarro,María Juliana Ballesta‐Martínez,Eulalia Valencia,Ana M. Bueno,Víctor Martínez‐Glez,Vanesa López‐González,Birutė Burnytė,Algirdas Utkus,Pablo Lapunzina,Víctor L. Ruiz‐Pérez	32
14	Array CGH detection of a novel cryptic deletion at 3q13 in a complex chromosome rearrangement 2014 ·Genomics ·I. López,María Juliana Ballesta‐Martínez,(unknown),(unknown),Rosario Domingo‐Jiménez,Vanesa López‐González,(unknown),Encarna Guillén‐Navarro	2
15	X-linked intellectual disability type Nascimento is a clinically distinct, probably underdiagnosed entity 2013 ·Orphanet Journal of Rare Diseases ·Johanna Christina Czeschik,Peter Bauer,Karin Buiting,Claudia Dufke,Encarna Guillén‐Navarro,Diana Johnson,Udo Koehler,Vanesa López‐González,Hermann‐Josef Lüdecke,Alison Male,Deborah Morrogh,Angelika Rieß,Andreas Tzschach,Dagmar Wieczorek,Alma Kuechler	17
16	Autosomal dominant oculoauriculovertebral spectrum and 14q23.1 microduplication 2013 ·American Journal of Medical Genetics Part A ·María Juliana Ballesta‐Martínez,Vanesa López‐González,(unknown),(unknown),Sixto García‐Miñáur,Encarna Guillén‐Navarro	35
17	Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndrome 2013 ·Orphanet Journal of Rare Diseases ·Fransiska Malfait,Sofie Symoens,Nathalie Goemans,Yolanda Gyftodimou,Eva Holmberg,Vanesa López‐González,Geert Mortier,Sheela Nampoothiri,Michael B. Petersen,Anne De Paepe	62
18	Hemodynamic and genetic analysis in children with idiopathic, heritable, and congenital heart disease associated pulmonary arterial hypertension 2013 ·Respiratory Research ·Nicole Pfarr,Christine Fischer,Nicola Ehlken,(unknown),Vanesa López‐González,Matthias Gorenflo,Alfred Hager,Katrin Hinderhofer,Oliver Miera,Christian Nagel,Dietmar Schranz,Ekkehard Grünig	39
19	Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum 2012 ·Human Mutation ·(unknown),Samia A. Temtamy,Mona Aglan,Eulalia Valencia,Víctor Martínez‐Glez,María Juliana Ballesta‐Martínez,Vanesa López‐González,Adel M. Ashour,Khalda Amr,Verónica Pulido,Encarna Guillén‐Navarro,Pablo Lapunzina,José A. Caparrós‐Martín,Víctor L. Ruiz‐Pérez	72
20	Rapp–Hodgkin syndrome and SHFM1 patients: Delineating the p63–Dlx5/Dlx6 pathway 2012 ·Gene ·(unknown),María Rosa Moya‐Quiles,María Juliana Ballesta‐Martínez,Vanesa López‐González,(unknown),Encarna Guillén‐Navarro,I. López	14

About Vanesa López‐González

Vanesa López‐González is a scholar working on Reproductive Medicine, Genetics and Developmental Biology, having authored 24 papers that have together received 532 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Reproductive Health and Technologies (4 papers) and Connective tissue disorders research (4 papers). The work is most often cited by research in Genetics (311 citations), Rheumatology (85 citations) and Molecular Biology (264 citations). Vanesa López‐González has collaborated with scholars based in Spain, Germany and United States. Frequent co-authors include Encarna Guillén‐Navarro, María Juliana Ballesta‐Martínez, Pablo Lapunzina, Sixto García‐Miñáur, Víctor L. Ruiz‐Pérez, Víctor Martínez‐Glez, Eulalia Valencia, Fransiska Malfait, Anne De Paepe and Geert Mortier. Their work appears in journals such as SHILAP Revista de lepidopterología, Gene and Genomics.

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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