Valeria Capra

6.9k total citations
146 papers, 3.7k citations indexed

About

Valeria Capra is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Valeria Capra has authored 146 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Molecular Biology, 60 papers in Genetics and 36 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Valeria Capra's work include Genomic variations and chromosomal abnormalities (21 papers), Fetal and Pediatric Neurological Disorders (19 papers) and Prenatal Screening and Diagnostics (18 papers). Valeria Capra is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Fetal and Pediatric Neurological Disorders (19 papers) and Prenatal Screening and Diagnostics (18 papers). Valeria Capra collaborates with scholars based in Italy, United States and Canada. Valeria Capra's co-authors include Patrizia De Marco, Elisa Merello, Armando Cama, Zoha Kibar, Philippe Gros, Andrea Rossi, Gianluca Piatelli, Samantha Mascelli, Maria Grazia Calevo and Alessandro Raso and has published in prestigious journals such as Nature, New England Journal of Medicine and Nature Genetics.

In The Last Decade

Valeria Capra

139 papers receiving 3.6k citations

Peers

Valeria Capra
Susan H. Blanton United States
Thomy de Ravel Belgium
Gabriele Gillessen‐Kaesbach Germany
Mustafa Tekin United States
Athena M. Cherry United States
Ahmad S. Teebi Canada
Carsten Bergmann Germany
Charles I. Scott United States
M. Cristina Digilio Italy
Marc Jeanpierre France
Susan H. Blanton United States
Valeria Capra
Citations per year, relative to Valeria Capra Valeria Capra (= 1×) peers Susan H. Blanton

Countries citing papers authored by Valeria Capra

Since Specialization
Citations

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

Fields of papers citing papers by Valeria Capra

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valeria Capra

This figure shows the co-authorship network connecting the top 25 collaborators of Valeria Capra. A scholar is included among the top collaborators of Valeria Capra 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 Valeria Capra. Valeria Capra is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Scala, Marcello, Yu Zhang, Mariasavina Severino, et al.. (2025). A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcifications. European Journal of Human Genetics. 34(3). 324–332. 1 indexed citations
2.
Haanpää, Maria K., John R. Pollard, Monica Traverso, et al.. (2024). Expanding the phenotype of UPF3B‐related disorder: Case reports and literature review. American Journal of Medical Genetics Part A. 194(6). e63534–e63534. 3 indexed citations
3.
Capra, Valeria, et al.. (2024). Congenital Nasal Bones Agenesis: Report of a Rare Malformation. SHILAP Revista de lepidopterología. 2024(1). 1849957–1849957. 1 indexed citations
4.
Schoch, Kelly, Sabine Uhrig, Saskia Biskup, et al.. (2024). A second hotspot for pathogenic exon-skipping variants in CDC45. European Journal of Human Genetics. 32(7). 786–794. 1 indexed citations
5.
Sidpra, Jai, Sniya Sudhakar, Asthik Biswas, et al.. (2024). International Consensus Statement on the Radiologic Evaluation of Dysraphic Malformations of the Spine and Spinal Cord. American Journal of Neuroradiology. 45(6). 673–680.
6.
Viaggi, Silvia, et al.. (2023). Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome. Genes. 14(4). 810–810. 1 indexed citations
7.
Fiaschi, Pietro, Gianluca Piatelli, Valeria Capra, et al.. (2023). Practical Algorithm for the Management of Multisutural Craniosynostosis with Associated Chiari Malformation and/or Hydrocephalus. Pediatric Neurosurgery. 58(2). 67–79. 6 indexed citations
8.
Iacomino, Michele, Monica Traverso, Mariasavina Severino, et al.. (2023). Refining the electroclinical spectrum of NPRL3‐related epilepsy: A novel multiplex family and literature review. Epilepsia Open. 8(4). 1314–1330. 6 indexed citations
9.
Geraldo, Ana Filipa, Cesar Alves, Domenico Tortora, et al.. (2022). Spinal involvement in pediatric familial cavernous malformation syndrome. Neuroradiology. 64(8). 1671–1679. 1 indexed citations
10.
Geraldo, Ana Filipa, Cesar Alves, Domenico Tortora, et al.. (2022). Natural history of familial cerebral cavernous malformation syndrome in children: a multicenter cohort study. Neuroradiology. 65(2). 401–414. 4 indexed citations
11.
Uccella, Sarà, Andrea Accogli, Domenico Tortora, et al.. (2019). Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development. Journal of Neurology. 266(5). 1167–1181. 9 indexed citations
12.
Tortora, Domenico, Mariasavina Severino, Mattia Pacetti, et al.. (2018). Noninvasive Assessment of Hemodynamic Stress Distribution after Indirect Revascularization for Pediatric Moyamoya Vasculopathy. American Journal of Neuroradiology. 39(6). 1157–1163. 7 indexed citations
13.
Pinto, Anna Maria, Eva Trevisson, Valeria Morbidoni, et al.. (2018). Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma. European Journal of Human Genetics. 26(7). 1026–1037. 16 indexed citations
14.
Accogli, Andrea, Marcello Scala, Annalisa Calcagno, et al.. (2018). CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations. European Journal of Medical Genetics. 62(3). 198–203. 22 indexed citations
15.
Scala, Marcello, Pietro Fiaschi, Valeria Capra, et al.. (2018). When and why is surgical revascularization indicated for the treatment of moyamoya syndrome in patients with RASopathies? A systematic review of the literature and a single institute experience. Child s Nervous System. 34(7). 1311–1323. 17 indexed citations
16.
Severino, Mariasavina, Andrea Righini, Domenico Tortora, et al.. (2017). MR Imaging Diagnosis of Diencephalic-Mesencephalic Junction Dysplasia in Fetuses with Developmental Ventriculomegaly. American Journal of Neuroradiology. 38(8). 1643–1646. 15 indexed citations
17.
Severino, Mariasavina, Domenico Tortora, Sarà Uccella, et al.. (2017). Structural Connectivity Analysis in Children with Segmental Callosal Agenesis. American Journal of Neuroradiology. 38(3). 639–647. 11 indexed citations
18.
Capra, Valeria, Mariasavina Severino, Andrea Rossi, et al.. (2013). Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1. American Journal of Medical Genetics Part A. 164(2). 495–499. 9 indexed citations
19.
Bachetti, Tiziana, Angela Robbiano, Sara Parodi, et al.. (2006). Brainstem Anomalies in Two Patients Affected by Congenital Central Hypoventilation Syndrome. American Journal of Respiratory and Critical Care Medicine. 174(6). 706–709. 20 indexed citations
20.
Haupt, Riccardo, et al.. (1995). Cytogenetics of the tissue involved in neural tube defects.. PubMed. 6(1). 49–53.

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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