Valentina Stanley

2.3k total citations
20 papers, 358 citations indexed

About

Valentina Stanley is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Valentina Stanley has authored 20 papers receiving a total of 358 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Valentina Stanley's work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomic variations and chromosomal abnormalities (3 papers). Valentina Stanley is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomic variations and chromosomal abnormalities (3 papers). Valentina Stanley collaborates with scholars based in United States, Egypt and Türkiye. Valentina Stanley's co-authors include Joseph G. Gleeson, Maha S. Zaki, Damir Musaev, Martin W. Breuss, Xiaoxu Yang, Anide Johansen, Rasim Özgür Rosti, Joseph G. Gleeson, Mahmoud Y. Issa and Sara A. Wirth and has published in prestigious journals such as Nature, Cell and Nature Communications.

In The Last Decade

Valentina Stanley

19 papers receiving 357 citations

Peers

Valentina Stanley

GENET

PHEOH

CMN

Sylvie Janssens Belgium

Alexandre D. Baffet France

Chiara Tocco France

Louisa S. Tang United States

Nicolas Fossat Australia

Christophe Audouard France

Paula Alexandre United Kingdom

Franco Stanzial Italy

Nathalie Krusy Belgium

Abdelhafid Natiq Morocco

Sylvie Janssens Belgium

Valentina Stanley

263 ×1.3

49 ×0.5

GENET

36 ×0.4

21 ×0.4

PHEOH

39 ×0.9

CMN

Citations per year, relative to Valentina Stanley Valentina Stanley (= 1×) peers Sylvie Janssens

Countries citing papers authored by Valentina Stanley

Since Specialization

Citations

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

Fields of papers citing papers by Valentina Stanley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valentina Stanley

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

Garcia, Camila Araújo Bernardino, Muhammad Zubair, Marcelo Volpon Santos, et al.. (2025). Identification of Novel Mosaic Variants in Focal Epilepsy-Associated Patients’ Brain Lesions. Genes. 16(4). 421–421.

Chung, Changuk, Xiaoxu Yang, Robert F. Hevner, et al.. (2024). Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain. Nature. 629(8011). 384–392. 16 indexed citations

Breuss, Martin W., Xiaoxu Yang, Valentina Stanley, et al.. (2022). Unbiased mosaic variant assessment in sperm: a cohort study to test predictability of transmission. eLife. 11. 7 indexed citations

Chai, Guoliang, Frederike L. Harms, Christian Casar, et al.. (2021). Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation. Brain. 145(4). 1551–1563. 11 indexed citations

Yang, Xiaoxu, Martin W. Breuss, Danny Antaki, et al.. (2021). Developmental and temporal characteristics of clonal sperm mosaicism. Cell. 184(18). 4772–4783.e15. 26 indexed citations

Rodríguez‐Soto, Ana E., Morgan Meads, Valentina Stanley, et al.. (2021). Evidence of maternal vascular malperfusion in placentas of women with congenital heart disease. Placenta. 117. 209–212. 4 indexed citations

Breuss, Martin W., Guoliang Chai, Valentina Stanley, et al.. (2021). Biallelic hypomorphic mutations in HEATR5B, encoding HEAT repeat-containing protein 5B, in a neurological syndrome with pontocerebellar hypoplasia. European Journal of Human Genetics. 29(6). 957–964. 3 indexed citations

Zaki, Maha S., Katherine Johnson, Jennifer McEvoy‐Venneri, et al.. (2020). Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability. Journal of Medical Genetics. 58(4). 237–246. 5 indexed citations

Wang, Lu, Zhen Li, Desirée E.C. Smith, et al.. (2020). Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly. Nature Communications. 11(1). 4038–4038. 55 indexed citations

10.

Segal, Michael M., Renee D. George, Peter Waltman, et al.. (2020). Clinician-centric diagnosis of rare genetic diseases: performance of a gene pertinence metric in decision support for clinicians. Orphanet Journal of Rare Diseases. 15(1). 191–191. 5 indexed citations

11.

Garcia, Camila Araújo Bernardino, Xiaoxu Yang, Laurel Ball, et al.. (2020). mTOR pathway somatic variants and the molecular pathogenesis of hemimegalencephaly. Epilepsia Open. 5(1). 97–106. 19 indexed citations

12.

Issa, Mahmoud Y., Valentina Stanley, Renee D. George, et al.. (2020). Molecular diagnosis in recessive pediatric neurogenetic disease can help reduce disease recurrence in families. BMC Medical Genomics. 13(1). 68–68. 6 indexed citations

13.

Li, Chunmei, Justine Rousseau, Ah Jung Heo, et al.. (2020). UBR7 functions with UBR5 in the Notch signaling pathway and is involved in a neurodevelopmental syndrome with epilepsy, ptosis, and hypothyroidism. The American Journal of Human Genetics. 108(1). 134–147. 13 indexed citations

14.

Shaheen, Ranad, Nan Jiang, Fatema Alzahrani, et al.. (2019). Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans. The American Journal of Human Genetics. 104(4). 731–737. 21 indexed citations

15.

Li, Hongda, Laura Saucedo-Cuevas, Ling Yuan, et al.. (2019). Zika Virus Protease Cleavage of Host Protein Septin-2 Mediates Mitotic Defects in Neural Progenitors. Neuron. 101(6). 1089–1098.e4. 60 indexed citations

16.

Breuss, Martin W., Valentina Stanley, Xiaoxu Yang, et al.. (2019). Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly. Journal of Medical Genetics. 57(4). 274–282. 6 indexed citations

17.

Breuss, Martin W., An Nguyen, Qiong Song, et al.. (2018). Mutations in LNPK, Encoding the Endoplasmic Reticulum Junction Stabilizer Lunapark, Cause a Recessive Neurodevelopmental Syndrome. The American Journal of Human Genetics. 103(2). 296–304. 22 indexed citations

18.

Marin‐Valencia, Isaac, Gaia Novarino, Anide Johansen, et al.. (2017). A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features. Journal of Medical Genetics. 55(1). 48–54. 35 indexed citations

19.

Marin‐Valencia, Isaac, Andreas Gerondopoulos, Maha S. Zaki, et al.. (2017). Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia. The American Journal of Human Genetics. 101(3). 441–450. 43 indexed citations

20.

Stanley, Valentina, et al.. (1987). Induction ofClonal Monocyte-Macrophage TumorsInVivobya Mousec-myc Retrovirus: Rearrangement oftheCSF-1Geneas a Secondary Transforming Event. 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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