🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Valentina Stanley

University of California San Diego

ORCID: 0000-0002-2212-7796
Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 5%percentile
0.522Author DataRank

Indexed papers

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Comprehensive multiomic profiling of somatic mutations in malformations of cortical development

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.07.487401
Top 37%
0.522DataRank
Top 37%11 citations

Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels +45 more

Papers

Driven by 21 papers — median percentile 63. Top paper: “Somatic mosaicism reveals clonal distributions of neocortical development”.

Somatic mosaicism reveals clonal distributions of neocortical development

Nature(2022)10.1038/s41586-022-04602-7
N/A
1.4DataRank · unranked
65 citations

Xiaoxu Yang, Johannes C. M. Schlachetzki, Danny Antaki, Addison J. Lana, Xin Xu +91 more

Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development

Nature Genetics(2023)10.1038/s41588-022-01276-9
N/A
0.709DataRank · unranked
112 citations

Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels +76 more

Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder

Nature Communications(2021)10.1038/s41467-021-22627-w
N/A
0.598DataRank · unranked
53 citations

Deepa Rajan, Tyler R. Fortuna, Eric N. Anderson, Caroline Ward, Youngha Lee +65 more

A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion

New England Journal of Medicine(2021)10.1056/nejmoa2033911
N/A
0.581DataRank · unranked
47 citations

Emmanuelle Szenker‐Ravi, Changuk Chung, Zhen Li, Lu Wang, Muznah Khatoo +25 more

Comprehensive multiomic profiling of somatic mutations in malformations of cortical development

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.07.487401
Top 37%
0.522DataRank
Top 37%11 citations

Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels +45 more

A relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome

European Journal of Human Genetics(2020)10.1038/s41431-020-00717-5
N/A
0DataRank · unranked
18 citations

Marcello Scala, Christian Beetz, Guy Helman, Valentina Stanley, Xiaoxu Yang +42 more

Clinician-centric diagnosis of rare genetic diseases: performance of a gene pertinence metric in decision support for clinicians

Orphanet Journal of Rare Diseases(2020)10.1186/s13023-020-01461-1
N/A
0DataRank · unranked
10 citations

Renee D. George, Peter Waltman, Ayman W. El‐Hattab, Kiely N. James, Valentina Stanley +2 more

Biallelic variants in HPDL, encoding 4-hydroxyphenylpyruvate dioxygenase-like protein, lead to an infantile neurodegenerative condition

Genetics in Medicine(2020)10.1038/s41436-020-01010-y
N/A
0DataRank · unranked
37 citations

Sangmoon Lee, Rudy Fabunan, Guoliang Chai, Maha S. Zaki, Ghada M. H. Abdel‐Salam +25 more

Biallelic loss of function variants in SYT2 cause a treatable congenital onset presynaptic myasthenic syndrome

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61765
N/A
0DataRank · unranked
29 citations

Payam Mohassel, Lucia Laugwitz, Maha S. Zaki, Erik‐Jan Kamsteeg, Reza Maroofian +24 more

Temporal stability of human sperm mosaic mutations results in life-long threat of transmission to offspring

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.14.339796
N/A
0DataRank · unranked
3 citations

Martin W. Breuss, Xin Xu, Danny Antaki, Kiely N. James, Valentina Stanley +13 more

Developmental and temporal characteristics of clonal sperm mosaicism

Cell(2021)10.1016/j.cell.2021.07.024
N/A
0DataRank · unranked
57 citations

Martin W. Breuss, Xin Xu, Danny Antaki, Kiely N. James, Valentina Stanley +13 more

Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation

Brain(2021)10.1093/brain/awab403
N/A
0DataRank · unranked
17 citations

Guoliang Chai, Pauline E. Schneeberger, Frederike L. Harms, Christian Casar, Minyue Qi +10 more

Biallelic hypomorphic mutations in HEATR5B, encoding HEAT repeat-containing protein 5B, in a neurological syndrome with pontocerebellar hypoplasia

European Journal of Human Genetics(2021)10.1038/s41431-021-00832-x
N/A
0DataRank · unranked
11 citations

Martin W. Breuss, Zinayida Schlachetzki, Guoliang Chai, Danica Ross, Valentina Stanley +7 more

Cell-type-resolved somatic mosaicism reveals clonal dynamics of the human forebrain

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.24.563814
N/A
0DataRank · unranked
4 citations

Xiaoxu Yang, Robert F. Hevner, Katie Kennedy, Keng Ioi Vong, Yang Liu +10 more

Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain

Nature(2024)10.1038/s41586-024-07292-5
N/A
0DataRank · unranked
54 citations

Xiaoxu Yang, Robert F. Hevner, Katie Kennedy, Keng Ioi Vong, Yang Liu +12 more

Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly

Nature Communications(2020)10.1038/s41467-020-17454-4
N/A
0DataRank · unranked
88 citations

Zhen Li, David Sievert, Desirée E.C. Smith, Marisa I. Mendes, Dillon Y. Chen +10 more

Risk of meningomyelocele mediated by the common 22q11.2 deletion

Science(2024)10.1126/science.adl1624
N/A
0DataRank · unranked
21 citations

Sangmoon Lee, Kit Sing Au, T. Blaine Crowley, Valeria Capra, Meade Haller +74 more

Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of function

Brain(2020)10.1093/brain/awaa063
N/A
0DataRank · unranked
81 citations

Andrew C. Edmondson, Sumeet A. Khetarpal, Viola Alesi, Maha S. Zaki, Kevin Rostásy +27 more

Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly

Neuron(2020)10.1016/j.neuron.2020.10.035
N/A
0DataRank · unranked
59 citations

A. Dinsmoor Webb, Chen Li, Danny Antaki, Sangmoon Lee, Martin W. Breuss +32 more

Loss of the neural-specific BAF subunit ACTL6B relieves repression of early response genes and causes recessive autism

Proceedings of the National Academy of Sciences(2020)10.1073/pnas.1908238117
N/A
0DataRank · unranked
68 citations

Lu Wang, A. Krokhotin, Jessica J. Walsh, Hongjie Li, Hirotaka Shoji +24 more

Molecular diagnosis in recessive pediatric neurogenetic disease can help reduce disease recurrence in families

BMC Medical Genomics(2020)10.1186/s12920-020-0714-1
N/A
0DataRank · unranked
14 citations

Zinayida Chechlacz, Valentina Stanley, Renee D. George, Jennifer McEvoy‐Venneri, Denice Belandres +7 more