Valerie A. Arboleda

Also affiliated with Broad Center, UCLA Jonsson Comprehensive Cancer Center

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 31 papers. Top paper: “Metabolic reprogramming and epigenetic changes of vital organs in SARS-CoV-2–induced systemic toxicity”.

Metabolic reprogramming and epigenetic changes of vital organs in SARS-CoV-2–induced systemic toxicity

JCI Insight(2020)10.1172/jci.insight.145027

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0DataRank · unranked

88 citations

Feiyang Ma, Tomohiro Yokota, Gustavo Garcia, Amelia Palermo, Yijie Wang +19 more

Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.019

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0DataRank · unranked

25 citations

Philipp Kirchner, Antje Wiesener, Irma van de Beek, Quinten Waisfisz, Mieke M. van Haelst +43 more

Rapid cost-effective viral genome sequencing by V-seq

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.15.252510

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0DataRank · unranked

13 citations

James Boocock, Jacob M. Tome, Sukantha Chandrasekaran, Evann E. Hilt, Yi Zhang +14 more

Massively scaled-up testing for SARS-CoV-2 RNA via next-generation sequencing of pooled and barcoded nasal and saliva samples

Nature Biomedical Engineering(2021)10.1038/s41551-021-00754-5

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0DataRank · unranked

78 citations

Laila Sathe, Chetan Munugala, Eric M. Jones, Molly Gasperini, Nathan B. Lubock +36 more

From chemoproteomic‐detected amino acids to genomic coordinates: insights into precise multi‐omic data integration

Molecular Systems Biology(2021)10.15252/msb.20209840

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0DataRank · unranked

24 citations

Heta S. Desai, Valerie A. Arboleda, Keriann M. Backus, Maria F. Palafox

Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanisms

Molecular Genetics & Genomic Medicine(2021)10.1002/mgg3.1809

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0DataRank · unranked

14 citations

Jessica Kianmahd, Meghna Singh, Maria F. Palafox, Angela Wei, Kathryn Elliott +40 more

Lower SARS-CoV-2 viral shedding following COVID-19 vaccination among healthcare workers in Los Angeles, California

Open Forum Infectious Diseases(2021)10.1093/ofid/ofab526

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0DataRank · unranked

5 citations

Michael A. Pfeffer, Valerie A. Arboleda, Omai B. Garner, Annabelle de St. Maurice, Benjamin von Bredow +4 more

Lean Principles to Improve Quality in High-Throughput COVID-19 Testing Using SwabSeq: A Barcoded Sequencing-Based Testing Platform

Laboratory Medicine(2021)10.1093/labmed/lmab069

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0DataRank · unranked

4 citations

Rosita Saul, Laila Sathe, Joanna Xie, Dawn Marquette, Valerie A. Arboleda +1 more

Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

Genome Medicine(2022)10.1186/s13073-022-01106-x

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0DataRank · unranked

51 citations

Yi Ding, Vidhya Venkateswaran, Arjun Bhattacharya, Kristin Boulier, Alec Chiu +21 more

DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes

European Journal of Human Genetics(2022)10.1038/s41431-022-01083-0

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0DataRank · unranked

28 citations

Eric Chater‐Diehl, Sanaa Choufani, Elizabeth Y Wei, Rebecca R. Kianmahd, Anna Yu +8 more

DMRscaler: a scale-aware method to identify regions of differential DNA methylation spanning basepair to multi-megabase features

BMC Bioinformatics(2022)10.1186/s12859-022-04899-1

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0DataRank · unranked

10 citations

Angela Wei, Valerie A. Arboleda, Leroy Bondhus

Polygenic risk scores of endo-phenotypes identify the effect of genetic background in congenital heart disease

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100112

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0DataRank · unranked

12 citations

Leroy Bondhus, Gentian Lluri, Jae Hoon Sul, Valerie A. Arboleda, Sarah Spendlove

Balancing the transcriptome: leveraging sample similarity to improve measures of gene specificity

Briefings in Bioinformatics(2022)10.1093/bib/bbac158

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0DataRank · unranked

1 citations

Roshni Varma, Y.I. Hernández, Valerie A. Arboleda, Leroy Bondhus

Health care utilization of fine-scale identity by descent clusters in a Los Angeles biobank

medRxiv(2022)10.1101/2022.07.12.22277520

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0DataRank · unranked

4 citations

Arya Boudaie, Ruhollah Shemirani, Ella Petter, Alec Chiu, Ruth Johnson +10 more

Multi-omics on truncating ASXL1 mutations in Bohring Opitz syndrome identify dysregulation of canonical and non-canonical Wnt signaling

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.15.520167

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0DataRank · unranked

3 citations

Angela Wei, Zain Awamleh, Meghna Singh, Aileen Ning, Analeyla Herrera +4 more

Electronic health record signatures identify undiagnosed patients with Common Variable Immunodeficiency Disease

medRxiv(2022)10.1101/2022.08.03.22278352

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0DataRank · unranked

1 citations

Alexis V. Stephens, Sergey Knyazev, Lisa A. Kohn, Malika Freund, Leroy Bondhus +7 more

ASXL1 mutations that cause Bohring Opitz Syndrome (BOS) or acute myeloid leukemia share epigenomic and transcriptomic signatures

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.15.519823

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0DataRank · unranked

1 citations

Zain Awamleh, Angela Wei, Bianca Russell, Rosanna Weksberg, Valerie A. Arboleda +1 more

The omics era: a nexus of untapped potential for Mendelian chromatinopathies

Human Genetics(2023)10.1007/s00439-023-02560-2

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0DataRank · unranked

20 citations

Valerie A. Arboleda, Aileen A. Nava

Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region

Nature Medicine(2023)10.1038/s41591-023-02425-1

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0DataRank · unranked

14 citations

Arya Boudaie, Ruhollah Shemirani, Joel Mefford, Ella Petter, Alec Chiu +14 more

KAT6A mutations in Arboleda-Tham syndrome drive epigenetic regulation of posterior HOXC cluster

Human Genetics(2023)10.1007/s00439-023-02608-3

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0DataRank · unranked

11 citations

Sarah Spendlove, Angela Wei, Leroy Bondhus, Aileen A. Nava, Francisca N. de Luna Vitorino +7 more

Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation

JCI Insight(2023)10.1172/jci.insight.167744

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0DataRank · unranked

13 citations

Angela Wei, Zain Awamleh, Meghna Singh, Aileen Ning, Analeyla Herrera +4 more

Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in LMOD2 Gene Causing Infantile Dilated Cardiomyopathy

Cells(2023)10.3390/cells12111455

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0DataRank · unranked

10 citations

Tania M. Larrinaga, Alden Huang, Frank Makhlouf, Xuedong Kang, Jonathan Su +13 more

KAT6A mutations drive transcriptional dysregulation of cell cycle and Autism risk genes in an Arboleda-Tham Syndrome cerebral organoid model

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.17.545322

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0DataRank · unranked

2 citations

Connor Jops, Celine K. Vuong, Samantha L. Niles-Jensen, Leroy Bondhus, Cameron J. Ong +4 more

KAT6A mutations in Arboleda-Tham syndrome drive epigenetic regulation of posterior HOXC cluster

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.08.03.550595

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0DataRank · unranked

0 citations

Sarah Spendlove, Angela Wei, Leroy Bondhus, Aileen A. Nava, Francisca N. de Luna Vitorino +7 more

Electronic health record signatures identify undiagnosed patients with common variable immunodeficiency disease

Science Translational Medicine(2024)10.1126/scitranslmed.ade4510

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0DataRank · unranked

32 citations

Alexis V. Stephens, Rachel Mester, Sergey Knyazev, Lisa A. Kohn, Malika Freund +9 more

ASXL1 truncating variants in BOS and myeloid leukemia drive shared disruption of Wnt-signaling pathways but have differential isoform usage of RUNX3

BMC Medical Genomics(2024)10.1186/s12920-024-02039-7

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0DataRank · unranked

3 citations

Zain Awamleh, Mili Sinvhal, Andrew C.A. Wan, Leroy Bondhus, Angela Wei +4 more

Increased Frequency of Clonal Hematopoiesis of Indeterminate Potential in Bloom Syndrome Probands and Carriers

medRxiv(2024)10.1101/2024.02.02.24302163

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0DataRank · unranked

0 citations

Angela Wei, Tsumugi Gebo, PC Boutros, Maeve Flanagan, Nicole Kucine +4 more

Increased frequency of clonal hematopoiesis of indeterminate potential in Bloom syndrome probands and carriers

Haematologica(2024)10.3324/haematol.2024.285239

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0DataRank · unranked

0 citations

Angela Wei, Tsumugi Gebo, Paul C. Boutros, Maeve Flanagan, Nicole Kucine +4 more

Prioritizing disease-associated missense variants with chemoproteomic-detected amino acids

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.017

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0DataRank · unranked

2 citations

Lisa M. Boatner, Blake R. Wilde, Heather R. Christofk, Keriann M. Backus, Valerie A. Arboleda +1 more

Investigating the sources of variable impact of pathogenic variants in monogenic metabolic conditions

Nature Communications(2025)10.1038/s41467-025-60339-7

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0DataRank · unranked

3 citations

Richard Border, Boyang Fu, Sinéad Cullina, Nadav Brandes, Seon-Kyeong Jang +7 more

Type-2 immune skewing in patients with disseminated coccidioidomycosis

medRxiv(2025)10.1101/2025.09.26.25336729

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0DataRank · unranked

2 citations

Smriti S. Nagarajan, Alexis V Stephens, Samantha L. Jensen, Anviksha Srivastava, Miguel A. Moreno Lastre +9 more