Angela Wei

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 11 papers. Top paper: “Investigating the sources of variable impact of pathogenic variants in monogenic metabolic conditions”.

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

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

N/A

0.208DataRank · unranked

3 citations

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

N/A

0DataRank · unranked

10 citations

Angela Wei, Valerie A. Arboleda, Leroy Bondhus

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

N/A

0DataRank · unranked

3 citations

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

N/A

0DataRank · unranked

1 citations

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

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

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

N/A

0DataRank · unranked

11 citations

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

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

N/A

0DataRank · unranked

14 citations

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

N/A

0DataRank · unranked

0 citations

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

N/A

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

N/A

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

N/A

0DataRank · unranked

0 citations

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

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

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

N/A

0DataRank · unranked

13 citations

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