Lingshuang Wu

Biochemistry, Genetics and Molecular BiologyNeuroscience

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 4 papers. Top paper: “Molecular Basis for Membrane Binding and Lipolysis Activation by ABHD5”.

Molecular Basis for Membrane Binding and Lipolysis Activation by ABHD5

The FASEB Journal(2022)10.1096/fasebj.2022.36.s1.l7703

N/A

0DataRank · unranked

1 citations

Vladyslava Sokolova, Dongyan Tan, Michael V. Airola, Lingshuang Wu

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

medRxiv(2024)10.1101/2024.07.04.24309755

N/A

0DataRank · unranked

0 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +65 more

DDHD2 possesses both lipase and transacylase capacities that remodel triglyceride acyl chains

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2500527122

N/A

0DataRank · unranked

3 citations

Yong‐Mi Choi, Mohyeddine Omrane, Jiyao Chai, Shujuan Gao, Abdou Rachid Thiam +3 more

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.016

N/A

0DataRank · unranked

2 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +66 more