Zhi‐Jie Xia

Nanjing University of Posts and Telecommunications

ORCID: 0000-0003-3018-1925

Also affiliated with Nanjing Medical University

MedicineBiochemistry, Genetics and Molecular Biology

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 6 papers. Top paper: “Defining the clinical phenotype of Saul–Wilson syndrome”.

Defining the clinical phenotype of Saul–Wilson syndrome

Genetics in Medicine(2020)10.1038/s41436-019-0737-1

N/A

0DataRank · unranked

21 citations

Wadih M. Zein, Laryssa A. Huryn, Andrea Merker, Seth Berger, William G. Wilson +26 more

A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.013

N/A

0DataRank · unranked

22 citations

Paulina Sosicka, François Fenaille, Annie Harroche, Sandrine Vuillaumier‐Barrot, Mindy Porterfield +27 more

Protease-dependent defects in N-cadherin processing drive PMM2-CDG pathogenesis

JCI Insight(2021)10.1172/jci.insight.153474

N/A

0DataRank · unranked

9 citations

Lynn Dukes‐Rimsky, Brijesh Kumar, Zhi‐Jie Xia, Tammie Dang, Mark A. Lehrman +6 more

Origin of cytoplasmic GDP-fucose determines its contribution to glycosylation reactions

The Journal of Cell Biology(2022)10.1083/jcb.202205038

N/A

0DataRank · unranked

26 citations

Bobby G. Ng, Lauren E. Pepi, Asif Shajahan, Maurice Wong, David A. Scott +7 more

GLUT1 is a highly efficient L-fucose transporter

Journal of Biological Chemistry(2022)10.1016/j.jbc.2022.102738

N/A

0DataRank · unranked

16 citations

Paulina Sosicka, Zhi‐Jie Xia, Hudson H. Freeze, Bobby G. Ng

Variants in WASHC3, a component of the WASH complex, cause short stature, variable neurodevelopmental abnormalities, and distinctive facial dysmorphism

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101915

N/A

0DataRank · unranked

1 citations

Julian C. Lui, Dana Marafi, Zhi‐Jie Xia, Ruchika Bhatia, Elaine Zhou +21 more