Xiangbin Ruan

ORCID: 0000-0002-6895-2070

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 2 papers. Top paper: “Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humans”.

Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humans

Genetics in Medicine(2021)10.1016/j.gim.2021.09.014

N/A

0DataRank · unranked

19 citations

Irena Feng, Ana Rita Costa, Rita Pinto‐Costa, Jennifer E. Neil, Oana Caluseriu +21 more

Variants in ADD1 Cause Intellectual Disability, Corpus Callosum Dysgenesis, and Ventriculomegaly in Humans

SSRN Electronic Journal(2021)10.2139/ssrn.3931622

N/A

0DataRank · unranked

0 citations

Irena Feng, Ana Rita Costa, Rita Pinto‐Costa, Jennifer Neil, Oana Caluseriu +16 more