Qiliang Ding

3PUBLICATIONS
3CO-AUTHORS
Foetal development and medicineGenomicsGene expression (incl. microarray and other genome-wide approaches)
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Publications (3)

|Apr 11, 2025
Artifacts, Not Differences in Sex Development, Are the Predominant Cause of Phenotypic Sex Discordance With Prenatal Cell-Free DNA Screening: A Review of 33 Cases.

Qiliang Ding, Nicole L Hoppman, Erik C Thorland

|Oct 13, 2023
Using whole genome sequence findings to assess gene-disease causality in cardiomyopathy and arrhythmia patients.

Aishwarya Rajesh Krishnan, Marci Lb Schwartz, Cherith Somerville

|Nov 15, 2022
SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing.

Qiliang Ding, Cherith Somerville, Roozbeh Manshaei

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Frequent Collaborators

1 joint publications

Aishwarya Rajesh Krishnan

1 joint publications

Marci Lb Schwartz

1 joint publications

Raymond H Kim