Qizong Lao

6PUBLICATIONS
10CO-AUTHORS
Developmental genetics (incl. sex determination)Cancer geneticsEpigenetics (incl. genome methylation and epigenomics)
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Journal

Publications (6)

|Oct 06, 2025
Clinical and Biochemical Phenotype Across the Genotypic Spectrum of 21-hydroxylase Deficiency in 457 Individuals.

Qizong Lao, Annie Schulman, Sarah Kulkarni

|Jul 27, 2025
Predicting Residual 21-Hydroxylase Enzymatic Activity in Pediatric and Adult Congenital Adrenal Hyperplasia Patients: Towards Individualized Therapy.

Davide Bindellini, Robin Michelet, Yersultan Mirasbekov

|May 09, 2023
Congenital adrenal hyperplasia due to two rare CYP21A2 variant alleles, including a novel attenuated CYP21A1P/CYP21A2 chimera.

Qizong Lao, Deepika D Burkardt, Sarah Kollender

|Apr 26, 2021
Letter to the Editor from Lao and Merke: "Ehlers-Danlos Syndrome: Molecular and Clirnical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal Hyperplasia".

Qizong Lao, Deborah P Merke

|Apr 07, 2021
Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras.

Qizong Lao, Deborah P Merke

|Dec 17, 2020
A TNXB splice donor site variant as a cause of hypermobility type Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia.

Qizong Lao, Ashwini Mallappa, Fabio Rueda Faucz

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Frequent Collaborators

6 joint publications

Deborah P Merke

2 joint publications

Deepika D Burkardt

1 joint publications

Ashwini Mallappa

1 joint publications

Sarah Kollender