Linyan Meng

6PUBLICATIONS
40CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Neurology and neuromuscular diseases
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Publications (6)

|Jul 04, 2024
AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders.

Dongxue Mao, Chaozhong Liu, Linhua Wang

|Sep 06, 2022
Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis.

Runjun D Kumar, Linyan Meng, Pengfei Liu

|Nov 27, 2021
Recommendations by the ClinGen Rett/Angelman-like expert panel for gene-specific variant interpretation methods.

Dianalee McKnight, Lora Bean, Izabela Karbassi

|Jan 14, 2021
MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia.

Linyan Meng, Pirjo Isohanni, Yunru Shao

|May 09, 2020
Clinical validity of expanded carrier screening: Evaluating the gene-disease relationship in more than 200 conditions.

Marie Balzotti, Linyan Meng, Dale Muzzey

|Nov 08, 2019
Truncating variants in UBAP1 associated with childhood-onset nonsyndromic hereditary spastic paraplegia.

Shen Gu, Chun-An Chen, Jill A Rosenfeld

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Frequent Collaborators

2 joint publications

Pengfei Liu

1 joint publications

Shen Gu

1 joint publications

Megan A Waldrop

1 joint publications

Aurora Pujol