Xiumin Wang

15PUBLICATIONS
36CO-AUTHORS
Neurology and neuromuscular diseasesGene mappingDevelopmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)Medical biochemistry - proteins and peptides (incl. medical proteomics)
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Publications (15)

|Sep 03, 2026
Phenotypic and genotypic characteristics of pediatric patients with neurofibromatosis type 1: a 12-year single-center cohort study.

|May 28, 2026
Clinical delineation and genotype-phenotype correlation of 84 pediatric patients with Cornelia de Lange syndrome: insights from a single-center Chinese study.

|Apr 15, 2026
Pediatric X-linked adrenoleukodystrophy: phenotypes, variants, and HSCT outcomes.

|Jan 16, 2026
International guideline on genetic testing of children with short stature.

Andrew Dauber, Alexander A L Jorge, Ola Nilsson

|Jan 08, 2026
Clinical and genetic spectrum of pediatric mitochondrial disorders in China: insights from a 47-case genetically confirmed cohort.

Fan Yang, Ruen Yao, Guoying Chang

|Dec 30, 2025
Alström syndrome: a cross-sectional and follow-up study of 127 patients in China, highlighting genetic variant spectrum and cardiac features.

Yiguo Huang, Libo Wang, Qianwen Zhang

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Frequent Collaborators

1 joint publications

Yijun Tang

1 joint publications

Jian Wang

1 joint publications

Guoying Chang

1 joint publications

Andrew Dauber