Publications by authors named "Ruobing Zou"

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Elucidation of the adaptability of seedlings from different provenances analyzing photosynthetic characteristics and anatomical structure.
Yufeng Liu, Ruobing Zou, Yanmeng Guo, Yu Ji, Mengyuan Li

PeerJ· September 2025

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Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.
Lijia Huang, Jodi Warman-Chardon, Melissa T Carter, Kathie L Friend, Tracy E Dudding, Ruobing Zou

Orphanet J Rare Dis· March 2022

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Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia.
Gabrielle Lemire, Bixia Zheng, Grace U Ediae, Ruobing Zou, Priya T Bhola

Am J Med Genet A· October 2021

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Concordance between whole-exome sequencing and clinical Sanger sequencing: implications for patient care.
Alison Hamilton, Martine Tétreault, David A Dyment, Ruobing Zou, Kristin Kernohan

Mol Genet Genomic Med· September 2016

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Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update.
Lijia Huang, Megan R Vanstone, Taila Hartley, Matthew Osmond, Nick Barrowman, Ruobing Zou

Hum Mutat· February 2016

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Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.
Lijia Huang, Jodi Warman Chardon, Melissa T Carter, Kathie L Friend, Tracy E Dudding, Ruobing Zou

Orphanet J Rare Dis· September 2012

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Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome.
Rebecca L Hood, Matthew A Lines, Sarah M Nikkel, Jeremy Schwartzentruber, Chandree Beaulieu, Ruobing Zou

Am J Hum Genet· February 2012

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Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.
David A Grimes, Fabin Han, Michel Panisset, Lemuel Racacho, Fengxia Xiao, Ruobing Zou

Mov Disord· July 2006

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