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Jian-Guo Zhang

Beijing Genomics Institute (BGI)

Shenzhen, Guangdong 518083

China

SCHOLARLY PAPERS

4

DOWNLOADS

269

TOTAL CITATIONS

0

Scholarly Papers (4)

1.

Revealing the Causal Association between Birth Physical Characteristics and Neurodevelopmental Disorders: Insights from Mendelian Randomization

Number of pages: 19 Posted: 27 Dec 2024
Chinese Academy of Sciences (CAS), University of Chinese Academy of Sciences, University of Chinese Academy of Sciences, University of Chinese Academy of Sciences, Beijing Genomics Institute (BGI), Chinese Academy of Sciences (CAS) - HIM-BGI Center and Chinese Academy of Sciences (CAS) - HIM-BGI Center
Downloads 94 (730,864)

Abstract:

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Intelligence (IQ), Tourette syndrome, Attention-deficit/hyperactivity disorder, Epilepsy

2.

A Cysteinyl-tRNA Synthetase Mutation Causes Novel Autosomal-Dominant Inheritance of a Parkinsonism/Spinocerebellar-Ataxia Complex

Number of pages: 23 Posted: 01 Apr 2021
Chinese Academy of Medical Sciences - Department of Neurology, Clinical Epidemiology Unit, Beijing Genomics Institute (BGI), Anhui Provincial Children's Hospital, Chinese Academy of Medical Sciences - Department of Neurology, Clinical Epidemiology Unit, Chinese Academy of Medical Sciences - Department of Radiology, Beijing Genomics Institute (BGI), Beijing Genomics Institute (BGI), Chinese Academy of Medical Sciences - Department of Neurology, Clinical Epidemiology Unit, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC) - Department of Radiology, University of Science and Technology of China (USTC) - Hefei National Laboratory for Physical Sciences at the Microscale, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC) - Department of Radiology, BGI-Shenzhen, Beijing Genomics Institute (BGI), Peking University Health Science Center - Department of Pathology, Beijing Genomics Institute (BGI) and University of Science and Technology of China (USTC) - Hefei National Laboratory for Physical Sciences at the Microscale
Downloads 81 (796,622)

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3.

Rare Damaging Variants in the Sex Differences of Congenital Heart Disease: An Exome Sequencing Study

Number of pages: 19 Posted: 01 Jul 2024
Capital Medical University - Echocardiography Medical Center, Capital Medical University - Echocardiography Medical Center, Beijing Genomics Institute (BGI), Capital Medical University, Capital Medical University - Echocardiography Medical Center, Capital Medical University - Echocardiography Medical Center, Capital Medical University, Capital Medical University - Beijing Anzhen Hospital, Capital Medical University - Echocardiography Medical Center, Capital Medical University - Echocardiography Medical Center, Capital Medical University - Echocardiography Medical Center, Capital Medical University - Echocardiography Medical Center, Capital Medical University - Echocardiography Medical Center, Capital Medical University - Echocardiography Medical Center, Government of the People's Republic of China - Army Medical University, Beijing University, Rizhao People's Hospital, Beijing Genomics Institute (BGI), Tsinghua University - Tsinghua-Peking Center for Life Sciences, Capital Medical University, Capital Medical University and Capital Medical University
Downloads 72 (860,052)

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Congenital heart disease, Sex difference, Whole exome sequencing, Sex-specific medicine, Pediatric, Neurodevelopmental defects

4.

A Phenotype-Specific Framework for Identifying the Eye Abnormalities Causative Nonsynonymous-Variants

Number of pages: 24 Posted: 18 May 2020
Beijing Genomics Institute (BGI), Beijing Genomics Institute (BGI), Beijing Genomics Institute (BGI), Beijing Genomics Institute (BGI), Chinese Academy of Sciences (CAS) - Institute of Biomedical and Health Engineering, Beijing Genomics Institute (BGI), Genomic Prediction, Inc., Beijing Genomics Institute (BGI), BGI-Shenzhen, Sonoma Academy, Beijing Genomics Institute (BGI) and Beijing Genomics Institute (BGI)
Downloads 22 (1,424,331)

Abstract:

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Variant Pathogenicity Predictor, Phenotype Specific, Practical Precision, Causative Variants, Eye Abnormalities