Works by Dong, Weilai
Results: 25
GemC1 is a critical switch for neural stem cell generation in the postnatal brain.
- Published in:
- Glia, 2019, v. 67, n. 12, p. 2360, doi. 10.1002/glia.23690
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- Publication type:
- Article
Simulation study on catalytic oxidation of low concentration mine gas in an oxidation device.
- Published in:
- Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-024-80225-4
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- Publication type:
- Article
Comprehensive Genetic Analysis of Follicular Thyroid Carcinoma Predicts Prognosis Independent of Histology.
- Published in:
- 2018
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- Publication type:
- journal article
Mutation spectrum of congenital heart disease in a consanguineous Turkish population.
- Published in:
- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 6, p. 1, doi. 10.1002/mgg3.1944
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- Publication type:
- Article
SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 9, p. N.PAG, doi. 10.1002/mgg3.892
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- Publication type:
- Article
DIAPH1 Variants in Non–East Asian Patients With Sporadic Moyamoya Disease.
- Published in:
- JAMA Neurology, 2021, v. 78, n. 8, p. 993, doi. 10.1001/jamaneurol.2021.1681
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- Publication type:
- Article
A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome.
- Published in:
- 2022
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- Publication type:
- Case Study
Clinical Biochemistry of Serum Troponin.
- Published in:
- Diagnostics (2075-4418), 2024, v. 14, n. 4, p. 378, doi. 10.3390/diagnostics14040378
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- Publication type:
- Article
A Novel Missense Mutation in ERCC8 Co-Segregates with Cerebellar Ataxia in a Consanguineous Pakistani Family.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 19, p. 3090, doi. 10.3390/cells11193090
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- Publication type:
- Article
Molecular Genetics and Complex Inheritance of Congenital Heart Disease.
- Published in:
- Genes, 2021, v. 12, n. 7, p. 1020, doi. 10.3390/genes12071020
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- Publication type:
- Article
Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3.
- Published in:
- Frontiers in Cellular Neuroscience, 2019, p. 1, doi. 10.3389/fncel.2019.00425
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- Publication type:
- Article
Network assisted analysis of De novo variants using protein-protein interaction information identified 46 candidate genes for congenital heart disease.
- Published in:
- PLoS Genetics, 2022, v. 18, n. 6, p. 1, doi. 10.1371/journal.pgen.1010252
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- Publication type:
- Article
M-DATA: A statistical approach to jointly analyzing de novo mutations for multiple traits.
- Published in:
- PLoS Genetics, 2021, v. 17, n. 11, p. 1, doi. 10.1371/journal.pgen.1009849
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- Publication type:
- Article
Exome Sequencing as a Potential Diagnostic Adjunct in Sporadic Congenital Hydrocephalus.
- Published in:
- JAMA Pediatrics, 2021, v. 175, n. 3, p. 310, doi. 10.1001/jamapediatrics.2020.4878
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- Publication type:
- Article
Clinical, demographic and genetic features of patients with congenital heart disease : A single center experience.
- Published in:
- Marmara Medical Journal, 2022, v. 35, n. 2, p. 159, doi. 10.5472/marumj.1120570
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- Publication type:
- Article
Identification of a dominant MYH11 causal variant in chronic intestinal pseudo‐obstruction: Results of whole‐exome sequencing.
- Published in:
- Clinical Genetics, 2019, v. 96, n. 5, p. 473, doi. 10.1111/cge.13617
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- Publication type:
- Article
TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 12, p. 4292, doi. 10.1093/brain/awae175
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- Publication type:
- Article
Statistical methods for assessing the effects of de novo variants on birth defects.
- Published in:
- Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00590-z
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- Publication type:
- Article
Correction to: A contiguous microdeletion syndrome at Xp22.13 with non-obstructive azoospermia and congenital cataracts.
- Published in:
- 2021
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- Publication type:
- Correction Notice
A contiguous microdeletion syndrome at Xp23.13 with non-obstructive azoospermia and congenital cataracts.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 2, p. 471, doi. 10.1007/s10815-019-01685-6
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- Publication type:
- Article
Dual inhibiting OCT4 and AKT potently suppresses the propagation of human cancer cells.
- Published in:
- Scientific Reports, 2017, p. 46246, doi. 10.1038/srep46246
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- Publication type:
- Article
Clonal evolution analysis of paired anaplastic and well‐differentiated thyroid carcinomas reveals shared common ancestor.
- Published in:
- Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 645, doi. 10.1002/gcc.22678
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- Publication type:
- Article
Integrative modeling of transmitted and de novo variants identifies novel risk genes for congenital heart disease.
- Published in:
- Quantitative Biology, 2021, v. 9, n. 2, p. 216, doi. 10.15302/J-QB-021-0248
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- Publication type:
- Article
Nonexercise machine learning models for maximal oxygen uptake prediction in national population surveys.
- Published in:
- Journal of the American Medical Informatics Association, 2023, v. 30, n. 5, p. 943, doi. 10.1093/jamia/ocad035
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- Publication type:
- Article
The Cost of Medications at a Student-Run Free Clinic in New Haven, Connecticut, 2021-2023.
- Published in:
- Preventing Chronic Disease, 2024, v. 21, p. 1, doi. 10.5888/pcd21.230277
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- Publication type:
- Article