Yajian Wang

7.

Xuliang Zhao, Weiwei Sun, Jian-an Jia, 1966, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

7.

Xuliang Zhao, Weiwei Sun, Jian-an Jia, 2020, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

IDDCA syndrome in a Chinese infant due to GNB5 biallelic mutations

Yajian Wang, Yuanyuan Xu, D. Jin, 2020, Journal of Human Genetics.

Mutation in BRAF and SMAD4 associated with resistance to neoadjuvant chemoradiation therapy in locally advanced rectal cancer

Yajian Wang, Du He, Xin Wang, 2019, Virchows Archiv.

De Novo Mutation of Paternal IGF2 Gene Causing Silver–Russell Syndrome in a Sporadic Patient

Yajian Wang, Deyun Liu, Xiu-An Yang, 2017, Front. Genet..

Compound heterozygous variants in MOGS inducing congenital disorders of glycosylation (CDG) IIb

Yajian Wang, Yuanyuan Xu, D. Jin, 2018, Journal of Human Genetics.

Humus Components and Biogenic Structures under Tropical Slash-and- 1 Burn Agriculture 2 3

Xuliang Zhao, Weiwei Sun, Jian-an Jia, 2010 .

Compound Heterozygous Mutations in ABCG5 or ABCG8 Causing Chinese Familial Sitosterolemia.

Weiwei Sun, Yajian Wang, Gong Zhang, 2020, The journal of gene medicine.

Prenatal ultrasound-assisted identification of multiple malformations caused by a deletion in the long-arm end of chromosome 7 and review of the literature

Xuliang Zhao, Weiwei Sun, Jian-an Jia, 2020, The Journal of Maternal-Fetal & Neonatal Medicine.

Performance validation of an amplicon-based targeted next-generation sequencing assay and mutation profiling of 648 Chinese colorectal cancer patients

Yingyong Hou, Yajian Wang, Huaiyin Shi, 2018, Virchows Archiv.

Whole-exome Sequencing Helps the Diagnosis and Treatment in Children with Neurodevelopmental Delay Accompanied Unexplained Dyspnea

Yajian Wang, Weiyue Gu, Yuanyuan Xu, 2018, Scientific Reports.

Whole-exome Sequencing Helps the Diagnosis and Treatment in Children with Neurodevelopmental Delay Accompanied Unexplained Dyspnea

Yajian Wang, Weiyue Gu, Yuanyuan Xu, 2018, Scientific Reports.

Novel NFU1 Variants Induced MMDS Behaved as Special Leukodystrophy in Chinese Sufferers

Yajian Wang, Tao Wang, D. Jin, 2017, Journal of Molecular Neuroscience.

Biallelic INTS1 Mutations Cause a Rare Neurodevelopmental Disorder in Two Chinese Siblings

Yajian Wang, De Wu, Xiu-An Yang, 2019, Journal of Molecular Neuroscience.

Usher syndrome type 2A complicated with glycogen storage disease type 3 due to paternal uniparental isodisomy of chromosome 1 in a sporadic patient

Weiwei Sun, Yajian Wang, Weiyue Gu, 2021, Molecular genetics & genomic medicine.

Novel NFU1 Variants Induced MMDS Behaved as Special Leukodystrophy in Chinese Sufferers

Yajian Wang, D. Jin, Tao Wang, 2017, Journal of Molecular Neuroscience.

Nutrient Control of Hunger by Extrinsic Gastrointestinal

Xuliang Zhao, Weiwei Sun, Jian-an Jia, 2013 .

Compound heterozygous variants in MOGS inducing congenital disorders of glycosylation (CDG) IIb

Yajian Wang, Yuanyuan Xu, D. Jin, 2018, Journal of Human Genetics.