B. Han

发表

Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes

Richard A Marini, Simon X. Xu, Nicole M. Russo-Ponsaran, 2019 .

Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2.

J. Seidman, M. Bitner-Glindzicz, Xiangyin Kong, 2010, American journal of human genetics.

Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64.

Wei Li, X. Liu, K. Wrzeszczynski, 2011, American journal of human genetics.

Newborn hearing concurrent genetic screening for hearing impairment-a clinical practice in 58,397 neonates in Tianjin, China.

X. Yi, J. Zou, B. Han, 2013, International journal of pediatric otorhinolaryngology.

Mutation Analysis of Slc26a4 in Mainland Chinese Patients with Enlarged Vestibular Aqueduct

X. Liu, D. Yan, B. Han, 2009, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

High frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorder

L. Lan, Z. Yin, J. Guan, 2016, Clinical genetics.

Identification of a novel mutation of PJVK in the Chinese non-syndromic hearing loss population with low prevalence of the PJVK mutations

L. Lan, B. Han, Lan Yu, 2015, Acta oto-laryngologica.

Correlation analysis of genotypes, auditory function, and vestibular size in Chinese children with enlarged vestibular aqueduct syndrome

L. Lan, B. Han, Qiuju Wang, 2013, Acta oto-laryngologica.

Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype–phenotype review for DFNA11

L. Lan, J. Guan, B. Han, 2018, Acta oto-laryngologica.

A novel mutation of SATB2 inhibits odontogenesis of human dental pulp stem cells through Wnt/β-catenin signaling pathway

B. Han, Yan-Heng Zhou, Ting Zhang, 2021, Stem Cell Research & Therapy.

Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China

Huanming Yang, Jian Wang, Zhiyu Peng, 2018, bioRxiv.

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

David T. Miller, O. Platt, Bai-Lin Wu, 2008, Genetics in Medicine.

Integrating de novo and inherited variants in over 42,607 autism cases identifies mutations in new moderate risk genes

William T. Harvey, Richard A Marini, Simon X. Xu, 2021, medRxiv.

Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss

Ling Yang, Xin Jin, L. Lan, 2013, PloS one.

Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

Richard A Marini, Simon X. Xu, Nicole M. Russo-Ponsaran, 2019, npj Genomic Medicine.

[Mutation screening of MITF gene in patients with Waardenburg syndrome type 2].

J. Chen, B. Han, Guo-jian Wang, 2008, Yi chuan = Hereditas.

Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family

Xuegong Zhang, P. Sham, J. Chen, 2014, Annals of human genetics.

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

B. Wu, B. Han, L. Wong, 2009, Journal of Translational Medicine.

Unilateral auditory neuropathy spectrum disorder

L. Lan, B. Han, Qiuju Wang, 2012, Acta oto-laryngologica.

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population

B. Han, L. Wong, E. Schmitt, 2007, Genetics in Medicine.

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

L. Lan, Z. Yin, J. Guan, 2016, Journal of Human Genetics.

Newborn genetic screening for high risk deafness-associated mutations with a new Tetra-primer ARMS PCR kit.

L. Lan, B. Han, Qiuju Wang, 2013, International journal of pediatric otorhinolaryngology.

Reproductive management through integration of PGD and MPS-based noninvasive prenatal screening/diagnosis for a family with GJB2-associated hearing impairment

L. Lan, Z. Yin, B. Han, 2015, Science China Life Sciences.

Psychiatric and Medical Profiles of Autistic Adults in the SPARK Cohort

Richard A Marini, Simon X. Xu, Nicole M. Russo-Ponsaran, 2020, Journal of Autism and Developmental Disorders.

A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family

L. Lan, J. Guan, B. Han, 2017, Chinese medical journal.

A novel AGK splicing mutation in a patient with Sengers syndrome and left ventricular non-compaction cardiomyopathy

B. Han, W. Yin, T. Tian, 2023, Pediatric Research.

[Prenatal diagnosis for hereditary deaf families assisted by genetic testing].

B. Han, Qiuju Wang, Guo-jian Wang, 2007, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

[Features of nationwide distribution and frequency of a common gap junction beta-2 gene mutation in China].

B. Han, Guo-jian Wang, Yongyi Yuan, 2007, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

[Frequency of SLC26A4 IVS7-2A > G mutation in patients with severe to profound hearing loss from different area and ethnic group in China].

B. Han, Yongyi Yuan, D. Kang, 2007, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

Targeted High-Throughput Sequencing Identifies Pathogenic Mutations in KCNQ4 in Two Large Chinese Families with Autosomal Dominant Hearing Loss

X. Yi, Ling Yang, L. Lan, 2014, PloS one.

Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss.

J. Chen, B. Han, Guo-jian Wang, 2008, Mitochondrion.

A Novel DFNA36 Mutation in TMC1 Orthologous to the Beethoven (Bth) Mouse Associated with Autosomal Dominant Hearing Loss in a Chinese Family

Ling Yang, Xin Jin, L. Lan, 2014, PloS one.

Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64.

Wei Li, X. Liu, K. Wrzeszczynski, 2011, American journal of human genetics.

Reproductive management through integration of PGD and MPS-based noninvasive prenatal screening/diagnosis for a family with GJB2-associated hearing impairment

L. Lan, Z. Yin, B. Han, 2015, Science China Life Sciences.

Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China

Huanming Yang, Jian Wang, Zhiyu Peng, 2018, Genetics in Medicine.

A novel mutation of SATB2 inhibits odontogenesis of human dental pulp stem cells through Wnt/β-catenin signaling pathway

B. Han, Yan-Heng Zhou, Ting Zhang, 2021, Stem Cell Research & Therapy.