An Integrated Nomogram Combining Deep Learning and Radiomics for Predicting Malignancy of Pulmonary Nodules Using CT‐Derived Nodules and Adipose Tissue: A Multicenter Study

Authors: Shidi Miao, Qifan Xuan, Hanbing Xie, Yuyang Jiang, Mengzhuo Sun, Wenjuan Huang, Jing Li, Hongzhuo Qi, Ao Li, Qiujun Wang, Zengyao Liu, Ruitao Wang

Source: Cancer Medicine, Vol 13, Iss 21, Pp n/a-n/a (2024)

Subject Terms: adipose tissue, computed tomography, deep learning, multicenter, multimodal, nomogram, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

File Description: electronic resource

Relation: https://doaj.org/toc/2045-7634

Access URL: https://doaj.org/article/a5a050eece7a4089b43a07b69931978c

Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected family

Authors: Jing Chen, Qinqin Xiang, Xiao Xiao, Bocheng Xu, Hanbing Xie, He Wang, Mei Yang, Shanling Liu

Source: BMC Medical Genomics, Vol 15, Iss 1, Pp 1-8 (2022)

Subject Terms: Osteogenesis imperfecta, Congenital contractural arachnodactyly syndrome, COL1A2, FBN2, Synergistic effect, Whole-exome sequencing, Internal medicine, RC31-1245, Genetics, QH426-470

File Description: electronic resource

Relation: https://doaj.org/toc/1755-8794

Access URL: https://doaj.org/article/204eeba8a5984a32b287603584d62ae8

NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism

Authors: Yuanyuan Xiao, Cong Zhou, Hanbing Xie, Shuang Huang, Jing Wang, Shanling Liu

Source: BMC Genomics, Vol 23, Iss 1, Pp 1-8 (2022)

Subject Terms: Oculocutaneous albinism, TYR, OCA2, Targeted NGS, Medical genomics, Nucleotide variations, Biotechnology, TP248.13-248.65, Genetics, QH426-470

File Description: electronic resource

Relation: https://doaj.org/toc/1471-2164

Access URL: https://doaj.org/article/7c66af441edc4399b5431a089d995b0d

Compound heterozygous splicing variants in KIAA0586 cause fetal short‐rib thoracic dysplasia and cerebellar malformation: Use of exome sequencing in prenatal diagnosis

Authors: Qianying Zhao, Bocheng Xu, Qinqin Xiang, Yu Tan, Hanbing Xie, Qianqian Gao, Lingyi Wen, He Wang, Mei Yang, Shanling Liu

Source: Molecular Genetics & Genomic Medicine, Vol 11, Iss 3, Pp n/a-n/a (2023)

Subject Terms: exome sequencing, Joubert syndrome, KIAA0586, prenatal diagnosis, short‐rib thoracic dysplasia, splicing variants, Genetics, QH426-470

File Description: electronic resource

Relation: https://doaj.org/toc/2324-9269

Access URL: https://doaj.org/article/747ef8f32f524361b9c843ad4b2afcdb

Case Report: The compound heterozygotes variants in FLT4 causes autosomal recessive hereditary lymphedema in a Chinese family

Authors: Qinqin Xiang, Jing Chen, Xiao Xiao, Bocheng Xu, Hanbing Xie, He Wang, Mei Yang, Shanling Liu

Source: Frontiers in Genetics, Vol 14 (2023)

Subject Terms: FLT4, primary lymphedema, autosomal recessive, trio-whole-exome sequencing, case report, Genetics, QH426-470

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2023.1140406/full; https://doaj.org/toc/1664-8021

Access URL: https://doaj.org/article/75502509235f4cf686e5d6f4fd93a1a4

A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis

Authors: Qianying Zhao, Qinqin Xiang, Yu Tan, Xiao Xiao, Hanbing Xie, He Wang, Mei Yang, Shanling Liu

Source: Molecular Genetics & Genomic Medicine, Vol 10, Iss 10, Pp n/a-n/a (2022)

Subject Terms: classic Bartter syndrome, CLCNKB, exome sequencing, prenatal genetic diagnosis, Genetics, QH426-470

File Description: electronic resource

Relation: https://doaj.org/toc/2324-9269

Access URL: https://doaj.org/article/62773c4bd4a34284b58cb84555622736

A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case report

Authors: Cong Zhou, Yuanyuan Xiao, Hanbing Xie, Shanling Liu, Jing Wang

Source: BMC Medical Genomics, Vol 14, Iss 1, Pp 1-6 (2021)

Subject Terms: Hearing loss, USH2A, Variant, Disease-targeted gene panel, Next generation sequencing, Prenatal diagnosis, Internal medicine, RC31-1245, Genetics, QH426-470

File Description: electronic resource

Relation: https://doaj.org/toc/1755-8794

Access URL: https://doaj.org/article/0fae4972e65f43dc81b6bf09252bce3c

Ultrasound-guided transmuscular quadratus lumborum block reduced postoperative opioids consumptions in patients after laparoscopic hepatectomy: a three-arm randomized controlled trial

Authors: Mengya Pang, Guoliang Sun, Weifeng Yao, Shaoli Zhou, Ning Shen, Haofeng Liao, Hanbing Xie, Wanling Gao, Mian Ge

Source: BMC Anesthesiology, Vol 21, Iss 1, Pp 1-10 (2021)

Subject Terms: Postoperative analgesia, laparoscopic hepatectomy, Transmuscular quadratus lumborum block, oxycodone, Anesthesiology, RD78.3-87.3

File Description: electronic resource

Relation: https://doaj.org/toc/1471-2253

Access URL: https://doaj.org/article/666e5cd9ec244597bcdbcffbc14f93a9

Case Report: Novel Compound Heterozygous Variants in TRIOBP Associated With Congenital Deafness in a Chinese Family

Authors: Cong Zhou, Yuanyuan Xiao, Hanbing Xie, Jing Wang, Shanling Liu

Source: Frontiers in Genetics, Vol 12 (2021)

Subject Terms: TRIOBP, DFNB28, variation, hearing loss, next generation sequencing, Genetics, QH426-470

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2021.766973/full; https://doaj.org/toc/1664-8021

Access URL: https://doaj.org/article/916ef4ff7af94c7dbdbe0a9469e6bbf1

Identification of copy number variations among fetuses with ultrasound soft markers using next-generation sequencing

Authors: Jing Wang, Lin Chen, Cong Zhou, Li Wang, Hanbing Xie, Yuanyuan Xiao, Daishu Yin, Yang Zeng, Feng Tang, Yunyuan Yang, Hongmei Zhu, Xinlian Chen, Qian Zhu, Zhiying Liu, Hongqian Liu

Source: Scientific Reports, Vol 8, Iss 1, Pp 1-7 (2018)

Subject Terms: Medicine, Science

File Description: electronic resource

Relation: https://doaj.org/toc/2045-2322

Access URL: https://doaj.org/article/c04a9775f08a4724ba2f2486a69aa05e

Application of copy number variation sequencing for prenatal diagnosis in women at an advanced maternal age

Authors: Jing, Wang, Lin, Chen, Cong, Zhou, Li, Wang, Hanbing, Xie, Yuanyuan, Xiao, Hongmei, Zhu, Ting, Hu, Zhu, Zhang, Qian, Zhu

Source: Zhonghua yi xue yi chuan xue za zhi. 36(6):533-537

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN621116317&indx=1&recIds=ETOCRN621116317

Sudden Death in a Male Infant Due to Histiocytoid Cardiomyopathy: An Autopsy Case and Review of the Literature.

Authors: Hanbing Xie, Xueqin Chen, Ni Chen, Qiao Zhou, Xie, Hanbing, Chen, Xueqin, Chen, Ni, Zhou, Qiao

Source: American Journal of Forensic Medicine & Pathology; Mar2017, Vol. 38 Issue 1, p32-34, 3p

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