Fengxiao Bu

Fengxiao Bu

University of Iowa

H-index: 11

North America-United States

About Fengxiao Bu

Fengxiao Bu, With an exceptional h-index of 11 and a recent h-index of 11 (since 2020), a distinguished researcher at University of Iowa, specializes in the field of Genetics, Bioinformatics.

His recent articles reflect a diverse array of research interests and contributions to the field:

Molecular diagnosis, clinical evaluation and phenotypic spectrum of Townes-Brocks syndrome: insights from a large Chinese hearing loss cohort

Exploring noncoding variants in genetic diseases: from detection to functional insights

Identifying genetic factors of polycystic ovary syndrome in women with epilepsy: a whole-genome sequencing study

NCAD v1. 0: a database for non-coding variant annotation and interpretation

Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss

Identification of mobile element insertion from whole genome sequencing data using deep neural network model

seGMM: A new tool for gender determination from massively parallel sequencing data

DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing loss

Fengxiao Bu Information

University

Position

___

Citations(all)

1177

Citations(since 2020)

630

Cited By

839

hIndex(all)

11

hIndex(since 2020)

11

i10Index(all)

11

i10Index(since 2020)

11

Email

University Profile Page

Google Scholar

Fengxiao Bu Skills & Research Interests

Genetics

Bioinformatics

Top articles of Fengxiao Bu

Title

Journal

Author(s)

Publication Date

Molecular diagnosis, clinical evaluation and phenotypic spectrum of Townes-Brocks syndrome: insights from a large Chinese hearing loss cohort

Journal of Medical Genetics

Xiaohong Yan

Jing Wang

Wen Yang

Linke Li

Tian Shen

...

2024/1/31

Exploring noncoding variants in genetic diseases: from detection to functional insights

Ke Wu

Fengxiao Bu

Yang Wu

Gen Zhang

Xin Wang

...

2024/1/4

Identifying genetic factors of polycystic ovary syndrome in women with epilepsy: a whole-genome sequencing study

Neuroendocrinology

Wanlin Lai

Yiming Wu

Leihao Sha

Qi Lai

Ximeng Yang

...

2024/3/1

NCAD v1. 0: a database for non-coding variant annotation and interpretation

Journal of Genetics and Genomics

Xiaoshu Feng

Sihan Liu

Ke Li

Fengxiao Bu

Huijun Yuan

2024/2/1

Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss

Genome Medicine

Sihan Liu

Mingjun Zhong

Yu Huang

Qian Zhang

Ting Chen

...

2023/12/18

Identification of mobile element insertion from whole genome sequencing data using deep neural network model

bioRxiv

Xiaofei Xu

Yu Huang

Xuegang Wang

Jing Cheng

Huijun Yuan

...

2023/3/8

seGMM: A new tool for gender determination from massively parallel sequencing data

Frontiers in Genetics

Sihan Liu

Yuanyuan Zeng

Chao Wang

Qian Zhang

Meilin Chen

...

2022/3/3

DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing loss

Human genetics

Fengxiao Bu

Mingjun Zhong

Qinyi Chen

Yumei Wang

Xia Zhao

...

2022/4

High performance of a GPU-accelerated variant calling tool in genome data analysis

bioRxiv

Qian Zhang

Hao Liu

Fengxiao Bu

2021/12/13

See List of Professors in Fengxiao Bu University(University of Iowa)

Co-Authors

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