Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases

Rong Chen, Lisong Shi, Jörg Hakenberg, +27

Nature Biotechnology

Mendelian Childhood DiseasesMendelian DisorderGeneticsGenomes Identifies IndividualsGenetic Epidemiology +9

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9

Cristina M. Justice, Garima Yagnik, Yoonhee Kim, +30

Nature Genetics

SclerostinNonsyndromic Sagittal CraniosynostosisGenetic DisorderGeneticsGenetic Epidemiology +6

Cytogenomic identification and long-read single molecule real-time (SMRT) sequencing of a Bardet–Biedl Syndrome 9 (BBS9) deletion

Jennifer Reiner, Laura Rosa Pisani, Wanqiong Qiao, +10

npj Genomic Medicine

Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population

Lisong Shi, Cong Li, Chuchu Wang, +20

Human Genetics

EpidemiologyCardiovascular DiseaseGenetic DisorderGeneticsGenetic Epidemiology +8

CADgene: a comprehensive database for coronary artery disease genes

Hui Liu, Wei Liu, Yifang Liao, +7

Nucleic Acids Research

Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population

Pengyun Wang, Qinbo Yang, Xiaofen Wu, +17

Biochemical and Biophysical Research Communications

ChannelopathiesFunctional Dominant-negative MutationGenetic DisorderMedicineGenetics +7

Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population

Cong Li, Fan Wang, Yanzong Yang, +22

Human Genetics

Snp Rs2106261Zfhx3 GeneGenetic DisorderGeneticsGenetic Epidemiology +9

Assessment of Vibrational Non-Equilibrium Effect on Detonation Cell Size

Lisong Shi, Hua Shen, Peng Zhang, +2

Combustion Science and Technology

Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID population

Xiang Ren, Chengqi Xu, Chengxiong Zhan, +17

Clinica Chimica Acta

Genome-wide Association StudyAllelic VariantCardiovascular DiseaseMedicineGenetics +9

Disease-associated variants in different categories of disease located in distinct regulatory elements

Meng Ma, Ru Ying, Ling-Shiang Chuang, +8

BMC Genomics