1.TBX6 Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis. New England Journal of Medicine 2015;372:341-350. IF=79.2 2.Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella. American Journal of Human Genetics 2017;100(6):854-864. IF=8.8 3.Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella. Journal of Medical Genetics 2019;56(2):96-103. IF=5.7 4.lexity and correlation of dosage-sensitive genes with clinical severity in genomic disorders. Human Molecular Genetics 2017;26(10):1927-1941. IF=4.9 5.CNV instability associated with DNA replication dynamics: evidence for replicative mechanisms in CNV mutagenesis. Human Molecular Genetics 2015;24(6):1574-1583. IF=4.9 6. Jeesun Kim*, Hongbo Zhao*, Soojin Kim, Debra Hollowell, Kevin Lin, Yue Lu, Yoko Takata, Jianjun Shen & Taiping Chen. Maternal Setdb1 Is Required for Meiotic Progression and Preimplantation Development in Mouse. Plos Genetics 2016 Apr 12;12(4):e1005970. (*co-first author) (IF=5.54) 7.Soo Jin Kim*, Hongbo Zhao*, Swanand Hardikar1, Anup K. Singh, Margaret A. Goodel, Taiping Chen. A DNMT3A mutation common in AML exhibits dominant-negative effects in murine ES cells. Blood. 2013 Dec 12; 122(25):4086-9 (*co-first author) (IF=15.132)
近五年获奖情况 1.教育部自然科学奖 一等奖 基因组拷贝数变异的突变机理与致病机制研究 (主要完成人)张锋，邱贵兴，金力，吴志宏，徐书华，吴南，陈晓丽 2.药明康德生命化学研究奖 杰出成就奖 基因组拷贝数变异致生殖与发育疾病的机制研究 (主要完成人)张锋 3.转化医学奖励计划 转化医学创新奖 无 (主要完成人)张锋 | 
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