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Feng Zhang
Feng Zhang
Professor of Genetics, Fudan University
Geverifieerd e-mailadres voor fudan.edu.cn - Homepage
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Copy number variation in human health, disease, and evolution
F Zhang, W Gu, ME Hurles, JR Lupski
Annual review of genomics and human genetics 10, 451-481, 2009
13772009
Whole-genome sequencing in a patient with Charcot–Marie–Tooth neuropathy
JR Lupski, JG Reid, C Gonzaga-Jauregui, D Rio Deiros, DCY Chen, ...
New England Journal of Medicine 362 (13), 1181-1191, 2010
9042010
Mechanisms for human genomic rearrangements
W Gu, F Zhang, JR Lupski
Pathogenetics 1 (1), 4, 2008
7652008
Non-coding genetic variants in human disease
F Zhang, JR Lupski
Human molecular genetics 24 (R1), R102-R110, 2015
6212015
Genetic evidence supports demic diffusion of Han culture
B Wen, H Li, D Lu, X Song, F Zhang, Y He, F Li, Y Gao, X Mao, L Zhang, ...
Nature 431 (7006), 302-305, 2004
5172004
The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans
F Zhang, M Khajavi, AM Connolly, CF Towne, SD Batish, JR Lupski
Nature genetics 41 (7), 849-853, 2009
5162009
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements
P Liu, A Erez, SCS Nagamani, SU Dhar, KE Kołodziejska, ...
Cell 146 (6), 889-903, 2011
4552011
Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome
MB Ramocki, SU Peters, YJ Tavyev, F Zhang, C Carvalho, CP Schaaf, ...
Annals of neurology 66 (6), 771-782, 2009
3302009
Autism-like behaviours and germline transmission in transgenic monkeys overexpressing MeCP2
Z Liu, X Li, JT Zhang, YJ Cai, TL Cheng, C Cheng, Y Wang, CC Zhang, ...
Nature 530 (7588), 98-102, 2016
3202016
Complex human chromosomal and genomic rearrangements
F Zhang, CMB Carvalho, JR Lupski
Trends in Genetics 25 (7), 298-307, 2009
2982009
TBX6 Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis
N Wu, X Ming, J Xiao, Z Wu, X Chen, M Shinawi, Y Shen, G Yu, J Liu, ...
New England Journal of Medicine 372 (4), 341-350, 2015
2682015
Biallelic mutations in CFAP43 and CFAP44 cause male infertility with multiple morphological abnormalities of the sperm flagella
S Tang, X Wang, W Li, X Yang, Z Li, W Liu, C Li, Z Zhu, L Wang, J Wang, ...
The American Journal of Human Genetics 100 (6), 854-864, 2017
2542017
Increased LIS1 expression affects human and mouse brain development
W Bi, T Sapir, OA Shchelochkov, F Zhang, MA Withers, JV Hunter, T Levy, ...
Nature genetics 41 (2), 168-177, 2009
2442009
Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching
CMB Carvalho, F Zhang, P Liu, A Patel, T Sahoo, CA Bacino, C Shaw, ...
Human molecular genetics 18 (12), 2188-2203, 2009
2192009
Y chromosome evidence of earliest modern human settlement in East Asia and multiple origins of Tibetan and Japanese populations
H Shi, H Zhong, Y Peng, YL Dong, XB Qi, F Zhang, LF Liu, SJ Tan, RZ Ma, ...
BMC biology 6 (1), 45, 2008
1882008
Zinc-finger-nucleases mediate specific and efficient excision of HIV-1 proviral DNA from infected and latently infected human T cells
X Qu, P Wang, D Ding, L Li, H Wang, L Ma, X Zhou, S Liu, S Lin, X Wang, ...
Nucleic acids research 41 (16), 7771-7782, 2013
1852013
Assessing structural variation in a personal genome—towards a human reference diploid genome
AC English, WJ Salerno, OA Hampton, C Gonzaga-Jauregui, S Ambreth, ...
BMC genomics 16 (1), 286, 2015
1562015
Genetic structure of Hmong-Mien speaking populations in East Asia as revealed by mtDNA lineages
B Wen, H Li, S Gao, X Mao, Y Gao, F Li, F Zhang, Y He, Y Dong, Y Zhang, ...
Molecular Biology and Evolution 22 (3), 725-734, 2004
1562004
Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability
F Zhang, P Seeman, P Liu, MAJ Weterman, C Gonzaga-Jauregui, ...
The American Journal of Human Genetics 86 (6), 892-903, 2010
1482010
Microdeletions including YWHAE in the Miller–Dieker syndrome region on chromosome 17p13. 3 result in facial dysmorphisms, growth restriction, and cognitive impairment
SCS Nagamani, F Zhang, OA Shchelochkov, W Bi, Z Ou, F Scaglia, ...
Journal of medical genetics 46 (12), 825-833, 2009
1442009
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Artikelen 1–20