about
Y chromosome evidence of earliest modern human settlement in East Asia and multiple origins of Tibetan and Japanese populationsGenetic evidence supports demic diffusion of Han cultureGJB1/Connexin 32 whole gene deletions in patients with X-linked Charcot-Marie-Tooth disease.Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de LangeThe b2/b3 subdeletion shows higher risk of spermatogenic failure and higher frequency of complete AZFc deletion than the gr/gr subdeletion in a Chinese populationWhole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy.SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humansIncreased LIS1 expression affects human and mouse brain developmentAutism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome.Evaluation of copy number variation detection for a SNP array platform.Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLSEvolution in health and medicine Sackler colloquium: Genomic disorders: a window into human gene and genome evolution.Copy number variation in human health, disease, and evolution.Identification of copy number variation hotspots in human populations.Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangementsScreening of Duchenne muscular dystrophy (DMD) mutations and investigating its mutational mechanism in Chinese patients.High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile.Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability.Potocki-Lupski syndrome: a microduplication syndrome associated with oropharyngeal dysphagia and failure to thrive.A spatial analysis of genetic structure of human populations in China reveals distinct difference between maternal and paternal lineages.Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataract.X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3TBX6 null variants and a common hypomorphic allele in congenital scoliosis.Fifteen novel EIF2B1-5 mutations identified in Chinese children with leukoencephalopathy with vanishing white matter and a long term follow-up.Structural variation of the human genome: mechanisms, assays, and role in male infertilityCNV instability associated with DNA replication dynamics: evidence for replicative mechanisms in CNV mutagenesis.Frequency of nonallelic homologous recombination is correlated with length of homology: evidence that ectopic synapsis precedes ectopic crossing-over.Assessing structural variation in a personal genome-towards a human reference diploid genome.The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans.Complex human chromosomal and genomic rearrangements.Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han populationNon-coding genetic variants in human disease.Alu-specific microhomology-mediated deletion of the final exon of SPAST in three unrelated subjects with hereditary spastic paraplegia.MacroH2A1 associates with nuclear lamina and maintains chromatin architecture in mouse liver cells.Replicative mechanisms of CNV formation preferentially occur as intrachromosomal events: evidence from Potocki-Lupski duplication syndrome.Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs.Genetic studies of human diversity in East Asia.Increased genome instability in human DNA segments with self-chains: homology-induced structural variations via replicative mechanismsPartial deletions are associated with an increased risk of complete deletion in AZFc: a new insight into the role of partial AZFc deletions in male infertility.Zinc-finger-nucleases mediate specific and efficient excision of HIV-1 proviral DNA from infected and latently infected human T cells.
P50
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P50
description
genetics researcher at Fudan University
@en
հետազոտող
@hy
name
Feng Zhang
@ast
Feng Zhang
@en
Feng Zhang
@es
Feng Zhang
@nl
Feng Zhang
@sl
type
label
Feng Zhang
@ast
Feng Zhang
@en
Feng Zhang
@es
Feng Zhang
@nl
Feng Zhang
@sl
prefLabel
Feng Zhang
@ast
Feng Zhang
@en
Feng Zhang
@es
Feng Zhang
@nl
Feng Zhang
@sl
P108
P1053
C-7735-2009
P106
P2456
P2798
P31
P3829
P496
0000-0003-4556-8276
P569
2000-01-01T00:00:00Z