J. Cheung

发表

Murine segmental duplications are hot spots for chromosome and gene evolution.

S. Scherer, J. González, L. Armengol, 2005, Genomics.

Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence

J. R. MacDonald, S. Scherer, X. Estivill, 2003, Genome Biology.

Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements.

S. Scherer, L. Armengol, X. Estivill, 2003, Human molecular genetics.

Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletions.

Xavier Estivill, Joseph Cheung, Lluís Armengol, 2003, Human molecular genetics.

Comparative analysis of the paired immunoglobulin-like receptor (PILR) locus in six mammalian genomes: duplication, conversion, and the birth of new genes.

Michael D. Wilson, S. Scherer, B. Koop, 2006, Physiological genomics.

Duplication and relocation of the functional DPY19L2 gene within low copy repeats

S. Scherer, A. Carson, J. Cheung, 2006, BMC Genomics.

Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome.

Xavier Estivill, Joseph Cheung, Stephen W Scherer, 2002, Human molecular genetics.

A novel gene encoding a TIG multiple domain protein is a positional candidate for autosomal recessive polycystic kidney disease.

Z. Zhao, K. Tsuchiya, Guan-qing Wu, 2002, Genomics.

Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome.

S. Scherer, J. Vincent, A. Boright, 2001, American journal of human genetics.

A role for common fragile site induction in amplification of human oncogenes.

David I. Smith, S. Scherer, J. Vincent, 2002, Cancer cell.

Genomic analysis of five chromosome 7p deletion patients with Greig cephalopolysyndactyly syndrome (GCPS).

S. Scherer, J. Vincent, C. Windpassinger, 2006, European journal of medical genetics.

Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.

K Nakabayashi, S W Scherer, S. Scherer, 2001, Genomics.

Human Chromosome 7: DNA Sequence and Biology

Junjun Zhang, Nazneen Rahman, Alexander K. Hudek, 2003, Science.

The Blimp-1 gene regulatory region directs EGFP expression in multiple hematopoietic lineages and testis in mice

T. Jin, Mingyao Liu, C. Shi, 2008, Transgenic Research.

GATA1 mutations in transient leukemia and acute megakaryoblastic leukemia of Down syndrome.

S. Scherer, A. Zipursky, J. Cheung, 2003, Blood.

Recent segmental and gene duplications in the mouse genome

Junjun Zhang, Michael D. Wilson, Joseph Cheung, 2003, Genome Biology.

Discovery of the human genome sequence in the public and private databases

S. Scherer, J. Cheung, 2001, Current Biology.

The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript system.

Joseph Cheung, Stephen W Scherer, S. Scherer, 2002, Genomics.

Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans.

L. Tsui, R. Hegele, B. Koop, 2003, Human molecular genetics.

Duplication and relocation of the functional DPY19L2 gene within low copy repeats

S. Scherer, A. Carson, J. Cheung, 2006, BMC Genomics.