Yuan-qing Wu

发表

Comprehensive molecular characterization of human colon and rectal cancer

Steven J. M. Jones, Joshua M. Stuart, Brian D. O’Connor, 2012, Nature.

Comparative validation of the D. melanogaster modENCODE transcriptome annotation

James B. Brown, P. Bickel, Manolis Kellis, 2014, Genome research.

Refinement of the genomic structure of STX1A and mutation analysis in nondeletion Williams syndrome patients.

L. Shaffer, L. Tsui, B. Bejjani, 2002, American journal of medical genetics.

Loss of the Potassium Channel β‐Subunit Gene, KCNAB2, Is Associated with Epilepsy in Patients with 1p36 Deletion Syndrome

L. Shaffer, C. Kashork, Yuan-qing Wu, 2001, Epilepsia.

Human testis specifically expresses a homologue of the rodent T lymphocytes RT6 mRNA

Yuan-qing Wu, M. Mattei, A. Pawlak, 1996, FEBS letters.

A case of segmental paternal isodisomy of chromosome 14

L. Shaffer, Yuan-qing Wu, John P. Johnson, 2002, Human Genetics.

Allele-specific methylation of a functional CTCF binding site upstream of MEG3 in the human imprinted domain of 14q32

L. Shaffer, Yuan-qing Wu, A. Rosa, 2005, Chromosome Research.

Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions.

L. Shaffer, J. McPherson, Yuan-qing Wu, 1999, Human molecular genetics.

Molecular cloning, characterization and expression modulation of four ferritins in black carp Mylopharyngodon piceus in response to Aeromonas hydrophila challenge

Yuan-qing Wu, Jinyun Ye, Yuanyuan Xie, 2020 .

Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin.

L. Shaffer, J. Lupski, J. Korenberg, 1998, American journal of medical genetics.

Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11.

B. D. de Vries, A. V. D. van den Ouweland, P. Heutink, 1994, Human molecular genetics.

Meiotic human sperm cells express a leucine-rich homologue of Caenorhabditis elegans early embryogenesis gene, Zyg-11.

Yuan-qing Wu, G. Guellaen, A. Pawlak, 2001, Molecular human reproduction.

Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome.

L. Shaffer, J. Badano, Yuan-qing Wu, 2000, American journal of human genetics.