Xiao-Ning Chen

发表

The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

M. Gerstein, Fabian Grubert, L. Shaffer, 2009, Proceedings of the National Academy of Sciences.

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2

Georg Auburger, Iscia Lopes-Cendes, Julie R. Korenberg, 1996, Nature Genetics.

Chronic all-trans retinoic acid administration induced hyperactivity of HPA axis and behavioral changes in young rats

Jiang-Ning Zhou, Xiao-Ning Chen, L. Cai, 2010, European Neuropsychopharmacology.

A physical map of the human genome

D. Haussler, B. Trask, R. Wilson, 2001, Nature.

Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel

J. Korenberg, Shibo Li, G. Stetten, 2001, Genetics in medicine : official journal of the American College of Medical Genetics.

Down syndrome congenital heart disease: A narrowed region and a candidate gene

E. Zackai, N. Spinner, G. Lyons, 2001, Genetics in Medicine.

The Human Lumican Gene

J. Korenberg, P. Roughley, J. Grover, 1995, The Journal of Biological Chemistry.

The 200-kb segmental duplication on human chromosome 21 originates from a pericentromeric dissemination involving human chromosomes 2, 18 and 13.

J. Rossier, J. Korenberg, F. Chibon, 2003, Gene.

FISH analysis of terminal deletions in patients diagnosed with cri‐du‐chat syndrome

D. Grady, J. Overhauser, Xiao-Ning Chen, 1999, Clinical genetics.

Comparative Genome Hybridization

Julie R. Korenberg, J. Korenberg, Xiao-Ning Chen, 2002 .

BAC resource for molecular cytogenetics.

J. Korenberg, Xiao-Ning Chen, 2002, Methods in molecular biology.

Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.

Julie R Korenberg, J. Korenberg, G. Semenza, 2002, American journal of medical genetics.

Evolution of the mammalian G protein α subunit multigene family

B. Trask, M. Simon, J. Korenberg, 1992, Nature Genetics.

Refined physical map of the human PAX2/HOX11/NFKB2 cancer gene region at 10q24 and relocalization of the HPV6AI1 viral integration site to 14q13.3-q21.1

J. Korenberg, M. Eccles, A. Neri, 2003, BMC Genomics.

APP-BP1, a Novel Protein That Binds to the Carboxyl-terminal Region of the Amyloid Precursor Protein (*)

J. Korenberg, R. Neve, N. Chow, 1996, The Journal of Biological Chemistry.

William's syndrome: gene expression is related to parental origin and regional coordinate control

Jeremy C. Collette, A. Galaburda, U. Bellugi, 2009, Journal of Human Genetics.

Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on Chromosome 7q11.23

Rumiko Matsuoka, Ursula Bellugi, Julie R Korenberg, 2003, Genetics in Medicine.

VI. Genome Structure and Cognitive Map of Williams Syndrome

Rumiko Matsuoka, Ursula Bellugi, Julie R. Korenberg, 2000, Journal of Cognitive Neuroscience.

Deletion of chromosome 21 disturbs human brain

J. Korenberg, J. Moeschler, G. Barlow, 2006 .

Deletion of chromosome 21 disturbs human brain morphogenesis

J. Korenberg, J. Moeschler, G. Barlow, 2006, Genetics in Medicine.

Cryptic Translocation Identification in Human and Mouse Using Several Telomeric Multiplex FISH (TM-FISH) Strategies

J. Korenberg, P. Bray-Ward, D. Ward, 2001, Laboratory Investigation.

The Human Synaptotagmin IV Gene Defines an Evolutionary Break Point between Syntenic Mouse and Human Chromosome Regions but Retains Ligand Inducibility and Tissue Specificity*

J. Korenberg, H. Herschman, Xiao-Ning Chen, 2000, The Journal of Biological Chemistry.

Stress and glucocorticoids regulated corticotropin releasing factor in rat prefrontal cortex

Jiang-Ning Zhou, Xiao-Ning Chen, D. Tong, 2011, Molecular and Cellular Endocrinology.

The Involvement of Retinoic Acid Receptor-α in Corticotropin-Releasing Hormone Gene Expression and Affective Disorders

D. Swaab, Jiang-Ning Zhou, A. Bao, 2009, Biological Psychiatry.

Towards a full karyotype screening of interphase cells: ‘FISH and chip’ technology

Jan Smida, Jingly Fung, Julie R Korenberg, 2001, Molecular and Cellular Endocrinology.

Mammalian DSCAMs: roles in the development of the spinal cord, cortex, and cerebellum?

G. Lyons, J. Korenberg, G. Barlow, 2002, Biochemical and biophysical research communications.

Estrogen receptor-α and -β regulate the human corticotropin-releasing hormone gene through similar pathways

Jiang-Ning Zhou, Xiao-Ning Chen, Hong Zhu, 2008, Brain Research.

Is It Williams Syndrome? Gtf2ird1 Implicated in Visual–spatial Construction and Gtf2i in Sociability Revealed by High Resolution Arrays Materials and Methods Subject Deletion Analysis Cognitive-behavioral Analysis Results Physical and Developmental Features Deletion Analysis Neurocognitive Performan

U. Bellugi, J. Korenberg, D. Mills, 2022 .

Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans.

X. Chen, E. Vilain, A. Swain, 2001, American journal of human genetics.

A triple color FISH technique for mouse chromosome identification

J. Korenberg, D. Ward, J. Greally, 2001, Mammalian Genome.

Is it Williams syndrome? GTF2IRD1 implicated in visual–spatial construction and GTF2I in sociability revealed by high resolution arrays

U. Bellugi, J. Korenberg, D. Mills, 2009, American journal of medical genetics. Part A.