J. Korenberg

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DSCAM: a novel member of the immunoglobulin superfamily maps in a Down syndrome region and is involved in the development of the nervous system.

K. Yamakawa, Y. K. Huot, M. A. Haendelt, 1998, Human molecular genetics.

Abnormal Cortical Complexity and Thickness Profiles Mapped in Williams Syndrome

Agatha D. Lee, Jennifer A. Geaga, A. Toga, 2005, The Journal of Neuroscience.

Phosphofructokinase activity in fibroblasts aneuploid for chromosome 21

C. Epstein, J. Korenberg, K. G. Annerén, 1987, Human Genetics.

Integration of cytogenetic landmarks into the draft sequence of the human genome

D. Haussler, E. Birney, B. Trask, 2001, Nature.

Genetic Mapping of Brain Plasticity Across Development in Williams Syndrome: ERP Markers of Face and Language Processing

A. Galaburda, U. Bellugi, J. Korenberg, 2013, Developmental neuropsychology.

Down syndrome phenotypes: the consequences of chromosomal imbalance.

C. Disteche, X. Chen, J. Korenberg, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Specific cloning of human DNA as yeast artificial chromosomes by transformation-associated recombination.

X. Chen, J. Korenberg, V. Larionov, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Symmetry of Cortical Folding Abnormalities in Williams Syndrome Revealed by Surface-Based Analyses

D. V. van Essen, M. Raichle, A. Snyder, 2006, The Journal of Neuroscience.

Reward, salience, and attentional networks are activated by religious experience in devout Mormons

Jared A. Nielsen, Jeffrey S. Anderson, J. Korenberg, 2016, Social neuroscience.

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.

Abnormal brain synchrony in Down Syndrome☆

Guido Gerig, Jared A. Nielsen, Julie R. Korenberg, 2013, NeuroImage: Clinical.

Human genome organization: Alu, LINES, and the molecular structure of metaphase chromosome bands

Mary C. Rykowski, Julie R. Korenberg, J. Korenberg, 1988, Cell.

Evidence for superior parietal impairment in Williams syndrome

U Bellugi, S Eliez, A L Reiss, 2005, Neurology.

More Is Not Always Better: Increased Fractional Anisotropy of Superior Longitudinal Fasciculus Associated with Poor Visuospatial Abilities in Williams Syndrome

Ursula Bellugi, Brian W. Haas, Fumiko Hoeft, 2007, The Journal of Neuroscience.

Frontostriatal Dysfunction During Response Inhibition in Williams Syndrome

A. Galaburda, U. Bellugi, J. Korenberg, 2007, Biological Psychiatry.

Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome

Ursula Bellugi, Julie R. Korenberg, A. Galaburda, 1999, Trends in Neurosciences.

Defining the social phenotype in Williams syndrome: A model for linking gene, the brain, and behavior

Ursula Bellugi, Judy Reilly, Allan L Reiss, 2008, Development and Psychopathology.

Association between cerebral shape and social use of language in Williams syndrome

A. Galaburda, U. Bellugi, J. Korenberg, 2008, American journal of medical genetics. Part A.

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

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

Toward a molecular understanding of Down syndrome.

J. Korenberg, 1993, Progress in clinical and biological research.

Over-Expression of DSCAM and COL6A2 Cooperatively Generates Congenital Heart Defects

Kristen Jepsen, Karen Ocorr, Rolf Bodmer, 2011, PLoS genetics.

Structural organization of mouse peroxisome proliferator-activated receptor gamma (mPPAR gamma) gene: alternative promoter use and different splicing yield two mPPAR gamma isoforms.

X. Chen, J. Korenberg, J. Reddy, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Morphological differences in the mirror neuron system in Williams syndrome

E. Halgren, U. Bellugi, T. Brown, 2016, Social neuroscience.

Atypical hemispheric asymmetry in the perception of negative human vocalizations in individuals with Williams syndrome

U. Bellugi, J. Korenberg, D. Mills, 2010, Neuropsychologia.

Affiliative behavior in Williams syndrome: Social perception and real-life social behavior

R. Adolphs, U. Bellugi, J. Korenberg, 2010, Neuropsychologia.

The neurobiology of Williams syndrome: Cascading influences of visual system impairment?

A. Galaburda, U. Bellugi, J. Korenberg, 2006, Cellular and Molecular Life Sciences CMLS.

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

U. Bellugi, J. Korenberg, F. Rose, 2003 .

Williams syndrome: an exploration of neurocognitive and genetic features

U. Bellugi, J. Korenberg, E. Klima, 2001, Clinical Neuroscience Research.

Toward a cDNA map of the human genome.

M. Adams, J. Venter, X. Chen, 1995, Genomics.

Assignment1 of the GOV (Glioblastoma Overexpressed) gene to human chromosome band 19p13.2 by fluorescence in situ hybridization

J. Korenberg, X.-N. Chen, Z. Shi, 1999, Cytogenetic and Genome Research.

Isolation and characterization of the human MRE11 homologue.

X. Chen, J. Korenberg, D. Weaver, 1995, Genomics.

Patient-Empowerment Interactive Technologies

Craig B Caldwell, Julie R Korenberg, J. Korenberg, 2012, Science Translational Medicine.

Violence: heightened brain attentional network response is selectively muted in Down syndrome

Jared A. Nielsen, Jeffrey S. Anderson, G. Gerig, 2015, Journal of Neurodevelopmental Disorders.

Report and abstracts of the Sixth International Workshop on Human Chromosome 21 Mapping 1996. Cold Spring Harbor, New York, USA. May 6-8,1996.

John Quackenbush, R. Hubert, J. Korenberg, 1997, Cytogenetics and cell genetics.

Selection of a sublibrary enriched for a chromosome from total human bacterial artificial chromosome library using DNA from flow sorted chromosomes as hybridization probes.

M. Simon, X. Chen, J. Korenberg, 1995, Nucleic acids research.

Involvement of protein kinase Cepsilon (PKCepsilon) in thyroid cell death. A truncated chimeric PKCepsilon cloned from a thyroid cancer cell line protects thyroid cells from apoptosis.

X. Chen, J. Korenberg, J. Fagin, 1999, The Journal of biological chemistry.

Base ratio, DNA content, and quinacrine-brightness of human chromosomes.

J. Korenberg, W. Engels, William R. Engels, 1978, Proceedings of the National Academy of Sciences of the United States of America.

Down syndrome: The crucible for treating genomic imbalance

J. Korenberg, 2009, Genetics in Medicine.

Mapping Genetically Controlled Neural Circuits of Social Behavior and Visuo-Motor Integration by a Preliminary Examination of Atypical Deletions with Williams Syndrome

Brian W. Haas, A. Galaburda, U. Bellugi, 2014, PloS one.

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.

J. Korenberg, G. Gimelli, M. Digilio, 2000, Circulation.

Deletion of a 5cM Region at Chromosome 8 p 23 Is Associated With a Spectrum of Congenital Heart Defects

J. Korenberg, G. Gimelli, M. Digilio, 2000 .

A high-resolution PAC and BAC map of the SCA2 region.

S. Pulst, P. D. de Jong, X. Chen, 1997, Genomics.

Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.

L. Shaffer, J. Korenberg, V. Sutton, 1997, American journal of human genetics.

Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical map

S. Pulst, J. Korenberg, P. Jong, 1996, Human Genetics.

Purification and Properties of Human Cytosolic Folylpoly-γ-glutamate Synthetase and Organization, Localization, and Differential Splicing of Its Gene*

J. Korenberg, B. Shane, Yun-Jung Choi, 1996, The Journal of Biological Chemistry.

Hypothesis: familial Mediterranean fever--a genetic disorder of the lipocortin family?

J. Korenberg, J. Rotter, M. Shohat, 1989, American journal of medical genetics.

Evolution of the mammalian G protein alpha subunit multigene family.

B. Trask, M. Simon, X. Chen, 1992, Nature genetics.

Hot spots and functional organization of human chromosomes

J. Korenberg, C. Denniston, E. Therman, 1978, Human Genetics.

A comprehensive large-insert yeast artificial chromosome library for physical mapping of the mouse genome

E. Lander, X. Chen, J. Korenberg, 1996, Mammalian Genome.

Isolation, characterization, and regional mapping of microclones from a human chromosome 21 microdissection library.

J. Korenberg, J. Yu, R. Gemmill, 1992, American journal of human genetics.

Cloning of human cDNAs encoding mitochondrial and cytosolic serine hydroxymethyltransferases and chromosomal localization.

X. Chen, J. Korenberg, B. Shane, 1993, The Journal of biological chemistry.

Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia.

J. Korenberg, N. Heerema, M. Bull, 1994, American journal of medical genetics.

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.

Chromosomal localization of human genes for the LDL receptor family member glycoprotein 330 (LRP2) and its associated protein RAP (LRPAP1).

X. Chen, J. Korenberg, D. Strickland, 1994, Genomics.

The gene organization, chromosome location, and expression of a 55-kDa matrix protein (PRELP) of human articular cartilage.

X. Chen, J. Korenberg, P. Roughley, 1996, Genomics.

Localization of the human fibromodulin gene (FMOD) to chromosome 1q32 and completion of the cDNA sequence.

X. Chen, J. Korenberg, P. Roughley, 1994, Genomics.

Quantitative representation and description of intravoxel fiber complexity in HARDI

J. Korenberg, E. Hsu, C. Chu, 2015, Physics in medicine and biology.

Relative order and location of DNA sequences on chromosome 21 linked to familial Alzheimer disease.

S. Pulst, J. Korenberg, T. Yang-Feng, 1991, American journal of medical genetics.

Panel of aneuploid cell lines for physical mapping of the proximal long arm of human chromosome 21.

S. Pulst, J. Korenberg, 2005, American journal of medical genetics. Supplement.

Transient leukemia with trisomy 21: description of a case and review of the literature.

J. Korenberg, J. Graham, N. Fischel‐Ghodsian, 1995, American journal of medical genetics.

Localization of the tight junction protein gene TJP1 to human chromosome 15q13, distal to the Prader-Willi/Angelman region, and to mouse chromosome 7.

T. Mohandas, X. Chen, J. Korenberg, 1995, Genomics.

Chromosomal localization of murine and human oligodendrocyte-specific protein genes.

X. Chen, J. Korenberg, J. Bronstein, 1996, Genomics.

Identification and analysis of the human and murine putative chromatin structure regulator SUPT6H and Supt6h.

X. Chen, J. Korenberg, J. Cheng, 1996, Genomics.

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

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

Deletion of 20p 11.23----pter with normal growth hormone-releasing hormone genes.

S. Pulst, J. Korenberg, J. Graham, 1991, American journal of medical genetics.

Isolation and characterization of a candidate gene for progressive myoclonus epilepsy on 21q22.3.

K. Yamakawa, R. Hubert, X. Chen, 1995, Human molecular genetics.

Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12).

X. Chen, J. Korenberg, M. Geraghty, 2000, American journal of medical genetics.

Morphometry of anatomical shape complexes with dense deformations and sparse parameters

Guido Gerig, Alain Trouvé, Stanley Durrleman, 2014, NeuroImage.

6 – Chromosome Structure and Levels of Chromosome Organization

H. Ris, J. Korenberg, 1979 .

Giemsa technique for the detection of sister chromatid exchanges

J. Korenberg, E. Freedlender, 2004, Chromosoma.

Genetic marker family studies in familial Mediterranean fever (FMF) in Armenians

J. Korenberg, J. Rotter, G. Petersen, 1990, Clinical genetics.

The Human Lumican Gene

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

Stable ring chromosome 21: molecular and clinical definition of the lesion.

S. Pulst, J. Korenberg, D. Marshak, 1992, American journal of medical genetics.

Partial tetrasomy 21 in a male infant

X. Chen, J. Korenberg, L. Gaunt, 2000, Journal of medical genetics.

Confined placental chimerism: prenatal and postnatal cytogenetic and molecular analysis, and pregnancy outcome.

J. Korenberg, R. Schreck, T. Falik-Borenstein, 1994, American journal of medical genetics.

Sister chromatid differentiation in 5-bromo-2′-deoxyuridine-substituted chromosomes: A study with DNA-specific ligands and monoclonal antibody to histone H2B

J. Korenberg, J. Stockert, M. Ribas, 1994, Chromosome Research.

Prostaglandins E2 and E2 alpha are elevated in saliva of cystic fibrosis patients.

J. Korenberg, B. Rigas, W. Merrill, 1989, The American journal of gastroenterology.

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.

Targeted gene walking by low stringency polymerase chain reaction: assignment of a putative human brain sodium channel gene (SCN3A) to chromosome 2q24-31.

X. Chen, J. Korenberg, J. Andresen, 1994, Proceedings of the National Academy of Sciences of the United States of America.

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.

Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine.

B. Birren, L. Hui, X. Wu, 1999, Genome research.

Human cDNA mapping using a high-resolution R-banding technique and fluorescence in situ hybridization.

X. Chen, J. Korenberg, 1995, Cytogenetics and cell genetics.

Assignment of the human aggrecan gene (AGC1) to 15q26 using fluorescence in situ hybridization analysis.

X. Chen, J. Korenberg, P. Roughley, 1993, Genomics.

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.

Core Transcriptional Networks in Williams Syndrome: IGF1-PI3K-AKT-mTOR, MAPK and Actin Signaling at the Synapse Echo Autism.

J. Korenberg, R. Weiss, D. Dunn, 2021, Human molecular 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.

Gene structure and amino acid sequence of the human cone photoreceptor cGMP-phosphodiesterase alpha' subunit (PDEA2) and its chromosomal localization to 10q24.

J. Korenberg, D. Farber, J. Ye, 1995, Genomics.

Human lymphocyte-specific pp52 gene is a member of a highly conserved dispersed family.

C. Denny, X. Chen, J. Korenberg, 1993, Genomics.

DSCAM Deficiency Causes Loss of Pre-Inspiratory Neuron Synchroneity and Perinatal Death

K. Yamakawa, S. Itohara, J. Korenberg, 2009, The Journal of Neuroscience.

Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions.

J. Korenberg, D. Patterson, K. Gardiner, 1990, The EMBO journal.

Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype.

S. Pulst, J. Korenberg, T. Ikeuchi, 1990, American journal of human genetics.

BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21.

P. D. de Jong, M. Simon, R. Hubert, 1997, Genomics.

Down syndrome suppression of tumor growth and the role of the calcineurin inhibitor DSCR1

George Q. Daley, Julie R. Korenberg, Yoshiaki Okada, 2009, Nature.

Congenital gastric teratoma in Wiedemann-Beckwith syndrome.

J. Korenberg, J. Graham, L. Platt, 1991, American journal of medical genetics.

Physical and comparative mapping of distal mouse chromosome 16. 5 p5.

J. Korenberg, T. Wiltshire, R. Reeves, 1998, Genome research.

Title A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome Permalink

A. Galaburda, U. Bellugi, J. Korenberg, 2010 .

A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome

A. Galaburda, U. Bellugi, J. Korenberg, 2010, Journal of Neurodevelopmental Disorders.

Williams Syndrome: A Neurogenetic Model of Human Behavior

Allan L. Reiss, Ursula Bellugi, Julie R. Korenberg, 2006 .

Neural Correlates of Auditory Perception in Williams Syndrome: An fMRI Study

Gary H. Glover, Stephan Eliez, Allan L. Reiss, 2003, NeuroImage.

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.

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.

DSCAM: an endogenous promoter drives expression in the developing CNS and neural crest.

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

Use of a fluorescent-PCR reaction to detect genomic sequence copy number and transcriptional abundance.

D. Lashkari, J. Korenberg, D. Kurnit, 1996, Genome research.

Isolation and regional mapping of DNA sequences unique to human chromosome 21.

D. Cox, J. Korenberg, M. Croyle, 1987, American journal of human genetics.

Oxytocin and Vasopressin Are Dysregulated in Williams Syndrome, a Genetic Disorder Affecting Social Behavior

U. Bellugi, J. Korenberg, D. Slattery, 2012, PloS one.

From amplification to gene in thyroid cancer: a high-resolution mapped bacterial-artificial-chromosome resource for cancer chromosome aberrations guides gene discovery after comparative genome hybridization.

X. Chen, J. Korenberg, S. Chissoe, 1998, American journal of human genetics.

A high-fidelity physical map of human chromosome 21q in yeast artificial chromosomes.

X. Chen, J. Korenberg, D. Cohen, 1995, Genome research.

Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis.

C. Disteche, J. Korenberg, J R Korenberg, 1992, American journal of human genetics.

Using fluorescence in situ hybridization (FISH) in genome mapping.

X. Chen, J. Korenberg, T. Yang-Feng, 1992, Trends in biotechnology.

Down syndrome: toward a molecular definition of the phenotype.

C J Epstein, S. Pulst, C. Epstein, 2005, American journal of medical genetics. Supplement.

The Alzheimer amyloid precursor protein maps to human chromosome 21 bands q21.105-q21.05.

S. Pulst, J. Korenberg, R. Neve, 1989, Genomics.

Tetrasomy 21 pter-->q22.1 and Down syndrome: molecular definition of the region.

J. Korenberg, S. Schuffenhauer, R. Schipper, 1994, American journal of medical genetics.

The effect of BrdU incorporation on chromosome structure

H. Ris, J. Korenberg, 1975 .

The relationship between age and IQ in adults with Williams syndrome.

J. Korenberg, E. Klima, F. Rose, 2004, American journal of mental retardation : AJMR.

Protocols to establish genotype-phenotype correlations in Down syndrome.

E. Courchesne, C. Epstein, J. Korenberg, 1991, American journal of human genetics.

The social phenotype of Williams syndrome

U. Bellugi, J. Korenberg, A. Järvinen, 2013, Current Opinion in Neurobiology.

Characterization of a human chromosome 22 enriched bacterial artificial chromosome sublibrary.

M. Simon, X. Chen, J. Korenberg, 1995, Genetic analysis : biomolecular engineering.

VI. Genome Structure and Cognitive Map of Williams Syndrome

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

Mouse molecular cytogenetic resource: 157 BACs link the chromosomal and genetic maps.

B. Birren, X. Chen, J. Korenberg, 1999, Genome research.

Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia.

S. Pulst, J. Korenberg, D. Barker, 1991, American journal of medical genetics.

Molecular and cellular characterization of the Down syndrome critical region protein 2.

J. Korenberg, J. Vesa, D. Greenfield, 2005, Biochemical and biophysical research communications.

Intelligence in Williams Syndrome Is Related to STX1A, Which Encodes a Component of the Presynaptic SNARE Complex

E. Sobel, U. Bellugi, J. Korenberg, 2010, PloS one.

Localization of the human gene for fibulin-1 (FBLN1) to chromosome band 22q13.3.

X. Chen, J. Korenberg, W. Argraves, 1995, Cytogenetics and cell genetics.

Characterization of the human homologue of the mouse Tg737 candidate polycystic kidney disease gene.

X. Chen, J. Korenberg, L. Onuchic, 1995, Human molecular genetics.

3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry

Paul M. Thompson, Arthur W. Toga, Ming-Chang Chiang, 2007, NeuroImage.

Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer disease

S. Pulst, J. Korenberg, P. Fain, 1991, Human Genetics.

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.

A new HaeIII polymorphism at the D21S13 locus

S. Pulst, J. Korenberg, M. Ren, 1990, Human Genetics.

A new EcoRI polymorphism at the D21S13 locus

S. Pulst, J. Korenberg, M. Carbone, 1990, Human Genetics.

A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21.

J. Korenberg, G. Chenevix-Trench, J. Burn, 1993, American journal of human genetics.

Genomic organization, nucleotide sequence, biophysical properties, and localization of the voltage-gated K+ channel gene KCNA4/Kv1.4 to mouse chromosome 2/human 11p14 and mapping of KCNC1/Kv3.1 to mouse 7/human 11p14.3-p15.2 and KCNA1/Kv1.1 to human 12p13.

X. Chen, J. Korenberg, N. Copeland, 1994, Genomics.

Characterization of genomic and complementary DNA sequence of human C-reactive protein, and comparison with the complementary DNA sequence of serum amyloid P component.

J. Korenberg, A. Whitehead, P. Woo, 1985, The Journal of biological chemistry.

Cloning, characterization, and copy number of the murine survival motor neuron gene: homolog of the spinal muscular atrophy-determining gene.

J. Nadeau, X. Chen, J. Korenberg, 1997, Genome research.

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.

Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees: effects of marker allele frequencies on lod scores.

S. Pulst, J. Korenberg, P. Fain, 1993, American journal of medical genetics.

A bacterial artificial chromosome-based framework contig map of human chromosome 22q.

B. Birren, M. Simon, I. Dunham, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Cross-modal influences of affect across social and non-social domains in individuals with Williams syndrome

U. Bellugi, J. Korenberg, D. Mills, 2010, Neuropsychologia.

Formative Experiences: We Are Social – Therefore We Are: The Interplay of Mind, Culture, and Genetics in Williams Syndrome

U. Bellugi, J. Korenberg, J. Reilly, 2010 .

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 .

Deletion of 7q11.23 Genes and Williams Syndrome

A. Galaburda, U. Bellugi, C. Epstein, 2008 .

Nature and nurture: Williams syndrome across cultures.

U. Bellugi, J. Korenberg, N. Masataka, 2007, Developmental science.

Increased local gyrification mapped in Williams syndrome

Paul M. Thompson, Arthur W. Toga, Rebecca A. Dutton, 2006, NeuroImage.

“Everybody in the world is my friend” hypersociability in young children with Williams syndrome

Ursula Bellugi, U. Bellugi, J. Korenberg, 2004, American journal of medical genetics. Part A.

Affect, Social Behavior, and the Brain in Williams Syndrome

U. Bellugi, J. Korenberg, A. Reiss, 2007 .

A human neurodevelopmental model for Williams syndrome

Anders M. Dale, Fred H. Gage, Ursula Bellugi, 2016, Nature.

Relative sparing of primary auditory cortex in Williams Syndrome

Allan L. Reiss, Ursula Bellugi, Dorothy P. Holinger, 2005, Brain Research.

Down Syndrome Cell Adhesion Molecule is conserved in mouse and highly expressed in the adult mouse brain

G. Lyons, J. Korenberg, G. Barlow, 2002, Cytogenetic and Genome Research.

Serum amyloid A and P protein genes in familial Mediterranean fever.

J. Korenberg, J. Rotter, G. Petersen, 1990, Genomics.

Localization of the humanRGR opsin gene to chromosome 10q23

X. Chen, J. Korenberg, M. Jiang, 1996, Human Genetics.

Dentate gyrus mediates cognitive function in the Ts65Dn/DnJ mouse model of down syndrome

R. Kesner, J. Korenberg, Genevieve K. Smith, 2014, Hippocampus.

Isolation and chromosomal mapping of the human immunoglobulin-associated B29 gene (IGB).

A. A. Thompson, C. Denny, X. Chen, 1993, Genomics.

Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA.

L. Bolund, X. Chen, J. Korenberg, 1999, Genomics.

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

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

JH8, a gene highly homologous to the mouse jerky gene, maps to the region for childhood absence epilepsy on 8q24.

K. Yamakawa, X. Chen, J. Korenberg, 1998, Biochemical and biophysical research communications.

Rearrangement of chromosome 15 in the region q11.2----q12 in an individual with obesity syndrome and her normal mother.

T. Mohandas, J. Korenberg, D. Rimoin, 1990, American journal of medical genetics.

Reduced parietal and visual cortical activation during global processing in Williams syndrome

Ursula Bellugi, Dean Mobbs, Vinod Menon, 2007, Developmental medicine and child neurology.

A periodic tryptophan protein 2 gene homologue (PWP2H) in the candidate region of progressive myoclonus epilepsy on 21q22.3.

K. Yamakawa, J. Korenberg, D. Gao, 1996, Cytogenetics and cell genetics.

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.

Sensitivity of the Autonomic Nervous System to Visual and Auditory Affect Across Social and Non-Social Domains in Williams Syndrome

Benjamin R. Dering, U. Bellugi, J. Korenberg, 2012, Front. Psychology.

HAMILTON-JACOBI SKELETONS ON CORTICAL SURFACES WITH APPLICATIONS IN CHARACTERIZING THE GYRIFICATION PATTERN INWILLIAMS SYNDROME

Paul M. Thompson, Arthur W. Toga, Rebecca A. Dutton, 2007, 2007 4th IEEE International Symposium on Biomedical Imaging: From Nano to Macro.

Anomalous sylvian fissure morphology in Williams syndrome

Paul M. Thompson, Rebecca A. Dutton, Allan L. Reiss, 2006, NeuroImage.

To modulate or not to modulate: Differing results in uniquely shaped Williams syndrome brains

Allan L. Reiss, Ursula Bellugi, Mark A. Eckert, 2006, NeuroImage.

Use of 3-D cortical morphometry for mapping increased cortical gyrification and complexity in Williams syndrome

Paul M. Thompson, Arthur W. Toga, Rebecca A. Dutton, 2006, 3rd IEEE International Symposium on Biomedical Imaging: Nano to Macro, 2006..

Molecular mapping of the Down syndrome phenotype.

J. Korenberg, 1990, Progress in clinical and biological research.

The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17

S. Pulst, J. Korenberg, J. Graham, 1990, Human Genetics.

Molecular characterization of human neogenin, a DCC-related protein, and the mapping of its gene (NEO1) to chromosomal position 15q22.3-q23.

K. Yamakawa, X. Chen, J. Korenberg, 1997, Genomics.

The structure and chromosome location of the human chondroadherin gene (CHAD).

X. Chen, J. Korenberg, P. Roughley, 1997, Genomics.

Isolation, chromosomal localization, and sequence analysis of human chromosome 21 zinc finger domains.

X. Chen, J. Korenberg, Y. Bernstein, 1994, Genomics.

PCP4 maps between D21S345 and P31P10SP6 on chromosome 21q22.2-->q22.3.

R. Hubert, J. Korenberg, 1997, Cytogenetics and cell genetics.

Molecular cloning and chromosomal localization of one of the human glutamate receptor genes.

L. Hood, X. Chen, J. Korenberg, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Construction and characterization of a human chromosome 2-specific BAC library.

X. Chen, J. Korenberg, Q. Wu, 1994, Genomics.

Serial section registration of axonal confocal microscopy datasets for long-range neural circuit reconstruction

Tolga Tasdizen, Cameron Christensen, Elizabeth Jurrus, 2012, Journal of Neuroscience Methods.

Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes

A Mari, J. Korenberg, M. Digilio, 1999, Journal of medical genetics.

Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion

D. Cox, S. Pulst, C. Epstein, 1991, Human Genetics.

Structural integrity of the limbic–prefrontal connection: Neuropathological correlates of anxiety in Williams syndrome

E. Halgren, U. Bellugi, T. Brown, 2016, Social neuroscience.

Genome-Wide Analyses of Gene Expression in Williams Syndrome

J. Korenberg, 2009 .

rontostriatal Dysfunction During Response Inhibition n Williams Syndrome

A. Galaburda, U. Bellugi, J. Korenberg, 2006 .

Localization of human CREBBP (CREB binding protein) to 16p13.3 by fluorescence in situ hybridization.

X. Chen, J. Korenberg, 1995, Cytogenetics and Cell Genetics.

Molecular analysis of chromosome 21 in a patient with a phenotype of Down syndrome and apparently normal karyotype.

J. Korenberg, C. Wadelius, L. Zech, 1996, American journal of medical genetics.

Characterization of a highly conserved human homolog to the chicken neural cell surface protein Bravo/Nr-CAM that maps to chromosome band 7q31.

K. Yamakawa, X. Chen, J. Korenberg, 1996, Genomics.

A triple color FISH technique for mouse chromosome identification

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

Chromosome localization and RFLP analysis of PDC-E2: the major autoantigen of primary biliary cirrhosis.

J. Korenberg, R. Coppel, M. Patel, 1993, Autoimmunity.

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.

Down syndrome phenotypic mapping.

J. Korenberg, 1991, Progress in clinical and biological research.

Topology Preserving Atlas Construction from Shape Data without Correspondence Using Sparse Parameters

Guido Gerig, Alain Trouvé, Stanley Durrleman, 2012, MICCAI.

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.

Sensitivity of the Autonomic Nervous System to Visual and Auditory Affect Across Social and Non-Social Domains in Williams Syndrome

Benjamin R. Dering, U. Bellugi, J. Korenberg, 2012, Front. Psychology.

Quantitative representation and description of intravoxel fiber complexity in HARDI

J. Korenberg, E. Hsu, C. Chu, 2015, Physics in medicine and biology.

CHROMOSOME LOCALIZATION AND RFLP ANALYSIS OF CIRRHOSIS PDC-E2: THE MAJOR AUTOANTIGEN OF PRIMARY BILIARY

J. Korenberg, R. Coppel, M. Gershwin, 1993 .

Metrics for Uncertainty Analysis and Visualization of Diffusion Tensor Images

Raj Varma Kommaraju, Jeff M. Phillips, Chris R. Johnson, 2010, MIAR.

[Williams syndrome. A summary of cognitive, electrophysiological, anatomofunctional, microanatomical and genetic findings].

A. Galaburda, U. Bellugi, J. Korenberg, 2003, Revista de neurologia.

Formative Experiences: We Are Social – Therefore We Are: The Interplay of Mind, Culture, and Genetics in Williams Syndrome

U. Bellugi, J. Korenberg, J. Reilly, 2010 .