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Julie Korenberg

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Anna Järvinen; Julie R Korenberg; Dirk Neumann; Rowena Ng; Davide Crivelli; Benjamin Dering; Mark Grichanik; Ursula Bellugi
Sensitivity of the autonomic nervous system to visual and auditory affect across social and non-social domains in williams syndrome.
Anna Järvinen-Pasley; Ralph Adolphs; Anna Yam; Kiley J Hill; Mark Grichanik; Judy Reilly; Debra Mills; Allan L Reiss; Julie R Korenberg; Ursula Bellugi
Affiliative behavior in Williams syndrome: social perception and real-life social behavior.
Anna Järvinen-Pasley; Seth D Pollak; Anna Yam; Kiley J Hill; Mark Grichanik; Debra Mills; Allan L Reiss; Julie R Korenberg; Ursula Bellugi
Atypical hemispheric asymmetry in the perception of negative human vocalizations in individuals with Williams syndrome.

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All Publications

2012: Anna Järvinen; Julie R Korenberg; Dirk Neumann; Rowena Ng; Davide Crivelli; Benjamin Dering; Mark Grichanik; Ursula Bellugi
Sensitivity of the autonomic nervous system to visual and auditory affect across social and non-social domains in williams syndrome.
Frontiers in psychology 2012;3():343.
2010: Anna Järvinen-Pasley; Ralph Adolphs; Anna Yam; Kiley J Hill; Mark Grichanik; Judy Reilly; Debra Mills; Allan L Reiss; Julie R Korenberg; Ursula Bellugi
Affiliative behavior in Williams syndrome: social perception and real-life social behavior.
Neuropsychologia 2010;48(7):2110-9.
2010: Anna Järvinen-Pasley; Seth D Pollak; Anna Yam; Kiley J Hill; Mark Grichanik; Debra Mills; Allan L Reiss; Julie R Korenberg; Ursula Bellugi
Atypical hemispheric asymmetry in the perception of negative human vocalizations in individuals with Williams syndrome.
Neuropsychologia 2010;48(4):1047-52.
2010: Michael C Gao; Ursula Bellugi; Li Dai; Debra L Mills; Eric M Sobel; Kenneth Lange; Julie R Korenberg
Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex.
PloS one 2010;5(4):e10292.
2010: Anna Järvinen-Pasley; Bradley W Vines; Kiley J Hill; Anna Yam; Mark Grichanik; Debra Mills; Allan L Reiss; Julie R Korenberg; Ursula Bellugi
Cross-modal influences of affect across social and non-social domains in individuals with Williams syndrome.
Neuropsychologia 2010;48(2):456-66.
2008: Doron Gothelf; Yvonne M Searcy; Judy Reilly; Philip T Lai; Tope Lanre-Amos; Debra Mills; Julie R Korenberg; Albert Galaburda; Ursula Bellugi; Allan L Reiss
Association between cerebral shape and social use of language in Williams syndrome.
American journal of medical genetics. Part A 2008;146A(21):2753-61.
2008: Anna Järvinen-Pasley; Ursula Bellugi; Judy Reilly; Debra L Mills; Albert Galaburda; Allan L Reiss; Julie R Korenberg
Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.
Development and psychopathology 2008;20(1):1-35.
2007: Carol Zitzer-Comfort; Teresa Doyle; Nobuo Masataka; Julie R Korenberg; Ursula Bellugi
Nature and nurture: Williams syndrome across cultures.
Developmental science 2007;10(6):755-62.
2007: Fumiko Hoeft; Naama Barnea-Goraly; Brian W Haas; Golijeh Golarai; Derek Ng; Debra Mills; Julie R Korenberg; Ursula Bellugi; Albert M Galaburda; Allan L Reiss
More is not always better: increased fractional anisotropy of superior longitudinal fasciculus associated with poor visuospatial abilities in Williams syndrome.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2007;27(44):11960-5.
2007: Dean Mobbs; Mark A Eckert; Debra Mills; Julie R Korenberg; Ursula Bellugi; Albert M Galaburda; Allan L Reiss
Frontostriatal dysfunction during response inhibition in Williams syndrome.
Biological psychiatry 2007;62(3):256-61.
2007: Ming-Chang Chiang; Allan L Reiss; Agatha D Lee; Ursula Bellugi; Albert M Galaburda; Julie R Korenberg; Debra L Mills; Arthur W Toga; Paul M Thompson
3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry.
NeuroImage 2007;36(4):1096-109.
2007: Dean Mobbs; Mark A Eckert; Vinod Menon; Debra Mills; Julie R Korenberg; Albert M Galaburda; Fredric E Rose; Ursula Bellugi; Allan L Reiss
Reduced parietal and visual cortical activation during global processing in Williams syndrome.
Developmental medicine and child neurology 2007;49(6):433-8.
2006: Christian Gaser; Eileen Luders; Paul M Thompson; Agatha D Lee; Rebecca A Dutton; Jennifer A Geaga; Kiralee M Hayashi; Ursula Bellugi; Albert M Galaburda; Julie R Korenberg; Debra L Mills; Arthur W Toga; Allan L Reiss
Increased local gyrification mapped in Williams syndrome.
NeuroImage 2006;33(1):46-54.
2006: Mark A Eckert; Albert M Galaburda; Asya Karchemskiy; Alyssa Liang; Paul Thompson; Rebecca A Dutton; Agatha D Lee; Ursula Bellugi; Julie R Korenberg; Debra Mills; Fredric E Rose; Allan L Reiss
Anomalous sylvian fissure morphology in Williams syndrome.
NeuroImage 2006;33(1):39-45.
2006: Mark A Eckert; Adam Tenforde; Albert M Galaburda; Ursula Bellugi; Julie R Korenberg; Debra Mills; Allan L Reiss
To modulate or not to modulate: differing results in uniquely shaped Williams syndrome brains.
NeuroImage 2006;32(3):1001-7.
2006: Mark A Eckert; Albert M Galaburda; Debra L Mills; Ursula Bellugi; Julie R Korenberg; Allan L Reiss
The neurobiology of Williams syndrome: cascading influences of visual system impairment?
Cellular and molecular life sciences : CMLS 2006;63(16):1867-75.
2006: Guimei Yao; Xiao-Ning Chen; Laura Flores-Sarnat; Gillian M Barlow; Giandomenico Palka; John B Moeschler; Barbara McGillivray; Richard P Morse; Julie R Korenberg
Deletion of chromosome 21 disturbs human brain morphogenesis.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(1):1-7.
2005: Paul M Thompson; Agatha D Lee; Rebecca A Dutton; Jennifer A Geaga; Kiralee M Hayashi; Mark A Eckert; Ursula Bellugi; Albert M Galaburda; Julie R Korenberg; Debra L Mills; Arthur W Toga; Allan L Reiss
Abnormal cortical complexity and thickness profiles mapped in Williams syndrome.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2005;25(16):4146-58.
2005: Dorothy P Holinger; Ursula Bellugi; Debra L Mills; Julie R Korenberg; Allan L Reiss; Gordon F Sherman; Albert M Galaburda
Relative sparing of primary auditory cortex in Williams Syndrome.
Brain research 2005;1037(1-2):35-42.
2005: Jouni Vesa; Ying Brown; Danielle Greenfield; Julie R Korenberg
Molecular and cellular characterization of the Down syndrome critical region protein 2.
Biochemical and biophysical research communications 2005;328(1):235-42.
2005: Mark A Eckert; D Hu; Stephan Eliez; Ursula Bellugi; Albert M Galaburda; Julie R Korenberg; Debra Mills; Allan L Reiss
Evidence for superior parietal impairment in Williams syndrome.
Neurology 2005;64(1):152-3.
2004: Yvonne M Searcy; Alan Lincoln; Fredric E Rose; Edward S Klima; Nasim Bavar; Julie R Korenberg
The relationship between age and IQ in adults with Williams syndrome.
American journal of mental retardation : AJMR 2004;109(3):231-6.
2004: Teresa F Doyle; Ursula Bellugi; Julie R Korenberg; John Graham
"Everybody in the world is my friend" hypersociability in young children with Williams syndrome.
American journal of medical genetics. Part A 2004;124A(3):263-73.
2004: Xiao-Ning Chen; Julie R Korenberg
BAC mapping using fluorescence in situ hybridization.
Methods in molecular biology (Clifton, N.J.) 2004;255():131-41.
2003: Geoffroy Golfier; Frédéric Chibon; Alain Aurias; Xiao-Ning Chen; Julie R Korenberg; Jean Rossier; Marie-Claude Potier
The 200-kb segmental duplication on human chromosome 21 originates from a pericentromeric dissemination involving human chromosomes 2, 18 and 13.
Gene 2003;312():51-9.
2003: Hamao Hirota; Rumiko Matsuoka; Xiao-Ning Chen; Lora S Salandanan; Alan Lincoln; Fredric E Rose; Mariko Sunahara; Makiko Osawa; Ursula Bellugi; Julie R Korenberg
Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23.
Genetics in medicine : official journal of the American College of Medical Genetics 2003;5(4):311-21.
2003: Sheryl M Gough; Margaret McDonald; Xiao-Ning Chen; Julie R Korenberg; Antonino Neri; Tomas Kahn; Michael Eccles; Christine Morris
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.
BMC genomics 2003;4(1):9.
2003: Albert M Galaburda; Dorothy P Holinger; D Mills; A Reiss; Julie R Korenberg; Ursula Bellugi
[Williams syndrome. A summary of cognitive, electrophysiological, anatomofunctional, microanatomical and genetic findings].
Revista de neurologia 2003;36 Suppl 1():S132-7.
2003: Daniel J Levitin; Vinod Menon; J Eric Schmitt; Stephan Eliez; Christopher D White; Gary H Glover; Jay Kadis; Julie R Korenberg; Ursula Bellugi; Allan L Reiss
Neural correlates of auditory perception in Williams syndrome: an fMRI study.
NeuroImage 2003;18(1):74-82.
2002: Gillian M Barlow; Gary E Lyons; James A Richardson; Harvey B Sarnat; Julie R Korenberg
DSCAM: an endogenous promoter drives expression in the developing CNS and neural crest.
Biochemical and biophysical research communications 2002;299(1):1-6.
2002: Gillian M Barlow; Bruce Micales; Xiao-Ning Chen; Gary E Lyons; Julie R Korenberg
Mammalian DSCAMs: roles in the development of the spinal cord, cortex, and cerebellum?
Biochemical and biophysical research communications 2002;293(3):881-91.
2002: Colyn B Cargile; Denise Li-Meng Goh; Barbara K Goodman; Xiao-Ning Chen; Julie R Korenberg; Gregg L Semenza; George H Thomas
Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.
American journal of medical genetics 2002;109(2):133-8.
2002: Xiao-Ning Chen; Julie R Korenberg
BAC resource for molecular cytogenetics.
Methods in molecular biology (Clifton, N.J.) 2002;204():391-403.
2001: Octavian Henegariu; Judit Dunai; Xiao-Ning Chen; Julie R Korenberg; David C Ward; John M Greally
A triple color FISH technique for mouse chromosome identification.
Mammalian genome : official journal of the International Mammalian Genome Society 2001;12(6):462-5.
2001: Octavian Henegariu; S Artan; John M Greally; Xiao-Ning Chen; Julie R Korenberg; Gail H Vance; L Stubbs; Patricia Bray-Ward; David C Ward
Cryptic translocation identification in human and mouse using several telomeric multiplex fish (TM-FISH) strategies.
Laboratory investigation; a journal of technical methods and pathology 2001;81(4):483-91.
2001: Gillian M Barlow; Xiao-Ning Chen; Z Y Shi; Gary E Lyons; D M Kurnit; L Celle; Nancy B Spinner; Elaine Zackai; M J Pettenati; A J Van Riper; M J Vekemans; Corey H Mjaatvedt; Julie R Korenberg
Down syndrome congenital heart disease: a narrowed region and a candidate gene.
Genetics in medicine : official journal of the American College of Medical Genetics 2001;3(2):91-101.
2001: Cathy M Tuck-Muller; Barbara K Goodman; Shibo Li; Jose E Martinez; Xiao-Ning Chen; Wladimir Wertelecki; Julie R Korenberg; Gail Stetten
Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel.
Genetics in medicine : official journal of the American College of Medical Genetics 2001;3(2):126-31.
2001: Gillian M Barlow; Bruce Micales; Gary E Lyons; Julie R Korenberg
Down syndrome cell adhesion molecule is conserved in mouse and highly expressed in the adult mouse brain.
Cytogenetics and cell genetics 2001;94(3-4):155-62.
2000: Gregory D Ferguson; Xiao-Ning Chen; Julie R Korenberg; Harvey R Herschman
The human synaptotagmin IV gene defines an evolutionary break point between syntenic mouse and human chromosome regions but retains ligand inducibility and tissue specificity.
The Journal of biological chemistry 2000;275(47):36920-6.
2000: AM Slavotinek; Xiao-Ning Chen; A Jackson; L Gaunt; A Campbell; Jill Clayton-Smith; Julie R Korenberg
Partial tetrasomy 21 in a male infant.
Journal of medical genetics 2000;37(10):E30.
2000: Colyn B Cargile; Iain McIntosh; MV Clough; Julie Rutberg; Reza Yaghmai; Barbara K Goodman; Xiao-Ning Chen; Julie R Korenberg; George H Thomas; Michael T Geraghty
Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12).
American journal of medical genetics 2000;92(5):328-35.
2000: Julie R Korenberg; Xiao-Ning Chen; Hamao Hirota; Z Lai; Ursula Bellugi; D Burian; B Roe; R Matsuoka
VI. Genome structure and cognitive map of Williams syndrome.
Journal of cognitive neuroscience 2000;12 Suppl 1():89-107.
1999: Julie R Korenberg; Xiao-Ning Chen; Z Sun; Z Y Shi; S Ma; E Vataru; D Yimlamai; J S Weissenbach; H Shizuya; MI Simon; S S Gerety; H Nguyen; I S Zemsteva; L Hui; J Silva; X Wu; Bruce Birren; T J Hudson
Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine.
Genome research 1999;9(10):994-1001.
1999: Jeffrey A Knauf; R Elisei; Daria Mochly-Rosen; Tamar Liron; Xiao-Ning Chen; R Gonsky; Julie R Korenberg; James A Fagin
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.
The Journal of biological chemistry 1999;274(33):23414-25.
1999: Peter Ianakiev; Michael W Kilpatrick; C Dealy; R Kosher; Julie R Korenberg; Xiao-Ning Chen; Petros Tsipouras
A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24.
Biochemical and biophysical research communications 1999;261(1):64-70.
1999: Julie R Korenberg; Xiao-Ning Chen; K L Devon; D Noya; M L Oster-Granite; Bruce Birren
Mouse molecular cytogenetic resource: 157 BACs link the chromosomal and genetic maps.
Genome research 1999;9(5):514-23.
1999: Ursula Bellugi; L Lichtenberger; D Mills; Albert M Galaburda; Julie R Korenberg
Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome.
Trends in neurosciences 1999;22(5):197-207.
1999: Xiuqing Zhang; Huanming Yang; Morten J Corydon; X Zhang; S Pedersen; Julie R Korenberg; Xiao-Ning Chen; J Laporte; Niels Gregersen; Erik Niebuhr; G Liu; Lars Bolund
Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA.
Genomics 1999;57(1):144-51.
1998: Deborah E Cabin; J W McKee-Johnson; LE Matesic; Timothy Wiltshire; EE Rue; A E Mjaatvedt; Y K Huo; Julie R Korenberg; Roger H Reeves
Physical and comparative mapping of distal mouse chromosome 16. 5 p5.
Genome research 1998;8(9):940-50.
1998: X Chen; Jeffrey A Knauf; R Gonsky; M Wang; E H Lai; S Chissoe; James A Fagin; Julie R Korenberg
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.
American journal of human genetics 1998;63(2):625-37.
1998: Ryoji Morita; E Miyazaki; Chung Yan Fong; Xiao-Ning Chen; Julie R Korenberg; Antonio V Delgado-Escueta; Kazuhiro Yamakawa
JH8, a gene highly homologous to the mouse jerky gene, maps to the region for childhood absence epilepsy on 8q24.
Biochemical and biophysical research communications 1998;248(2):307-14.
1998: Kazuhiro Yamakawa; Y K Huot; M A Haendelt; RS Hubert; Xiao-Ning Chen; Gary E Lyons; Julie R Korenberg
DSCAM: a novel member of the immunoglobulin superfamily maps in a Down syndrome region and is involved in the development of the nervous system.
Human molecular genetics 1998;7(2):227-37.
1998: Xiao-Ning Chen; Z Y Shi; Julie R Korenberg; A Sehgal
Assignment of the GOV (Glioblastoma overexpressed) gene to human chromosome band 19p13.2 by fluorescence in situ hybridization.
Cytogenetics and cell genetics 1998;83(3-4):230-1.
1997: J Grover; Xiao-Ning Chen; Julie R Korenberg; P J Roughley
The structure and chromosome location of the human chondroadherin gene (CHAD).
Genomics 1997;45(2):379-85.
1997: T Nechiporuk; Alex Nechiporuk; S Sahba; Karla P Figueroa; H Shibata; Xiao-Ning Chen; Julie R Korenberg; P de Jong; Stef pulst
A high-resolution PAC and BAC map of the SCA2 region.
Genomics 1997;44(3):321-9.
1997: J Vielmetter; Xiao-Ning Chen; Frank Miskevich; R P Lane; K Yamakawa; Julie R Korenberg; WJ Dreyer
Molecular characterization of human neogenin, a DCC-related protein, and the mapping of its gene (NEO1) to chromosomal position 15q22.3-q23.
Genomics 1997;41(3):414-21.
1997: RS Hubert; S Mitchell; Xiao-Ning Chen; K Ekmekji; C Gadomski; Z Sun; D Noya; U J Kim; C Chen; H Shizuya; M Simon; P J de Jong; Julie R Korenberg
BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21.
Genomics 1997;41(2):218-26.
1997: CJ DiDonato; Xiao-Ning Chen; D Noya; Julie R Korenberg; J H Nadeau; Louise R Simard
Cloning, characterization, and copy number of the murine survival motor neuron gene: homolog of the spinal muscular atrophy-determining gene.
Genome research 1997;7(4):339-52.
1997: Julie R Korenberg; Jaakko Aaltonen; C Brahe; Deborah E Cabin; N Creau; Jean-Maurice Delabar; J Doering; Katheleen Gardiner; RS Hubert; JH Ives; AM Kessling; J Kudoh; R Lafrenière; Y Murakami; M Ohira; M Ohki; D Patterson; Marie-Claude Potier; John Quackenbush; Roger H Reeves; Y Sakaki; N Shimizu; E Soeda; Christine Van Broeckhoven; Marie-Laure Yaspo
Report and abstracts of the Sixth International Workshop on Human Chromosome 21 Mapping 1996. Cold Spring Harbor, New York, USA. May 6-8,1996.
Cytogenetics and cell genetics 1997;79(1-2):21-52.
1997: RS Hubert; Julie R Korenberg
PCP4 maps between D21S345 and P31P10SP6 on chromosome 21q22.2-->q22.3.
Cytogenetics and cell genetics 1997;78(1):44-5.
1996: J Grover; Xiao-Ning Chen; Julie R Korenberg; A D Recklies; Peter J Roughley
The gene organization, chromosome location, and expression of a 55-kDa matrix protein (PRELP) of human articular cartilage.
Genomics 1996;38(2):109-17.
1996: Stef pulst; Alex Nechiporuk; T Nechiporuk; Suzana Gispert; Xiao-Ning Chen; I Lopes-Cendes; S Pearlman; S Starkman; G Orozco-Diaz; A Lunkes; P DeJong; G A Rouleau; Georg Auburger; Julie R Korenberg; C Figueroa; S Sahba
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
Nature genetics 1996;14(3):269-76.
1996: M L Haldi; C Strickland; P Lim; V VanBerkel; X Chen; D Noya; Julie R Korenberg; Z Husain; J Miller; Eric S Lander
A comprehensive large-insert yeast artificial chromosome library for physical mapping of the mouse genome.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(10):767-9.
1996: R P Lane; Xiao-Ning Chen; K Yamakawa; J Vielmetter; Julie R Korenberg; W J Dreyer
Characterization of a highly conserved human homolog to the chicken neural cell surface protein Bravo/Nr-CAM that maps to chromosome band 7q31.
Genomics 1996;35(3):456-65.
1996: UJ Kim; H Shizuya; H L Kang; S S Choi; C L Garrett; L J Smink; Bruce Birren; Julie R Korenberg; Carl Bruder; M I Simon
A bacterial artificial chromosome-based framework contig map of human chromosome 22q.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(13):6297-301.
1996: J M Bronstein; C A Kozak; Xiao-Ning Chen; S Wu; Michael Danciger; Julie R Korenberg; Debora B Farber
Chromosomal localization of murine and human oligodendrocyte-specific protein genes.
Genomics 1996;34(2):255-7.
1996: Xiao-Ning Chen; Julie R Korenberg; M Jiang; D Shen; H K Fong
Localization of the human RGR opsin gene to chromosome 10q23.
Human genetics 1996;97(6):720-2.
1996: Bruce Birren; Y Tachi-iri; UJ Kim; M Nguyen; H Shizuya; Julie R Korenberg; M I Simon
A human chromosome 22 fosmid resource: mapping and analysis of 96 clones.
Genomics 1996;34(1):97-106.
1996: T Nechiporuk; Alex Nechiporuk; X Guan; R Frederick; Karla P Figueroa; I Chumakov; Julie R Korenberg; P J de Jong; Stef pulst
Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical map.
Human genetics 1996;97(4):462-7.
1996: K Yamakawa; D Q Gao; Julie R Korenberg
A periodic tryptophan protein 2 gene homologue (PWP2H) in the candidate region of progressive myoclonus epilepsy on 21q22.3.
Cytogenetics and cell genetics 1996;74(1-2):140-5.
1995: Julie R Korenberg; Xiao-Ning Chen; S Mitchell; S Fannin; S Gerwehr; D Cohen; I Chumakov
A high-fidelity physical map of human chromosome 21q in yeast artificial chromosomes.
Genome research 1995;5(5):427-43.
1995: UJ Kim; H Shizuya; Xiao-Ning Chen; L Deaven; S Speicher; J Solomon; Julie R Korenberg; M I Simon
Characterization of a human chromosome 22 enriched bacterial artificial chromosome sublibrary.
Genetic analysis : biomolecular engineering 1995;12(2):73-9.
1995: S Bhatt; R Schreck; John M Graham; Julie R Korenberg; C G Hurvitz; Nathan Fischel-Ghodsian
Transient leukemia with trisomy 21: description of a case and review of the literature.
American journal of medical genetics 1995;58(4):310-4.
1995: Julie R Korenberg; Xiao-Ning Chen; M D Adams; J C Venter
Toward a cDNA map of the human genome.
Genomics 1995;29(2):364-70.
1995: J Grover; Xiao-Ning Chen; Julie R Korenberg; Peter J Roughley
The human lumican gene. Organization, chromosomal location, and expression in articular cartilage.
The Journal of biological chemistry 1995;270(37):21942-9.
1995: Yijun Zhu; Chao Qi; Julie R Korenberg; Xiao-Ning Chen; D Noya; M Sambasiva Rao; Janardan K Reddy
Structural organization of mouse peroxisome proliferator-activated receptor gamma (mPPAR gamma) gene: alternative promoter use and different splicing yield two mPPAR gamma isoforms.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(17):7921-5.
1995: Natik I Piriev; A S Viczian; J Ye; B Kerner; Julie R Korenberg; Debora B Farber
Gene structure and amino acid sequence of the human cone photoreceptor cGMP-phosphodiesterase alpha' subunit (PDEA2) and its chromosomal localization to 10q24.
Genomics 1995;28(3):429-35.
1995: UJ Kim; H Shizuya; L Deaven; Xiao-Ning Chen; Julie R Korenberg; M I Simon
Selection of a sublibrary enriched for a chromosome from total human bacterial artificial chromosome library using DNA from flow sorted chromosomes as hybridization probes.
Nucleic acids research 1995;23(10):1838-9.
1995: K Yamakawa; S Mitchell; RS Hubert; Xiao-Ning Chen; S Colbern; Y K Huo; C Gadomski; UJ Kim; Julie R Korenberg
Isolation and characterization of a candidate gene for progressive myoclonus epilepsy on 21q22.3.
Human molecular genetics 1995;4(4):709-16.
1995: Julie R Korenberg; Xiao-Ning Chen; H Tran; Scott Argraves
Localization of the human gene for fibulin-1 (FBLN1) to chromosome band 22q13.3.
Cytogenetics and cell genetics 1995;68(3-4):192-3.
1995: Julie R Korenberg; Xiao-Ning Chen
Human cDNA mapping using a high-resolution R-banding technique and fluorescence in situ hybridization.
Cytogenetics and cell genetics 1995;69(3-4):196-200.
1995: Xiao-Ning Chen; Julie R Korenberg
Localization of human CREBBP (CREB binding protein) to 16p13.3 by fluorescence in situ hybridization.
Cytogenetics and cell genetics 1995;71(1):56-7.
1994: M Wang; Xiao-Ning Chen; S Shouse; J Manson; Q Wu; R Li; J Wrestler; D Noya; Z G Sun; Julie R Korenberg
Construction and characterization of a human chromosome 2-specific BAC library.
Genomics 1994;24(3):527-34.
1994: Robert Sztrolovics; Xiao-Ning Chen; J Grover; Peter J Roughley; Julie R Korenberg
Localization of the human fibromodulin gene (FMOD) to chromosome 1q32 and completion of the cDNA sequence.
Genomics 1994;23(3):715-7.
1994: Julie R Korenberg; Kelley M Argraves; Xiao-Ning Chen; H Tran; Dudley K Strickland; Scott Argraves
Chromosomal localization of human genes for the LDL receptor family member glycoprotein 330 (LRP2) and its associated protein RAP (LRPAP1).
Genomics 1994;22(1):88-93.
1994: Julie R Korenberg; Xiao-Ning Chen; R Schipper; Z Sun; Rivkah Gonsky; S Gerwehr; N Carpenter; C Daumer; P Dignan; C Disteche
Down syndrome phenotypes: the consequences of chromosomal imbalance.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(11):4997-5001.
1994: T C Falik-Borenstein; Julie R Korenberg; R R Schreck
Confined placental chimerism: prenatal and postnatal cytogenetic and molecular analysis, and pregnancy outcome.
American journal of medical genetics 1994;50(1):51-6.
1993: J Sainz; M Rasmussen; Alex Nechiporuk; Henrik Vissing; X Cheng; Julie R Korenberg; Stef pulst
Dinucleotide repeat polymorphism at the D22S351 locus.
Human molecular genetics 1993;2(10):1749.
1993: Alex Nechiporuk; P Fain; E Kort; L E Nee; E Frommelt; R J Polinsky; Julie R Korenberg; Stef pulst
Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees: effects of marker allele frequencies on lod scores.
American journal of medical genetics 1993;48(1):63-6.
1993: Julie R Korenberg; Xiao-Ning Chen; K Doege; J Grover; Peter J Roughley
Assignment of the human aggrecan gene (AGC1) to 15q26 using fluorescence in situ hybridization analysis.
Genomics 1993;16(2):546-8.
1993: W J Wood; AA Thompson; Julie R Korenberg; Xiao-Ning Chen; William A. May; Randolph Wall; Christopher T Denny
Isolation and chromosomal mapping of the human immunoglobulin-associated B29 gene (IGB).
Genomics 1993;16(1):187-92.
1993: William A. May; Julie R Korenberg; Xiao-Ning Chen; L Lunsford; W J Wood; A Thompson; Randolph Wall; Christopher T Denny
Human lymphocyte-specific pp52 gene is a member of a highly conserved dispersed family.
Genomics 1993;15(3):515-20.
1993: Julie R Korenberg
Toward a molecular understanding of Down syndrome.
Progress in clinical and biological research 1993;384():87-115.
1992: Thomas Wilkie; D J Gilbert; Anne S Olsen; Xiao-Ning Chen; T T Amatruda; Julie R Korenberg; Barbara J Trask; P de Jong; Randall R Reed; M I Simon
Evolution of the mammalian G protein alpha subunit multigene family.
Nature genetics 1992;1(2):85-91.
1992: Julie R Korenberg; C Bradley; C M Disteche
Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis.
American journal of human genetics 1992;50(2):294-302.
1992: T C Falik-Borenstein; T M Pribyl; Stef pulst; Daniel L Van Dyke; L Weiss; M L Chu; J Kraus; D Marshak; Julie R Korenberg
Stable ring chromosome 21: molecular and clinical definition of the lesion.
American journal of medical genetics 1992;42(1):22-8.
1991: Stef pulst; T Yang-Feng; Julie R Korenberg
Relative order and location of DNA sequences on chromosome 21 linked to familial Alzheimer disease.
American journal of medical genetics 1991;41(4):454-9.
1991: Stef pulst; V M Riccardi; P Fain; Julie R Korenberg
Familial spinal neurofibromatosis: clinical and DNA linkage analysis.
Neurology 1991;41(12):1923-7.
1991: C Puckett; C M Gomez; Julie R Korenberg; H Tung; T J Meier; Xiao-Ning Chen; Leroy Hood
Molecular cloning and chromosomal localization of one of the human glutamate receptor genes.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(17):7557-61.
1991: Stef pulst; T Pribyl; David Barker; V M Riccardi; M Ren; H Yaari; Julie R Korenberg
Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia.
American journal of medical genetics 1991;40(1):84-7.
1991: Julie R Korenberg; D K Kalousek; G Anneren; Stef pulst; J G Hall; C J Epstein; D R Cox
Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion.
Human genetics 1991;87(2):112-8.
1991: Stef pulst; P Fain; V Cohn; L E Nee; R J Polinsky; Julie R Korenberg
Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer disease.
Human genetics 1991;87(2):159-61.
1991: T C Falik-Borenstein; Julie R Korenberg; I Davos; L D Platt; S Gans; B Goodman; R Schreck; J M Graham
Congenital gastric teratoma in Wiedemann-Beckwith syndrome.
American journal of medical genetics 1991;38(1):52-7.
1990: Tamy Shohat; Mordechai Shohat; G M Petersen; R S Sparkes; D Langfield; J Bickal; Julie R Korenberg; A D Schwabe; Jerome I Rotter
Genetic marker family studies in familial Mediterranean fever (FMF) in Armenians.
Clinical genetics 1990;38(5):332-9.
1990: Mordechai Shohat; Tamy Shohat; David L Rimoin; T Mohandas; John R Heckenlively; R Ellen Magenis; M B Davidson; Julie R Korenberg
Rearrangement of chromosome 15 in the region q11.2----q12 in an individual with obesity syndrome and her normal mother.
American journal of medical genetics 1990;37(2):173-7.
1990: Stef pulst; Julie R Korenberg; M Ren; J Greenwald
A new HaeIII polymorphism at the D21S13 locus.
Human genetics 1990;85(6):671.
1990: Mordechai Shohat; Tamy Shohat; Jerome I Rotter; M Schlesinger; G M Petersen; T Pribyl; GEORGE SACK; A D Schwabe; Julie R Korenberg
Serum amyloid A and P protein genes in familial Mediterranean fever.
Genomics 1990;8(1):83-9.
1990: Julie R Korenberg; H Kawashima; Stef pulst; T Ikeuchi; N Ogasawara; K Yamamoto; S A Schonberg; R West; L Allen; E Magenis
Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype.
American journal of human genetics 1990;47(2):236-46.
1990: Stef pulst; J M Graham; P Fain; David Barker; T Pribyl; Julie R Korenberg
The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17.
Human genetics 1990;85(1):12-4.
1990: Stef pulst; Julie R Korenberg; J Greenwald; M Carbone
A new EcoRI polymorphism at the D21S13 locus.
Human genetics 1990;84(6):580.
1990: Julie R Korenberg; H Kawashima; Stef pulst; L Allen; E Magenis; C J Epstein
Down syndrome: toward a molecular definition of the phenotype.
American journal of medical genetics. Supplement 1990;7():91-7.
1990: Julie R Korenberg
Molecular mapping of the Down syndrome phenotype.
Progress in clinical and biological research 1990;360():105-15.
1990: Stef pulst; Julie R Korenberg
Panel of aneuploid cell lines for physical mapping of the proximal long arm of human chromosome 21.
American journal of medical genetics. Supplement 1990;7():137-40.
1989: M Shohat; Julie R Korenberg; A D Schwabe; J I Rotter
Hypothesis: familial Mediterranean fever--a genetic disorder of the lipocortin family?
American journal of medical genetics 1989;34(2):163-7.
1989: Julie R Korenberg; Stef pulst; R L Neve; R West
The Alzheimer amyloid precursor protein maps to human chromosome 21 bands q21.105-q21.05.
Genomics 1989;5(1):124-7.
1988: Julie R Korenberg; M C Rykowski
Human genome organization: Alu, lines, and the molecular structure of metaphase chromosome bands.
Cell 1988;53(3):391-400.