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Papers authored by Korenberg JR

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Down syndrome: The crucible for treating genomic imbalance.

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Korenberg JR

Genetics in medicine : official journal of the American College of Medical Genetics 11(9):617-9, 2009 Sep - Who cited this? | PubMed ID: 19690507 | Fulltext

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

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Korbel JO, Tirosh-Wagner T, Urban AE, Chen XN, Kasowski M, Dai L, Grubert F, Erdman C, Gao MC, Lange K, Sobel EM, Barlow GM, Aylsworth AS, Carpenter NJ, Clark RD, Cohen MY,

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Proceedings of the National Academy of Sciences of the United States of America 106(29):12031-6, 2009 Jul 21 - Who cited this? | PubMed ID: 19597142 | Fulltext

Down's syndrome suppression of tumour growth and the role of the calcineurin inhibitor DSCR1.

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Baek KH, Zaslavsky A, Lynch RC, Britt C, Okada Y, Siarey RJ, Lensch MW, Park IH, Yoon SS, Minami T, Korenberg JR, Folkman J, Daley GQ, Aird WC, Galdzicki Z, and Ryeom S

Nature 459(7250):1126-30, 2009 Jun 25 - Who cited this? | PubMed ID: 19458618 | Fulltext

DSCAM deficiency causes loss of pre-inspiratory neuron synchroneity and perinatal death.

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Amano K, Fujii M, Arata S, Tojima T, Ogawa M, Morita N, Shimohata A, Furuichi T, Itohara S, Kamiguchi H, Korenberg JR, Arata A, and Yamakawa K

The Journal of neuroscience : the official journal of the Society for Neuroscience 29(9):2984-96, 2009 Mar 4 - Who cited this? | PubMed ID: 19261893 | Fulltext

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

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Dai L, Bellugi U, Chen XN, Pulst-Korenberg AM, Järvinen-Pasley A, Tirosh-Wagner T, Eis PS, Graham J, Mills D, Searcy Y, and Korenberg JR

American journal of medical genetics. Part A 149A(3):302-14, 2009 Feb 1 - Who cited this? | PubMed ID: 19205026 | Fulltext

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

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Collette JC, Chen XN, Mills DL, Galaburda AM, Reiss AL, Bellugi U, and Korenberg JR

Journal of human genetics 54(4):193-8, 2009 - Who cited this? | PubMed ID: 19282872 | Fulltext

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

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Gothelf D, Searcy YM, Reilly J, Lai PT, Lanre-Amos T, Mills D, Korenberg JR, Galaburda A, Bellugi U, and Reiss AL

American journal of medical genetics. Part A 146A(21):2753-61, 2008 Nov 1 - Who cited this? | PubMed ID: 18924169 | Fulltext

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

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Järvinen-Pasley A, Bellugi U, Reilly J, Mills DL, Galaburda A, Reiss AL, and Korenberg JR

Development and psychopathology 20(1):1-35, 2008 - Who cited this? | PubMed ID: 18211726 | Fulltext

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

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Chiang MC, Reiss AL, Lee AD, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, and Thompson PM

NeuroImage 36(4):1096-109, 2007 Jul 15 - Who cited this? | PubMed ID: 17512756 | Fulltext

Anomalous sylvian fissure morphology in Williams syndrome.

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Eckert MA, Galaburda AM, Karchemskiy A, Liang A, Thompson P, Dutton RA, Lee AD, Bellugi U, Korenberg JR, Mills D, Rose FE, and Reiss AL

NeuroImage 33(1):39-45, 2006 Oct 15 - Who cited this? | PubMed ID: 16876437 | Fulltext

Increased local gyrification mapped in Williams syndrome.

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Gaser C, Luders E, Thompson PM, Lee AD, Dutton RA, Geaga JA, Hayashi KM, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, and Reiss AL

NeuroImage 33(1):46-54, 2006 Oct 15 - Who cited this? | PubMed ID: 16901723 | Fulltext

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

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Eckert MA, Tenforde A, Galaburda AM, Bellugi U, Korenberg JR, Mills D, and Reiss AL

NeuroImage 32(3):1001-7, 2006 Sep - Who cited this? | PubMed ID: 16806978 | Fulltext

The neurobiology of Williams syndrome: cascading influences of visual system impairment?.

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Eckert MA, Galaburda AM, Mills DL, Bellugi U, Korenberg JR, and Reiss AL

Cellular and molecular life sciences : CMLS 63(16):1867-75, 2006 Aug - Who cited this? | PubMed ID: 16810457 | Fulltext

Deletion of chromosome 21 disturbs human brain morphogenesis.

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Yao G, Chen XN, Flores-Sarnat L, Barlow GM, Palka G, Moeschler JB, McGillivray B, Morse RP, and Korenberg JR

Genetics in medicine : official journal of the American College of Medical Genetics 8(1):1-7, 2006 Jan - Who cited this? | PubMed ID: 16418593 | Fulltext

Abnormal cortical complexity and thickness profiles mapped in Williams syndrome.

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Thompson PM, Lee AD, Dutton RA, Geaga JA, Hayashi KM, Eckert MA, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, and Reiss AL

The Journal of neuroscience : the official journal of the Society for Neuroscience 25(16):4146-58, 2005 Apr 20 - Who cited this? | PubMed ID: 15843618 | Fulltext

Relative sparing of primary auditory cortex in Williams Syndrome.

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Holinger DP, Bellugi U, Mills DL, Korenberg JR, Reiss AL, Sherman GF, and Galaburda AM

Brain research 1037(1-2):35-42, 2005 Mar 10 - Who cited this? | PubMed ID: 15777750 | Fulltext

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

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Vesa J, Brown Y, Greenfield D, and Korenberg JR

Biochemical and biophysical research communications 328(1):235-42, 2005 Mar 4 - Who cited this? | PubMed ID: 15670775 | Fulltext

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

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Searcy YM, Lincoln AJ, Rose FE, Klima ES, Bavar N, and Korenberg JR

American journal of mental retardation : AJMR 109(3):231-6, 2004 May - Who cited this? | PubMed ID: 15072519 | Fulltext

"Everybody in the world is my friend" hypersociability in young children with Williams syndrome.

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Doyle TF, Bellugi U, Korenberg JR, and Graham J

American journal of medical genetics. Part A 124(3):263-73, 2004 Jan 30 - Who cited this? | PubMed ID: 14708099 | Fulltext

BAC mapping using fluorescence in situ hybridization.

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Chen XN and Korenberg JR

Methods in molecular biology (Clifton, N.J.) 255:131-41, 2004 - Who cited this? | PubMed ID: 15020820 | Fulltext

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.

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Gough SM, McDonald M, Chen XN, Korenberg JR, Neri A, Kahn T, Eccles MR, and Morris CM

BMC genomics 4(1):9, 2003 Mar 3 - Who cited this? | PubMed ID: 12697057 | Fulltext

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

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Galaburda AM, Holinger D, Mills D, Reiss A, Korenberg JR, and Bellugi U

Revista de neurologia 36 Suppl 1:S132-7, 2003 Feb - Who cited this? | PubMed ID: 12599114 | Fulltext

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

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Hirota H, Matsuoka R, Chen XN, Salandanan LS, Lincoln A, Rose FE, Sunahara M, Osawa M, Bellugi U, and Korenberg JR

Genetics in medicine : official journal of the American College of Medical Genetics 5(4):311-21, 2003 - Who cited this? | PubMed ID: 12865760 | Fulltext

Neural correlates of auditory perception in Williams syndrome: an fMRI study.

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Levitin DJ, Menon V, Schmitt JE, Eliez S, White CD, Glover GH, Kadis J, Korenberg JR, Bellugi U, and Reiss AL

NeuroImage 18(1):74-82, 2003 Jan - Who cited this? | PubMed ID: 12507445 | Fulltext

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

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Barlow GM, Lyons GE, Richardson JA, Sarnat HB, and Korenberg JR

Biochemical and biophysical research communications 299(1):1-6, 2002 Nov 22 - Who cited this? | PubMed ID: 12435380 | Fulltext

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

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Barlow GM, Micales B, Chen XN, Lyons GE, and Korenberg JR

Biochemical and biophysical research communications 293(3):881-91, 2002 May 10 - Who cited this? | PubMed ID: 12051741 | Fulltext

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

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Cargile CB, Goh DL, Goodman BK, Chen XN, Korenberg JR, Semenza GL, and Thomas GH

American journal of medical genetics 109(2):133-8, 2002 Apr 22 - Who cited this? | PubMed ID: 11977162 | Fulltext

BAC resource for molecular cytogenetics.

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Chen XN and Korenberg JR

Methods in molecular biology (Clifton, N.J.) 204:391-403, 2002 - Who cited this? | PubMed ID: 12397812 | Fulltext

Towards a full karyotype screening of interphase cells: 'FISH and chip' technology.

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Weier H, Munné S, Lersch RA, Hsieh H, Smida J, Chen X, Korenberg JR, Pedersen RA, and Fung J

Molecular and cellular endocrinology 183 Suppl 1:S41-5, 2001 Oct 22 - Who cited this? | PubMed ID: 11576731 | Fulltext

A triple color FISH technique for mouse chromosome identification.

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Henegariu O, Dunai J, Chen XN, Korenberg JR, Ward DC, and Greally JM

Mammalian genome : official journal of the International Mammalian Genome Society 12(6):462-5, 2001 Jun - Who cited this? | PubMed ID: 11353394 | Fulltext

Cryptic translocation identification in human and mouse using several telomeric multiplex fish (TM-FISH) strategies.

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Henegariu O, Artan S, Greally JM, Chen XN, Korenberg JR, Vance GH, Stubbs L, Bray-Ward P, and Ward DC

Laboratory investigation; a journal of technical methods and pathology 81(4):483-91, 2001 Apr - Who cited this? | PubMed ID: 11304567 | Fulltext

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

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Cheung VG, Nowak N, Jang W, Kirsch IR, Zhao S, Chen XN, Furey TS, Kim UJ, Kuo WL, Olivier M, Conroy J, Kasprzyk A, Massa H, Yonescu R, Sait S, Thoreen C,

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Nature 409(6822):953-8, 2001 Feb 15 - Who cited this? | PubMed ID: 11237021 | Fulltext

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

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Barlow GM, Chen XN, Shi ZY, Lyons GE, Kurnit DM, Celle L, Spinner NB, Zackai E, Pettenati MJ, Van Riper AJ, Vekemans MJ, Mjaatvedt CH, and Korenberg JR

Genetics in medicine : official journal of the American College of Medical Genetics 3(2):91-101, 2001 - Who cited this? | PubMed ID: 11280955 | Fulltext

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

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Tuck-Muller CM, Goodman BK, Li S, Martinez JE, Chen XN, Wertelecki W, Korenberg JR, and Stetten G

Genetics in medicine : official journal of the American College of Medical Genetics 3(2):126-31, 2001 - Who cited this? | PubMed ID: 11280950 | Fulltext

Down syndrome cell adhesion molecule is conserved in mouse and highly expressed in the adult mouse brain.

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Barlow GM, Micales B, Lyons GE, and Korenberg JR

Cytogenetics and cell genetics 94(3-4):155-62, 2001 - Who cited this? | PubMed ID: 11856873 | Fulltext

The human synaptotagmin IV gene defines an evolutionary break point between syntenic mouse and human chromosome regions but retains ligand inducibility and tissue specificity.

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Ferguson GD, Chen XN, Korenberg JR, and Herschman HR

The Journal of biological chemistry 275(47):36920-6, 2000 Nov 24 - Who cited this? | PubMed ID: 10938284 | Fulltext

Partial tetrasomy 21 in a male infant.

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Slavotinek AM, Chen XN, Jackson A, Gaunt L, Campbell A, Clayton-Smith J, and Korenberg JR

Journal of medical genetics 37(10):E30, 2000 Oct - Who cited this? | PubMed ID: 11015462 | Fulltext

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

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Giglio S, Graw SL, Gimelli G, Pirola B, Varone P, Voullaire L, Lerzo F, Rossi E, Dellavecchia C, Bonaglia MC, Digilio MC, Giannotti A, Marino B, Carrozzo R, Korenberg JR, Danesino C,

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Circulation 102(4):432-7, 2000 Jul 25 - Who cited this? | PubMed ID: 10908216 | Fulltext

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

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Cargile CB, McIntosh I, Clough MV, Rutberg J, Yaghmai R, Goodman BK, Chen XN, Korenberg JR, Thomas GH, and Geraghty MT

American journal of medical genetics 92(5):328-35, 2000 Jun 19 - Who cited this? | PubMed ID: 10861662 | Fulltext

VI. Genome structure and cognitive map of Williams syndrome.

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Korenberg JR, Chen XN, Hirota H, Lai Z, Bellugi U, Burian D, Roe B, and Matsuoka R

Journal of cognitive neuroscience 12 Suppl 1:89-107, 2000 - Who cited this? | PubMed ID: 10953236 | Fulltext

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

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Korenberg JR, Chen XN, Sun Z, Shi ZY, Ma S, Vataru E, Yimlamai D, Weissenbach JS, Shizuya H, Simon MI, Gerety SS, Nguyen H, Zemsteva IS, Hui L, Silva J, Wu X,

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Genome research 9(10):994, 1999 Oct - Who cited this? | PubMed ID: 10523528 | Fulltext

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.

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Knauf JA, Elisei R, Mochly-Rosen D, Liron T, Chen XN, Gonsky R, Korenberg JR, and Fagin JA

The Journal of biological chemistry 274(33):23414-25, 1999 Aug 13 - Who cited this? | PubMed ID: 10438519 | Fulltext

A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24.

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Ianakiev P, Kilpatrick MW, Dealy C, Kosher R, Korenberg JR, Chen XN, and Tsipouras P

Biochemical and biophysical research communications 261(1):64-70, 1999 Jul 22 - Who cited this? | PubMed ID: 10405324 | Fulltext

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

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Bellugi U, Lichtenberger L, Mills D, Galaburda A, and Korenberg JR

Trends in neurosciences 22(5):197-207, 1999 May - Who cited this? | PubMed ID: 10322491 | Fulltext

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

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Korenberg JR, Chen XN, Devon KL, Noya D, Oster-Granite ML, and Birren BW

Genome research 9(5):514-23, 1999 May - Who cited this? | PubMed ID: 10330132 | Fulltext

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

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Zhang X, Yang H, Corydon MJ, Zhang X, Pedersen S, Korenberg JR, Chen XN, Laporte J, Gregersen N, Niebuhr E, Liu G, and Bolund L

Genomics 57(1):144-51, 1999 Apr 1 - Who cited this? | PubMed ID: 10191094 | Fulltext

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

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Cabin DE, McKee-Johnson JW, Matesic LE, Wiltshire T, Rue EE, Mjaatvedt AE, Huo YK, Korenberg JR, and Reeves RH

Genome research 8(9):940-50, 1998 Sep - Who cited this? | PubMed ID: 9750193 | Fulltext

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.

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Chen X, Knauf JA, Gonsky R, Wang M, Lai EH, Chissoe S, Fagin JA, and Korenberg JR

American journal of human genetics 63(2):625-37, 1998 Aug - Who cited this? | PubMed ID: 9683604 | Fulltext

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

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Morita R, Miyazaki E, Fong CY, Chen XN, Korenberg JR, Delgado-Escueta AV, and Yamakawa K

Biochemical and biophysical research communications 248(2):307-14, 1998 Jul 20 - Who cited this? | PubMed ID: 9675132 | Fulltext

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

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Wu YQ, Sutton VR, Nickerson E, Lupski JR, Potocki L, Korenberg JR, Greenberg F, Tassabehji M, and Shaffer LG

American journal of medical genetics 78(1):82-9, 1998 Jun 16 - Who cited this? | PubMed ID: 9637430 | Fulltext

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