Julie Korenberg, MD PhD - Publications

Affiliations: 
Pediatrics University of California, Los Angeles, Los Angeles, CA 

178 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Ferguson MA, Nielsen JA, King JB, Dai L, Giangrasso DM, Holman R, Korenberg JR, Anderson JS. Reward, Salience, and Attentional Networks are Activated by Religious Experience in Devout Mormons. Social Neuroscience. PMID 27834117 DOI: 10.1080/17470919.2016.1257437  0.6
2016 Chailangkarn T, Trujillo CA, Freitas BC, Hrvoj-Mihic B, Herai RH, Yu DX, Brown TT, Marchetto MC, Bardy C, McHenry L, Stefanacci L, Järvinen A, Searcy YM, DeWitt M, Wong W, ... ... Korenberg JR, et al. A human neurodevelopmental model for Williams syndrome. Nature. PMID 27509850 DOI: 10.1038/nature19067  0.56
2015 Sun CY, Chu CY, Liu WY, Hsu EW, Korenberg JR, Zhu YM. Quantitative representation and description of intravoxel fiber complexity in HARDI. Physics in Medicine and Biology. 60: 8417-8436. PMID 26464329 DOI: 10.1088/0031-9155/60/21/8417  0.88
2015 Ng R, Brown TT, Erhart M, Järvinen AM, Korenberg JR, Bellugi U, Halgren E. Morphological differences in the mirror neuron system in Williams syndrome. Social Neuroscience. 1-12. PMID 26230578 DOI: 10.1080/17470919.2015.1070746  0.88
2015 Ng R, Brown TT, Järvinen AM, Erhart M, Korenberg JR, Bellugi U, Halgren E. Structural integrity of the limbic-prefrontal connection: Neuropathological correlates of anxiety in Williams syndrome. Social Neuroscience. 1-6. PMID 26214361 DOI: 10.1080/17470919.2015.1057294  0.88
2015 Anderson JS, Treiman SM, Ferguson MA, Nielsen JA, Edgin JO, Dai L, Gerig G, Korenberg JR. Violence: heightened brain attentional network response is selectively muted in Down syndrome. Journal of Neurodevelopmental Disorders. 7: 15. PMID 26131023 DOI: 10.1186/s11689-015-9112-y  0.56
2015 Ng R, Brown TT, Erhart M, Järvinen AM, Korenberg JR, Bellugi U, Halgren E. Morphological differences in the mirror neuron system in Williams syndrome Social Neuroscience. DOI: 10.1080/17470919.2015.1070746  0.88
2014 Hoeft F, Dai L, Haas BW, Sheau K, Mimura M, Mills D, Galaburda A, Bellugi U, Korenberg JR, Reiss AL. Mapping genetically controlled neural circuits of social behavior and visuo-motor integration by a preliminary examination of atypical deletions with Williams syndrome. Plos One. 9: e104088. PMID 25105779 DOI: 10.1371/journal.pone.0104088  0.88
2014 Durrleman S, Prastawa M, Charon N, Korenberg JR, Joshi S, Gerig G, Trouvé A. Morphometry of anatomical shape complexes with dense deformations and sparse parameters. Neuroimage. 101: 35-49. PMID 24973601 DOI: 10.1016/j.neuroimage.2014.06.043  0.88
2014 Smith GK, Kesner RP, Korenberg JR. Dentate gyrus mediates cognitive function in the Ts65Dn/DnJ mouse model of Down syndrome. Hippocampus. 24: 354-62. PMID 24339224 DOI: 10.1002/hipo.22229  0.88
2013 Mills DL, Dai L, Fishman I, Yam A, Appelbaum LG, St George M, Galaburda A, Bellugi U, Korenberg JR. Genetic mapping of brain plasticity across development in Williams syndrome: ERP markers of face and language processing. Developmental Neuropsychology. 38: 613-42. PMID 24219698 DOI: 10.1080/87565641.2013.825617  0.88
2013 Anderson JS, Nielsen JA, Ferguson MA, Burback MC, Cox ET, Dai L, Gerig G, Edgin JO, Korenberg JR. Abnormal brain synchrony in Down Syndrome. Neuroimage. Clinical. 2: 703-15. PMID 24179822 DOI: 10.1016/j.nicl.2013.05.006  0.88
2013 Järvinen A, Korenberg JR, Bellugi U. The social phenotype of Williams syndrome. Current Opinion in Neurobiology. 23: 414-22. PMID 23332975 DOI: 10.1016/j.conb.2012.12.006  0.88
2012 Durrleman S, Prastawa M, Korenberg JR, Joshi S, Trouvé A, Gerig G. Topology preserving atlas construction from shape data without correspondence using sparse parameters. Medical Image Computing and Computer-Assisted Intervention : Miccai ... International Conference On Medical Image Computing and Computer-Assisted Intervention. 15: 223-30. PMID 23286134  0.88
2012 Järvinen A, Dering B, Neumann D, Ng R, Crivelli D, Grichanik M, Korenberg JR, Bellugi U. Sensitivity of the autonomic nervous system to visual and auditory affect across social and non-social domains in williams syndrome. Frontiers in Psychology. 3: 343. PMID 23049519 DOI: 10.3389/fpsyg.2012.00343  0.88
2012 Bruggers CS, Altizer RA, Kessler RR, Caldwell CB, Coppersmith K, Warner L, Davies B, Paterson W, Wilcken J, D'Ambrosio TA, German ML, Hanson GR, Gershan LA, Korenberg JR, Bulaj G. Patient-empowerment interactive technologies. Science Translational Medicine. 4: 152ps16. PMID 22993292 DOI: 10.1126/scitranslmed.3004009  0.88
2012 Dai L, Carter CS, Ying J, Bellugi U, Pournajafi-Nazarloo H, Korenberg JR. Oxytocin and vasopressin are dysregulated in Williams Syndrome, a genetic disorder affecting social behavior. Plos One. 7: e38513. PMID 22719898 DOI: 10.1371/journal.pone.0038513  0.88
2012 Hogrebe L, Paiva AR, Jurrus E, Christensen C, Bridge M, Dai L, Pfeiffer RL, Hof PR, Roysam B, Korenberg JR, Tasdizen T. Serial section registration of axonal confocal microscopy datasets for long-range neural circuit reconstruction. Journal of Neuroscience Methods. 207: 200-10. PMID 22465678 DOI: 10.1016/j.jneumeth.2012.03.002  0.88
2011 Grossman TR, Gamliel A, Wessells RJ, Taghli-Lamallem O, Jepsen K, Ocorr K, Korenberg JR, Peterson KL, Rosenfeld MG, Bodmer R, Bier E. Over-expression of DSCAM and COL6A2 cooperatively generates congenital heart defects. Plos Genetics. 7: e1002344. PMID 22072978 DOI: 10.1371/journal.pgen.1002344  0.88
2011 Hogrebe L, Paiva ARC, Jurrus E, Christensen C, Bridge M, Korenberg JR, Tasdizen T. Trace driven registration of neuron confocal microscopy stacks Proceedings - International Symposium On Biomedical Imaging. 1345-1348. DOI: 10.1109/ISBI.2011.5872649  0.88
2011 Leng Z, Korenberg JR, Roysam B, Tasdizen T. A rapid 2-D centerline extraction method based on tensor voting Proceedings - International Symposium On Biomedical Imaging. 1000-1003. DOI: 10.1109/ISBI.2011.5872570  0.88
2011 Carey JC, Golabi M, Korenberg JR. In memoriam: Charles J. Epstein American Journal of Medical Genetics, Part A. DOI: 10.1002/ajmg.a.34126  0.88
2010 Mimura M, Hoeft F, Kato M, Kobayashi N, Sheau K, Piggot J, Mills D, Galaburda A, Korenberg JR, Bellugi U, Reiss AL. A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome. Journal of Neurodevelopmental Disorders. 2: 93-98. PMID 21304831 DOI: 10.1007/s11689-009-9041-8  0.88
2010 Gao MC, Bellugi U, Dai L, Mills DL, Sobel EM, Lange K, Korenberg JR. Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex. Plos One. 5: e10292. PMID 20422020 DOI: 10.1371/journal.pone.0010292  0.88
2010 Järvinen-Pasley A, Adolphs R, Yam A, Hill KJ, Grichanik M, Reilly J, Mills D, Reiss AL, Korenberg JR, Bellugi U. Affiliative behavior in Williams syndrome: social perception and real-life social behavior. Neuropsychologia. 48: 2110-9. PMID 20385151 DOI: 10.1016/j.neuropsychologia.2010.03.032  0.88
2010 Järvinen-Pasley A, Pollak SD, Yam A, Hill KJ, Grichanik M, Mills D, Reiss AL, Korenberg JR, Bellugi U. Atypical hemispheric asymmetry in the perception of negative human vocalizations in individuals with Williams syndrome. Neuropsychologia. 48: 1047-52. PMID 20005238 DOI: 10.1016/j.neuropsychologia.2009.12.002  0.88
2010 Järvinen-Pasley A, Vines BW, Hill KJ, Yam A, Grichanik M, Mills D, Reiss AL, Korenberg JR, Bellugi U. Cross-modal influences of affect across social and non-social domains in individuals with Williams syndrome. Neuropsychologia. 48: 456-66. PMID 19822162 DOI: 10.1016/j.neuropsychologia.2009.10.003  0.88
2010 Zitzer-Comfort C, Reilly J, Korenberg JR, Bellugi U. We are social – therefore we are: The interplay of mind, culture, and genetics in Williams syndrome Formative Experiences: the Interaction of Caregiving, Culture, and Developmental Psychobiology. 136-166. DOI: 10.1017/CBO9780511711879.010  0.88
2010 Jiao F, Phillips JM, Stinstra J, Krüger J, Varma R, Hsu E, Korenberg J, Johnson CR. Metrics for uncertainty analysis and visualization of diffusion tensor images Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 6326: 179-190. DOI: 10.1007/978-3-642-15699-1_19  0.88
2009 Korenberg JR. Down syndrome: the crucible for treating genomic imbalance. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 11: 617-9. PMID 19690507 DOI: 10.1097/GIM.0b013e3181b765e7  0.88
2009 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, ... ... Korenberg JR, et al. The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies. Proceedings of the National Academy of Sciences of the United States of America. 106: 12031-6. PMID 19597142 DOI: 10.1073/pnas.0813248106  0.88
2009 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, et al. Down's syndrome suppression of tumour growth and the role of the calcineurin inhibitor DSCR1. Nature. 459: 1126-30. PMID 19458618 DOI: 10.1038/nature08062  0.88
2009 Collette JC, Chen XN, Mills DL, Galaburda AM, Reiss AL, Bellugi U, Korenberg JR. William's syndrome: gene expression is related to parental origin and regional coordinate control. Journal of Human Genetics. 54: 193-8. PMID 19282872 DOI: 10.1038/jhg.2009.5  0.88
2009 Amano K, Fujii M, Arata S, Tojima T, Ogawa M, Morita N, Shimohata A, Furuichi T, Itohara S, Kamiguchi H, Korenberg JR, Arata A, Yamakawa K. DSCAM deficiency causes loss of pre-inspiratory neuron synchroneity and perinatal death. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 2984-96. PMID 19261893 DOI: 10.1523/JNEUROSCI.3624-08.2009  0.88
2009 Dai L, Bellugi U, Chen XN, Pulst-Korenberg AM, Järvinen-Pasley A, Tirosh-Wagner T, Eis PS, Graham J, Mills D, Searcy Y, Korenberg JR. Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays. American Journal of Medical Genetics. Part A. 149: 302-14. PMID 19205026 DOI: 10.1002/ajmg.a.32652  0.88
2008 Gothelf D, Searcy YM, Reilly J, Lai PT, Lanre-Amos T, Mills D, Korenberg JR, Galaburda A, Bellugi U, Reiss AL. Association between cerebral shape and social use of language in Williams syndrome. American Journal of Medical Genetics. Part A. 146: 2753-61. PMID 18924169 DOI: 10.1002/ajmg.a.32507  0.88
2008 Järvinen-Pasley A, Bellugi U, Reilly J, Mills DL, Galaburda A, Reiss AL, Korenberg JR. Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior. Development and Psychopathology. 20: 1-35. PMID 18211726 DOI: 10.1017/S0954579408000011  0.88
2007 Hoeft F, Barnea-Goraly N, Haas BW, Golarai G, Ng D, Mills D, Korenberg J, Bellugi U, Galaburda A, Reiss AL. 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. 27: 11960-5. PMID 17978036 DOI: 10.1523/JNEUROSCI.3591-07.2007  0.88
2007 Zitzer-Comfort C, Doyle T, Masataka N, Korenberg J, Bellugi U. Nature and nurture: Williams syndrome across cultures. Developmental Science. 10: 755-62. PMID 17973792 DOI: 10.1111/j.1467-7687.2007.00626.x  0.88
2007 Mobbs D, Eckert MA, Menon V, Mills D, Korenberg J, Galaburda AM, Rose FE, Bellugi U, Reiss AL. Reduced parietal and visual cortical activation during global processing in Williams syndrome. Developmental Medicine and Child Neurology. 49: 433-8. PMID 17518929 DOI: 10.1111/j.1469-8749.2007.00433.x  0.88
2007 Chiang MC, Reiss AL, Lee AD, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, Thompson PM. 3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry. Neuroimage. 36: 1096-109. PMID 17512756 DOI: 10.1016/j.neuroimage.2007.04.024  0.88
2007 Mobbs D, Eckert MA, Mills D, Korenberg J, Bellugi U, Galaburda AM, Reiss AL. Frontostriatal dysfunction during response inhibition in Williams syndrome. Biological Psychiatry. 62: 256-61. PMID 16996488 DOI: 10.1016/j.biopsych.2006.05.041  0.88
2007 Bellugi U, Järvinen-Pasley A, Doyle TF, Reilly J, Reiss AL, Korenberg JR. Affect, social behavior, and the brain in Williams syndrome Current Directions in Psychological Science. 16: 99-104. DOI: 10.1111/j.1467-8721.2007.00484.x  0.88
2007 Shi Y, Reiss AL, Lee AD, Dutton RA, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Dinov I, Thompson PM, Toga AW. Hamilton-jacobi skeletons on cortical surfaces with applications in characterizing the gyrification pattern in williams syndrome 2007 4th Ieee International Symposium On Biomedical Imaging: From Nano to Macro - Proceedings. 660-663. DOI: 10.1109/ISBI.2007.356938  0.88
2006 Gaser C, Luders E, Thompson PM, Lee AD, Dutton RA, Geaga JA, Hayashi KM, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, Reiss AL. Increased local gyrification mapped in Williams syndrome. Neuroimage. 33: 46-54. PMID 16901723 DOI: 10.1016/j.neuroimage.2006.06.018  0.88
2006 Eckert MA, Galaburda AM, Karchemskiy A, Liang A, Thompson P, Dutton RA, Lee AD, Bellugi U, Korenberg JR, Mills D, Rose FE, Reiss AL. Anomalous sylvian fissure morphology in Williams syndrome. Neuroimage. 33: 39-45. PMID 16876437 DOI: 10.1016/j.neuroimage.2006.05.062  0.88
2006 Eckert MA, Galaburda AM, Mills DL, Bellugi U, Korenberg JR, Reiss AL. The neurobiology of Williams syndrome: cascading influences of visual system impairment? Cellular and Molecular Life Sciences : Cmls. 63: 1867-75. PMID 16810457 DOI: 10.1007/s00018-005-5553-x  0.88
2006 Eckert MA, Tenforde A, Galaburda AM, Bellugi U, Korenberg JR, Mills D, Reiss AL. To modulate or not to modulate: differing results in uniquely shaped Williams syndrome brains. Neuroimage. 32: 1001-7. PMID 16806978 DOI: 10.1016/j.neuroimage.2006.05.014  0.88
2006 Van Essen DC, Dierker D, Snyder AZ, Raichle ME, Reiss AL, Korenberg J. Symmetry of cortical folding abnormalities in Williams syndrome revealed by surface-based analyses. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 5470-83. PMID 16707799 DOI: 10.1523/JNEUROSCI.4154-05.2006  0.88
2006 Yao G, Chen XN, Flores-Sarnat L, Barlow GM, Palka G, Moeschler JB, McGillivray B, Morse RP, Korenberg JR. Deletion of chromosome 21 disturbs human brain morphogenesis. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 8: 1-7. PMID 16418593 DOI: 10.1097/01.gim.0000195892.60506.3f  0.88
2006 Tosun D, Reiss AL, Lee AD, Dutton RA, Hayashi KM, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, Thompson PM. Use of 3-D cortical morphometry for mapping increased cortical gyrification and complexity in Williams syndrome 2006 3rd Ieee International Symposium On Biomedical Imaging: From Nano to Macro - Proceedings. 2006: 1172-1175.  0.88
2005 Thompson PM, Lee AD, Dutton RA, Geaga JA, Hayashi KM, Eckert MA, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, Toga AW, Reiss AL. Abnormal cortical complexity and thickness profiles mapped in Williams syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 4146-58. PMID 15843618 DOI: 10.1523/JNEUROSCI.0165-05.2005  0.88
2005 Holinger DP, Bellugi U, Mills DL, Korenberg JR, Reiss AL, Sherman GF, Galaburda AM. Relative sparing of primary auditory cortex in Williams Syndrome. Brain Research. 1037: 35-42. PMID 15777750 DOI: 10.1016/j.brainres.2004.11.038  0.88
2005 Vesa J, Brown Y, Greenfield D, Korenberg JR. Molecular and cellular characterization of the Down syndrome critical region protein 2. Biochemical and Biophysical Research Communications. 328: 235-42. PMID 15670775 DOI: 10.1016/j.bbrc.2004.09.226  0.88
2005 Eckert MA, Hu D, Eliez S, Bellugi U, Galaburda A, Korenberg J, Mills D, Reiss AL. Evidence for superior parietal impairment in Williams syndrome. Neurology. 64: 152-3. PMID 15642924 DOI: 10.1212/01.WNL.0000148598.63153.8A  0.88
2004 Searcy YM, Lincoln AJ, Rose FE, Klima ES, Bavar N, Korenberg JR. The relationship between age and IQ in adults with Williams syndrome. American Journal of Mental Retardation : Ajmr. 109: 231-6. PMID 15072519 DOI: 10.1352/0895-8017(2004)109<231:TRBAAI>2.0.CO;2  0.88
2004 Chen XN, Korenberg JR. BAC mapping using fluorescence in situ hybridization. Methods in Molecular Biology (Clifton, N.J.). 255: 131-41. PMID 15020820 DOI: 10.1385/1-59259-752-1:131  0.88
2004 Doyle TF, Bellugi U, Korenberg JR, Graham J. "Everybody in the world is my friend" hypersociability in young children with Williams syndrome. American Journal of Medical Genetics. Part A. 124: 263-73. PMID 14708099 DOI: 10.1002/ajmg.a.20416  0.88
2003 Golfier G, Chibon F, Aurias A, Chen XN, Korenberg J, Rossier J, Potier MC. The 200-kb segmental duplication on human chromosome 21 originates from a pericentromeric dissemination involving human chromosomes 2, 18 and 13. Gene. 312: 51-9. PMID 12909340 DOI: 10.1016/S0378-1119(03)00673-5  0.88
2003 Hirota H, Matsuoka R, Chen XN, Salandanan LS, Lincoln A, Rose FE, Sunahara M, Osawa M, Bellugi U, Korenberg JR. 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. 5: 311-21. PMID 12865760 DOI: 10.1097/01.GIM.0000076975.10224.67  0.88
2003 Gough SM, McDonald M, Chen XN, Korenberg JR, Neri A, Kahn T, Eccles MR, Morris CM. 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. 4: 9. PMID 12697057  0.88
2003 Galaburda AM, Holinger D, Mills D, Reiss A, Korenberg JR, Bellugi U. [Williams syndrome. A summary of cognitive, electrophysiological, anatomofunctional, microanatomical and genetic findings]. Revista De Neurologia. 36: S132-7. PMID 12599114  0.88
2003 Levitin DJ, Menon V, Schmitt JE, Eliez S, White CD, Glover GH, Kadis J, Korenberg JR, Bellugi U, Reiss AL. Neural correlates of auditory perception in Williams syndrome: an fMRI study. Neuroimage. 18: 74-82. PMID 12507445 DOI: 10.1006/nimg.2002.1297  0.88
2003 Gough SM, McDonald M, Chen XN, Korenberg JR, Neri A, Kahn T, Eccles MR, Morris CM. Refined physical map of the human PAX2/HOX11/NFKB2 cancer gene region at 10q24 and relocalization of the HPV6AIL viral integration site to 14q13.3-q21.1 Bmc Genomics. 4. DOI: 10.1186/1471-2164-4-9  0.88
2002 Barlow GM, Lyons GE, Richardson JA, Sarnat HB, Korenberg JR. DSCAM: an endogenous promoter drives expression in the developing CNS and neural crest. Biochemical and Biophysical Research Communications. 299: 1-6. PMID 12435380 DOI: 10.1016/S0006-291X(02)02548-2  0.88
2002 Chen XN, Korenberg JR. BAC resource for molecular cytogenetics. Methods in Molecular Biology (Clifton, N.J.). 204: 391-403. PMID 12397812 DOI: 10.1385/1-59259-300-3:391  0.88
2002 Barlow GM, Micales B, Chen XN, Lyons GE, Korenberg JR. Mammalian DSCAMs: roles in the development of the spinal cord, cortex, and cerebellum? Biochemical and Biophysical Research Communications. 293: 881-91. PMID 12051741 DOI: 10.1016/S0006-291X(02)00307-8  0.88
2002 Cargile CB, Goh DL, Goodman BK, Chen XN, Korenberg JR, Semenza GL, Thomas GH. Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome. American Journal of Medical Genetics. 109: 133-8. PMID 11977162 DOI: 10.1002/ajmg.10323  0.88
2001 Barlow GM, Micales B, Lyons GE, Korenberg JR. Down syndrome cell adhesion molecule is conserved in mouse and highly expressed in the adult mouse brain. Cytogenetics and Cell Genetics. 94: 155-62. PMID 11856873  0.88
2001 Weier H, Munné S, Lersch RA, Hsieh H, Smida J, Chen X, Korenberg JR, Pedersen RA, Fung J. Towards a full karyotype screening of interphase cells: 'FISH and chip' technology. Molecular and Cellular Endocrinology. 183: S41-5. PMID 11576731 DOI: 10.1016/S0303-7207(01)00566-4  0.88
2001 Henegariu O, Dunai J, Chen XN, Korenberg JR, Ward DC, Greally JM. A triple color FISH technique for mouse chromosome identification. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 462-5. PMID 11353394 DOI: 10.1007/s003350020038  0.88
2001 Henegariu O, Artan S, Greally JM, Chen XN, Korenberg JR, Vance GH, Stubbs L, Bray-Ward P, Ward DC. Cryptic translocation identification in human and mouse using several telomeric multiplex fish (TM-FISH) strategies. Laboratory Investigation; a Journal of Technical Methods and Pathology. 81: 483-91. PMID 11304567  0.88
2001 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, Korenberg JR. Down syndrome congenital heart disease: a narrowed region and a candidate gene. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 3: 91-101. PMID 11280955  0.88
2001 Tuck-Muller CM, Goodman BK, Li S, Martinez JE, Chen XN, Wertelecki W, Korenberg JR, Stetten G. 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. 3: 126-31. PMID 11280950  0.88
2001 Cargile CB, Goh DLM, Goodman BK, Chen XN, Korenberg JR, Semenza GL, Thomas GH. Intrasubthalamic injection of 6-hydroxydopamine induces changes in the firing rate and pattern of subthalamic nucleus neurons in the rat Synapse. 40: 145-153. PMID 11252026 DOI: 10.1002/syn.1036  0.88
2001 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, ... ... Korenberg JR, et al. Integration of cytogenetic landmarks into the draft sequence of the human genome. Nature. 409: 953-8. PMID 11237021 DOI: 10.1038/35057192  0.88
2001 Bellugi U, Korenberg JR, Klima ES. Williams syndrome: An exploration of neurocognitive and genetic features Clinical Neuroscience Research. 1: 217-229. DOI: 10.1016/S1566-2772(01)00008-1  0.88
2000 Slavotinek AM, Chen XN, Jackson A, Gaunt L, Campbell A, Clayton-Smith J, Korenberg JR. Partial tetrasomy 21 in a male infant. Journal of Medical Genetics. 37: E30. PMID 11015462  0.88
2000 Korenberg JR, Chen XN, Hirota H, Lai Z, Bellugi U, Burian D, Roe B, Matsuoka R. VI. Genome structure and cognitive map of Williams syndrome. Journal of Cognitive Neuroscience. 12: 89-107. PMID 10953236  0.88
2000 Ferguson GD, Chen XN, Korenberg JR, Herschman HR. 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. 275: 36920-6. PMID 10938284 DOI: 10.1074/jbc.M005801200  0.88
2000 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, et al. Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects. Circulation. 102: 432-7. PMID 10908216  0.88
2000 Cargile CB, McIntosh I, Clough MV, Rutberg J, Yaghmai R, Goodman BK, Chen XN, Korenberg JR, Thomas GH, Geraghty MT. Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12). American Journal of Medical Genetics. 92: 328-35. PMID 10861662 DOI: 10.1002/1096-8628(20000619)92:5<328::AID-AJMG7>3.0.CO;2-P  0.88
1999 Botta A, Novelli G, Mari A, Novelli A, Sabani M, Korenberg J, Osborne LR, Digilio MC, Giannotti A, Dallapiccola B. Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes. Journal of Medical Genetics. 36: 478-80. PMID 10874638  0.88
1999 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, et al. Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine. Genome Research. 9: 994-1001. PMID 10523528 DOI: 10.1101/gr.9.10.994  0.88
1999 Knauf JA, Elisei R, Mochly-Rosen D, Liron T, Chen XN, Gonsky R, Korenberg JR, Fagin JA. 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. 274: 23414-25. PMID 10438519 DOI: 10.1074/jbc.274.33.23414  0.88
1999 Ianakiev P, Kilpatrick MW, Dealy C, Kosher R, Korenberg JR, Chen XN, Tsipouras P. A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24. Biochemical and Biophysical Research Communications. 261: 64-70. PMID 10405324 DOI: 10.1006/bbrc.1999.0963  0.88
1999 Korenberg JR, Chen XN, Devon KL, Noya D, Oster-Granite ML, Birren BW. Mouse molecular cytogenetic resource: 157 BACs link the chromosomal and genetic maps. Genome Research. 9: 514-23. PMID 10330132  0.88
1999 Bellugi U, Lichtenberger L, Mills D, Galaburda A, Korenberg JR. Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome. Trends in Neurosciences. 22: 197-207. PMID 10322491 DOI: 10.1016/S0166-2236(99)01397-1  0.88
1999 Zhang X, Yang H, Corydon MJ, Zhang X, Pedersen S, Korenberg JR, Chen XN, Laporte J, Gregersen N, Niebuhr E, Liu G, Bolund L. Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA. Genomics. 57: 144-51. PMID 10191094 DOI: 10.1006/geno.1999.5741  0.88
1998 Chen XN, Shi ZY, Korenberg JR, Sehgal A. Assignment of the GOV (Glioblastoma overexpressed) gene to human chromosome band 19p13.2 by fluorescence in situ hybridization. Cytogenetics and Cell Genetics. 83: 230-1. PMID 10072586  0.88
1998 Cabin DE, McKee-Johnson JW, Matesic LE, Wiltshire T, Rue EE, Mjaatvedt AE, Huo YK, Korenberg JR, Reeves RH. Physical and comparative mapping of distal mouse chromosome 16. 5 p5. Genome Research. 8: 940-50. PMID 9750193  0.88
1998 Chen X, Knauf JA, Gonsky R, Wang M, Lai EH, Chissoe S, Fagin JA, Korenberg JR. 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. 63: 625-37. PMID 9683604 DOI: 10.1086/301973  0.88
1998 Morita R, Miyazaki E, Fong CY, Chen XN, Korenberg JR, Delgado-Escueta AV, Yamakawa K. 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. 248: 307-14. PMID 9675132 DOI: 10.1006/bbrc.1998.8947  0.88
1998 Wu YQ, Sutton VR, Nickerson E, Lupski JR, Potocki L, Korenberg JR, Greenberg F, Tassabehji M, Shaffer LG. Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin. American Journal of Medical Genetics. 78: 82-9. PMID 9637430 DOI: 10.1002/(SICI)1096-8628(19980616)78:1<82::AID-AJMG17>3.0.CO;2-K  0.88
1998 Yamakawa K, Huot YK, Haendelt MA, Hubert R, Chen XN, Lyons GE, Korenberg JR. 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. 7: 227-37. PMID 9426258 DOI: 10.1093/hmg/7.2.227  0.88
1997 Korenberg JR, Aaltonen J, Brahe C, Cabin D, Creau N, Delabar JM, Doering J, Gardiner K, Hubert RS, Ives J, Kessling A, Kudoh J, Lafrenière R, Murakami Y, Ohira M, et al. 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. 79: 21-52. PMID 9533011  0.88
1997 Hubert RS, Korenberg JR. PCP4 maps between D21S345 and P31P10SP6 on chromosome 21q22.2-->q22.3. Cytogenetics and Cell Genetics. 78: 44-5. PMID 9345904  0.88
1997 Grover J, Chen XN, Korenberg JR, Roughley PJ. The structure and chromosome location of the human chondroadherin gene (CHAD). Genomics. 45: 379-85. PMID 9344663 DOI: 10.1006/geno.1997.4951  0.88
1997 Shapira SK, McCaskill C, Northrup H, Spikes AS, Elder FF, Sutton VR, Korenberg JR, Greenberg F, Shaffer LG. Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome. American Journal of Human Genetics. 61: 642-50. PMID 9326330 DOI: 10.1086/515520  0.88
1997 Nechiporuk T, Nechiporuk A, Sahba S, Figueroa K, Shibata H, Chen XN, Korenberg JR, de Jong P, Pulst SM. A high-resolution PAC and BAC map of the SCA2 region. Genomics. 44: 321-9. PMID 9325053 DOI: 10.1006/geno.1997.4886  0.88
1997 Vielmetter J, Chen XN, Miskevich F, Lane RP, Yamakawa K, Korenberg JR, Dreyer WJ. Molecular characterization of human neogenin, a DCC-related protein, and the mapping of its gene (NEO1) to chromosomal position 15q22.3-q23. Genomics. 41: 414-21. PMID 9169140 DOI: 10.1006/geno.1997.4688  0.88
1997 Hubert RS, Mitchell S, Chen XN, Ekmekji K, Gadomski C, Sun Z, Noya D, Kim UJ, Chen C, Shizuya H, Simon M, de Jong PJ, Korenberg JR. BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21. Genomics. 41: 218-26. PMID 9143497 DOI: 10.1006/geno.1997.4657  0.88
1997 DiDonato CJ, Chen XN, Noya D, Korenberg JR, Nadeau JH, Simard LR. Cloning, characterization, and copy number of the murine survival motor neuron gene: homolog of the spinal muscular atrophy-determining gene. Genome Research. 7: 339-52. PMID 9110173  0.88
1997 Chen LH, Liu ML, Hwang HY, Chen LS, Korenberg J, Shane B. Human methionine synthase. cDNA cloning, gene localization, and expression. The Journal of Biological Chemistry. 272: 3628-34. PMID 9013615 DOI: 10.1074/jbc.272.6.3628  0.88
1997 Korenberg JR, Aaltonen J, Brahe C, Cabin D, Creau N, Delabar JM, Doering J, Gardiner K, Hubert RS, Ives J, Kessling A, Kudoh J, Lafreniere R, Murakami Y, Ohira M, et al. Sixth International Workshop on Human Chromosome 21 Mapping 1996, New York, May 6-8 1996: Report Cytogenetics and Cell Genetics. 79: 22-34.  0.88
1996 Thompson AD, Braun BS, Arvand A, Stewart SD, May WA, Chen E, Korenberg J, Denny C. EAT-2 is a novel SH2 domain containing protein that is up regulated by Ewing's sarcoma EWS/FLI1 fusion gene. Oncogene. 13: 2649-58. PMID 9000139  0.88
1996 Grover J, Chen XN, Korenberg JR, Recklies AD, Roughley PJ. The gene organization, chromosome location, and expression of a 55-kDa matrix protein (PRELP) of human articular cartilage. Genomics. 38: 109-17. PMID 8954791 DOI: 10.1006/geno.1996.0605  0.88
1996 Chiang PW, Song WJ, Wu KY, Korenberg JR, Fogel EJ, Van Keuren ML, Lashkari D, Kurnit DM. Use of a fluorescent-PCR reaction to detect genomic sequence copy number and transcriptional abundance. Genome Research. 6: 1013-26. PMID 8908521  0.88
1996 Pulst SM, Nechiporuk A, Nechiporuk T, Gispert S, Chen XN, Lopes-Cendes I, Pearlman S, Starkman S, Orozco-Diaz G, Lunkes A, DeJong P, Rouleau GA, Auburger G, Korenberg JR, Figueroa C, et al. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nature Genetics. 14: 269-76. PMID 8896555 DOI: 10.1038/ng1196-269  0.88
1996 Yamakawa K, Gao DQ, Korenberg JR. A periodic tryptophan protein 2 gene homologue (PWP2H) in the candidate region of progressive myoclonus epilepsy on 21q22.3. Cytogenetics and Cell Genetics. 74: 140-5. PMID 8893822  0.88
1996 Haldi ML, Strickland C, Lim P, VanBerkel V, Chen X, Noya D, Korenberg JR, Husain Z, Miller J, Lander ES. 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. 7: 767-9. PMID 8854865  0.88
1996 Nechiporuk T, Nechiporuk A, Guan X, Frederick R, Figueroa K, Chumakov I, Korenberg JR, de Jong PJ, Pulst SM. Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical map. Human Genetics. 97: 462-7. PMID 8834243 DOI: 10.1007/s004390050073  0.88
1996 Ahlbom BE, Goetz P, Korenberg JR, Pettersson U, Seemanova E, Wadelius C, Zech L, Annerén G. Molecular analysis of chromosome 21 in a patient with a phenotype of Down syndrome and apparently normal karyotype. American Journal of Medical Genetics. 63: 566-72. PMID 8826436 DOI: 10.1002/(SICI)1096-8628(19960628)63:4<566::AID-AJMG10>3.0.CO;2-G  0.88
1996 Lane RP, Chen XN, Yamakawa K, Vielmetter J, Korenberg JR, Dreyer WJ. Characterization of a highly conserved human homolog to the chicken neural cell surface protein Bravo/Nr-CAM that maps to chromosome band 7q31. Genomics. 35: 456-65. PMID 8812479 DOI: 10.1006/geno.1996.0385  0.88
1996 Chiang PW, Wang S, Smithivas P, Song WJ, Ramamoorthy S, Hillman J, Puett S, Van Keuren ML, Crombez E, Kumar A, Glover TW, Miller DE, Tsai CH, Blackburn CC, Chen XN, ... ... Korenberg JR, et al. Identification and analysis of the human and murine putative chromatin structure regulator SUPT6H and Supt6h. Genomics. 34: 328-33. PMID 8786132 DOI: 10.1006/geno.1996.0294  0.88
1996 Kim UJ, Shizuya H, Kang HL, Choi SS, Garrett CL, Smink LJ, Birren BW, Korenberg JR, Dunham I, Simon MI. 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. 93: 6297-301. PMID 8692809 DOI: 10.1073/pnas.93.13.6297  0.88
1996 Chen L, Qi H, Korenberg J, Garrow TA, Choi YJ, Shane B. Purification and properties of human cytosolic folylpoly-gamma-glutamate synthetase and organization, localization, and differential splicing of its gene. The Journal of Biological Chemistry. 271: 13077-87. PMID 8662720 DOI: 10.1074/jbc.271.22.13077  0.88
1996 Bronstein JM, Kozak CA, Chen XN, Wu S, Danciger M, Korenberg JR, Farber DB. Chromosomal localization of murine and human oligodendrocyte-specific protein genes. Genomics. 34: 255-7. PMID 8661061 DOI: 10.1006/geno.1996.0278  0.88
1996 Birren BW, Tachi-iri Y, Kim UJ, Nguyen M, Shizuya H, Korenberg JR, Simon MI. A human chromosome 22 fosmid resource: mapping and analysis of 96 clones. Genomics. 34: 97-106. PMID 8661029 DOI: 10.1006/geno.1996.0246  0.88
1996 Chen XN, Korenberg JR, Jiang M, Shen D, Fong HK. Localization of the human RGR opsin gene to chromosome 10q23. Human Genetics. 97: 720-2. PMID 8641686 DOI: 10.1007/s004390050126  0.88
1996 Chow N, Korenberg JR, Chen XN, Neve RL. APP-BP1, a novel protein that binds to the carboxyl-terminal region of the amyloid precursor protein. The Journal of Biological Chemistry. 271: 11339-46. PMID 8626687 DOI: 10.1074/jbc.271.19.11339  0.88
1996 Larionov V, Kouprina N, Graves J, Chen XN, Korenberg JR, Resnick MA. Specific cloning of human DNA as yeast artificial chromosomes by transformation-associated recombination. Proceedings of the National Academy of Sciences of the United States of America. 93: 491-6. PMID 8552668 DOI: 10.1073/pnas.93.1.491  0.88
1996 Chen XN, Mitchell S, Gerwehr S, Sun Z, Hubert R, Kim UJ, Shizuya H, Wu X, Silva J, Birren B, Hudson TJ, De Jong P, Lander E, Simon M, Korenberg JR. An integrated BAC/PAC molecular cytogenetic resource for human genetics: Applications to disease Journal of Investigative Medicine. 44: 105A.  0.88
1996 Yamakawa K, Gao DQ, Mitchell S, Lyons G, Kim U, Lehesjoki AE, De La Chapelle A, Korenberg JR. Candidate genes for progressive myoclonus epilepsy on 21Q22.3 Journal of Investigative Medicine. 44: 116A.  0.88
1995 Mohandas TK, Chen XN, Rowe LB, Birkenmeier EH, Fanning AS, Anderson JM, Korenberg JR. Localization of the tight junction protein gene TJP1 to human chromosome 15q13, distal to the Prader-Willi/Angelman region, and to mouse chromosome 7. Genomics. 30: 594-7. PMID 8825647 DOI: 10.1006/geno.1995.1281  0.88
1995 Korenberg JR, Chen XN, Mitchell S, Fannin S, Gerwehr S, Cohen D, Chumakov I. A high-fidelity physical map of human chromosome 21q in yeast artificial chromosomes. Genome Research. 5: 427-43. PMID 8808464  0.88
1995 Korenberg JR, Chen XN, Adams MD, Venter JC. Toward a cDNA map of the human genome. Genomics. 29: 364-70. PMID 8666383 DOI: 10.1006/geno.1995.9993  0.88
1995 Kim UJ, Shizuya H, Chen XN, Deaven L, Speicher S, Solomon J, Korenberg J, Simon MI. Characterization of a human chromosome 22 enriched bacterial artificial chromosome sublibrary. Genetic Analysis : Biomolecular Engineering. 12: 73-9. PMID 8574897 DOI: 10.1016/1050-3862(95)00121-2  0.88
1995 Bhatt S, Schreck R, Graham JM, Korenberg JR, Hurvitz CG, Fischel-Ghodsian N. Transient leukemia with trisomy 21: description of a case and review of the literature. American Journal of Medical Genetics. 58: 310-4. PMID 8533839 DOI: 10.1002/ajmg.1320580404  0.88
1995 Petrini JH, Walsh ME, DiMare C, Chen XN, Korenberg JR, Weaver DT. Isolation and characterization of the human MRE11 homologue. Genomics. 29: 80-6. PMID 8530104 DOI: 10.1006/geno.1995.1217  0.52
1995 Korenberg JR, Chen XN, Tran H, Argraves WS. Localization of the human gene for fibulin-1 (FBLN1) to chromosome band 22q13.3. Cytogenetics and Cell Genetics. 68: 192-3. PMID 7842734  0.52
1995 Kim UJ, Shizuya H, Deaven L, Chen XN, Korenberg JR, Simon MI. 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. 23: 1838-9. PMID 7784194 DOI: 10.1093/nar/23.10.1838  0.88
1995 Korenberg JR, Chen XN. Human cDNA mapping using a high-resolution R-banding technique and fluorescence in situ hybridization. Cytogenetics and Cell Genetics. 69: 196-200. PMID 7698011  0.52
1995 Grover J, Chen XN, Korenberg JR, Roughley PJ. The human lumican gene. Organization, chromosomal location, and expression in articular cartilage. The Journal of Biological Chemistry. 270: 21942-9. PMID 7665616  0.88
1995 Zhu Y, Qi C, Korenberg JR, Chen XN, Noya D, Rao MS, Reddy JK. 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. 92: 7921-5. PMID 7644514  0.52
1995 Yamakawa K, Mitchell S, Hubert R, Chen XN, Colbern S, Huo YK, Gadomski C, Kim UJ, Korenberg JR. Isolation and characterization of a candidate gene for progressive myoclonus epilepsy on 21q22.3. Human Molecular Genetics. 4: 709-16. PMID 7633421 DOI: 10.1093/hmg/4.4.709  0.88
1995 Schrick JJ, Onuchic LF, Reeders ST, Korenberg J, Chen XN, Moyer JH, Wilkinson JE, Woychik RP. Characterization of the human homologue of the mouse Tg737 candidate polycystic kidney disease gene. Human Molecular Genetics. 4: 559-67. PMID 7633404  0.52
1995 Chen XN, Korenberg JR. Localization of human CREBBP (CREB binding protein) to 16p13.3 by fluorescence in situ hybridization. Cytogenetics and Cell Genetics. 71: 56-7. PMID 7606928  0.52
1995 Palmer CG, Blouin JL, Bull MJ, Breitfeld P, Vance GH, Van Meter T, Weaver DD, Heerema NA, Colbern SG, Korenberg JR. Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia. American Journal of Medical Genetics. 57: 527-36. PMID 7573123 DOI: 10.1002/ajmg.1320570403  0.88
1995 Korenberg JR. Mental modelling. Nature Genetics. 11: 109-11. PMID 7550329 DOI: 10.1038/ng1095-109  0.88
1995 Piriev NI, Viczian AS, Ye J, Kerner B, Korenberg JR, Farber DB. Gene structure and amino acid sequence of the human cone photoreceptor cGMP-phosphodiesterase alpha' subunit (PDEA2) and its chromosomal localization to 10q24. Genomics. 28: 429-35. PMID 7490077 DOI: 10.1006/geno.1995.1171  0.88
1994 Korenberg JR, Chen XN, Schipper R, Sun Z, Gonsky R, Gerwehr S, Carpenter N, Daumer C, Dignan P, Disteche C. Down syndrome phenotypes: the consequences of chromosomal imbalance. Proceedings of the National Academy of Sciences of the United States of America. 91: 4997-5001. PMID 8197171  0.52
1994 Falik-Borenstein TC, Korenberg JR, Schreck RR. Confined placental chimerism: prenatal and postnatal cytogenetic and molecular analysis, and pregnancy outcome. American Journal of Medical Genetics. 50: 51-6. PMID 8160753 DOI: 10.1002/ajmg.1320500112  0.88
1994 Malo MS, Srivastava K, Andresen JM, Chen XN, Korenberg JR, Ingram VM. Targeted gene walking by low stringency polymerase chain reaction: assignment of a putative human brain sodium channel gene (SCN3A) to chromosome 2q24-31. Proceedings of the National Academy of Sciences of the United States of America. 91: 2975-9. PMID 8159690  0.88
1994 Malo MS, Blanchard BJ, Andresen JM, Srivastava K, Chen XN, Li X, Jabs EW, Korenberg JR, Ingram VM. Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24. Cytogenetics and Cell Genetics. 67: 178-86. PMID 8062593 DOI: 10.1159/000133818  0.88
1994 Ghozi MC, Weiss Y, Chen XN, Bernstein Y, Dafni N, Korenberg JR, Groner Y. Isolation, chromosomal localization, and sequence analysis of human chromosome 21 zinc finger domains. Genomics. 20: 487-9. PMID 8034323 DOI: 10.1006/geno.1994.1205  0.52
1994 Wymore RS, Korenberg JR, Kinoshita KD, Aiyar J, Coyne C, Chen XN, Hustad CM, Copeland NG, Gutman GA, Jenkins NA. 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. Genomics. 20: 191-202. PMID 8020965  0.52
1994 Korenberg JR, Argraves KM, Chen XN, Tran H, Strickland DK, Argraves WS. Chromosomal localization of human genes for the LDL receptor family member glycoprotein 330 (LRP2) and its associated protein RAP (LRPAP1). Genomics. 22: 88-93. PMID 7959795 DOI: 10.1006/geno.1994.1348  0.52
1994 Sztrolovics R, Chen XN, Grover J, Roughley PJ, Korenberg JR. Localization of the human fibromodulin gene (FMOD) to chromosome 1q32 and completion of the cDNA sequence. Genomics. 23: 715-7. PMID 7851907 DOI: 10.1006/geno.1994.1567  0.52
1994 Wang M, Chen XN, Shouse S, Manson J, Wu Q, Li R, Wrestler J, Noya D, Sun ZG, Korenberg J. Construction and characterization of a human chromosome 2-specific BAC library. Genomics. 24: 527-34. PMID 7713504  0.52
1993 Garrow TA, Brenner AA, Whitehead VM, Chen XN, Duncan RG, Korenberg JR, Shane B. Cloning of human cDNAs encoding mitochondrial and cytosolic serine hydroxymethyltransferases and chromosomal localization. The Journal of Biological Chemistry. 268: 11910-6. PMID 8505317  0.88
1993 Wood WJ, Thompson AA, Korenberg J, Chen XN, May W, Wall R, Denny CT. Isolation and chromosomal mapping of the human immunoglobulin-associated B29 gene (IGB). Genomics. 16: 187-92. PMID 8486355 DOI: 10.1006/geno.1993.1157  0.88
1993 May W, Korenberg JR, Chen XN, Lunsford L, Wood WJ, Thompson A, Wall R, Denny CT. Human lymphocyte-specific pp52 gene is a member of a highly conserved dispersed family. Genomics. 15: 515-20. PMID 8468046 DOI: 10.1006/geno.1993.1102  0.88
1993 Nechiporuk A, Fain P, Kort E, Nee LE, Frommelt E, Polinsky RJ, Korenberg JR, Pulst SM. 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. 48: 63-6. PMID 8357039 DOI: 10.1002/ajmg.1320480113  0.88
1993 Korenberg JR, Chen XN, Doege K, Grover J, Roughley PJ. Assignment of the human aggrecan gene (AGC1) to 15q26 using fluorescence in situ hybridization analysis. Genomics. 16: 546-8. PMID 8314595 DOI: 10.1006/geno.1993.1228  0.52
1993 Sainz J, Rasmussen M, Nechiporuk A, Vissing H, Cheng X, Korenberg JR, Pulst SM. Dinucleotide repeat polymorphism at the D22S351 locus. Human Molecular Genetics. 2: 1749. PMID 8268946 DOI: 10.1093/hmg/2.10.1749  0.88
1992 Korenberg JR, Yang-Feng T, Schreck R, Chen XN. Using fluorescence in situ hybridization (FISH) in genome mapping. Trends in Biotechnology. 10: 27-32. PMID 1367928 DOI: 10.1016/0167-7799(92)90163-P  0.88
1992 Falik-Borenstein TC, Pribyl TM, Pulst SM, Van Dyke DL, Weiss L, Chu ML, Kraus J, Marshak D, Korenberg JR. Stable ring chromosome 21: molecular and clinical definition of the lesion. American Journal of Medical Genetics. 42: 22-8. PMID 1308361 DOI: 10.1002/ajmg.1320420107  0.88
1992 Wilkie TM, Gilbert DJ, Olsen AS, Chen XN, Amatruda TT, Korenberg JR, Trask BJ, de Jong P, Reed RR, Simon MI. Evolution of the mammalian G protein alpha subunit multigene family. Nature Genetics. 1: 85-91. PMID 1302014 DOI: 10.1038/ng0592-85  0.88
1991 Korenberg JR, Kalousek DK, Anneren G, Pulst SM, Hall JG, Epstein CJ, Cox DR. Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion. Human Genetics. 87: 112-8. PMID 2066097 DOI: 10.1007/BF00204163  0.88
1991 Falik-Borenstein TC, Korenberg JR, Davos I, Platt LD, Gans S, Goodman B, Schreck R, Graham JM. Congenital gastric teratoma in Wiedemann-Beckwith syndrome. American Journal of Medical Genetics. 38: 52-7. PMID 2012133 DOI: 10.1002/ajmg.1320380113  0.88
1991 Pulst SM, Pribyl T, Barker DF, Riccardi VM, Ren M, Yaari H, Korenberg JR. Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia. American Journal of Medical Genetics. 40: 84-7. PMID 1909491 DOI: 10.1002/ajmg.1320400117  0.88
1991 Shohat M, Herman V, Melmed S, Neufeld N, Schreck R, Pulst S, Graham JM, Rimoin DL, Korenberg JR. Deletion of 20p 11.23----pter with normal growth hormone-releasing hormone genes. American Journal of Medical Genetics. 39: 56-63. PMID 1867266 DOI: 10.1002/ajmg.1320390113  0.88
1991 Epstein CJ, Korenberg JR, Annerén G, Antonarakis SE, Aymé S, Courchesne E, Epstein LB, Fowler A, Groner Y, Huret JL. Protocols to establish genotype-phenotype correlations in Down syndrome. American Journal of Human Genetics. 49: 207-35. PMID 1829580  0.88
1991 Pulst SM, Yang-Feng T, Korenberg JR. Relative order and location of DNA sequences on chromosome 21 linked to familial Alzheimer disease. American Journal of Medical Genetics. 41: 454-9. PMID 1776637 DOI: 10.1002/ajmg.1320410415  0.88
1991 Pulst SM, Riccardi VM, Fain P, Korenberg JR. Familial spinal neurofibromatosis: clinical and DNA linkage analysis. Neurology. 41: 1923-7. PMID 1745350  0.88
1991 Pulst SM, Fain P, Cohn V, Nee LE, Polinsky RJ, Korenberg JR. Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer disease. Human Genetics. 87: 159-61. PMID 1676700 DOI: 10.1007/BF00204173  0.88
1991 Puckett C, Gomez CM, Korenberg JR, Tung H, Meier TJ, Chen XN, Hood L. 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. 88: 7557-61. PMID 1652753  0.88
1990 Shohat T, Shohat M, Petersen GM, Sparkes RS, Langfield D, Bickal J, Korenberg JR, Schwabe AD, Rotter JI. Genetic marker family studies in familial Mediterranean fever (FMF) in Armenians. Clinical Genetics. 38: 332-9. PMID 2282713  0.88
1990 Pulst SM, Graham JM, Fain P, Barker D, Pribyl T, Korenberg JR. The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17. Human Genetics. 85: 12-4. PMID 2162805 DOI: 10.1007/BF00276318  0.88
1990 Korenberg JR, Kawashima H, Pulst SM, Ikeuchi T, Ogasawara N, Yamamoto K, Schonberg SA, West R, Allen L, Magenis E. Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype. American Journal of Human Genetics. 47: 236-46. PMID 2143053  0.88
1990 Pulst SM, Korenberg JR. Panel of aneuploid cell lines for physical mapping of the proximal long arm of human chromosome 21. American Journal of Medical Genetics. Supplement. 7: 137-40. PMID 2127362  0.88
1990 Shohat M, Shohat T, Rotter JI, Schlesinger M, Petersen GM, Pribyl T, Sack G, Schwabe AD, Korenberg JR. Serum amyloid A and P protein genes in familial Mediterranean fever. Genomics. 8: 83-9. PMID 1981994 DOI: 10.1016/0888-7543(90)90228-M  0.88
1990 Pulst SM, Korenberg JR, Ren M, Greenwald J. A new HaeIII polymorphism at the D21S13 locus. Human Genetics. 85: 671. PMID 1977689 DOI: 10.1007/BF00193597  0.88
1990 Pulst SM, Korenberg JR, Greenwald J, Carbone M. A new EcoRI polymorphism at the D21S13 locus. Human Genetics. 84: 580. PMID 1970976 DOI: 10.1007/BF00210815  0.88
1989 Rigas B, Korenberg JR, Merrill WW, Levine L. Prostaglandins E2 and E2 alpha are elevated in saliva of cystic fibrosis patients. The American Journal of Gastroenterology. 84: 1408-12. PMID 2816873  0.88
1989 Korenberg JR, Pulst SM, Neve RL, West R. The Alzheimer amyloid precursor protein maps to human chromosome 21 bands q21.105-q21.05. Genomics. 5: 124-7. PMID 2527801 DOI: 10.1016/0888-7543(89)90095-5  0.88
1978 Korenberg JR, Therman E, Denniston C. Hot spots and functional organization of human chromosomes. Human Genetics. 43: 13-22. PMID 78886 DOI: 10.1007/BF00396473  0.88
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