Julie Korenberg, MD PhD - Publications

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

36 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, 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  0.497
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  0.307
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  0.562
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  0.609
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  0.561
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  0.555
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  0.557
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  0.553
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  0.603
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  0.579
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  0.612
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  0.354
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  0.606
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  0.607
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  0.603
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  0.318
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  0.522
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  0.605
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  0.582
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  0.566
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  0.581
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  0.476
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  0.32
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.  0.524
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  0.599
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  0.696
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  0.601
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  0.302
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  0.618
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  0.354
2003 Galaburda AM, Holinger D, Mills D, Reiss A, Korenberg JR, Bellugi U. El síndrome de Williams. Un resumen de hallazgos cognitivos, electrofisiológicos, anatomofuncionales, microanatómicos y genéticos Revista De NeurologíA. 36: 132. DOI: 10.33588/Rn.36S1.2003070  0.465
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 DOI: 10.1162/089892900562002  0.34
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 DOI: 10.1136/Jmg.36.6.478  0.396
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  0.576
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 DOI: 10.1093/Hmg/4.4.559  0.315
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  0.323
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