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Julie R. Korenberg

Julie R. Korenberg

D-Index & Metrics

Genetics

D-Index
69
Citations
19645
World Ranking
2336
National Ranking
1056

Overview

Julie R. Korenberg is affiliated with the University of Utah in the United States. Their research predominantly spans several interconnected fields, including neuroscience and psychology, with a strong focus on developmental and cellular neuroscience, as well as social and cognitive psychology.

The scientist's work addresses multiple specialized topics, among which are:

  • Williams Syndrome Research
  • Nuclear Receptors and Signaling
  • Neuroendocrine regulation and behavior
  • Cognitive Abilities and Testing
  • Congenital heart defects research
  • Coronary Artery Anomalies

Their recent publications reflect this range of interests and include the following:

  • Core transcriptional networks in Williams syndrome: IGF1-PI3K-AKT-mTOR, MAPK and actin signaling at the synapse echo autism, 2021, published in Human Molecular Genetics
  • Oxytocin and our place in the universe, 2024, published in Comprehensive Psychoneuroendocrinology
  • Brain lateralization for perceiving direction of motion is reversed in Williams syndrome and related to BUD23, 2025, published in Scientific Reports

Frequent co-authors of Korenberg include:

  • Li Dai
  • Robert B. Weiss
  • Diane M. Dunn
  • Anna Ramirez
  • Sharan Paul

The main publication venues where their work has appeared are:

  • Human Molecular Genetics
  • Comprehensive Psychoneuroendocrinology
  • Scientific Reports

Best Publications

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

    Stefan M. Pulst;Alex Nechiporuk;Alex Nechiporuk;Tamilla Nechiporuk;Tamilla Nechiporuk;Suzana Gispert

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

    Yijun Zhu;Chao Qi;Julie R. Korenberg;Xiao Ning Chen

  • Down syndrome phenotypes: the consequences of chromosomal imbalance

    J R Korenberg;X N Chen;R Schipper;Z Sun

  • A physical map of the human genome.

    John Douglas Mcpherson;Marco Marra;Marco Marra;La Deana Hillier;Robert H. Waterston

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

    Julie R. Korenberg;Julie R. Korenberg;Mary C. Rykowski

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

    Ursula Bellugi;Liz Lichtenberger;Debra Mills;Albert Galaburda

  • Giemsa technique for the detection of sister chromatid exchanges

    Julie R. Korenberg;Elizabeth F. Freedlender

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

    Jan O. Korbel;Tal Tirosh-Wagner;Alexander Eckehart Urban;Xiao Ning Chen

  • VI. Genome Structure and Cognitive Map of Williams Syndrome

    Julie R. Korenberg;Xiao-Ning Chen;Hamao Hirota;Zona Lai

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

    Kwan Hyuck Baek;Alexander Zaslavsky;Ryan C. Lynch;Carmella Britt

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

    V. G. Cheung;N. Nowak;W. Jang;I. R. Kirsch

  • Abnormal cortical complexity and thickness profiles mapped in Williams syndrome.

    Paul M. Thompson;Agatha D. Lee;Rebecca A. Dutton;Jennifer A. Geaga

  • Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region

    Kouzin Kamino;Harry T. Orr;Haydeh Payami;Ellen M. Wijsman

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

    Teresa F. Doyle;Ursula Bellugi;Julie R. Korenberg;Julie R. Korenberg;John Graham

  • Evolution of the mammalian G protein α subunit multigene family

    Thomas M. Wilkie;Debra J. Gilbert;Anne S. Olsen;Xiao-Ning Chen

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

    Julie R. Korenberg;Hiroko Kawashima;Stefan M. Pulst;T. Ikeuchi

  • DSCAM: A Novel Member of the Immunoglobulin Superfamily Maps in a Down Syndrome Region and is Involved in the Development of the Nervous System

    Kazuhiro Yamakawa;Yong Kang Huo;Melissa A. Haendel;René Hubert

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

    Fumiko Hoeft;Naama Barnea-Goraly;Brian W. Haas;Golijeh Golarai

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

    Stuart K. Shapira;Christopher McCaskill;Hope Northrup;Aimee S. Spikes

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

    P Woo;J R Korenberg;A S Whitehead

Frequent Co-Authors

Ursula Bellugi
Ursula Bellugi Salk Institute for Biological Studies
Debra L. Mills
Debra L. Mills Bangor University
Allan L. Reiss
Allan L. Reiss Stanford University
Albert M. Galaburda
Albert M. Galaburda Beth Israel Deaconess Medical Center
Stefan M. Pulst
Stefan M. Pulst University of Utah
Kazuhiro Yamakawa
Kazuhiro Yamakawa Nagoya City University
Judy Reilly
Judy Reilly San Diego State University
Mark A. Eckert
Mark A. Eckert Medical University of South Carolina
Melvin I. Simon
Melvin I. Simon California Institute of Technology
Fumiko Hoeft
Fumiko Hoeft University of Connecticut

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