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Genetics

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106
Citations
36439
World Ranking
607
National Ranking
305

Molecular Biology

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106
Citations
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430
National Ranking
246

Medicine

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105
Citations
36295
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6823
National Ranking
3601

Overview

Paul J. Hagerman is affiliated with the University of California, Davis, in the United States. Their research primarily focuses on Biochemistry, Genetics, and Molecular Biology, with notable contributions to Genetics and Neurodevelopmental Disorders and Autism Spectrum Disorder Research.

The scientist's work spans several main topics including:

  • Genetics and Neurodevelopmental Disorders
  • Autism Spectrum Disorder Research
  • Congenital heart defects research
  • Ubiquitin and proteasome pathways
  • Genomic variations and chromosomal abnormalities
  • Endoplasmic Reticulum Stress and Disease
  • Epigenetics and DNA Methylation

Paul J. Hagerman has published extensively in subfields such as:

  • Genetics
  • Molecular Biology
  • Cognitive Neuroscience
  • Cell Biology
  • Oncology

Frequent publication venues for their work include:

  • Frontiers in Molecular Biosciences
  • Cells
  • Genes
  • Current Opinion in Neurology
  • Movement Disorders Clinical Practice

Among their recent papers are:

  • "Fragile X-associated tremor/ataxia syndrome: pathophysiology and management," 2021, Current Opinion in Neurology
  • "Women with Fragile X-associated Tremor/Ataxia Syndrome," 2020, Movement Disorders Clinical Practice
  • "Fragile X syndrome," 2021, Current Biology
  • "Elevated FMR1-mRNA and lowered FMRP - A double-hit mechanism for psychiatric features in men with FMR1 premutations," 2020, Translational Psychiatry
  • "Human Cerebral Cortex Proteome of Fragile X-Associated Tremor/Ataxia Syndrome," 2021, Frontiers in Molecular Biosciences

Paul J. Hagerman frequently collaborates with other researchers. Notable frequent co-authors include:

  • Randi J. Hagerman
  • Flora Tassone
  • Jamie L. Randol
  • Andrea Schneider
  • Kyoungmi Kim

Best Publications

  • Flexibility of DNA

    Paul J. Hagerman

  • Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

    Randi J Hagerman;M. Leehey;W. Heinrichs;Flora Tassone

  • Sequence-directed curvature of DNA.

    Paul J. Hagerman

  • Elevated levels of FMR1 mRNA in carrier males : A new mechanism of involvement in the fragile-X syndrome

    Flora Tassone;Randi J. Hagerman;Randi J. Hagerman;Annette K. Taylor;Louise W. Gane

  • Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates

    Sébastien Jacquemont;Randi J. Hagerman;Maureen Leehey;Jim Grigsby

  • Fragile X syndrome

    Randi J. Hagerman;Elizabeth Berry-Kravis;Heather Cody Hazlett;Donald B. Bailey

  • The fragile-X premutation: a maturing perspective.

    Paul J. Hagerman;Randi J. Hagerman

  • Penetrance of the Fragile X–Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population

    Sébastien Jacquemont;Randi J. Hagerman;Maureen A. Leehey;Deborah A. Hall

  • Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS)

    C. M. Greco;Robert F Berman;Ryan Martin;Flora Tassone

  • Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers.

    C. M. Greco;Randi J Hagerman;Flora Tassone;A. E. Chudley

  • Autism profiles of males with fragile X syndrome.

    Susan W. Harris;David R Hessl;Beth Goodlin-Jones;Jessica A Ferranti

  • The fragile X prevalence paradox

    Paul J Hagerman

  • Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction

    James A. Brunberg;Sebastien Jacquemont;Randi J. Hagerman;Elizabeth M. Berry-Kravis

  • Fragile-X–Associated Tremor/Ataxia Syndrome (FXTAS) in Females with the FMR1 Premutation

    Randi J Hagerman;B. R. Leavitt;F. Farzin;S. Jacquemont

  • Investigation of the flexibility of DNA using transient electric birefringence.

    Paul J. Hagerman

  • Protein composition of the intranuclear inclusions of FXTAS

    C. K. Iwahashi;D. H. Yasui;H. J. An;C. M. Greco

  • Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation.

    Faraz Farzin;Hazel Perry;David R Hessl;Danuta Loesch

  • Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients

    Chantal Sellier;Frédérique Rau;Yilei Liu;Flora Tassone

  • Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome

    Randi J Hagerman;Paul J Hagerman

  • Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Authors' reply

    David G. Munoz;R. J. Hagerman;C. Greco;S. Jacquemont

Frequent Co-Authors

Randi J Hagerman
Randi J Hagerman University of California, Davis
Flora Tassone
Flora Tassone University of California, Davis
Jim Grigsby
Jim Grigsby University of Colorado Denver
David R Hessl
David R Hessl University of California, Davis
Elizabeth Berry-Kravis
Elizabeth Berry-Kravis Rush University Medical Center
Sébastien Jacquemont
Sébastien Jacquemont University of Montreal
Isaac N. Pessah
Isaac N. Pessah University of California, Davis
Susan M. Rivera
Susan M. Rivera University of California, Davis
Rob Willemsen
Rob Willemsen Erasmus University Rotterdam
Robert F. Berman
Robert F. Berman University of California, Davis

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