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Medicine

D-Index
103
Citations
35476
World Ranking
7418
National Ranking
3878

Overview

Hugo W. Moser was a researcher primarily affiliated with the Kennedy Krieger Institute in the United States. Their academic work spanned key areas within biochemistry, genetics, and molecular biology, as well as medicine.

Their research included contributions to specific subfields such as physiology, molecular biology, and cell biology. These subfields complemented their broader investigations, offering insights into complex biological processes.

Moser's main topics of study focused on lysosomal storage disorders research, sphingolipid metabolism and signaling, and cellular transport and secretion. These topics highlight their interest in understanding cellular mechanisms and disease pathways related to lysosomal function and lipid biochemistry.

  • Lysosomal Storage Disorders Research
  • Sphingolipid Metabolism and Signaling
  • Cellular Transport and Secretion

The scientist frequently collaborated with others during their career, including coauthors Michael Beck and Konrad Sandhoff.

  • Michael Beck
  • Konrad Sandhoff

Best Publications

  • Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

    Jean Mosser;Anne-Marie Douar;Claude-Olivier Sarde;Petra Kioschis

  • Dendritic Anomalies in Disorders Associated with Mental Retardation

    Walter E. Kaufmann;Hugo W. Moser;Hugo W. Moser

  • X-linked adrenoleukodystrophy.

    Hugo W Moser;Hugo W Moser;Asif Mahmood;Gerald V Raymond

  • Imaging cortical association tracts in the human brain using diffusion-tensor-based axonal tracking.

    Susumu Mori;Walter E. Kaufmann;Christos Davatzikos;Bram Stieltjes

  • Adrenoleukodystrophy: phenotype, genetics, pathogenesis and therapy.

    H W Moser

  • Peroxisome biogenesis disorders.

    Steven J. Steinberg;Gabriele Dodt;Gerald V. Raymond;Nancy E. Braverman

  • Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders

    Gabriele Dodt;Nancy Braverman;Candice Wong;Ann Moser

  • Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata.

    Nancy Braverman;Gary Steel;Cassandra Obie;Ann Moser

  • Adrenoleukodystrophy Increased plasma content of saturated very long chain fatty acids

    Hugo W. Moser;Hugo W. Moser;Ann B. Moser;Karen K. Frayer;Winston Chen

  • Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening

    Lena Bezman;Ann B. Moser;Gerald V. Raymond;Piero Rinaldo

  • Cerebral X-linked adrenoleukodystrophy: the international hematopoietic cell transplantation experience from 1982 to 1999.

    Charles Peters;Lawrence R. Charnas;Ye Tan;Richard S. Ziegler

  • Long-term effect of bone-marrow transplantation for childhood-onset cerebral X-linked adrenoleukodystrophy

    Elsa G Shapiro;W. Krivit;L. Lockman;I. Jambaqué

  • Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls

    Ann B. Moser;Nancy Kreiter;Lena Bezman;Shou en Lu

  • ABCD1 mutations and the X‐linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations

    Stephan Kemp;Aurora Pujol;Hans R. Waterham;Björn M. Van Geel

  • Adrenoleukodystrophy: a scoring method for brain MR observations.

    D. J. Loes;S. Hite;H. Moser;A. E. Stillman

  • The cerebrohepatorenal (Zellweger) syndrome. Increased levels and impaired degradation of very-long-chain fatty acids and their use in prenatal diagnosis.

    Ann E. Moser;Inderjit Singh;Inderjit Singh;Inderjit Singh;Frank R. Brown;Frank R. Brown;Frank R. Brown;George I. Solish;George I. Solish;George I. Solish

  • Adrenoleukodystrophy: survey of 303 cases: biochemistry, diagnosis, and therapy

    Hugo W. Moser;Ann E. Moser;Inderjit Singh;P. O'Neill

  • Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells

    Barbara R. Migeon;Hugo W. Moser;Ann B. Moser;Joyce Axelman

  • A mouse model for X-linked adrenoleukodystrophy

    Jyh Feng Lu;Ann M. Lawler;Paul A. Watkins;James M. Powers

  • Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome.

    Jutta Gärtner;Hugo Moser;David Valle

Frequent Co-Authors

Ann B. Moser
Ann B. Moser Kennedy Krieger Institute
Paul A. Watkins
Paul A. Watkins Kennedy Krieger Institute
David Valle
David Valle Johns Hopkins University School of Medicine
Ronald J.A. Wanders
Ronald J.A. Wanders University of Amsterdam
William Krivit
William Krivit University of Minnesota
Peter C.M. van Zijl
Peter C.M. van Zijl Kennedy Krieger Institute
H. van den Bosch
H. van den Bosch Utrecht University
J. M. Tager
J. M. Tager University of Amsterdam
John M. Opitz
John M. Opitz University of Utah
James F. Reynolds
James F. Reynolds Monash University

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Best Scientists Citing Hugo W. Moser