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Simon G. Gregory

Simon G. Gregory

D-Index & Metrics

Genetics

D-Index
68
Citations
67642
World Ranking
2378
National Ranking
1069

Overview

Simon G. Gregory is affiliated with Duke University in the United States. Their research spans multiple fields, primarily Medicine and Biochemistry, Genetics and Molecular Biology. Within these main areas, their work touches on subfields such as Molecular Biology, Immunology, Cancer Research, Pulmonary and Respiratory Medicine, and Genetics.

The researcher's recent publications reflect a broad interest in biological mechanisms and medical conditions. Selected recent papers include:

  • Synovial cell cross-talk with cartilage plays a major role in the pathogenesis of osteoarthritis, 2020, Scientific Reports
  • Human distal lung maps and lineage hierarchies reveal a bipotent progenitor, 2022, Nature
  • Intranasal Oxytocin in Children and Adolescents with Autism Spectrum Disorder, 2021, New England Journal of Medicine
  • Erythromyeloid progenitors give rise to a population of osteoclasts that contribute to bone homeostasis and repair, 2020, Nature Cell Biology
  • Meteorin-like facilitates skeletal muscle repair through a Stat3/IGF-1 mechanism, 2020, Nature Metabolism

Frequent topics studied by Simon G. Gregory include:

  • Neuroendocrine regulation and behavior
  • Glioma Diagnosis and Treatment
  • Immune cells in cancer
  • Single-cell and spatial transcriptomics
  • Infant Health and Development
  • Immune Cell Function and Interaction
  • Prostate Cancer Treatment and Research

The scientist has collaborated often with several co-authors, including:

  • David M. Ashley
  • Vaibhav Jain
  • Giselle Y. López
  • Karen Abramson
  • Emily Hocke

Simon G. Gregory's publications are well represented in a variety of venues. The most frequent publication outlets include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Neuro-Oncology
  • Scientific Reports
  • Cancer Research
  • JCI Insight

The research encompasses work on immune mechanisms, cancer biology, molecular genetics, and pulmonary medicine, alongside applications of single-cell and spatial transcriptomics. This variety indicates a multidisciplinary approach connecting cellular biology with clinical implications.

Best Publications

  • Initial sequencing and analysis of the human genome.

    Eric S. Lander;Lauren M. Linton;Bruce Birren;Chad Nusbaum

  • Initial sequencing and comparative analysis of the mouse genome.

    Robert H. Waterston;Kerstin Lindblad-Toh;Ewan Birney;Jane Rogers

  • Identification of the breast cancer susceptibility gene BRCA2

    Wooster R;Bignell G;Lancaster J;Swift S

  • Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

    H Ueda;Howson Jmm.;L Esposito;J Heward

  • Risk alleles for multiple sclerosis identified by a genomewide study.

    David A. Hafler;Alastair Compston;Stephen Sawcer;Mark J. Daly

  • The DNA sequence of the human X chromosome

    Mark T Ross;Darren V Grafham;Alison J Coffey;Steven Scherer

  • A high resolution HLA and SNP haplotype map for disease association studies in the extended human MHC

    Paul I W de Bakker;Gil McVean;Pardis C Sabeti;Marcos M Miretti

  • Interleukin 7 receptor α chain (IL7R) shows allelic and functional association with multiple sclerosis

    Simon G. Gregory;Silke Schmidt;Puneet Seth;Jorge R. Oksenberg

  • A physical map of the human genome.

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

  • LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

    Sue Shackleton;David J. Lloyd;Stephen N.J. Jackson;Richard Evans

  • Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.

    Simon G Gregory;Jessica J Connelly;Aaron J Towers;Jessica Johnson

  • Interleukin-2 gene variation impairs regulatory T cell function and causes autoimmunity

    Jun Yamanouchi;Dan Rainbow;Pau Serra;Sarah Howlett

  • A stress response pathway regulates DNA damage through β2-adrenoreceptors and β-arrestin-1.

    Makoto R. Hara;Jeffrey J. Kovacs;Erin J. Whalen;Sudarshan Rajagopal

  • The DNA sequence and biological annotation of human chromosome 1

    S. G. Gregory;S. G. Gregory;K. F. Barlow;K. E. McLay;R. Kaul

  • A physical map of the mouse genome.

    Simon G Gregory;Mandeep Sekhon;Jacqueline Schein;Shaying Zhao

  • A high-density screen for linkage in multiple sclerosis.

    Sawcer S;Ban M;Maranian M;Yeo Tw

  • Prospective Multicenter Validation of Androgen Receptor Splice Variant 7 and Hormone Therapy Resistance in High-Risk Castration-Resistant Prostate Cancer: The PROPHECY Study

    Andrew J. Armstrong;Susan Halabi;Jun Luo;David M. Nanus

  • Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness

    Valentina Labay;Tal Raz;Dana Baron;Hanna Mandel

  • Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome.

    Ruti Parvari;Eli Hershkovitz;Nili Grossman;Rafael Gorodischer

  • Erratum: Identification of the breast cancer susceptibility gene BRCA2

    Richard Wooster;Graham Bignell;Jonathan Lancaster;Sally Swift

Frequent Co-Authors

Svati H. Shah
Svati H. Shah Duke University
Elizabeth R. Hauser
Elizabeth R. Hauser Duke University
William E. Kraus
William E. Kraus Duke University
Allison E. Ashley-Koch
Allison E. Ashley-Koch Duke University
Jeffery M. Vance
Jeffery M. Vance University of Miami
Margaret A. Pericak-Vance
Margaret A. Pericak-Vance University of Miami
Jane Rogers
Jane Rogers Earlham Institute
Lisa F. Barcellos
Lisa F. Barcellos University of California, Berkeley
Stephen L. Hauser
Stephen L. Hauser University of California, San Francisco

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