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Genetics

D-Index
60
Citations
14895
World Ranking
3143
National Ranking
385

Overview

Robin M. Winter was affiliated with Northwick Park Hospital in the United Kingdom. Their research contributed primarily to the fields of Medicine and Physics and Astronomy, with specific focus on Radiology, Nuclear Medicine and Imaging as well as Atomic and Molecular Physics, and Optics.

The scientist's work encompassed two main thematic areas: Medical Imaging Techniques and Applications, and Atomic and Subatomic Physics Research. Additionally, their research included aspects of Radiomics and Machine Learning in Medical Imaging.

Winter's publication record includes contributions to the repository arXiv (Cornell University), where their recent paper titled "A novel imaging setup for hybrid radiotherapy tailored PET/MR in patients with head and neck cancer" was published in 2024.

  • A novel imaging setup for hybrid radiotherapy tailored PET/MR in patients with head and neck cancer, 2024, arXiv (Cornell University)

Collaborations featured a number of frequent co-authors, including:

  • Ola Engelsen
  • O. J. Bratting
  • Njål Brekke
  • Jostein Sæterstøl
  • O. Sæther

These collaborations indicate an interdisciplinary approach bridging clinical medicine and imaging physics.

Winter's scientific contributions spanned investigations of advanced imaging technologies as applied to cancer radiotherapy and the integration of PET/MR systems, as well as research in atomic and subatomic physics relevant to medical imaging techniques.

Best Publications

  • Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

    A K Ryan;J A Goodship;D I Wilson;N Philip

  • Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.

    Andrew O.M. Wilkie;Andrew O.M. Wilkie;Sarah F. Slaney;Sarah F. Slaney;Michael Oldridge;Michael D. Poole

  • Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome.

    William Reardon;Robin M. Winter;Paul Rutland;Louise J. Pulleyn

  • Subtle chromosomal rearrangements in children with unexplained mental retardation.

    Samantha J L Knight;Regina Regan;Alison Nicod;Sharon W Horsley

  • Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.

    P Rutland;L J Pulleyn;W Reardon;M Baraitser

  • Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome

    M.V. Bell;M.C. Hirst;Y. Nakahori;R.N. MacKinnon

  • Identification of the gene for oral-facial-digital type I syndrome.

    Maria I. Ferrante;Sally A. Feather;Alessandro Bulfone;Victoria Wright

  • Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis

    Deborah J. Shears;Humberto J. Vassal;Frances R. Goodman;Rodger W. Palmer

  • Clinical studies on submicroscopic subtelomeric rearrangements: a checklist.

    B B A de Vries;S M White;S J L Knight;R Regan

  • Telomeres: a diagnosis at the end of the chromosomes

    L.B.A. de Vries;R. Winter;A. Schinzel;C.M.A. van Ravenswaaij-Arts

  • 3D analysis of facial morphology

    Peter Hammond;Tim J. Hutton;Judith E. Allanson;Linda E. Campbell

  • Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes.

    Xiao Ping Zhou;Heather Hampel;Hannelore Thiele;Robert J. Gorlin

  • The mutational spectrum in Waardenburg syndrome

    Mayada Tassabehji;Valerie E. Newton;Xue Zhong Liu;Xue Zhong Liu;Angela Brady

  • Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract

    F. R. Goodman;S. Mundlos;Y. Muragaki;D. Donnai

  • Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype.

    A K Ryan;K Bartlett;P Clayton;S Eaton

  • Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases

    H. Annika Siitonen;Outi Kopra;Helena Kääriäinen;Henna Haravuori

  • Clinical phenotype of desmosterolosis

    David R. FitzPatrick;Jean W. Keeling;Margaret J. Evans;Alex E. Kan

  • Identification of mutations in CUL7 in 3-M syndrome

    Céline Huber;Dora Dias-Santagata;Anna Glaser;James O'Sullivan

  • A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation.

    M. E. Pembrey;R. M. Winter;K. E. Davies;John M. Opitz

  • Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome

    M Oldridge;A O Wilkie;S F Slaney;Poole

Frequent Co-Authors

Sue Malcolm
Sue Malcolm University College London
William Reardon
William Reardon Children's Health Ireland
Peter J. Scambler
Peter J. Scambler University College London
Louise Brueton
Louise Brueton Northwick Park Hospital
Dian Donnai
Dian Donnai University of Manchester
Kay E. Davies
Kay E. Davies University of Oxford
Andrew O.M. Wilkie
Andrew O.M. Wilkie University of Oxford
James F. Reynolds
James F. Reynolds Monash University
Raoul C.M. Hennekam
Raoul C.M. Hennekam University of Amsterdam
John M. Opitz
John M. Opitz University of Utah

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