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Medicine

D-Index
78
Citations
22330
World Ranking
18044
National Ranking
759

Research.com Recognitions

  • 2011 - Fellow of the Royal Society of Canada Academy of Science

Overview

Judith G. Hall is a researcher affiliated with the University of British Columbia in Canada. Their academic work lies predominantly in the field of Medicine, with a focus on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Pulmonary and Respiratory Medicine, and Surgery. The scope of their research covers multiple topics including Neurogenetic and Muscular Disorders Research, Prenatal Screening and Diagnostics, Genomics and Rare Diseases, Assisted Reproductive Technology and Twin Pregnancy, Congenital Anomalies and Fetal Surgery, BRCA gene mutations in cancer, and Genomic variations and chromosomal abnormalities.

The research contributions of Judith G. Hall include numerous recent papers such as:

  • "Recurrent constellations of embryonic malformations re-conceptualized as an overlapping group of disorders with shared pathogenesis" (2020) published in American Journal of Medical Genetics Part A
  • "The spectrum of brain malformations and disruptions in twins" (2020) published in American Journal of Medical Genetics Part A
  • "Perspectives on the future of dysmorphology" (2022) published in American Journal of Medical Genetics Part A
  • "Common data elements for arthrogryposis multiplex congenita: An international framework" (2024) published in Developmental Medicine & Child Neurology
  • "Deformations associated with arthrogryposis" (2021) published in American Journal of Medical Genetics Part A

Judith G. Hall frequently co-authors with several researchers, including:

  • Nicholas G. Martin
  • Jeffrey M. Craig
  • Yoon-Mi Hur
  • Jaakko Kaprio
  • Cornelis B. Lambalk

The venues where Judith G. Hall publishes most often encompass:

  • Twin Research and Human Genetics (13 publications)
  • American Journal of Medical Genetics Part A (11 publications)
  • American Journal of Medical Genetics Part C Seminars in Medical Genetics (7 publications)
  • Developmental Medicine & Child Neurology (3 publications)
  • UNC Libraries (2 publications)

An award received by Judith G. Hall includes election as a Fellow of the Royal Society of Canada in 2011 under the Academy of Science category.

Best Publications

  • Maternal and fetal sequelae of anticoagulation during pregnancy

    Judith G. Hall;Richard M. Pauli;Kathleen M. Wilson

  • International Nosology of Heritable Disorders of Connective Tissue, Berlin, 1986.

    P. Beighton;A. de Paepe;D. Danks;G. Finidori

  • Genomic imprinting: review and relevance to human diseases.

    J G Hall

  • Errors of morphogenesis: concepts and terms. Recommendations of an international working group.

    J. Spranger;K. Benirschke;J.G. Hall;W. Lenz

  • Evidence for multi‐site closure of the neural tube in humans

    Margot I. Van Allen;Dagmar K. Kalousek;Gerold F. Chernoff;Diana Juriloff

  • Review and hypotheses: somatic mosaicism: observations related to clinical genetics.

    Hall Jg

  • Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly—a new syndrome? Part I: Clinical, causal, and pathogenetic considerations

    J. G. Hall;P. D. Pallister;S. K. Clarren;J. B. Beckwith

  • Handbook of Normal Physical Measurements

    Judith G. Hall;Ursula G. Froster-Iskenius;Judith E. Allanson

  • Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach, and general aspects.

    Judith G. Hall

  • STANDARD GROWTH CURVES FOR ACHONDROPLASIA

    William A. Horton;Jerome I. Rotter;David L. Rimoin;Charles I. Scott

  • The distal arthrogryposes: delineation of new entities--review and nosologic discussion.

    J. G. Hall;S. D. Reed;G. Greene

  • Human Malformations and Related Anomalies

    Roger E. Stevenson;Judith G. Hall

  • Noonan Syndrome: The Changing Phenotype

    J. E. Allanson;J. G. Hall;H. E. Hughes;M. Preus

  • Arthrogryposis (multiple congenital contractures): diagnostic approach to etiology, classification, genetics, and general principles.

    Judith G. Hall

  • Health supervision for children with achondroplasia.

    Tracy L. Trotter;Judith G. Hall

  • Osteogenesis imperfecta type III. Delineation of the phenotype with reference to genetic heterogeneity

    D. O. Sillence;K. K. Barlow;A. P. Garber;J. G. Hall

  • X-linked cutis laxa: defective cross-link formation in collagen due to decreased lysyl oxidase activity.

    Byers Ph;Siegel Rc;Holbrook Ka;Narayanan As

  • Klinefelter syndrome: Expanding the phenotype and identifying new research directions

    Joe Leigh Simpson;Felix de la Cruz;Ronald S Swerdloff;Carole Samango-Sprouse

  • Apnea and sudden unexpected death in infants with achondroplasia

    Richard M. Pauli;Charles I. Scott;E. Robert Wassman;Enid F. Gilbert

  • Analysis of Pena Shokeir phenotype.

    Hall Jg

Frequent Co-Authors

John M. Opitz
John M. Opitz University of Utah
James F. Reynolds
James F. Reynolds Monash University
John M. Graham
John M. Graham Cedars-Sinai Medical Center
David L. Rimoin
David L. Rimoin Cedars-Sinai Medical Center
Kenneth L. Jones
Kenneth L. Jones University of California, San Diego
Holger Hoehn
Holger Hoehn University of Würzburg
William A. Horton
William A. Horton Shriners Hospitals for Children - Erie
Peter H. Byers
Peter H. Byers University of Washington
Donna E. Stewart
Donna E. Stewart University of Toronto
Roger E. Stevenson
Roger E. Stevenson Clemson University

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