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Bernard G. Forget

Bernard G. Forget

D-Index & Metrics

Molecular Biology

D-Index
68
Citations
13016
World Ranking
1538
National Ranking
779

Overview

Bernard G. Forget is affiliated with Yale University in the United States, contributing to the field of Medicine with a specific focus on Geriatrics and Gerontology. Their research emphasizes Pharmaceutical Practices and Patient Outcomes, reflecting an interest in improving medication management especially in elderly populations.

Recent scholarly work includes the paper titled "4CPS-227 Pharmaceutical review and pharmaceutical intervention in a nursing home to enhance the medication management of residents," published in 2024 in the venue Section 4: Clinical pharmacy services.

Frequent coauthors in their research include:

  • Eugénie Castex
  • V Frapart
  • Luisa Bertin
  • J Siauve

Publication activities are primarily concentrated in the venue Section 4: Clinical pharmacy services, where they have contributed at least one paper.

Their main research topics are centered around Pharmaceutical Practices and Patient Outcomes, which suggests a professional interest in the optimization of pharmacy-related clinical services and the impact of these interventions on patient health, particularly in geriatric care settings.

Best Publications

  • The structure and evolution of the human β-globin gene family

    Argiris Efstratiadis;James W. Posakony;Tom Maniatis;Richard M. Lawn

  • Short interspersed repetitive DNA elements in eucaryotes: transposable DNA elements generated by reverse transcription of RNA pol III transcripts?

    Pudur Jagadeeswaran;Bernard G. Forget;Sherman M. Weissman

  • Molecular basis of hereditary persistence of fetal hemoglobin

    Bernard G. Forget

  • Full-length sequence of the cDNA for human erythroid beta-spectrin.

    John C. Winkelmann;Jan Gowth Chang;William T. Tse;Alphonse L. Scarpa

  • Human beta-globin messenger RNA. III. Nucleotide sequences derived from complementary DNA.

    C A Marotta;J T Wilson;B G Forget;S M Weissman

  • Nucleotide Sequence of KB Cell 5S RNA

    Bernard G. Forget;Sherman M. Weissman

  • Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.

    Stefan W. Eber;Jennifer M. Gonzalez;Marcia L. Lux;Alphonse L. Scarpa

  • Base substitution in an intervening sequence of a beta+-thalassemic human globin gene

    R. A. Spritz;P. Jagadeeswaran;Prabhakara V Choudary;P. A. Biro

  • Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8.

    Samuel E. Lux;William T. Tse;Joan C. Menninger;Kathryn M. John

  • A point mutation in the A γ -globin gene promoter in Greek hereditary persistence of fetal haemoglobin

    Francis S. Collins;Francis S. Collins;James E. Metherall;Minoru Yamakawa;Julian Pan

  • Embryonic-fetal erythroid characteristics of a human leukemic cell line

    Edward J. Benz;Mary J. Murnane;Barry L. Tonkonow;Brian W. Berman

  • Erythroid and nonerythroid spectrins

    John C. Winkelmann;Bernard G. Forget

  • The gene for the human erythropoietin receptor: analysis of the coding sequence and assignment to chromosome 19p

    John C. Winkelmann;Laura A. Penny;Larry L. Deaven;Bernard G. Forget

  • Classification of the Disorders of Hemoglobin

    Bernard G. Forget;H. Franklin Bunn

  • Complete nucleotide sequence of the human δ-globin gene

    Richard A. Spritz;Jon K. Deriel;Bernard G. Forget;Sherman M. Weissman

  • G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene

    Francis S. Collins;Christian J. Stoeckert;Graham R. Serjeant;Bernard G. Forget

  • Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man

    Dorothy Tuan;Elise Feingold;Marsha Newman;Sherman M. Weissman

  • Reverse transcription and direct amplification of cellular RNA transcripts by Taq polymerase

    William T. Tse;Bernard G. Forget

  • Molecular evolution of human and rabbit beta-globin mRNAs.

    Fotis C. Kafatos;Argiris Efstratiadis;Bernard G. Forget;Sherman M. Weissman

  • Disorders of Hemoglobin: The Molecular Basis of α Thalassemia

    Martin H. Steinberg;Bernard G. Forget;Douglas R. Higgs;David J. Weatherall

Frequent Co-Authors

Patrick G. Gallagher
Patrick G. Gallagher Yale University
Sherman M. Weissman
Sherman M. Weissman Yale University
Samuel E. Lux
Samuel E. Lux Harvard University
Edward J. Benz
Edward J. Benz Harvard University
David H.K. Chui
David H.K. Chui Boston University
Martin H. Steinberg
Martin H. Steinberg Boston University
Jon S. Morrow
Jon S. Morrow Yale University
Richard A. Spritz
Richard A. Spritz University of Colorado Denver
Francis S. Collins
Francis S. Collins National Institutes of Health
David W. Speicher
David W. Speicher The Wistar Institute

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