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Biology and Biochemistry

D-Index
46
Citations
7316
World Ranking
18963
National Ranking
7745

Overview

David F. Bishop is affiliated with the Icahn School of Medicine at Mount Sinai in the United States. Their research focuses primarily on the fields of Medicine and Biochemistry, Genetics and Molecular Biology, with subfields including Molecular Biology, Rheumatology, Physiology, Pulmonary and Respiratory Medicine, and Cardiology and Cardiovascular Medicine.

The topics central to their work encompass Porphyrin Metabolism and Disorders, Heme Oxygenase-1 and Carbon Monoxide, Folate and B Vitamins Research, Erythrocyte Function and Pathophysiology, Blood properties and coagulation, as well as Lipid metabolism and disorders.

Among recent publications, notable papers include the 2020 article "Human aminolevulinate synthase structure reveals a eukaryotic-specific autoinhibitory loop regulating substrate binding and product release" published in Nature Communications, and another 2020 paper titled "X-linked macrocytic dyserythropoietic anemia in females with an ALAS2 mutation" featured in the Journal of Clinical Investigation.

Frequent co-authors collaborating with David F. Bishop are:

  • H. Bailey
  • G.A. Bezerra
  • Jason R. Marcero
  • Siladitya Padhi
  • William R. Foster

Publications are also frequently found in these venues:

  • Nature Communications
  • Journal of Clinical Investigation

Best Publications

  • An atypical variant of Fabry's disease with manifestations confined to the myocardium.

    von Scheidt W;Eng Cm;Fitzmaurice Tf;Erdmann E

  • Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation

    Soumeya Bekri;Gyula Kispal;Gyula Kispal;Gyula Kispal;Heike Lange;Edward Fitzsimons

  • Human alpha-galactosidase A: nucleotide sequence of a cDNA clone encoding the mature enzyme.

    David F. Bishop;David H. Calhoun;Harold S. Bernstein;Petros Hantzopoulos

  • Acute Porphyrias in the USA: Features of 108 Subjects from Porphyrias Consortium

    Herbert L. Bonkovsky;Vinaya C. Maddukuri;Cemal Yazici;Karl E. Anderson

  • Structural organization of the human alpha-galactosidase A gene: further evidence for the absence of a 3' untranslated region.

    David F. Bishop;Ruth Kornreich;Robert J. Desnick

  • Human δ-aminolevulinate synthase: Assignment of the housekeeping gene to 3p21 and the erythroid-specific gene to the X chromosome

    David F. Bishop;Ann S. Henderson;Kenneth H. Astrin

  • Overexpression of human alpha-galactosidase A results in its intracellular aggregation, crystallization in lysosomes, and selective secretion.

    Y A Ioannou;D F Bishop;R J Desnick

  • Nucleotide sequence of the human α-galactosidase A gene

    Ruth Kornreich;Robert J. Desnick;David F. Bishop

  • Fabry disease: six gene rearrangements and an exonic point mutation in the alpha-galactosidase gene.

    H S Bernstein;D F Bishop;K H Astrin;R Kornreich

  • Enzymatic defect in "X-linked" sideroblastic anemia: molecular evidence for erythroid delta-aminolevulinate synthase deficiency.

    Philip D. Cotter;Martin Baumann;David F. Bishop

  • Identification of point mutations in the alpha-galactosidase A gene in classical and atypical hemizygotes with Fabry disease.

    H Sakuraba;A Oshima;Y Fukuhara;M Shimmoto

  • Alpha-galactosidase A gene rearrangements causing Fabry disease. Identification of short direct repeats at breakpoints in an Alu-rich gene.

    R Kornreich;D F Bishop;R J Desnick

  • Affinity purification of alpha-galactosidase A from human spleen, placenta, and plasma with elimination of pyrogen contamination. Properties of the purified splenic enzyme compared to other forms.

    D F Bishop;R J Desnick

  • Human delta-aminolevulinate dehydratase: nucleotide sequence of a full-length cDNA clone

    James G. Wetmur;David F. Bishop;Christopher Cantelmo;Robert J. Desnick

  • δ-Aminolevulinic Acid Dehydratase Isozymes and Lead Toxicitya

    K. H. Astrin;D. F. Bishop;J. G. Wetmur;B. Kaul

  • Neuroaxonal dystrophy due to lysosomal alpha-N-acetylgalactosaminidase deficiency.

    Detlev Schindler;David F. Bishop;David E. Wolfe;Anne M. Wang

  • Enzyme therapy in Fabry disease: differential in vivo plasma clearance and metabolic effectiveness of plasma and splenic alpha-galactosidase A isozymes

    Robert J. Desnick;Kenneth J. Dean;Gregory Grabowski;David F. Bishop

  • Uroporphyrinogen III synthase erythroid promoter mutations in adjacent GATA1 and CP2 elements cause congenital erythropoietic porphyria

    Constanza Solis;Gerardo I. Aizencang;Kenneth H. Astrin;David F. Bishop

  • Late-onset X-linked sideroblastic anemia. Missense mutations in the erythroid delta-aminolevulinate synthase (ALAS2) gene in two pyridoxine-responsive patients initially diagnosed with acquired refractory anemia and ringed sideroblasts.

    P. D. Cotter;A. May;E. J. Fitzsimons;T. Houston

  • Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females.

    Mario Cazzola;Mario Cazzola;Mario Cazzola;Alison May;Alison May;Alison May;Gaetano Bergamaschi;Gaetano Bergamaschi;Gaetano Bergamaschi;Paola Cerani;Paola Cerani;Paola Cerani

Frequent Co-Authors

Robert J. Desnick
Robert J. Desnick Icahn School of Medicine at Mount Sinai
James G. Wetmur
James G. Wetmur Icahn School of Medicine at Mount Sinai
Shih-Feng Tsai
Shih-Feng Tsai National Health Research Institutes
Charles C. Sweeley
Charles C. Sweeley Michigan State University
Herbert L. Bonkovsky
Herbert L. Bonkovsky Wake Forest University
Andrej Hasilik
Andrej Hasilik Philipp University of Marburg
John A. Martignetti
John A. Martignetti Icahn School of Medicine at Mount Sinai
Vijay G. Sankaran
Vijay G. Sankaran Harvard University
Vern L. Schramm
Vern L. Schramm Albert Einstein College of Medicine
Harry A. Dailey
Harry A. Dailey University of Georgia

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