Bernard G. Forget

9.3k citations

162 papers · 7.5k indexed · 1 hit paper · h-index 51

Impact in

Genetics top 0.1%
- Hemoglobinopathies and Related Disorders
Hematology top 0.5%
- Iron Metabolism and Disorders

Papers in

Genetics 68
- Hemoglobinopathies and Related Disorders 66
Hematology 46
- Iron Metabolism and Disorders 20

Co-authors: Sherman M. Weissman S M Weissman Patrick G. Gallagher Pudur Jagadeeswaran Jon K. deRiel William Tse John T. Wilson S Weissman
Journals: Journal of Biological Chemistry (17 papers)Blood (16 papers)Proceedings of the National Academy of Sciences (9 papers)Annals of the New York Academy of Sciences (8 papers)Journal of Clinical Investigation (7 papers)
Partner nations: United States France Canada

In The Last Decade

Bernard G. Forget

162 papers receiving 7.0k citations

Hit Papers

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The Structure and Evolution of the Human /?-Globin Gene Family 1980 · 253 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

1980 The Structure and Evolution of the Human /?-Globin Gene Family

Peers

Countries citing papers authored by Bernard G. Forget

Since Specialization

Citations

This map shows the geographic impact of Bernard G. Forget's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Bernard G. Forget with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernard G. Forget more than expected).

Fields of papers citing papers by Bernard G. Forget

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bernard G. Forget. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Bernard G. Forget. The network helps show where Bernard G. Forget may publish in the future.

Co-authors

The 25 scholars most cited alongside Bernard G. Forget, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Bernard G. Forget Line = papers co-authored together Bernard G. Forget links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Massive splenic infarction in an adolescent with hemoglobin S‐HPFH Pediatric Blood & Cancer ·Akarawit Eiamsamarng, Bernard G. Forget, David H.K. Chui, Hongyuan Luo, Farzana Pashankar	2012	5
2	Preface Hematology/Oncology Clinics of North America ·Bernard G. Forget	2010	1
3	Cytokine signals through STAT3 promote expression of granulocyte secondary granule proteins in 32D cells Experimental Hematology ·Lei Wang, Murat O. Arcasoy, Stephanie S. Watowich, Bernard G. Forget	2005	10
4	The homeodomain gene Pitx2 is expressed in primitive hematopoietic stem/progenitor cells but not in their differentiated progeny Experimental Hematology ·Barbara Degar, M Zdybiewska, Becky McCorkle, Peter J. Quesenberry, Sherman M. Weissman, Bernard G. Forget	2001	20
5	A Human β-Spectrin Gene Promoter Directs High Level Expression in Erythroid but Not Muscle or Neural Cells Journal of Biological Chemistry ·Patrick G. Gallagher, Denise E. Sabatino, Marc Romana, Amanda P. Cline, Lisa Garrett, David M. Bodine, Bernard G. Forget	1999	27
6	Molecular Basis of Hereditary Persistence of Fetal Hemoglobin Annals of the New York Academy of Sciences ·Bernard G. Forget	1998	215
7	Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia. Journal of Clinical Investigation ·Patrick G. Gallagher, Mary Jane Petruzzi, Scott A. Weed, Zhigang Zhang, Sally L. Marchesi, Narla Mohandas, Jon S. Morrow, Bernard G. Forget	1997	31
8	High Levels of Human γ-Globin Gene Expression in Adult Mice Carrying a Transgene of Deletion-Type Hereditary Persistence of Fetal Hemoglobin Molecular and Cellular Biology ·Murat O. Arcasoy, Marc Romana, Mary E. Fabry, Gert Feistritzer, Ronald L. Nagel, Bernard G. Forget	1997	27
9	Amino-acid substitution in α-spectrin commonly coinherited with nondominant hereditary spherocytosis American Journal of Hematology ·William Tse, Patrick G. Gallagher, Vinicius Pioli Zanetin, Yongping Wang, Lori K. Benoit, David W. Speicher, John C. Winkelmann, Peter Agre, Bernard G. Forget, Sally L. Marchesi	1997	15
10	Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis American Journal of Hematology ·Laurette Morlé, Muriel Bozon, Nicole Alloisio, Agnès Vallier, Sandrine Hayette, Keming Yang, T Almodovar Salas, N Philippe, Bernard G. Forget, J. Delaunay	1997	17
11	Structure and Organization of the Human Ankyrin-1 Gene Journal of Biological Chemistry ·Patrick G. Gallagher, William Tse, A L Scarpa, Samuel E. Lux, Bernard G. Forget	1997	62
12	Genetic basis of the polymorphisms of the αI domain of spectrin American Journal of Hematology ·Patrick G. Gallagher, Marc Romana, Clara Wong, Bernard G. Forget	1997	2
13	Hematologically Important Mutations: Band 3 and Protein 4.2 Variants in Hereditary Spherocytosis Blood Cells Molecules and Diseases ·Claudia Grzywacz, Bernard G. Forget	1997	30
14	Structure, Organization, and Expression of the Human Band 7.2b Gene, a Candidate Gene for Hereditary Hydrocytosis Journal of Biological Chemistry ·Patrick G. Gallagher, Bernard G. Forget	1995	43
15	The Gene for Human Erythrocyte Membrane Protein Band 7.2 (EPB72) Maps to 9q33-q34 Centromeric to the Philadelphia Chromosome Translocation Breakpoint Region Genomics ·Patrick G. Gallagher, Madhvi B. Upender, David C. Ward, Bernard G. Forget	1993	10
16	The exon-intron organization of the human erythrocyte α-spectrin gene Genomics ·Leszek Kotula, Lisa D. Laury‐Kleintop, Louise C. Showe, Kenneth E. Sahr, Alban J. Linnenbach, Bernard G. Forget, Peter J. Curtis	1991	27
17	Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8 Nature ·Samuel E. Lux, William Tse, Joan C. Menninger, Kathryn M. John, Peter C. Harris, O Shalev, Robert R. Chilcote, Sally L. Marchesi, Paul C. Watkins, Vann Bennett, MARIA SOUZA, Francis S. Collins, Uta Francke, David C. Ward, Bernard G. Forget	1990	161
18	Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin New England Journal of Medicine ·Fernando Ferreira Costa, Peter Agre, Paul C. Watkins, John C. Winkelmann, Tang K. Tang, K M John, Samuel E. Lux, Bernard G. Forget	1990	59
19	Cloning and Nucleotide Sequence Analysis of Human Embryonic ζ-Globin cDNA DNA ·Michel Cohen‐Solal, Omar Alidmat, Jon K. deRiel, Mary Jo Murnane, Bernard G. Forget	1982	16
20	Waldenström's macroglobulinemia with generalized amyloidosis. PubMed ·Bernard G. Forget, Zhang Yunhong, H. Sheldon	1966	35

About Bernard G. Forget

Bernard G. Forget is a scholar working on Genetics, Hematology, Physiology, Genetics and Molecular Biology, having authored 162 papers that have together received 7.5k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (66 papers), Erythrocyte Function and Pathophysiology (62 papers), RNA modifications and cancer (25 papers), Blood properties and coagulation (24 papers), RNA and protein synthesis mechanisms (20 papers), Iron Metabolism and Disorders (20 papers), Pancreatic function and diabetes (19 papers) and DNA and Nucleic Acid Chemistry (17 papers). The work is most often cited by research in Genetics (2.8k citations), Hematology (1.8k citations), Physiology (2.0k citations), Molecular Biology (4.0k citations) and Cell Biology (720 citations). Bernard G. Forget has collaborated with scholars based in United States, France and Canada. Frequent co-authors include Sherman M. Weissman, S M Weissman, Patrick G. Gallagher, Pudur Jagadeeswaran, Jon K. deRiel, William Tse, John T. Wilson, S Weissman, Martin H. Steinberg and Edward J. Benz. Their work appears in journals such as Journal of Biological Chemistry, Blood, Proceedings of the National Academy of Sciences, Annals of the New York Academy of Sciences and Journal of Clinical Investigation.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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