BG Forget

1.8k citations

63 papers · 1.7k · h-index 25

Impact in

Genetics top 1%
- Hemoglobinopathies and Related Disorders
- Diabetes and associated disorders
Hematology top 2%
- Iron Metabolism and Disorders
- Blood groups and transfusion

Papers in

Genetics 32
- Hemoglobinopathies and Related Disorders 30
- Diabetes and associated disorders 6
Physiology 28
- Erythrocyte Function and Pathophysiology 28

Co-authors: EJ Jr Benz (8 shared papers)William Tse (4 shared papers)PG Gallagher (8 shared papers)S M Weissman (2 shared papers)M Garbarz (3 shared papers)DG Nathan (4 shared papers)J. Delaunay (7 shared papers)FS Collins (5 shared papers)
Journals: Blood (44 papers)Journal of Clinical Investigation (4 papers)Proceedings of the National Academy of Sciences (4 papers)Journal of Biological Chemistry (2 papers)Cold Spring Harbor Symposia on Quantitative Biology (1 paper)
Partner nations: United States France Morocco

In The Last Decade

BG Forget

62 papers receiving 1.6k citations

Peers

Countries citing papers authored by BG Forget

Since Specialization

Citations

This map shows the geographic impact of BG 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 BG Forget with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites BG Forget more than expected).

Fields of papers citing papers by BG Forget

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by BG 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 BG Forget. The network helps show where BG Forget may publish in the future.

Co-authors

The 25 scholars most cited alongside BG 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 BG Forget Line = papers co-authored together BG Forget links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 63 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Embryonic-fetal erythroid characteristics of a human leukemic cell line. Proceedings of the National Academy of Sciences ·EJ Jr Benz, Mary Jo Murnane, B L Tonkonow, Brian Berman, Eric Michael Mazur, Cesira Cavallesco, T Jenko, Edward L. Snyder, BG Forget, R Hoffman	1980	162
2	RNA polymerase III transcriptional units are interspersed among human non-alpha-globin genes. Proceedings of the National Academy of Sciences ·Craig H. Duncan, P A Biro, Prabhakara V. Choudary, James T. Elder, Richard R.‐C. Wang, BG Forget, J. Kim de Riel, S M Weissman	1979	130
3	Intranuclear defect in beta-globin mRNA accumulation due to a premature translation termination codon Blood ·K Takeshita, BG Forget, A Scarpa, EJ Jr Benz	1984	96
4	Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association. Journal of Clinical Investigation ·William Tse, Marie‐Christine Lecomte, Fernando Ferreira Costa, M Garbarz, C Feo, Pierre Boivin, D Dhermy, BG Forget	1990	95
5	Beta-thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the beta-globin gene Blood ·C Wong, Stylianos E. Antonarakis, SC Goff, SH Orkin, BG Forget, DG Nathan, PJ Giardina, HH Jr Kazazian	1989	64
6	The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene cluster Blood ·EA Feingold, BG Forget	1989	64
7	A new mutation in IVS-1 of the human beta globin gene causing beta thalassemia due to abnormal splicing Blood ·GF Atweh, Sze Chuen Cesar Wong, Robin Reed, Stylianos E. Antonarakis, DE Zhu, PK Ghosh, Tom Maniatis, BG Forget, HH Jr Kazazian	1987	60
8	Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1. Journal of Clinical Investigation ·Pamela S. Becker, William Tse, Samuel E. Lux, BG Forget	1993	56
9	Hemin control of heme biosynthesis and catabolism in a human leukemia cell line Blood ·Ronald Hoffman, N Ibrahim, MJ Murnane, A Diamond, BG Forget, R D Levere	1980	55
10	Induction of erythropoietic colonies in a human chronic myelogenous leukemia cell line Blood ·Robert S. Hoffman, MJ Murnane, EJ Jr Benz, Rainer Prohaska, Victoria Floyd, Nicholas Dainiak, BG Forget, Heinz Furthmayr	1979	53
11	Developmental regulation of human gamma- and beta-globin genes in the absence of the locus control region Blood ·Joëlle Starck, Rudraditya Sarkar, Marc Romana, Ankur Bhargava, AL Scarpa, Masatake Tanaka, JW Chamberlain, S Weissman, BG Forget	1994	48
12	Molecular cloning of the cDNA for human erythrocyte beta-spectrin Blood ·JC Winkelmann, TL Leto, Watkins Pc, Roger L. Eddy, TB Shows, AJ Linnenbach, KE Sahr, N Kathuria, Marchesi Vt, BG Forget	1988	46
13	Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron. The EMBO Journal ·James E. Metherall, FS Collins, J. Pan, S M Weissman, BG Forget	1986	42
14	Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe). Journal of Clinical Investigation ·Laurette Morlé, Anne‐Françoise Roux, Nicole Alloisio, B Pothier, Joëlle Starck, Luc Denoroy, François Morlé, R.-C. Rudigoz, BG Forget, J. Delaunay	1990	40
15	Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population Blood ·FS Collins, CD Boehm, PG Waber, CJ Jr Stoeckert, S Weissman, BG Forget, HH Jr Kazazian	1984	38
16	Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families Blood ·AF Roux, François Morlé, Djamel Guetarni, P Colonna, Kenneth E. Sahr, BG Forget, J. Delaunay, Jacqueline Godet	1989	37
17	Hemoglobin synthesis in human BFU-E and CFU-E-derived erythroid colonies Blood ·BJ Clarke, DG Nathan, BP Alter, BG Forget, DG Hillman, D Housman	1979	37
18	Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks Blood ·PG Waber, MA Bender, RE Gelinas, C. Kattamis, A Karaklis, K. Sofroniadou, G. Stamatoyannopoulos, FS Collins, BG Forget, HH Jr Kazazian	1986	36
19	Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain Blood ·Laurette Morlé, François Morlé, AF Roux, Jacqueline Godet, BG Forget, Luc Denoroy, M Garbarz, D Dhermy, R Kastally, J. Delaunay	1989	35
20	Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation. Journal of Clinical Investigation ·M Garbarz, William Tse, PG Gallagher, C. Picat, Marie‐Christine Lecomte, Francis Galibert, D Dhermy, BG Forget	1991	32

About BG Forget

BG Forget is a scholar working on Genetics, Physiology, Molecular Biology, Hematology and Pulmonary and Respiratory Medicine, having authored 63 papers that have together received 1.7k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (30 papers), Erythrocyte Function and Pathophysiology (28 papers), Iron Metabolism and Disorders (12 papers), RNA modifications and cancer (12 papers), Blood properties and coagulation (11 papers), DNA and Nucleic Acid Chemistry (11 papers), RNA and protein synthesis mechanisms (7 papers) and Diabetes and associated disorders (6 papers). The work is most often cited by research in Genetics (619 citations), Hematology (456 citations), Physiology (692 citations), Molecular Biology (797 citations) and Genetics (287 citations). BG Forget has collaborated with scholars based in United States, France and Morocco. Frequent co-authors include EJ Jr Benz, William Tse, PG Gallagher, S M Weissman, M Garbarz, DG Nathan, J. Delaunay, FS Collins, Edward L. Snyder and Pierre Boivin. Their work appears in journals such as Blood, Journal of Clinical Investigation, Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Cold Spring Harbor Symposia on Quantitative Biology.

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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