BG Forget

1.8k citations

63 papers · 1.7k · h-index 25

Impact in

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

Papers in

Genetics 33
- Hemoglobinopathies and Related Disorders 30
- Diabetes and associated disorders 6
Hematology 22
- Iron Metabolism and Disorders 12

Co-authors: EJ Jr Benz (8 shared papers)William T. Tse (4 shared papers)PG Gallagher (8 shared papers)S M Weissman (2 shared papers)Michel Garbarz (3 shared papers)FS Collins (5 shared papers)Jean Delaunay (7 shared papers)DG Nathan (4 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)The EMBO Journal (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	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, Paul Andrew Biro, Prabhakara V. Choudary, James T. Elder, Richard R.‐C. Wang, BG Forget, J. Kim de Riel, S M Weissman	1979	128
3	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 T. Tse, Marie‐Christine Lecomte, Fernando Ferreira Costa, Michel Garbarz, C Feo, Pierre Boivin, Didier Dhermy, BG Forget	1990	94
4	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	93
5	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	65
6	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, Stuart H. Orkin, BG Forget, DG Nathan, PJ Giardina, HH Jr Kazazian	1989	63
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	1987	59
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 Sue Becker, William T. Tse, Samuel E. Lux, BG Forget	1993	57
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	54
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	52
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	1994	49
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	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, Jun‐Ping Pan, S M Weissman, BG Forget	1986	43
14	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	40
15	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, Brigitte Pothier, Joëlle Starck, Luc Denoroy, François Morlé, René Charles Rudigoz	1990	40
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, Jean 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	36
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, Christos Kattamis, A Karaklis, K. Sofroniadou, George Stamatoyannopoulos, FS Collins	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, Michel Garbarz, Didier Dhermy	1989	36
20	The structure of hemoglobin Indianapolis [beta112(G14) arginine]. An unstable variant detectable only by isotopic labeling. Journal of Biological Chemistry ·Junius G. Adams, Martin H. Steinberg, Laurence A. Boxer, Robert L. Baehner, BG Forget, G.A. Tsistrakis	1979	32

About BG Forget

BG Forget is a scholar working on Genetics, Hematology, Physiology, Molecular Biology and Genetics, 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), DNA and Nucleic Acid Chemistry (11 papers), Blood properties and coagulation (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 (632 citations), Hematology (461 citations), Physiology (702 citations), Molecular Biology (792 citations) and Genetics (291 citations). BG Forget has collaborated with scholars based in United States, France and Morocco. Frequent co-authors include EJ Jr Benz, William T. Tse, PG Gallagher, S M Weissman, Michel Garbarz, FS Collins, Jean Delaunay, DG Nathan, Edward L. Snyder and Fernando Ferreira Costa. Their work appears in journals such as Blood, Journal of Clinical Investigation, Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The EMBO Journal.

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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