BG Forget

1.8k citations

63 papers · 1.6k indexed · h-index 24

Genetics top 1%
- Hemoglobinopathies and Related Disorders 30
- Diabetes and associated disorders 6
Hematology top 2%
- Iron Metabolism and Disorders 12
Physiology top 5%
- Erythrocyte Function and Pathophysiology 28
Molecular Biology top 10%
- RNA modifications and cancer 12
- DNA and Nucleic Acid Chemistry 11
- RNA and protein synthesis mechanisms 7
Genetics top 10%
- Hemoglobinopathies and Related Disorders 30
- Diabetes and associated disorders 6
Pulmonary and Respiratory Medicine
- Blood properties and coagulation 11

Co-authors: EJ Jr Benz William Tse PG Gallagher S M Weissman M Garbarz DG Nathan FS Collins J. Delaunay
Cited by: Genetics Hematology Physiology
Journals: Blood (44 papers)Journal of Clinical Investigation (4 papers)Proceedings of the National Academy of Sciences (4 papers)
Partner nations: United States France Morocco

In The Last Decade

BG Forget

62 papers receiving 1.5k 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-authorship network

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

#	Work
1	Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis. PubMed ·Patrick G. Gallagher,Leszek Kotula,Yao Lin,Sally L. Marchesi,Peter J. Curtis,David W. Speicher,BG Forget	1996	7
2	Developmental regulation of human gamma- and beta-globin genes in the absence of the locus control region Blood ·Joëlle Starck,Rudraditya Sarkar,Marc Romana,K. Sjoberg,中島浩一,Masatake Tanaka,M. P. DOYLE,S Weissman,BG Forget	1994	1
3	Increased expression of the G gamma and A gamma globin genes associated with a mutation in the A gamma enhancer Blood ·Günay Balta,Ashley Matan,S. Takegawa,Elvia Willyono,Thalia Papayannopoulou,BG Forget,Şule Kısakürek	1994	7
4	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	52
5	Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion Blood ·PG Gallagher,М. О. Компанець,Lori K. Benoit,C. C. B.,Andrew Krause,BG Forget	1993	12
6	The pathophysiology and molecular genetics of beta thalassemia. PubMed ·BG Forget	1993	13
7	Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self- association site Blood ·Nicole Alloisio,R Wilmotte,Laurette Morlé,Faouzi Baklouti,J Maréchal,A. Vucinic-Superina,Luc Denoroy,Carlo V. Feo,BG Forget,R Kastally,J. Delaunay	1992	14
8	A structurally abnormal erythropoietin receptor gene in a human erythroleukemia cell line. PubMed ·Amanda E.M Browne,K. Harris,Lucas Penny,BG Forget,Toshio Kitamura,J C Winkelmann	1992	20
9	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	30
10	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	36
11	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,О. В. Позднякова,Pierre Boivin,周学兰,BG Forget	1990	90
12	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 ·Fouad A Ali,BG Forget	1989	60
13	A new mutation in IVS-1 of the human beta globin gene causing beta thalassemia due to abnormal splicing Blood ·Şule Kısakürek,A. K. D. Bhalerao,N. T. Ashimbaeva,Stylianos E. Antonarakis,D.M.I. Verreth,Ph. Pott,張盈盈張盈盈,BG Forget,Memona Khan	1987	0
14	The beta-globin gene on the Chinese delta beta-thalassemia chromosome carries a promoter mutation Blood ·Şule Kısakürek,Xiaoxiang Zhu,Ashley Matan,顾彬,Memona Khan,BG Forget	1987	1
15	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	40
16	A novel basis for delta beta-thalassemia in a Chinese family Blood ·Şule Kısakürek,Juan Marcos Castro-Tapia,BG Forget	1986	8
17	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,Revathy Raja,S Weissman,BG Forget,Zulfanul Qahfi	1984	38
18	Sequences of Human Repetitive DNA, Non- -globin Genes, and Major Histocompatibility Locus Genes: II. Sequences of Non- -globin Genes in Man Cold Spring Harbor Symposia on Quantitative Biology ·Pudur Jagadeeswaran,Junxiao Pan,BG Forget,S Weissman	1983	9
19	Embryonic-fetal erythroid characteristics of a human leukemic cell line. Proceedings of the National Academy of Sciences ·EJ Jr Benz,Mary Jo Murnane,R. B. Hall,Brian Berman,Eric Michael Mazur,Pengfei Zhou,Irina Marchesini,Edward L. Snyder,BG Forget,Shoji Kazahari	1980	161
20	Hemoglobin synthesis in human BFU-E and CFU-E-derived erythroid colonies Blood ·Alexis Laszczuk,DG Nathan,BP Alter,BG Forget,Zhao Weil,P. Pardasani	1979	37

About BG Forget

BG Forget is a scholar working on Genetics, Hematology and Physiology, having authored 63 papers that have together received 1.6k 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 (607 citations), Hematology (439 citations) and Physiology (652 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, FS Collins, J. Delaunay, Eric Michael Mazur and Edward L. Snyder. 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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