Bernard G. Forget - Concepedia

Author

Bernard G. Forget

Also Known As

B FORGET, B Forget, B G Forget, B. Forget, B. G. FORGET, B. G. Forget, B.G. Forget, BERNARD G. FORGET, Bernard Forget, Bernard G Forget

212

Publications

9.3K

Citations

H-Index

111

Concepts

All Affiliations

Yale University Harvard University Boston Children's Hospital Massachusetts Institute of Technology Dana-Farber Cancer Institute

About

Bernard G. Forget is an author at Yale University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	38	67	4.6K
2	Natural Sciences	24	31	2.2K
3	Health Sciences	8	8	511
4	Engineering	2	2	59
5	Public Health	1	1	55

Bernard G. Forget

116

Publications

7.6K

Citations

H-Index

Page 1

	Year	Citations
Insertion of synthetic copies of human globin genes into bacterial plasmids John T. Wilson, Lois B. Wilson, Jon K. deRiel, Nucleic Acids Research	1978	346
The Structure and Evolution of the Human /?-Globin Gene Family Argiris Efstratiadis, James W. Posakony, Tom Maniatis, Tom ManiatisGenetic DisorderNatural SciencesGeneticsArgiris Efstratiadis Department	1980	290
Nucleotide Sequence of KB Cell 5 <i>S</i> RNA Bernard G. Forget, Sherman M. Weissman Science	1967	240
Full-length sequence of the cDNA for human erythroid beta-spectrin. J C Winkelmann, Jan‐Gowth Chang, William Tse, Journal of Biological Chemistry	1990	237
Base substitution in an intervening sequence of a beta+-thalassemic human globin gene. Richard A. Spritz, Pudur Jagadeeswaran, Prabhakara V. Choudary, Proceedings of the National Academy of Sciences Base ChangeGenetic DisorderNatural SciencesGeneticsHematology	1981	232
Human beta-globin messenger RNA. III. Nucleotide sequences derived from complementary DNA. Charles A. Marotta, John T. Wilson, Bernard G. Forget, Journal of Biological Chemistry	1977	222
Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis Stefan Eber, Jennifer M. Reingle González, Marcia L. Lux, Nature Genetics Major CauseDevelopmental BiologyGenetic DisorderGeneticsMolecular Genetics	1996	216
Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8 Samuel E. Lux, William Tse, Joan C. Menninger, Nature Genetic DisorderGeneticsHematologyPathologyMolecular Genetics	1990	213
A point mutation in the Aγ-globin gene promoter in Greek hereditary persistence of fetal haemoglobin Francis S. Collins, James E. Metherall, Minoru Yamakawa, Nature Heme HomeostasisGenetic DisorderNatural SciencesGeneticsHematology	1985	189
Ankyrin binds to the 15th repetitive unit of erythroid and nonerythroid beta-spectrin. Scott P. Kennedy, Stephen L. Warren, Bernard G. Forget, The Journal of Cell Biology Developmental BiologySignal TransductionBiochemistryNonerythroid Beta-spectrinMedicine	1991	170

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