PG Gallagher - Concepedia

Author

PG Gallagher

Yale University

Also Known As

P G GALLAGHER, P G Gallagher, P.G. Gallagher, PG Gallagher, Patrick G Gallagher

Publications

468

Citations

H-Index

Concepts

All Affiliations

Yale University Inserm

About

PG Gallagher is an author at Yale University specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	268
2	Natural Sciences	4	4	101
3	Cell Biology	4	4	91
4	Health Sciences	2	2	69
5	Biology	1	1	34

PG Gallagher

Publications

442

Citations

H-Index

Page 1

	Year	Citations
Spectrin genes in health and disease. PG Gallagher, Forget Bg PubMed Disease MechanismMedicineGeneticsGenetic EpidemiologySpectrin Genes	1993	53
Disorders of the erythrocyte membrane PG Gallagher Medical Entomology and Zoology Erythrocyte MembraneMembrane TransportPhysiologyHematologyHistopathology	1998	45
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis. Patricia B. Jenkins, Ghassan K. Abou‐Alfa, D Dhermy, Journal of Clinical Investigation GeneticsBlood CellMolecular BiologyMolecular GeneticsUnaffected Family Members	1996	42
Case-control analysis of endemic <i>Serratia marcescens</i> bacteremia in a neonatal intensive care unit M. J Bizzarro, Louise‐Marie Dembry, Robert S. Baltimore, Archives of Disease in Childhood Fetal & Neonatal	2006	35
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. M Garbarz, William Tse, PG Gallagher, Journal of Clinical Investigation GeneticsMolecular BiologyPathologyGene CharacterizationMolecular Genetics	1991	34
Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide PB Floyd, PG Gallagher, LA Valentino, Blood	1991	31
An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216) WT Tse, PG Gallagher, B Pothier, Blood	1991	26
Clinical and molecular aspects of disorders of the erythrocyte membrane skeleton. PG Gallagher, WT Tse, Forget Bg PubMed Clinical DisordersPhysiologyHistopathologyHematologyPathology	1990	24
Late-onset Leclercia adecarboxylata sepsis in a premature neonate Melissa U. Nelson, Yelena Maksimova, Vincent Schulz, Journal of Perinatology NeonatologyPathogenesisPediatricsSepsisPremature Neonate	2013	23
Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide PB Floyd, PG Gallagher, LA Valentino, Blood	1991	23

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