PG Gallagher

468 total citations
21 papers, 379 citations indexed

About

PG Gallagher is a scholar working on Physiology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, PG Gallagher has authored 21 papers receiving a total of 379 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Physiology, 8 papers in Pulmonary and Respiratory Medicine and 6 papers in Genetics. Recurrent topics in PG Gallagher's work include Erythrocyte Function and Pathophysiology (17 papers), Blood properties and coagulation (8 papers) and Diabetes and associated disorders (4 papers). PG Gallagher is often cited by papers focused on Erythrocyte Function and Pathophysiology (17 papers), Blood properties and coagulation (8 papers) and Diabetes and associated disorders (4 papers). PG Gallagher collaborates with scholars based in United States, France and Canada. PG Gallagher's co-authors include BG Forget, Louise‐Marie Dembry, D Dhermy, A L Scarpa, Robert S. Baltimore, Melissa B. Davis, M Garbarz, Marc Romana, Bernard G. Forget and William Tse and has published in prestigious journals such as Journal of Clinical Investigation, Blood and Archives of Disease in Childhood Fetal & Neonatal.

In The Last Decade

PG Gallagher

21 papers receiving 373 citations

Peers

Countries citing papers authored by PG Gallagher

Since Specialization

Citations

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

Fields of papers citing papers by PG Gallagher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of PG Gallagher

This figure shows the co-authorship network connecting the top 25 collaborators of PG Gallagher. A scholar is included among the top collaborators of PG Gallagher based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with PG Gallagher. PG Gallagher is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Late-onset Leclercia adecarboxylata sepsis in a premature neonate 2013 ·Journal of Perinatology ·(unknown), Yelena Maksimova, Vincent Schulz, Matthew J. Bizzarro, PG Gallagher	12
2	Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred 2011 ·Blood Cells Molecules and Diseases ·Brett L. Houston, Teresa Zelinski, Sara J. Israels, Gail Coghlan, B.N. Chodirker, PG Gallagher, Donald S. Houston, Ryan Zarychanski	17
3	Case-control analysis of endemic Serratia marcescens bacteremia in a neonatal intensive care unit 2006 ·Archives of Disease in Childhood Fetal & Neonatal ·(unknown), Louise‐Marie Dembry, Robert S. Baltimore, PG Gallagher	26
4	Assignment<footref rid="foot01"><sup>1</sup></footref> of the 2P domain, acid-sensitive potassium channel OAT1 gene KCNK3 to human chromosome bands 2p24.1→p23.3 and murine 5B by in situ hybridization 1999 ·Cytogenetic and Genome Research ·(unknown), Patricia Bray‐Ward, Steven A. Goldstein, PG Gallagher	6
5	Disorders of the erythrocyte membrane 1998 ·Medical Entomology and Zoology ·PG Gallagher	39
6	A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis. 1996 ·Journal of Clinical Investigation ·(unknown), Ghassan K. Abou‐Alfa, D Dhermy, E Bursaux, Carlo V. Feo, A L Scarpa, Samuel E. Lux, M Garbarz, Bernard G. Forget, PG Gallagher	31
7	The lethal hemolytic mutation in beta I sigma 2 spectrin Providence yields a null phenotype in neonatal skeletal muscle. 1996 ·PubMed ·Scott A. Weed, Paul R. Stabach, Calvin E. Oyer, PG Gallagher, Jon S. Morrow	9
8	cDNA structure, tissue-specific expression, and chromosomal localization of the murine band 7.2b gene 1995 ·Blood ·PG Gallagher, Marc Romana, (unknown), (unknown)	18
9	Localization of the human α-fodrin gene (SPTAN1) to 9q33→q34 by fluorescence in situ hybridization 1994 ·Cytogenetic and Genome Research ·Madhvi B. Upender, PG Gallagher, Randall T. Moon, David C. Ward, Bernard G. Forget	6
10	Spectrin St Louis and the alpha LELY allele [letter] 1994 ·Blood ·PG Gallagher, BG Forget	14
11	Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion 1993 ·Blood ·PG Gallagher, (unknown), Lori K. Benoit, (unknown), (unknown), BG Forget	12
12	Spectrin genes in health and disease. 1993 ·PubMed ·PG Gallagher, (unknown)	44
13	Large numbers of alternatively spliced isoforms of the regulatory region of human erythrocyte ankyrin. 1992 ·PubMed ·PG Gallagher, (unknown), (unknown), (unknown), (unknown)	10
14	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. 1991 ·Journal of Clinical Investigation ·M Garbarz, William Tse, PG Gallagher, C. Picat, Marie‐Christine Lecomte, Francis Galibert, D Dhermy, BG Forget	30
15	Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide 1991 ·Blood ·(unknown), PG Gallagher, (unknown), Melissa B. Davis, (unknown), BG Forget	17
16	An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216) 1991 ·Blood ·(unknown), PG Gallagher, B Pothier, (unknown), A L Scarpa, J. Delaunay, BG Forget	4
17	Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide 1991 ·Blood ·(unknown), PG Gallagher, (unknown), Melissa B. Davis, (unknown), BG Forget	25
18	A defect in alpha-spectrin mRNA accumulation in hereditary pyropoikilocytosis. 1991 ·PubMed ·PG Gallagher, (unknown), (unknown), (unknown), (unknown)	10
19	An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216) 1991 ·Blood ·(unknown), PG Gallagher, B Pothier, (unknown), A L Scarpa, J. Delaunay, BG Forget	23
20	Clinical and molecular aspects of disorders of the erythrocyte membrane skeleton. 1990 ·PubMed ·PG Gallagher, (unknown), (unknown)	19

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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