Patrick G. Gallagher

Author

Also Known As

Cho, Alex H, Kathleen A. Martin, Laura Silvestri, P G Gallagher, P Gallagher, P. G. Gallagher, P.G. Gallagher, PATRICK G. GALLAGHER, Patrick G Gallagher, Patrick G. Gallagher

405

Publications

14.1K

Citations

H-Index

158

Concepts

All Affiliations

Yale University National Institutes of Health National Human Genome Research Institute New York Blood Center Pediatrics and Genetics

About

Patrick G. Gallagher is an author at Yale University specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	33	49	3K
2	Health Sciences	10	10	450
3	Natural Sciences	10	10	353
4	Public Health	3	3	104
5	Social Sciences	1	1	224

Patrick G. Gallagher

143

Publications

10.3K

Citations

H-Index

Page 1

	Year	Citations
Hereditary spherocytosis Silverio Perrotta, Patrick G. Gallagher, Narla Mohandas The Lancet	2008	579
Seventy-Five Years of Neonatal Sepsis at Yale: 1928–2003 Matthew J. Bizzarro, Craig Raskind, Robert S. Baltimore, PEDIATRICS	2005	465
Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis Ryan Zarychanski, Vincent Schulz, Brett L. Houston, Blood	2012	440
Global transcriptome analyses of human and murine terminal erythroid differentiation Xiuli An, Vincent Schulz, Jie Li, Blood	2014	354
Sites of Regulated Phosphorylation that Control K-Cl Cotransporter Activity Jesse Rinehart, Yelena Maksimova, Jessica E. Tanis, Cell Molecular PhysiologySignal TransductionRegulated PhosphorylationPhysiologyCellular Biochemistry	2009	286
Changing Patterns in Neonatal<i>Escherichia coli</i>Sepsis and Ampicillin Resistance in the Era of Intrapartum Antibiotic Prophylaxis Matthew J. Bizzarro, Louise‐Marie Dembry, Robert S. Baltimore, PEDIATRICS	2008	263
Efficacy of ECT: a meta-analysis P G Janicak, John M. Davis, Robert D. Gibbons, American Journal of Psychiatry Meta-analysisPsychiatryClinical EffectivenessPsychotropic MedicationMood Symptom	1985	224
Altered erythrocyte endothelial adherence and membrane phospholipid asymmetry in hereditary hydrocytosis Patrick G. Gallagher, Seon Hee Chang, Michael P. Rettig, Blood	2003	221
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
Nonstochastic Reprogramming from a Privileged Somatic Cell State Shangqin Guo, Xiaoyuan Zi, Vincent Schulz, Cell Cellular AutomatonCell ReprogrammingSystems Biology	2014	182

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