Michael J. Gambello - Concepedia

Author

Michael J. Gambello

Also Known As

M Gambello, M J Gambello, M. Gambello, M. J. Gambello, M.J. Gambello, Michael Gambello, Michael J Gambello, Michael J. Gambello, Roberto Espana

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Emory University Baylor College of Medicine The University of Texas Health Science Center at Houston University of California, Los Angeles University of British Columbia

About

Michael J. Gambello is an author at Emory University specializing in medicine, pediatrics, and newborn screening.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	1.5K
2	Education	1	1	29
3	Natural Sciences	1	1	715
4	Biochemistry	1	1	25
5	Cell Biology	1	1	236

Michael J. Gambello

Publications

Citations

H-Index

Page 1

	Year	Citations
Cloning and characterization of the Pseudomonas aeruginosa lasR gene, a transcriptional activator of elastase expression Michael J. Gambello, Barbara H. Iglewski Journal of Bacteriology Lasr GeneFunctional Lasr GeneNatural SciencesVirulence FactorProtein Biosynthesis	1991	715
Contribution of specific Pseudomonas aeruginosa virulence factors to pathogenesis of pneumonia in a neonatal mouse model of infection H B Tang, Emily DiMango, Ruth Bryan, Infection and Immunity Neonatal Mouse ModelMedical MicrobiologyPseudomonas Aeruginosa ProductsLung InflammationStrain Pao I.e.	1996	397
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway Gregory M. Enns, Vandana Shashi, Matthew N. Bainbridge, Genetics in Medicine GeneticsEndocytic PathwayProtein DegradationInherited DisorderMolecular Genetics	2014	236
<i>Pseudomonas aeruginosa</i> LasA: a second elastase under the transcriptional control of <i>lasR</i> D S Toder, Michael J. Gambello, Barbara H. Iglewski Molecular Microbiology	1991	187
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis Karin Weiss, Hayley P. Lazar, Alina Kurolap, Genetics in Medicine Mendelian DisorderGenetic DisorderGeneticsGenotype–phenotype CorrelationsGenetic Epidemiology	2019	97
Natural history and genotype‐phenotype correlations in 72 individuals with <i>SATB2</i>‐associated syndrome Yuri A. Zárate, Constance Smith‐Hicks, Carol L. Greene, American Journal of Medical Genetics Part A	2018	73
Kuskokwim Syndrome, a Recessive Congenital Contracture Disorder, Extends the Phenotype of<i>FKBP10</i> Mutations Aileen M. Barnes, Geraldine Duncan, MaryAnn Weis, Human Mutation	2013	61
Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome Melissa M. Murphy, T. Lindsey Burrell, Joseph F. Cubells, BMC Psychiatry	2018	52
Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care Rossana Sanchez Russo, Michael J. Gambello, Melissa M. Murphy, Genetics in Medicine	2021	46
Increased parental anxiety and a benign clinical course: Infants identified with short-chain acyl-CoA dehydrogenase deficiency and isobutyryl-CoA dehydrogenase deficiency through newborn screening in Georgia Roa Sadat, Patricia Hall, Angela Wittenauer, Molecular Genetics and Metabolism NeonatologyNewborn ScreeningEarly Childhood DevelopmentPediatricsParental Anxiety	2019	29

Page 1