Brian Kirmse - Concepedia

Author

Brian Kirmse

University of Mississippi Medical Center ORCID

Also Known As

B. Kirmse, Brian Kirmse, Brian M Kirmse, Brian M. Kirmse, Kirmse, Brian M., Lene Rottensten, Parikh, Sunil

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

University of Mississippi Medical Center Jackson Memorial Hospital Icahn School of Medicine at Mount Sinai Children's National Inserm

About

Brian Kirmse is an author at University of Mississippi Medical Center specializing in medicine, pediatrics, and hiv.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	13	823
2	Public Health	2	2	28
3	Cell Biology	2	2	51
4	Health Sciences	1	1	15
5	Natural Sciences	1	1	36

Brian Kirmse

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
The incidence of urea cycle disorders Marshall Summar, Stefan Koelker, Debra Freedenberg, Molecular Genetics and Metabolism UrologyMedicineFemale UrologyMenopauseChronic Kidney Disease	2013	308
Newborn screening and early biochemical follow-up in combined methylmalonic aciduria and homocystinuria, cblC type, and utility of methionine as a secondary screening analyte James D. Weisfeld‐Adams, Mark A. Morrissey, Brian Kirmse, Molecular Genetics and Metabolism UrologyMedicineCombined Methylmalonic AciduriaBioanalysisSecondary Screening Analyte	2009	130
Study of <i>LPIN1</i>, <i>LPIN2</i> and <i>LPIN3</i> in rhabdomyolysis and exercise‐induced myalgia Caroline Michot, Laurence Hubert, Norma B. Romero, Journal of Inherited Metabolic Disease	2012	89
Factors Associated with Positive SARS-CoV-2 Test Results in Outpatient Health Facilities and Emergency Departments Among Children and Adolescents Aged <18 Years — Mississippi, September–November 2020 Charlotte V. Hobbs, Lora Martin, Sara Kim, MMWR Morbidity and Mortality Weekly Report	2020	83
Novel first-dose adverse drug reactions during a phase I trial of olipudase alfa (recombinant human acid sphingomyelinase) in adults with Niemann–Pick disease type B (acid sphingomyelinase deficiency) Margaret M. McGovern, Melissa Wasserstein, Brian Kirmse, Genetics in Medicine	2015	75
High prevalence of structural heart disease in children with cblC-type methylmalonic aciduria and homocystinuria Laurie E. Profitlich, Brian Kirmse, Melissa Wasserstein, Molecular Genetics and Metabolism Cblc-type Methylmalonic AciduriaHeart FailureStructural Heart DiseaseCardiovascular DiseasePediatric Heart Disease	2009	72
HIV Protease Inhibitors Inhibit the Development of Preerythrocytic-Stage<i>Plasmodium</i>Parasites Charlotte V. Hobbs, Tatiana Voza, Alida Coppi, The Journal of Infectious Diseases Protease InhibitorsParasite DevelopmentMedicineHuman RetrovirusMalaria	2008	58
Genome sequencing as a first-line diagnostic test for hospitalized infants Kevin M. Bowling, Michelle L. Thompson, Candice R. Finnila, Genetics in Medicine Early DiagnosisNeonatologyNewborn ScreeningPatient SafetyPediatrics	2021	54
Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement Rebecca C. Ahrens‐Nicklas, Lars Schlotawa, Andrea Ballabio, Molecular Genetics and Metabolism Complex CareInherited Metabolic DiseaseMultiple Sulfatase DeficiencyClinical DiseaseConsensus Statement	2018	50
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder Sukhleen Kour, Deepa Rajan, Tyler R. Fortuna, Nature Communications	2021	50

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