Sarah Zimmerman - Concepedia

Author

Sarah Zimmerman

Cincinnati Children's Hospital Medical Center ORCID

Also Known As

S. Zimmerman, S.L. Zimmerman, Sarah L Zimmerman, Sarah L. Zimmerman, Sarah Zimmerman

Publications

Citations

H-Index

Concepts

All Affiliations

Cincinnati Children's Hospital Medical Center Yale University University of Cincinnati Wake Forest University University of Cincinnati Medical Center

About

Sarah Zimmerman is an author at Cincinnati Children's Hospital Medical Center specializing in medicine, public health, and public health nutrition.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	284
2	Public Health	3	3	174
3	Health Sciences	1	1	10
4	Natural Sciences	1	1	74
5	Biochemistry	1	1	74

Sarah Zimmerman

Publications

951

Citations

H-Index

Page 1

	Year	Citations
Familial pulmonary alveolar proteinosis caused by mutations in <i>CSF2RA</i> Takuji Suzuki, Takuro Sakagami, Bruce K. Rubin, The Journal of Experimental Medicine	2008	296
X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome Ke Liu, Biji T. Kurien, Sarah Zimmerman, Arthritis & Rheumatology	2015	169
Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationships Kristen L. Sund, Sarah Zimmerman, Cameron Thomas, Genetics in Medicine Genome-wide Association StudyGenetic AnalysisGenetic TestingGenetic DisorderMedicine	2012	90
Excretion and conservation of glycerol, and expression of aquaporins and glyceroporins, during cold acclimation in Cope's gray tree frog<i>Hyla chrysoscelis</i> Sarah Zimmerman, James Frisbie, David L. Goldstein, American Journal of Physiology-Regulatory, Integrative and Comparative Physiology Cellular PhysiologyLow PermeabilityOsmoregulationAnimal PhysiologyGray Tree Frogs	2006	74
A 2015 global update on folic acid‐preventable spina bifida and anencephaly Annelise C. Arth, Vijaya Kancherla, Helena Pachón, Birth Defects Research Part A Clinical and Molecular Teratology NutritionBrain DevelopmentPublic Health NutritionGlobal UpdateBackground Spina Bifida	2016	74
The clinical phenotype of children with Fanconi anemia caused by biallelic <i>FANCD1/BRCA2</i> mutations Kasiani C. Myers, Stella M. Davies, Richard E. Harris, Pediatric Blood & Cancer	2011	50
Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly Jill A. Rosenfeld, Kyae Hyung Kim, Brad Angle, Molecular Syndromology GeneticsLargest DuplicationMendelian DisorderCarrier Family MembersCraniofacial Anomalies	2012	46
A new frontonasal dysplasia syndrome associated with deletion of the <i>SIX2</i> gene Robert B. Hufnagel, Sarah Zimmerman, Laura A. Krueger, American Journal of Medical Genetics Part A	2015	40
Periprocedural Pericardial Effusion Complicating Transcatheter Left Atrial Appendage Occlusion: A Report From the NCDR LAAO Registry Matthew J. Price, Miguel Valderrábano, Sarah Zimmerman, Circulation Cardiovascular Interventions	2022	37
Watchman device migration and embolization: A report from the NCDR LAAO Registry Daniel J. Friedman, James V. Freeman, Sarah Zimmerman, Journal of Cardiovascular Electrophysiology	2023	18

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