Wendy E. Smith - Concepedia

Author

Wendy E. Smith

Also Known As

Hilde Olivié, Rutsch, Frank, W Smith, W. E. Smith, W. Edwin Smith, W. Smith, W.E. Smith, Wendy E Smith, Wendy E. Smith, Wendy Smith

Publications

5.9K

Citations

H-Index

Concepts

All Affiliations

Maine Medical Center University of Minnesota Maine Medical Center Icahn School of Medicine at Mount Sinai Children's Hospital of Philadelphia

About

Wendy E. Smith is an author at Maine Medical Center specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	20	3.8K
2	Biochemistry	3	3	556
3	Social Sciences	2	2	683
4	Public Health	1	1	15
5	Clinical Nutrition	1	1	692

Wendy E. Smith

Publications

5.4K

Citations

H-Index

Page 1

	Year	Citations
Phenylalanine hydroxylase deficiency: diagnosis and management guideline Jerry Vockley, Hans C. Andersson, Kevin M. Antshel, Genetics in Medicine MedicineClinical NutritionPathologyAdrenal DiseaseMetabolism	2014	692
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay Santhosh Girirajan, Jill A. Rosenfeld, Gregory M. Cooper, Nature Genetics Developmental BiologyTwo-hit ModelGeneticsDevelopmental ScienceGlobal Developmental Delay	2010	669
Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification Frank Rutsch, Nico Ruf, Sucheta M. Vaingankar, Nature Genetics Developmental BiologyGeneticsPathologyInfantile Arterial CalcificationVascular Biology	2003	592
Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients Regina Ensenauer, Adewale Adeyinka, Heather C. Flynn, The American Journal of Human Genetics CytogeneticsGenetic DisorderGeneticsMolecular AnalysisPathology	2003	376
Recombinant human acid α-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial Andrea Amalfitano, A. Resai Bengur, Richard P. Morse, Genetics in Medicine Translational MedicineBiochemistryInherited Metabolic DiseaseGlycobiologyPediatrics	2001	346
Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum Can Be Caused by Mutations in Either ENPP1 or ABCC6 Yvonne Nitschke, Geneviève Baujat, Ulrike Botschen, The American Journal of Human Genetics MechanobiologyDevelopmental AnomalyEither Enpp1Arterial CalcificationGenetics	2011	335
Shiga Toxin 1 Triggers a Ribotoxic Stress Response Leading to p38 and JNK Activation and Induction of Apoptosis in Intestinal Epithelial Cells Wendy E. Smith, Anne Kane, Sausan T. Campbell, Infection and Immunity	2003	189
Identification of a Recurrent Microdeletion at 17q23.1q23.2 Flanked by Segmental Duplications Associated with Heart Defects and Limb Abnormalities Blake C. Ballif, Aaron Theisen, Jill A. Rosenfeld, The American Journal of Human Genetics Heart DefectsDevelopmental BiologyGenetic DisorderSegmental DuplicationsGenetics	2010	166
TBX5 Genetic Testing Validates Strict Clinical Criteria for Holt-Oram Syndrome Deborah A. McDermott, Michael Bressan, Jié He, Pediatric Research Genetic DisorderGeneticsGenetic EpidemiologyTuberous SclerosisHolt-oram Syndrome	2005	150
Shiga Toxins Induce, Superinduce, and Stabilize a Variety of C-X-C Chemokine mRNAs in Intestinal Epithelial Cells, Resulting in Increased Chemokine Expression Cheleste M. Thorpe, Wendy E. Smith, Bryan P. Hurley, Infection and Immunity	2001	143

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