Wendy E. Smith

5.9k citations

40 papers · 2.3k indexed · 1 hit paper · h-index 20

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Endocrinology top 5%

Papers in ⓘ

Clinical Biochemistry 17
- Metabolism and Genetic Disorders 17
Physiology 14
- Diet and metabolism studies 9
- Lysosomal Storage Disorders Research 5

Co-authors: Cheleste M. Thorpe (3 shared papers)David W. K. Acheson (2 shared papers)Jerry Vockley (6 shared papers)Susan A. Berry (8 shared papers)Dianne M. Frazier (2 shared papers)Kevin M. Antshel (1 shared paper)Barbara K. Burton (2 shared papers)Nancy Braverman (1 shared paper)
Journals: Molecular Genetics and Metabolism (5 papers)Genetics in Medicine (5 papers)Critical Care Clinics (5 papers)Infection and Immunity (3 papers)The Journal of Pediatrics (2 papers)
Partner nations: United States Canada United Kingdom

In The Last Decade

Wendy E. Smith

39 papers receiving 2.2k citations

Hit Papers

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Phenylalanine hydroxylase deficiency: diagnosis and management guideline 2014 · 465 citations

Peers

Countries citing papers authored by Wendy E. Smith

Since Specialization

Citations

This map shows the geographic impact of Wendy E. Smith's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Wendy E. Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wendy E. Smith more than expected).

Fields of papers citing papers by Wendy E. Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wendy E. Smith. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Wendy E. Smith. The network helps show where Wendy E. Smith may publish in the future.

Co-authors

The 25 scholars most cited alongside Wendy E. Smith, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Wendy E. Smith Line = papers co-authored together Wendy E. Smith links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 40 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Phenylalanine hydroxylase deficiency: diagnosis and management guideline Genetics in Medicine ·Jerry Vockley, Hans C. Andersson, Kevin M. Antshel, Nancy Braverman, Barbara K. Burton, Dianne M. Frazier, John J. Mitchell, Wendy E. Smith, Barry H. Thompson, Susan A. Berry Hit paper breakdown →	2014	465
2	Recombinant human acid α-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial Genetics in Medicine ·Andrea Amalfitano, A. Resai Bengur, Richard P. Morse, Joseph M. Majure, Laura E. Case, Deborah L. Veerling, Joanne Mackey, Priya S. Kishnani, Wendy E. Smith, Alison McVie‐Wylie, Jennifer A. Sullivan, George Hoganson, John A. Phillips, G. Bradley Schaefer, Joel Charrow, Russell E. Ware, Edward H. Bossen, Yuan-Tsong Chen	2001	293
3	Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients The American Journal of Human Genetics ·Regina Ensenauer, Adewale Adeyinka, Heather C. Flynn, Virginia V. Michels, Noralane M. Lindor, D. Brian Dawson, Erik C. Thorland, Cindy Pham Lorentz, Jennifer Goldstein, Marie McDonald, Wendy E. Smith, Elba Simon-Fayard, Alan A. Alexander, Anita S. Kulharya, Rhett P. Ketterling, Robin D. Clark, Syed M. Jalal	2003	265
4	Shiga Toxin 1 Triggers a Ribotoxic Stress Response Leading to p38 and JNK Activation and Induction of Apoptosis in Intestinal Epithelial Cells Infection and Immunity ·Wendy E. Smith, Anne Kane, Sausan T. Campbell, David W. K. Acheson, Brent Cochran, Cheleste M. Thorpe	2003	154
5	Shiga Toxins Induce, Superinduce, and Stabilize a Variety of C-X-C Chemokine mRNAs in Intestinal Epithelial Cells, Resulting in Increased Chemokine Expression Infection and Immunity ·Cheleste M. Thorpe, Wendy E. Smith, Bryan P. Hurley, David W. K. Acheson	2001	116
6	TBX5 Genetic Testing Validates Strict Clinical Criteria for Holt-Oram Syndrome Pediatric Research ·Deborah A. McDermott, Michael Bressan, Jié He, Joseph S. Lee, Salim Aftimos, Martina Brueckner, Fiona J. Gilbert, Gail E. Graham, Mark Hannibal, Jeffrey W. Innis, Mary Ella Pierpont, Annick Raas‐Rothschild, Alan Shanske, Wendy E. Smith, Robert H. Spencer, Martin G. St. John-Sutton, Lionel Van Maldergem, Darrel Waggoner, Matthew P. Weber, Craig T. Basson	2005	104
7	Unmasked Adult-Onset Urea Cycle Disorders in the Critical Care Setting Critical Care Clinics ·Marshall Summar, Frances Barr, Sheila Dawling, Wendy E. Smith, Brendan Lee, Rani H. Singh, William J. Rhead, Lisa Sniderman King, Brian W. Christman	2005	92
8	Secretion of a wheat α-amylase expressed in yeast Nature ·Steven J. Rothstein, Colin M. Lazarus, Wendy E. Smith, David C. Baulcombe, Anthony A. Gatenby	1984	89
9	Recombinant human acid ??-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial Genetics in Medicine ·Andrea Amalfitano, A. Resai Bengur, Richard P. Morse, Joseph M. Majure, Laura E. Case, Deborah L. Veerling, Joanne Mackey, Priya S. Kishnani, Wendy E. Smith, Alison McVie‐Wylie, Jennifer A. Sullivan, George Hoganson, John A. Phillips, G. Bradley Schaefer, Joel Charrow, Russell E. Ware, Edward H. Bossen, Yuan‐Tsong Chen	2001	73
10	Rare Disorders of Metabolism with Elevated Butyryl- and Isobutyryl-Carnitine Detected by Tandem Mass Spectrometry Newborn Screening Pediatric Research ·Dwight D. Koeberl, Sarah P. Young, Niels Gregersen, Jerry Vockley, Wendy E. Smith, Daniel K. Benjamin, Yan An, S. D. Weavil, Shu Chaing, Deeksha Bali, Marie McDonald, Priya S. Kishnani, Ying-Tsong Chen, David S. Millington	2003	68
11	Urea Cycle Disorders: Clinical Presentation Outside the Newborn Period Critical Care Clinics ·Wendy E. Smith, Priya S. Kishnani, Brendan Lee, Rani H. Singh, William J. Rhead, Lisa Sniderman King, Michael C. Smith, Marshall Summar	2005	66
12	Evaluation of 3‐methylcrotonyl‐CoA carboxylase deficiency detected by tandem mass spectrometry newborn screening Journal of Inherited Metabolic Disease ·Dwight D. Koeberl, David S. Millington, Wendy E. Smith, S. D. Weavil, Joseph Muenzer, Shawn E. McCandless, Priya S. Kishnani, Marie McDonald, Shu Chaing, Anne Boney, Elizabeth Moore, Dianne M. Frazier	2003	62
13	Borrelia burgdorferi-Induced Expression of Matrix Metalloproteinases from Human Chondrocytes Requires Mitogen-Activated Protein Kinase and Janus Kinase/Signal Transducer and Activator of Transcription Signaling Pathways Infection and Immunity ·Aruna K. Behera, Cheleste M. Thorpe, J. Michael Kidder, Wendy E. Smith, Ethan Hildebrand, Linden T. Hu	2004	48
14	Ammonia Control in Children Ages 2 Months through 5 Years with Urea Cycle Disorders: Comparison of Sodium Phenylbutyrate and Glycerol Phenylbutyrate The Journal of Pediatrics ·Wendy E. Smith, George A. Díaz, Uta Lichter‐Konecki, Susan A. Berry, Cary O. Harding, Shawn E. McCandless, Cindy LeMons, Joe Mauney, Klara Dickinson, Dion F. Coakley, Tristen Moors, Masoud Mokhtarani, Bruce F. Scharschmidt, Brendan Lee	2013	33
15	8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients American Journal of Medical Genetics Part A ·John Barber, Jill A. Rosenfeld, Nicola Foulds, Sophie Laird, Mark S. Bateman, N. Simon Thomas, Samantha Baker, Viv Maloney, Arayamparambil C. Anilkumar, Wendy E. Smith, Valerie Banks, Sara Ellingwood, Yara Kharbutli, Lakshmi Mehta, Keith Eddleman, Michael Marble, Regina M. Zambrano, John A. Crolla, Allen N. Lamb	2013	33
16	Nutritional Management of Urea Cycle Disorders Critical Care Clinics ·Rani H. Singh, William J. Rhead, Wendy E. Smith, Brendan Lee, Lisa Sniderman King, Marshall Summar	2005	30
17	Distinctive phenotype in 9 patients with deletion of chromosome 1q24‐q25 American Journal of Medical Genetics Part A ·Deepika Burkardt, Jill A. Rosenfeld, Maria Helgeson, Brad Angle, Valerie Banks, Wendy E. Smith, Karen W. Gripp, Jessica Moline, Rocio Moran, Dmitriy M. Niyazov, Cathy A. Stevens, Elaine H. Zackai, Robert Roger Lebel, Douglas G. Ashley, Nancy Kramer, Ralph S. Lachman, John M. Graham	2011	29
18	Glycerol phenylbutyrate treatment in children with urea cycle disorders: Pooled analysis of short and long-term ammonia control and outcomes Molecular Genetics and Metabolism ·Susan A. Berry, Uta Lichter‐Konecki, George A. Díaz, Shawn E. McCandless, William J. Rhead, Wendy E. Smith, Cynthia LeMons, Sandesh C.S. Nagamani, Dion F. Coakley, Masoud Mokhtarani, Bruce F. Scharschmidt, Brendan Lee	2014	27
19	Medical genetics education in the midst of the COVID‐19 pandemic: Shared resources American Journal of Medical Genetics Part A ·Debra S. Regier, Wendy E. Smith, Heather M. Byers	2020	23
20	Electroconvulsive Therapy: A Canadian Perspective The Canadian Journal of Psychiatry ·Wendy E. Smith, Alex Richman	1984	23

About Wendy E. Smith

Wendy E. Smith is a scholar working on Clinical Biochemistry, Physiology, Genetics, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 40 papers that have together received 2.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (17 papers), Diet and metabolism studies (9 papers), Neonatal Health and Biochemistry (7 papers), Lysosomal Storage Disorders Research (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Muscle metabolism and nutrition (4 papers), Congenital heart defects research (4 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). The work is most often cited by research in Clinical Biochemistry (806 citations), Endocrinology (166 citations), Rheumatology (415 citations), Physiology (710 citations) and Biochemistry (132 citations). Wendy E. Smith has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Cheleste M. Thorpe, David W. K. Acheson, Jerry Vockley, Susan A. Berry, Dianne M. Frazier, Kevin M. Antshel, Barbara K. Burton, Nancy Braverman, Hans C. Andersson and John J. Mitchell. Their work appears in journals such as Molecular Genetics and Metabolism, Genetics in Medicine, Critical Care Clinics, Infection and Immunity and The Journal of Pediatrics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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