David A. Wenger

13.0k citations

221 papers · 9.2k indexed · 1 hit paper · h-index 55

Impact in

Physiology top 0.1%
- Lysosomal Storage Disorders Research
- Calcium signaling and nucleotide metabolism
Cell Biology top 0.5%
- Cellular transport and secretion

Papers in

Physiology 180
- Lysosomal Storage Disorders Research 170
Cell Biology 40
- Cellular transport and secretion 30

Co-authors: Mohammad A. Rafi Paola Luzi Martha Sattler Koji Inui Peter G. Pentchev Marcella Comly Marie T. Vanier Joanne Kurtzberg
Journals: Molecular Genetics and Metabolism (15 papers)Journal of Inherited Metabolic Disease (10 papers)Clinica Chimica Acta (8 papers)The Journal of Pediatrics (7 papers)Human Mutation (7 papers)
Partner nations: United States France Japan

In The Last Decade

David A. Wenger

220 papers receiving 8.9k citations

Hit Papers

align trajectories log scale

Transplantation of Umbilical-Cord Blood in Babies with Infantile Krabbe's Disease 2005 · 522 citations

Peers

Countries citing papers authored by David A. Wenger

Since Specialization

Citations

This map shows the geographic impact of David A. Wenger'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 David A. Wenger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David A. Wenger more than expected).

Fields of papers citing papers by David A. Wenger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David A. Wenger. 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 David A. Wenger. The network helps show where David A. Wenger may publish in the future.

Co-authors

The 25 scholars most cited alongside David A. Wenger, 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 David A. Wenger Line = papers co-authored together David A. Wenger links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood‐onset beta‐mannosidosis Molecular Genetics & Genomic Medicine ·Troy C. Lund, Weston P. Miller, Julie B. Eisengart, Katrina Simmons, Laura Pollard, Deborah L. Renaud, David A. Wenger, Marc C. Patterson, Paul J. Orchard	2019	5
2	Diagnostic challenges in Salla disease Jessica N. Hartley, Michael S. Salman, Frances Booth, Lorne E. Seargeant, David A. Wenger, Jens Wrogemann, Aizeddin Mhanni	2013	1
3	GM2 gangliosidosis associated with a HEXA missense mutation in Japanese Chin dogs: A potential model for Tay Sachs disease Molecular Genetics and Metabolism ·Douglas N. Sanders, Rong Zeng, David A. Wenger, Gary S. Johnson, Gayle C. Johnson, Jared E. Decker, Martin L. Katz, Simon R. Platt, Dennis P. O’Brien	2012	18
4	Extended Normal Life After AAVrh10-mediated Gene Therapy in the Mouse Model of Krabbe Disease Molecular Therapy ·Mohammad A. Rafi, Han Zhi Rao, Paola Luzi, Mark Curtis, David A. Wenger	2012	82
5	Effects of treatments on inflammatory and apoptotic markers in the CNS of mice with globoid cell leukodystrophy Brain Research ·Paola Luzi, Ronnie M. Abraham, Mohammad A. Rafi, Mark Curtis, D. Craig Hooper, David A. Wenger	2009	60
6	Cord-Blood Transplants from Unrelated Donors in Patients with Hurler's Syndrome New England Journal of Medicine ·Susan Staba, Maria L. Escolar, Michele D. Poe, Young Kim, Paul Martin, Paul Szabolcs, June Allison-Thacker, Susan Wood, David A. Wenger, Pablo Rubinstein, John J. Hopwood, William Krivit, Joanne Kurtzberg	2004	329
7	Psychosine-induced apoptosis in a mouse oligodendrocyte progenitor cell line is mediated by caspase activation Neuroscience Letters ·Mariam Zaka, David A. Wenger	2004	78
8	Krabbe Disease: Genetic Aspects and Progress toward Therapy Molecular Genetics and Metabolism ·David A. Wenger, Mohammad A. Rafi, Paola Luzi, Jeffrey Datto, Elvira Costantino‐Ceccarini	2000	157
9	Niemann-Pick C disease : insight from studies on mutated NPC1 gene and protein M. T. Vanier, Gilles Millat, Christophe Marçais, Catherine Tomasetto, Mohammad A. Rafi, Tohru Yamamoto, Kosaku Ohno, David A. Wenger	1999	1
10	Transduction of Cultured Oligodendrocytes from Normal and Twitcher Mice by a Retroviral Vector Containing Human Galactocerebrosidase (GALC) cDNA Neurochemical Research ·Elvira Costantino‐Ceccarini, Alice Luddi, Margherita Volterrani, Michelina Strazza, Mohammad A. Rafi, David A. Wenger	1999	21
11	Globoid cell leukodystrophy in Cairn and West Highland white terriers Journal of Heredity ·David A. Wenger	1999	50
12	MRI and electrophysiological abnormalities in a case of canine globoid cell leucodystrophy Journal of Small Animal Practice ·Francesca Cozzi, Charles H. Vite, David A. Wenger, Teresa Victoria, Mark E. Haskins	1998	24
13	Multiple mutations in the GALC gene in a patient with adult‐onset krabbe disease Annals of Neurology ·Paola Luzi, Mohammad A. Rafi, David A. Wenger	1996	44
14	Infantile Sialic Acid Storage Disease: A Rare Cause of Cytoplasmic Vacuolation in Pediatric Patients Pediatric Pathology & Laboratory Medicine ·Laura P. Hale, Cosmas J. M. van de Ven, David A. Wenger, William D. Bradford, Stephen G. Kahler	1995	14
15	Structure and organization of the human galactocerebrosidase (GALC) gene Genomics ·Paola Luzi, Mohammad A. Rafi, David A. Wenger	1995	71
16	Mutations in the lysosomal beta-galactosidase gene that cause the adult form of GM1 gangliosidosis. PubMed ·Supriya Chakraborty, Mohammad A. Rafi, David A. Wenger	1994	28
17	Clinical and Biochemical Studies in an American Child with Sialuria Biochemical Medicine and Metabolic Biology ·Donna M. Krasnewich, Frank Tietze, W. Kŕause, Robert K. Pretzlaff, David A. Wenger, Vaibhav A. Diwadkar, W. A. Gahl	1993	15
18	Leukocyte sonicates as a source for both enzyme assay and DNA amplification for mutational analysis of certain lysosomal disorders Clinica Chimica Acta ·Eileen Louie, Mohammad A. Rafi, David A. Wenger	1991	9
19	Use of 4‐methylumbelliferyl‐6‐sulpho‐2‐acetamido‐2‐deoxy‐β‐D‐glucopyranoside for prenatal diagnosis of tay‐sachs disease using chorionic villi Prenatal Diagnosis ·Eugene E. Grebner, David A. Wenger	1987	7
20	Prenatal diagnosis of Krabbe disease: Galactosylceramide metabolism in cultured amniotic fluid cells The Journal of Pediatrics ·Tooru Kudoh, David A. Wenger	1982	5

About David A. Wenger

David A. Wenger is a scholar working on Physiology, Cell Biology, Physiology, Developmental Neuroscience and Organic Chemistry, having authored 221 papers that have together received 9.2k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (170 papers), Carbohydrate Chemistry and Synthesis (48 papers), Glycosylation and Glycoproteins Research (48 papers), Trypanosoma species research and implications (32 papers), Cellular transport and secretion (30 papers), Glycogen Storage Diseases and Myoclonus (20 papers), RNA regulation and disease (18 papers) and Sphingolipid Metabolism and Signaling (14 papers). The work is most often cited by research in Physiology (6.4k citations), Physiology (708 citations), Cell Biology (2.0k citations), Neurology (528 citations) and Developmental Neuroscience (257 citations). David A. Wenger has collaborated with scholars based in United States, France and Japan. Frequent co-authors include Mohammad A. Rafi, Paola Luzi, Martha Sattler, Koji Inui, Peter G. Pentchev, Marcella Comly, Marie T. Vanier, Joanne Kurtzberg, William Krivit and Maria L. Escolar. Their work appears in journals such as Molecular Genetics and Metabolism, Journal of Inherited Metabolic Disease, Clinica Chimica Acta, The Journal of Pediatrics and Human Mutation.

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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