George Hoganson

3.7k citations

50 papers · 2.1k indexed · h-index 21

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Physiology top 5%
- Lysosomal Storage Disorders Research

Papers in

Clinical Biochemistry 17
- Metabolism and Genetic Disorders 17
Biochemistry 5

Co-authors: Bryan B. Fuller Ken Iozumi Mark Allen Everett Joel Charrow Peter C. Johnson Massimo Zeviani M. DiRocco Graziella Uziel
Journals: Molecular Genetics and Metabolism (5 papers)The Journal of Pediatrics (3 papers)Genetics in Medicine (3 papers)Journal of Inherited Metabolic Disease (3 papers)Pediatric Research (3 papers)
Partner nations: United States Canada China

In The Last Decade

George Hoganson

50 papers receiving 2.0k citations

Peers

Countries citing papers authored by George Hoganson

Since Specialization

Citations

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

Fields of papers citing papers by George Hoganson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by George Hoganson. 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 George Hoganson. The network helps show where George Hoganson may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Multisite Oral Amoxicillin Challenges During Pediatric Emergency Department Visits JAMA Pediatrics ·David Vyles, George Hoganson, Constance McAneney, Mariana Castells, Elizabeth J. Phillips, Alexis Visotcky, David C. Brousseau	2023	1
2	Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDG Genetics in Medicine ·Peter Witters, R.L. Toennisson, Rita Barone, Katrin Õunap, Ramona Salvarinova, Sabine Grønborg, George Hoganson, Fernando Scaglia, Andrea M. Lewis, Mari Mori, Jolanta Sykut‐Cegielska, Andrew C. Edmondson, Miao He, Éva Morava	2020	56
3	Newborn Screening for Lysosomal Storage Disorders in Illinois: The Initial 15-Month Experience The Journal of Pediatrics ·Barbara K. Burton, Joel Charrow, George Hoganson, Alfons Sureda Carrión, Brad T. Tinkle, Stephen R. Braddock, Michael Schneider, Dorothy K. Grange, محمد أحمد محمود شلبی شلبی, 哲史奥田, Rebecca Barnett, Rong Shao, Khaja Basheeruddin, George J. Dizikes	2017	139
4	Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndrome Journal of Human Genetics ·Julia Ma Morán del Pozo, Jennifer Keller‐Ramey, Amy Knight Johnson, Jennifer A. Lee, Daniel B. Magner, Pratibha Dumane, Yendi Fernanda Ayala Pérez, I. Seong, Zejuan Li, Yeison Mejías Vásquez, Soma Das, Rachel Laframboise, William J. Capps, Ian D. Krantz, Sarah E. Noon, George Hoganson, Jennifer Burton, Christian P. Schaaf, Daniela del Gaudio	2017	10
5	Internal Carotid Artery Dissection After a Roller Coaster Ride in a 4-Year-Old: Case Report and Review of the Literature Pediatric Neurology ·Amre Nouh, 季希富, Thomas Grobelny, George Hoganson, Bhuvaneswar Reddy Kunduru, José Biller	2014	5
6	Enzymatic activity of methionine adenosyltransferase variants identified in patients with persistent hypermethioninemia Molecular Genetics and Metabolism ·Joaquín Fernández‐Irigoyen, Enrique Santamaría, Yin‐Hsiu Chien, Wuh‐Liang Hwu, Stanley H. Korman, Hanna Faghfoury, Andreas Schulze, George Hoganson, Sally P. Stabler, Robert H. Allen, Conrad Wagner, S. Harvey Mudd, Fernando J. Corrales	2010	24
7	Zonisamide Ameliorates Symptoms of Secondary Paroxysmal Dystonia Pediatric Neurology ·Robert T. Egel, George Hoganson, Prerika Agarwal, Lotfi Khemiri	2010	7
8	Infantile systemic hyalinosis Journal of the American Academy of Dermatology ·Helen T. Shin, Amy S. Paller, George Hoganson, Judith P. Willner, Mary Wu Chang, Seth J. Orlow	2004	29
9	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, Jessica Ivette Carbajal Suárez, 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
10	Canine Heparan Sulfate Sulfamidase and the Molecular Pathology Underlying Sanfilippo Syndrome Type A in Dachshunds Genomics ·Elena L. Aronovich, K. Paige Carmichael, Hiroki Morizono, Ioannis G. Koutlas, Minerva Deanching, George Hoganson, Andrea Fischer, Chester B. Whitley	2000	20
11	Very‐long‐chain acyl‐CoA dehydrogenase subunit assembles to the dimer form on mitochondrial inner membrane FEBS Letters ·Masayoshi Souri, Toshifumi Aoyama, George Hoganson, Takashi Hashimoto	1998	33
12	Correlation of severity and outcome with plasma sterol levels in variants of the Smith-Lemli-Opitz syndrome The Journal of Pediatrics ·G. Stephen Tint, Gerald Salen, Ashok K. Batta, Sarah Shefer, Mira Irons, Ellen Roy Elias, Dianne Abuelo, Virginia P. Johnson, Marie Lambert, Richard A. Lutz, Carolyn Schanen, Colleen A. Morris, George Hoganson, W. H. Thomin	1995	117
13	Identification of a novel exonic mutation at -13 from 5' splice site causing exon skipping in a girl with mitochondrial acetoacetyl-coenzyme A thiolase deficiency. Journal of Clinical Investigation ·Toshiyuki Fukao, Seiji Yamaguchi, Yoshitaka Isaka, T Orii, George Hoganson, Takashi Hashimoto	1994	33
14	Clinical and Pathologic Findings in 2 Siblings with Congenital Nephrotic Syndrome Fetal Diagnosis and Therapy ·Pius, Miguel Farolan, 日本経済長期研究グル-プ, J. Hörnschemeyer, Seh Woong Chung, George Hoganson	1994	6
15	Hormonal Regulation of Melanogenesis in Mouse Melanoma and in Human Melanocytes Annals of the New York Academy of Sciences ·Bryan B. Fuller, Deepa Rungta, Ken Iozumi, George Hoganson, Attila Györkös, Dayan Nahotto, George Émerson Pereira Farias, K. Owens	1993	21
16	Role of Tyrosinase as the Determinant of Pigmentation in Cultured Human Melanocytes Journal of Investigative Dermatology ·Ken Iozumi, George Hoganson, Arifin Arifin, Mark Allen Everett, Bryan B. Fuller	1993	218
17	Tentative assignment of gene for oto‐palato‐digital syndrome to distal Xq (Xq26–q28) American Journal of Medical Genetics ·David I. Hoar, L. Leigh Field, J. P. Hiegel, George Hoganson, Beverly R. Rollnick, Joe J. Hoo	1992	12
18	Phylogenetic comparisons of the branched-chain α-ketoacid dehydrogenase complex Comparative Biochemistry and Physiology Part B Comparative Biochemistry ·Richard S. Eisenstein, Robert H. Miller, George Hoganson, Alfred E. Harper	1990	4
19	The human RD protein is closely related to nuclear RNA-binding proteins and has been highly conserved Gene ·Carol S. Surowy, George Hoganson, John J. Gosink, Kathleen M. Strunk, Richard A. Spritz	1990	30
20	Biopterin Synthesis Defects: Problems in Diagnosis PEDIATRICS ·George Hoganson, Stanley Berlow, Seymour Kaufman, Sheldon Milstien, Marie Vetter, Reuben Matalon, Edwin W. Naylor, William E. Seifert	1984	17

About George Hoganson

George Hoganson is a scholar working on Clinical Biochemistry, Biochemistry, Physiology, Molecular Biology and Cell Biology, having authored 50 papers that have together received 2.1k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (10 papers), Lysosomal Storage Disorders Research (10 papers), melanin and skin pigmentation (5 papers), Neonatal Health and Biochemistry (4 papers), Diet and metabolism studies (4 papers), Biochemical Analysis and Sensing Techniques (4 papers) and RNA and protein synthesis mechanisms (3 papers). The work is most often cited by research in Clinical Biochemistry (587 citations), Physiology (687 citations), Cell Biology (394 citations), Rheumatology (352 citations) and Molecular Biology (1.0k citations). George Hoganson has collaborated with scholars based in United States, Canada and China. Frequent co-authors include Bryan B. Fuller, Ken Iozumi, Mark Allen Everett, Joel Charrow, Peter C. Johnson, Massimo Zeviani, M. DiRocco, Graziella Uziel, Stefano DiDonato and Darryl C. DeVivo. Their work appears in journals such as Molecular Genetics and Metabolism, The Journal of Pediatrics, Genetics in Medicine, Journal of Inherited Metabolic Disease and Pediatric Research.

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