Ingrid Tein

4.2k citations

88 papers · 3.1k indexed · h-index 36

Impact in

Clinical Biochemistry top 0.05%
- Metabolism and Genetic Disorders
Biochemistry top 1%
- Amino Acid Enzymes and Metabolism

Papers in ⓘ

Clinical Biochemistry 64
- Metabolism and Genetic Disorders 64
Biochemistry 9

Co-authors: Anne‐Marie Lamhonwah (18 shared papers)Darryl C. De Vivo (8 shared papers)Frank Merante (5 shared papers)Lee Benson (6 shared papers)S. DiMauro (6 shared papers)B. H. Robinson (2 shared papers)Greg D. Wells (5 shared papers)Cameron Ackerley (4 shared papers)
Journals: Biochemical and Biophysical Research Communications (9 papers)Molecular Genetics and Metabolism (7 papers)Neurology (6 papers)Journal of Inherited Metabolic Disease (6 papers)Pediatric Research (5 papers)
Partner nations: Canada United States United Kingdom

In The Last Decade

Ingrid Tein

87 papers receiving 3.0k citations

Peers

Countries citing papers authored by Ingrid Tein

Since Specialization

Citations

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

Fields of papers citing papers by Ingrid Tein

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Ingrid Tein, 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 Ingrid Tein Line = papers co-authored together Ingrid Tein 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 88 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Pyridoxine dependent epilepsy and antiquitin deficiency Molecular Genetics and Metabolism ·Sylvia Stöckler, Barbara Plecko, Sídney M. Gospe, Marion B. Coulter-Mackie, Mary Connolly, Clara van Karnebeek, Saadet Mercimek‐Mahmutoglu, Hans Hartmann, Gunter Scharer, Eduard A. Struijs, Ingrid Tein, Cornelis Jakobs, Peter T. Clayton, Johan L.K. Van Hove	2011	214
2	Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake Annals of Neurology ·Charles A. Stanley, Susan Deleeuw, Paul M. Coates, C. Vianey‐Liaud, P. Divry, Jean‐Paul Bonnefont, Jean‐Marie Saudubray, Morey W. Haymond, Friedrich K. Trefz, Galen N. Breningstall, Rebecca S. Wappner, D. J. Byrd, Claude Sansaricq, Ingrid Tein, Warren D. Grover, David Valle, S. Lane Rutledge, William R. Treem	1991	163
3	Impaired Skin Fibroblast Carnitine Uptake in Primary Systemic Carnitine Deficiency Manifested by Childhood Carnitine-Responsive Cardiomyopathy Pediatric Research ·Ingrid Tein, Darryl C. De Vivo, F Z Bierman, P Pulver, Linda J. De Meirleir, Ljerka Cvitanović-Šojat, Roberta A Pagon, Enrico Bertini, Carlo Dionisi‐Vici, Serenella Servidei, S. DiMauro	1990	147
4	l‐Carnitine Supplementation in Childhood Epilepsy: Current Perspectives Epilepsia ·Darryl C. De Vivo, Timothy P. Bohan, David L. Coulter, Fritz E. Dreifuss, Robert Greenwood, Douglas R. Nordli, W. Donald Shields, Carl E. Stafstrom, Ingrid Tein	1998	117
5	Carnitine transport: Pathophysiology and metabolism of known molecular defects Journal of Inherited Metabolic Disease ·Ingrid Tein	2003	105
6	Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene. PubMed ·Frank Merante, Ingrid Tein, Lee Benson, B. H. Robinson	1994	104
7	NovelOCTN2mutations: No genotype–phenotype correlations: Early carnitine therapy prevents cardiomyopathy American Journal of Medical Genetics ·Anne‐Marie Lamhonwah, S. E. Olpin, R. J. Pollitt, Christine Vianey‐Saban, P. Divry, Nathalie Guffon, G. T. N. Besley, Russell Onizuka, Linda J. De Meirleir, Ljerka Cvitanović-Šojat, Ivo Barić, Carlo Dionisi‐Vici, Ksenija Fumić, Miljenka Maradin, Ingrid Tein	2002	93
8	Novel localization of OCTN1, an organic cation/carnitine transporter, to mammalian mitochondria Biochemical and Biophysical Research Communications ·Anne‐Marie Lamhonwah, Ingrid Tein	2006	89
9	An additional mitochondrial tRNAIle point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy Human Mutation ·Frank Merante, Tomoko Myint, Ingrid Tein, Lee Benson, B. H. Robinson	1996	86
10	Cystic fibrosis transmembrane conductance regulator in human muscle: Dysfunction causes abnormal metabolic recovery in exercise Annals of Neurology ·Anne‐Marie Lamhonwah, Christine E. Bear, Ling Jun Huan, Patrick Kim Chiaw, Cameron Ackerley, Ingrid Tein	2010	85
11	Mitochondrial encephalomyopathy, lactic acidosis, stroke‐like episodes (MELAS): Clinical, radiological, pathological, and genetic observations Annals of Neurology ·Betty Koo, Laurence E. Becker, Sylvester Chuang, Frank Merante, Brian H. Robinson, Daune MacGregor, Ingrid Tein, Vincent B. Ho, Douglas A. McGreal, John R. Wherrett, William J. Logan	1993	81
12	The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level Human Genetics ·Christina B. Pedersen, Steen Kølvraa, Agnete Kølvraa, Vibeke Stenbroen, Margrethe Kjeldsen, Regina Ensenauer, Ingrid Tein, Dietrich Matern, Piero Rinaldo, Christine Vianey‐Saban, Antònia Ribes, W. Lehnert, Ernst Christensen, Thomas J. Corydon, Brage Storstein Andresen, Søren Vang, Lars Bolund, Jerry Vockley, Peter Bross, Niels Gregersen	2008	73
13	Bioenergetic provision of energy for muscular activity Paediatric Respiratory Reviews ·Greg D. Wells, Hiran Selvadurai, Ingrid Tein	2009	65
14	Fatty acid oxidation abnormalities in childhood-onset spinal muscular atrophy: Primary or secondary defect(s)? Pediatric Neurology ·Ingrid Tein, Avril Sloane, Elizabeth Donner, Dennis C. Lehotay, David S. Millington, Richard I. Kelley	1995	64
15	Skeletal Muscle Metabolic Dysfunction in Obesity and Metabolic Syndrome Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Greg D. Wells, Michael D. Noseworthy, Jill Hamilton, Mark Tarnopolski, Ingrid Tein	2008	58
16	Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlation. Journal of Clinical Investigation ·Jamal A. Ibdah, Ingrid Tein, Carlo Dionisi‐Vici, Malcolm J. Bennett, Lodewijk IJlst, B Gibson, Ronald J. A. Wanders, Arnold W. Strauss	1998	57
17	A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn’s disease locus (IBD5) Biochemical and Biophysical Research Communications ·Anne‐Marie Lamhonwah, Jennifer Skaug, Stephen W. Scherer, Ingrid Tein	2003	57
18	Short‐chainL‐3‐hydroxyacyl‐CoA dehydrogenase deficiency in muscle: A new cause for recurrent myoglobinuria and encephalopathy Annals of Neurology ·Ingrid Tein, Darryl C. De Vivo, Daniel E. Hale, J. T. R. Clarke, Howard M. Zinman, Ronnald Laxer, A Shore, S. DiMauro	1991	57
19	Short-chain acyl–CoA dehydrogenase deficiency Neurology ·Ingrid Tein, Robert H. A. Haslam, William J. Rhead, Michael J. Bennett, L E Becker, Jerry Vockley	1999	54
20	Expression patterns of the organic cation/carnitine transporter family in adult murine brain Brain and Development ·Anne Marie Lamhonwah, Cynthia Hawkins, Carolyn Tam, Jeannie Hsiu Ding Wong, Lydia Mai, Ingrid Tein	2007	53

About Ingrid Tein

Ingrid Tein is a scholar working on Clinical Biochemistry, Biochemistry, Molecular Biology, Rheumatology and Pediatrics, Perinatology and Child Health, having authored 88 papers that have together received 3.1k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (64 papers), Mitochondrial Function and Pathology (49 papers), Peroxisome Proliferator-Activated Receptors (10 papers), Diet and metabolism studies (10 papers), Muscle metabolism and nutrition (7 papers), ATP Synthase and ATPases Research (6 papers), Biochemical and Molecular Research (6 papers) and RNA modifications and cancer (6 papers). The work is most often cited by research in Clinical Biochemistry (1.9k citations), Biochemistry (363 citations), Molecular Biology (1.8k citations), Pediatrics, Perinatology and Child Health (466 citations) and Rheumatology (312 citations). Ingrid Tein has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Anne‐Marie Lamhonwah, Darryl C. De Vivo, Frank Merante, Lee Benson, S. DiMauro, B. H. Robinson, Greg D. Wells, Cameron Ackerley, Carlo Dionisi‐Vici and Daune MacGregor. Their work appears in journals such as Biochemical and Biophysical Research Communications, Molecular Genetics and Metabolism, Neurology, Journal of Inherited Metabolic Disease and Pediatric Research.

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