Anne‐Marie Lamhonwah

Author

Hospital for Sick Children

Also Known As

Anne-Marie LamHonWah, Anne-Marie Lamhonwah, Anne‐Marie Lamhonwah

Publications

962

Citations

H-Index

Concepts

All Affiliations

Hospital for Sick Children University of Toronto SickKids Foundation Montreal Children's Hospital Aarhus University Hospital

About

Anne‐Marie Lamhonwah is an author at Hospital for Sick Children specializing in medicine, natural sciences, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	13	562
2	Natural Sciences	7	7	291
3	Biochemistry	5	5	283
4	Cell Biology	3	3	77
5	Cellular Physiology	1	1	23

Anne‐Marie Lamhonwah

Publications

891

Citations

H-Index

Page 1

	Year	Citations
Novel<i>OCTN2</i>mutations: No genotype–phenotype correlations: Early carnitine therapy prevents cardiomyopathy Anne‐Marie Lamhonwah, S. E. Olpin, R. J. Pollitt, American Journal of Medical Genetics	2002	119
Cystic fibrosis transmembrane conductance regulator in human muscle: Dysfunction causes abnormal metabolic recovery in exercise Anne‐Marie Lamhonwah, Christine E. Bear, Ling Jun Huan, Annals of Neurology	2010	108
Novel localization of OCTN1, an organic cation/carnitine transporter, to mammalian mitochondria Anne‐Marie Lamhonwah, Ingrid Tein Biochemical and Biophysical Research Communications Mammalian MitochondriaOrganic Cation/carnitine TransporterMitochondrial FunctionBiochemistryNatural Sciences	2006	102
A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn’s disease locus (IBD5) Anne‐Marie Lamhonwah, Jennifer Skaug, Stephen W. Scherer, Biochemical and Biophysical Research Communications Disease LocusBiochemistryCrohn ’Gastrointestinal PharmacologyMedicine	2003	70
OCTN3 is a mammalian peroxisomal membrane carnitine transporter Anne‐Marie Lamhonwah, Cameron Ackerley, A Tilups, Biochemical and Biophysical Research Communications BiochemistryNatural SciencesMembrane TransportPhysiologyMembrane Biology	2005	64
Carnitine Uptake Defect: Frameshift Mutations in the Human Plasmalemmal Carnitine Transporter Gene Anne‐Marie Lamhonwah, Ingrid Tein Biochemical and Biophysical Research Communications Carnitine Uptake DefectMedicineGeneticsInherited Metabolic DiseasePhysiology	1998	64
Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin Ingrid Tein, Orly Elpeleg, Bruria Ben‐Zeev, Molecular Genetics and Metabolism Candidate Founder MutationAshkenazi Jewish OriginGenetic DisorderGeneticsClinical Heterogeneity	2007	62
Sequence homology around the biotin-binding site of human propionyl-CoA carboxylase and pyruvate carboxylase Anne‐Marie Lamhonwah, Frank Quan, Roy A. Gravel Archives of Biochemistry and Biophysics	1987	35
Vulnerability to Oxidative Stress In Vitro in Pathophysiology of Mitochondrial Short-Chain Acyl-CoA Dehydrogenase Deficiency: Response to Antioxidants Zarazuela Zolkipli, Christina B. Pedersen, Anne‐Marie Lamhonwah, PLoS ONE	2011	33
Isolation and expression of a full-length cDNA encoding the human GM2 activator protein Bei Xie, Beth McInnes, Kuldeep Neote, Biochemical and Biophysical Research Communications Full-length CdnaProtein ExpressionNatural SciencesGeneticsGene Structure	1991	30

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