Marie Lambert - Concepedia

Author

Marie Lambert

Centre Hospitalier Universitaire Sainte-Justine

Also Known As

Lambert Marie, Lambert, Marie, MARIE LAMBERT, Marie Lambert

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Centre Hospitalier Universitaire Sainte-Justine Université de Montréal McGill University Centre Hospitalier de l’Université de Montréal Hospital for Sick Children

About

Marie Lambert is an author at Centre Hospitalier Universitaire Sainte-Justine specializing in medicine, pediatrics, and inherited metabolic disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	483
2	Health Sciences	2	2	71
3	Education	1	1	16
4	Engineering	1	1	18
5	Management	1	1	16

Marie Lambert

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Hyperornithinaemia- hyperammonaemia- homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter Jose A. Camacho, Cassandra Obie, Barbara J. Biery, Nature Genetics Mitochondrial Ornithine TransporterUrologyMendelian DisorderMitochondrial FunctionGenetic Disorder	1999	204
Treatment of Familial Hypercholesterolemia in Children and Adolescents: Effect of Lovastatin Marie Lambert, Paul-J. Lupien, Claude Gagné, PEDIATRICS	1996	159
Diagnostic Accuracy of Blood Lactate-to-Pyruvate Molar Ratio in the Differential Diagnosis of Congenital Lactic Acidosis François‐Guillaume Debray, Grant A. Mitchell, Pierre Allard, Clinical Chemistry	2007	127
Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex Teresa Costa, Marie Lambert, Ikuko Teshima, American Journal of Medical Genetics	1998	90
Influence of methylenetetrahydrofolate reductase genotype, age, vitamin B-12, and folate status on plasma homocysteine in children Edgard Delvin, Rima Rozen, Aïcha Mérouani, American Journal of Clinical Nutrition Vitamin NutritionNutritionPlasma HomocysteineMethylenetetrahydrofolate Reductase GenotypeMedicine	2000	65
Outcome of individuals with low-moderate methylmalonic aciduria detected through a neonatal screening program Lisa C. Sniderman, Marie Lambert, Robert Giguère, The Journal of Pediatrics Early DiagnosisUrologyNeonatologyLow-moderate Methylmalonic AciduriaNeonatal Screening Program	1999	64
Associations Between Children’s Diets and Features of Their Residential and School Neighbourhood Food Environments Andraea Van Hulst, Trade A. Barnett, Lise Gauvin, Canadian Journal of Public Health Food ChoiceNutritionLocal Food SystemsDiet QualityTheir Residential	2012	53
Homozygous hypomorphic <i>BRCA2</i> variant in primary ovarian insufficiency without cancer or Fanconi anaemia trait Sandrine Caburet, Abdelkader Heddar, Elodie Dardillac, Journal of Medical Genetics	2020	44
Geographic distribution of French‐Canadian low‐density lipoprotein receptor gene mutations in the Province of Quebec Marie‐Claude Vohl, Sital Moorjan, Madeleine Roy, Clinical Genetics	1997	42
Autosomal dominant polycystic kidney disease in the fetus Jacques L. Michaud, Pierre Russo, Andrée Grignon, American Journal of Medical Genetics UrologyMedicineKidney FailureRenal PathologyFetal Adpkd Kidneys	1994	42

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