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Louis Dallaire

Observed names: Dallaire, L., Dallaire, Louis, Dallaire, Louis M., L DALLAIRE, L Dallaire, L. DALLAIRE, L. Dallaire
Observed institutions: University of Vermont, Children's Hospital of Wisconsin, Université de Sherbrooke, University of British Columbia, Johns Hopkins University, University of Antwerp, Medical College of Wisconsin, Douglas Mental Health University Institute, Montreal Children's Hospital, North York General Hospital, Santa Clara Valley Medical Center, Centre Hospitalier Universitaire de Sherbrooke, Centre Hospitalier Universitaire Sainte-Justine, Credit Valley Hospital, Royal Victoria Hospital, Centre Hospitalier Universitaire Amiens-Picardie, Hôtel-Dieu de Québec, Stanford Medicine, Centre hospitalier de l'Université Laval, Montreal Clinical Research Institute, CHU Sainte-Justine Research Center, Université de Picardie Jules Verne, McGill University, Université de Montréal, Stanford University
OpenAlex ID: A5111895003
Fluorometric assay of neuraminidase with a sodium (4-methylumbelliferyl-α-d-N-acetylneuraminate) substrate
1979 · M. Potier, L. Mameli, et al. · Analytical Biochemistry · 816
Trisomy Recurrence: A Reconsideration Based on North American Data
2004 · Dorothy Warburton, Louis Dallaire, et al. · The American Journal of Human Genetics · 248
Prenatal diagnosis of genetic disease in Canada: report of a collaborative study.
1976 · N E Simpson, L Dallaire, et al. · PubMed Central · 242
Neurologic Crises in Hereditary Tyrosinemia
1990 · Grant Mitchell, Jean Larochelle, et al. · New England Journal of Medicine · 230
Cloning, expression and chromosomal mapping of human lysosomal sialidase and characterization of mutations in sialidosis
1997 · Alexey V. Pshezhetsky, Catherine Richard, et al. · Nature Genetics · 215
Age-specific distribution of plasma amino acid concentrations in a healthy pediatric population
1997 · Nathalie Lepage, Nancy McDonald, et al. · Clinical Chemistry · 148
Multiple atresias and a new syndrome of hereditary multiple atresias involving the gastrointestinal tract from stomach to rectum
1973 · F.M. Guttman, P. Braun, et al. · Journal of Pediatric Surgery · 143
Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in Québec
2012 · Jean Larochelle, Fernando Alvarez, et al. · Molecular Genetics and Metabolism · 137
Comparative behavioral, biochemical and pigmentary effects of MPTP, MPP+ and paraquat in rana pipiens
1985 · A. Barbeau, L. Dallaire, et al. · Life Sciences · 119
Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex
1998 · Teresa Costa, Marie Lambert, et al. · American Journal of Medical Genetics · 91
Fetal congenital diaphragmatic hernia: accuracy of sonography in the diagnosis and prediction of the outcome after birth.
1996 · L Guibaud, D Filiatrault, et al. · American Journal of Roentgenology · 71
Recommendations on the use of folic acid supplementation to prevent the recurrence of neural tube defects. Clinical Teratology Committee, Canadian College of Medical Geneticists.
1993 · M I Van Allen, F C Fraser, et al. · PubMed Central · 70
Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria
1986 · Grant A. Mitchell, David Watkins, et al. · The Journal of Pediatrics · 63
Reactivity of amniotic fluid alpha-fetoprotein with concanavallin A in diagnosis of neural tube defects.
1979 · C J Smith, P C Kelleher, et al. · BMJ · 60
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New amphibian models for the study of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)
1985 · A. Barbeau, L. Dallaire, et al. · Life Sciences · 58
Dicarboxylic aminoaciduria: An inborn error of amino acid conservation
1977 · Serge B. Melançon, Louis Dallaire, et al. · The Journal of Pediatrics · 57
Annex 6: Chromosome mosaicism in CVS and amniocentesis samples
1992 · I. E. Teshima, D. K. Kalousek, et al. · Prenatal Diagnosis · 52
The composition of preterm milk in relation to the degree of prematurity
1984 · G Lepage, S Collet, et al. · American Journal of Clinical Nutrition · 50
Prenatal detection of intestinal obstruction: deficient amniotic fluid disaccharidases in affected fetuses
1980 · P. R. Morin, M. Potier, et al. · Clinical Genetics · 49
Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance.
1969 · L Dallaire · Journal of Medical Genetics · 48
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Club foot, an adverse outcome of early amniocentesis: disruption or deformation?
1999 · S A Farrell, A M Summers, et al. · Journal of Medical Genetics · 47
De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype
1999 · Fr�d�rique Tihy, Emmanuelle Lemyre, et al. · American Journal of Medical Genetics · 46
Prenatal diagnosis of hereditary tyrosinaemia: Measurement of succinylacetone in amniotic fluid
1982 · R. Gagné, A. Lescault, et al. · Prenatal Diagnosis · 46
Autosomal dominant polycystic kidney disease in the fetus
1994 · Jacques Michaud, Pierre Russo, et al. · American Journal of Medical Genetics · 43
Parental reaction and adaptability to the prenatal diagnosis of fetal defect or genetic disease leading to pregnancy interruption
1995 · L. Dallaire, G. Lortie, et al. · Prenatal Diagnosis · 42
Works count: 171
Citation count: 4,506
H-index: 32
I10-index: 73
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