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M. St‐Louis

Observed names: M St-Louis, M. St-Louis
Institution: Héma-Québec
OpenAlex ID: A5113594140
Tyrosine and its catabolites: from disease to cancer.
1996 · R M Tanguay, R Jorquera, et al. · Acta Biochimica Polonica · 66
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Identification of a stop mutation in five Finnish patients suffering from hereditary tyrosinemia type I
1994 · M. St-Louis, B. Leclerc, et al. · Human Molecular Genetics · 50
Set‐up and routine use of a database of 10 555 genotyped blood donors to facilitate the screening of compatible blood components for alloimmunized patients
2009 · J. Perreault, J. Lavoie, et al. · Vox Sanguinis · 46
Génotypage de 21 000 donneurs de sang au Québec et analyse du RHD
2010 · M. St-Louis, J. Perreault, et al. · Transfusion Clinique et Biologique · 30
Genotyping for red blood cell polymorphisms
2008 · C. E. Van Der Schoot, M. De Haas, et al. · Vox Sanguinis · 23
Weak D type 42 cases found in individuals of European descent
2011 · M. St-Louis, M. Richard, et al. · Immunohematology · 18
Consortium for Blood Group Genes (CBGG): 2009 report
2010 · G.A. Denomme, C.M Westhoff, et al. · Immunohematology · 16
PCR ‐free blood group genotyping using a nanobiosensor
2014 · D. Brouard, O. Ratelle, et al. · Vox Sanguinis · 11
Alloimmunization of patients by blood units harboring distinct DEL variants
2013 · M. St-Louis, A. Lebrun, et al. · Immunohematology · 10
A new SEMA7A variant found in Native Americans with alloantibody
2010 · M. Richard, J. St‐Laurent, et al. · Vox Sanguinis · 8
Red blood cell antigen portrait of self‐identified Black donors in Quebec
2014 · M. St‐Louis, J. Constanzo‐Yanez, et al. · Transfusion Medicine · 4
A LU:−16 individual with antibodies
2017 · C. Éthier, C. Parent, et al. · Immunohematology
Strong association between a splice mutation (IVS12+5G{r_arrow}A) and haplotype 6 in hereditary tyrosinemia type I
1994 · Robert M. Tanguay, M. St‐Louis, et al. · The American Journal of Human Genetics
Works count: 13
Citation count: 282
H-index: 9
I10-index: 9
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