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Christian Allen Drouin

Observed names: C A Drouin, Christian A. Drouin, Drouin CA
Observed institution: Hôtel-Dieu de Québec
OpenAlex ID: A5080898566
Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord
2008 · Alexandre Montpetit, Stéphanie Côté, et al. · PLoS Genetics · 178
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MEDNIK syndrome: a novel defect of copper metabolism treatable by zinc acetate therapy
2013 · Diego Martinelli, Lorena Travaglini, et al. · Brain · 156
Expanding the Clinical Phenotype Associated WithELOVL4Mutation
2014 · Maxime Cadieux-Dion, Maude Turcotte-Gauthier, et al. · JAMA Neurology · 128
Pluripotent stem cell-derived bile canaliculi-forming hepatocytes to study genetic liver diseases involving hepatocyte polarity
2019 · Arend W. Overeem, Karin Klappe, et al. · Journal of Hepatology · 47
Rothmund-Thomson syndrome with osteosarcoma
1993 · Christian A. Drouin, Eric Mongrain, et al. · Journal of the American Academy of Dermatology · 45
An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22
2004 · Thomas G. Saba, Alexandre Montpetit, et al. · Human Genetics · 43
The association of Buschke-Ollendorf syndrome and nail-patella syndrome
2002 · Christian Allen Drouin, Hugues Grenon · Journal of the American Academy of Dermatology · 21
[Recurrence of erosive pustular scalp dermatosis after a skin graft].
1999 · C A Drouin, R A Cloutier · PubMed · 15
La première maladie génétique québécoise : le syndrome de Clouston
2015 · Christian A. Drouin · Érudit (Université de Montréal)
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Le patrimoine génétique germanique des Québécois
2012 · Christian A. Drouin · Érudit (Université de Montréal)
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A new locus for pure Spinocerebellar Ataxia associated with Erythrokeratodermia maps to chromosome 6p12.3-16.1
2009 · Turcotte Gauthier M, Nguyen DK, et al. · Institutional Research Information System University of Turin (University of Turin)
Works count: 11
Citation count: 633
H-index: 8
I10-index: 8
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