Publications by authors named "Nancy Laurin"

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Processing biological samples from simulated radiological terrorist events using Rapid DNA instruments.
Chantal J Frégeau, Nancy Laurin

Forensic Sci Int· January 2024

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Comparative analysis of two Rapid DNA technologies for the processing of blood and saliva-based samples.
Nancy Laurin, Hélène Boulianne, Chantal Frégeau

Forensic Sci Int Genet· November 2023

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New incompatibilities uncovered using the Promega DNA IQ™ chemistry.
Nancy Laurin, Florence Célestin, Meagan Clark, Della Wilkinson, Brian Yamashita

Forensic Sci Int· December 2015

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An Accelerated Analytical Process for the Development of STR Profiles for Casework Samples.
Nancy Laurin, Chantal J Frégeau

J Forensic Sci· July 2015

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The Qiagen Investigator® Quantiplex HYres as an alternative kit for DNA quantification.
Chantal J Frégeau, Nancy Laurin

Forensic Sci Int Genet· May 2015

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Population genetic data of the AmpFℓSTR® Identifiler® Plus and PowerPlex® 16 HS STR loci in four Canadian populations.
Nancy Laurin, Emmanuel Milot

Int J Legal Med· March 2014

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Performance of Identifiler Direct and PowerPlex 16 HS on the Applied Biosystems 3730 DNA Analyzer for processing biological samples archived on FTA cards.
Nancy Laurin, Anick DeMoors, Chantal Frégeau

Forensic Sci Int Genet· September 2012

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Development of a fast PCR protocol enabling rapid generation of AmpFℓSTR® Identifiler® profiles for genotyping of human DNA.
Amanda Foster, Nancy Laurin

Investig Genet· March 2012

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Optimization and validation of a fast amplification protocol for AmpFlSTR® Profiler Plus® for rapid forensic human identification.
Nancy Laurin, Chantal Frégeau

Forensic Sci Int Genet· January 2012

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Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region.
Nancy Laurin, Karen G Wigg, Yu Feng, Paul Sandor, Cathy L Barr

Am J Med Genet B Neuropsychiatr Genet· January 2009

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Association study for genes at chromosome 5p13-q11 in attention deficit hyperactivity disorder.
Nancy Laurin, Jonghun Lee, Abel Ickowicz, Tejaswee Pathare, Molly Malone

Am J Med Genet B Neuropsychiatr Genet· July 2008

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No evidence for genetic association between DARPP-32 (PP1R1B) polymorphisms and attention deficit hyperactivity disorder.
Nancy Laurin, Abel Ickowicz, Tejaswee Pathare, Molly Malone, Rosemary Tannock

Am J Med Genet B Neuropsychiatr Genet· April 2008

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Investigation of the G protein subunit Galphaolf gene (GNAL) in attention deficit/hyperactivity disorder.
Nancy Laurin, Abel Ickowicz, Tejaswee Pathare, Molly Malone, Rosemary Tannock

J Psychiatr Res· January 2008

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Association study of the brain-derived neurotropic factor (BDNF) gene in attention deficit hyperactivity disorder.
Jonghun Lee, Nancy Laurin, Jennifer Crosbie, Abel Ickowicz, Tejaswee Pathare

Am J Med Genet B Neuropsychiatr Genet· December 2007

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Sequestosome 1: mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone.
Jean Morissette, Nancy Laurin, Jacques P Brown

J Bone Miner Res· December 2006

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The functional landscape of mouse gene expression.
Wen Zhang, Quaid D Morris, Richard Chang, Ofer Shai, Malina A Bakowski, Nancy Laurin

J Biol· September 2006

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Human hormone-sensitive lipase (HSL): expression in white fat corrects the white adipose phenotype of HSL-deficient mice.
Mélanie Fortier, Krishnakant Soni, Nancy Laurin, Shu Pei Wang, Pascale Mauriège

J Lipid Res· September 2005

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Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone.
Nancy Laurin, Jacques P Brown, Jean Morissette, Vincent Raymond

Am J Hum Genet· June 2002

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