H. Daoud

V. Meininger, F. Salachas, J. Bouchard, 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis

J. Bouchard, G. Rouleau, W. Camu, 2011, Neurobiology of Aging.

Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum

M. Lassonde, G. Rouleau, A. Dionne‐Laporte, 2015, European Journal of Human Genetics.

Frailty predicts adverse outcomes in older patients undergoing transcatheter aortic valve replacement (TAVR). From the National Inpatient Sample.

L. Klein, H. Daoud, M. Abdel-Rahman, 2021, Cardiovascular revascularization medicine : including molecular interventions.

Impact of Sex Differences on Outcomes of Peripheral Artery Disease Intervention (From a Nationwide Sample).

H. Daoud, A. Volgman, Saria S. Awadalla, 2020, The American journal of cardiology.

Autism and Nonsyndromic Mental Retardation Associated with a De Novo Mutation in the NLGN4X Gene Promoter Causing an Increased Expression Level

C. Barthélémy, P. Vourc'h, C. Andres, 2009, Biological Psychiatry.

Association of long ATXN2 CAG repeat sizes with increased risk of amyotrophic lateral sclerosis.

V. Meininger, G. Rouleau, W. Camu, 2011, Archives of neurology.

Association of Long ATXN 2 CAG Repeat Sizes With Increased Risk of Amyotrophic Lateral Sclerosis

V. Meininger, G. Rouleau, W. Camu, 2011 .

Investigation of C9orf72 repeat expansions in Parkinson's disease

N. Jodoin, G. Rouleau, S. Chouinard, 2013, Neurobiology of Aging.

Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism

A. Vanderver, B. Brais, C. Stevens, 2013, Journal of Medical Genetics.

Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patients

V. Meininger, G. Rouleau, W. Camu, 2013, Neurobiology of Aging.

Mosaic KRAS mutation in a patient with encephalocraniocutaneous lipomatosis and renovascular hypertension

K. Boycott, B. Chung, H. Daoud, 2018, American journal of medical genetics. Part A.

Parent–child exome sequencing identifiesa de novo truncating mutation in TCF4 in non‐syndromic intellectual disability

G. Rouleau, G. Rouleau, F. Hamdan, 2013, Clinical genetics.

National trends of outcomes in transcatheter aortic valve replacement (TAVR) through transapical versus endovascular approach: From the National Inpatient Sample (NIS).

L. Klein, A. Shroff, H. Daoud, 2020, Cardiovascular revascularization medicine : including molecular interventions.

In-hospital outcomes of transapical versus surgical aortic valve replacement: from the U.S. national inpatient sample

L. Klein, H. Daoud, Alejandro Sanchez-Nadales, 2021, Journal of geriatric cardiology : JGC.

Novel FUS deletion in a patient with juvenile amyotrophic lateral sclerosis.

J. Langlais, B. Brais, G. Rouleau, 2012, Archives of neurology.

Mutations in FUS cause FALS and SALS in French and French Canadian populations

V. Meininger, F. Salachas, J. Bouchard, 2009, Neurology.

Genetic analysis of SIGMAR1 as a cause of familial ALS with dementia

G. Rouleau, M. Strong, W. Camu, 2012, European Journal of Human Genetics.

Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis

J. Bouchard, G. Rouleau, W. Camu, 2012, Neurobiology of Aging.

Motor neuron disease: A role for ubiquilin 2 mutations in neurodegeneration

G. Rouleau, H. Daoud, 2011, Nature Reviews Neurology.

Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis

J. Bouchard, G. Rouleau, W. Camu, 2011, Journal of Human Genetics.

UBQLN2 mutations are rare in French and French–Canadian amyotrophic lateral sclerosis

V. Meininger, F. Salachas, J. Bouchard, 2012, Neurobiology of Aging.

Chromosome 9p21 in amyotrophic lateral sclerosis: the plot thickens

G. Rouleau, P. Dion, V. Belzil, 2010, The Lancet Neurology.

C9orf72 Repeat Expansions in Rapid Eye Movement Sleep Behaviour Disorder

A. Desautels, R. Postuma, J. Montplaisir, 2014, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Coronary artery disease (CAD) risk factor analysis in an age-stratified hospital population with systemic lupus erythematosus (SLE)

H. Daoud, M. Abdel-Rahman, D. Levinson, 2020, International Journal of Cardiology. Hypertension.

Resolution of refractory hypotension and anuria in a premature newborn with loss‐of‐function of ACE

K. Boycott, D. Bulman, E. Bareke, 2015, American journal of medical genetics. Part A.

Acute Coronary Syndrome (ACS) due to Coronary Artery Embolism in a Patient with Atrial Fibrillation

H. Daoud, A. Abugroun, Surender Kumar, 2019, Case reports in cardiology.

Rates of revascularization and PCI:CABG ratio: a new indicator predicting in-hospital mortality in acute coronary syndromes

L. Klein, H. Daoud, A. Abugroun, 2021, Coronary artery disease.

Infective endocarditis and brain abscess secondary to Aggregatibacter aphrophilus

H. Daoud, A. Abugroun, O. Olanipekun, 2019, IDCases.

Detailed Biochemical and Bioenergetic Characterization of FBXL4-Related Encephalomyopathic Mitochondrial DNA Depletion.

M. Holcik, P. Chakraborty, J. Brophy, 2015, JIMD reports.

De Novo Balanced Translocation t (7;16) (p22.1; p11.2) Associated with Autistic Disorder

H. Daoud, H. Chaabouni, R. Zemni, 2008, Journal of biomedicine & biotechnology.

De Novo SYNGAP1 Mutations in Nonsyndromic Intellectual Disability and Autism

J. Lacaille, J. Milunsky, M. Krebs, 2011, Biological Psychiatry.

ATXN2 trinucleotide repeat length correlates with risk of ALS

Ashley R. Jones, J. Hardy, Yi-Chung Lee, 2017, Neurobiology of Aging.

Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.

J. Bouchard, Andrew W. Folkmann, G. Rouleau, 2015, Human molecular genetics.

Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis

V. Meininger, G. Rouleau, W. Camu, 2008, Journal of Medical Genetics.

Genetics of motor neuron disorders: new insights into pathogenic mechanisms

G. Rouleau, P. Dion, H. Daoud, 2009, Nature Reviews Genetics.

Adopting High-Resolution Allele Frequencies Substantially Expedites Variant Interpretation in Genetic Diagnostic Laboratories.

M. Ghani, J. McGowan-Jordan, H. Daoud, 2019, The Journal of molecular diagnostics : JMD.

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia

Robert H. Brown, R. Petersen, B. Boeve, 2016, Nature Communications.

A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population

M. Palkovits, P. Vourc'h, C. Andres, 2015, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis.

G. Rouleau, D. Spiegelman, É. Henrion, 2011, Archives of neurology.

Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR)

Nasim Vasli, Matthew S. Lebo, Matthew S Lebo, 2017, Genetics in Medicine.

Giant right atrium: a long-term complication of rheumatic heart disease

H. Daoud, Walid Ibrahim, M. Taha, 2020, Oxford medical case reports.

Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients.

Guy A Rouleau, Ute Woehlbier, Robert H. Brown, 2015, Gene.

Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation

A. Rötig, P. Vourc'h, C. Andres, 2008, Human Genetics.

Genetic linkage analysis of schizophrenia using chromosome 11q13-24 markers in Israeli pedigrees.

R. Ebstein, B. Lerer, S. Whatley, 1995, American journal of medical genetics.

Exploring the 7p22.1 Chromosome as a Candidate Region for Autism

H. Daoud, H. Chaabouni, S. Briault, 2010, Journal of biomedicine & biotechnology.

Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia.

G. Rouleau, A. Dionne‐Laporte, G. Patrinos, 2015, European journal of medical genetics.

The Creatine Transporter Gene Paralogous at 16p11.2 Is Expressed in Human Brain

H. Daoud, H. Chaabouni, R. Zemni, 2008, Comparative and functional genomics.

Exome sequencing reveals SPG11 mutations causing juvenile ALS

G. Rouleau, A. Dionne‐Laporte, P. Dion, 2012, Neurobiology of Aging.

A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories

C. van Broeckhoven, C. Shaw, P. Andersen, 2014, Journal of Medical Genetics.

No TARDBP mutations in a French Canadian population of patients with Parkinson disease.

G. Rouleau, J. Rivière, P. Dion, 2009, Archives of neurology.

Identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delay

Hwanho Choi, Michael A McDonough, Christopher J Schofield, 2015, Journal of Medical Genetics.

Spontaneous Celiac Artery Dissection Presenting With Splenic Infarction: A Case Report

H. Daoud, A. Natarajan, Habeeb Khalaf, 2018, Gastroenterology research.

Analysis of the UNC13A gene as a risk factor for sporadic amyotrophic lateral sclerosis.

G. Rouleau, W. Camu, P. Dion, 2010, Archives of neurology.

Reinterpretation of sequence variants: one diagnostic laboratory’s experience, and the need for standard guidelines

Caitlin Chisholm, Hussein Daoud, Mahdi Ghani, 2017, Genetics in Medicine.

CORONARY ARTERY DISEASE RISK FACTOR ANALYSIS IN AN AGE-STRATIFIED HOSPITAL POPULATION WITH SYSTEMIC LUPUS ERYTHEMATOSUS

H. Daoud, D. Levinson, Manar M. Elhassan, 2020 .

Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.

J. Bouchard, Andrew W. Folkmann, G. Rouleau, 2015, Human Molecular Genetics.

A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population

M. Palkovits, P. Vourc'h, C. Andres, 2015, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration.

Mutations in FUS cause FALS and SALS in French and French Canadian populations

V. Meininger, F. Salachas, J. Bouchard, 2009, Neurology.

Analysis of the UNC13A gene as a risk factor for sporadic amyotrophic lateral sclerosis.

G. Rouleau, W. Camu, P. Dion, 2010, Archives of neurology.

Analysis of DPP6 and FGGY as candidate genes for amyotrophic lateral sclerosis

G. Rouleau, P. Dion, H. Daoud, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Association of long ATXN2 CAG repeat sizes with increased risk of amyotrophic lateral sclerosis.

V. Meininger, G. Rouleau, W. Camu, 2011, Archives of neurology.

A role for ubiquilin 2 mutations in neurodegeneration.

G. Rouleau, H. Daoud, 2011, Nature reviews. Neurology.

Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis.

G. Rouleau, D. Spiegelman, W. Camu, 2011, Archives of neurology.

Impact of Center Procedural Volume on Mortality and Readmission Rates Following Pericardiectomy in the United States.

H. Daoud, R. Walters, Venkata S. Pajjuru, 2023, The American journal of cardiology.

No effect on SOD1 splicing by TARDP or FUS mutations.

G. Rouleau, P. Dion, V. Belzil, 2011, Archives of neurology.