Mohamad Saad

发表

GIGI-Quick: a fast approach to impute missing genotypes in genome-wide association family data

Ehsan Ullah, Alejandro Q. Nato, Ellen M. Wijsman, 2018, Bioinform..

Association score testing for rare variants and binary traits in family data with shared controls

Ellen M. Wijsman, Mohamad Saad, E. Wijsman, 2019, Briefings Bioinform..

Nonlinear control of a one flexible link in the vertical plane

Mohamad Saad, M. Saad, 2007, 2007 IEEE International Conference on Systems, Man and Cybernetics.

State-feedback and Linear Quadratic regulator applied to a single-link flexible manipulator

Mohamad Saad, Walid Ghie, Mariam Baroudi, 2009, 2009 IEEE International Conference on Robotics and Biomimetics (ROBIO).

Modal analysis of assumed-mode models of a flexible slewing beam

Ouassima Akhrif, Mohamad Saad, Lahcen Saydy, 2006, Int. J. Model. Identif. Control..

Robust noncollocated passive models of a flexible link with uncertain payload and joint inertia

Ouassima Akhrif, Lahcen Saydy, Mohamad Saad, 2000, ICECS 2000. 7th IEEE International Conference on Electronics, Circuits and Systems (Cat. No.00EX445).

Application of robust design of a PI controller using guardian maps

Azeddine Kaddouri, Mohamad Saad, Patrick Jodouin, 2009, 2009 Canadian Conference on Electrical and Computer Engineering.

Modélisation et commande d'un robot flexible

Ouassima Akhrif, Lahcen Saydy, Mohamad Saad, 1994 .

KinVis: a visualization tool to detect cryptic relatedness in genetic datasets

Ehsan Ullah, Michaël Aupetit, Arun Das, 2018, Bioinform..

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinsons disease (vol 22, pg 1696, 2013)

Mohamad Saad, Nicholas W. Wood, Gibbs, 2013 .

GIGI2: A Fast Approach for Parallel Genotype Imputation in Large Pedigrees

Ehsan Ullah, Ellen M. Wijsman, Khalid Kunji, 2019, bioRxiv.

Single-marker and multi-marker mixed models for polygenic score analysis in family-based data

Mohamad Saad, Andrés Legarra, Nora Bohossian, 2014, BMC Proceedings.

Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis

Erika Salvi, Mohamad Saad, Eric Hachulla, 2011, PLoS genetics.

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

Mohamad Saad, Nicholas W Wood, Manu Sharma, 2011, The Lancet.

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

Nicholas Eriksson, Margaret Sutherland, Mohamad Saad, 2015, Neurobiology of Aging.

Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

Jean-François Dartigues, Günther Deuschl, Yoav Ben-Shlomo, 2017, Genome Biology.

Genetic comorbidities in Parkinson's disease.

Mohamad Saad, Anette Schrag, Thomas Gasser, 2014, Human molecular genetics.

Whole genome sequencing of Caribbean Hispanic families with late‐onset Alzheimer's disease

James Jaworski, Mohamad Saad, Eric Boerwinkle, 2018, Annals of clinical and translational neurology.

Use of support vector machines for disease risk prediction in genome‐wide association studies: Concerns and opportunities

Andreas Zell, Andreas Jahn, Mohamad Saad, 2012, Human mutation.

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.

Mohamad Saad, Peter Holmans, Nicholas W Wood, 2013, Human molecular genetics.

Power of Family‐Based Association Designs to Detect Rare Variants in Large Pedigrees Using Imputed Genotypes

Mohamad Saad, Ellen M Wijsman, E. Wijsman, 2014, Genetic epidemiology.

Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.

Mohamad Saad, Alexandra Durr, Christophe Tzourio, 2011, Human molecular genetics.