Author details

Full Name

Ahmed Bouhouche

Affiliation

Medical School and Pharmacy, University Mohammed V in Rabat

ORCID

Career Start Year

1993

Papers

H Index

Expertise

CM4AI Collaborator

Trey Ideker (CM4AI)

PMID	Paper Title	Journal Title	Published Year
37256495	Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients.	J Mol Neurosci	2023
35281597	Novel <i>ITGB2</i> Mutation Is Responsible for a Severe Form of Leucocyte Adhesion Deficiency Type 1.	Biomed Res Int	2022
32557143	Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease.	J Mol Neurosci	2021
34133966	Identification of the novel SDR42E1 gene that affects steroid biosynthesis associated with the oculocutaneous genital syndrome.	Exp Eye Res	2021
32131761	Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report.	BMC Med Genet	2020
33343949	A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia.	Case Rep Genet	2020
33045815	Characterization of Recessive Parkinson Disease in a Large Multicenter Study.	Ann Neurol	2020
29525037	Association of vitamin D status with multiple sclerosis in a case-control study from Morocco.	Rev Neurol (Paris)	2018
30108543	Deep Brain Stimulation in Moroccan Patients With Parkinson's Disease: The Experience of Neurology Department of Rabat.	Front Neurol	2018
30581635	Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing.	Case Rep Genet	2018
29670566	Non-Motor Symptoms of Parkinson's Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients.	Front Neurol	2018
28723952	Evidence for prehistoric origins of the G2019S mutation in the North African Berber population.	PLoS One	2017
28465860	<i>LRRK2</i> G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's Disease.	Parkinsons Dis	2017
29163333	Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel.	Front Neurol	2017
27153400	Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.	Am J Hum Genet	2016
27508872	Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents.	Cell Metab	2016
27413743	A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism.	Biomed Res Int	2016
27259058	Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.	Am J Hum Genet	2016
26958025	Clinical and genetic data of Huntington disease in Moroccan patients.	Afr Health Sci	2015
24482476	Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.	Science	2014
24319291	KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction.	J Med Genet	2014
23180398	CLN6 p.I154del mutation causing late infantile neuronal ceroid lipofuscinosis in a large consanguineous Moroccan family.	Indian J Pediatr	2013
23993422	[Juvenile Huntington disease: A case study].	Arch Pediatr	2013
23712319	Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan family.	Eur J Med Genet	2013
22436252	An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3.	BMC Med Genet	2012
23176821	Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.	Am J Hum Genet	2012
18758830	A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22.	Neurogenetics	2009
17503452	Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description.	Am J Med Genet B Neuropsychiatr Genet	2007
18062449	A novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families.	Can J Neurol Sci	2007
17347251	Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.	Brain	2007
17273843	A novel locus for autosomal recessive spastic ataxia on chromosome 17p.	Hum Genet	2007
16333315	Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1.	Eur J Hum Genet	2006
16775368	Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease.	Neuromolecular Med	2006
16924012	Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations.	Neurology	2006
16399879	Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia.	J Med Genet	2006
15786464	Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).	Ann Neurol	2005
12687498	Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma.	Am J Hum Genet	2003
14586604	High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients.	J Neurol	2003
12039660	Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families.	J Neurol Sci	2002
10602360	Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1.	Eur J Hum Genet	1999
29086979	The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33.	Ann N Y Acad Sci	1999
29086961	The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33.	Ann N Y Acad Sci	1999
10441578	A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.	Am J Hum Genet	1999
10586271	The autosomal recessive form of CMT disease linked to 5q31-q33.	Ann N Y Acad Sci	1999
10586230	The autosomal recessive form of CMT disease linked to 5q31-q33.	Ann N Y Acad Sci	1999
9221057	[The role of quinine chlorhydrate in the conditioned inhibition of the tarsal reflex in Drosophila melanogaster].	Can J Exp Psychol	1995
8126596	Immunocytochemical and learning studies of a Drosophila melanogaster neurological mutant, no-bridgeKS49 as an approach to the possible role of the central complex.	J Neurogenet	1993

1 - 47 of 47

Abdoulaye Yalcouy??

University of Cape Town

Career Start Year 2017

Number of shared co-authors 0

James M Polke

National Hospital for Neurology and Neurosurgery

Career Start Year 2005

Number of shared co-authors 4

Saskia Biskup

Center for Genomics and Transcriptomics (CeGaT)

Career Start Year 2004

Number of shared co-authors 8

Jana Vandrovcova

UCL Queen Square Institute of Neurology

Career Start Year 2004

Number of shared co-authors 6

Fowzan S Alkuraya

King Faisal Specialist Hospital and Research Center

Career Start Year 2001

Number of shared co-authors 18

Francesca Mari

Institute de Pathologie et de Genetique ASBL

Career Start Year 2000

Number of shared co-authors 2

Wojciech Wiszniewski

Oregon Health & Sciences University

Career Start Year 1998

Number of shared co-authors 4

Kym M Boycott

Children's Hospital of Eastern Ontario

Career Start Year 1996

Number of shared co-authors 11

Enza Maria Valente

University of Pavia

Career Start Year 1996

Number of shared co-authors 28

Andrea H N??meth

University of Oxford

Career Start Year 1993

Number of shared co-authors 10

Franco Stanzial

Genetic Counseling Service - Regional Hospital of Bolzano

Career Start Year 1993

Number of shared co-authors 14

Rafa?? P??oski

Medical University of Warsaw

Career Start Year 1992

Number of shared co-authors 5

Peter Hedera

University of Louisville

Career Start Year 1992

Number of shared co-authors 1

Patrizia Rizzu

German Center for Neurodegenerative Diseases

Career Start Year 1991

Number of shared co-authors 5

Henry Houlden

Institute of Neurology, University College London (UCL)

Career Start Year 1991

Number of shared co-authors 23

Isabella Moroni

Fondazione IRCCS Istituto Neurologico Carlo Besta

Career Start Year 1990

Number of shared co-authors 17

Irma J??rvel??

University of Helsinki

Career Start Year 1989

Number of shared co-authors 0

Andrea Haworth

UCL Queen Square Institute of Neurology

Career Start Year 1989

Number of shared co-authors 0

Nicholas W Wood

UCL Queen Square Institute of Neurology

Career Start Year 1988

Number of shared co-authors 9

Peter Heutink

German Center for Neurodegenerative Diseases (DZNE).

Career Start Year 1988

Number of shared co-authors 6

Lefkos T Middleton

Ageing Epidemiology Research Unit, School of Public Health, Imperial College London

Career Start Year 1988

Number of shared co-authors 3

Dong-Hui Chen

University of Washington School of Medicine

Career Start Year 1988

Number of shared co-authors 0

Han G Brunner

Maastricht University Medical Centre

Career Start Year 1987

Number of shared co-authors 9

Hubert J M Smeets

Maastricht University Medical Centre+

Career Start Year 1987

Number of shared co-authors 1

Alessandra Renieri

University of Siena

Career Start Year 1984

Number of shared co-authors 4

Xavier Estivill

Sidra Medical Center

Career Start Year 1983

Number of shared co-authors 3

Irenaeus F M de Coo

Unit Clinical Genomics, Maastricht University

Career Start Year 1982

Number of shared co-authors 0

Thomas Meitinger

Technical University of Munich, Institute of Human Genetics

Career Start Year 1982

Number of shared co-authors 11

Enrico Bertini

IRCCS Bambino Gesu Children's Research Hospital

Career Start Year 1978

Number of shared co-authors 23

Thomas D Bird

University of Washington School of Medicine

Career Start Year 1965

Number of shared co-authors 7

row(s) 1 - 30 of 30

Ali Benomar

Medical School and Pharmacy, University Mohammed V in Rabat

Co-authored papers 28

Naima Bouslam

Specialties Hospital

Co-authored papers 25

Alexis Brice

Sorbonne University, Paris Brain Institute - ICM, Inserm, CNRS

Co-authored papers 18

Alexandra Durr

Sorbonne University, Paris Brain Institute - ICM, Inserm, CNRS

Co-authored papers 6

Giovanni Stevanin

Sorbonne University, Paris Brain Institute - ICM, Inserm, CNRS

Co-authored papers 6

Sylvain Hanein

Institute of Genetic Diseases, INSERM UMR1163, Imagine and Paris Descartes University

Co-authored papers 3

Sylvie Forlani

ICM DNA and Cell Bank CNRS UMR7225, INSERM U1127, Sorbonne University

Co-authored papers 2

Laure Raymond

Sorbonne Universite, Institut du Cerveau-Paris Brain Institute-ICM, Inserm, CNRS

Co-authored papers 2

Maha S Zaki

Human Genetics and Genome Research Institute, National Research Centre

Co-authored papers 2

Guy A Rouleau

McGill University, Canada Montreal Neurological Institute and Hospital

Co-authored papers 2

Joseph G Gleeson

University of California

Co-authored papers 2

Ahmet Okay Caglayan

Yale School of Medicine

Co-authored papers 1

YoSon Park

University of Pennsylvania - Perelman School of Medicine

Co-authored papers 1

Faezeh Mojahedi

Blood Borne Infections Research Center, Academic Center for Education

Co-authored papers 1

Emily G Spencer

Scripps Research Translational Institute

Co-authored papers 1

Ghada M H Abdel-Salam

Human Genetics and Genome Research Institute, National Research Centre

Co-authored papers 1

Andrew B Singleton

National Institute on Aging

Co-authored papers 1

Sekar Kathiresan

Co-authored papers 1

Asl??han Tolun

Istanbul Technical University

Co-authored papers 1

Andrew C Edmondson

Co-authored papers 1

Stacey Gabriel

Broad Institute of MIT and Harvard

Co-authored papers 1

Daniel J Rader

Co-authored papers 1

Massimo Mascaro

Howard Hughes Medical Institute, University of California

Co-authored papers 1

Jumana Y Al-Aama

King AbdulAziz University

Co-authored papers 1

Mostafa Abdellateef

Center for Brain Development, University of California

Co-authored papers 1

Laila Selim

Cairo University

Co-authored papers 1

H??lya Kayserili

Istanbul University

Co-authored papers 1

Bita Bozorgmehri

Co-authored papers 1

Alice A Koh

Howard Hughes Medical Institute, University of California

Co-authored papers 1

Naiara Akizu

University of Pennsylvania

Co-authored papers 1

1 - 30

Author Details

Column Actions

Recommended Authors

Collaborators