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Alexandre Dionne‐Laporte

Observed names: A Dionne‐Laporte, Alexandre DIonne-Laporte, Alexandre Dionne-Laporte, Dionne Laporte, Alexandre, Dionne-Laporte, Alexandre
Institution: McGill University
Observed institutions: University of Hawaiʻi at Mānoa, Montreal Neurological Institute and Hospital, University of Hawaii System, Centre Hospitalier de l’Université de Montréal, CHU Sainte-Justine Research Center, McGill University Research Centre for Studies in Aging, McGill University, Université de Montréal
OpenAlex ID: A5112311925
The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus)
2008 · Ray Ming, Shaobin Hou, et al. · Nature · 1,109
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Increased exonic de novo mutation rate in individuals with schizophrenia
2011 · Simon L Girard, Julie Gauthier, et al. · Nature Genetics · 445
De Novo Mutations in Moderate or Severe Intellectual Disability
2014 · Fadi F. Hamdan, Myriam Srour, et al. · PLoS Genetics · 429
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Draft genome sequence of the rubber tree Hevea brasiliensis
2013 · Ahmad Yamin Abdul Rahman, Abhilash O Usharraj, et al. · BMC Genomics · 283
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Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy
2014 · Kristopher T Kahle, Nancy D Merner, et al. · EMBO Reports · 201
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Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor
2012 · Nancy D. Merner, Simon L. Girard, et al. · The American Journal of Human Genetics · 190
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Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia
2013 · Amir Boukhris, Rebecca Schule, et al. · The American Journal of Human Genetics · 188
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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
2016 · Ziv Gan-Or, Naima Bouslam, et al. · The American Journal of Human Genetics · 123
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Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia
2015 · Marie Coutelier, Cyril Goizet, et al. · Brain · 114
Exome sequencing reveals SPG11 mutations causing juvenile ALS
2011 · Hussein Daoud, Sirui Zhou, et al. · Neurobiology of Aging · 110
SMPD1 mutations, activity, and α‐synuclein accumulation in Parkinson's disease
2019 · Roy N. Alcalay, Victoria Mallett, et al. · Movement Disorders · 108
Loss of Association of REEP2 with Membranes Leads to Hereditary Spastic Paraplegia
2014 · Typhaine Esteves, Alexandra Durr, et al. · The American Journal of Human Genetics · 107
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De novo variants in sporadic cases of childhood onset schizophrenia
2015 · Amirthagowri Ambalavanan, Simon L Girard, et al. · European Journal of Human Genetics · 98
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Loss-of-function de novo mutations play an important role in severe human neural tube defects
2015 · Philippe Lemay, Marie-Claude Guyot, et al. · Journal of Medical Genetics · 76
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Joubert Syndrome in French Canadians and Identification of Mutations in CEP104
2015 · Myriam Srour, Fadi F. Hamdan, et al. · The American Journal of Human Genetics · 73
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RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population
2016 · Sirui Zhou, Amirthagowri Ambalavanan, et al. · The American Journal of Human Genetics · 72
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Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis
2015 · Claire S. Leblond, Ziv Gan-Or, et al. · Neurobiology of Aging · 70
De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Callosum, Axon, Cardiac, Ocular, and Genital Defects
2019 · Andrea Accogli, Sara Calabretta, et al. · The American Journal of Human Genetics · 58
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Global characterization of copy number variants in epilepsy patients from whole genome sequencing
2018 · Jean Monlong, Simon L. Girard, et al. · PLoS Genetics · 56
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Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia
2018 · Boris Chaumette, Vladimir Ferrafiat, et al. · Molecular Psychiatry · 53
Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease
2016 · Jay P. Ross, Nicolas Dupre, et al. · Neurobiology of Aging · 48
Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma
2017 · Barbara Rivera, Massimo Di Iorio, et al. · Cancer Research · 43
Rare deleterious variants in GRHL3 are associated with human spina bifida
2017 · Philippe Lemay, Patrizia De Marco, et al. · Human Mutation · 37
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Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum
2015 · Loubna Jouan, Bouchra Ouled Amar Bencheikh, et al. · European Journal of Human Genetics · 34
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Whole exome sequencing identifies novel predisposing genes in neural tube defects
2018 · Philippe Lemay, Patrizia De Marco, et al. · Molecular Genetics & Genomic Medicine · 31
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Works count: 68
Citation count: 4,581
H-index: 26
I10-index: 47
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