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You searched for +publisher:"McGill University" +contributor:("Guy Rouleau"). Showing records 1 – 6 of 6 total matches.

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McGill University

1. Dona, Michèle. Protein interactions in hereditary spastic paraplegia's molecular mechanism.

Degree: MS, Department of Medicine, 2017, McGill University

Hereditary spastic paraplegias (HSP) is a group of genetic disorder that cause progressive and generally severe lower extremity spasticity and weakness. These symptoms are usually… (more)

Subjects/Keywords: Medicine

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APA (6th Edition):

Dona, M. (2017). Protein interactions in hereditary spastic paraplegia's molecular mechanism. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile145602.pdf

Chicago Manual of Style (16th Edition):

Dona, Michèle. “Protein interactions in hereditary spastic paraplegia's molecular mechanism.” 2017. Masters Thesis, McGill University. Accessed June 25, 2019. http://digitool.library.mcgill.ca/thesisfile145602.pdf.

MLA Handbook (7th Edition):

Dona, Michèle. “Protein interactions in hereditary spastic paraplegia's molecular mechanism.” 2017. Web. 25 Jun 2019.

Vancouver:

Dona M. Protein interactions in hereditary spastic paraplegia's molecular mechanism. [Internet] [Masters thesis]. McGill University; 2017. [cited 2019 Jun 25]. Available from: http://digitool.library.mcgill.ca/thesisfile145602.pdf.

Council of Science Editors:

Dona M. Protein interactions in hereditary spastic paraplegia's molecular mechanism. [Masters Thesis]. McGill University; 2017. Available from: http://digitool.library.mcgill.ca/thesisfile145602.pdf


McGill University

2. Ambalavanan, Amirthagowri. Genetic risk factors of childhood onset schizophrenia.

Degree: PhD, Department of Human Genetics, 2017, McGill University

Schizophrenia is a severe psychiatric disorder that affects approximately 1% of the general population. Childhood Onset Schizophrenia (COS) is a rare form of schizophrenia diagnosed… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Ambalavanan, A. (2017). Genetic risk factors of childhood onset schizophrenia. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile146920.pdf

Chicago Manual of Style (16th Edition):

Ambalavanan, Amirthagowri. “Genetic risk factors of childhood onset schizophrenia.” 2017. Doctoral Dissertation, McGill University. Accessed June 25, 2019. http://digitool.library.mcgill.ca/thesisfile146920.pdf.

MLA Handbook (7th Edition):

Ambalavanan, Amirthagowri. “Genetic risk factors of childhood onset schizophrenia.” 2017. Web. 25 Jun 2019.

Vancouver:

Ambalavanan A. Genetic risk factors of childhood onset schizophrenia. [Internet] [Doctoral dissertation]. McGill University; 2017. [cited 2019 Jun 25]. Available from: http://digitool.library.mcgill.ca/thesisfile146920.pdf.

Council of Science Editors:

Ambalavanan A. Genetic risk factors of childhood onset schizophrenia. [Doctoral Dissertation]. McGill University; 2017. Available from: http://digitool.library.mcgill.ca/thesisfile146920.pdf


McGill University

3. Mohtashami, Sadaf. Expression and proteomic analysis of KlFlA/25B in hereditary sensory and autonomic neuropathies type ll.

Degree: MS, Department of Medicine, 2017, McGill University

Hereditary sensory and autonomic neuropathies (HSANs) form a group of rare disorders that are characterized by variable sensory and autonomic dysfunctions. HSAN type II (HSAN-II)… (more)

Subjects/Keywords: Medicine

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APA (6th Edition):

Mohtashami, S. (2017). Expression and proteomic analysis of KlFlA/25B in hereditary sensory and autonomic neuropathies type ll. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile148602.pdf

Chicago Manual of Style (16th Edition):

Mohtashami, Sadaf. “Expression and proteomic analysis of KlFlA/25B in hereditary sensory and autonomic neuropathies type ll.” 2017. Masters Thesis, McGill University. Accessed June 25, 2019. http://digitool.library.mcgill.ca/thesisfile148602.pdf.

MLA Handbook (7th Edition):

Mohtashami, Sadaf. “Expression and proteomic analysis of KlFlA/25B in hereditary sensory and autonomic neuropathies type ll.” 2017. Web. 25 Jun 2019.

Vancouver:

Mohtashami S. Expression and proteomic analysis of KlFlA/25B in hereditary sensory and autonomic neuropathies type ll. [Internet] [Masters thesis]. McGill University; 2017. [cited 2019 Jun 25]. Available from: http://digitool.library.mcgill.ca/thesisfile148602.pdf.

Council of Science Editors:

Mohtashami S. Expression and proteomic analysis of KlFlA/25B in hereditary sensory and autonomic neuropathies type ll. [Masters Thesis]. McGill University; 2017. Available from: http://digitool.library.mcgill.ca/thesisfile148602.pdf


McGill University

4. Quoibion, Amélie. m6A RNA methylation and TARDBP, a gene implicated in amyotrophic lateral sclerosis.

Degree: MS, Department of Human Genetics, 2017, McGill University

N6-methyladenosine (m6A) is a reversible epigenetic post-transcriptional modification of RNA. The addition of methyl groups on adenosine implicates a N6-adenosine-methyltransferase complex constituted of two methyltransferase-like… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Quoibion, A. (2017). m6A RNA methylation and TARDBP, a gene implicated in amyotrophic lateral sclerosis. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile148652.pdf

Chicago Manual of Style (16th Edition):

Quoibion, Amélie. “m6A RNA methylation and TARDBP, a gene implicated in amyotrophic lateral sclerosis.” 2017. Masters Thesis, McGill University. Accessed June 25, 2019. http://digitool.library.mcgill.ca/thesisfile148652.pdf.

MLA Handbook (7th Edition):

Quoibion, Amélie. “m6A RNA methylation and TARDBP, a gene implicated in amyotrophic lateral sclerosis.” 2017. Web. 25 Jun 2019.

Vancouver:

Quoibion A. m6A RNA methylation and TARDBP, a gene implicated in amyotrophic lateral sclerosis. [Internet] [Masters thesis]. McGill University; 2017. [cited 2019 Jun 25]. Available from: http://digitool.library.mcgill.ca/thesisfile148652.pdf.

Council of Science Editors:

Quoibion A. m6A RNA methylation and TARDBP, a gene implicated in amyotrophic lateral sclerosis. [Masters Thesis]. McGill University; 2017. Available from: http://digitool.library.mcgill.ca/thesisfile148652.pdf

5. Cruceanu, Cristiana. Investigation of genetic and molecular susceptibility factors for bipolar disorder.

Degree: PhD, Department of Human Genetics, 2016, McGill University

Bipolar disorder (BD) is a psychiatric condition characterized by at least two episodes of clinically significantly disturbed mood, energy, and activity. Given its debilitating nature,… (more)

Subjects/Keywords: Human Genetics

…Turecki1# 1 McGill Group for Suicide Studies, Douglas Hospital, McGill University, Montreal… …studies described here were performed under the co-supervision of Drs. Gustavo Turecki and Guy… …Rouleau. Chapter 1 contains a review of the literature covering topics such as the… 

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APA (6th Edition):

Cruceanu, C. (2016). Investigation of genetic and molecular susceptibility factors for bipolar disorder. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile143584.pdf

Chicago Manual of Style (16th Edition):

Cruceanu, Cristiana. “Investigation of genetic and molecular susceptibility factors for bipolar disorder.” 2016. Doctoral Dissertation, McGill University. Accessed June 25, 2019. http://digitool.library.mcgill.ca/thesisfile143584.pdf.

MLA Handbook (7th Edition):

Cruceanu, Cristiana. “Investigation of genetic and molecular susceptibility factors for bipolar disorder.” 2016. Web. 25 Jun 2019.

Vancouver:

Cruceanu C. Investigation of genetic and molecular susceptibility factors for bipolar disorder. [Internet] [Doctoral dissertation]. McGill University; 2016. [cited 2019 Jun 25]. Available from: http://digitool.library.mcgill.ca/thesisfile143584.pdf.

Council of Science Editors:

Cruceanu C. Investigation of genetic and molecular susceptibility factors for bipolar disorder. [Doctoral Dissertation]. McGill University; 2016. Available from: http://digitool.library.mcgill.ca/thesisfile143584.pdf


McGill University

6. Diaz Anzaldua, Adriana. Genetic investigation of Tourette syndrome in the French Canadian population.

Degree: PhD, Department of Biology, 2004, McGill University

Tourette syndrome (TS) is a childhood-onset neuropsychiatric disorder characterized by multiple motor and one or more phonic tics. TS affects all races and ethnic groups… (more)

Subjects/Keywords: Biology  – Genetics

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Diaz Anzaldua, A. (2004). Genetic investigation of Tourette syndrome in the French Canadian population. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile18194.pdf

Chicago Manual of Style (16th Edition):

Diaz Anzaldua, Adriana. “Genetic investigation of Tourette syndrome in the French Canadian population.” 2004. Doctoral Dissertation, McGill University. Accessed June 25, 2019. http://digitool.library.mcgill.ca/thesisfile18194.pdf.

MLA Handbook (7th Edition):

Diaz Anzaldua, Adriana. “Genetic investigation of Tourette syndrome in the French Canadian population.” 2004. Web. 25 Jun 2019.

Vancouver:

Diaz Anzaldua A. Genetic investigation of Tourette syndrome in the French Canadian population. [Internet] [Doctoral dissertation]. McGill University; 2004. [cited 2019 Jun 25]. Available from: http://digitool.library.mcgill.ca/thesisfile18194.pdf.

Council of Science Editors:

Diaz Anzaldua A. Genetic investigation of Tourette syndrome in the French Canadian population. [Doctoral Dissertation]. McGill University; 2004. Available from: http://digitool.library.mcgill.ca/thesisfile18194.pdf

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