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M Maillard

Showing results (111-120 of 140) with videos related to

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Neuroimage|September 9, 2019
Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number VariationsAlonso Cárdenas-de-la-Parra, Sandra Martin-Brevet, Clara Moreau, et al.
Translational Psychiatry|February 14, 2024
Pervasive alterations of intra-axonal volume and network organization in young children with a 16p11.2 deletionAnne M Maillard, David Romascano, Julio E Villalón-Reina, et al.
Genes|January 21, 2023
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease ResearchLauren K White, T Blaine Crowley, Brenda Finucane, et al.
Journal of Intellectual Disability Research : JIDR|February 22, 2022
The COVID-19 pandemic's impact on worry and medical disruptions reported by individuals with chromosome 22q11.2 copy number variants and their caregiversL K White, T B Crowley, B Finucane, et al.
Molecular Psychiatry|November 26, 2014
The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesityA M Maillard, A Ruef, F Pizzagalli, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|October 2, 2010
Fatal Apophysomyces elegans infection transmitted by deceased donor renal allograftsB D Alexander, W A Schell, A M Siston, et al.
Translational Psychiatry|February 5, 2021
The psychiatric phenotypes of 1q21 distal deletion and duplicationStefanie C Linden, Cameron J Watson, Jacqueline Smith, et al.
Translational Psychiatry|July 6, 2021
Correction: The psychiatric phenotypes of 1q21 distal deletion and duplicationStefanie C Linden, Cameron J Watson, Jacqueline Smith, et al.
Translational Psychiatry|March 7, 2019
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
American Journal of Human Genetics|May 5, 2015
A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 PathologyEugenia Migliavacca, Christelle Golzio, Katrin Männik, et al.
Pageof 14

Showing results (111-120 of 140) with videos related to

Sort By:
Pageof 14
Neuroimage|September 9, 2019
Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number VariationsAlonso Cárdenas-de-la-Parra, Sandra Martin-Brevet, Clara Moreau, et al.
Translational Psychiatry|February 14, 2024
Pervasive alterations of intra-axonal volume and network organization in young children with a 16p11.2 deletionAnne M Maillard, David Romascano, Julio E Villalón-Reina, et al.
Genes|January 21, 2023
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease ResearchLauren K White, T Blaine Crowley, Brenda Finucane, et al.
Journal of Intellectual Disability Research : JIDR|February 22, 2022
The COVID-19 pandemic's impact on worry and medical disruptions reported by individuals with chromosome 22q11.2 copy number variants and their caregiversL K White, T B Crowley, B Finucane, et al.
Molecular Psychiatry|November 26, 2014
The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesityA M Maillard, A Ruef, F Pizzagalli, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|October 2, 2010
Fatal Apophysomyces elegans infection transmitted by deceased donor renal allograftsB D Alexander, W A Schell, A M Siston, et al.
Translational Psychiatry|February 5, 2021
The psychiatric phenotypes of 1q21 distal deletion and duplicationStefanie C Linden, Cameron J Watson, Jacqueline Smith, et al.
Translational Psychiatry|July 6, 2021
Correction: The psychiatric phenotypes of 1q21 distal deletion and duplicationStefanie C Linden, Cameron J Watson, Jacqueline Smith, et al.
Translational Psychiatry|March 7, 2019
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
American Journal of Human Genetics|May 5, 2015
A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 PathologyEugenia Migliavacca, Christelle Golzio, Katrin Männik, et al.
Pageof 14