Leila Kushan (L Kushan)

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 31

Top Venues

Nature communications

Research square

bioRxiv : the preprint server for biology

Molecular psychiatry

David Geffen School of Medicine at UCLA

Universiteit Utrecht (MSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

David Geffen School of Medicine at UCLA

United States

Project Manager :: Semel Institute for Neuroscience and Human Behavior

Education History

Universiteit Utrecht

Netherlands

MSC :: Neuroscience and Cognition

University of California Los Angeles

United States

BSC :: Neuroscience

Publications

Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Author Correction: Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Filomena Grazia Alvino, S Gini, A Minetti, Marco Pagani, D Sastre-Yagüe, Noemi Barsotti, A Elizabeth de Guzman, Charles H Schleifer, Alexia Stuefer, Leila Kushan, Caterina Montani, Alberto Galbusera, Francesco Papaleo, Michael V Lombardo, M Pasqualetti, Carrie E Bearden, Alessandro Gozzi
Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndrome. bioRxiv : the preprint server for biology (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Filomena Grazia Alvino, S Gini, A Minetti, Marco Pagani, D Sastre-Yagüe, Noemi Barsotti, A Elizabeth de Guzman, Charles H Schleifer, Alexia Stuefer, Leila Kushan, Caterina Montani, Alberto Galbusera, Francesco Papaleo, Michael V Lombardo, Massimo Pasqualetti, Carrie E Bearden, Alessandro Gozzi
Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndrome. bioRxiv : the preprint server for biology (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Filomena Grazia Alvino, S Gini, A Minetti, Marco Pagani, D Sastre-Yagüe, Noemi Barsotti, A Elizabeth de Guzman, Charles H Schleifer, Alexia Stuefer, Leila Kushan, Caterina Montani, Alberto Galbusera, Francesco Papaleo, Michael V Lombardo, Massimo Pasqualetti, Carrie E Bearden, Alessandro Gozzi
Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndrome. bioRxiv : the preprint server for biology (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Filomena Grazia Alvino, S Gini, A Minetti, Marco Pagani, D Sastre-Yagüe, Noemi Barsotti, A Elizabeth de Guzman, Charles H Schleifer, Alexia Stuefer, Leila Kushan, Caterina Montani, Alberto Galbusera, Francesco Papaleo, Michael V Lombardo, Massimo Pasqualetti, Carrie E Bearden, Alessandro Gozzi
Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndrome. bioRxiv : the preprint server for biology (2024)
Filomena Grazia Alvino, S Gini, A Minetti, Marco Pagani, D Sastre-Yagüe, Noemi Barsotti, A Elizabeth de Guzman, Charles H Schleifer, Alexia Stuefer, Leila Kushan, Caterina Montani, Alberto Galbusera, Francesco Papaleo, Michael V Lombardo, Massimo Pasqualetti, Carrie E Bearden, Alessandro Gozzi
Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndrome. bioRxiv : the preprint server for biology (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Kaustubh Supekar, Carlo de Los Angeles, Srikanth Ryali, Leila Kushan, Charles H Schleifer, Gabriela Repetto, Nicolas A Crossley, Tony Simon, Carrie E Bearden, Vinod Menon
Robust and replicable functional brain signatures of 22q11.2 deletion syndrome and associated psychosis: a deep neural network-based multi-cohort study. Molecular psychiatry (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Author Correction: Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert Zatorre, Sebastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. bioRxiv : the preprint server for biology (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Jasmine Modasi, Vahe Khachadourian, Kathleen O'Hora, Leila Kushan, Theodore F Robles, Grant S Shields, Eva Velthorst, Carrie E Bearden
Associations between acute and chronic lifetime stressors and psychosis-risk symptoms in individuals with 22q11.2 copy number variants. Psychological medicine (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Jakub Kopal, Kuldeep Kumar, Karin Saltoun, Claudia Modenato, Clara A Moreau, Sandra Martin-Brevet, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Petra Tamer, Elise Douard, Anne M Maillard, Borja Rodríguez-Herreros, Aurèlie Pain, Sonia Richetin, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida E Sønderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Sébastien Jacquemont, Danilo Bzdok
Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence. Nature human behaviour (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Maria Jalbrzikowski, Amy Lin, Ariana Vajdi, Vardui Grigoryan, Leila Kushan, Christopher R K Ching, Charles Schleifer, Rebecca A Hayes, Stephanie A Chu, Catherine A Sugar, Jennifer K Forsyth, Carrie E Bearden
Longitudinal trajectories of cortical development in 22q11.2 copy number variants and typically developing controls. Molecular psychiatry 27 (10) (2022)
Elisabeth Neuhaus, Elke Hattingen, Stella Blasel, Eike Steidl, N Polomac, Felix Rosenow, Theodor Ruber, Eva Herrmann, C Ecker, Leila Kushan, Amy Lin, A Vajdi, Carrie E Bearden, Alina Jurcoane
Heterotopia in Individuals with 22q11.2 Deletion Syndrome. AJNR. American journal of neuroradiology 42 (11) (2021)
Clara A Moreau, Sebastian G W Urchs, Kuldeep Kumar, Pierre Orban, Catherine Schramm, Guillaume Dumas, Aurélie Labbe, Guillaume Huguet, Elise Douard, Pierre-Olivier Quirion, Amy Lin, Leila Kushan, Stephanie Grot, David Luck, Adrianna Mendrek, Stephane Potvin, Emmanuel Stip, Thomas Bourgeron, Alan C Evans, Carrie E Bearden, Pierre Bellec, Sebastien Jacquemont
Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia. Nature communications 11 (1) (2020)

Leila Kushan.css-eqlu8i{font-size:small;padding-left:4px;} (L Kushan)

Publication Activity (10 Years)

Top Topics

Top Venues

Leila Kushan (L Kushan)