Schleifer, Charles H.; Chang, Sarah E.; Amir, Carolyn M.; O'Hora, Kathleen P.; Fung, Hoki; Kang, Jee Won D.; Kushan-Wells, Leila; Daly, Eileen; Di Fabio, Fabio; Frascarelli, Marianna; Gudbrandsen, Maria; Kates, Wendy R.; Murphy, Declan; Addington, Jean; Anticevic, Alan; Cadenhead, Kristin S.; Cannon, Tyrone D.; Cornblatt, Barbara A.; Keshavan, Matcheri; Mathalon, Daniel H.; Perkins, Diana O.; Stone, William S.; Walker, Elaine; Woods, Scott W.; Uddin, Lucina Q.; Kumar, Kuldeep; Hoftman, Gil D.; Bearden, Carrie E.

Differential inflammatory profiles in carriers of reciprocal 22q11.2 copy number variants

PSYCHONEUROENDOCRINOLOGY

IF3.6

2024-11-011

OAAI

Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications

22 q11.2和16 p11.2缺失和重复的神经认知特征

MOLECULAR PSYCHIATRY

IF10.1

2024-07-240

OAAI

Gur, Ruben C.; Bearden, Carrie E.; Jacquemont, Sebastien; Swillen, Ann; van Amelsvoort, Therese; van den Bree, Marianne; Vorstman, Jacob; Sebat, Jonathan; Ruparel, Kosha; Gallagher, Robert Sean; Mcclellan, Emily; White, Lauren; Crowley, Terrence Blaine; Giunta, Victoria; Kushan, Leila; O'Hora, Kathleen; Verbesselt, Jente; Vandensande, Ans; Vingerhoets, Claudia; van Haelst, Mieke; Hall, Jessica; Harwood, Janet; Chawner, Samuel J. R. A.; Patel, Nishi; Palad, Katrina; Hong, Oanh; Guevara, James; Martin, Charles Olivier; Jizi, Khadije; Belanger, Anne-Marie; Scherer, Stephen W.; Bassett, Anne S.; McDonald-McGinn, Donna M.; Gur, Raquel E.

DISRUPTED NREM SLEEP PHYSIOLOGY LINKED TO 22Q11.2 DELETION SYNDROME

SLEEP

IF4.9

2024-04-200

PRE

Robust and replicable functional brain signatures of 22q11.2 deletion syndrome and associated psychosis: a deep neural network-based multi-cohort study

22 q11.2缺失综合征和相关精神病的强大且可复制的功能性脑特征: 一项基于深度神经网络的多队列研究

MOLECULAR PSYCHIATRY

IF10.1

2024-04-120

PRE

Using rare genetic mutations to revisit structural brain asymmetry (vol 15, 2639, 2024)

使用罕见的基因突变来重新审视结构性大脑不对称 (第15卷，2639，2024)

NATURE COMMUNICATIONS

IF15.7

2024-04-100

OAAI

Kopal, Jakub; Kumar, Kuldeep; Shafighi, Kimia; Saltoun, Karin; Modenato, Claudia; Moreau, Clara A.; Huguet, Guillaume; Jean-Louis, Martineau; Martin, Charles-Olivier; Saci, Zohra; Younis, Nadine; Douard, Elise; Jizi, Khadije; Beauchamp-Chatel, Alexis; Kushan, Leila; Silva, Ana I.; van den Bree, Marianne B. M.; Linden, David E. J.; Owen, Michael J.; Hall, Jeremy; Lippe, Sarah; Draganski, Bogdan; Sonderby, Ida E.; Andreassen, Ole A.; Glahn, David C.; Thompson, Paul M.; Bearden, Carrie E.; Zatorre, Robert; Jacquemont, Sebastien; Bzdok, Danilo

Using rare genetic mutations to revisit structural brain asymmetry

使用罕见的基因突变来重新审视大脑结构的不对称性

NATURE COMMUNICATIONS

IF15.7

2024-03-261

OAAI

Effects of gene dosage and development on subcortical nuclei volumes in individuals with 22q11.2 copy number variations

NEUROPSYCHOPHARMACOLOGY

IF7.1

2024-03-022

OAAI

Longitudinal Development of Thalamocortical Functional Connectivity in 22q11.2 Deletion Syndrome

BIOLOGICAL PSYCHIATRY-COGNITIVE NEUROSCIENCE AND NEUROIMAGING

IF4.8

2024-02-014

OAAI

Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome

基于源的形态计量学揭示了22 q11.2缺失综合征的结构性脑模式异常

HUMAN BRAIN MAPPING

IF3.3

2024-01-124

OAAI

Ge, Ruiyang; Ching, Christopher R. K.; Bassett, Anne S.; Kushan, Leila; Antshel, Kevin M.; van Amelsvoort, Therese; Bakker, Geor; Butcher, Nancy J.; Campbell, Linda E.; Chow, Eva W. C.; Craig, Michael; Crossley, Nicolas A.; Cunningham, Adam; Daly, Eileen; Doherty, Joanne L.; Durdle, Courtney A.; Emanuel, Beverly S.; Fiksinski, Ania; Forsyth, Jennifer K.; Fremont, Wanda; Goodrich-Hunsaker, Naomi J.; Gudbrandsen, Maria; Gur, Raquel E.; Jalbrzikowski, Maria; Kates, Wendy R.; Lin, Amy; Linden, David E. J.; Mccabe, Kathryn L.; McDonald-McGinn, Donna; Moss, Hayley; Murphy, Declan G.; Murphy, Kieran C.; Owen, Michael J.; Villalon-Reina, Julio E.; Repetto, Gabriela M.; Roalf, David R.; Ruparel, Kosha; Schmitt, J. Eric; Schuite-Koops, Sanne; Angkustsiri, Kathleen; Sun, Daqiang; Vajdi, Ariana; van den Bree, Marianne; Vorstman, Jacob; Thompson, Paul M.; Vila-Rodriguez, Fidel; Bearden, Carrie E.

Distinct neurocognitive profiles and clinical phenotypes associated with copy number variation at the 22q11.2 locus

AUTISM RESEARCH

IF5.6

2023-11-233

OAAI

Associations between acute and chronic lifetime stressors and psychosis-risk symptoms in individuals with 22q11.2 copy number variants

PSYCHOLOGICAL MEDICINE

IF5.5

2023-04-201

OAAI

Neurobehavioral risk factors influence prevalence and severity of hazardous substance use in youth at genetic and clinical high risk for psychosis

FRONTIERS IN PSYCHIATRY