المؤلفون: Moore, Tyler M, Salzer, Deby, Bearden, Carrie E, Calkins, Monica E, Kates, Wendy R, Kushan, Leila, Gallagher, Robert Sean, Frumer, Dafna Sofrin, Weinberger, Ronnie, McDonald-McGinn, Donna M, Gur, Raquel E, Gothelf, Doron

المصدر: Journal of Neurodevelopmental Disorders. 13(1)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Clinical Sciences, Pediatric, Clinical Research, Mental health, Adolescent, Adult, Autism Spectrum Disorder, Child, DiGeorge Syndrome, Female, Humans, Male, Marfan Syndrome, Psychotic Disorders, Reproducibility of Results, Young Adult, Velocardiofacial syndrome, DiGeorge, Subthreshold psychotic symptoms, Structured Interview for Prodromal Syndromes, Scale of Prodromal Symptoms, Inter-rater reliability, Psychosis risk syndrome, Neurosciences, Psychology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/6m66k192
https://escholarship.org/content/qt6m66k192/qt6m66k192.pdf

المؤلفون: Forsyth, Jennifer K, Mennigen, Eva, Lin, Amy, Sun, Daqiang, Vajdi, Ariana, Kushan-Wells, Leila, Ching, Christopher RK, Villalon-Reina, Julio E, Thompson, Paul M, Jonas, Rachel K, Pacheco-Hansen, Laura, Bakker, Geor, van Amelsvoort, Therese, Antshel, Kevin M, Fremont, Wanda, Kates, Wendy R, Campbell, Linda E, McCabe, Kathryn L, Craig, Michael C, Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M, Murphy, Declan G, Murphy, Kieran C, Fiksinski, Ania, Koops, Sanne, Vorstman, Jacob, Crowley, T Blaine, Emanuel, Beverly S, Gur, Raquel E, McDonald-McGinn, Donna M, Roalf, David R, Ruparel, Kosha, Schmitt, J Eric, Zackai, Elaine H, Durdle, Courtney A, Goodrich-Hunsaker, Naomi J, Simon, Tony J, Bassett, Anne S, Butcher, Nancy J, Chow, Eva WC, Vila-Rodriguez, Fidel, Cunningham, Adam, Doherty, Joanne L, Linden, David E, Moss, Hayley, Owen, Michael J, van den Bree, Marianne, Crossley, Nicolas A, Repetto, Gabriela M, Bearden, Carrie E

المصدر: Cerebral Cortex. 31(7)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Neurosciences, Pediatric, Human Genome, Congenital Structural Anomalies, Genetics, Rare Diseases, Biotechnology, Clinical Research, 2.1 Biological and endogenous factors, 22q11 Deletion Syndrome, Brain Cortical Thickness, Case-Control Studies, Cerebral Cortex, DNA Copy Number Variations, Gene Expression Profiling, Gene Expression Regulation, Developmental, Haploinsufficiency, Humans, Magnetic Resonance Imaging, MicroRNAs, Mitochondrial Proteins, RNA-Binding Proteins, Receptors, Purinergic P2, copy number variant, cortical thickness, DGCR8, gene expression, surface area, 22q11.2 ENIGMA Consortium, Psychology, Cognitive Sciences, Experimental Psychology, Biological psychology, Cognitive and computational psychology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/9jb3j2c6
https://escholarship.org/content/qt9jb3j2c6/qt9jb3j2c6.pdf

المؤلفون: 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.

المساهمون: Psychosociale zorg patientenzorg

مصطلحات موضوعية: 22q11 deletion syndrome, gray matter volume, magnetic resonnance imaging, source-based morphometry, Anatomy, Radiological and Ultrasound Technology, Radiology Nuclear Medicine and imaging, Neurology, Clinical Neurology

وصف الملف: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/454238

الاتاحة: https://dspace.library.uu.nl/handle/1874/454238

المؤلفون: McBride, Haley, Jhawar, Nandini, Boucicaut, Laurie, Bearden, Carrie E., Kates, Wendy R., Woolf‐King, Sarah E., Antshel, Kevin M.

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics ; volume 195, issue 6 ; ISSN 1552-4841 1552-485X

الاتاحة: http://dx.doi.org/10.1002/ajmg.b.32973
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.32973

المؤلفون: Chawner, Samuel JRA, Doherty, Joanne L, Anney, Richard JL, Antshel, Kevin M, Bearden, Carrie E, Bernier, Raphael, Chung, Wendy K, Clements, Caitlin C, Curran, Sarah R, Cuturilo, Goran, Fiksinski, Ania M, Gallagher, Louise, Goin-Kochel, Robin P, Gur, Raquel E, Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R, Kushan, Leila, Maillard, Anne M, McDonald-McGinn, Donna M, Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T, Green-Snyder, LeeAnne, Vorstman, Jacob A, Wenger, Tara L, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne BM

المصدر: American Journal of Psychiatry. 178(1)

مصطلحات موضوعية: Clinical Research, Genetics, Prevention, Human Genome, Intellectual and Developmental Disabilities (IDD), Behavioral and Social Science, Autism, Pediatric, Brain Disorders, Mental Health, Genetic Testing, Aetiology, 2.1 Biological and endogenous factors, Autistic Disorder, Child, DNA Copy Number Variations, Gene Deletion, Genetic Association Studies, Genetic Predisposition to Disease, Heterozygote, Humans, Interview, Psychological, Male, Prevalence, Risk Factors, Severity of Illness Index, IMAGINE-ID Consortium, Copy Number Variants, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/97g4x8h8

المؤلفون: Davies, Robert W, Fiksinski, Ania M, Breetvelt, Elemi J, Williams, Nigel M, Hooper, Stephen R, Monfeuga, Thomas, Bassett, Anne S, Owen, Michael J, Gur, Raquel E, Morrow, Bernice E, McDonald-McGinn, Donna M, Swillen, Ann, Chow, Eva WC, van den Bree, Marianne, Emanuel, Beverly S, Vermeesch, Joris R, van Amelsvoort, Therese, Arango, Celso, Armando, Marco, Campbell, Linda E, Cubells, Joseph F, Eliez, Stephan, Garcia-Minaur, Sixto, Gothelf, Doron, Kates, Wendy R, Murphy, Kieran C, Murphy, Clodagh M, Murphy, Declan G, Philip, Nicole, Repetto, Gabriela M, Shashi, Vandana, Simon, Tony J, Suñer, Damiàn Heine, Vicari, Stefano, Scherer, Stephen W, Bearden, Carrie E, Vorstman, Jacob AS

المصدر: Nature Medicine. 26(12)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Health Sciences, Genetics, Schizophrenia, Serious Mental Illness, Behavioral and Social Science, Prevention, Brain Disorders, Clinical Research, Mental Health, Aetiology, 2.1 Biological and endogenous factors, Mental health, Adolescent, Adult, Aged, Child, Child, Preschool, Cognitive Dysfunction, Cohort Studies, DiGeorge Syndrome, Female, Genetic Variation, Humans, Intellectual Disability, Male, Middle Aged, Multifactorial Inheritance, Phenotype, Risk Factors, Young Adult, International 22q11.2 Brain and Behavior Consortium, Medical and Health Sciences, Immunology, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/2sg8q3hf

المؤلفون: Villalón-Reina, Julio E, Martínez, Kenia, Qu, Xiaoping, Ching, Christopher RK, Nir, Talia M, Kothapalli, Deydeep, Corbin, Conor, Sun, Daqiang, Lin, Amy, Forsyth, Jennifer K, Kushan, Leila, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Jonas, Rachel K, van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy R, Antshel, Kevin M, Fremont, Wanda, Campbell, Linda E, McCabe, Kathryn L, Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M, Murphy, Declan, Craig, Michael, Emanuel, Beverly, McDonald-McGinn, Donna M, Vorstman, Jacob AS, Fiksinski, Ania M, Koops, Sanne, Ruparel, Kosha, Roalf, David, Gur, Raquel E, Eric Schmitt, J, Simon, Tony J, Goodrich-Hunsaker, Naomi J, Durdle, Courtney A, Doherty, Joanne L, Cunningham, Adam C, van den Bree, Marianne, Linden, David EJ, Owen, Michael, Moss, Hayley, Kelly, Sinead, Donohoe, Gary, Murphy, Kieran C, Arango, Celso, Jahanshad, Neda, Thompson, Paul M, Bearden, Carrie E

المصدر: Molecular Psychiatry. 25(11)

مصطلحات موضوعية: Paediatrics, Biomedical and Clinical Sciences, Pediatric, Congenital Structural Anomalies, Brain Disorders, Biomedical Imaging, Mental Health, Clinical Research, Rare Diseases, Neurosciences, Mental health, Adolescent, Adult, Anisotropy, Child, DiGeorge Syndrome, Diffusion Magnetic Resonance Imaging, Female, Humans, Male, Middle Aged, White Matter, Young Adult, Biological Sciences, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry, Clinical sciences, Biological psychology, Clinical and health psychology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3st981z8
https://escholarship.org/content/qt3st981z8/qt3st981z8.pdf

المؤلفون: Sun, Daqiang, Ching, Christopher RK, Lin, Amy, Forsyth, Jennifer K, Kushan, Leila, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Villalon-Reina, Julio E, Qu, Xiaoping, Jonas, Rachel K, van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy R, Antshel, Kevin M, Fremont, Wanda, Campbell, Linda E, McCabe, Kathryn L, Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M, Murphy, Declan, Craig, Michael, Vorstman, Jacob, Fiksinski, Ania, Koops, Sanne, Ruparel, Kosha, Roalf, David R, Gur, Raquel E, Schmitt, J Eric, Simon, Tony J, Goodrich-Hunsaker, Naomi J, Durdle, Courtney A, Bassett, Anne S, Chow, Eva WC, Butcher, Nancy J, Vila-Rodriguez, Fidel, Doherty, Joanne, Cunningham, Adam, van den Bree, Marianne BM, Linden, David EJ, Moss, Hayley, Owen, Michael J, Murphy, Kieran C, McDonald-McGinn, Donna M, Emanuel, Beverly, van Erp, Theo GM, Turner, Jessica A, Thompson, Paul M, Bearden, Carrie E

المصدر: Molecular Psychiatry. 25(8)

مصطلحات موضوعية: Biological Psychology, Biomedical and Clinical Sciences, Psychology, Clinical Research, Mental Health, Genetics, Mental Illness, Rare Diseases, Congenital Structural Anomalies, Neurosciences, Brain Disorders, Biomedical Imaging, Schizophrenia, Serious Mental Illness, Pediatric, 2.1 Biological and endogenous factors, Mental health, Adolescent, Adult, Cerebral Cortex, Chromosome Deletion, DiGeorge Syndrome, Female, Gray Matter, Humans, Magnetic Resonance Imaging, Male, Psychotic Disorders, Young Adult, Biological Sciences, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry, Clinical sciences, Biological psychology, Clinical and health psychology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/26s9n67w
https://escholarship.org/content/qt26s9n67w/qt26s9n67w.pdf

المؤلفون: Ching, Christopher RK, Gutman, Boris A, Sun, Daqiang, Villalon Reina, Julio, Ragothaman, Anjanibhargavi, Isaev, Dmitry, Zavaliangos-Petropulu, Artemis, Lin, Amy, Jonas, Rachel K, Kushan, Leila, Pacheco-Hansen, Laura, Vajdi, Ariana, Forsyth, Jennifer K, Jalbrzikowski, Maria, Bakker, Geor, van Amelsvoort, Therese, Antshel, Kevin M, Fremont, Wanda, Kates, Wendy R, Campbell, Linda E, McCabe, Kathryn L, Craig, Michael C, Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M, Murphy, Declan G, Murphy, Kieran C, Fiksinski, Ania, Koops, Sanne, Vorstman, Jacob, Crowley, T Blaine, Emanuel, Beverly S, Gur, Raquel E, McDonald-McGinn, Donna M, Roalf, David R, Ruparel, Kosha, Schmitt, J Eric, Zackai, Elaine H, Durdle, Courtney A, Goodrich-Hunsaker, Naomi J, Simon, Tony J, Bassett, Anne S, Butcher, Nancy J, Chow, Eva WC, Vila-Rodriguez, Fidel, Cunningham, Adam, Doherty, Joanne, Linden, David E, Moss, Hayley, Owen, Michael J, van den Bree, Marianne, Crossley, Nicolas A, Repetto, Gabriela M, Thompson, Paul M, Bearden, Carrie E

المصدر: American Journal of Psychiatry. 177(7)

مصطلحات موضوعية: Clinical Research, Serious Mental Illness, Brain Disorders, Mental Health, Schizophrenia, Clinical Trials and Supportive Activities, Neurosciences, 2.1 Biological and endogenous factors, Aetiology, Mental health, Adolescent, Adult, Atrophy, Brain, Brain Mapping, Case-Control Studies, Child, DiGeorge Syndrome, Female, Humans, Hypertrophy, Magnetic Resonance Imaging, Male, Mental Disorders, Middle Aged, Psychotic Disorders, Young Adult, 22q11.2 Deletion Syndrome, Copy Number Variant, Neuroanatomy, Neurodevelopment, Psychosis, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/2zz5f98w

المؤلفون: Zhao, Yingjie, Diacou, Alexander, Johnston, H Richard, Musfee, Fadi I, McDonald-McGinn, Donna M, McGinn, Daniel, Crowley, T Blaine, Repetto, Gabriela M, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R, Kates, Wendy R, Digilio, M Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne, Moss, Hayley, Owen, Michael J, Murphy, Kieran C, Murphy, Clodagh M, Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J, Shprintzen, Robert J, Campbell, Linda, Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Consortium, International 22q11 2 Brain and Behavior, Antonarakis, Stylianos E, Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, María Angeles, Epstein, Michael P, Evers, Rens, Fernandez, Luis, Fritsch, Rosemarie, Algas, Fernando García, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S, Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Teresa, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther DA, Vergaelen, Elfi, Warren, Steve T, Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong, Zwick, Michael, Bearden, Carrie E, Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob AS, Gothelf, Doron, Zackai, Elaine, Agopian, AJ, Gur, Raquel E, Bassett, Anne S, Emanuel, Beverly S, Goldmuntz, Elizabeth, Mitchell, Laura E, Wang, Tao, Morrow, Bernice E

المصدر: American Journal of Human Genetics. 106(1)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Epidemiology, Health Sciences, Clinical Research, Human Genome, Heart Disease, Cardiovascular, Pediatric, Aetiology, 2.1 Biological and endogenous factors, Case-Control Studies, Chromosome Deletion, Chromosomes, Human, Pair 22, Cohort Studies, Female, Genome-Wide Association Study, Heart Defects, Congenital, Humans, Linkage Disequilibrium, Male, Phenotype, Polymorphism, Single Nucleotide, Proto-Oncogene Mas, Segmental Duplications, Genomic, International 22q11.2 Brain and Behavior Consortium, CRKL, DiGeorge syndrome, TBX1, chromosome 22q11.2 deletion syndrome, complex trait, congenital heart disease, conotruncal heart defects, copy number variation, genetic association, genetic modifier, haploinsufficiency, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/38b9f8cx

المؤلفون: Zhao, Yingjie, Guo, Tingwei, Fiksinski, Ania, Breetvelt, Elemi, McDonald‐McGinn, Donna M, Crowley, Terrence B, Diacou, Alexander, Schneider, Maude, Eliez, Stephan, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris, Chow, Eva WC, Gothelf, Doron, Duijff, Sasja, Evers, Rens, Amelsvoort, Thérèse A, Bree, Marianne, Owen, Michael, Niarchou, Maria, Bearden, Carrie E, Ornstein, Claudia, Pontillo, Maria, Buzzanca, Antonino, Vicari, Stefano, Armando, Marco, Murphy, Kieran C, Murphy, Clodagh, Garcia‐Minaur, Sixto, Philip, Nicole, Campbell, Linda, Morey‐Cañellas, Jaume, Raventos, Jasna, Rosell, Jordi, Heine‐Suner, Damian, Shprintzen, Robert J, Gur, Raquel E, Zackai, Elaine, Emanuel, Beverly S, Wang, Tao, Kates, Wendy R, Bassett, Anne S, Vorstman, Jacob AS, Morrow, Bernice E, Consortium, on behalf of the International 22q11 2 Brain and Behavior

المصدر: American Journal of Medical Genetics Part A. 176(10)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Clinical Sciences, Genetics, Acquired Cognitive Impairment, Clinical Research, Brain Disorders, Pediatric, Adolescent, Adult, Child, Chromosome Deletion, Chromosomes, Human, Pair 22, DiGeorge Syndrome, Female, Humans, Intellectual Disability, Intelligence Tests, Male, 22q11.2 deletion syndrome, deletion size, intellectual disability, IQ, low copy repeat, segmental duplication, International 22q11.2 Brain and Behavior Consortium, Clinical sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/6nj7d39k

المؤلفون: Guo, Tingwei, Diacou, Alexander, Nomaru, Hiroko, McDonald-McGinn, Donna M, Hestand, Matthew, Demaerel, Wolfram, Zhang, Liangtian, Zhao, Yingjie, Ujueta, Francisco, Shan, Jidong, Montagna, Cristina, Zheng, Deyou, Crowley, Terrence B, Kushan-Wells, Leila, Bearden, Carrie E, Kates, Wendy R, Gothelf, Doron, Schneider, Maude, Eliez, Stephan, Breckpot, Jeroen, Swillen, Ann, Vorstman, Jacob, Zackai, Elaine, Benavides Gonzalez, Felipe, Repetto, Gabriela M, Emanuel, Beverly S, Bassett, Anne S, Vermeesch, Joris R, Marshall, Christian R, Morrow, Bernice E

المصدر: Human Molecular Genetics. 27(7)

مصطلحات موضوعية: Rare Diseases, Pediatric, Biotechnology, Genetics, Congenital, Alleles, Chromosome Deletion, Chromosome Mapping, Chromosomes, Human, Pair 22, DiGeorge Syndrome, Female, Humans, Male, Meiosis, International Chromosome 22q11.2, International 22q11.2 Brain and Behavior Consortia, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/8w2197nk

المؤلفون: Zhao, Yingjie, Wang, Yujue, Shi, Lijie, McDonald-McGinn, Donna M., Crowley, T. Blaine, McGinn, Daniel E., Tran, Oanh T., Miller, Daniella, Lin, Jhih Rong, Zackai, Elaine, Johnston, H. Richard, Chow, Eva W.C., Vorstman, Jacob A.S., Vingerhoets, Claudia, van Amelsvoort, Therese, Gothelf, Doron, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Eliez, Stephan, Schneider, Maude, van den Bree, Marianne B.M., Owen, Michael J., Kates, Wendy R., Repetto, Gabriela M., Shashi, Vandana, Schoch, Kelly, Bearden, Carrie E., Digilio, M. Cristina, Unolt, Marta, Putotto, Carolina, Marino, Bruno, Pontillo, Maria, Armando, Marco, Vicari, Stefano, Angkustsiri, Kathleen, Campbell, Linda, Busa, Tiffany, Heine-Suñer, Damian, Murphy, Kieran C., Murphy, Declan, García-Miñaúr, Sixto, Fernández, Luis, Zhang, Zhengdong D., Goldmuntz, Elizabeth, Gur, Raquel E., Emanuel, Beverly S., Zheng, Deyou, Marshall, Christian R., Morrow, B.E.

المصدر: Zhao , Y , Wang , Y , Shi , L , McDonald-McGinn , D M , Crowley , T B , McGinn , D E , Tran , O T , Miller , D , Lin , J R , Zackai , E , Johnston , H R , Chow , E W C , Vorstman , J A S , Vingerhoets , C , van Amelsvoort , T , Gothelf , D , Swillen , A , Breckpot , J , Vermeesch , J R , Eliez , S , Schneider , M , van den Bree ....

الاتاحة: https://cris.maastrichtuniversity.nl/en/publications/5c26b31a-58b8-48fd-807e-167fcdfdd379
https://doi.org/10.1038/s41525-023-00363-y

المؤلفون: Guo, Tingwei, Repetto, Gabriela M, McDonald McGinn, Donna M, Chung, Jonathan H, Nomaru, Hiroko, Campbell, Christopher L, Blonska, Anna, Bassett, Anne S, Chow, Eva WC, Mlynarski, Elisabeth E, Swillen, Ann, Vermeesch, Joris, Devriendt, Koen, Gothelf, Doron, Carmel, Miri, Michaelovsky, Elena, Schneider, Maude, Eliez, Stephan, Antonarakis, Stylianos E, Coleman, Karlene, Tomita-Mitchell, Aoy, Mitchell, Michael E, Digilio, M Cristina, Dallapiccola, Bruno, Marino, Bruno, Philip, Nicole, Busa, Tiffany, Kushan-Wells, Leila, Bearden, Carrie E, Piotrowicz, Małgorzata, Hawuła, Wanda, Roberts, Amy E, Tassone, Flora, Simon, Tony J, van Duin, Esther DA, van Amelsvoort, Thérèse A, Kates, Wendy R, Zackai, Elaine, Johnston, H Richard, Cutler, David J, Agopian, AJ, Goldmuntz, Elizabeth, Mitchell, Laura E, Wang, Tao, Emanuel, Beverly S, Morrow, Bernice E

المصدر: Circulation Genomic and Precision Medicine. 10(5)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Cardiovascular Medicine and Haematology, Genetics, Rare Diseases, Congenital Structural Anomalies, Clinical Research, Human Genome, Heart Disease, Cardiovascular, Pediatric, 2.1 Biological and endogenous factors, Aetiology, Congenital, Chromatin, Chromosomes, Human, Pair 5, DiGeorge Syndrome, Genetic Loci, Genome-Wide Association Study, Genotype, High-Throughput Nucleotide Sequencing, Humans, Linkage Disequilibrium, MEF2 Transcription Factors, Oligonucleotide Array Sequence Analysis, Phenotype, Polymorphism, Single Nucleotide, Receptors, G-Protein-Coupled, Sequence Analysis, DNA, Tetralogy of Fallot, chromosomes, DiGeorge syndrome, genotype, ivelo-cardio-facial syndrome, tetralogy of Fallot, International 22q11.2 Consortium/Brain and Behavior Consortium*, Medical Biotechnology, Cardiorespiratory Medicine and Haematology, Cardiovascular System & Hematology, Cardiovascular medicine and haematology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/7hp1507k

المؤلفون: Weisman, Omri, Guri, Yael, Gur, Raquel E, McDonald-McGinn, Donna M, Calkins, Monica E, Tang, Sunny X, Emanuel, Beverly, Zackai, Elaine H, Eliez, Stephan, Schneider, Maude, Schaer, Marie, Kates, Wendy R, Antshel, Kevin M, Fremont, Wanda, Shashi, Vandana, Hooper, Stephen R, Armando, Marco, Vicari, Stefano, Pontillo, Maria, Kushan, Leila, Jalbrzikowski, Maria, Bearden, Carrie E, Cubells, Joseph F, Ousley, Opal Y, Walker, Elaine F, Simon, Tony J, Stoddard, Joel, Niendam, Tara A, van den Bree, Marianne BM, Gothelf, Doron

المصدر: Schizophrenia Bulletin. 43(5)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Clinical Sciences, Behavioral and Social Science, Mental Health, Serious Mental Illness, Brain Disorders, Neurosciences, Clinical Research, Pediatric, Clinical Trials and Supportive Activities, Mental health, Adolescent, Adult, Anxiety Disorders, Attention Deficit Disorder with Hyperactivity, Child, Cognitive Dysfunction, Comorbidity, DiGeorge Syndrome, Humans, Middle Aged, Prodromal Symptoms, Psychotic Disorders, Young Adult, velocardiofacial syndrome, subthreshold psychotic symptoms, structured interview for prodromal syndromes, anxiety disorder, global assessment of functioning, attention deficit, hyperactivity disorder, IQ, DiGeorge syndrome, International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome, attention deficit/hyperactivity disorder, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry, Clinical sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/7bf8368m

المؤلفون: Schreiner, Matthew, Forsyth, Jennifer K, Karlsgodt, Katherine H, Anderson, Ariana E, Hirsh, Nurit, Kushan, Leila, Uddin, Lucina Q, Mattiacio, Leah, Coman, Ioana L, Kates, Wendy R, Bearden, Carrie E

المصدر: Cerebral cortex (New York, N.Y. : 1991). 27(6)

مصطلحات موضوعية: Gyrus Cinguli, Parietal Lobe, Nerve Net, Humans, DiGeorge Syndrome, Oxygen, Magnetic Resonance Imaging, Case-Control Studies, Cohort Studies, Psychotic Disorders, Psychiatric Status Rating Scales, Neuropsychological Tests, Motion, Adolescent, Child, Female, Male, Young Adult, Connectome, intrinsic connectivity networks, machine learning, psychosis, resting state functional MRI, velocardiofacial syndrome, Clinical Research, Prevention, Serious Mental Illness, Brain Disorders, Pediatric, Neurosciences, Mental Health, Mental health, Psychology, Cognitive Sciences, Experimental Psychology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/91b245dw

المؤلفون: Mattiaccio, Leah M, Coman, Ioana L, Schreiner, Matthew J, Antshel, Kevin M, Fremont, Wanda P, Bearden, Carrie E, Kates, Wendy R

المصدر: Journal of Neurodevelopmental Disorders. 8(1)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Neurosciences, Brain Disorders, Serious Mental Illness, Mental Health, Clinical Research, Behavioral and Social Science, Basic Behavioral and Social Science, Aetiology, 4.1 Discovery and preclinical testing of markers and technologies, Detection, screening and diagnosis, 2.3 Psychological, social and economic factors, Mental health, 22q11.2 deletion syndrome, ICA, Resting-state fMRI, Schizophrenia, Psychology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3h1387df
https://escholarship.org/content/qt3h1387df/qt3h1387df.pdf

المؤلفون: Mlynarski, Elisabeth E, Xie, Michael, Taylor, Deanne, Sheridan, Molly B, Guo, Tingwei, Racedo, Silvia E, McDonald-McGinn, Donna M, Chow, Eva WC, Vorstman, Jacob, Swillen, Ann, Devriendt, Koen, Breckpot, Jeroen, Digilio, Maria Cristina, Marino, Bruno, Dallapiccola, Bruno, Philip, Nicole, Simon, Tony J, Roberts, Amy E, Piotrowicz, Małgorzata, Bearden, Carrie E, Eliez, Stephan, Gothelf, Doron, Coleman, Karlene, Kates, Wendy R, Devoto, Marcella, Zackai, Elaine, Heine-Suñer, Damian, Goldmuntz, Elizabeth, Bassett, Anne S, Morrow, Bernice E, Emanuel, Beverly S, International Chromosome 22q11.2 Consortium

المصدر: Human genetics. 135(3)

مصطلحات موضوعية: International Chromosome 22q11.2 Consortium, Chromosomes, Human, Pair 22, Humans, Heart Defects, Congenital, DiGeorge Syndrome, Chromosome Deletion, DNA Copy Number Variations, Genotyping Techniques, Human Genome, Rare Diseases, Heart Disease, Cardiovascular, Pediatric, Clinical Research, Prevention, Genetics, Congenital Structural Anomalies, 2.1 Biological and endogenous factors, Congenital, Genetics & Heredity, Complementary and Alternative Medicine, Paediatrics and Reproductive Medicine

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/49g9k7pj

المؤلفون: Psychosociale zorg patientenzorg, 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.

URL: https://doi.org/10.1002/hbm.26553
http://hdl.handle.net/1874/454238
https://dspace.library.uu.nl/handle/1874/454238
http://www.scopus.com/inward/record.url?scp=85182249725&partnerID=8YFLogxK
1065-9471
Human Brain Mapping
45
1
e26553

المؤلفون: Sønderby, Ida E, Ching, Christopher R K, Ayesa-Arriola, Rosa, Thompson, Paul M, Bearden, Carrie E, Andreassen, Ole A, Group, ENIGMA-CNV Working, 2 Deletion Syndrome Working Group, ENIGMA 22q11., Bernard, Manon, Blackburn, Nicholas B, Bøen, Rune, de Geus, Eco, de Zwarte, Sonja M C, Bakker, Geor, Forti, Marta Di, Frei, Oleksandr, Fukunaga, Masaki, Hehir-Kwa, Jayne Y, Hillegers, Manon H J, Hoffmann, Per, Homuth, Georg, Jahanshad, Neda, Koops, Sanne, Kumar, Kuldeep, Bassett, Anne S, Kikuchi, Masataka, Le Hellard, Stephanie, Leu, Costin, Murray, Robin M, Naerland, Terje, Nyberg, Lars, Ophoff, Roel A, Pike, G Bruce, Sando, Sigrid B, Shin, Jean, Boomsma, Dorret I, Shumskaya, Elena, Sisodiya, Sanjay M, Steen, Vidar M, Teumer, Alexander, Uhlmann, Anne, Wright, Margaret J, Antshel, Kevin M, Campbell, Linda E, Crossley, Nicolas A, Crowley, T Blaine, Bülow, Robin, Daly, Eileen, Fiksinski, Ania M, Forsyth, Jennifer K, Fremont, Wanda, Goodrich-Hunsaker, Naomi J, Gudbrandsen, Maria, Jonas, Rachel K, Kates, Wendy R, Lin, Amy, McCabe, Kathryn L, Butcher, Nancy J, Moss, Hayley, Murphy, Declan G, Murphy, Kieran C, Owen, Michael J, Ruparel, Kosha, Simon, Tony J, van Amelsvoort, Therese, Vorstman, Jacob A S, Calhoun, Vince D, Caspers, Svenja, Chow, Eva W C, Cichon, Sven, Thomopoulos, Sophia I, Ciufolini, Simone, Craig, Michael C, Crespo-Facorro, Benedicto, Cunningham, Adam C, Dale, Anders M, Dazzan, Paola, de Zubicaray, Greig I, Djurovic, Srdjan, Doherty, Joanne L, Donohoe, Gary, van der Meer, Dennis, Draganski, Bogdan, Durdle, Courtney A, Ehrlich, Stefan, Emanuel, Beverly S, Espeseth, Thomas, Fisher, Simon E, Ge, Tian, Glahn, David C, Grabe, Hans J, Gur, Raquel E, Sun, Daqiang, Gutman, Boris A, Haavik, Jan, Håberg, Asta K, Hansen, Laura A, Hashimoto, Ryota, Hibar, Derrek P, Holmes, Avram J, Hottenga, Jouke-Jan, Hulshoff Pol, Hilleke E, Jalbrzikowski, Maria, Villalon-Reina, Julio E, Knowles, Emma E M, Kushan, Leila, Linden, David E J, Liu, Jingyu, Lundervold, Astri J, Martin-Brevet, Sandra, Martínez, Kenia, Mather, Karen A, Mathias, Samuel R, McDonald-McGinn, Donna M, Agartz, Ingrid, McRae, Allan F, Medland, Sarah E, Moberget, Torgeir, Modenato, Claudia, Monereo Sánchez, Jennifer, Moreau, Clara A, Mühleisen, Thomas W, Paus, Tomas, Pausova, Zdenka, Prieto, Carlos, Amunts, Katrin, Ragothaman, Anjanibhargavi, Reinbold, Céline S, Reis Marques, Tiago, Repetto, Gabriela M, Reymond, Alexandre, Roalf, David R, Rodriguez-Herreros, Borja, Rucker, James J, Sachdev, Perminder S, Schmitt, James E, Arango, Celso, Schofield, Peter R, Silva, Ana I, Stefansson, Hreinn, Stein, Dan J, Tamnes, Christian K, Tordesillas-Gutiérrez, Diana, Ulfarsson, Magnus O, Vajdi, Ariana, van 't Ent, Dennis, van den Bree, Marianne B M, Armstrong, Nicola J, Vassos, Evangelos, Vázquez-Bourgon, Javier, Vila-Rodriguez, Fidel, Walters, G Bragi, Wen, Wei, Westlye, Lars T, Wittfeld, Katharina, Zackai, Elaine H, Stefánsson, Kári, Jacquemont, Sebastien

المصدر: Human brain mapping 43(1), 300-328 (2022). doi:10.1002/hbm.25354

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Brain: diagnostic imaging, Brain: growth & development, Brain: pathology, DNA Copy Number Variations, Humans, Magnetic Resonance Imaging, Mental Disorders: diagnostic imaging, Mental Disorders: genetics, Mental Disorders: pathology, Multicenter Studies as Topic, Neurodevelopmental Disorders: diagnostic imaging, Neurodevelopmental Disorders: genetics, Neurodevelopmental Disorders: pathology, Neuroimaging, brain structural imaging, copy number variant, diffusion tensor imaging, evolution, genetics-first approach, neurodevelopmental disorders, psychiatric disorders

جغرافية الموضوع: DE

Relation: info:eu-repo/semantics/altIdentifier/pmid/pmid:33615640; info:eu-repo/semantics/altIdentifier/issn/1065-9471; info:eu-repo/semantics/altIdentifier/issn/1097-0193; https://pub.dzne.de/record/155631; https://pub.dzne.de/search?p=id:%22DZNE-2021-00799%22

الاتاحة: https://pub.dzne.de/record/155631
https://pub.dzne.de/search?p=id:%22DZNE-2021-00799%22