日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Genetic overlap between idiopathic scoliosis and schizophrenia in the general population

普通人群中特发性脊柱侧弯与精神分裂症的遗传重叠

de Reuver, Steven; Engchuan, Worrawat; Safarian, Nickie; Zarrei, Mehdi; Vorstman, Jacob A S; Castelein, René M; Breetvelt, Elemi J

A normative chart for cognitive development in a genetically selected population

基因选择人群认知发展规范图表

Fiksinski, Ania M; Bearden, Carrie E; Bassett, Anne S; Kahn, René S; Zinkstok, Janneke R; Hooper, Stephen R; Tempelaar, Wanda; McDonald-McGinn, Donna; Swillen, Ann; Emanuel, Beverly; Morrow, Bernice; Gur, Raquel; Chow, Eva; van den Bree, Marianne; Vermeesch, Joris; Warren, Stephen; Owen, Michael; van Amelsvoort, Therese; Eliez, Stephan; Gothelf, Doron; Arango, Celso; Kates, Wendy; Simon, Tony; Murphy, Kieran; Repetto, Gabriela; Suner, Damian Heine; Vicari, Stefano; Cubells, Joseph; Armando, Marco; Philip, Nicole; Campbell, Linda; Garcia-Minaur, Sixto; Schneider, Maude; Shashi, Vandana; Vorstman, Jacob; Breetvelt, Elemi J

Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model

高风险遗传模型中家庭内部因素对维度神经行为特征的影响

Fiksinski, Ania M; Heung, Tracy; Corral, Maria; Breetvelt, Elemi J; Costain, Gregory; Marshall, Christian R; Kahn, Rene S; Vorstman, Jacob A S; Bassett, Anne S

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

22q11.2缺失存在时,精神分裂症风险的遗传因素

Cleynen, Isabelle; Engchuan, Worrawat; Hestand, Matthew S; Heung, Tracy; Holleman, Aaron M; Johnston, H Richard; Monfeuga, Thomas; McDonald-McGinn, Donna M; Gur, Raquel E; Morrow, Bernice E; Swillen, Ann; Vorstman, Jacob A S; Bearden, Carrie E; Chow, Eva W C; van den Bree, Marianne; Emanuel, Beverly S; Vermeesch, Joris R; Warren, Stephen T; Owen, Michael J; Chopra, Pankaj; Cutler, David J; Duncan, Richard; Kotlar, Alex V; Mulle, Jennifer G; Voss, Anna J; Zwick, Michael E; Diacou, Alexander; Golden, Aaron; Guo, Tingwei; Lin, Jhih-Rong; Wang, Tao; Zhang, Zhengdong; Zhao, Yingjie; Marshall, Christian; Merico, Daniele; Jin, Andrea; Lilley, Brenna; Salmons, Harold I; Tran, Oanh; Holmans, Peter; Pardinas, Antonio; Walters, James T R; Demaerel, Wolfram; Boot, Erik; Butcher, Nancy J; Costain, Gregory A; Lowther, Chelsea; Evers, Rens; van Amelsvoort, Therese A M J; van Duin, Esther; Vingerhoets, Claudia; Breckpot, Jeroen; Devriendt, Koen; Vergaelen, Elfi; Vogels, Annick; Crowley, T Blaine; McGinn, Daniel E; Moss, Edward M; Sharkus, Robert J; Unolt, Marta; Zackai, Elaine H; Calkins, Monica E; Gallagher, Robert S; Gur, Ruben C; Tang, Sunny X; Fritsch, Rosemarie; Ornstein, Claudia; Repetto, Gabriela M; Breetvelt, Elemi; Duijff, Sasja N; Fiksinski, Ania; Moss, Hayley; Niarchou, Maria; Murphy, Kieran C; Prasad, Sarah E; Daly, Eileen M; Gudbrandsen, Maria; Murphy, Clodagh M; Murphy, Declan G; Buzzanca, Antonio; Fabio, Fabio Di; Digilio, Maria C; Pontillo, Maria; Marino, Bruno; Vicari, Stefano; Coleman, Karlene; Cubells, Joseph F; Ousley, Opal Y; Carmel, Miri; Gothelf, Doron; Mekori-Domachevsky, Ehud; Michaelovsky, Elena; Weinberger, Ronnie; Weizman, Abraham; Kushan, Leila; Jalbrzikowski, Maria; Armando, Marco; Eliez, Stéphan; Sandini, Corrado; Schneider, Maude; Béna, Frédérique Sloan; Antshel, Kevin M; Fremont, Wanda; Kates, Wendy R; Belzeaux, Raoul; Busa, Tiffany; Philip, Nicole; Campbell, Linda E; McCabe, Kathryn L; Hooper, Stephen R; Schoch, Kelly; Shashi, Vandana; Simon, Tony J; Tassone, Flora; Arango, Celso; Fraguas, David; García-Miñaúr, Sixto; Morey-Canyelles, Jaume; Rosell, Jordi; Suñer, Damià H; Raventos-Simic, Jasna; Epstein, Michael P; Williams, Nigel M; Bassett, Anne S

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

利用常见遗传变异研究22q11.2缺失综合征的表型表达和风险预测

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 W C; 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 A S

9. DOES BIOLOGY READ THE DSM? TRANSDIAGNOSTIC FINDINGS IN PSYCHOSIS AND IMPLICATIONS FOR TREATMENT

9. 生物学是否解读了《精神疾病诊断与统计手册》(DSM)?精神病跨诊断的发现及其对治疗的启示

Poe, S Lucy; Gill, Kelly E; Brucato, Gary; Corcoran, Cheryl M; Girgis, Ragy R; Sigvard, Anne; Tangmose, Karen; Bojesen, Kirsten Borup; Jessen, Kasper; Nielsen, Mette Ødegaard; Fuglø, Dan; Jensen, Lars Thorbjørn; Rostrup, Egill; Glenthøj, Birte; Bryce, Shayden; Ponsford, Jennie; Lee, Stuart; Tan, Eric; Carruthers, Sean; Lawrence, Richard; Rossell, Susan; Wenneberg, Christina; Broberg, Brian; Rostrup, Egill; Glenthøj, Louise Birkedal; Glenthoj, Birte; Nordentoft, Merete; Kristensen, Tina Dam; Geaghan, Michael; Cairns, Murray; Dazzan, Paola; Reinders, AAT Simone; Shatzi, Vasiliki; Carletti, Francesco; Arango, Celso; Fleischhacker, Wolfgang; Galderisi, Silvana; Mucci, Armida; Glenthoj, Birte; Egerton, Alice; Barker, Gareth; Leucht, Stefan; Meyer-Lindenberg, Andreas; Kahn, René S; Rujescu, Dan; Sommer, Iris; Winter, Inge; McGuire, Philip; Ganapathiraju, Madhavi; Balakrishnan, Narayanaswamy; Calvo, Ana; O’Hanlon, Erik; Coughlan, Helen; Kelleher, Ian; Clarke, Mary; Cannon, Mary; Klauser, Paul; Baumann, Philipp S; Fournier, Margot; Xin, Lijing; Griffa, Alessandra; Cleusix, Martine; Jenni, Raoul; Cuenod, Michel; Hagmann, Patric; Conus, Philippe; Do, Kim Q; Jessen, Kasper; Rostrup, Egill; Mandl, Rene C W; Nielsen, Mette Ø; Bak, Nikolaj; Fagerlund, Birgitte; Glenthøj, Birte Y; Ebdrup, Bjørn H; Martins-De-Souza, Daniel; Webster, Maree; Weickert, Cynthia Shannon; Thorup, Anne Amalie; Hemager, Nicoline; Ellersgaard, Ditte V; Christiani, Camilla Jerlang; Burton, Birgitte Klee; Spang, Katrine S; Gregersen, Maja; Søndergaard, Anne; Gantriis, Ditte L; Greve, Aja; Jepsen, Jens Richardt; Mors, Ole; von Plessen, Kerstin; Nordentoft, Merete; Bloomfield, Michael; Hilker, Rikke; Nielsen, Mette; Legind, Christian; Jensen, Maria H; Anhøj, Simon; Broberg, Brian; Fagerlund, Birgitte; Nordentoft, Merete; Glenthøj, Birte; Kruiper, Caitlyn; Glenthoj, Birte; Oranje, Bob; Tangmose, Karen; Nielsen, Mette Odegård; Sigvard, Anne; Jessen, Kasper; Bojesen, Kirsten; Bjerregaard, Marie; Rostrup, Egill; Glenthoj, Birte; Selten, Iris; Rydkjaer, Jacob; Pagsberg, Anne Katrine; Fagerlund, Birgitte; Glenthoj, Birte; Jepsen, Jens Richardt Møllegaard; Oranje, Bob; Pau, Soldevila-Matias; Carlos, González-Vivas; Gracián, García-Martí; Olga, Soprano-Ros; Luis, Martí-Bonmatí; Benedicto, Crespo-Facorro; Julio, Sanjuán; González-Rodríguez, Alexandre; Estrada, Francesc; Monreal, José Antonio; Palao, Diego; Labad, Javier; van Themaat, Anna Hester Ver Loren; Jepsen, Jens Richardt Møllegaard; Christiani, Camilla; Nordentoft, Merete; Nielsen, Mette; Rostrup, Egill; Hilker, Rikke; Legind, Christian; Jensen, Maria H; Anhøj, Simon; Broberg, Brian V; Fagerlund, Birgitte; Glenthøj, Birte; Nordentoft, Merete; Hemager, Nicoline; Christiani, Camilla Jerlang; Ellersgaard, Ditte V; Greve, Aja; Gantriis, Ditte Lou; Burton, Birgitte Klee; Spang, Katrine; von Plessen, Kerstin; Møllegaard Jepsen, Jens Richardt; Mors, Ole; Thorup, Anne Amalie; Bojesen, Kirsten; Broberg, Brian; Jessen, Kasper; Sigvard, Anne; Tangmose, Karen; Nielsen, Mette Ødegaard; Rostrup, Egill; Glenthoj, Birte; Ania, Fiksinski; Breetvelt, Elemi; Vorstman, Jacob; Chow, Eva; Lee, Erin; Palmer, Lisa; Boot, Erik; Butcher, Nancy; Kahn, Rene; Bassett, Anne; Weickert, Cynthia Shannon; Gehr, Johannes; Glenthoj, Birte; Nielsen, Mette; Gregersen, Maja; Clemmensen, Lars; Søndergaard, Anne; Christiani, Camilla Jerlang; Hemager, Nicoline; Ellersgaard, Ditte; Spang, Katrine Søborg; Greve, Aja; Gantriis, Ditte Lou; Knudsen, Christina Bruun; Andreassen, Anna Krogh; Veddum, Lotte; Stadsgaard, Henriette Brockdorff; Bliksted, Vibeke Fuglsang; Mors, Ole; Plessen, Kerstin J; Nordentoft, Merete; Jepsen, Jens Richardt Møllegaard; Thorup, Anne A E; Andersen, Gitte; Schæbel, Helle; Wulff, Sanne; Glenthøj, Birte; Nielsen, Mette Ødegaard; Lemvigh, Cecilie; Jepsen, Jens Richardt Møllegaard; Fagerlund, Birgitte; Pagsberg, Anne Katrine; Glenthoj, Birte; Rydkjaer, Jacob; Oranje, Bob; Teigset, Charlotte; Mohn, Christine; Rund, Bjorn; Langbein, Kerstin; Fleischer, Christian; Kuhnt, Katrin; Smesny, Stefan; Stabell, Lena; Gjestad, Rolf; Kroken, Rune; Løberg, Else-Marie; Jørgensen, Hugo A; Johnsen, Erik; Park, Sohee; Legind, Christian; Broberg, Brian; Mandl, Rene; Brouwer, Rachel; Anhøj, Simon; Hilker, Rikke; Jensen, Maria H; McGuire, Philip; Hulshoff Pol, Hilleke E; Fagerlund, Birgitte; Rostrup, Egill; Glenthoj, Birte; Meador-Woodruff, James; Owen, Michael

Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects

在1427名22q11.2缺失综合征患者中,智商差异部分取决于缺失类型。

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 W C; Gothelf, Doron; Duijff, Sasja; Evers, Rens; van Amelsvoort, Thérèse A; van den 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 A S; Morrow, Bernice E

Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome

了解22q11.2缺失综合征的儿童精神表型

Fiksinski, Ania M; Schneider, Maude; Murphy, Clodagh M; Armando, Marco; Vicari, Stefano; Canyelles, Jaume M; Gothelf, Doron; Eliez, Stephan; Breetvelt, Elemi J; Arango, Celso; Vorstman, Jacob A S

Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal study

22q11.2缺失综合征中的自闭症谱系障碍和精神病风险:一项前瞻性纵向研究的结果

Fiksinski, A M; Breetvelt, E J; Duijff, S N; Bassett, A S; Kahn, R S; Vorstman, J A S

Early interventions in risk groups for schizophrenia: what are we waiting for?

对精神分裂症高危人群进行早期干预:我们还在等什么?

Sommer, Iris E; Bearden, Carrie E; van Dellen, Edwin; Breetvelt, Elemi J; Duijff, Sasja N; Maijer, Kim; van Amelsvoort, Therese; de Haan, Lieuwe; Gur, Raquel E; Arango, Celso; Díaz-Caneja, Covadonga M; Vinkers, Christiaan H; Vorstman, Jacob As