Year |
Citation |
Score |
2024 |
Ge R, Ching CRK, Bassett AS, Kushan L, Antshel KM, van Amelsvoort T, Bakker G, Butcher NJ, Campbell LE, Chow EWC, Craig M, Crossley NA, Cunningham A, Daly E, Doherty JL, et al. Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human Brain Mapping. 45: e26553. PMID 38224541 DOI: 10.1002/hbm.26553 |
0.617 |
|
2023 |
Gur R, Bearden C, Jacquemont S, Jizi K, van TA, van den Bree M, Vorstman J, Sebat J, Ruparel K, Gallagher R, Swillen A, McClellan E, White L, Crowley T, Giunta V, ... ... Bassett A, et al. Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research Square. PMID 38234766 DOI: 10.21203/rs.3.rs-3393845/v1 |
0.36 |
|
2023 |
Freud LR, Galloway S, Crowley TB, Moldenhauer J, Swillen A, Breckpot J, Borrell A, Vora NL, Cuneo B, Hoffman H, Gilbert L, Nowakowska B, Geremek M, Kutkowska-Kaźmierczak A, Vermeesch JR, ... ... Bassett A, et al. Prenatal versus Postnatal Diagnosis of 22q11.2 Deletion Syndrome: Cardiac and Non-Cardiac Outcomes through 1 Year of Age. American Journal of Obstetrics and Gynecology. PMID 37717890 DOI: 10.1016/j.ajog.2023.09.005 |
0.306 |
|
2023 |
Zhao Y, Wang Y, Shi L, McDonald-McGinn DM, Crowley TB, McGinn DE, Tran OT, Miller D, Lin JR, Zackai E, Johnston HR, Chow EWC, Vorstman JAS, Vingerhoets C, van Amelsvoort T, ... ... Bassett AS, et al. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. Npj Genomic Medicine. 8: 17. PMID 37463940 DOI: 10.1038/s41525-023-00363-y |
0.325 |
|
2023 |
Bassett AS, McDonald-McGinn DM, Boot E, Óskarsdóttir S, Yuen RKC. Approaches to studying the impact of 22q11.2 copy number variants. American Journal of Human Genetics. 110: 1216-1218. PMID 37419092 DOI: 10.1016/j.ajhg.2023.05.008 |
0.305 |
|
2023 |
Lin JR, Zhao Y, Jabalameli MR, Nguyen N, Mitra J, Swillen A, Vorstman JAS, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, Owen MJ, Williams NM, Bassett AS, McDonald-McGinn DM, et al. Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. Molecular Psychiatry. PMID 36869225 DOI: 10.1038/s41380-023-02009-y |
0.47 |
|
2023 |
Óskarsdóttir S, Boot E, Crowley TB, Loo JCY, Arganbright JM, Armando M, Baylis AL, Breetvelt EJ, Castelein RM, Chadehumbe M, Cielo CM, de Reuver S, Eliez S, Fiksinski AM, Forbes BJ, ... ... Bassett AS, et al. Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100338. PMID 36729053 DOI: 10.1016/j.gim.2022.11.006 |
0.329 |
|
2023 |
Boot E, Óskarsdóttir S, Loo JCY, Crowley TB, Orchanian-Cheff A, Andrade DM, Arganbright JM, Castelein RM, Cserti-Gazdewich C, de Reuver S, Fiksinski AM, Klingberg G, Lang AE, Mascarenhas MR, Moss EM, ... ... Bassett AS, et al. Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100344. PMID 36729052 DOI: 10.1016/j.gim.2022.11.012 |
0.32 |
|
2023 |
Blagowidow N, Nowakowska B, Schindewolf E, Grati FR, Putotto C, Breckpot J, Swillen A, Crowley TB, Loo JCY, Lairson LA, Óskarsdóttir S, Boot E, Garcia-Minaur S, Cristina Digilio M, Marino B, ... ... Bassett AS, et al. Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes. 14. PMID 36672900 DOI: 10.3390/genes14010160 |
0.343 |
|
2022 |
Bassett AS. Clinical genetics of schizophrenia and related neuropsychiatric disorders. Psychiatry Research. 319: 114992. PMID 36463725 DOI: 10.1016/j.psychres.2022.114992 |
0.426 |
|
2022 |
Palmer LD, McManus Z, Heung T, McAlpine G, Blagojevic C, Corral M, Bassett AS. Reproductive Outcomes in Adults with 22q11.2 Deletion Syndrome. Genes. 13. PMID 36421801 DOI: 10.3390/genes13112126 |
0.321 |
|
2022 |
Wen J, Trost B, Engchuan W, Halvorsen M, Pallotto LM, Mitina A, Ancalade N, Farrell M, Backstrom I, Guo K, Pellecchia G, Thiruvahindrapuram B, Giusti-Rodriguez P, Rosen JD, Li Y, ... ... Bassett AS, et al. Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia. Molecular Psychiatry. PMID 36380236 DOI: 10.1038/s41380-022-01857-4 |
0.367 |
|
2022 |
Heung T, Conroy B, Malecki S, Ha J, Boot E, Corral M, Bassett AS. Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome. Genes. 13. PMID 36360275 DOI: 10.3390/genes13112038 |
0.392 |
|
2022 |
McGinn DE, Crowley TB, Heung T, Tran O, Moss E, Zackai EH, Emanuel BS, Chow EWC, Morrow BE, Swillen A, Bassett AS, McDonald-McGinn DM. Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome. Genes. 13. PMID 36292685 DOI: 10.3390/genes13101800 |
0.311 |
|
2022 |
Campbell IM, Crowley TB, Jobaliya C, Bailey A, McGinn DE, Gaiser K, Bassett A, Gur RE, Morrow B, Emanuel BS, Franco AT, French D, Zackai EH, McDonald-McGinn DM, Lambert MP. Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression. Clinical Genetics. PMID 36075864 DOI: 10.1111/cge.14227 |
0.356 |
|
2022 |
Drmic IE, MacKinnon Modi B, McConnell B, Jilderda S, Hoang N, Noor A, Bassett AS, Speevak M, Stavropoulos DJ, Carter MT. Neurodevelopmental functioning in probands and non-proband carriers of 22q11.2 microduplication. American Journal of Medical Genetics. Part A. PMID 35899837 DOI: 10.1002/ajmg.a.62916 |
0.401 |
|
2022 |
Pasternak M, Shirzadi Z, Mutsaerts HJ, Boot E, Butcher NJ, MacIntosh BJ, Heung T, Bassett AS, Masellis M. Elevated regional cerebral blood flow in adults with 22q11.2 deletion syndrome. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 1-15. PMID 35748435 DOI: 10.1080/15622975.2022.2093969 |
0.663 |
|
2022 |
Mojarad BA, Engchuan W, Trost B, Backstrom I, Yin Y, Thiruvahindrapuram B, Pallotto L, Mitina A, Khan M, Pellecchia G, Haque B, Guo K, Heung T, Costain G, Scherer SW, ... ... Bassett AS, et al. Genome-wide tandem repeat expansions contribute to schizophrenia risk. Molecular Psychiatry. PMID 35546631 DOI: 10.1038/s41380-022-01575-x |
0.386 |
|
2022 |
Ying S, Heung T, Zhang Z, Yuen RKC, Bassett AS. Schizophrenia Risk Mediated by microRNA Target Genes Overlapped by Genome-Wide Rare Copy Number Variation in 22q11.2 Deletion Syndrome. Frontiers in Genetics. 13: 812183. PMID 35495153 DOI: 10.3389/fgene.2022.812183 |
0.347 |
|
2021 |
Breetvelt EJ, Smit KC, van Setten J, Merico D, Wang X, Vaartjes I, Bassett AS, Boks MPM, Szatmari P, Scherer SW, Kahn RS, Vorstman JAS. A Regional Burden of Sequence-Level Variation in the 22q11.2 Region Influences Schizophrenia Risk and Educational Attainment. Biological Psychiatry. PMID 35063188 DOI: 10.1016/j.biopsych.2021.11.019 |
0.335 |
|
2021 |
Sønderby IE, Ching CRK, Thomopoulos SI, van der Meer D, Sun D, Villalon-Reina JE, Agartz I, Amunts K, Arango C, Armstrong NJ, Ayesa-Arriola R, Bakker G, Bassett AS, Boomsma DI, Bülow R, et al. Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs. Human Brain Mapping. PMID 33615640 DOI: 10.1002/hbm.25354 |
0.662 |
|
2021 |
Mojarad BA, Yin Y, Manshaei R, Backstrom I, Costain G, Heung T, Merico D, Marshall CR, Bassett AS, Yuen RKC. Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia. Translational Psychiatry. 11: 84. PMID 33526774 DOI: 10.1038/s41398-021-01211-2 |
0.391 |
|
2021 |
Fiksinski AM, Heung T, Corral M, Breetvelt EJ, Costain G, Marshall CR, Kahn RS, Vorstman JAS, Bassett AS. Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model. Psychological Medicine. 1-9. PMID 33443009 DOI: 10.1017/S0033291720005279 |
0.309 |
|
2020 |
Davies RW, Fiksinski AM, Breetvelt EJ, Williams NM, Hooper SR, Monfeuga T, Bassett AS, Owen MJ, Gur RE, Morrow BE, McDonald-McGinn DM, Swillen A, Chow EWC, van den Bree M, Emanuel BS, et al. Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. Nature Medicine. PMID 33169016 DOI: 10.1038/s41591-020-1103-1 |
0.431 |
|
2020 |
Van L, Heung T, Malecki SL, Fenn C, Tyrer A, Sanches M, Chow EWC, Boot E, Corral M, Dash S, George SR, Bassett AS. 22q11.2 microdeletion and increased risk for type 2 diabetes. Eclinicalmedicine. 26: 100528. PMID 33089125 DOI: 10.1016/J.Eclinm.2020.100528 |
0.468 |
|
2020 |
Buijs PC, Bassett AS, Gold DA, Boot E. Cognitive behavioral therapy in 22q11.2 deletion syndrome: A case study of two young adults with an anxiety disorder. Journal of Intellectual Disabilities : Joid. 1744629520942374. PMID 32772800 DOI: 10.1177/1744629520942374 |
0.421 |
|
2020 |
Loo JCY, Boot E, Corral M, Bassett AS. Personalized medical information card for adults with 22q11.2 deletion syndrome: An initiative to improve communication between patients and healthcare providers. Journal of Applied Research in Intellectual Disabilities : Jarid. PMID 32407568 DOI: 10.1111/Jar.12747 |
0.354 |
|
2020 |
Boot E, Mentzel TQ, Palmer LD, van Harten PN, Marras C, Lang AE, Bassett AS. Age-Related Parkinsonian Signs in Microdeletion 22q11.2. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 32386091 DOI: 10.1002/Mds.28080 |
0.486 |
|
2020 |
van Mil S, Heung T, Malecki S, Van L, Chang J, Breetvelt E, Wald R, Oechslin E, Silversides C, Bassett AS. Impact of a 22q11.2 microdeletion on adult all-cause mortality in tetralogy of Fallot. The Canadian Journal of Cardiology. PMID 32348848 DOI: 10.1016/J.Cjca.2020.04.019 |
0.452 |
|
2020 |
Ching CRK, Gutman BA, Sun D, Villalon Reina J, Ragothaman A, Isaev D, Zavaliangos-Petropulu A, Lin A, Jonas RK, Kushan L, Pacheco-Hansen L, Vajdi A, Forsyth JK, Jalbrzikowski M, Bakker G, ... ... Bassett AS, et al. Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness. The American Journal of Psychiatry. appiajp201919060583. PMID 32046535 DOI: 10.1176/Appi.Ajp.2019.19060583 |
0.707 |
|
2020 |
Cleynen I, Engchuan W, Hestand MS, Heung T, Holleman AM, Johnston HR, Monfeuga T, McDonald-McGinn DM, Gur RE, Morrow BE, Swillen A, Vorstman JAS, Bearden CE, Chow EWC, van den Bree M, ... ... Bassett AS, et al. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry. PMID 32015465 DOI: 10.1038/S41380-020-0654-3 |
0.756 |
|
2020 |
Homans JF, de Reuver S, Heung T, Silversides CK, Oechslin EN, Houben ML, McDonald-McGinn DM, Kruyt MC, Castelein RM, Bassett AS. The Role of 22q11.2 Deletion Syndrome in the Relationship between Congenital Heart Disease and Scoliosis. The Spine Journal : Official Journal of the North American Spine Society. PMID 31958577 DOI: 10.1016/J.Spinee.2020.01.006 |
0.475 |
|
2019 |
Vervoort L, Demaerel W, Rengifo LY, Odrzywolski A, Vergaelen E, Hestand MS, Breckpot J, Devriendt K, Swillen A, McDonald-McGinn DM, Fiksinski AM, Zinkstok JR, Morrow BE, Heung T, Vorstman JAS, ... Bassett AS, et al. Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins. Human Molecular Genetics. 28: 3724-3733. PMID 31884517 DOI: 10.1093/Hmg/Ddz166 |
0.462 |
|
2019 |
Zhao Y, Diacou A, Johnston HR, Musfee FI, McDonald-McGinn DM, McGinn D, Crowley TB, Repetto GM, Swillen A, Breckpot J, Vermeesch JR, Kates WR, Digilio MC, Unolt M, Marino B, ... ... Bassett AS, et al. Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. American Journal of Human Genetics. PMID 31870554 DOI: 10.1016/J.Ajhg.2019.11.010 |
0.471 |
|
2019 |
Zarrei M, Burton CL, Engchuan W, Young EJ, Higginbotham EJ, MacDonald JR, Trost B, Chan AJS, Walker S, Lamoureux S, Heung T, Mojarad BA, Kellam B, Paton T, Faheem M, ... ... Bassett AS, et al. A large data resource of genomic copy number variation across neurodevelopmental disorders. Npj Genomic Medicine. 4: 26. PMID 31602316 DOI: 10.1038/S41525-019-0098-3 |
0.348 |
|
2019 |
Zinkstok JR, Boot E, Bassett AS, Hiroi N, Butcher NJ, Vingerhoets C, Vorstman JAS, van Amelsvoort TAMJ. Neurobiological perspective of 22q11.2 deletion syndrome. The Lancet. Psychiatry. PMID 31395526 DOI: 10.1016/S2215-0366(19)30076-8 |
0.727 |
|
2019 |
Malecki SL, Van Mil S, Graffi J, Breetvelt E, Corral M, Boot E, Chow EWC, Sanches M, Verma AA, Bassett AS. A genetic model for multimorbidity in young adults. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31363180 DOI: 10.1038/S41436-019-0603-1 |
0.426 |
|
2019 |
Van L, Heung T, Graffi J, Ng E, Malecki S, Van Mil S, Boot E, Corral M, Chow EWC, Hodgkinson KA, Silversides C, Bassett AS. All-cause mortality and survival in adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30948858 DOI: 10.1038/S41436-019-0509-Y |
0.451 |
|
2019 |
Vlaskamp DRM, Bassett AS, Sullivan JE, Robblee J, Sadleir LG, Scheffer IE, Andrade DM. Schizophrenia is a later-onset feature of PCDH19 Girls Clustering Epilepsy. Epilepsia. 60: 429-440. PMID 30828795 DOI: 10.1111/Epi.14678 |
0.375 |
|
2019 |
Boot E, Bassett AS, Marras C. 22q11.2 Deletion Syndrome-Associated Parkinson's Disease. Movement Disorders Clinical Practice. 6: 11-16. PMID 30746410 DOI: 10.1002/Mdc3.12687 |
0.462 |
|
2019 |
Costain G, Walker S, Argiropoulos B, Baribeau DA, Bassett AS, Boot E, Devriendt K, Kellam B, Marshall CR, Prasad A, Serrano MA, Stavropoulos DJ, Twede H, Vermeesch JR, Vorstman JAS, et al. Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders. Journal of Neurodevelopmental Disorders. 11: 3. PMID 30732576 DOI: 10.1186/S11689-019-9263-3 |
0.349 |
|
2019 |
Vingerhoets C, van Oudenaren MJF, Bloemen OJN, Boot E, van Duin EDA, Evers LJM, Fiksinski AM, Breetvelt EJ, Palmer LD, Vergaelen E, Vogels A, Meijer C, Booij J, de Haan L, ... ... Bassett AS, et al. Low prevalence of substance use in people with 22q11.2 deletion syndrome. The British Journal of Psychiatry : the Journal of Mental Science. 1-7. PMID 30604657 DOI: 10.1192/Bjp.2018.258 |
0.491 |
|
2019 |
Monfeuga T, Epstein MP, Holleman AM, Cleynen I, Johnston H, Zhao Y, McDonald-McGinn DM, Gur RE, Warren ST, Vermeesch J, Emanuel BS, Morrow BE, Bassett AS, Williams N. 7Schizophrenia Polygenic Risk Score Analysis In 22Q11.2 Deletion Syndrome European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.014 |
0.56 |
|
2018 |
Rezazadeh A, Bercovici E, Kiehl TR, Chow EW, Krings T, Bassett AS, Andrade DM. Periventricular nodular heterotopia in 22q11.2 deletion and frontal lobe migration. Annals of Clinical and Translational Neurology. 5: 1314-1322. PMID 30480026 DOI: 10.1002/Acn3.641 |
0.499 |
|
2018 |
Zhao Y, Guo T, Fiksinski A, Breetvelt E, McDonald-McGinn DM, Crowley TB, Diacou A, Schneider M, Eliez S, Swillen A, Breckpot J, Vermeesch J, Chow EWC, Gothelf D, Duijff S, ... ... Bassett AS, et al. Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects. American Journal of Medical Genetics. Part A. PMID 30289625 DOI: 10.1002/Ajmg.A.40359 |
0.434 |
|
2018 |
Sumitomo A, Horike K, Hirai K, Butcher N, Boot E, Sakurai T, Nucifora FC, Bassett AS, Sawa A, Tomoda T. A mouse model of 22q11.2 deletions: Molecular and behavioral signatures of Parkinson's disease and schizophrenia. Science Advances. 4: eaar6637. PMID 30116778 DOI: 10.1126/Sciadv.Aar6637 |
0.699 |
|
2018 |
Fiksinski AM, Breetvelt EJ, Lee YJ, Boot E, Butcher N, Palmer L, Chow EWC, Kahn RS, Vorstman JAS, Bassett AS. Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia. Psychological Medicine. 1-8. PMID 30064532 DOI: 10.1017/S0033291718001824 |
0.702 |
|
2018 |
Sun D, Ching CRK, Lin A, Forsyth JK, Kushan L, Vajdi A, Jalbrzikowski M, Hansen L, Villalon-Reina JE, Qu X, Jonas RK, van Amelsvoort T, Bakker G, Kates WR, Antshel KM, ... ... Bassett AS, et al. Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size. Molecular Psychiatry. PMID 29895892 DOI: 10.1038/S41380-018-0078-5 |
0.706 |
|
2018 |
Butcher NJ, Boot E, Lang AE, Andrade D, Vorstman J, McDonald-McGinn D, Bassett AS. Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series. American Journal of Medical Genetics. Part A. PMID 29777584 DOI: 10.1002/Ajmg.A.38708 |
0.732 |
|
2018 |
Boot E, Butcher NJ, Udow S, Marras C, Mok KY, Kaneko S, Barrett MJ, Prontera P, Berman BD, Masellis M, Dufournet B, Nguyen K, Charles P, Mutez E, Danaila T, ... ... Bassett AS, et al. Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2. Neurology. PMID 29752303 DOI: 10.1212/Wnl.0000000000005660 |
0.62 |
|
2018 |
Palmer LD, Butcher NJ, Boot E, Hodgkinson KA, Heung T, Chow EWC, Guna A, Crowley TB, Zackai E, McDonald-McGinn DM, Bassett AS. Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome. American Journal of Medical Genetics. Part A. 176: 936-944. PMID 29575622 DOI: 10.1002/Ajmg.A.38645 |
0.674 |
|
2018 |
Manley W, Moreau MP, Azaro M, Siecinski SK, Davis G, Buyske S, Vieland V, Bassett AS, Brzustowicz L. Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype. Plos One. 13: e0194233. PMID 29529098 DOI: 10.1371/Journal.Pone.0194233 |
0.424 |
|
2018 |
Unolt M, Barry J, Digilio MC, Marino B, Bassett A, Oechslin E, Low DW, Belasco JB, Kallish S, Sullivan K, Zackai EH, McDonald-McGinn DM. Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome. European Journal of Medical Genetics. PMID 29447908 DOI: 10.1016/J.Ejmg.2018.02.006 |
0.466 |
|
2018 |
Buijs PCM, Bassett AS, Boot E. Non-pharmacological treatment of psychiatric disorders in individuals with 22q11.2 deletion syndrome; a systematic review. American Journal of Medical Genetics. Part A. PMID 29363845 DOI: 10.1002/Ajmg.A.38612 |
0.403 |
|
2018 |
Guo T, Diacou A, Hiroko N, McDonald-McGinn DM, Hestand M, Demaerel W, Zhang L, Zhao Y, Ujueta F, Shan J, Montagna C, Zheng D, Crowley TB, Kushan-Wells L, Bearden CE, ... ... Bassett AS, et al. Deletion size analysis of 1,680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2. Human Molecular Genetics. PMID 29361080 DOI: 10.1093/Hmg/Ddy028 |
0.476 |
|
2018 |
Ania F, Vorstman J, Bassett A, Breetvelt E. S132. A NORMATIVE CHART FOR THE TRAJECTORY OF COGNITIVE FUNCTIONING IN INDIVIDUALS AT HIGH RISK FOR SCHIZOPHRENIA: LONGITUDINAL FINDINGS FROM THE INTERNATIONAL BRAIN AND BEHAVIOR CONSORTIUM ON 22Q11.2 DELETION SYNDROME Schizophrenia Bulletin. 44: S376-S377. DOI: 10.1093/Schbul/Sby018.919 |
0.489 |
|
2018 |
Ania F, Breetvelt E, Vorstman J, Chow E, Lee E, Palmer L, Boot E, Butcher N, Kahn R, Bassett A. F72. NEUROCOGNITION AND ADAPTIVE FUNCTIONING IN THE 22Q11.2 DELETION SYNDROME MODEL OF SCHIZOPHRENIA Schizophrenia Bulletin. 44: S247-S247. DOI: 10.1093/schbul/sby017.603 |
0.686 |
|
2018 |
Fiksinski A, Breetvelt E, Vorstman J, Lee E, Boot E, Butcher N, Palmer L, Chow E, Kahn R, Bassett A. F207. Neurocognition and Adaptive Functioning in the 22q11.2 Deletion Syndrome Model of Schizophrenia Biological Psychiatry. 83: S319. DOI: 10.1016/J.Biopsych.2018.02.821 |
0.712 |
|
2018 |
Fiksinski A, Vorstman J, Bassett A, Breetvelt E. S210. A Normative Chart for the Trajectory of Cognitive Functioning in a Genetically Selected Population: Longitudinal Findings From the International Brain and Behavior Consortium on 22q11.2 Deletion Syndrome Biological Psychiatry. 83: S429. DOI: 10.1016/J.Biopsych.2018.02.1102 |
0.397 |
|
2017 |
Lowther C, Merico D, Costain G, Waserman J, Boyd K, Noor A, Speevak M, Stavropoulos DJ, Wei J, Lionel AC, Marshall CR, Scherer SW, Bassett AS. Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia. Genome Medicine. 9: 105. PMID 29187259 DOI: 10.1186/S13073-017-0488-Z |
0.495 |
|
2017 |
Guo T, Repetto GM, McDonald McGinn DM, Chung JH, Nomaru H, Campbell CL, Blonska A, Bassett AS, Chow EWC, Mlynarski EE, Swillen A, Vermeesch J, Devriendt K, Gothelf D, Carmel M, et al. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. Circulation. Cardiovascular Genetics. 10. PMID 29025761 DOI: 10.1161/Circgenetics.116.001690 |
0.376 |
|
2017 |
Borlot F, Regan BM, Bassett AS, Stavropoulos DJ, Andrade DM. Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability. Jama Neurology. PMID 28846756 DOI: 10.1001/Jamaneurol.2017.1775 |
0.308 |
|
2017 |
Gur RE, Bassett AS, McDonald-McGinn DM, Bearden CE, Chow E, Emanuel BS, Owen M, Swillen A, Van den Bree M, Vermeesch J, Vorstman JAS, Warren S, Lehner T, Morrow B. A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium. Molecular Psychiatry. PMID 28761081 DOI: 10.1038/Mp.2017.161 |
0.543 |
|
2017 |
Bassett AS, Lowther C, Merico D, Costain G, Chow EWC, van Amelsvoort T, McDonald-McGinn D, Gur RE, Swillen A, Van den Bree M, Murphy K, Gothelf D, Bearden CE, Eliez S, Kates W, et al. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome. The American Journal of Psychiatry. appiajp201716121417. PMID 28750581 DOI: 10.1176/Appi.Ajp.2017.16121417 |
0.596 |
|
2017 |
Bassett AS, Scherer SW. Copy Number Variation in Tourette Syndrome. Neuron. 94: 1041-1043. PMID 28641101 DOI: 10.1016/J.Neuron.2017.06.017 |
0.307 |
|
2017 |
Wither RG, Borlot F, MacDonald A, Butcher NJ, Chow EWC, Bassett AS, Andrade DM. 22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy. Epilepsia. PMID 28448680 DOI: 10.1111/Epi.13748 |
0.648 |
|
2017 |
Butcher NJ, Merico D, Zarrei M, Ogura L, Marshall CR, Chow EWC, Lang AE, Scherer SW, Bassett AS. Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease. Plos One. 12: e0173944. PMID 28430790 DOI: 10.1371/Journal.Pone.0173944 |
0.639 |
|
2017 |
Butcher NJ, Marras C, Pondal M, Rusjan P, Boot E, Christopher L, Repetto GM, Fritsch R, Chow EW, Masellis M, Strafella AP, Lang AE, Bassett AS. Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease. Brain : a Journal of Neurology. PMID 28369257 DOI: 10.1093/Brain/Awx053 |
0.689 |
|
2017 |
Van L, Boot E, Bassett AS. Update on the 22q11.2 deletion syndrome and its relevance to schizophrenia. Current Opinion in Psychiatry. PMID 28230630 DOI: 10.1097/Yco.0000000000000324 |
0.588 |
|
2017 |
Fiksinski AM, Breetvelt EJ, Duijff SN, Bassett AS, Kahn RS, Vorstman JA. Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal study. Schizophrenia Research. PMID 28119035 DOI: 10.1016/J.Schres.2017.01.032 |
0.519 |
|
2017 |
Baharnoori M, Mandell DM, Andrade DM, Chow EWC, Bassett AS, Kiehl T. Periventricular nodular heterotopia and bilateral intraventricular xanthogranulomas in 22q11.2 deletion syndrome Human Pathology: Case Reports. 9: 55-57. DOI: 10.1016/J.Ehpc.2016.09.003 |
0.536 |
|
2016 |
Mak CCY, Chow PC, Liu APY, Chan KYK, Chu YWY, Mok GTK, Leung GKC, Yeung KS, Chau AKT, Lowther C, Scherer SW, Marshall CR, Bassett AS, Chung BHY. De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients. Npj Genomic Medicine. 1: 16033. PMID 29263819 DOI: 10.1038/Npjgenmed.2016.33 |
0.48 |
|
2016 |
Costain G, Silversides CK, Bassett AS. The importance of copy number variation in congenital heart disease. Npj Genomic Medicine. 1: 16031. PMID 28706735 DOI: 10.1038/Npjgenmed.2016.31 |
0.43 |
|
2016 |
Bassett AS, Costain G, Marshall CR. Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal setting. Prenatal Diagnosis. PMID 27718271 DOI: 10.1002/Pd.4935 |
0.528 |
|
2016 |
Voll SL, Boot E, Butcher NJ, Cooper S, Heung T, Chow EW, Silversides CK, Bassett AS. Obesity in adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27537705 DOI: 10.1038/Gim.2016.98 |
0.636 |
|
2016 |
Lowther C, Speevak M, Armour CM, Goh ES, Graham GE, Li C, Zeesman S, Nowaczyk MJ, Schultz LA, Morra A, Nicolson R, Bikangaga P, Samdup D, Zaazou M, Boyd K, ... ... Bassett AS, et al. Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27195815 DOI: 10.1038/Gim.2016.54 |
0.333 |
|
2016 |
Isles AR, Ingason A, Lowther C, Walters J, Gawlick M, Stöber G, Rees E, Martin J, Little RB, Potter H, Georgieva L, Pizzo L, Ozaki N, Aleksic B, Kushima I, ... ... Bassett A, et al. Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. Plos Genetics. 12: e1005993. PMID 27153221 DOI: 10.1371/Journal.Pgen.1005993 |
0.542 |
|
2016 |
Mlynarski EE, Xie M, Taylor D, Sheridan MB, Guo T, Racedo SE, McDonald-McGinn DM, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, ... ... Bassett AS, et al. Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome. Human Genetics. PMID 26742502 DOI: 10.1007/S00439-015-1623-9 |
0.439 |
|
2015 |
McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, Zackai EH, Emanuel BS, Vermeesch JR, Morrow BE, Scambler PJ, Bassett AS. 22q11.2 deletion syndrome. Nature Reviews. Disease Primers. 1: 15071. PMID 27189754 DOI: 10.1038/nrdp.2015.71 |
0.396 |
|
2015 |
Costain G, Lionel AC, Ogura L, Marshall CR, Scherer SW, Silversides CK, Bassett AS. Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries. International Journal of Cardiology. 204: 115-121. PMID 26655555 DOI: 10.1016/J.Ijcard.2015.11.127 |
0.306 |
|
2015 |
Costain G, Roche SL, Scherer SW, Silversides CK, Bassett AS. Rare copy number variations in an adult with transposition of the great arteries emphasize the importance of updated genetic assessments in syndromic congenital cardiac disease. International Journal of Cardiology. 203: 516-518. PMID 26551885 DOI: 10.1016/J.Ijcard.2015.10.216 |
0.329 |
|
2015 |
Gross SJ, Stosic M, McDonald-McGinn DM, Bassett AS, Norvez A, Dhamankar R, Kobara K, Kirkizlar E, Zimmermann B, Wayham N, Babiarz JE, Ryan A, Jinnett KN, Demko Z, Benn P. Clinical Experience with Single-Nucleotide Polymorphism-Based Noninvasive Prenatal Screening for 22q11.2 Deletion Syndrome. Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology. PMID 26396068 DOI: 10.1002/Uog.15754 |
0.41 |
|
2015 |
Merico D, Zarrei M, Costain G, Ogura L, Alipanahi B, Gazzellone MJ, Butcher NJ, Thiruvahindrapuram B, Nalpathamkalam T, Chow EW, Andrade DM, Frey BJ, Marshall CR, Scherer SW, Bassett AS. Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome. G3 (Bethesda, Md.). 5: 2453-61. PMID 26384369 DOI: 10.1534/G3.115.021345 |
0.731 |
|
2015 |
Guna A, Butcher NJ, Bassett AS. Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms. Journal of Neurodevelopmental Disorders. 7: 18. PMID 26137170 DOI: 10.1186/S11689-015-9113-X |
0.7 |
|
2015 |
Boot E, Butcher NJ, Vorstman JA, van Amelsvoort TA, A Fung WL, Bassett AS. Pharmacological Treatment of 22q11.2 Deletion Syndrome-related Psychoses. Pharmacopsychiatry. PMID 26091278 DOI: 10.1055/S-0035-1554645 |
0.696 |
|
2015 |
Van L, Butcher NJ, Costain G, Ogura L, Chow EW, Bassett AS. Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26087175 DOI: 10.1038/Gim.2015.84 |
0.745 |
|
2015 |
Hashemi B, Bassett A, Chitayat D, Chong K, Feldman M, Flanagan J, Goobie S, Kawamura A, Lowther C, Prasad C, Siu V, So J, Tung S, Speevak M, Stavropoulos DJ, et al. Deletion of 15q11.2(BP1-BP2) region: Further evidence for lack of phenotypic specificity in a pediatric population. American Journal of Medical Genetics. Part A. PMID 25946043 DOI: 10.1002/Ajmg.A.37134 |
0.471 |
|
2015 |
Mlynarski EE, Sheridan MB, Xie M, Guo T, Racedo SE, McDonald-McGinn DM, Gai X, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, ... ... Bassett AS, et al. Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome. American Journal of Human Genetics. 96: 753-64. PMID 25892112 DOI: 10.1016/J.Ajhg.2015.03.007 |
0.424 |
|
2015 |
Butcher NJ, Fung WL, Fitzpatrick L, Guna A, Andrade DM, Lang AE, Chow EW, Bassett AS. Response to clozapine in a clinically identifiable subtype of schizophrenia. The British Journal of Psychiatry : the Journal of Mental Science. 206: 484-91. PMID 25745132 DOI: 10.1192/Bjp.Bp.114.151837 |
0.64 |
|
2015 |
Vorstman JA, Breetvelt EJ, Duijff SN, Eliez S, Schneider M, Jalbrzikowski M, Armando M, Vicari S, Shashi V, Hooper SR, Chow EW, Fung WL, Butcher NJ, Young DA, McDonald-McGinn DM, ... ... Bassett AS, et al. Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome. Jama Psychiatry. 72: 377-85. PMID 25715178 DOI: 10.1001/Jamapsychiatry.2014.2671 |
0.704 |
|
2015 |
Boot E, Butcher NJ, van Amelsvoort TA, Lang AE, Marras C, Pondal M, Andrade DM, Fung WL, Bassett AS. Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome. American Journal of Medical Genetics. Part A. 167: 639-45. PMID 25684639 DOI: 10.1002/Ajmg.A.36928 |
0.685 |
|
2015 |
Chan C, Costain G, Ogura L, Silversides CK, Chow EW, Bassett AS. Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome. Journal of Genetic Counseling. PMID 25579115 DOI: 10.1007/S10897-014-9811-7 |
0.47 |
|
2015 |
Fung WL, Butcher NJ, Costain G, Andrade DM, Boot E, Chow EW, Chung B, Cytrynbaum C, Faghfoury H, Fishman L, García-Miñaúr S, George S, Lang AE, Repetto G, Shugar A, ... ... Bassett AS, et al. Practical guidelines for managing adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 25569435 DOI: 10.1038/Gim.2014.175 |
0.695 |
|
2015 |
Lowther C, Costain G, Stavropoulos DJ, Melvin R, Silversides CK, Andrade DM, So J, Faghfoury H, Lionel AC, Marshall CR, Scherer SW, Bassett AS. Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 149-57. PMID 25077648 DOI: 10.1038/Gim.2014.83 |
0.556 |
|
2015 |
Warnica W, Merico D, Costain G, Alfred SE, Wei J, Marshall CR, Scherer SW, Bassett AS. Copy number variable microRNAs in schizophrenia and their neurodevelopmental gene targets. Biological Psychiatry. 77: 158-66. PMID 25034949 DOI: 10.1016/J.Biopsych.2014.05.011 |
0.428 |
|
2015 |
Carter M, MacKinnon B, Jilderda S, Falcon J, Swaroop P, Dale B, Noor A, Bassett AS, Stavropoulos DJ, Drmic I. MG-105 Delineating the phenotypes associated with the 15q11.2 BP1-BP2 deletion: Preliminary trends in psychometric evaluation Journal of Medical Genetics. 52: A2.3-A3. DOI: 10.1136/Jmedgenet-2015-103578.6 |
0.446 |
|
2015 |
Lowther C, Speevak M, Armour C, Goh E, Graham G, Li C, Zeesman S, Nowaczyk MJ, Schultz L, Morra A, Nicolson R, Rajguru M, Goobie S, Tarnopolsky MA, Prasad C, ... ... Bassett AS, et al. MG-123 Exonic and intronic NRXN1 deletions: Novel genotype-phenotype correlations Journal of Medical Genetics. 52: A9.1-A9. DOI: 10.1136/Jmedgenet-2015-103578.23 |
0.387 |
|
2014 |
Baker K, Costain G, Fung WL, Bassett AS. Chromosomal microarray analysis-a routine clinical genetic test for patients with schizophrenia. The Lancet. Psychiatry. 1: 329-31. PMID 26360988 DOI: 10.1016/S2215-0366(14)70308-6 |
0.491 |
|
2014 |
Merico D, Costain G, Butcher NJ, Warnica W, Ogura L, Alfred SE, Brzustowicz LM, Bassett AS. MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome. Frontiers in Neurology. 5: 238. PMID 25484875 DOI: 10.3389/Fneur.2014.00238 |
0.699 |
|
2014 |
Costain G, Lionel AC, Fu F, Stavropoulos DJ, Gazzellone MJ, Marshall CR, Scherer SW, Bassett AS. Adult neuropsychiatric expression and familial segregation of 2q13 duplications. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 337-44. PMID 24807792 DOI: 10.1002/Ajmg.B.32236 |
0.555 |
|
2014 |
Cheung EN, George SR, Costain GA, Andrade DM, Chow EW, Silversides CK, Bassett AS. Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome. Clinical Endocrinology. 81: 190-6. PMID 24735350 DOI: 10.1111/Cen.12466 |
0.473 |
|
2014 |
Lowther C, Costain G, Melvin R, Stavropoulos DJ, Lionel AC, Marshall CR, Scherer SW, Bassett AS. Adult expression of a 3q13.31 microdeletion. Molecular Cytogenetics. 7: 23. PMID 24650298 DOI: 10.1186/1755-8166-7-23 |
0.586 |
|
2014 |
Schneider M, Debbané M, Bassett AS, Chow EW, Fung WL, van den Bree M, Owen M, Murphy KC, Niarchou M, Kates WR, Antshel KM, Fremont W, McDonald-McGinn DM, Gur RE, Zackai EH, et al. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. The American Journal of Psychiatry. 171: 627-39. PMID 24577245 DOI: 10.1176/Appi.Ajp.2013.13070864 |
0.436 |
|
2014 |
Chin-Yee NJ, Costain G, Swaby JA, Silversides CK, Bassett AS. Reproductive fitness and genetic transmission of tetralogy of Fallot in the molecular age. Circulation. Cardiovascular Genetics. 7: 102-9. PMID 24563425 DOI: 10.1161/Circgenetics.113.000328 |
0.308 |
|
2014 |
Costain G, Bassett AS. Individualizing recurrence risks for severe mental illness: epidemiologic and molecular genetic approaches. Schizophrenia Bulletin. 40: 21-3. PMID 24045037 DOI: 10.1093/Schbul/Sbt133 |
0.489 |
|
2014 |
Cheung EN, George SR, Andrade DM, Chow EW, Silversides CK, Bassett AS. Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 40-4. PMID 23765047 DOI: 10.1038/Gim.2013.71 |
0.418 |
|
2014 |
Costain G, Esplen MJ, Toner B, Scherer SW, Meschino WS, Hodgkinson KA, Bassett AS. Evaluating genetic counseling for individuals with schizophrenia in the molecular age. Schizophrenia Bulletin. 40: 78-87. PMID 23236078 DOI: 10.1093/Schbul/Sbs138 |
0.475 |
|
2014 |
Karas DJ, Costain G, Chow EW, Bassett AS. Perceived burden and neuropsychiatric morbidities in adults with 22q11.2 deletion syndrome. Journal of Intellectual Disability Research : Jidr. 58: 198-210. PMID 23106770 DOI: 10.1111/J.1365-2788.2012.01639.X |
0.453 |
|
2014 |
Costain G, Esplen MJ, Toner B, Hodgkinson KA, Bassett AS. Evaluating genetic counseling for family members of individuals with schizophrenia in the molecular age. Schizophrenia Bulletin. 40: 88-99. PMID 23104866 DOI: 10.1093/Schbul/Sbs124 |
0.439 |
|
2014 |
Merico D, Costain G, Butcher N, Warnica W, Ogura L, Alfred SE, Brzustowicz L, Bassett AS. MicroRNA target genes and risk for schizophrenia in 22q11.2 deletion syndrome Frontiers in Neurology. 5. DOI: 10.3389/Fneur.2014.00221 |
0.724 |
|
2014 |
Bassett AS. 22Q11.2 DELETION SYNDROME AS A GENETIC MODEL FOR SCHIZOPHRENIA Schizophrenia Research. 153: S76. DOI: 10.1016/S0920-9964(14)70245-2 |
0.576 |
|
2013 |
Costain G, McDonald-McGinn DM, Bassett AS. Prenatal genetic testing with chromosomal microarray analysis identifies major risk variants for schizophrenia and other later-onset disorders. The American Journal of Psychiatry. 170: 1498. PMID 24306343 DOI: 10.1176/Appi.Ajp.2013.13070880 |
0.507 |
|
2013 |
Yuen T, Chow EW, Silversides CK, Bassett AS. Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome. Schizophrenia Research. 151: 221-5. PMID 24262682 DOI: 10.1016/J.Schres.2013.10.041 |
0.515 |
|
2013 |
Butcher NJ, Kiehl TR, Hazrati LN, Chow EW, Rogaeva E, Lang AE, Bassett AS. Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications. Jama Neurology. 70: 1359-66. PMID 24018986 DOI: 10.1001/Jamaneurol.2013.3646 |
0.652 |
|
2013 |
Andrade DM, Krings T, Chow EW, Kiehl TR, Bassett AS. Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 40: 652-6. PMID 23968937 DOI: 10.1017/S0317167100014876 |
0.366 |
|
2013 |
Costain G, Lionel AC, Merico D, Forsythe P, Russell K, Lowther C, Yuen T, Husted J, Stavropoulos DJ, Speevak M, Chow EW, Marshall CR, Scherer SW, Bassett AS. Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays. Human Molecular Genetics. 22: 4485-501. PMID 23813976 DOI: 10.1093/Hmg/Ddt297 |
0.481 |
|
2013 |
Delio M, Guo T, McDonald-McGinn DM, Zackai E, Herman S, Kaminetzky M, Higgins AM, Coleman K, Chow C, Jalbrzikowski M, Jarlbrzkowski M, Bearden CE, Bailey A, Vangkilde A, Olsen L, ... ... Bassett A, et al. Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. American Journal of Human Genetics. 92: 439-47. PMID 23453669 DOI: 10.1016/j.ajhg.2013.01.018 |
0.474 |
|
2013 |
Lionel AC, Vaags AK, Sato D, Gazzellone MJ, Mitchell EB, Chen HY, Costain G, Walker S, Egger G, Thiruvahindrapuram B, Merico D, Prasad A, Anagnostou E, Fombonne E, Zwaigenbaum L, ... ... Bassett AS, et al. Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures. Human Molecular Genetics. 22: 2055-66. PMID 23393157 DOI: 10.1093/Hmg/Ddt056 |
0.439 |
|
2013 |
Costain G, Bassett AS. Incomplete knowledge of the clinical context as a barrier to interpreting incidental genetic research findings. The American Journal of Bioethics : Ajob. 13: 58-60. PMID 23391068 DOI: 10.1080/15265161.2012.754063 |
0.304 |
|
2013 |
Vorstman JA, Breetvelt EJ, Thode KI, Chow EW, Bassett AS. Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion. Schizophrenia Research. 143: 55-9. PMID 23153825 DOI: 10.1016/J.Schres.2012.10.010 |
0.571 |
|
2013 |
Dolcetti A, Silversides CK, Marshall CR, Lionel AC, Stavropoulos DJ, Scherer SW, Bassett AS. 1q21.1 Microduplication expression in adults. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 282-9. PMID 23018752 DOI: 10.1038/Gim.2012.129 |
0.542 |
|
2012 |
Brzustowicz LM, Bassett AS. miRNA-mediated risk for schizophrenia in 22q11.2 deletion syndrome. Frontiers in Genetics. 3: 291. PMID 23248646 DOI: 10.3389/Fgene.2012.00291 |
0.552 |
|
2012 |
Costain G, Bassett AS. Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era. The Application of Clinical Genetics. 5: 1-18. PMID 23144566 DOI: 10.2147/Tacg.S21953 |
0.509 |
|
2012 |
Herman SB, Guo T, McGinn DM, Blonska A, Shanske AL, Bassett AS, Chow EW, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, et al. Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. American Journal of Medical Genetics. Part A. 158: 2781-7. PMID 23034814 DOI: 10.1002/Ajmg.A.35512 |
0.441 |
|
2012 |
Costain G, Bassett AS. The ever-evolving concept of clinical significance and the potential for sins of omission in genetic research. The American Journal of Bioethics : Ajob. 12: 22-4. PMID 22974025 DOI: 10.1080/15265161.2012.699142 |
0.332 |
|
2012 |
Silversides CK, Lionel AC, Costain G, Merico D, Migita O, Liu B, Yuen T, Rickaby J, Thiruvahindrapuram B, Marshall CR, Scherer SW, Bassett AS. Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways. Plos Genetics. 8: e1002843. PMID 22912587 DOI: 10.1371/Journal.Pgen.1002843 |
0.455 |
|
2012 |
Martin N, Mikhaelian M, Cytrynbaum C, Shuman C, Chitayat DA, Weksberg R, Bassett AS. 22q11.2 deletion syndrome: attitudes towards disclosing the risk of psychiatric illness. Journal of Genetic Counseling. 21: 825-34. PMID 22833231 DOI: 10.1007/S10897-012-9517-7 |
0.523 |
|
2012 |
Butcher NJ, Chow EW, Costain G, Karas D, Ho A, Bassett AS. Functional outcomes of adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 14: 836-43. PMID 22744446 DOI: 10.1038/Gim.2012.66 |
0.688 |
|
2012 |
Husted JA, Ahmed R, Chow EW, Brzustowicz LM, Bassett AS. Early environmental exposures influence schizophrenia expression even in the presence of strong genetic predisposition. Schizophrenia Research. 137: 166-8. PMID 22381191 DOI: 10.1016/J.Schres.2012.02.009 |
0.465 |
|
2012 |
Costain G, Chow EW, Ray PN, Bassett AS. Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome. Journal of Intellectual Disability Research : Jidr. 56: 641-51. PMID 22142442 DOI: 10.1111/J.1365-2788.2011.01510.X |
0.488 |
|
2011 |
Costain G, Chow EW, Silversides CK, Bassett AS. Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions. Journal of Medical Genetics. 48: 819-24. PMID 22051516 DOI: 10.1136/Jmedgenet-2011-100440 |
0.524 |
|
2011 |
Guo T, McDonald-McGinn D, Blonska A, Shanske A, Bassett AS, Chow E, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, Dallapiccola B, et al. Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Human Mutation. 32: 1278-89. PMID 21796729 DOI: 10.1002/Humu.21568 |
0.415 |
|
2011 |
Philip N, Bassett A. Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome Behavior Genetics. 41: 403-412. PMID 21573985 DOI: 10.1007/S10519-011-9468-Z |
0.487 |
|
2011 |
Bassett AS, McDonald-McGinn DM, Devriendt K, Digilio MC, Goldenberg P, Habel A, Marino B, Oskarsdottir S, Philip N, Sullivan K, Swillen A, Vorstman J. Practical guidelines for managing patients with 22q11.2 deletion syndrome. The Journal of Pediatrics. 159: 332-9.e1. PMID 21570089 DOI: 10.1016/J.Jpeds.2011.02.039 |
0.345 |
|
2011 |
Bassett AS. Parental origin, DNA structure, and the schizophrenia spectrum. The American Journal of Psychiatry. 168: 350-3. PMID 21474594 DOI: 10.1176/Appi.Ajp.2011.11010173 |
0.462 |
|
2011 |
Chow EW, Ho A, Wei C, Voormolen EH, Crawley AP, Bassett AS. Association of schizophrenia in 22q11.2 deletion syndrome and gray matter volumetric deficits in the superior temporal gyrus. The American Journal of Psychiatry. 168: 522-9. PMID 21362743 DOI: 10.1176/Appi.Ajp.2010.10081230 |
0.566 |
|
2011 |
Swaby JA, Silversides CK, Bekeschus SC, Piran S, Oechslin EN, Chow EW, Bassett AS. Complex congenital heart disease in unaffected relatives of adults with 22q11.2 deletion syndrome. The American Journal of Cardiology. 107: 466-71. PMID 21257016 DOI: 10.1016/J.Amjcard.2010.09.045 |
0.481 |
|
2011 |
Piran S, Bassett AS, Grewal J, Swaby JA, Morel C, Oechslin EN, Redington AN, Liu PP, Silversides CK. Patterns of cardiac and extracardiac anomalies in adults with tetralogy of fallot. American Heart Journal. 161: 131-7. PMID 21167345 DOI: 10.1016/J.Ahj.2010.09.015 |
0.42 |
|
2011 |
Costain G, Silversides CK, Marshall CR, Shago M, Costain N, Bassett AS. 13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature review. International Journal of Cardiology. 146: 134-9. PMID 20598760 DOI: 10.1016/J.Ijcard.2010.05.070 |
0.475 |
|
2010 |
Simmons TR, Flax JF, Azaro MA, Hayter JE, Justice LM, Petrill SA, Bassett AS, Tallal P, Brzustowicz LM, Bartlett CW. Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families. Human Heredity. 70: 232-44. PMID 20948219 DOI: 10.1159/000320367 |
0.357 |
|
2010 |
Fung WLA, McEvilly R, Fong J, Silversides C, Chow E, Bassett A. Elevated prevalence of generalized anxiety disorder in adults with 22q11.2 deletion syndrome American Journal of Psychiatry. 167: 998. PMID 20693476 DOI: 10.1176/Appi.Ajp.2010.09101463 |
0.403 |
|
2010 |
Bassett AS, Costain G, Fung WL, Russell KJ, Pierce L, Kapadia R, Carter RF, Chow EW, Forsythe PJ. Clinically detectable copy number variations in a Canadian catchment population of schizophrenia. Journal of Psychiatric Research. 44: 1005-9. PMID 20643418 DOI: 10.1016/J.Jpsychires.2010.06.013 |
0.53 |
|
2010 |
Costain G, Ho A, Crawley AP, Mikulis DJ, Brzustowicz LM, Chow EW, Bassett AS. Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: a preliminary report. Schizophrenia Research. 122: 81-4. PMID 20638248 DOI: 10.1016/J.Schres.2010.06.014 |
0.532 |
|
2010 |
Husted JA, Ahmed R, Chow EW, Brzustowicz LM, Bassett AS. Childhood trauma and genetic factors in familial schizophrenia associated with the NOS1AP gene. Schizophrenia Research. 121: 187-92. PMID 20541371 DOI: 10.1016/J.Schres.2010.05.021 |
0.447 |
|
2010 |
Bassett AS, Scherer SW, Brzustowicz LM. Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease. The American Journal of Psychiatry. 167: 899-914. PMID 20439386 DOI: 10.1176/Appi.Ajp.2009.09071016 |
0.544 |
|
2010 |
Voormolen EH, Wei C, Chow EW, Bassett AS, Mikulis DJ, Crawley AP. Voxel-based morphometry and automated lobar volumetry: the trade-off between spatial scale and statistical correction. Neuroimage. 49: 587-96. PMID 19619660 DOI: 10.1016/J.Neuroimage.2009.07.018 |
0.345 |
|
2009 |
Ng MY, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah, Holmans PA, Escamilla M, Wildenauer DB, Williams NM, Laurent C, ... ... Bassett AS, et al. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Molecular Psychiatry. 14: 774-85. PMID 19349958 DOI: 10.1038/Mp.2008.135 |
0.503 |
|
2009 |
Wratten NS, Memoli H, Huang Y, Dulencin AM, Matteson PG, Cornacchia MA, Azaro MA, Messenger J, Hayter JE, Bassett AS, Buyske S, Millonig JH, Vieland VJ, Brzustowicz LM. Identification of a schizophrenia-associated functional noncoding variant in NOS1AP. The American Journal of Psychiatry. 166: 434-41. PMID 19255043 DOI: 10.1176/Appi.Ajp.2008.08081266 |
0.384 |
|
2009 |
Bassett AS, Chow EW, Husted J, Hodgkinson KA, Oechslin E, Harris L, Silversides C. Premature death in adults with 22q11.2 deletion syndrome. Journal of Medical Genetics. 46: 324-30. PMID 19246480 DOI: 10.1136/Jmg.2008.063800 |
0.447 |
|
2009 |
Zaleski C, Bassett AS, Tam K, Shugar AL, Chow EW, McPherson E. The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome. American Journal of Medical Genetics. Part A. 149: 525-8. PMID 19208384 DOI: 10.1002/Ajmg.A.32650 |
0.465 |
|
2009 |
Husted JA, Lim S, Chow EW, Greenwood C, Bassett AS. Heritability of neurocognitive traits in familial schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 845-53. PMID 19180565 DOI: 10.1002/Ajmg.B.30907 |
0.388 |
|
2009 |
Vorstman JA, Chow EW, Ophoff RA, van Engeland H, Beemer FA, Kahn RS, Sinke RJ, Bassett AS. Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 430-3. PMID 18646052 DOI: 10.1002/Ajmg.B.30827 |
0.565 |
|
2009 |
Kiehl TR, Chow EW, Mikulis DJ, George SR, Bassett AS. Neuropathologic features in adults with 22q11.2 deletion syndrome. Cerebral Cortex (New York, N.Y. : 1991). 19: 153-64. PMID 18483005 DOI: 10.1093/Cercor/Bhn066 |
0.52 |
|
2008 |
Bassett AS, Marshall CR, Lionel AC, Chow EW, Scherer SW. Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome. Human Molecular Genetics. 17: 4045-53. PMID 18806272 DOI: 10.1093/Hmg/Ddn307 |
0.594 |
|
2008 |
Brzustowicz LM, Bassett AS. Phenotype matters: the case for careful characterization of relevant traits. The American Journal of Psychiatry. 165: 1096-8. PMID 18765489 DOI: 10.1176/Appi.Ajp.2008.08060897 |
0.493 |
|
2008 |
Bassett AS, Chow EW. Schizophrenia and 22q11.2 deletion syndrome. Current Psychiatry Reports. 10: 148-57. PMID 18474208 DOI: 10.1007/S11920-008-0026-1 |
0.577 |
|
2008 |
Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, Kupprion C, Ramadanova K, Thierfelder L, McKenna W, Gallagher B, Morris-Larkin L, Bassett AS, Parfrey PS, Young TL. Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene. American Journal of Human Genetics. 82: 809-21. PMID 18313022 DOI: 10.1016/J.Ajhg.2008.01.010 |
0.361 |
|
2008 |
Kapadia RK, Bassett AS. Recognizing a common genetic syndrome: 22q11.2 deletion syndrome. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 178: 391-3. PMID 18268261 DOI: 10.1503/Cmaj.071300 |
0.405 |
|
2008 |
Fung WL, Chow EW, Webb GD, Gatzoulis MA, Bassett AS. Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease. International Journal of Cardiology. 131: 51-8. PMID 18191243 DOI: 10.1016/J.Ijcard.2007.08.141 |
0.487 |
|
2007 |
Husted JA, Driezen P, Chow EW, Bassett AS. Sibship characteristics in a familial sample with genetic susceptibility to schizophrenia. Schizophrenia Research. 95: 248-9. PMID 17629677 DOI: 10.1093/Aje/163.Suppl_11.S218-B |
0.434 |
|
2007 |
Bassett AS, Caluseriu O, Weksberg R, Young DA, Chow EW. Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome. Biological Psychiatry. 61: 1135-40. PMID 17217925 DOI: 10.1016/J.Biopsych.2006.07.038 |
0.499 |
|
2007 |
Weksberg R, Stachon AC, Squire JA, Moldovan L, Bayani J, Meyn S, Chow E, Bassett AS. Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome. Human Genetics. 120: 837-45. PMID 17028864 DOI: 10.1007/S00439-006-0242-X |
0.51 |
|
2006 |
Logue MW, Brzustowicz LM, Bassett AS, Chow EW, Vieland VJ. A posterior probability of linkage-based re-analysis of schizophrenia data yields evidence of linkage to chromosomes 1 and 17. Human Heredity. 62: 47-54. PMID 17019084 DOI: 10.1159/000096035 |
0.494 |
|
2006 |
Chow EW, Watson M, Young DA, Bassett AS. Neurocognitive profile in 22q11 deletion syndrome and schizophrenia. Schizophrenia Research. 87: 270-8. PMID 16753283 DOI: 10.1016/J.Schres.2006.04.007 |
0.501 |
|
2006 |
Caluseriu O, Mirza G, Ragoussis J, Chow EW, MacCrimmon D, Bassett AS. Schizophrenia in an adult with 6p25 deletion syndrome. American Journal of Medical Genetics. Part A. 140: 1208-13. PMID 16642507 DOI: 10.1002/Ajmg.A.31222 |
0.488 |
|
2006 |
Talkowski ME, Seltman H, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin AP, Deshpande SN, Egan MF, Gill M, Kendler KS, Kirov G, Heston LL, et al. Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biological Psychiatry. 60: 152-62. PMID 16631129 DOI: 10.1016/J.Biopsych.2006.02.015 |
0.348 |
|
2006 |
Husted JA, Greenwood CM, Bassett AS. Heritability of schizophrenia and major affective disorder as a function of age, in the presence of strong cohort effects. European Archives of Psychiatry and Clinical Neuroscience. 256: 222-9. PMID 16331352 DOI: 10.1007/S00406-005-0629-Z |
0.418 |
|
2005 |
Weksberg R, Hughes S, Moldovan L, Bassett AS, Chow EW, Squire JA. A method for accurate detection of genomic microdeletions using real-time quantitative PCR. Bmc Genomics. 6: 180. PMID 16351727 DOI: 10.1186/1471-2164-6-180 |
0.411 |
|
2005 |
Bassett AS, Chow EW, Husted J, Weksberg R, Caluseriu O, Webb GD, Gatzoulis MA. Clinical features of 78 adults with 22q11 Deletion Syndrome. American Journal of Medical Genetics. Part A. 138: 307-13. PMID 16208694 DOI: 10.1002/Ajmg.A.30984 |
0.456 |
|
2005 |
Moore SJ, Green JS, Fan Y, Bhogal AK, Dicks E, Fernandez BA, Stefanelli M, Murphy C, Cramer BC, Dean JC, Beales PL, Katsanis N, Bassett AS, Davidson WS, Parfrey PS. Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: a 22-year prospective, population-based, cohort study. American Journal of Medical Genetics. Part A. 132: 352-60. PMID 15637713 DOI: 10.1002/Ajmg.A.30406 |
0.369 |
|
2005 |
Saviouk V, Chow EW, Bassett AS, Brzustowicz LM. Tumor necrosis factor promoter haplotype associated with schizophrenia reveals a linked locus on 1q44. Molecular Psychiatry. 10: 375-83. PMID 15340354 DOI: 10.1038/Sj.Mp.4001582 |
0.518 |
|
2004 |
Greenwood CM, Husted J, Bomba MD, Hodgkinson KA, Bassett AS. Elevated rates of schizophrenia in a familial sample with mental illness and intellectual disability. Journal of Intellectual Disability Research : Jidr. 48: 531-9. PMID 15312053 DOI: 10.1111/J.1365-2788.2004.00621.X |
0.459 |
|
2004 |
MartÃn B, Fañanás L, Gutiérrez B, Chow EW, Bassett AS. Dermatoglyphic profile in 22q deletion syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 128: 46-9. PMID 15211630 DOI: 10.1002/Ajmg.B.30034 |
0.512 |
|
2004 |
Brzustowicz LM, Simone J, Mohseni P, Hayter JE, Hodgkinson KA, Chow EW, Bassett AS. Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22. American Journal of Human Genetics. 74: 1057-63. PMID 15065015 DOI: 10.1086/420774 |
0.532 |
|
2003 |
Chow EW, Husted J, Weksberg R, Bassett AS. Postmaturity in a genetic subtype of schizophrenia. Acta Psychiatrica Scandinavica. 108: 260-8. PMID 12956826 DOI: 10.1034/J.1600-0447.2003.00124.X |
0.47 |
|
2003 |
Bassett AS, Chow EW, AbdelMalik P, Gheorghiu M, Husted J, Weksberg R. The schizophrenia phenotype in 22q11 deletion syndrome. The American Journal of Psychiatry. 160: 1580-6. PMID 12944331 DOI: 10.1176/Appi.Ajp.160.9.1580 |
0.506 |
|
2003 |
Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, ... ... Bassett AS, et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. American Journal of Human Genetics. 73: 34-48. PMID 12802786 DOI: 10.1086/376549 |
0.537 |
|
2003 |
AbdelMalik P, Husted J, Chow EW, Bassett AS. Childhood head injury and expression of schizophrenia in multiply affected families. Archives of General Psychiatry. 60: 231-6. PMID 12622655 DOI: 10.1001/Archpsyc.60.3.231 |
0.387 |
|
2003 |
Gheorghiu M, Chow E, Bassett A. Childhood behaviour in a 22Q deletion syndrome subtype of schizophrenia Schizophrenia Research. 60: 81. DOI: 10.1016/S0920-9964(03)80627-8 |
0.489 |
|
2003 |
Chow E, Weksberg R, Bassett A. Impulsivity and aggression in 22Q11 deletion syndrome and schizophrenia Schizophrenia Research. 60: 79. DOI: 10.1016/S0920-9964(03)80621-7 |
0.487 |
|
2003 |
Caluseriu O, Tayyeb T, Chow E, Bassett A. Clozapine-associated seizures in a 22Q deletion syndrome subtype of schizophrenia Schizophrenia Research. 60: 79. DOI: 10.1016/S0920-9964(03)80620-5 |
0.433 |
|
2003 |
Bassett AS, Chow E, AbdelMalik P, Gheorghiu M, Husted J, Weksberg R. The schizophrenia phenotype in 22Q deletion syndrome Schizophrenia Research. 60: 78. DOI: 10.1016/S0920-9964(03)80618-7 |
0.577 |
|
2003 |
AbdelMalik P, Bassett A, Husted J, Chow E. Childhood head injury and illness expression in familial schizophrenia Schizophrenia Research. 60: 77. DOI: 10.1016/S0920-9964(03)80613-8 |
0.372 |
|
2002 |
Brzustowicz LM, Hayter JE, Hodgkinson KA, Chow EW, Bassett AS. Fine mapping of the schizophrenia susceptibility locus on chromosome 1q22. Human Heredity. 54: 199-209. PMID 12771552 DOI: 10.1159/000070665 |
0.506 |
|
2002 |
Bassett AS, Chow EW, Vieland VJ, Brzustowicz L. Is schizophrenia linked to chromosome 1q? Science (New York, N.Y.). 298: 2277; author reply 2. PMID 12494945 DOI: 10.1126/Science.1076508 |
0.531 |
|
2002 |
Bassett AS, Chow EW, Weksberg R, Brzustowicz L. Schizophrenia and genetics: new insights. Current Psychiatry Reports. 4: 307-14. PMID 12126600 DOI: 10.1007/S11920-996-0051-X |
0.519 |
|
2002 |
Bartlett CW, Flax JF, Logue MW, Vieland VJ, Bassett AS, Tallal P, Brzustowicz LM. A major susceptibility locus for specific language impairment is located on 13q21. American Journal of Human Genetics. 71: 45-55. PMID 12048648 DOI: 10.1086/341095 |
0.345 |
|
2002 |
Waterwort DM, Bassett AS, Brzustowicz LM. Recent advances in the genetics of schizophrenia. Cellular and Molecular Life Sciences : Cmls. 59: 331-48. PMID 11915947 DOI: 10.1007/S00018-002-8426-6 |
0.569 |
|
2002 |
Chow EW, Zipursky RB, Mikulis DJ, Bassett AS. Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome. Biological Psychiatry. 51: 208-15. PMID 11839363 DOI: 10.1016/S0006-3223(01)01246-X |
0.568 |
|
2002 |
Zwaigenbaum L, Chow E, Bassett A, Farrell S. Behavioural Disorders in Children with Cleft Palate and 22Q11 Deletion Syndrome Paediatrics & Child Health. 7: 56A-56A. DOI: 10.1093/pch/7.suppl_A.56Aa |
0.307 |
|
2001 |
Scutt LE, Chow EW, Weksberg R, Honer WG, Bassett AS. Patterns of dysmorphic features in schizophrenia. American Journal of Medical Genetics. 105: 713-23. PMID 11803519 DOI: 10.1002/Ajmg.1612 |
0.426 |
|
2001 |
Bassett AS, Chow EW, O'Neill S, Brzustowicz LM. Genetic insights into the neurodevelopmental hypothesis of schizophrenia. Schizophrenia Bulletin. 27: 417-30. PMID 11596844 DOI: 10.1093/Oxfordjournals.Schbul.A006884 |
0.477 |
|
2001 |
Kopala LC, Good KP, Morrison K, Bassett AS, Alda M, Honer WG. Impaired olfactory identification in relatives of patients with familial schizophrenia. The American Journal of Psychiatry. 158: 1286-90. PMID 11481164 DOI: 10.1176/Appi.Ajp.158.8.1286 |
0.396 |
|
2001 |
Lazier K, Chow EW, AbdelMalik P, Scutt LE, Weksberg R, Bassett AS. Low platelet count in a 22q11 deletion syndrome subtype of schizophrenia. Schizophrenia Research. 50: 177-80. PMID 11439238 DOI: 10.1016/S0920-9964(00)00159-6 |
0.477 |
|
2001 |
Bassett AS, Chow EW, Waterworth DM, Brzustowicz L. Genetic insights into schizophrenia. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 46: 131-7. PMID 11280081 DOI: 10.1177/070674370104600203 |
0.492 |
|
2001 |
Hodgkinson KA, Murphy J, O'Neill S, Brzustowicz L, Bassett AS. Genetic counselling for schizophrenia in the era of molecular genetics. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 46: 123-30. PMID 11280080 DOI: 10.1177/070674370104600202 |
0.456 |
|
2001 |
Bassett AS. Psychiatric genetics in the 21st century. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 46: 121-2. PMID 11280079 DOI: 10.1177/070674370104600201 |
0.311 |
|
2001 |
Bassett AS, Chow EWC, Brzustowicz L. The genetics of schizophrenia Neuroscience News. 4: 20-26. |
0.353 |
|
2000 |
Bassett AS, Chow EW, Weksberg R. Chromosomal abnormalities and schizophrenia. American Journal of Medical Genetics. 97: 45-51. PMID 10813803 DOI: 10.1002/(Sici)1096-8628(200021)97:1<45::Aid-Ajmg6>3.0.Co;2-9 |
0.562 |
|
2000 |
Brzustowicz LM, Hodgkinson KA, Chow EW, Honer WG, Bassett AS. Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22. Science (New York, N.Y.). 288: 678-82. PMID 10784452 DOI: 10.1126/Science.288.5466.678 |
0.572 |
|
2000 |
Nicolson R, Murphy K, Chow E, Zipursky R, Bassett A. 379. 22q11 deletion syndrome (velocardiofacial syndrome) and schizophrenia: a genetic subtype? Biological Psychiatry. 47: S115-S116. DOI: 10.1016/S0006-3223(00)00643-0 |
0.559 |
|
1999 |
Chow EW, Mikulis DJ, Zipursky RB, Scutt LE, Weksberg R, Bassett AS. Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia. Biological Psychiatry. 46: 1436-42. PMID 10578458 DOI: 10.1016/S0006-3223(99)00150-X |
0.533 |
|
1999 |
Bassett AS, Chow EW. 22q11 deletion syndrome: a genetic subtype of schizophrenia. Biological Psychiatry. 46: 882-91. PMID 10509171 DOI: 10.1016/S0006-3223(99)00114-6 |
0.563 |
|
1999 |
Cohen E, Chow EW, Weksberg R, Bassett AS. Phenotype of adults with the 22q11 deletion syndrome: A review. American Journal of Medical Genetics. 86: 359-65. PMID 10494092 DOI: 10.1002/(Sici)1096-8628(19991008)86:4<359::Aid-Ajmg10>3.0.Co;2-V |
0.405 |
|
1999 |
Brzustowicz LM, Honer WG, Chow EW, Little D, Hogan J, Hodgkinson K, Bassett AS. Linkage of familial schizophrenia to chromosome 13q32. American Journal of Human Genetics. 65: 1096-103. PMID 10486329 DOI: 10.1086/302579 |
0.531 |
|
1999 |
Chow E, Young D, Janiszewski E, Tso A, Weksberg R, Bassett AS. Neurocognitive functioning in adult patients with 22q11 deletion syndrome and schizophrenia Genetic Counseling. 10: 112. |
0.463 |
|
1999 |
Bassett AS, Chow E, Scltt L, Hüücmmün K, Weksberg R. Adult phenotype of 22q11 deletion syndrome and schizophrenia Genetic Counseling. 10: 111-112. |
0.485 |
|
1998 |
Bassett AS. Progress on the genetics of schizophrenia. Journal of Psychiatry & Neuroscience : Jpn. 23: 270-3. PMID 9846030 |
0.357 |
|
1998 |
Neves-Pereira M, Bassett AS, Honer WG, Lang D, King NA, Kennedy JL. No evidence for linkage of the CHRNA7 gene region in Canadian schizophrenia families. American Journal of Medical Genetics. 81: 361-3. PMID 9754620 DOI: 10.1002/(Sici)1096-8628(19980907)81:5<361::Aid-Ajmg3>3.0.Co;2-W |
0.407 |
|
1998 |
Bassett AS, Hodgkinson K, Chow EW, Correia S, Scutt LE, Weksberg R. 22q11 deletion syndrome in adults with schizophrenia. American Journal of Medical Genetics. 81: 328-37. PMID 9674980 DOI: 10.1002/(Sici)1096-8628(19980710)81:4<328::Aid-Ajmg10>3.0.Co;2-N |
0.591 |
|
1998 |
Husted J, Scutt LE, Bassett AS. Paternal transmission and anticipation in schizophrenia. American Journal of Medical Genetics. 81: 156-62. PMID 9613855 DOI: 10.1002/(Sici)1096-8628(19980328)81:2<156::Aid-Ajmg6>3.0.Co;2-U |
0.384 |
|
1998 |
Petronis A, Vincent J, Paterson A, Bassett A, Honer W, Gottesman I, Fuller Torrey E, Meltzer H, Lieberman J, Kennedy J. Search for unstable DNA in schizophrenia Schizophrenia Research. 29: 135. DOI: 10.1016/S0920-9964(97)88642-2 |
0.384 |
|
1998 |
Scutt L, Correia S, Chow E, Hogan J, Hodgkinson K, Jones C, Honer W, Kaegi S, Weksberg R, Bassett A. Delineating a 22q11 deletion subtype of schizophrenia Schizophrenia Research. 29: 131. DOI: 10.1016/S0920-9964(97)88631-8 |
0.468 |
|
1998 |
Bassett A, Hodgkinson K, Chow E, Scutt L, Weksberg R. 22q11.2 deletion syndrome and schizophrenia Schizophrenia Research. 29: 131. DOI: 10.1016/S0920-9964(97)88630-6 |
0.489 |
|
1997 |
Erlenmeyer-Kimling L, Adamo UH, Rock D, Roberts SA, Bassett AS, Squires-Wheeler E, Cornblatt BA, Endicott J, Pape S, Gottesman II. The New York High-Risk Project. Prevalence and comorbidity of axis I disorders in offspring of schizophrenic parents at 25-year follow-up. Archives of General Psychiatry. 54: 1096-102. PMID 9400345 DOI: 10.1001/Archpsyc.1997.01830240052008 |
0.355 |
|
1997 |
Brzustowicz LM, Honer WG, Chow EW, Hogan J, Hodgkinson K, Bassett AS. Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p. American Journal of Human Genetics. 61: 1388-96. PMID 9399881 DOI: 10.1086/301623 |
0.479 |
|
1997 |
Smith GN, Flynn SW, Kopala LC, Bassett AS, Lapointe JS, Falkai P, Honer WG. A comprehensive method of assessing routine CT scans in schizophrenia. Acta Psychiatrica Scandinavica. 96: 395-401. PMID 9395159 DOI: 10.1111/J.1600-0447.1997.Tb09935.X |
0.373 |
|
1997 |
King N, Bassett AS, Honer WG, Masellis M, Kennedy JL. Absence of linkage for schizophrenia on the short arm of chromosome 5 in multiplex Canadian families. American Journal of Medical Genetics. 74: 472-4. PMID 9342193 DOI: 10.1002/(Sici)1096-8628(19970919)74:5<472::Aid-Ajmg2>3.0.Co;2-Q |
0.47 |
|
1997 |
Vicente AM, Macciardi F, Verga M, Bassett AS, Honer WG, Bean G, Kennedy JL. NCAM and schizophrenia: genetic studies. Molecular Psychiatry. 2: 65-9. PMID 9154219 DOI: 10.1038/Sj.Mp.4000235 |
0.477 |
|
1997 |
Lang DJ, Bassett AS, Falkai P, Smith GN, Lapointe JS, Honer WG. Sylvian fissure and middle cranial fossae asymmetries in families with schizophrenia Schizophrenia Research. 24: 150. DOI: 10.1016/S0920-9964(97)82429-2 |
0.427 |
|
1997 |
Bassett A, Scutt L, Correia S, Bomba M, Husted J. Anticipation and imprinting in schizophrenia: Results from a large representative Canadian archival sample Schizophrenia Research. 24: 54. DOI: 10.1016/S0920-9964(97)82155-X |
0.421 |
|
1997 |
Bury A, Chow E, Weksberg R, Correia S, Scutt L, Bassett A. Velocardiofacial syndrome (VCFS) in schizophrenia: Cognitive features Schizophrenia Research. 24: 53. DOI: 10.1016/S0920-9964(97)82152-4 |
0.43 |
|
1997 |
Hodgkinson K, Chow E, Correia S, Scutt L, McAlduff J, Beatty B, Squire J, Weksberg R, Bassett A. Velo-Cardio-Facial Syndrome: A true genetic subtype of schizophrenia? Schizophrenia Research. 24: 53. DOI: 10.1016/S0920-9964(97)82151-2 |
0.393 |
|
1997 |
Bassett A, Honer W, Chow E, McAlduff J, Hodgkinson K, Kirkham S, Brzustowicz L. A susceptibility locus for schizophrenia on chromosome 6 using positive symptom scores as quantitative traits Schizophrenia Research. 24: 50. DOI: 10.1016/S0920-9964(97)82143-3 |
0.362 |
|
1996 |
O'Malley MP, Bassett AS, Honer WG, Kennedy JL, King N, Berg D. Linkage analysis between schizophrenia and the Darier's disease region on 12q. Psychiatric Genetics. 6: 187-90. PMID 9149323 DOI: 10.1097/00041444-199624000-00003 |
0.521 |
|
1996 |
Bassett AS, Chow EW, Bury A, Ali F, Haylock CA, Smith GN, Lapointe JS, Honer WG. Increased head circumference in schizophrenia. Biological Psychiatry. 40: 1173-5. PMID 8931921 DOI: 10.1016/S0006-3223(96)00288-0 |
0.37 |
|
1996 |
Bassett AS, Bury A, Hodgkinson KA, Honer WG. Reproductive fitness in familial schizophrenia. Schizophrenia Research. 21: 151-60. PMID 8885043 DOI: 10.1016/0920-9964(96)00018-7 |
0.466 |
|
1996 |
Honer WG, Bassett AS, Falkai P, Beach TG, Lapointe JS. A case study of temporal lobe development in familial schizophrenia. Psychological Medicine. 26: 191-5. PMID 8643758 |
0.354 |
|
1996 |
Wakem P, Ikeda S, Haake A, Polakowska R, Ewing N, Sarret Y, Duvic M, Berg D, Bassett A, Kennedy JL, Tuskis A, Epstein EH, Goldsmith LA. Localization of the Darier Disease Gene to a 2-cM Portion of 12q23-24.1 Journal of Investigative Dermatology. 106: 365-367. PMID 8601743 DOI: 10.1111/1523-1747.Ep12343145 |
0.344 |
|
1996 |
Brzustowicz LM, Honer WG, McAlduff J, Hodgkinson K, Ricketts AR, Bassett AS. Evidence for a locus on chromosome 6p related to positive symptom scores in Canadian families with schizophrenia Psychiatric Genetics. 6: 137. DOI: 10.1097/00041444-199623000-00010 |
0.453 |
|
1996 |
Kopala L, Bassett A, Morrison K, Good K, Honer W. Olfactory deficits in familial schizophrenia Schizophrenia Research. 18: 244. DOI: 10.1016/0920-9964(96)85741-0 |
0.409 |
|
1996 |
Honer W, Bassett A, Squires-Wheeler E, Falkai P, Smith G, Lapointe J, Canero C, Lang D. The temporal lobes, reversed asymmetry, and schizophrenia genetics Schizophrenia Research. 18: 184. DOI: 10.1016/0920-9964(96)85578-2 |
0.33 |
|
1995 |
Honer WG, Bassett AS, Squires-Wheeler E, Falkai P, Smith GN, Lapointe JS, Canero C, Lang DJ. The temporal lobes, reversed asymmetry and the genetics of schizophrenia. Neuroreport. 7: 221-4. PMID 8742456 DOI: 10.1097/00001756-199512290-00053 |
0.447 |
|
1995 |
Erlenmeyer-Kimling L, Squires-Wheeler E, Adamo UH, Bassett AS, Cornblatt BA, Kestenbaum CJ, Rock D, Roberts SA, Gottesman II. The New York High-Risk Project. Psychoses and cluster A personality disorders in offspring of schizophrenic parents at 23 years of follow-up. Archives of General Psychiatry. 52: 857-65. PMID 7575106 DOI: 10.1001/Archpsyc.1995.03950220067013 |
0.375 |
|
1995 |
Kennedy JL, Berg D, Bassett AS, Roy R, King N, Perkins M. Genetic linkage for Darier disease (keratosis follicularis). American Journal of Medical Genetics. 55: 307-10. PMID 7537018 DOI: 10.1002/Ajmg.1320550312 |
0.403 |
|
1995 |
Petronis A, Sasaki T, Bassett A, Honer W, Kennedy J. Search for unstable DNA in schizophrenia families demonstrating evidence for genetic anticipation Schizophrenia Research. 15: 46. DOI: 10.1016/0920-9964(95)95149-4 |
0.415 |
|
1995 |
Vicente A, Sasaki T, King N, Barr C, Bassett A, Honer W, Macciardi F, Kennedy J. Genetic testing of the neurodevelopment hypothesis of schizophrenia Schizophrenia Research. 15: 42. DOI: 10.1016/0920-9964(95)95136-W |
0.441 |
|
1995 |
Honer WG, Bassett AS, Canero C, Smith GN, Lapointe JS, Squires-Wheeler E, Falkai P. The temporal lobe in families with schizophrenia: Effects of diagnosis and family of origin Schizophrenia Research. 15: 41. DOI: 10.1016/0920-9964(95)95131-R |
0.377 |
|
1995 |
Hodgkinson KA, Macgregor DJ, Shuman C, Bassett AS. The provision of genetic counselling for persons with schizophrenia and their relatives Schizophrenia Research. 15: 40. DOI: 10.1016/0920-9964(95)95130-2 |
0.45 |
|
1994 |
Bassett AS, Honer WG. Evidence for anticipation in schizophrenia. American Journal of Human Genetics. 54: 864-70. PMID 8178826 |
0.378 |
|
1994 |
Chow EW, Bassett AS, Weksberg R. Velo-cardio-facial syndrome and psychotic disorders: implications for psychiatric genetics. American Journal of Medical Genetics. 54: 107-12. PMID 8074160 DOI: 10.1002/Ajmg.1320540205 |
0.525 |
|
1994 |
Bassett AS, Bury A, Honer WG. Testing Liddle's three-syndrome model in families with schizophrenia. Schizophrenia Research. 12: 213-21. PMID 8054313 DOI: 10.1016/0920-9964(94)90031-0 |
0.423 |
|
1994 |
Sidenberg DG, Berg D, Bassett AS, King N, Petronis A, Kamble AB, Kennedy JL. Genetic linkage evaluation of twenty-four loci in an eastern Canadian family segregating Darier's disease (keratosis follicularis). Journal of the American Academy of Dermatology. 31: 27-30. PMID 8021367 DOI: 10.1016/S0190-9622(94)70130-X |
0.384 |
|
1994 |
Honer WG, Bassett AS, Smith GN, Lapointe JS, Falkai P. Temporal lobe abnormalities in multigenerational families with schizophrenia. Biological Psychiatry. 36: 737-43. PMID 7858069 DOI: 10.1016/0006-3223(94)90084-1 |
0.412 |
|
1993 |
Bassett AS, Collins EJ, Nuttall SE, Honer WG. Positive and negative symptoms in families with schizophrenia. Schizophrenia Research. 11: 9-19. PMID 8297809 DOI: 10.1016/0920-9964(93)90033-F |
0.446 |
|
1993 |
Sidenberg DG, Bassett AS, Demchyshyn L, Niznik HB, Macciardi F, Kamble AB, Honer WG, Kennedy JL. New polymorphism for the human serotonin 1D receptor variant (5-HT1D beta) not linked to schizophrenia in five Canadian pedigrees. Human Heredity. 43: 315-8. PMID 8104876 DOI: 10.1159/000154150 |
0.394 |
|
1993 |
Petronis A, Bassett A, Sidenberg D, Kamble A, Honer W, Macciardi F, Kennedy J. Investigation of genetic risk factors for schizophrenia on 11q Schizophrenia Research. 9: 122. DOI: 10.1016/0920-9964(93)90183-J |
0.533 |
|
1993 |
Kennedy J, Van Tol H, Petronis A, Sidenberg D, Macciardi F, Honer W, Bassett A. Dopamine D4 receptor gene variants and schizophrenia Schizophrenia Research. 9: 119. DOI: 10.1016/0920-9964(93)90173-G |
0.377 |
|
1993 |
Jones C, Bassett A, McGillivray B, Weksberg R, Roy R, MacEwan G, Smith G, Lang M, Homer W. Physical anomalies in schizophrenia Schizophrenia Research. 9: 118. DOI: 10.1016/0920-9964(93)90170-N |
0.309 |
|
1992 |
Honer WG, Bassett AS, MacEwan GW, Hurwitz T, Li DK, Hilal S, Prohovnik I. Structural brain imaging abnormalities associated with schizophrenia and partial trisomy of chromosome 5. Psychological Medicine. 22: 519-24. PMID 1615118 DOI: 10.1017/S0033291700030464 |
0.464 |
|
1992 |
Bassett AS. Chromosomal aberrations and schizophrenia. Autosomes. The British Journal of Psychiatry : the Journal of Mental Science. 161: 323-34. PMID 1393302 DOI: 10.1192/Bjp.161.3.323 |
0.543 |
|
1991 |
Kopala LC, Clark CC, Bassett A. Olfactory deficits in schizophrenia and chromosome 5. Biological Psychiatry. 29: 732-733. PMID 2054445 DOI: 10.1016/0006-3223(91)90151-B |
0.465 |
|
1991 |
Bassett AS. Linkage analysis of schizophrenia: challenges and promise. Social Biology. 38: 189-96. PMID 1801200 DOI: 10.1080/19485565.1991.9988787 |
0.501 |
|
1991 |
Honer W, Bassett A, MacEwan G, Hurwitz T, Li D, Hilal S, Prohovnik I. Structural brain imaging in partial trisomy chromosome 5 with schizophrenia Schizophrenia Research. 4: 278. DOI: 10.1016/0920-9964(91)90144-G |
0.325 |
|
1991 |
Bassett A, Collins E, Honer W, McAlduff J, Forsythe P. Genetic linkage analysis study of schizophrenia in Canadian families: Clinical assessment results Schizophrenia Research. 4: 249. DOI: 10.1016/0920-9964(91)90093-7 |
0.451 |
|
1991 |
Bassett A. Chromosomal aberrations and schizophrenia Schizophrenia Research. 4: 248-249. DOI: 10.1016/0920-9964(91)90092-6 |
0.493 |
|
1990 |
Honer WG, Bassett AS, Kopala L, Kennedy JL. A genotype-phenotype research strategy for schizophrenia. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 35: 776-83. PMID 2282633 DOI: 10.1177/070674379003500910 |
0.436 |
|
1990 |
McGillivray BC, Bassett AS, Langlois S, Pantzar T, Wood S. Familial 5q11.2----q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia. American Journal of Medical Genetics. 35: 10-3. PMID 1967903 DOI: 10.1002/ajmg.1320350103 |
0.458 |
|
1989 |
Bassett AS. Chromosome 5 and schizophrenia: implications for genetic linkage studies. Schizophrenia Bulletin. 15: 393-402. PMID 2814372 DOI: 10.1093/schbul/15.3.393 |
0.401 |
|
1989 |
Gilliam TC, Freimer NB, Kaufmann CA, Powchik PP, Bassett AS, Bengtsson U, Wasmuth JJ. Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia. Genomics. 5: 940-4. PMID 2591972 DOI: 10.1016/0888-7543(89)90138-9 |
0.4 |
|
1989 |
Bassett AS. Eye Tracking Dysfunction is Associated With Partial Trisomy of Chromosome 5 and Schizophrenia: A Response-Reply Archives of General Psychiatry. 46: 757. DOI: 10.1001/archpsyc.1989.01810080087014 |
0.374 |
|
1988 |
Iacono WG, Bassett AS, Jones BD. Eye tracking dysfunction is associated with partial trisomy of chromosome 5 and schizophrenia. Archives of General Psychiatry. 45: 1140-1. PMID 3196143 DOI: 10.1001/archpsyc.1988.01800360088014 |
0.393 |
|
1988 |
Bassett AS, McGillivray BC, Jones BD, Pantzar JT. Partial trisomy chromosome 5 cosegregating with schizophrenia. Lancet. 1: 799-801. PMID 2895320 |
0.414 |
|
Show low-probability matches. |